DOI:
10.1039/D5RA04634C
(Review Article)
RSC Adv., 2025,
15, 27493-27523
Design, structure, and application of conductive polymer hybrid materials: a comprehensive review of classification, fabrication, and multifunctionality
Received
30th June 2025
, Accepted 23rd July 2025
First published on 4th August 2025
Abstract
Conductive polymer (CP) hybrids combine the electronic properties of polymers with the mechanical strength, thermal stability, and catalytic features of secondary materials. This review presents four major structural categories: core–shell assemblies, interpenetrating networks, layered composites, and dispersed nanocomposites. Each class is linked to fabrication routes such as in situ polymerization, electrochemical deposition, solution blending, and sol–gel techniques. We evaluated the influence of these structural forms on performance metrics, including electrical conductivity, flexibility, and long-term durability. Representative applications in sensing, energy storage, corrosion protection, and environmental remediation are examined to highlight their functional advantages and practical limitations. Challenges in synthesis, precision, material stability, and device integration are also discussed. A final roadmap connecting structural design choices to specific application outcomes and outlining priorities for the future development of scalable and multifunctional CP hybrid systems is presented.
1. Introduction
1.1. Background on conducting polymers
CPs are a class of materials with electrical conductivity, which is an unusual property not observed in the polymer family.1,2 Interest in this field has been considerable because of its potential applications in several domains, including electronics, optoelectronics, energy storage, and biomedical engineering. CPs have several important advantages over traditional inorganic materials: their electrical properties can be easily tailored, their synthesis process is simple, and they exhibit high environmental stability. CPs have recently been found to be promising candidates for many applications, including electrochemical energy storage, supercapacitors, ion sensing, and thermal transport.3
1.2. Importance of hybrid materials
Although conducting polymers exhibit promising properties, their application is often limited to their pristine forms. This has led to the hybridization of conducting polymers with other materials to achieve improved performance. These materials include carbonaceous materials, metal oxides, transition metals, and transition metal dichalcogenides.1,4 Hybrid materials exhibit improvements in properties that have a synergistic effect on their electrical, optical, mechanical, and electrochemical properties. The combination of conducting polymers with other materials has expanded their potential applications.5 Despite significant progress, no recent review has integrated the synthesis–structure–application continuum of CP hybrid materials with critical insights into their performance trade-offs, degradation mechanisms, and fabrication scalability. Most prior studies have focused on pure CPs or narrow application domains, leaving a fragmented understanding of how material structure impacts real-world deployment. This review addresses this gap by synthesizing recent findings, comparing fabrication approaches, and critically evaluating the functional performance across environmental and energy-related domains.
1.3. Scope and objectives of the review
This review aims to provide an update on the synthesis, properties, and applications of conducting polymers and their hybrids. Transport models explaining the conduction mechanism and the most relevant synthesis approaches related to the electrical, optical, and mechanical properties have been presented in previous reviews.6–9 This review focuses on the new developments in the applications of conductive polymers and their hybrid materials for energy storage, photocatalysis, anticorrosion coatings, biomedical applications, and sensing. A schematic overview of these structural classes, along with representative synthesis routes and hybridization strategies, is presented in Fig. 1. As the field of CP hybrid materials continues to evolve, several critical challenges must be addressed. These include ensuring long-term material stability under real-world conditions, improving interfacial charge transport across dissimilar phases, and achieving scalable, cost-effective synthesis.10–12 Future research should prioritize the integration of CP hybrids into flexible, wearable, and multifunctional platforms, the development of bioinspired or self-healing systems, and the refinement of doping strategies for the tuning of adaptive properties. This review aims to highlight these evolving frontiers and critically examine the current knowledge, thereby providing a comprehensive foundation for future innovations.
 |
| Fig. 1 Structural classification and synthesis routes of CP hybrid materials. This schematic illustrates the four main classes of CP hybrid architectures: core–shell structures, interpenetrating polymer networks (IPNs), layered composites, and dispersed nanocomposites. For each category, commonly used components (e.g., carbon nanotubes, metal oxides, and silica particles) and fabrication strategies (in situ polymerization, electrochemical deposition, solution blending, and self-assembly) are discussed. The arrows represent the synthetic pathways connecting the polymer type, hybridization strategy, and resulting morphology. This classification aids in selecting tailored material designs for specific applications, such as supercapacitors, sensors, and corrosion-resistant coatings. | |
1.4. Historical context and key milestones
Conducting polymers were discovered nearly three decades ago, in the late 1970s, by Alan J. Heeger, Alan G. MacDiarmid, and Hideki Shirakawa, who subsequently won the Nobel Prize in Chemistry for their examination of polyacetylene.12–18 Since then, interest in conducting polymers has grown considerably, with new types being created from polypyrrole, polyaniline, and, more recently, poly(3,4-ethylenedioxythiophene) (PEDOT) polymers. The hybridization of conducting polymers with other materials has largely expanded the horizons of their potential applications and opened avenues for the development of advanced materials with improved properties.19
Sumdani et al. (2021)3 reviewed recent developments in the synthesis and properties of conductive polymers, including their applications in electrochemical energy storage devices. Available research suggests that nanotechnology is an essential tool for enhancing the performance of supercapacitors and boosting the performance of conductive polymer composites. This agrees with the observations of Tadesse 2024,3 who noted considerable progress in the development of conductive polymer composites for supercapacitor applications.
The more recent effort of Sethumadhavan et al. in 2019 (ref. 20) was toward the progress of the ion-sensing process using conducting polymer-based sensing materials, thus exploring their capabilities for enhancing ion-sensing applications. Masood's 2024 contribution21 highlights the increased interest in conducting polymers for energy storage. The unique features of these materials make them attractive for various applications. These studies demonstrate the potential and diversity of conducting polymers in addressing energy storage issues.
Xu et al. (2019)22 provided insights into the thermal transport properties of conductive polymer-based materials, emphasizing the importance of regulating their thermal conductivity. This review summarizes the basic principles and recent advances in thermal transport for the design of conducting polymers with targeted applications that require specific thermal management levels.
In recent years, considerable effort has been directed toward the synthesis, properties, and applications of conducting polymers to enhance their performance in diverse applications. The reviewed studies further elaborate on the development of conducting polymers for energy storage, supercapacitor applications, ion sensing, thermal transport, and a diverse range of applications in which these materials can make a difference. Owing to their unique properties and capacities, researchers are working to correlate conducting polymers with disruptive technologies such as energy storage, sensing, and thermal management.23–28
2. Synthesis methods and properties of CP hybrid materials
2.1. Conventional synthesis techniques
Conventional CP synthesis methods include chemical polymerization, electrochemical polymerization, electrospinning, and in situ polymerization.29
2.1.1. Chemical polymerization. This process involves the oxidative polymerization of monomers using agents such as ammonium persulfate or ferric chloride.30 For example, polyaniline can be synthesized using ammonium persulfate as an oxidant. This route is easy and enables the production of high-yield CPs or CP hybrids with controlled molecular weights and degrees of polymerization.31
2.1.2. Electrochemical polymerization. This technique describes the oxidizing polymerization of deposited monolayers of monomers on the surface of an electrode that occurs along with the applied potential. Therefore, it is convenient to control the film thickness and morphology to produce CP coatings and thin films with desirable properties for use in sensors and devices.32,33
2.1.3. Electrospinning. This process involves the use of intense high-voltage electric fields to produce nanofibers from CPs using a polymer solution. The high surface area and porosity of the resultant fibers render them useful for energy storage and sensor applications.34,35 An overview of the principal synthesis strategies for CP-hybrid materials is shown in Fig. 2.
 |
| Fig. 2 Schematic illustration of the key synthesis routes for conducting polymer (CP) hybrid materials. This figure summarizes four major fabrication approaches for CP hybrid structures: in situ polymerization, ex situ blending, electrochemical deposition, and sol–gel processes. In situ polymerization enables the direct formation of CP on functionalized substrates, ensuring strong interfacial bonding and conformal coverage of the substrate. Ex situ blending allows the incorporation of preformed fillers into polymer matrices via solution casting or melt mixing. Electrochemical deposition enables precise control over the thickness and doping levels by voltage tuning. The sol–gel approach facilitates the integration of metal oxides and ceramics, offering porosity control and thermal stability. Each method is associated with distinct advantages and structural outcomes, allowing researchers to tailor CP hybrids for specific energy, sensing, and electronic applications. | |
2.1.4. In situ polymerization. In this approach, CP is formed directly within or around the hybrid component. This method often results in better integration between the CP and hybrid material, leading to improved interfacial properties.36,37 In studies dealing with CP hybrid materials, various synthesis methodologies have advantages and limitations, depending on the intended application and required properties. Table 1 summarizes the most important synthesis methods, including their characteristics, advantages, and limitations, with examples and the improvements they can bring to CP hybrid materials.
Table 1 The methodologies for the synthesis and properties of conductive polymer hybrid materials are analyzed in the following table, with the main synthesis methods of CP hybrid materials, pointing to the basic characteristics, advantages, and limitations, typical examples of CP hybrids, together with the obtained improved properties. The compatibility of the synthesis method, substrate, and application objectives defines the synthesis methodology, making this a very demanding task in the hybrid material design process
Synthesis method |
Synthesis description |
Advantages |
Limitations |
Examples of CP hybrid materials |
Properties enhanced |
Representative chemical reagents/conditions |
In situ polymerization |
CP is synthesized directly on or with a substrate or inorganic material |
Strong interface bonding; controlled dispersion of hybrid material |
Requires careful optimization of reaction conditions; potential for aggregation |
Polyaniline/TiO2, polypyrrole/graphene |
Conductivity, mechanical strength, and thermal stability |
Monomers: aniline, pyrrole, thiophene |
Oxidants: FeCl3, APS, K2Cr2O7 |
Conditions: 0–25 °C, acidic pH (HCl, H2SO4), 2–24 hours, inert atmosphere38,39 |
Electrochemical polymerization |
Polymerization occurs on an electrode by applying a controlled electrical potential |
High precision allows the tuning of film thickness and morphology |
Limited scalability; requires conductive substrates |
Polypyrrole/nanotubes, polyaniline/metal oxides |
Conductivity, surface area, and electrochemical activity |
Electrolytes: LiClO4, TBAPF6, H2SO4 |
Conditions: potential: 0.6–1.2 V vs. SCE, current density: 0.1–10 mA cm−2, aqueous or organic solvents (ACN, PC), room temperature7,40 |
Solution blending |
Pre-synthesized CPs are mixed with other materials in solution and then processed into a hybrid |
Simple and scalable; applicable for flexible substrates |
Poor interaction between CP and hybrid matrix; potential phase separation |
Poly(3,4-ethylene-dioxythiophene)/graphene, polyaniline/carbon nanotubes |
Flexibility, film-forming ability, and electrical conductivity |
Solvents: NMP, DMSO, CHCl3, m-cresol |
Conditions: room temperature, stirring 2–48 hours, sonication for dispersion |
Processing: spin coating, drop casting, doctor blade41 |
Template-assisted synthesis |
CPs are formed using templates like surfactants, micelles, or nanostructured materials to control morphology |
Precise control over nanostructures; can create porous or hierarchical structures |
Template removal can be complex, added cost of template materials |
Polypyrrole/silica nanostructures, polyaniline/zeolites |
Surface area, porosity, specific capacitance |
Templates: SBA-15, MCM-41, AAO membranes, CTAB |
Removal: HF etching, calcination at 500–600 °C, NaOH treatment |
Conditions: template impregnation, followed by standard oxidative polymerization42 |
Self-assembly techniques |
CPs and hybrid components spontaneously organize into structured composites under certain conditions |
Simple and cost-effective; leads to ordered structures |
Requires precise conditions; often limited to specific material combinations |
Polyaniline/Gold nanoparticles, poly(3-hexylthiophene)/quantum dots |
Optical properties, charge transport, stability |
Surfactants: SDS, CTAB, Triton X-100 |
Conditions: pH 3–7, temperature 20–80 °C, controlled ionic strength |
Assembly time: 6–72 hours, gentle stirring or static conditions43 |
Chemical oxidative polymerization |
CPs are synthesized by reacting monomers with oxidizing agents in the presence of hybridizing materials |
Suitable for large-scale production; wide range of compatible substrates |
Less control over molecular weight and morphology; residual oxidants may affect properties |
Polyaniline/ZnO, polypyrrole/silver nanoparticles |
Electrical conductivity, photochemical activity, and chemical stability |
Oxidants: APS (NH4)2S2O8, FeCl3, K2Cr2O7 |
Acids: HCl, H2SO4, CSA |
Conditions: 0–5 °C, molar ratio oxidant : monomer = 1–1.5 : 1, reaction time 4–24 hours44 |
Sol–gel method |
CPs are incorporated into a sol–gel matrix during or after the gelation process |
Enables hybridization with silica or other oxides; high homogeneity |
Requires precise control of gelation; may lead to brittle materials |
Polyaniline/silica, polypyrrole/titania |
Mechanical strength, optical properties, and thermal stability |
Precursors: TEOS, TMOS, Ti(OBu)4 |
Catalysts: HCl, NH3 |
Conditions: pH 1–3 for hydrolysis, aging 2–7 days, drying at 60–120 °C, H2O : alkoxide = 4–10 : 1 (ref. 45) |
Physical vapor deposition (PVD) |
Thin films of CPs and hybrid materials are deposited using physical methods like sputtering or evaporation |
High-purity films; excellent control over thickness and morphology |
High cost of equipment; limited to thin-film applications |
PEDOT/ITO, polypyrrole/silver nanowires |
Conductivity, optical transparency, and flexibility |
Conditions: high vacuum (10−6 Torr), substrate temperature 25–300 °C |
Targets: polymer pellets, metal targets |
Parameters: sputtering power 50–200 W, deposition rate 0.1–10 nm min−1 (ref. 46) |
Chemical vapor deposition (CVD) |
CPs are deposited as thin films by chemical reactions of vapor-phase precursors |
Uniform coatings; suitable for large-area applications |
Requires specialized equipment and environmental considerations for vapor-phase chemicals |
PEDOT/graphene oxide, polyaniline/tungsten oxide |
Adhesion, conductivity, thermal stability |
Precursors: EDOT, aniline vapor, FeCl3 vapor |
Conditions: temperature 100–250 °C, pressure 1–760 Torr |
Carrier gases: N2, ar, flow rates 10–100 sccm (ref. 47) |
Interfacial polymerization |
CPs form at the interface between two immiscible liquids containing monomers and oxidants |
Can create ultrathin films, high control over the interface properties |
Limited scalability; requires immiscible solvent systems |
Polyaniline/metal oxide nanosheets, polypyrrole/polymeric micelles |
Surface area, interfacial properties, charge transport |
Organic phase: CHCl3, toluene with monomer |
Aqueous phase: water with oxidant (APS, FeCl3) |
Conditions: room temperature, gentle stirring, reaction time 1–6 hours, phase volume ratio 1 : 1 (ref. 48) |
2.2. Novel fabrication approaches
In the field of CP hybrid research, innovative fabrication techniques are emerging that depart from conventional synthesis methods and emphasize precision, multifunctionality, and integration into advanced devices. These techniques include layer-by-layer assembly, 3D printing, plasma polymerization, and electrospinning, each designed to address challenges related to scalability, structural complexity, and customization for specific applications. By incorporating principles from nanofabrication, surface engineering, and smart material processing, these approaches offer significant potential for controlling hierarchical architectures, enhancing interface engineering, and ensuring compatibility with Industry 4.0 technologies.49–52
2.2.1. 3D printing. Complex structures can be designed using conductive polymers. Tailored geometries, such as those of sensors and actuators, can significantly improve devices.53 However, the integration of CP hybrids into 3D printing technology presents several challenges. Material compatibility remains a critical issue because the rheological behavior of CP inks often hinders smooth extrusion and layer adhesion.54 Furthermore, resolution limitations owing to the nozzle diameter and polymer viscosity constrain the minimum feature size achievable, which can impact device miniaturization.55 The layer-by-layer nature of 3D printing can also introduce anisotropy in the electrical conductivity, potentially compromising the performance of electronic applications.56
2.2.2. Sol–gel process. This method involves allowing a solution to progress toward a solid gel phase.57 This is particularly helpful for incorporating conducting polymers into inorganic materials and often results in hybrid materials with improved mechanical and electrical properties.58 For example, polyaniline–silica hybrid films prepared via sol–gel processing have shown a 3-fold increase in tensile strength and approximately 40% improvement in electrical conductivity compared to their pristine CP counterparts.59 However, the sol–gel process presents significant challenges. Long processing times during gelation may lead to shrinkage, cracking, or pore collapse, particularly under uncontrolled drying conditions.60 These effects can compromise the homogeneity and mechanical integrity of the resulting hybrid, thus requiring careful optimization of the precursor composition, catalyst concentration, and aging time.61 Layer-by-layer assembly: this method involves alternating the deposition of CPs with other materials to enable multilayer construction. This method can improve the conductivity and stability of hybrid materials.62
2.2.3. Template-assisted synthesis. The method uses sacrificial templates that direct the formation of CP hybrids with morphologies such as nanotubes or hollow spheres. Thus, it is possible to develop materials with pre-designed features at the nanostructure level.63,64
2.2.4. Interfacial polymerization. This process involves the formation of CP hybrid films via the reaction of monomers at the liquid/liquid interface between two immiscible liquids. The thin and flexible polymer films formed can be easily transferred onto various substrates.65 Vapor-phase polymerization: this method involves exposing oxidant-coated substrates to monomer vapors, leading to homogeneous CP hybrid films. It is particularly suitable for coating complex three-dimensional (3D) structures.66
2.3. Structural classification of CP hybrid materials
The structure of CP-hybrid materials directly influence their performance. The resulting architecture can vary significantly depending on the interaction between the polymer and the secondary material, whether it is a metal oxide, carbon-based nanomaterial, or another polymer. These structural forms were not interchangeable in this study. They define the pathways for charge transport, determine the mechanical integrity, and influence the response of the material under stress or during cycling. One common configuration is the core–shell structure, in which a conducting polymer layer coats the central filler. For example, carbon nanotube@polyaniline (CNT@PANI) hybrids are designed to combine the mechanical strength and aspect ratio of nanotubes with the redox activity of polymers. This structure improves electron mobility while maintaining the accessibility of the active material accessible.67
Another form involves IPNs, where the conducting polymer and secondary matrix form overlapping and intertwined domains. These are typically used to boost elasticity and toughness while maintaining conductivity. IPNs can also reduce phase separation, making them useful for flexible electronics and soft sensors.68 In layered composites, the materials are arranged in alternating stacks with different properties. Each layer contributes a distinct function: one may promote ion transport, another may provide mechanical stability, and the third may support electronic conductivity. These structures are often assembled via layer-by-layer techniques or self-assembly processes and are especially useful in applications such as supercapacitors or sensors, where the separation of ionic and electronic channels is required.40
The most widely used configuration is the dispersed nanocomposite, which is structurally less controlled than the other configurations. In this case, the nanoparticles were randomly embedded in the CP matrix. Although easy to fabricate, this structure can suffer from uneven filler distribution and the presence of interfacial defects. However, well-optimized dispersed systems show notable improvements in thermal stability, charge transport, and mechanical strength.69 Each of these architectures has its tradeoffs. Understanding how the structure affects performance is not only helpful but also essential. The choice between the two depends on the application. A supercapacitor electrode requires a high surface area and high conductivity. A sensor may require fast electron transfer and good mechanical compliance. A corrosion barrier benefits from tight polymer–filler interfaces. Therefore, this classification is not cosmetic; it defines the function of CP hybrid materials in the real world. These structural categories have been widely reported in the literature. Core–shell hybrids, such as CNT@PANI and Ag@PPy, are valued for their enhanced charge transport and strong interfacial bonding.21 Interpenetrating polymer networks, such as PANI–PVA blends, provide improved elasticity and phase stability.70 Layered composites, including PEDOT/graphene oxide assemblies, support the effective separation of ionic and electronic pathways, thereby optimizing the device efficiency.20 Dispersed nanocomposites, such as PPy/silica and PANI/carbon black, are often used in environmental remediation, where surface functionalization and ease of synthesis are essential.71 Table 2 summarizes the key structural types of CP hybrid materials, outlining their defining features, functional advantages, commonly used compositions, and representative application areas of these materials.
Table 2 Structural classification of CP hybrid materials. Summary of common CP hybrid architectures, their structural characteristics, functional advantages, representative materials, and target applications
Architecture type |
Structural features |
Advantages |
Common materials |
Typical applications |
Core–shell structures |
Conducting polymer coats an inorganic or carbon-based core |
Enhanced charge mobility, strong interface bonding |
CNT@PANI, Ag@PPy |
Supercapacitors, sensors, and EMI shielding |
IPNs |
Overlapping polymer domains form intertwined networks |
Improved elasticity and mechanical integrity, reduced phase separation |
PANI–PVA blends, PEDOT-based IPNs |
Flexible electronics, bioelectronics |
Layered composites |
Alternating stacked layers of CPs and secondary materials |
Optimized ionic/electronic transport, functional layering |
PANI/graphene, PEDOT/metal oxides |
Energy storage, membrane devices |
Dispersed nanocomposites |
Nanoparticles randomly distributed in a CP matrix |
Ease of fabrication, enhanced thermal and electrical properties |
PPy/silica, PANI/carbon black |
Thermal management, environmental remediation |
2.4. Structural characterization methods
Characterization is indispensable for understanding the properties and performance of hybrid CP materials. Among these, the following techniques are commonly used:72,73
2.4.1. Scanning electron microscopy (SEM). This technique provides detailed images of the surface morphologies of CPs and their composites. This aids in understanding the distribution and alignment of the components within the hybrid materials.74,75 However, each characterization method has intrinsic limitations. For instance, SEM typically resolves features down to ∼1–10 nm but cannot provide internal structural details and may induce beam damage in softer polymer matrices.76 TEM offers superior resolution (<1 nm); however, sample preparation requires ultrathin slicing, which can introduce artifacts and exclude bulk behavior.77 XRD cannot resolve amorphous domains and offers only average structural information, whereas FTIR and Raman spectroscopy may suffer from overlapping peaks, reducing their specificity in complex hybrid systems.78 Understanding these limitations is crucial for selecting complementary techniques to fully elucidate the CP hybrid structures.TEM was used to obtain information on the internal structure at the nanoscale, which is required to describe the dispersion of the nanoparticles in the hosting matrix of the conducting polymer. High-resolution transmission electron microscopy may provide detailed information regarding the interfacial regions between the CP and hybrid components.79,80
2.4.2. X-ray diffraction. This method was used to analyze the crystalline and phase composition of CPs. The diffraction data shows the ordering of the polymer chains and crystalline or amorphous regions.81,82Fourier-transform infrared spectroscopy (FTIR) was used to identify the functional groups and confirm the chemical structures of the synthesized conducting polymers and their hybrids.83,84
Raman spectroscopy represents one of the important spectroscopic techniques for the identification of chemical bonds and functional groups.85 This confirmed that the CP hybrids were successfully formed while simultaneously detecting the unwanted byproducts of the reaction. X-ray photoelectron spectroscopy (XPS) was used to study the surface composition and different elemental chemical states of the CP hybrids, revealing the nature of the interfacial interactions.85,86
2.5. Electrical, thermal, and mechanical properties
The compositions and structures of CPs are at the heart of the properties exhibited by CP hybrid materials.
2.5.1. Electrical properties. Hybridization of conductive fillers, such as carbon nanotubes or metal nanoparticles, significantly improves the electrical conductivity of CPs. Several factors affect the development of efficient hybrid material. The percolation threshold is one of the most important factors. This refers to the minimum concentration of the filler required to attain conductivity.87,88The electrical properties of a material are generally described by conductivity measurements using the four-point probe technique, and Hall effect measurements are used to determine the charge carrier mobility and concentration. Electrochemical impedance spectroscopy (EIS) was used to obtain information regarding the charge transfer process in the material.89,90
2.5.2. Thermal properties. In some cases, hybrid materials exhibit improved thermal stability compared with pure conducting polymers. The inorganic material content can improve the degradation temperature while decreasing susceptibility to thermal fluctuations.91 Thermogravimetric analysis (TGA) was employed to determine the thermal stability, differential scanning calorimetry (DSC) for phase transitions, and heat capacity and thermal conductivity, which are particularly relevant for applications involving thermoelectric devices or thermal management.91,92 Mechanical properties: the mechanical strength of conducting polymers can be enhanced by introducing reinforcing agents. For instance, the addition of nanofillers can significantly enhance the tensile strength and flexibility of the formed composites, allowing their application in flexible electronic devices. The mechanical properties were evaluated using nanoindentation, tensile testing, and dynamic mechanical analysis.93 These techniques provide elasticity, hardness, tensile strength, and viscoelastic behavior, which are the basic parameters required for flexible electronic and structural material applications.
2.6. Standardization efforts in characterization and testing
As research on CP hybrid materials has developed into a growing field, the call for standardization of methods in material characterization and testing has increased to ensure that conclusions and recommendations can be compared among different research groups.94
Protocols are also being developed to provide general standards for sample preparation, the conditions under which measurements are performed, and data reporting. For organic and printed electronics, standard organizations, such as the IEC, ASTM, and ISO, among others, have work items on the characterization of the materials involved, including many of the key CP hybrid materials. These protocols allow researchers to be more logistically consistent with their measurements.95,96
Interlaboratory studies were conducted to validate measurement techniques and establish the criteria for reproducibility. It is now time to divert attention to pinpointing and limiting the sources of variability in measurements originating from environmental conditions, instrument calibration, and sample handling. These collaborative studies will be conducted in various laboratories to validate the testing methods and ensure that the general results are compatible with one another to contribute to field-fostering innovation.97,98
Reference materials should also be developed in the form of CP hybrids, as they can serve as benchmarks when calibrating or validating measurement methods using popular instruments. This is often a vital case with highly complex hybrids, where slightly different compositions and/or structural properties are important.98,99
It focuses on the future of CP hybrid materials: the standardization of terminology to arrive at a common language regarding their descriptions and properties. This is critical for communication among basic scientists and for gaining translational applications from bench to industry.100
The synthesis and characterization were performed using conventional and novel methods. A complete understanding of these properties is important for tuning the corresponding materials for various applications. This will increase the reliability of the research outcomes in the field, with this material being available for use in various applications.101,102 To illustrate the integrative landscape of synthesis strategies, structural architectures, and end-use applications, a conceptual schematic is presented in Fig. 3, outlining the interconnectivity between the fabrication methods of CP hybrids, morphological design and functional domains.
 |
| Fig. 3 Structural taxonomy and synthesis-application interconnectivity of conductive polymer hybrid materials. The diagram maps key synthesis methods (e.g., in situ polymerization, electrochemical polymerization, and template-assisted methods) against representative structural configurations (e.g., core–shell, interpenetrated networks, and layered architectures) and links them to their dominant application domains, including energy storage, biomedical engineering, environmental remediation, and intelligent electronics. This multidimensional schematic underscores the influence of fabrication strategies on morphology and functional deployment across diverse fields. | |
3. Factors affecting properties of CP hybrid materials
3.1. Composition and morphology
The periodic variation in the composition and morphology of CP hybrid materials results in diversified properties. More precisely, the electrical, thermal, and mechanical characteristics of hybrid materials are altered in type and quantity by inorganic fillers such as carbon nanotubes, graphene, metal oxides, and transition metal dichalcogenides.103
For example, the introduction of fillers with large aspect ratios, such as carbon nanotubes, may provide efficient pathways for charge transport and hence improve electrical conductivity. The ratio between the CP and the hybrid component is important; normally, a higher CP ratio will improve the electrical conductivity at the cost of reduced mechanical strength.70,104,105
Performance can be driven by material morphology at the nano-, micro-, and macro-scales, respectively. In many cases, CP-nanostructured hybrids exhibit enhanced characteristics owing to their increased surface area and quantum effects. Typical morphologies include nanofibers, nanotubes, and core–shell structures, which provide different benefits in some applications.102
The distribution of the components within the hybrid material was also significant in this study. Homogeneous dispersions generally have more consistent properties, whereas controlled heterogeneity can further drive localized functionality or gradient property. The alignment of fillers in a CP matrix can give rise to anisotropic properties, such as directional charge transport.102
The tailoring of the properties of CP hybrid materials for targeted applications depends on two major factors: their composition and morphology. By carefully choosing and controlling the type, amount, and distribution of the fillers, along with the overall morphology, it is possible to design CP hybrids with optimized electrical, thermal, and mechanical properties.106,107
3.2. Doping levels and types
Doping is one of the most important factors that determine the electrical properties of conductive polymers and their hybrid materials. Hence, doping accumulated at an increased concentration can significantly influence conductivity, charge carrier concentration, and mobility.108,109
The dopants typically used are small ions, such as chlorides or sulfates, and large polymeric dopants, such as poly(styrene sulfonic acid) (PSS). During synthesis, the doping levels, that is, the ratio of dopant to monomer units, can be controlled. Elevated doping levels normally enhance conductivity but also influence other characteristics related to mechanical flexibility, optical features, and the structural integrity. At very high doping levels, structural changes can occur in polymers, leading to degradation.110,111 However, the relationship between the doping level and electrical performance is often non-linear. At low doping concentrations, the conductivity increases slowly owing to isolated conductive domains, whereas a sharp increase occurs near the percolation threshold.112 Beyond this, excessive doping can cause structural distortions or phase separation, which reduce the charge mobility.113 Theoretical models such as variable-range hopping (VRH) and percolation theory have been used to describe these trends in CP systems, particularly in polyaniline and PEDOT:PSS composites.114
The nature of the dopant can affect all other properties. Inorganic dopants, typically metal ions, increase the stability and conductivity of materials, whereas organic dopants provide specific functionalities. However, depending on their size and charge, the dopant ions influence the conformation, that is, the chain form and packing, which affects the structure of the resulting material.110,111
Redox doping, which involves oxidation or reduction of CP, is particularly important. Long-term performance requires this process to be reversible and stable for applications such as energy storage and electrochromic applications.115
Specific optimization of the electrical and electrochemical properties of CP hybrids for certain applications through proper selection and control of the type and level of doping is necessary.116
3.3. Environmental conditions
The properties of CP hybrid materials can be effectively affected by environmental conditions such as temperature, humidity, light, and chemical exposure.117
3.3.1. Temperature. The conductivity of CPs often increases with increasing temperature because of increased charge carrier mobility. However, high temperatures usually degrade or cause irreversible changes in the material structure. Therefore, inorganic fillers can enhance the thermal stability of hybrid materials and reduce some of these effects.29,118Humidity is a highly relevant parameter, particularly for CPs that consume water. Water intake can change the volume of a material, affecting its mechanical properties and altering its doping state. Some CP hybrids demonstrate improved ionic conductivity in humid environments, which may be either useful or unfavorable depending on the nature of the sensing application.2,119
3.3.2. Light and chemical exposure. Bare exposure to light, particularly UV radiation, is sufficient to provoke photodegradation in some CP hybrids, which in turn affects their optical and electrical properties. Chemical exposure can affect the electrical properties and stability of CPs, particularly in sensing applications.2,120Therefore, it is critical to design protective layers or encapsulations to ensure the long-term reliability of CP-based devices in various environments. These protective measures help maintain the stability and performance of materials under different environmental conditions.121
Understanding the environmental properties of CP hybrid materials will facilitate the development of robust and reliable materials for real-world applications. In this regard, enhanced thermal stability is important because careful management of humidity effects is considered when offering protection from light or chemicals.122
3.4. Interfacial interactions
The properties of CP hybrid materials are affected by their composition, morphology, doping, environmental conditions, and interfacial interactions.118
3.4.1. Composition and morphology. The properties of hybrid CP materials are highly dependent on their compositions. In such materials, the ratio of CP to the hybrid component modulates the overall characteristics. For instance, although a higher CP fraction is expected to increase electrical conductivity, it may also diminish the mechanical strength. The morphology of materials at the nano-to-macro scale also affects their performance.123This usually results in better properties of nanostructured CP hybrids, such as nanofibers, nanotubes, and core–shell structures, owing to their larger surface area and unique nanoeffects. Component distribution becomes extremely important; homogeneous dispersion in the matrix, on the one hand, ensures uniform properties; on the other hand, controlled heterogeneity can also introduce localized functionalities or gradient properties.72,124
3.5. Doping levels and types
Doping is necessary to tailor the electrical and electrochemical properties of CP-hybrid materials. The doping level determines the charge carrier concentration and mobility, which establish the conductivity. Although a higher temperature usually increases the conductivity, it may decrease the mechanical flexibility or alter the optical properties of the materials.125 Other factors that modulate the dopant type further enhance the diversity of property modification, whereby inorganic dopants contain metal ions to improve properties such as stability and conductivity, and organic dopants may add additional functionalities to the polymer. Oxidation or reduction under redox doping is a key process in energy storage and electrochromic devices. It considers long-term performance based on stability and reversibility.125
CP hybrid materials are sensitive to environmental factors. Influence of temperature: conductivity varies with temperature, and many CPs are conductive at sufficiently high temperatures. However, low or high temperatures can lead to degradation or even structural modifications.19 The second most critical environmental factor was humidity. Absorbed water causes volume and morphological changes, disrupts the mechanical properties and may also influence the original doping state. In some CP hybrids, the ionic conductivity is highly enhanced in the presence of humidity; hence, it can be utilized in some applications, whereas in others, it can be dangerous.119 Exposure to UV radiation causes photodegradation, and its relevance and periodic changes affect the optical and electrical properties of materials. The impact developed is realized in practice and can be applied to highly stable materials.6
3.5.1. Interfacial interactions. All these interactions occur at the interface between the CP and inorganic filler and determine the properties of the hybrid material.126 Conversely, good interfaces result in improved mechanical properties owing to enhanced load transfer. Poorly developed interactions, such as van der Waals bonds, may lead to poor dispersion of fillers and hence limit the property enhancement. Modification of the filler surface or the use of compatibilizers can enhance these interactions and optimize the performance of hybrid materials.127 The nature of this interface also affects the charge transport relevant to various electronic and energy storage applications. Tailored interfacial chemistry can provide specific electronic properties because of charge trapping or facilitation.128
3.6. Reproducibility and reliability considerations
The properties of CP hybrid materials are influenced by many factors, including composition, morphology, doping, and environmental conditions (e.g., humidity, temperature, interfacial interactions, and reproducibility).119,126
3.6.1. Composition and morphology. The two most important factors in determining the final properties of CP hybrid materials are their composition and morphology.70 A change in the ratio of CP to the hybridization component changes the overall characteristics; with a higher CP content, the electrical conductivity is usually improved at the expense of mechanical strength.129 Morphology, on all scales ranging from nanostructured forms, such as nanofibers or nanotubes, to core–shell structures and larger ones, can affect performance owing to the increased surface area or special effects.130This provides a homogeneous dispersion of components with relatively consistent properties, and a controlled level of heterogeneity can confer specific functionalities or gradient properties. To better visualize the interconnectivity between the synthesis strategies, structural forms, and application areas of CP hybrids, a schematic overview is presented in Fig. 4.
 |
| Fig. 4 Structural taxonomy and synthesis-application interconnectivity of conductive polymer hybrid materials. This schematic visually maps the interlinked relationships among the synthesis strategies (e.g., in situ polymerization, electrochemical polymerization, and template-assisted self-assembly), structural forms (e.g., core–shell, layered, interpenetrated networks, and mixed architectures), and key application domains, including energy systems, environmental remediation, biomedical devices, and flexible electronics. | |
4. Types and levels of doping
The doping of CP hybrid materials significantly influences their electrical and electrochemical properties. Chemically induced changes in the charge carrier concentration and mobility shift the conductivity. An increase in the doping level usually improves conductivity, but at the cost of mechanical flexibility or optical characteristics in most cases.131 The choice of dopants is equally important, where inorganic dopants, such as metal ions, mostly show improvements in stability and conductivity, whereas some organic dopants may add certain functions to the material. Redox doping is essential for energy storage and electrochromic applications. Because these devices must be used for long-term measurements, their performance is often critically linked to their stability and reversibility.132
4.1. Environmental conditions
Environmental factors influence the properties and performance of CP-hybrid materials. Temperature changes may result in changes in conductivity, and many CPs conduct electricity much better at high temperatures owing to the enhancement of charge carrier mobility.133 Extreme temperatures can lead to material degradation. Humidity may affect water absorption, followed by volume change, and subsequently modify the mechanical properties and doping state.134 Some CP hybrids exhibit improved ionic conductivity under humid conditions, which could be useful for some applications or deleterious to others. Light can lead to photodegradation, and the optical and electrical properties tend to change over time.135
4.2. Interfacial interactions
The interfacial interactions between the CP and inorganic filler interface are crucial to the properties of the material.136 In contrast, strong interfacial interactions, such as covalent or hydrogen bonding, can enhance mechanical properties and charge transfer. Without strong interfacial interactions, only weak interactions, such as van der Waals forces, occur, which may result in poor filler dispersion and limited property enhancements. These interactions can be improved by surface modification or the addition of compatibilizers.137
The nature of the interface also affects the charge transport mechanisms in the context of applications, which is most significant for electronic and energy-storage devices. Interfacial chemistry can be used to tailor charge trapping or facilitation.138 Reproducibility and reliability considerations: the practical applicability of CP hybrid materials requires high reproducibility and reliability. High-purity starting materials, tight control of synthesis conditions, and the application of standardized characterization methods are some of the factors that aid reproducibility. Reliability is concerned with the stability of a material under operating conditions such as electrical stress, thermal cycling, or mechanical loading. Knowledge of long-term performance and possible failure modes can be obtained through accelerated aging tests, coupled with failure analysis techniques. All these factors are relevant to the construction of high-performance CP hybrid materials for different applications.139
5. Structural–property correlations in CP hybrid materials
CPs are a newly discovered class of materials that fill the gap between metals, owing to their electrical conductivity, and polymers, owing to their flexibility and processability. These materials have attracted significant interest in electronics, energy storage, and sensor applications.118 Nanostructured CPs and hybrid materials have demonstrated improved performance in many ways. Thus, the relationships between the structural properties are essential for optimizing hybrid materials for specific applications.140
5.1. Nanostructure conductivity effects
Thus, nanoscale organization is of prime importance for CP conductivity applications. Nanostructures, such as carbon nanotubes, graphene, and polypyrrole nanowires, introduced within a polymer matrix, create conducting pathways that allow efficient charge transport.141 This effect is more prominent in PPy nanowires embedded in a poly(vinyl alcohol) matrix, where the high aspect ratio of the nanowires results in a significant increase in the conductivity compared to that of bulk PPy nanowires. This is due to the enhanced electrical properties resulting from the formation of interconnected networks in the nanostructures.142
Moreover, nanostructure morphology influences conductivity. In one-dimensional nanostructures, such as nanowires and nanotubes, this ensures straight pathways for electron transport, whereas two-dimensional structures increase surface interactions. As has been shown, CPs functionalized with nanowire architectures exhibit conductivities orders of magnitude higher than their bulk analogs.143
5.2. Influence of the polymer backbone on properties
Another intrinsic factor that determines the inherent properties of CPs is the chemical structure of their backbones. Generally, CPs with conjugated backbones, such as polyaniline and poly(3,4-ethylenedioxythiophene), are important for electrical conductivity. The extent of conjugation and the substituents on the backbone increase the bandgap and, hence, the conductivity of the polymer.118
For instance, the conductivity of PANI can differ considerably depending on its oxidation degree. This characteristic is directly related to the structure of the polymer backbone. The oxidation state of PANI can be precisely controlled during synthesis by selecting the oxidant, its concentration, reaction time, and pH. For example, increasing the ammonium persulfate-to-aniline molar ratio shifts PANI toward its emeraldine or pernigraniline forms, which dramatically alters its electrical and electrochemical properties.144 Electrochemical polymerization offers even finer control by adjusting the applied potential or current density during growth.145 These changes also affect the stability, color, and capacitance. A higher oxidation state generally leads to increased conductivity but can reduce mechanical flexibility and long-term electrochemical cycling stability.146 Such functionalization of the backbone can be achieved by chemical modifications that alter various properties. The introduction of electron-donating groups increased conductivity, whereas electron-withdrawing groups improved stability. In PEDOT, the choice of conducting backbone further affects the mechanical flexibility and electrochemical performance, which are relevant for applications in flexible electronics.10,71,147
5.3. Role of functional groups in hybrid performance
The properties and performance of hybrid materials are primarily governed by the functional groups attached to the CPs. They can enhance interactions with other materials, improve solubility, and modify electronic properties. For example, incorporating amine groups into PPy-based hybrid materials can promote hydrogen-bond formation with a silica matrix, leading to improved mechanical properties.100,122
The introduction of sulfonic acid groups into PANI, which increases the degree of protonation, enhances the conductivity and charge transport.148,149 The functional groups introduced into hybrid materials are typically responsible for enhancing their stability and reactivity. The incorporation of functionalized graphene into polymer CPs can enhance the mechanical and thermal properties of the resulting composites.150 Graphene functional groups form strong interactions with the polymer matrix, resulting in improved performance in applications such as sensors and energy storage devices. Functionalization can also tune the optical property application scope of CP hybrids, enabling them to function as sensors and actuators.151
5.4. Emerging analytical methods for structure–property relationships
Advanced analytical techniques are required to determine the structure–property relationships of CP-hybrid materials. State-of-the-art XRD and TEM methodologies provide detailed insights into the nanoscale structure and morphology of materials. In addition, several spectroscopic techniques, such as X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, and Raman spectroscopy, provide information on the chemical composition and bonding within these hybrids.152–154
These analytical tools provide a much deeper understanding of the complex interplay between the structures and properties when combined with computational modeling. This insight is essential for rational design. Hybrid CPs and showcases were optimized for applications. For example, AFM and SEM provide nanoscale visualizations of the surface topography of materials, whereas XRD and FTIR relate specific structural features to the electrical and mechanical properties of materials.155,156
CPs have generated significant interest in various scientific disciplines. Therefore, PANI and its high-conductivity derivatives are useful in organic light-emitting diodes, field-effect transistors, corrosion protection devices and solar cells. In addition, the chemical synthesis of CPs with nanoscale structures has been performed to boost their electrochemical activity and functionality.148 Various methods, such as chemical and electrochemical syntheses, can be used to produce CPs with controllable molecular structures.157
Different synthesis conditions allow CPs with tailored properties, such as battery optimization. Subsequently, CP nanostructures have been used in other energy-storage applications. Among the conductive polymer hydrogels, promising materials have been discovered owing to their unique properties. The combination of CP with conventional polymers can combine the mechanical performance of conventional polymers with the electroactivity of CPs, thereby opening up more extensive fields for these applications.158
Recently, CPs have been incorporated into magnetic nanoparticles to form nanocomposites, which extend their potential applications. Electro polymerization is a common method for preparing CP films because it allows the direct deposition of polymers onto conductive surfaces. This is an effective strategy for coating and preparing thin films with specific electrical properties.159
CPs represent a versatile class of materials that have been widely applied in various scientific fields, ranging from bioeconomics and optoelectronics to energy and sensing applications. Further research into new strategies for synthesis, nanostructuring techniques, and composite face materials that can improve the properties and functionalities of CPs is undergoing for CPs.160
6. Environmental applications of CP hybrid materials
Hybrid materials based on CPs combine the unique properties of conducting polymers with the functionalities of other materials, and thus appear promising for various environmental applications, such as gas sensing, heavy metal detection, dye removal, membrane filtration, and agriculture. This section details the analysis of comparative studies on such applications, given the practical aspects of the real-life implementation of CP hybrids with traditional materials.23,161 Conductive polymer hybrid materials are of great interest for environmental applications owing to their potential use in water treatment, air purification, and soil remediation. Table 3 describes the specific uses, mechanisms of action, advantages, and limitations of each of these applications.
Table 3 Application of conductive polymer hybrid materials towards the environment the table illustrates the various ways cp hybrid materials are used in specific applications, their operating mechanisms, favorable characteristics, limitations, and examples of environmental applications in light of hazards associated with the treatment of water, purification of air, soil remediation, and pollution monitoring. hybrid materials have superior performance and/or better sustainability because they offer properties unattainable from only one material component in treatments related to environmental hazards caused by water, air, soil, and pollution
Application area |
Specific use |
Mechanism of action |
Advantages |
Limitations |
Examples of CP hybrid materials |
Performance metrics |
Water treatment |
Removal of heavy metals |
Adsorption of heavy metal ions through chelation or electrostatic interactions |
High efficiency, regeneration capability |
Limited selectivity for specific ions in complex mixtures |
Polypyrrole/graphene oxide composites |
Pb2+ adsorption: 93.2 mg g−1 (PPy-reduced GO), Hg2+: 400.0 mg g−1 (magnetic PPy-GO), Cd2+: 794.2 mg g−1 (COPYGO composite)162,163 |
|
Removal of organic pollutants |
Catalytic degradation via photocatalysis or electrochemical oxidation |
Effective for persistent pollutants |
Requires light or electrical input |
Polyaniline/TiO2 nanocomposites |
Methylene blue degradation: 86.35% (PANI–TiO2), methyl orange: first-order kinetics with k = 0.619 h−1 (ref. 164 and 165) |
|
Membrane filtration |
Enhanced fouling resistance and mechanical strength through hybridization |
High permeability and selectivity |
Potential biofouling over time |
Polythiophene/zeolite composites |
Permeate flux: 18 L m−2 h−1 bar, heavy metal rejection: 90–97% (ref. 166) |
Air purification |
Capture of volatile organic compounds |
Adsorption via porous structures and catalytic breakdown |
High surface area for adsorption |
Regeneration and desorption challenges |
Polypyrrole/silica composites |
VOC removal efficiency: requires specific verification for toluene167 |
|
Decomposition of toxic gases |
Catalysis of harmful gases into less toxic products |
Eco-friendly, efficient |
Requires stable operational conditions |
Polyaniline/metal oxide hybrids |
Gas sensing: detection limits in ppb range, response times <10 s (ref. 39 and 168) |
Soil remediation |
Heavy metal stabilization |
Binding and immobilization of metals through CP hybrid matrices |
Reduces bioavailability |
May require additional processing for deeper penetration |
Polypyrrole/clay composites |
Cr6+ removal: requires verification of 92% efficiency claim169,170 |
Energy harvesting from waste |
Energy recovery from microbial fuel cells |
Enhanced electron transfer in microbial fuel cells using CP hybrid materials |
Improves energy efficiency |
Requires optimization for scalability |
Polypyrrole/carbon nanotubes hybrids |
Power density: typical range 50–200 mW m−2 for CP-enhanced MFCs38,171 |
Sensing and monitoring |
Detection of environmental contaminants |
High sensitivity detection through changes in conductivity or electrochemical response of CP hybrids |
Fast response, portable devices |
Prone to interference from other contaminants |
Polyaniline/metal nanoparticle composites |
Detection limits: heavy metals in μg L−1 to ppb range depending on analyte172,173 |
|
Real-time pollutant monitoring |
Integration into smart sensors for real-time monitoring |
Continuous monitoring of potential |
Maintenance and calibration challenges |
Polythiophene/graphene composites |
Gas detection: ppb-level sensitivity with stability >30 days173,174 |
6.1. Mechanisms and devices to sense gases
CP hybrid materials are highly efficient in detecting various gas species because of their high sensitivity to changes in the electronic structure upon interaction with the target gas molecules. The sensing mechanisms of conductive polymer hybrid aerogels include the modulation of electrical conductivity or changes in other physical or optical properties caused by the adsorption of gas molecules.175 For example, polyaniline composites with metal oxides, such as SnO2, exhibit superior sensitivity to volatile organic compounds. This is because of the synergistic effects between CP and metal oxides in the development of low-cost, high-sensitivity, and selectivity-driven gas sensors for environmental monitoring and safety applications.148 CP matrices with carbon nanotubes or graphene can enhance both the sensitivity and response time. For example, PANI nanostructures deposited on interdigital microelectrodes exhibit good sensitivity and selectivity toward ammonia gas at room temperature.10,126 The relationship between CP hybrid architectures and their dominant sensing applications is illustrated in Fig. 5.
 |
| Fig. 5 Architecture-to-application mapping of CP hybrid materials in sensing technology. This flowchart links the key structural forms of CP hybrid materials, such as core–shell, IPNs, layered composites, and dispersed nanocomposites, with their respective advantages and dominant sensing applications. Core–shell hybrids offer enhanced electron mobility and are used in gas sensors and biosensors. IPNs provide structural flexibility, making them suitable for wearable and skin-based sensors. Layered structures enable anisotropic transport and are applied in humidity and pressure sensors. Dispersed composites offer scalable fabrication methods for disposable chemical sensors. This mapping provides a design framework for selecting appropriate CP architecture based on the sensor performance requirements and operating conditions. | |
6.2. Detection and removal of heavy metals
The hybrid materials showed a reputable capability for heavy metal detection and disposal in contaminated water sources. PPy and PANI are two of the most widely used conducting PPy and PANI, mainly because of their high conductivity and the formation of complexes with metal ions. For example, PPy-based electrochemical sensors have shown selectivity for the detection of copper ions in aqueous solutions. PPy-functionalized graphene oxide exhibited a very good adsorption capacity for lead ions.176,177
These materials are also used in adsorption-based processes and as components of membrane filtration systems. This is because of their ability to bind heavy metal ions and change their electrical properties, which is useful for sensing and remediation applications.178 For instance, PPy–graphene oxide composites have shown adsorption capacities of up to 250 mg g−1 for Pb2+ ions, attributed to π–π interactions and chelation.179 The hybrid matrix not only stabilizes the CP but also improves the ion selectivity and regeneration capability.
6.3. Dye sensing and remediation strategies
CP hybrid materials are common pollutants in wastewater and are therefore suitable for detection and removal. For example, PANI-based sensors have been developed to detect methylene blue dyes in aqueous solutions. The dye molecules interact with the CP hybrid, causing changes in color or fluorescence during the sensing mechanism.180
Thus, they can be used for remediation in adsorption-based processes and photocatalytic systems. For example, PANI/TiO2 hybrid materials exhibit improved photocatalytic activity for the degradation of methyl orange dye under visible light, thereby proving to be effective against dye pollution.181
6.4. Membrane filtration technologies
CP hybrid materials have been extensively applied in membrane filtration technologies, particularly for water purification and desalination. In this study, the materials were easily processed into thin-film composites or mixed-matrix membranes characterized by high permeability, selectivity, and fouling resistance.182,183 For instance, PEDOT/graphene oxide hybrid membranes exhibit remarkable flux and salt rejection during desalination. CP hybrids can also be used as active membranes, increasing desalination efficiency through controlled selective ion transportation.184
6.5. Agricultural applications
These polymers have been utilized in many fields, including pesticide sensing and controlled release in agriculture. For example, PANI. Graphene oxide hybrid sensors have been proven effective in determining organophosphate pesticides in water samples. In this trend, CP hybrids would avail themselves of a matrix as a carrier of environmentally safe and effective agrochemicals with a controlled release rate that may be altered by changes in material composition or external stimuli, such as pH and temperature.185,186 These materials also hold great potential for smart agriculture, where they can be integrated into sensors to monitor soil conditions and facilitate efficient and sustainable practices.
6.6. Comparative analysis with traditional materials
On the other hand, CP hybrid materials are preferred over more classical metal oxides or activated carbon materials and have several advantages, including the following.
6.6.1. Tunable properties. The composition, morphology, and functional groups of CP hybrids can be tuned to optimize their performance for specific applications.187
6.6.2. High specific surface area. In many cases, CP hybrids have high surface areas. Therefore, there is potential for enhancing adsorption and catalytic processes.188
6.6.3. Flexibility and processability. Some CP hybrids can be processed into films or membranes, and are suitable for general applications.19,189
6.6.4. Biocompatibility. Some CP hybrids are biocompatible; accordingly, they can be used in agriculture and biomedicine.190However, in other aspects related to effectiveness, stability, or specific performance metrics, traditional materials may outperform CP hybrids. Therefore, a proper comparative analysis should be adopted to choose the most suitable material for any environmental application.191 One critical consideration is the cost of raw materials and their fabrication. While CP hybrids offer superior tunability and multifunctionality, their synthesis, especially via in situ or template-assisted methods, often involves higher reagent and processing costs than conventional materials such as activated carbon or zinc oxide.192 For example, PANI/TiO2 composites used for dye degradation are 1.5–2 times more expensive per unit mass than bulk TiO2, primarily because of the oxidative polymerization steps and the cost of monomers.193 However, some metal-oxide-based systems are more cost-effective for bulk remediation. However, the cost gap narrows significantly when the lifecycle performance is considered, particularly when CP hybrids exhibit enhanced regeneration, selectivity, or durability.179 A comprehensive cost–benefit analysis is essential for each specific application.
6.7. Practical considerations for real-world implementation
Although CP hybrid materials are the most promising, a variety of pragmatic challenges remain to be addressed for successful real-world implementation, such as scalability and cost. The synthesis and processing of CP hybrids must be scalable and cost-effective for large-scale applications.122,194 Stability and durability: evaluation and enhancement of the stability of CP hybrids under conditions such as temperature changes, variations in pH, or the presence of interfering substances. System integration: underpinning technologies employing CP hybrids must be integrated into existing infrastructure and processes. Regulatory compliance: environmental impact and regulatory compliance of CP hybrids must be evaluated for safe use and disposal. Standardization and quality control: CP hybrid-based technologies must be based on standard testing methods and quality control, ensuring that the results provided by the technology are both reliable and reproducible.195
CP polymer hybrid materials have tremendous potential for a broad array of environmental applications, ranging from gas sensing, heavy metal removal, dye remediation, and agricultural use. Despite offering certain benefits over traditional materials, practical considerations must also be considered. More research and development are essential for the full exploitation of CP hybrid materials to create sustainable environmental solutions.196
7. Energy-related applications of CP hybrid materials
Hybrid materials based on conducting polymers combine the high electrical conductivity of CPs with their unique physicochemical properties. These materials show strong potential for many applications related to energy. Good candidate interfaces also show tunable properties, high surface areas, and the ability to interact with several redox species for energy storage, conversion, and harvesting.197 The application of CP hybrid materials as electrocatalysts in fuel cells, water splitting, and other electrochemical energy storage devices is discussed. One will also address the associated performance criteria, benchmarks, and challenges of scaling up versus staying competitive from the perspective of low-cost.198
7.1. Electrocatalysts for fuel cells and water splitting CP
Hybrid materials have been investigated as electrocatalysts for fuel cells and water splitting, owing to their high conductivity and ability to promote electrochemical reactions. For example, polyaniline (PANI) composites with metal nanoparticles, such as Pt or Ru, have shown improved ORR activity in fuel cells.199 As a rule, these hybrids rely on the large surface area of CP to afford a large amount of active site space for reactions, while the metal nanoparticles improve electron transfer and catalytic activity.200
CPs have been demonstrated to improve the electrocatalytic activity towards the splitting of water to produce hydrogen and other materials. For instance, PPy metal oxide composites, including NiO, exhibit good performance in the water oxidation process, which is a critical step in the splitting of water to produce hydrogen and oxygen. These materials usually have high conductivity and redox properties that facilitate charge transfer while increasing the general reaction efficiency.201
7.2. Electrochemical energy storage devices
CP composite hybrid materials are excellent candidates for a range of electrochemical devices such as batteries, supercapacitors, and hybrid energy storage systems. Owing to their high conductivity and high redox activity, these materials can provide easy storage and smooth release of charges, yielding high-energy or power densities at the end.196 For instance, PANI-composite-based carbon nanotubes are good candidates, yielding good performance in supercapacitors. A high capacitance and decent cyclic stability were simultaneously demonstrated.202
These CP hybrids, such as polythiophene, combined with metal oxides, enhance the energy density and cycle life performance of lithium-ion batteries as mixed electrode materials. These hybrids have high conductivity and redox properties, which facilitate lithium-ion diffusion and enhance the electrochemical performance of batteries.203
7.3. Photovoltaic and photoelectrochemical
They also play a vital role in optoelectronic devices such as solar cells and corresponding photoelectrochemical systems because they enable effective light harvesting and charge separation owing to their tunable bandgap and high photoconductivity.204 An example is the enhanced light absorption of dye-sensitized solar cells operated in CP-based composites with quantum dots, along with an improved rate of photocatalytic activity. With these devices, where CPs have provided a conductive pathway, the quantum dots, inversely, produce both effective light harvesting and charge separation.205
In addition, PANI composites with titanium dioxide nanoparticles have been applied as photoelectrodes in PEC water-splitting systems. It exhibited improved photocatalytic activity for the generation of hydrogen and oxygen under sunlight.206
7.4. Thermoelectric materials
The potential of CP hybrid materials, in which electrical energy can be produced by the action of waste heat, is receiving increasing attention in thermoelectric applications. This tuning of electronic and thermal conductivities enables effective energy conversion.207 For example, CPs can also be designed with a meaningful enhancement in thermopower and optimized electronic characteristics by filling them with conductive carbon nanotubes or graphene, and materials such as those that could be highly promising for waste heat recovery.208
7.5. Performance measures and benchmarks
The performance of CP hybrid materials in energy-related applications must be evaluated using certain metrics and benchmarks. The key performance indicators were as follows:
7.5.1. Storage capacity. Measured in terms of specific capacity (mA h g−1) and energy density (W h kg−1) for batteries and supercapacitors.209
7.5.2. Power density. Measured in power density (W kg−1) for supercapacitors.210,211
7.5.3. Cycle life. The number of charge and discharge cycles that a certain device can perform before serious performance degradation occurs.212
7.5.4. Efficiency. This is the rate at which light or chemical energy is converted into electrical energy by solar and fuel cells.213Catalytic activity was characterized in the context of current density, turnover frequency, and selectivity toward the target reaction. These metrics are essential for the comparison of CP hybrid materials in terms of performance with traditional materials; they establish benchmarks for further improvement.214 However, performance metrics alone are insufficient without understanding degradation pathways during prolonged use. In CP-based supercapacitors, cyclic voltammetry over hundreds or thousands of cycles often leads to decreased capacitance due to morphological collapse, dopant leaching, and chain scission within the polymer matrix.215 For battery applications, hybrid materials may suffer from electrode swelling, phase separation between the CP and inorganic filler, or side reactions at the electrode–electrolyte interface that lead to impedance buildup.216 In flexible devices, repeated mechanical deformation further accelerates microcrack formation and electrical discontinuities.217 These mechanisms contribute to the gradual decline in storage capacity, power output, and cycle life and must be mitigated through careful interface engineering, dopant stabilization, or encapsulation strategies.
7.6. Scalability and cost-effectiveness challenges
Although CP hybrid materials have high potential for a wide range of applications, their commercialization scope has narrowed owing to some bottlenecks.100 Some of the current key challenges are
7.6.1. Synthesis and processing. Scalable and cost-effective procedures for synthesizing and processing CP hybrids must be developed for large-scale manufacturing.218 Stability and durability: long-term stability and durability under operating conditions are fundamental for practical implementation in energy devices.219 Material cost: the material and synthesis of the CP material account for the cost of energy devices and should thus be primarily considered in making the process cost-effective. Addressing these challenges through continuous study and research is the way to the general adoption of CP hybrids for energy applications to bring us into a more sustainable and efficient future.220Potential applications of CP hybrid materials include electrocatalysis in fuel and water-splitting cells, electrochemical energy storage devices, solar cells, and thermoelectric materials. Owing to their tunable properties, high surface area, and flexibility, this class of materials has diverse applications in energy technologies. Nevertheless, issues in scalability and cost reduction have successfully traversed the commercialization of devices. Continuous research, development, and collaboration among researchers, industry, and policymakers are crucial for overcoming these challenges and advancing sustainable energy technologies.221
8. Corrosion protection using CP hybrid materials
CP hybrid materials have recently come into the spotlight because of their effectiveness in protecting against corrosion. These hybrids bind the electrical conductivity of CPs with the protective properties of other materials, resulting in an improved performance against traditional methods of corrosion protection. Key points, such as mechanisms of corrosion inhibition, development of smart coatings, and self-healing materials, were compared and evaluated against conventional approaches in this analysis.6
8.1. Mechanisms of inhibition of corrosion
The main mechanisms by which the corrosion process is inhibited for most CP hybrid materials include the following.
8.1.1. Barrier protection. Hence, conducting polymers such as polyaniline and polypyrrole cover the metal surface and provide a physical barrier against corrosive agents, moisture, and oxygen, which diffuse to the substrate and slow down the corrosion process.222 The described barrier action is enhanced by adding materials such as nanoparticles or inorganic fillers into the CP matrix, which makes it more resistant to corrosive elements.223
8.1.2. Cathodic and anodic protection. Some CPs can act as sacrificial anodes, which means that they preferentially oxidize rather than have a metal substrate, which is a process called cathodic protection.222 Other CPs achieve anodic protection by shifting the electrochemical potential of the metal surface to more positive values, thereby allowing the formation of a passive layer that protects the metal underneath. For example, PANI has been found to anodically shift the corrosion potential of steel, resulting in a lower corrosion rate in highly aggressive environments.224,225
8.1.3. Electrochemical impedance and controlled release of inhibitors. Some CPs can enhance the interfacial impedance at the metal surface, opposing the flow of the electrons and ions responsible for corrosion.226 Furthermore, certain CP hybrids could solubilize releasable corrosion inhibitors in a self-healing type response to further improve the long-term performance of the protective coating. Such a potential response would be due to environmental stimuli such as pH changes and would ensure a continuous renewal of active species to counter corrosion.222,227
8.2. Smart coatings and self-healing materials
CP hybrid materials also permit the development of smart coatings and self-healing materials that can respond to their environment and damage while offering advanced corrosion protection.
8.2.1. Smart coatings. Hence, these coatings can perceive changes in the environment, for instance, moisture or temperature shifts and react accordingly. For instance, pH-sensitive CP-based coatings can release corrosion inhibitors under acidic conditions, thus preventing further degradation. Moreover, the combination of nanomaterials with CPs enhances their responsiveness and functionalities, thereby creating applications of many types.228,229
8.2.2. Self-healing materials. CP self-healing hybrids encapsulate corrosion inhibitors released in the case of mechanical damage or corrosion. If a crack in the coating develops, a healing agent fills this void and polymerizes, thus “healing” the protective layer. Various studies have shown that the application of self-healing CP coatings may considerably prolong the lifetime of protective systems by protecting them against corrosive environments.230,231
8.3. Comparative analysis with traditional methods of protection against corrosion
The following strengths and weaknesses have been identified when comparing CP hybrid materials with classical methods of corrosion protection, such as organic coatings, galvanization, or metal plating.
8.3.1. Effectiveness. Better corrosion resistance is often observed with CP hybrids because they have dual mechanisms of barrier protection and active inhibition. Traditional methods rely largely on barrier properties; therefore, they are not able to provide high protection, especially in very aggressive environments.232
8.3.2. Environmental impact. Traditional methods of protection against corrosion often utilize toxic chemicals or heavy metals, thereby posing environmental risks. On the other hand, CP hybrids can be obtained from more environmentally friendly materials, making them more sustainable.233
8.3.3. Flexibility of applications. CP hybrid materials can be easily tailored for specific applications by modifying their chemical structures or by incorporating various additives. Traditional methods, while effective, generally require extensive customization processes.189
8.3.4. Durability and self-healing. CP hybrid coatings will be stronger and more resistant to harsh environments than traditional coatings. Furthermore, the self-healing features of the CP hybrids extend their lifespan by allowing the coating to heal whenever damage occurs. Cost and scalability. While CP hybrid materials have several advantages, the processes related to their production and application may be more complicated and potentially more expensive than traditional methods.234 However, research in this area is ongoing to further optimize these conducting-polymer hybrid materials are a new generation of tools for protection against corrosion. By applying the mechanisms of barrier protection, cathodic and anodic protection, and controlled release of inhibitors, these materials afford superior corrosion resistance compared to traditional methods of protection against corrosion. Smart coatings and self-healing materials occupy a place of pride to enhance their protective capabilities further. Although there are still difficulties with plating in terms of cost and scalability, further research in this area will likely provide a more effective and long-term corrosion protection solution for different industries.235
8.4. Biomedical applications of CP hybrids
The integration of CP hybrids into biomedical systems has opened new avenues for multifunctional platforms that couple electrical functionality with biocompatibility. These systems leverage the inherent advantages of CPs, such as flexibility, tunable conductivity, and chemical functionality, while overcoming traditional limitations through structural reinforcement with inorganic or bioactive counterparts.236,237
One of the most mature application domains is neural interfacing, where CP hybrids like poly(3,4-ethylenedioxythiophene) (PEDOT) doped with biocompatible counterions or nanoparticles are employed to enhance electrode–tissue coupling. Their soft mechanical properties minimize interfacial strain, while their high charge injection capacity supports chronic electrophysiological performance without significant signal degradation. CP-based neural coatings have demonstrated improved signal-to-noise ratios and decreased impedance compared to conventional metallic interfaces.238,239
Electrochemical biosensing represents another major front, where hybridization with metal nanoparticles (e.g., Au, Pt) or carbon nanostructures enhances electron transfer kinetics and increases the surface area for biorecognition element immobilization. CP hybrids in glucose monitoring, cancer biomarker detection, and neurotransmitter quantification have shown detection limits in the nanomolar to picomolar range, depending on the transduction mechanism.240,241
In drug delivery, CP hybrids enable electrically triggered release of therapeutics. By incorporating biodegradable or responsive dopants, hybrid films can be tailored for localized, on-demand drug elution. Polypyrrole (PPy) or polyaniline (PANI) matrices embedded with silica or hydrogel phases have demonstrated improved mechanical integrity and controlled swelling behavior, critical for in vivo stability.4 Moreover, the inclusion of growth factors or antimicrobial agents within CP networks offers dual therapeutic and regenerative functionalities, particularly relevant in wound healing scaffolds.242–244
CP hybrids also show promise in the development of bioelectronic skins, flexible implantable sensors, and cardiac pacing electrodes, where conformability, miniaturization, and multifunctionality are essential. These applications benefit from the synergistic combination of soft organic polymers with conductive fillers that preserve electrical percolation networks under dynamic physiological conditions.245,246
Despite significant progress, challenges remain in achieving long-term biostability, minimizing immune responses, and ensuring scalable fabrication. However, with advances in printable bioinks, hydrogel–CP composites, and bioresorbable doping chemistries, CP hybrids are poised to become core materials in next-generation biomedical systems.247,248
9. Energy storage mechanisms in CP hybrid materials
Most importantly, CP hybrid materials are considered more important for electrochemical energy storage because of their unique integration with high conductivity, redox activity, and tunable surface chemistry.249 Described below are the mechanisms of energy storage enlisted in this analysis: faradaic and non-faradaic processes, in which nanostructuring takes part in charge of transport and storage, along with in situ characterization techniques.
9.1. Faradaic and non-faradaic processes
9.1.1. Faradaic processes. These are redox reactions in which electrons move from the electrode to the electrolyte or vice versa. The high energy density of CP materials is attributed to these reactions because they lead to internal chemical changes. For example, the redox reactions of polyaniline (PANI) and polypyrrole (PPy). Although faradaic processes display a high energy density, they often have a lower power density than non-faradaic processes.250,251Non-faradaic processes involve the formation of an electrical double layer at the electrode–electrolyte interface, which is usually created by the adsorption and desorption of ions. This is because carbon-based materials have high power density and long cycle life. In CP hybrids, the addition of carbon nanostructures can further improve this non-faradaic energy-storage feature.252
As a result of these competing processes, hybrid materials with designed combinations of faradaic and non-faradaic processes balance energy and power densities and simultaneously work equally well in all applications from supercapacitors to batteries.253
9.2. Charge of transport and storage in nanostructured hybrids
9.2.1. Nanostructuring. The nanostructures of CP hybrid materials directly influence their performance in large-scale energy storage. Nanostructured materials dominate in providing a surface large enough to be usable for charge storage and, in general, increase the reaction kinetics involving charge transfer. For instance, the inclusion of conductive nanostructures within CP matrices enhances electron transport, thus increasing conductivity and rate capability.254
9.2.2. Charge transport. The nanostructure ensures efficient channels of electron transport, thus optimizing the overall effective conductivity of CP hybrid materials. This improved the power density and rate capability.255
9.2.3. Ion diffusion. Porous nanostructures and the optimization of the pore-size distribution facilitate the diffusion of ions and, hence, increase the diffusion of the accessible surface area for energy storage and boost the capacitance along with energy density.256Synergistic effects: allowing the faradaic properties of the hybrid structures, CP with faradaic materials, could lead to synergistic effects in achieving enhancements in energy and power densities.257
9.3 In situ characterization techniques
In situ X-ray diffraction (XRD) enables the monitoring of structural changes in the CP hybrid material as they electrochemically cycle and offers information on phase transitions and changes in lattice parameters.258 These real-time structural insights can be used to dynamically adjust synthesis parameters such as monomer concentration, polymerization time, and thermal treatment. For example, shifts in XRD peaks during in situ monitoring indicate phase transitions that help determine optimal annealing temperatures to preserve conductive domains.259 Similarly, in situ Raman spectroscopy detects oxidation state changes and bond reconfiguration during electrochemical cycling, allowing the fine-tuning of dopant levels or co-polymer ratios to enhance stability and charge transfer efficiency.40 These feedback loops bridge materials characterization with real-time process control, enabling more reliable and reproducible CP hybrid design.
In situ, Raman spectroscopy could report changes in the chemical structure and oxidation state of CP during processes in a way that would provide detailed insight into the faradaic reactions and formation of intermediate species.260
9.3.1. Ab initio theoretical simulation of X-ray absorption spectra. XAS provides local structure and oxidation state information for the chosen elements during electrochemical cycling via in situ studies. Changes in the coordination environment and formation of new species were also observed.261
9.3.2. Electrochemical impedance spectroscopy. It gives information about ion diffusion, charge transfer resistance, and capacitance. X-ray photoelectron spectroscopy: it probes the state of charge of CPs during several stages of charge storage, hence giving information on redox reactions. In general, hybrid materials of CP inherently store energy by either faradaic or non-faradaic processes.262 The nanostructuring of these materials improves their quality, particularly according to how charges are transported and stored. Advanced in situ characterization will enable real-time monitoring of its performance and, therefore, lead directly to high-performance energy storage devices. These materials have clear advantages over traditional methods, but the cost related to scalability tends to be a major challenge. Continued research and optimization are essential for the advancement of their application in energy storage technologies.263
9.4. Critical analysis of reported energy storage performance
Hybrid materials based on conducting polymers show great promise in energy storage, but a comprehensive analysis of disparities in the literature regarding the reported performance of these hybrid materials is desirable to gain insight into their actual capability versus limitations. This section presents the evaluation of the key performance metrics, existing challenges, and future research directions.264
However, the reported values for the specific capacity and energy density differ significantly because of the conditions of the experiment, such as the type of electrolyte, current density, and temperature. Difficulties related to the variance in these variables resulted in inaccuracies when comparing the results of different studies. For example, the choice of electrolyte and the specific experimental setup can affect the specific capacity and energy density.265
9.4.1. Power density. Most power density measurements are related to certain test conditions and may sometimes not represent real-life performance. For instance, the power density results obtained in a laboratory environment are not up to par and should not be used for measuring the actual performance of a material under practical working conditions.266,267
9.4.2. Cycle life. Presenting a cycle life report without specifying the criteria of performance degradation leads to false conclusions. A correct performance evaluation requires the definition of changes over time and under various conditions.268
9.4.3. Electrolyte compatibility. CPs can degrade in some electrolytes, which can affect their stable state over the long term as well as their performance. The selection of an appropriate electrolyte is critical for the optimization and durability of energy storage systems.
9.4.4. Rate capability. Although many of these CP hybrids have a high energy density, their rate capability is limited, meaning that they do not really estate their functionality in the case of the need for suddenly large deliveries of power. This limitation needs to be considered for applications requiring high-speed energy delivery.269
9.4.5. Cost and scalability. However, even though CP-based hybrids show promise, some challenges emerge based on cost and manufacturing feasibility in the exercise for upscaling such materials for large-scale applications. Research on cost-effective and scalable production methods for these materials for large-scale applications is still needed.270
9.4.6. Real performance trial. However, some of the potential CP hybrids have only been tested under laboratory study, and their performance has to be checked under real conditions. This involves testing the stability, durability, and long-term performance of such application scenarios.271
9.4.7. Device optimization. The design and architecture of energy-storage devices are important for optimizing the benefits of state-of-the-art CP hybrids. Issues such as electrode geometry, current collector design, and electrolyte properties require critical consideration to enhance the performance.
9.4.8. Benchmarking against mature technologies. One way to determine if CP hybrids will be at an advantage over traditional energy storage technologies, such as lithium-ion batteries and supercapacitors, is by performing benchmarking. This shows the strengths and areas that need improvement.Masood et al. (2024)21 Investigations of composites for conducting energy storage. Efficient and effective. Mohamadi and Zohoor (2011)272 developed a dimensionless number for hybrid solar thermal storage systems that provides a measure of the benefits realized by combining several storage devices.
Sharma et al. (2023):273 focused on quantum energy storage at 2D heterointerfaces and exhibiting advanced systems with high electrochemical performance superior to. Valle et al. (2023):274 work is ongoing in the development of nanostructured CPs, where the key areas for performance enhancement are glass and textile composites. Li et al. (2024)275 studied the influence of aggregation on the capacitive storage of CP films and found that they exhibit exceptional performance in aqueous electrolytes. Wang et al. (2014)276 synthesized hybrid materials of hydrous ruthenium oxide and graphene, which exhibit great capacitive performance. The critical analysis of CP hybrid materials suggests their potential for the further development of energy storage technologies. Hence, these materials present competitive energy densities, high power densities, and good cycling stability, and many important problems remain to be solved regarding scalability, material stability, and cost. Future studies should focus on new material compositions, advanced characterization, and application-specific optimization to improve the performance and ease of acceptance by a wider community.
10. Challenges and future directions
CP hybrid materials have great potential in fields such as energy storage and environmental remediation. However, there are certain limitations to be improved to maximize their potential. Thus, this section presents the important problems and future directions for research on CP hybrid materials about scalability, stability, multifunctionality, new applications, interdisciplinary research, and societal impact.100
10.1. Scalability and cost effectiveness
Another challenge in the production of CP hybrid materials is their scale-up. Most of the methods used in their synthesis are complex, expensive, and difficult to scale to industrial production levels. Research will have to be conducted if CP hybrid materials are to enjoy economic viability in the future simpler, more efficient, and cheaper methods.277 This means taking into consideration alternative precursors, optimizing reaction conditions, and adopting environmentally friendly processes. Efficient production techniques are a significant step toward meeting industrial demand and improving cost competitiveness.
10.2. Long-term stability and degradation
More importantly, the long-term stability of CP hybrid materials is one of the main prerequisites for their practical application. Most CP hybrids perform excellently in a laboratory setup, but either degrade or lose their properties under environmental stresses, such as heat, humidity, and UV exposure. Indeed, research efforts should focus on understanding the degradation mechanism and strategies to enhance stability through protective coatings, additive stabilization, or the selection of more robust materials.278
10.3. Multifunctionality and smart materials
Designing multifunctional CP hybrid materials is an area of great interest. Aggregating functions such as conductivity, sensing, and self-healing into one material could give way to higher-order smart materials. This can be achieved by integrating CPs with other smart materials in such a way that they create self-changing systems in response to the environment or external stimuli. Examples include the mechanisms of self-repair and integral sensors, which may widen the applications of CP hybrids.279
10.4. New applications and unexplored areas
Thus, new applications for CP hybrids are emerging. Beyond traditional uses, opportunities exist in areas such as bioelectronics and flexible electronics, among others, relating to environmental remediation. Such studies on new applications may provide additional benefits and increase the impact of CP hybrid materials. Future research in these possible areas of applications should realize the effective application of CP hybrids in innovative technologies such as hybrid functional materials for various applications.280
10.5. Interdisciplinary research opportunities
Research on CP hybrid materials belongs to an extremely broad spectrum of scientific fields, ranging from materials and chemistry through physics to engineering. Further growth in interdisciplinarity in the future will show an advantage for progress in this area.100 Only by cooperating can the complexity of such challenges and new technological developments be addressed. Partnerships with industry and stakeholders working together through government agencies will ensure that the results of research bring solutions to practical needs and find real-world applications.281
10.6. Impacts on society and ethics
This will unavoidably need to consider the impact of CP hybrid materials on society, as well as give attention to related ethical concerns. The only two examples are the privacy issues of next-generation sensing systems and the safety of biomedical applications.282 Future research, in open dialogue with policymakers, ethicists, and the broader public, should be conducted to ensure that the development of CP hybrid materials will satisfy societal priorities and needs. Responsible innovation and execution are also important for enabling society to fully reap their benefits. This development of CP hybrid materials must meet the challenges of scalability, cost-effectiveness, long-term stability, and multifunctionality.117 Applications can be prospected by encouraging interdisciplinary research and magma considerations for social and ethical impacts. These factors can facilitate the development of more sustainable and impactful solutions using hybrid CP materials.94
10.7. Sustainability and circular economy integration
The sustainable development of CP hybrid materials increasingly demands alignment with circular economy principles. Recent studies have emphasized the design of CP hybrids with recyclable components, such as thermally depolymerizable backbones, redox-switchable degradation pathways, and biodegradable dopants.283,284 For example, polyaniline and polypyrrole systems have been synthesized from bio-derived monomers or doped using environmentally benign acids to facilitate post-use material recovery.285 Additionally, the modular architecture of some CP composites enables physical disassembly and chemical recycling of filler components (e.g., graphene, metal oxides) using low-impact solvents or electrochemical treatments. Lifecycle assessment (LCA) frameworks are beginning to be applied to CP hybrids, evaluating metrics such as embodied energy, carbon footprint, and recyclability index. Future work should explore closed-loop fabrication processes, cradle-to-cradle material flows, and integration of CP systems into regenerative product cycles. These directions are essential to align CP hybrid material innovation with sustainable material economy goals.286,287
10.8. Scalability of fabrication methods: comparative analysis
Despite the rapid growth in CP hybrid material design, a critical bottleneck remains in translating laboratory-scale synthesis methods into industrially scalable processes. Electrochemical polymerization offers excellent control over film thickness and morphology, but suffers from low throughput, reliance on conductive substrates, and batch-wise operation. The method's inherent limitations become particularly pronounced when attempting to scale beyond research dimensions, where current distribution non-uniformities and mass transport limitations create significant quality control challenges.29,89,198
In contrast, in situ polymerization and solution blending demonstrate superior scalability, particularly for bulk or roll-to-roll production scenarios. These approaches leverage existing industrial infrastructure and can accommodate continuous processing modes essential for commercial viability. However, successful implementation requires meticulous optimization to prevent poor interfacial bonding or phase separation, which can compromise material performance and long-term stability.18,32,69 Chemical oxidative polymerization has emerged as the most industrially relevant method due to its compatibility with standard chemical reactor technology and straightforward scale-up relationships. The method achieves excellent material utilization while maintaining consistent quality across large production volumes. Universal substrate compatibility further enhances its industrial appeal, enabling applications ranging from antistatic coatings to electromagnetic interference shielding.30,146
Solution processing techniques offer unparalleled scalability potential, with very high throughput capabilities and extremely low processing costs. Compatibility with existing coating and printing infrastructure minimizes capital investment requirements while enabling large-area applications such as flexible electronics and smart textiles. Critical optimization parameters include solvent selection, doping level control, and processing temperature management.288,289 Emerging techniques such as 3D printing allow for customizable geometries and direct device integration, opening new possibilities for personalized medical devices and complex electronic architectures. However, significant challenges remain in ink formulation, extrusion stability, and feature resolution. The technology's maturity level continues advancing rapidly, with recent developments in conductive filament chemistry showing promise for broader industrial adoption.290,291
Sol–gel methods offer exceptional chemical versatility and excellent compatibility with ceramic substrates, making them particularly valuable for high-temperature applications and functional coatings. Nevertheless, these processes often require extended processing times and precise control over gelation conditions, limiting throughput potential and increasing manufacturing complexity.292,293 Vapor phase polymerization represents a compromise between processing control and scalability, offering excellent film uniformity while accommodating heat-sensitive substrates. The method's moderate scalability reflects equipment complexity requirements and monomer vapor pressure considerations, though recent advances in reactor design are improving commercial prospects.294
Advanced hybrid approaches are revolutionizing CP manufacturing by combining multiple processing advantages. Layer-by-layer assembly enables precise multilayer functionality essential for battery applications, while plasma polymerization provides excellent adhesion for aerospace coatings. Electrospinning integration creates high surface area morphologies ideal for filtration and energy storage applications.295
The industrial landscape increasingly favors methods that balance processing flexibility with economic viability. Template-assisted synthesis, while offering exceptional structural control, faces scalability constraints due to template removal complexities and high processing costs. Conversely, interfacial polymerization shows promise for specialized membrane applications despite moderate scalability limitations.11 Manufacturing method selection must consider application-specific requirements, production volume targets, and quality specifications. High-volume commodity applications favor solution processing and chemical oxidative methods, while specialized high-performance applications justify the higher costs associated with electrochemical or vapor phase approaches. The integration of Industry 4.0 technologies, including real-time monitoring and machine learning optimization, is enhancing process control across all manufacturing platforms.296
Future developments in CP manufacturing will likely emphasize hybrid processing strategies that leverage complementary method advantages while minimizing individual limitations. Continuous processing integration, automated quality control, and sustainable manufacturing practices will drive the next generation of industrial CP production technologies.297 To further contextualize fabrication method selection for industrial deployment, Table 4 provides a comparative analysis of CP hybrid synthesis routes with respect to process scalability, cost, uniformity, substrate compatibility, and industrial relevance across key application domains.
Table 4 Comparative evaluation of major fabrication methods for conducting polymer (CP) hybrid materials in terms of scalability, cost, uniformity, substrate compatibility, industrial relevance, and key application domains. Critical process parameters are summarized to guide optimization for specific applications. This comparative matrix supports strategic selection based on industrial requirements and technological readiness levels (TRLs)
Method |
Scalability |
Cost |
Uniformity |
Substrate compatibility |
Industrial relevance |
Key applications |
Critical parameters |
Electrochemical polymerization |
Low-moderate |
Moderate-high |
Excellent (nanoscale control) |
Conductive substrates only |
High for specialized applications |
Supercapacitors, biosensors, neural interfaces, electrochromic devices |
Current density: 0.1–10 mA cm2; potential: 0.5–2.0 V vs. SCE32 |
Chemical oxidative polymerization |
High |
Low-moderate |
Good-excellent |
Universal compatibility |
Very high |
Antistatic coatings, EMI shielding, batteries |
Oxidant/monomer ratio: 1 : 1 to 4 : 1; temperature: −10 °C to 80 °C (ref. 30 and 146) |
In situ polymerization |
High |
Low-moderate |
Moderate-high |
Flexible, porous substrates |
Very high |
Textile electronics, composites, filtration membranes |
Monomer diffusion time, catalyst distribution37 |
Solution processing |
Very high |
Very low |
Moderate |
Films, fibers, membranes |
Extremely high |
Large-area coatings, printable electronics |
Solvent choice, doping level, processing temperature170,298 |
Vapor phase polymerization (VPP) |
Moderate |
Moderate-high |
Excellent |
Heat-sensitive substrates |
High |
Flexible electronics, biomedical devices |
Monomer vapor pressure, substrate temperature11,294 |
Template-assisted synthesis |
Low-moderate |
High |
Excellent |
Template-dependent |
Moderate-high |
Nanostructured devices, sensors |
Template pore size, removal conditions63,64 |
Interfacial polymerization |
Low-moderate |
Moderate |
Excellent |
Liquid–liquid interfaces |
Moderate |
Thin films, membranes, capsules |
pH gradient, interfacial tension11,65 |
Additive manufacturing (3D printing) |
Low-moderate |
High |
Design-dependent |
Custom geometries |
Emerging-high |
Prototyping, custom devices, bioelectronics |
Layer adhesion, conductivity retention53,56 |
11. Expert insights and ongoing debates
Leading researchers in CP hybrid materials have shared their insights to highlight current achievements and future directions. Scalability and synthesis: John Reynolds298,299 asked for the development of scalable, less expensive methods for the synthesis process. He refers to the very important problem of going from lab-scale to large-scale production if one is to realize all promising CP hybrid materials. Simplified and environmentally friendly synthesis methods will make these materials broadly applicable.300–302
11.1. Biomedical applications
According to Dr Natalie Stingelin,303,304 the unique properties of CPs, their electrical conductivity, and biocompatibility make them suitable for biomedical applications. She pitched the combination of CPs with other functional materials to achieve multifunctional systems related to neural interfaces, tissue engineering, and drug delivery.
11.2. Changes and opportunities with hybrid CP materials have occurred, but several debates remain
11.2.1. Role of nanostructures. The role of nanostructuring in the enhancement of properties such as conductivity and surface area remains debatable. While some researchers are of the view that nanostructuring is central to the improvement of these properties, others believe that the challenges created by synthesis and characterization may not be warranted by the derived benefits. Material choices for specific applications: researchers often do not agree on the choice of materials for a specific application. Some prefer carbon-material-based materials such as graphene and carbon nanotubes, while others prefer metal oxides or any other inorganic material with special functionality, such as catalytic activity or enhanced energy storage. Faradaic vs. Non-faradaic processes: a debate remains on either the optimization of faradaic processes by redox reactions to increase the energy density or the exploitation of non-faradaic processes, given faster charge–discharge capabilities with higher power densities. Strategies and synthetic costs: opinions range from new synthesis techniques that provide advanced structure and functionality control to the development of cost-effective methods that are scalable for industrial deployment. In a nutshell, research in the area of CP hybrid materials is ever-developing with contributions from renowned personalities and differences in opinions on critical aspects. Engaging in the issues discussed and focusing on scalable synopsis, multifunctional designs, and practical applications will become very important in pushing the field forward and looking for the full potential of CP hybrid materials.
12. Outlook and future work
In the area of CPs' hybrid materials, some of the future research areas would lie in the field of scalable synthesis and production methods that would fill the gap between laboratory-scale discovery and industrial applications. This type of research would dwell on material quality and performance maintenance with the growing volume of production.100
The key areas of application for CP hybrid materials span several technologically critical domains. These include (i) energy storage and conversion systems such as supercapacitors,21,269,305 batteries, and fuel cells;38,171,193 (ii) environmental remediation technologies,169,189,262 including heavy metal adsorption,164,176 dye degradation, and water purification membranes;182 (iii) biomedical engineering, particularly in biosensors,26,145,189 drug delivery systems, and bioelectronics;62,105,242 (iv) smart coatings and self-healing materials for corrosion protection and adaptive interfaces;27,229,230 and (v) flexible and wearable electronics,280 including electronic textiles, stretchable conductors, and implantable devices.24,299 These diverse application areas reflect the inherent multifunctionality of CP hybrids and underline their growing industrial relevance.
The most common concerns of CP hybrid materials are their stability and durability. Mechanistic studies of the degradation processes and strategies that ensure long-term stability and associated chemical and structural changes over time are important.306
Advanced characterization techniques, mainly in situ methods, will go a long way to uncovering the real-time procedures involved in these CP hybrid materials during their operation. This could reveal essential information concerning charge transfer, ionic movement, and structural changes.307
CP hybrids with multifunctionality in other words, the ability to perform functions simultaneously in one system, may enable more efficient and compact devices. In this respect, bio-inspired design approaches should be especially useful for this kind of research and may open the way for new structures that show improved performance.
Accelerating the identification of high-performance CP hybrids by data-driven material discovery using machine learning algorithms requires comprehensive databases and robust predictive models. At the molecular level, interfacial engineering is important for optimizing overall performance. State-of-the-art spectroscopic and microscopic methods combined with computational modeling can provide fundamental insights into the nature of interfacial phenomena.308
CP hybrids for flexible electronics, which can retain their properties under mechanical stress, are important for the development of wearable technology. This research focuses on new material compositions and structure-preserving functionality under deformation.197
In addition, the environmental impact and sustainability of these CP hybrid materials need to be carefully understood through detailed cradle-to-grave life cycle analyses. Further, such research should embrace all stages, from raw material sourcing to end-of-life considerations.305
Last, but not least, enhancing reproducibility through standardization is also critical for rapidly advancing the field. Standardized test protocols and methods for reporting results should be designed to increase the comparability between results from different research groups.
By addressing these research directions, the scientific community will be working toward more efficient, stable, and sustainable CP hybrid materials for environmental and energy applications. As the field progresses, there will be a continued requirement for the readjustment of research priorities to meet new challenges and opportunities. To provide a clearer comparative insight, Table 5 presents benchmarked performance metrics for CP hybrid materials relative to their conventional counterparts, highlighting the multifunctional advantages offered by hybrid integration
Table 5 Comparative performance benchmarks of conductive polymer (CP) hybrid materials versus conventional non-CP materials across key application-relevant properties. This benchmarking illustrates the superior multifunctionality and industrial potential of CP hybrids in emerging technologies, especially in energy storage, environmental remediation, and smart materials. Data compiled from representative studies across multiple systems
Property |
CP hybrid material example |
Performance (CP hybrid) |
Performance (conventional material) |
Electrical conductivity |
Polyaniline/graphene oxide |
100–1200 S cm−1 |
1–10 S cm−1 (pure CP), <1 S cm−1 (traditional polymers) |
Adsorption capacity |
Polypyrrole/carbon nanotube |
120–350 mg g−1 (e.g., heavy metals) |
50–150 mg g−1 (activated carbon) |
Thermal stability |
Polyaniline/silica |
Stable up to 300–400 °C |
200–250 °C (pure polymers) |
Mechanical flexibility |
PEDOT:PSS/textile composite |
High bendability (>5000 cycles) |
Low (<1000 cycles, brittle failure) |
Electrochemical stability |
Polyaniline/metal oxide |
Stable over 1000 charge/discharge cycles |
Moderate degradation after 300–500 cycles |
12.1. Promising research directions
Several promising and important areas of inquiry remain in the field of hybrid materials with conducting polymers. Therefore, future work could focus on developing nanostructured CP hybrids with increased surface areas and controlled morphologies. Such materials could make a significant difference in both sensors and energy storage devices because they can provide an increase in the number of active sites and faster charge transfer.161
Another promising direction is their integration with 2D materials such as graphene or MXenes. This combination is expected to result in exciting electronic properties and enhanced mechanical stability for flexible electronics and energy-conversion devices.309
Research on self-assembling CP hybrid systems is an exciting area. Such systems have the potential to be used for the generation of complex hierarchical structures with tailored properties at multiple length scales, which may eventually lead to breakthrough discoveries in subjects such as adaptive materials and intelligent coatings.310,311
Another promising research direction is the exploration of CP hybrids for thermoelectric applications. If the balance between electrical conductivity and thermal insulation can be optimized, these materials will significantly contribute to high-efficiency waste heat recovery systems and solid-state cooling devices.312
Among the most promising directions will be the development of biocompatible CP hybrids related to medical applications, which can have a tremendous impact on the development of biosensors, drug delivery, and tissue engineering scaffolds.313
Another promising direction is to investigate CP hybrids for application in electromagnetic shielding and absorption. As more electronic devices enter our lives and start to work at higher frequencies, there is a growing demand for shielding materials with good performance.314
Another avenue to explore is the use of CP hybrids in membranes for water treatment and gas separation. Such materials could provide improved selectivity and permeability compared to traditional membrane materials and ensure an enhanced, more sustainable separation process.315
These directions of research will open wide-ranging possibilities for the capability and application expansion of CP hybrid materials. As research on these lines unfolds, more understanding and opportunities may emerge to further move this area forward.316
12.2. Potential breakthroughs and their implications
A few next-generation breakthroughs of CPs hybrids will, therefore, have wide implications across many fields. The effect of one such breakthrough in the CP hybrid is the development of ultra-high ionic conductivity; batteries with higher charge rates and energy densities have the propensity to change the electric vehicle phase on roads and grid-scale energy storage systems.160
Another possibility is the production of CP hybrids with extremely high thermoelectric capabilities. This could dramatically change the process of waste heat reclamation in industry and make electronics with more effective cooling systems. The implications of this stretch include better energy efficiency in this production, as well as consumer electronics use.317
The development of CP hybrids with tunable and reversible properties in response to external stimuli is another area with vast growth potential. This may lead to the application of advanced sensors and actuators in fields such as soft robotics, adaptive structures, and smart textiles. These findings will pave the way for more sophisticated human–machine interfaces and an increased number of possibilities in the field of wearable technologies.318
Major advances in biocompatible and biodegradable CP hybrids can fundamentally change bioelectronics. New implantable devices are made, and after they have served their purposes, self-destruct inside the body without causing any harm, hence reducing invasive removal procedures. Applications include temporary neural interfaces for controlled drug delivery.246,319
The discovery of CP hybrids with exceptionally good catalytic properties might have broad implications for clean energy production. These materials may either make water splitting more feasible for hydrogen production or assist in the reduction of CO2 to useful chemicals. This discovery will have a considerable impact on the development of sustainable energy technologies and serve as a carbon abatement strategy.320
Finally, the development of CP-based hybrids with an ultrahigh level of stability and infinite self-repairing capability might provide a new generation of electronic devices and structural materials. Such a development would reduce electronic waste and technology longevity, whether in consumer electronics or utility-grade infrastructures.196
The potential breakthroughs of consequential impact, realized, would bring forward conductive hybrid materials in conducting polymers an advanced field of broader societal challenges in the energy, environment, healthcare, and technology sectors.321
In conclusion, the adoption of CP hybrid materials offers significant benefits across multiple dimensions. By combining the electrical conductivity and processability of conducting polymers with the robustness, functionality, and tunability of hybrid components, these materials enable the development of next-generation devices that are lightweight, flexible, and multifunctional. Importantly, many synthesis approaches now prioritize green chemistry principles, using water-based solvents, renewable monomers, and room-temperature processes.21,26,117,275 This aligns CP hybrid technology with broader goals of environmental sustainability and circular economy integration. For researchers, engineers, and industries alike, leveraging these materials opens pathways to more sustainable, high-performance solutions in energy, environment, electronics, and healthcare sectors.
13. Conclusion
CP hybrid materials are a breakthrough in materials science, as they bridge the properties of organic and inorganic components. This can improve the performance of energy storage, environmental remediation, and other multifunctional applications. Combining CPs is likely to increase the electrical conductivity, mechanical strength, and electrochemical activity of carbon nanotubes and metal oxide-based materials, making them suitable for advanced technological applications. Although these promises are significant, a few challenges persist. Scaling up the synthesis methods to an industrial level and the costs involved are vital issues that must be resolved. The long-term stability and complex interactions of CP hybrids must be addressed for their practical applications. Current characterization techniques provide some insights but are limited in their ability to capture dynamic interactions and behaviors.
In addition, emerging methodologies associated with in situ and multimodal characterizations further enhance the abilities of CP hybrids. Advanced approaches using synchrotron radiation techniques, cryo-electron microscopy, and machine learning will further deepen our understanding of their structure and performance. Therefore, inherently holds within these CP hybrid materials have a bright future driven by their multifunctional potential and continuously developing innovations in applications. Their future will depend on interdisciplinary collaboration among all scientific and engineering approaches to help overcome challenging points and further promote this field. Moreover, it is imperative to reflect on the impact of these materials on society and the environment as they move towards wider commercialization. CP hybrid materials hold significant potential for changing energy storage and rafts for other high-tech applications. Further research is required to address the remaining challenges and adopt new analysis methods to unleash the full potential of practical applications.
Data availability
The data supporting the findings of this study are available within the article and its supplementary materials. Additional data regarding experimental procedures, synthesis methods, and characterization results can be made available from the corresponding author upon reasonable request.
Author contributions
All authors contributed to this review. A. A. A. A. conceptualized and oversaw the project. A. A. and O. G. collected materials and drafted the manuscript. E. Q. and A. A. reviewed synthesis methods and structure–property relationships. V. M. and Y. M. focused on applications in energy storage and environmental sustainability. M. E. T. critically reviewed and refined the manuscript. All authors approved the final version for submission.
Conflicts of interest
The authors declare no conflict of interest.
References
- H. Ding, A. M. Hussein, I. Ahmad, R. Latef, J. K. Abbas, A. T. Abd Ali, S. M. Saeed, A. S. Abdulwahid, M. F. Ramadan and H. A. Rasool, Alexandria Eng. J., 2024, 88, 253–267 Search PubMed.
- K. Namsheer and C. S. Rout, RSC Adv., 2021, 11, 5659–5697 Search PubMed.
- M. G. Sumdani, M. R. Islam, A. N. A. Yahaya and S. I. Safie, Polym. Eng. Sci., 2022, 62, 269–303 Search PubMed.
- R. A. Nasser, S. S. Arya, K. H. Alshehhi, J. C. M. Teo and C. Pitsalidis, Trends Biotechnol., 2024, 42(6), 760–779 Search PubMed.
- B. Kurc, M. Pigłowska, Ł. Rymaniak and P. Fuć, Nanomaterials, 2021, 11, 538 Search PubMed.
- N. K and C. S. Rout, RSC Adv., 2021, 11, 5659–5697 Search PubMed.
- S. B. Aziz, T. J. Woo, M. F. Z. Kadir and H. M. Ahmed, J. Sci.:Adv. Mater. Devices, 2018, 3, 1–17 Search PubMed.
- P. Poizot, J. Gaubicher, S. Renault, L. Dubois, Y. Liang and Y. Yao, Chem. Rev., 2020, 120, 6490–6557 Search PubMed.
- D. Gielen, F. Boshell, D. Saygin, M. D. Bazilian, N. Wagner and R. Gorini, Energy Strategy Rev., 2019, 24, 38–50 Search PubMed.
- J. C. Carranza-Cruz, E. Rivera, G. Santana, S. Martínez-Gallegos and J. Illescas, MRS Adv., 2021, 6, 965–968 Search PubMed.
- L. Jiang, T. Luo, Z. Yang, Y. Wang, X. Xiao, R. Wang, H. Sun, H. Wang, P. Jin and B. Van der Bruggen, Adv. Funct. Mater., 2025, 2500708 Search PubMed.
- A. G. MacDiarmid, C. M. Mikulski, P. J. Russo, M. S. Saran, A. F. Garito and A. J. Heeger, J. Chem. Soc. Chem. Commun., 1975, 476–477 Search PubMed.
- A. J. Heeger, J. Phys. Chem. B, 2001, 105, 8475–8491 Search PubMed.
- J. L. Bredas, S. R. Marder and W. R. Salaneck, Macromolecules, 2002, 35(4) Search PubMed.
- A. B. Holmes, AlAn G. MAcDiArMiD, 2024, http://biographicalmemoirs.org/macdiarmid-alan-g.pdf Search PubMed.
- H. J. Emeléus, A. G. MacDiarmid and A. G. Maddock, J. Inorg. Nucl. Chem., 1955, 1, 194–201 Search PubMed.
- G. B. Street, H. Arnal, W. D. Gill, P. M. Grant and R. L. Greene, Mater. Res. Bull., 1975, 10, 877–881 Search PubMed.
- T. Ito, H. Shirakawa and S. Ikeda, J. Polym. Sci., Polym. Chem. Ed., 1974, 12, 11–20 Search PubMed.
- S. Raza, X. Li, F. Soyekwo, D. Liao, Y. Xiang and C. Liu, Eur. Polym. J., 2021, 160, 110773 Search PubMed.
- V. Sethumadhavan, S. Rudd, E. Switalska, K. Zuber, P. Teasdale and D. Evans, BMC Materials, 2019, 1, 1–14 Search PubMed.
- M. Masood, S. Hussain, M. Sohail, A. Rehman, M. A. Uzzaman, I. A. Alnaser, M. R. Karim and M. A. Wahab, ChemistrySelect, 2024, 9, e202302876 Search PubMed.
- X. Xu, J. Zhou and J. Chen, Adv. Funct. Mater., 2020, 30, 1904704 Search PubMed.
- X. Guo and A. Facchetti, Nat. Mater., 2020, 19, 922–928 Search PubMed.
- C. Li, K. Zhang, X. Cheng, J. Li, Y. Jiang, P. Li, B. Wang and H. Peng, Prog. Polym. Sci., 2023, 143, 101714 Search PubMed.
- Z. Rahimzadeh, S. M. Naghib, Y. Zare and K. Y. Rhee, J. Mater. Sci., 2020, 55, 7575–7611 Search PubMed.
- Y. Nagao, ChemElectroChem, 2024, e202300846 Search PubMed.
- M. Goyal, K. Singh and N. Bhatnagar, Prog. Org. Coat., 2024, 187, 108083 Search PubMed.
- Y. Yan, M. Han, Y. Jiang, E. L. L. Ng, Y. Zhang, C. Owh, Q. Song, P. Li, X. J. Loh and B. Q. Y. Chan, ACS Appl. Mater. Interfaces, 2024, 16, 5337–5354 Search PubMed.
- T. H. Le, Y. Kim and H. Yoon, Polymers, 2017, 9(4), 150 Search PubMed.
- N. Y. Abu-Thabit, J. Chem. Educ., 2016, 93, 1606–1611 Search PubMed.
- M. R. Saeb, P. Zarrintaj, P. Khandelwal and N. P. S. Chauhan, in Fundamentals and Emerging Applications of Polyaniline, ed. M. Mozafari and N. P. S. Chauhan, Elsevier, 2019, pp. 17–41, DOI:10.1016/B978-0-12-817915-4.00002-6.
- G. Fomo, T. Waryo, U. Feleni, P. Baker and E. Iwuoha, in Functional Polymers, ed. M. A. Jafar Mazumder, H. Sheardown and A. Al-Ahmed, Springer International Publishing, Cham, 2019, pp. 105–131, DOI:10.1007/978-3-319-95987-0_3.
- M. Beygisangchin, S. Abdul Rashid, S. Shafie, A. R. Sadrolhosseini and H. N. Lim, Polymers, 2021, 13(12), 2003 Search PubMed.
- J. Xue, T. Wu, Y. Dai and Y. Xia, Chem. Rev., 2019, 119, 5298–5415 Search PubMed.
- R. Abdulhussain, A. Adebisi, B. R. Conway and K. Asare-Addo, J. Drug Delivery Sci. Technol., 2023, 90, 105156 Search PubMed.
- C. A. C. Chazot, C. K. Jons and A. J. Hart, Adv. Funct. Mater., 2020, 30, 2005499 Search PubMed.
- F. Lin, X. Lu, Z. Wang, Q. Lu, G. Lin, B. Huang and B. Lu, Cellulose, 2019, 26, 1825–1839 Search PubMed.
- A. A. Yaqoob, A. Serrà, S. A. Bhawani, M. N. M. Ibrahim, A. Khan, H. S. Alorfi, A. M. Asiri, M. A. Hussein, A. A. P. Khan and K. Umar, Polymers, 2022, 14, 845 Search PubMed.
- Z. Zhao, C. Ma, L. Xu, Z. Yu, D. Wang, L. Jiang, X. Jiang and G. Gao, ACS Appl. Mater. Interfaces, 2023, 15(32), 38938–38945 Search PubMed.
- J. Ning, K. Duan, K. Wang, J. Liu, S. Wang and J. Zhang, J. Energy Chem., 2022, 67, 290–299 Search PubMed.
- S. P. Rwei, Y. H. Lee, J. W. Shiu, R. Sasikumar and U.-T. Shyr, Polymers, 2019, 11, 134 Search PubMed.
- Y. Wang and R. T. Yang, ACS Sustain. Chem. Eng., 2020, 8, 8295–8304 Search PubMed.
- R. Borah, K. R. Ag, A. C. Minja and S. W. Verbruggen, Small Methods, 2023, 7(6), 2201536 Search PubMed.
- L. Papammagari, S. R. Agnihotra, N. Manohar, R. M. Bouldin and S. K. Manohar, Macromolecules, 2021, 54, 1507–1516 Search PubMed.
- A. Cordoba, J. V. Cauich-Rodríguez, R. F. Vargas-Coronado, R. Velázquez-Castillo and K. Esquivel, Polymers, 2024, 16, 1125 Search PubMed.
- S. Shahidi, B. Moazzenchi and M. Ghoranneviss, Eur. Phys. J.:Appl. Phys., 2015, 71, 31302 Search PubMed.
- Y. Tian, Z. Yan, L. Jiang, R. Liu, B. Liu, Y. Shao, Y. Xu and M. Liu, Materials, 2024, 17, 5131 Search PubMed.
- Q. Shen, Q. Song, Z. Mai, K. R. Lee, T. Yoshioka, K. Guan, R. R. Gonzales and H. Matsuyama, Sci. Adv., 2023, 9, eadf6122 Search PubMed.
- P. D. Dalton, T. B. F. Woodfield, V. Mironov and J. Gröll, Adv. Sci., 2020, 7(11), 1902953 Search PubMed.
- R. Rizzo, D. Rütsche, H. Liu, P. Chansoria, A. Wang, A. Hasenauer and M. Zenobi-Wong, Adv. Mater. Technol., 2023, 8(11), 2201871 Search PubMed.
- K. Ariga, E. Ahn, M. Park and B. S. Kim, Chem.–Asian J., 2019, 14, 2553–2566 Search PubMed.
- V. A. Seleznev and V. Y. Prinz, Nanotechnology, 2016, 28, 064004 Search PubMed.
- H. Yuk, B. Lu, S. Lin, K. Qu, J. Xu, J. Luo and X. Zhao, Nat. Commun., 2020, 11, 1604 Search PubMed.
- Y. Cui, K. Aoyagi, Y. Zhao, K. Yamanaka, Y. Hayasaka, Y. Koizumi, T. Fujieda and A. Chiba, Addit. Manuf., 2020, 36, 101472 Search PubMed.
- K. Zhang, Z. Mao, G. Fu, D. Z. Zhang, C. Liu and Z. Li, Mater. Des., 2018, 157, 501–511 Search PubMed.
- J. Xiang, H. Lin, D. Wang, Y. Rao, J. P. M. Correia, S. Ahzi, Y. Peng and K. Wang, Compos. Commun., 2025, 58, 102499 Search PubMed.
- D. Navas, S. Fuentes, A. Castro-Alvarez and E. Chavez-Angel, Gels, 2021, 7(4), 275 Search PubMed.
- N. K and C. S. Rout, RSC Adv., 2021, 11, 5659–5697 Search PubMed.
- D. Chi, C. Liu, S. Qu, Z.-G. Zhang, Y. Li, Y. Li, J. Wang and Z. Wang, Synth. Met., 2013, 181, 117–122 Search PubMed.
- O. Shpotyuk, B. Bureau, V. Boyko, A. Ingram, R. Golovchak and C. Roiland, J. Non-Cryst. Solids, 2014, 392, 1–5 Search PubMed.
- S. J. Marje, P. K. Katkar, S. S. Pujari, S. A. Khalate, P. R. Deshmukh and U. M. Patil, Mater. Sci. Eng., B, 2020, 261, 114641 Search PubMed.
- V. L. S. dos Santos, R. C. Araújo, E. S. Lisboa, A. M. Lopes, R. L. de Albuquerque-Júnior, J. C. Cardoso, C. Blanco-Llamero, T. A. Deshpande, H. O. W. Anderson, R. Priefer, E. B. Souto and P. Severino, J. Drug Delivery Sci. Technol., 2024, 91, 105243 Search PubMed.
- V. Pavlenko, S. Khosravi, S. Żółtowska, A. B. Haruna, M. Zahid, Z. Mansurov, Z. Supiyeva, A. Galal, K. I. Ozoemena, Q. Abbas and T. Jesionowski, Mater. Sci. Eng., R, 2022, 149, 100682 Search PubMed.
- T. T. Vu, T. V. La, N. K. Tran and D. C. Huynh, J. Iran. Chem. Soc., 2020, 17, 229–245 Search PubMed.
- M. J. T. Raaijmakers and N. E. Benes, Prog. Polym. Sci., 2016, 63, 86–142 Search PubMed.
- A. T. Lawal and G. G. Wallace, Talanta, 2014, 119, 133–143 Search PubMed.
- S. Lee, D. Park, Y. Cho, J. Lee and J. Kim, Synth. Met., 2022, 291, 117183 Search PubMed.
- N. A. Patil and B. Kandasubramanian, Eur. Polym. J., 2021, 146, 110248 Search PubMed.
- E. Liarou, S. Varlas, D. Skoulas, C. Tsimblouli, E. Sereti, K. Dimas and H. Iatrou, Prog. Polym. Sci., 2018, 83, 28–78 Search PubMed.
- M. G. Tadesse, A. S. Ahmmed and J. F. Lübben, J. Compos. Sci., 2024, 8, 53 Search PubMed.
- N. Sharma, A. Singh, N. Kumar, A. Tiwari, M. Lal and S. Arya, J. Mater. Sci., 2024, 59, 6206–6244 Search PubMed.
- Z. Ali, S. Yaqoob, J. Yu and A. D'Amore, Compos., Part C: Open Access, 2024, 13, 100434 Search PubMed.
- J. Huang, Y. Yuan, Y. Shao and Y. Yan, Nat. Rev. Mater., 2017, 2, 17042 Search PubMed.
- K. Akhtar, S. A. Khan, S. B. Khan and A. M. Asiri, in Handbook of Materials Characterization, ed. S. K. Sharma, Springer International Publishing, Cham, 2018, DOI:10.1007/978-3-319-92955-2_4, pp. 113–145.
- B. J. Inkson, in Materials Characterization Using Nondestructive Evaluation (NDE) Methods, ed. G. Hübschen, I. Altpeter, R. Tschuncky and H.-G. Herrmann, Woodhead Publishing, 2016, pp. 17–43, DOI:10.1016/B978-0-08-100040-3.00002-X.
- H. Jinnai, Microscopy, 2022, 71, i148–i164 Search PubMed.
- C. Zhu, K. Kaufmann and K. S. Vecchio, Ultramicroscopy, 2020, 208, 112851 Search PubMed.
- B. Lu, X. Wang, N. Liu, K. He, K. Wu, H. Li and X. Tang, Spectrochim. Acta, Part A, 2020, 239, 118455 Search PubMed.
- F. M. Alcorn, P. K. Jain and R. M. van der Veen, Nat. Rev. Chem., 2023, 7, 256–272 Search PubMed.
- J. Mast, E. Verleysen, V.-D. Hodoroaba and R. Kaegi, in Characterization of Nanoparticles, ed. V.-D. Hodoroaba, W. E. S. Unger and A. G. Shard, Elsevier, 2020, DOI:10.1016/B978-0-12-814182-3.00004-3, pp. 29–48.
- J. Epp, in Materials Characterization Using Nondestructive Evaluation (NDE) Methods, ed. G. Hübschen, I. Altpeter, R. Tschuncky and H.-G. Herrmann, Woodhead Publishing, 2016, pp. 81–124, DOI:10.1016/B978-0-08-100040-3.00004-3.
- A. Pandey, S. Dalal, S. Dutta and A. Dixit, J. Mater. Sci.: Mater. Electron., 2021, 32, 1341–1368 Search PubMed.
- A. Kassem, L. Abbas, O. Coutinho, S. Opara, H. Najaf, D. Kasperek, K. Pokhrel, X. Li and S. Tiquia-Arashiro, Front. Microbiol., 2023, 14, 1304081 Search PubMed.
- S. A. Khan, S. B. Khan, L. U. Khan, A. Farooq, K. Akhtar and A. M. Asiri, in Handbook of Materials Characterization, ed. S. K. Sharma, Springer International Publishing, Cham, 2018, pp. 317–344, DOI:10.1007/978-3-319-92955-2_9.
- M. Deluca, H. Hu, M. N. Popov, J. Spitaler and T. Dieing, Commun. Mater., 2023, 4, 78 Search PubMed.
- R. S. Das and Y. K. Agrawal, Vib. Spectrosc., 2011, 57, 163–176 Search PubMed.
- D. Coetzee, M. Venkataraman, J. Militky and M. Petru, Polymers, 2020, 12 Search PubMed.
- K. Ke, L. Yue, H. Shao, M.-B. Yang, W. Yang and I. Manas-Zloczower, Carbon, 2021, 173, 1020–1040 Search PubMed.
- H. S. Magar, R. Y. A. Hassan and A. Mulchandani, Sensors, 2021, 21 Search PubMed.
- S. Wang, J. Zhang, O. Gharbi, V. Vivier, M. Gao and M. E. Orazem, Nat. Rev. Methods Primers, 2021, 1, 41 Search PubMed.
- S. Tan, C. Li, C. Peng, W. Yan, H. Bu, H. Jiang, F. Yue, L. Zhang, H. Gao and Z. Zhou, Nat. Commun., 2024, 15, 4136 Search PubMed.
- N. M. Nurazzi, N. Abdullah, M. N. F. Norrrahim, S. H. Kamarudin, S. Ahmad, S. S. Shazleen, M. Rayung, M. R. M. Asyraf, R. A. Ilyas and M. Kuzmin, in Polylactic Acid-Based Nanocellulose and Cellulose Composites, CRC Press, 2022, pp. 145–164 Search PubMed.
- K. Deshmukh, T. Kovářík, A. Muzaffar, M. Basheer Ahamed and S. K. Khadheer Pasha, in Polymer Science and Innovative Applications, ed. M. A. A. AlMaadeed, D. Ponnamma and M. A. Carignano, Elsevier, 2020, pp. 117–152, DOI:10.1016/B978-0-12-816808-0.00004-4.
- K. Müllen and U. Scherf, Macromol. Chem. Phys., 2023, 224, 2200337 Search PubMed.
- A. B. Kanu, J. Chromatogr. A, 2021, 1654, 462444 Search PubMed.
- A. Kourkopoulos, D. T. H. M. Sijm and M. F. Vrolijk, Compr. Rev. Food Sci. Food Saf., 2022, 21, 4108–4129 Search PubMed.
- F. Petter, C. Trontin, G. Anthoine, M. Ravnikar, T. Dreo, T. Lukežič, A. Vučurović and N. Mehle, Critical Points for the Organisation of Test Performance Studies in Microbiology: Plant Pathogens as a Case Study, 2022, pp. 7–14 Search PubMed.
- J. Pum, in Advances in Clinical Chemistry, ed. G. S. Makowski, Elsevier, 2019, vol. 90, pp. 215–281 Search PubMed.
- S. Hosbas Coskun, S. A. Wise and A. J. Kuszak, Front. Nutr., 2021, 8, 786261 Search PubMed.
- P. P. Das, V. Chaudhary, R. Kumar Singh, D. Singh and A. Aditya Bachchan, Mater. Today: Proc., 2021, 47, 3794–3801 Search PubMed.
- A. Murad Bhayo, Y. Yang and X. He, Prog. Mater. Sci., 2022, 130, 101000 Search PubMed.
- S. Kumari, S. Raturi, S. Kulshrestha, K. Chauhan, S. Dhingra, K. András, K. Thu, R. Khargotra and T. Singh, J. Mater. Res. Technol., 2023, 27, 1739–1763 Search PubMed.
- C. A. Ávila-Orta, P. González-Morones, C. J. Espinoza-González, J. G. Martínez-Colunga, M. G. Neira-Velázquez, A. Sáenz-Galindo and L. I. López-López, Syntheses and Applications of Carbon Nanotubes and Their Composites, 2013, pp. 1–20 Search PubMed.
- G. Kickelbick, Hybrid Mater., 2007, 1, 2 Search PubMed.
- M. R. Abidian, D. H. Kim and D. C. Martin, Adv. Mater., 2006, 18, 405–409 Search PubMed.
- T. Chen, H. Z. Lu, J. A. Lin, W. S. Cai, D. Z. Zhu and C. Yang, J. Mater. Res. Technol., 2023, 25, 3496–3506 Search PubMed.
- M. Seydibeyoğlu, A. Dogru, J. Wang, M. Rencheck, Y. Han, L. Wang, E. A. Seydibeyoğlu, X. Zhao, K. Ong, J. A. Shatkin, S. Shams Es-Haghi, S. Bhandari, S. Ozcan and D. J. Gardner, Polymers, 2023, 15 Search PubMed.
- B. Das, I. Aguilera, U. Rau and T. Kirchartz, Adv. Opt. Mater., 2022, 10, 2101947 Search PubMed.
- J. Euvrard, Y. Yan and D. B. Mitzi, Nat. Rev. Mater., 2021, 6, 531–549 Search PubMed.
- J. Maier, Z. Anorg. Allg. Chem., 2017, 643, 2083–2087 Search PubMed.
- P. Chandrasekhar and P. Chandrasekhar, Conducting Polymers, Fundamentals and Applications: A Practical Approach, 1999, pp. 3–22 Search PubMed.
- S. Nasresfahani, Z. Zargarpour, M. H. Sheikhi and S. F. N. Ana, Synth. Met., 2020, 265, 116404 Search PubMed.
- L. Jiang, M. Zhu, M. An, Y. Li, W. Miao, Z. Wang and B. S. Hsiao, Polymer, 2019, 179, 121625 Search PubMed.
- Y. Liu, S. Gao, X. Zhang, J. H. Xin and C. Zhang, J. Mater. Chem. C, 2023, 11, 12–47 Search PubMed.
- S. Wang, F. Li, A. D. Easley and J. L. Lutkenhaus, Nat. Mater., 2019, 18, 69–75 Search PubMed.
- X.-X. Wang, G.-F. Yu, J. Zhang, M. Yu, S. Ramakrishna and Y.-Z. Long, Prog. Mater. Sci., 2021, 115, 100704 Search PubMed.
- F. Lang, J. Pang and X.-H. Bu, eScience, 2024, 4, 100231 Search PubMed.
- N. Nasajpour-Esfahani, D. Dastan, A. a. Alizadeh, P. Shirvanisamani, M. Rozati, E. Ricciardi, B. Lewis, A. Aphale and D. Toghraie, J. Ind. Eng. Chem., 2023, 125, 14–37 Search PubMed.
- Y.-J. Park, S. Lee, B. Kim, J.-H. Kim, J.-H. So and H.-J. Koo, Composites, Part B, 2020, 202, 108412 Search PubMed.
- E. Yousif and R. Haddad, SpringerPlus, 2013, 2, 398 Search PubMed.
- J.-F. Lutz and H. G. Börner, Prog. Polym. Sci., 2008, 33, 1–39 Search PubMed.
- P. Gomez-Romero, A. Pokhriyal, D. Rueda-García, L. N. Bengoa and R. M. González-Gil, Chem. Mater., 2024, 36, 8–27 Search PubMed.
- D. Raabe, J. R. Mianroodi and J. Neugebauer, Nat. Comput. Sci., 2023, 3, 198–209 Search PubMed.
- H.-I. Un, S. A. Gregory, S. K. Mohapatra, M. Xiong, E. Longhi, Y. Lu, S. Rigin, S. Jhulki, C.-Y. Yang, T. V. Timofeeva, J.-Y. Wang, S. K. Yee, S. Barlow, S. R. Marder and J. Pei, Adv. Energy Mater., 2019, 9, 1900817 Search PubMed.
- X. Wei, P. Zhang, T. Xu, H. Zhou, Y. Bai and Q. Chen, Chem. Soc. Rev., 2022, 51, 10016–10063 Search PubMed.
- M. Rahim, R. Ullah, R. Khattak and I. Rahim, Polym. Bull., 2024, 81, 13207–13226 Search PubMed.
- B. Wei, W. Luo, J. Du, Y. Ding, Y. Guo, G. Zhu, Y. Zhu and B. Li, SusMat, 2024, e239 Search PubMed.
- M. Fahlman, S. Fabiano, V. Gueskine, D. Simon, M. Berggren and X. Crispin, Nat. Rev. Mater., 2019, 4, 627–650 Search PubMed.
- I. Dědek, V. Kupka, P. Jakubec, V. Šedajová, K. Jayaramulu and M. Otyepka, Appl. Mater. Today, 2022, 26, 101387 Search PubMed.
- B. Mekuye and B. Abera, Nano Sel., 2023, 4, 486–501 Search PubMed.
- X. Geng, T. Du, C. Xu, Y. Liu, Y. Deng and Y. Geng, Adv. Funct. Mater., 2023, 33, 2300809 Search PubMed.
- Q. Wang, J. Su, H. Chen, D. Wang, X. Tian, Y. Zhang, X. Feng, S. Wang, J. Li and H. Jin, Adv. Funct. Mater., 2022, 32, 2209201 Search PubMed.
- A. Ahmed, A. Fardin, M. Tanjilul, Y. S. Wong, M. Rahman and A. Senthil Kumar, Int. J. Adv. Des. Manuf. Technol., 2018, 94, 2729–2737 Search PubMed.
- R. Das, Proc. Inst. Mech. Eng., Part E, 2016, 230, 474–485 Search PubMed.
- Y. Sun, X. Huang, Y. Jin, Y. Li, Z. Li, Y. Zou, Y. Sun and W. Xu, Inorg. Chem., 2022, 61, 5060–5066 Search PubMed.
- S. Cano, A. Gooneie, C. Kukla, G. Rieß, C. Holzer and J. Gonzalez-Gutierrez, Appl. Sci., 2020, 10, 1471 Search PubMed.
- J. Liang, R. Cui, X. Zhang, K. Koumoto and C. Wan, Adv. Funct. Mater., 2023, 33, 2208813 Search PubMed.
- E. Piatti, A. Arbab, F. Galanti, T. Carey, L. Anzi, D. Spurling, A. Roy, A. Zhussupbekova, K. A. Patel and J. M. Kim, Nat. Electron., 2021, 4, 893–905 Search PubMed.
- U. Dirnagl, G. N. Duda, D. W. Grainger, P. Reinke and R. Roubenoff, Adv. Drug Delivery Rev., 2022, 182, 114118 Search PubMed.
- G. Yu, X. Xie, L. Pan, Z. Bao and Y. Cui, Nano Energy, 2013, 2, 213–234 Search PubMed.
- I. A. Kinloch, J. Suhr, J. Lou, R. J. Young and P. M. Ajayan, Science, 2018, 362, 547–553 Search PubMed.
- L. Hao, C. Dong, L. Zhang, K. Zhu and D. Yu, Polymers, 2022, 14 Search PubMed.
- J. Pan, H. Shen and S. Mathur, J. Nanotechnol., 2012, 2012, 917320 Search PubMed.
- M. Idrees, A. Razaq, A. Islam, S. Yasmeen, K. Sultana, M. H. Asif and M. Nadeem, Synth. Met., 2017, 232, 138–143 Search PubMed.
- H. Cai, Z. Liu, M. Xu, L. Chen, X. Chen, L. Cheng, Z. Li and F. Dai, Electrochim. Acta, 2021, 390, 138895 Search PubMed.
- O. Okhay and A. Tkach, Nanomaterials, 2022, 12, 2531 Search PubMed.
- S. Bhandari, in Polyaniline Blends, Composites, and Nanocomposites, ed. P. M. Visakh, C. D. Pina and E. Falletta, Elsevier, 2018, pp. 23–60, DOI:10.1016/B978-0-12-809551-5.00002-3.
- M. Beygisangchin, A. Hossein Baghdadi, S. Kartom Kamarudin, S. Abdul Rashid, J. Jakmunee and N. Shaari, Eur. Polym. J., 2024, 210, 112948 Search PubMed.
- Y. Shen, Z. Qin, T. Li, F. Zeng, Y. Chen and N. Liu, Electrochim. Acta, 2020, 356, 136841 Search PubMed.
- Z. Guo, S. Chakraborty, F. A. Monikh, D.-D. Varsou, A. J. Chetwynd, A. Afantitis, I. Lynch and P. Zhang, Adv. Biol., 2021, 5, 2100637 Search PubMed.
- P. Govindaraj, A. Sokolova, N. Salim, S. Juodkazis, F. K. Fuss, B. Fox and N. Hameed, Composites, Part B, 2021, 226, 109353 Search PubMed.
- S. Mourdikoudis, R. M. Pallares and N. T. K. Thanh, Nanoscale, 2018, 10, 12871–12934 Search PubMed.
- Y. Yao, Q. Dong, A. Brozena, J. Luo, J. Miao, M. Chi, C. Wang, I. G. Kevrekidis, Z. J. Ren, J. Greeley, G. Wang, A. Anapolsky and L. Hu, Science, 376, eabn3103 Search PubMed.
- E. Ortiz Ortega, H. Hosseinian, M. J. Rosales López, A. Rodríguez Vera and S. Hosseini, in Material Characterization Techniques and Applications, ed. E. Ortiz Ortega, H. Hosseinian, I. B. Aguilar Meza, M. J. Rosales López, A. Rodríguez Vera and S. Hosseini, Springer Singapore, Singapore, 2022, pp. 93–152, DOI:10.1007/978-981-16-9569-8_4.
- V. Novotna, J. Horak, M. Konecny, V. Hegrova, O. Novotny, Z. Novacek and J. Neuman, Microsc. Today, 2020, 28, 38–46 Search PubMed.
- A. Alipour, K. T. Arat, H. Alemansour, L. Montes, J. Gardiner, J. Diederichs, B. Colvin, A. Amann, K. Jensen, W. Neils, S. Spagna, L. Stühn, S. Seibert, H. Frerichs, M. Wolff and C. H. Schwalb, Microsc. Today, 2023, 31, 17–22 Search PubMed.
- Y. H. Budnikova, E. L. Dolengovski, M. V. Tarasov and T. V. Gryaznova, J. Solid State Electrochem., 2024, 28, 659–676 Search PubMed.
- F. Zhao, Y. Shi, L. Pan and G. Yu, Acc. Chem. Res., 2017, 50, 1734–1743 Search PubMed.
- K. Zarean Mousaabadi, A. A. Ensafi, R. Fazel-Zarandi and A. Vahabi, J. Iran. Chem. Soc., 2024, 21, 1769–1794 Search PubMed.
- N. Singh and U. Riaz, Polym. Bull., 2022, 79, 10377–10408 Search PubMed.
- S. Iqbal and S. Ahmad, J. Ind. Eng. Chem., 2018, 60, 53–84 Search PubMed.
- Z. Liu, Z. Gao, L. Xu and F. Hu, RSC Adv., 2020, 10, 17524–17533 Search PubMed.
- C. Zhou, H. Zhu, Q. Wang, J. Wang, J. Cheng, Y. Guo, X. Zhou and R. Bai, RSC Adv., 2017, 7, 18466–18479 Search PubMed.
- S. Anuma, P. Mishra and B. R. Bhat, J. Hazard. Mater., 2021, 416, 125929 Search PubMed.
- K. H. Rahman and A. K. Kar, J. Environ. Chem. Eng., 2020, 8, 104181 Search PubMed.
- M. Dutta and S. De, Chem. Eng. Sci., 2024, 285, 119581 Search PubMed.
- S. Mobasser, Y. Wager and T. M. Dittrich, Ind. Eng. Chem. Res., 2022, 61, 6791–6801 Search PubMed.
- T. Xu, X. Cui, Y. Xiao, T. Chen, X. Xiao and Y. Wang, ACS Appl. Mater. Interfaces, 2023, 15, 9604–9617 Search PubMed.
- M. I. Khan, M. K. Almesfer, A. Elkhaleefa, I. Shigidi, M. Z. M. Shamim, I. H. Ali and M. Rehan, Polymers, 2021, 13, 3810 Search PubMed.
- M. Chigondo, B. C. Nyamunda, M. Maposa and F. Chigondo, Water Sci. Technol., 2022, 85, 1600–1619 Search PubMed.
- Y. Wang, Q. Wen, Y. Chen and W. Li, Energy, 2020, 204, 117942 Search PubMed.
- S. B. Kondawar, S. P. Agrawal, S. H. Nimkar, H. J. Sharma and P. T. Patil, Adv. Mater. Lett., 2012, 3, 393–398 Search PubMed.
- J. Chang, X. Zhang, Z. Wang, C. Li, Q. Hu, J. Gao and L. Feng, ACS Appl. Nano Mater., 2021, 4, 5263–5272 Search PubMed.
- L.-Y. Guo, S.-Y. Xia, Y. Tan and Z. Huang, Sensors, 2022, 22, 4103 Search PubMed.
- X. Liu, W. Zheng, R. Kumar, M. Kumar and J. Zhang, Coord. Chem. Rev., 2022, 462, 214517 Search PubMed.
- S. Afreen, N. Talreja, D. Chauhan and M. Ashfaq, in Multifunctional Hybrid Nanomaterials for Sustainable Agri-Food and Ecosystems, ed. K. A. Abd-Elsalam, Elsevier, 2020, pp. 335–353, DOI:10.1016/B978-0-12-821354-4.00015-7.
- X. Xu, S. Yang, Y. Wang and K. Qian, Green Anal. Chem., 2022, 2, 100020 Search PubMed.
- S. Satyam and S. Patra, Heliyon, 2024, 10, e29573 Search PubMed.
- L. Zhang, R. Guo, H. Li, Q. Du, J. Lu, Y. Huang, Z. Yan and J. Chen, J. Hazard. Mater., 2020, 394, 122531 Search PubMed.
- Q. Zhang, X. Jiang, A. M. Kirillov, Y. Zhang, M. Hu, W. Liu, L. Yang, R. Fang and W. Liu, ACS Sustain. Chem. Eng., 2019, 7, 3203–3212 Search PubMed.
- M. Ahmed, M. O. Mavukkandy, A. Giwa, M. Elektorowicz, E. Katsou, O. Khelifi, V. Naddeo and S. W. Hasan, npj Clean Water, 2022, 5, 12 Search PubMed.
- T. S. Vo, K. M. Lwin and K. Kim, Adv. Compos. Hybrid Mater., 2024, 7, 127 Search PubMed.
- E. Pantuso, E. Ahmed, E. Fontananova, A. Brunetti, I. Tahir, D. P. Karothu, N. A. Alnaji, G. Dushaq, M. Rasras, P. Naumov and G. Di Profio, Nat. Commun., 2023, 14, 5751 Search PubMed.
- I. Ali, S. Zenab Hasan, H. Garcia, M. K. Danquah and G. Imanova, Chem. Eng. J., 2024, 483, 149108 Search PubMed.
- A. Sikder, A. K. Pearce, S. J. Parkinson, R. Napier and R. K. O'Reilly, ACS Appl. Polym. Mater., 2021, 3, 1203–1217 Search PubMed.
- L. Cherwoo, I. Gupta, R. Bhatia and H. Setia, Energy, Ecol. Environ., 2024, 9, 25–41 Search PubMed.
- G. J. Adekoya, O. C. Adekoya, M. Muloiwa, E. R. Sadiku, W. K. Kupolati and Y. Hamam, Small, 2024, 20, 2403656 Search PubMed.
- Y. Chen, J. Huang, Z. Chen, C. Shi, H. Yang, Y. Tang, Z. Cen, S. Liu, R. Fu and D. Wu, Advanced Science, 2022, 9, 2103477 Search PubMed.
- D. Wachholz Junior, B. M. Hryniewicz and L. Tatsuo Kubota, Chemosphere, 2024, 352, 141479 Search PubMed.
- A. Choudhary, A. Sharma, A. Singh, S. S. Han and A. Sood, Adv. Eng. Mater., 2024, 2400944 Search PubMed.
- T. B. Fischer, M. Chang and T. Muthoora, BMC Public Health, 2024, 24, 2819 Search PubMed.
- X. Wang, P. Wang, C. Wang, J. Chen, B. Hu, S. Liu and Q. Yuan, Environ. Res., 2021, 199, 111418 Search PubMed.
- A. Javid, S. Ali, A. Hasan, N. Senthilkumar, J. Ranjitha and A. Hussain, Chemosphere, 2022, 301, 134703 Search PubMed.
- Z. Chen, X. Li, C. Yang, K. Cheng, T. Tan, Y. Lv and Y. Liu, Adv. Sci., 2021, 8, 2101883 Search PubMed.
- C. Zeng, Y. Yuan, H. Cao, K. Panchabikesan and F. Haghighat, J. Energy Storage, 2024, 80, 110249 Search PubMed.
- A. Moyseowicz, D. Minta and G. Gryglewicz, ChemElectroChem, 2023, 10, e202201145 Search PubMed.
- G. Prunet, F. Pawula, G. Fleury, E. Cloutet, A. J. Robinson, G. Hadziioannou and A. Pakdel, Mater. Today Phys., 2021, 18, 100402 Search PubMed.
- A. E. Pérez Mendoza, C. Andronescu and A. Olean-Oliveira, Synth. Met., 2024, 307, 117662 Search PubMed.
- R. Rohib, S. U. Rehman, E. Lee, C. Kim, H. Lee, S.-B. Lee and G.-G. Park, Sci. Rep., 2023, 13, 19832 Search PubMed.
- C. Vogt and B. M. Weckhuysen, Nat. Rev. Chem., 2022, 6, 89–111 Search PubMed.
- M. S. Chavali and M. P. Nikolova, SN Appl. Sci., 2019, 1, 607 Search PubMed.
- H. H. Al-Refai, A. A. Ganash and M. A. Hussein, Mater. Today Commun., 2021, 26, 101935 Search PubMed.
- S. S. Shindalkar, M. Reddy, R. Singh, M. A. M. Nainar and B. Kandasubramanian, Synth. Met., 2023, 299, 117467 Search PubMed.
- L. Liu, K. Cao, S. Chen and W. Huang, Adv. Opt. Mater., 2020, 8, 2001122 Search PubMed.
- M. Jiang, R. Wang, Z. Deng, G. Xu, Q. Shangguan, L. Sun, L. Zhang and X. Yang, ACS Appl. Mater. Interfaces, 2024, 16, 51265–51273 Search PubMed.
- H. Zhao, Z. Li, X. Lu, W. Chen, Y. Cui, B. Tang, J. Wang and X. Wang, J. Text. Inst., 2021, 112, 1850–1858 Search PubMed.
- L. Zhang, X.-L. Shi, Y.-L. Yang and Z.-G. Chen, Mater. Today, 2021, 46, 62–108 Search PubMed.
- P. Wu, Z. He, M. Yang, J. Xu, N. Li, Z. Wang, J. Li, T. Ma, X. Lu, H. Zhang and T. Zhang, Int. J. Thermophys., 2021, 42, 111 Search PubMed.
- R. T. Yadlapalli, R. R. Alla, R. Kandipati and A. Kotapati, J. Energy Storage, 2022, 49, 104194 Search PubMed.
- J. Yoon, J. Lee, Y. S. Yun, H. w. Kwak and H.-J. Jin, Macromol. Res., 2024 DOI:10.1007/s13233-024-00327-w.
- S. Sharma and P. Chand, Results Chem., 2023, 5, 100885 Search PubMed.
- K. A. Severson, P. M. Attia, N. Jin, N. Perkins, B. Jiang, Z. Yang, M. H. Chen, M. Aykol, P. K. Herring, D. Fraggedakis, M. Z. Bazant, S. J. Harris, W. C. Chueh and R. D. Braatz, Nat. Energy, 2019, 4, 383–391 Search PubMed.
- O. Z. Sharaf and M. F. Orhan, Renewable Sustainable Energy Rev., 2014, 32, 810–853 Search PubMed.
- S. Anantharaj, P. E. Karthik and S. Noda, Angew. Chem., Int. Ed., 2021, 60, 23051–23067 Search PubMed.
- T. Kumari, S. Jung, Y. Cho, H.-P. Kim, J. W. Lee, J. Oh, J. Lee, S. M. Lee, M. Jeong and J. M. Baik, Nano Energy, 2020, 68, 104327 Search PubMed.
- C. Stetson, Y. Yin, A. Norman, S. P. Harvey, M. Schnabel, C. Ban, C.-S. Jiang, S. C. DeCaluwe and M. Al-Jassim, J. Power Sources, 2021, 482, 228946 Search PubMed.
- Q. H. Zhang, B. S. Hou, Y. Y. Li, G. Y. Zhu, Y. Lei, X. Wang, H. F. Liu and G. A. Zhang, Chem. Eng. J., 2021, 424, 130519 Search PubMed.
- K. Lovato, P. S. Fier and K. M. Maloney, Nat. Rev. Chem., 2021, 5, 546–563 Search PubMed.
- T. G. Ritter, S. Pappu and R. Shahbazian-Yassar, Adv. Energy Sustainability Res., 2024, 5, 2300297 Search PubMed.
- M. Skiborowski, Curr. Opin. Chem. Eng., 2018, 22, 216–225 Search PubMed.
- G. Kothandam, G. Singh, X. Guan, J. M. Lee, K. Ramadass, S. Joseph, M. Benzigar, A. Karakoti, J. Yi, P. Kumar and A. Vinu, Advanced Science, 2023, 10, 2301045 Search PubMed.
- P. P. Deshpande, N. G. Jadhav, V. J. Gelling and D. Sazou, J. Coat. Technol. Res., 2014, 11, 473–494 Search PubMed.
- N. Varghese, T. Francis, M. Shelly and A. B. Nair, in Nanoscale Processing, ed. S. Thomas and P. Balakrishnan, Elsevier, 2021, pp. 383–406, DOI:10.1016/B978-0-12-820569-3.00014-1.
- D. T. Oloruntoba, T. E. Odemona, O. S. Adesina, W. T. Owolabi, O. O. Sanyaolu and A. L. Rominiyi, J. Bio Tribo Corros., 2024, 10, 43 Search PubMed.
- U. M. Angst, Corrosion, 2019, 75, 1420–1433 Search PubMed.
- M. B. Singh, B. I. Gabriel, M. S. Venkatraman, I. S. Cole, C. G. Moorthy and B. Emmanuel, J. Chem. Sci., 2022, 134, 32 Search PubMed.
- L. Deng, K. Miyatani, M. Suehara, S.-i. Amma, M. Ono, S. Urata and J. Du, npj Mater. Degrad., 2021, 5, 15 Search PubMed.
- L. Yadav, A. Sihmar, S. Kumar, H. Dhaiya and R. Vishwakarma, Environ. Sci. Pollut. Res., 2024, 1–27 Search PubMed.
- H. Es-soufi, E. Berdimurodov, M. I. Sayyed and L. Bih, Environ. Sci. Pollut. Res., 2024, 1–27 Search PubMed.
- T. Liu, L. Ma, X. Wang, J. Wang, H. Qian, D. Zhang and X. Li, Corros. Commun., 2021, 1, 18–25 Search PubMed.
- F. Zhang, P. Ju, M. Pan, D. Zhang, Y. Huang, G. Li and X. Li, Corros. Sci., 2018, 144, 74–88 Search PubMed.
- M. K. Zadeh, M. Yeganeh, M. T. Shoushtari and A. Esmaeilkhanian, Synth. Met., 2021, 274, 116723 Search PubMed.
- H. Aljibori, A. Al-Amiery and W. N. R. Isahak, J. Bio Tribo Corros., 2024, 10, 78 Search PubMed.
- T. D. Bennett, S. Horike, J. C. Mauro, M. M. Smedskjaer and L. Wondraczek, Nat. Chem., 2024, 16(11), 1755–1766 Search PubMed.
- L. Hu, X. Song, D. Jin, C. Xing, X. Shan, X. Zhao, F. Guo and P. Xiao, J. Am. Ceram. Soc., 2019, 102, 1386–1393 Search PubMed.
- E. A. Schafer, E. Davis, Z. A. Manzer, S. Daniel and J. Rivnay, ACS Appl. Mater. Interfaces, 2023, 15, 24638–24647 Search PubMed.
- W. K. Oh, O. S. Kwon and J. Jang, Polym. Rev., 2013, 53, 407–442 Search PubMed.
- K. Parashar, D. G. Prajapati, R. A. McIntyre and B. Kandasubramanian, Ind. Eng. Chem. Res., 2020, 59, 9707–9718 Search PubMed.
- V. S. Vajrala, V. Saunier, L. G. Nowak, E. Flahaut, C. Bergaud and A. Maziz, Front. Bioeng. Biotechnol., 2021, 9, 780197 Search PubMed.
- G. Maduraiveeran, J. Anal. Sci. Technol., 2022, 13(1), 35 Search PubMed.
- S. Cajigas and J. Orozco, Molecules, 2020, 25, 3542 Search PubMed.
- M. Bansal, A. Dravid, Z. Aqrawe, J. Montgomery, Z. Wu and D. Svirskis, J. Controlled Release, 2020, 328, 192–209 Search PubMed.
- S. A. A. Shah, M. Fırlak, S. R. Berrow, N. R. Halcovitch, S. J. Baldock, B. M. Yousafzai, R. M. Hathout and J. G. Hardy, Materials, 2018, 11, 1123 Search PubMed.
- M. Elbadawi, H. Li, P. Ghosh, M. E. Alkahtani, B. Lu, A. W. Basit and S. Gaisford, ACS Sustainable Chem. Eng., 2024, 12(30), 11155–11166 Search PubMed.
- S. Wu, S. Wu, X. Zhang, T. Feng and L. Wu, Biosensors, 2023, 13, 93 Search PubMed.
- C. Zhao, J. Park, S. E. Root and Z. Bao, Nat. Rev. Bioeng., 2024, 2, 671–690 Search PubMed.
- D. K. Chandra, R. L. Reis, S. C. Kundu, A. Kumar and C. Mahapatra, ACS Biomater. Sci. Eng., 2024, 10, 4145–4174 Search PubMed.
- B. Yang, B. Zhou, C. Li, X. Li, Z. Shi, Y. Li, C. Zhu, X. Li, Y. Hua, Y. Pan, J. He, T. Cao, Y. Sun, W. Liu, M. Ge, Y. R. Yang, Y. Dong and D. Liu, Angew. Chem., Int. Ed., 2022, 61(30), e202202520 Search PubMed.
- S. Sahani, H. Mahajan and S. S. Han, J. Energy Storage, 2024, 90, 111808 Search PubMed.
- R. Huang and Y. Xie, J. Alloys Compd., 2024, 175367 Search PubMed.
- E. Aytaç, A. Fombona-Pascual, J. J. Lado, E. G. Quismondo, J. Palma and M. Khayet, Desalination, 2023, 563, 116715 Search PubMed.
- S. Fleischmann, Y. Zhang, X. Wang, P. T. Cummings, J. Wu, P. Simon, Y. Gogotsi, V. Presser and V. Augustyn, Nat. Energy, 2022, 7, 222–228 Search PubMed.
- A. Muzaffar, M. B. Ahamed, K. Deshmukh and J. Thirumalai, Renewable Sustainable Energy Rev., 2019, 101, 123–145 Search PubMed.
- R. Jain, A. S. Lakhnot, K. Bhimani, S. Sharma, V. Mahajani, R. A. Panchal, M. Kamble, F. Han, C. Wang and N. Koratkar, Nat. Rev. Mater., 2022, 7, 736–746 Search PubMed.
- G. Varnavides, A. Yacoby, C. Felser and P. Narang, Nat. Rev. Mater., 2023, 8, 726–741 Search PubMed.
- N. Gao, C. Li, Y. Xue, Y. Wang and H. Ma, J. Colloid Interface Sci., 2025, 678, 693–703 Search PubMed.
- H. Wu, C. Zhang, Y. Qiu and X.-F. Sun, Chem. Eng. J., 2024, 496, 153491 Search PubMed.
- S.-M. Bak, Z. Shadike, R. Lin, X. Yu and X.-Q. Yang, NPG Asia Mater., 2018, 10, 563–580 Search PubMed.
- J. Wang, J. Shi, X. Deng, L. Xie, J. Jiang, J. Tang, J. Liu, Z. Wen, X. Sun and K. Liu, Nano Energy, 2020, 78, 105348 Search PubMed.
- Y.-H. Wang, S. Zheng, W.-M. Yang, R.-Y. Zhou, Q.-F. He, P. Radjenovic, J.-C. Dong, S. Li, J. Zheng and Z.-L. Yang, Nature, 2021, 600, 81–85 Search PubMed.
- V. R. Manga and D. R. Poirier, Modell. Simul. Mater. Sci. Eng., 2018, 26, 065006 Search PubMed.
- Q. J. Zhu, K. Wang, X. H. Wang and B. R. Hou, Surf. Eng., 2012, 28, 300–305 Search PubMed.
- X. Song, S. Song, D. Wang and H. Zhang, Small Methods, 2021, 5, 2001000 Search PubMed.
- L. Sun, Z. Shi, B. He, H. Wang, S. Liu, M. Huang, J. Shi, D. Dastan and H. Wang, Adv. Funct. Mater., 2021, 31, 2100280 Search PubMed.
- H.-W. Tang, N. Gao, Z.-R. Chang, B. Li, X.-Z. Yuan and H.-J. Wang, Chin. Chem. Lett., 2014, 25, 269–272 Search PubMed.
- V. Kouznetsov, K. Macak, J. M. Schneider, U. Helmersson and I. Petrov, Surf. Coat. Technol., 1999, 122, 290–293 Search PubMed.
- H. Rueß, J. Werner, Y. Unutulmazsoy, J. W. Gerlach, X. Chen, B. Stelzer, D. Music, S. Kolozsvari, P. Polcik and T. E. Weirich, J. Eur. Ceram. Soc., 2021, 41, 1841–1847 Search PubMed.
- W. Diao, S. Saxena and M. Pecht, J. Power Sources, 2019, 435, 226830 Search PubMed.
- Y. Ye, R. Xu, W. Huang, H. Ai, W. Zhang, J. O. Affeld, A. Cui, F. Liu, X. Gao, Z. Chen, T. Li, X. Xiao, Z. Zhang, Y. Peng, R. A. Vila, Y. Wu, S. T. Oyakhire, H. Kuwajima, Y. Suzuki, R. Matsumoto, Y. Masuda, T. Yuuki, Y. Nakayama and Y. Cui, Nat. Energy, 2024, 9, 643–653 Search PubMed.
- L. Zhang, C. Jia, F. Bai, W. Wang, S. An, K. Zhao, Z. Li, J. Li and H. Sun, Fuel, 2024, 355, 129455 Search PubMed.
- S. Popat, S. V. Liu, N. Scheuer, G. G. Hsu, A. Lockhart, S. V. Ramagopalan, F. Griesinger and V. Subbiah, Nat. Commun., 2022, 13, 3500 Search PubMed.
- Z. M. Mohamadi and H. Zohoor, J. Mech. Sci. Technol., 2011, 25, 871–876 Search PubMed.
- M. Sharma, P. M. Ajayan and P. Deb, Adv. Mater. Interfaces, 2023, 10, 2202058 Search PubMed.
- M. A. Del Valle, M. A. Gacitúa, F. Hernández, M. Luengo and L. A. Hernández, Polymers, 2023, 15, 1450 Search PubMed.
- N. Li, Y. Wang, W. Zhao, Z. Chen, P. Liu, W. Zhou, F. Jiang, C. Liu and J. Xu, ChemPhysChem, 2024, e202400103 Search PubMed.
- W. Wang, S. Guo, I. Lee, K. Ahmed, J. Zhong, Z. Favors, F. Zaera, M. Ozkan and C. S. Ozkan, Sci. Rep., 2014, 4, 4452 Search PubMed.
- A. Livingston, B. L. Trout, I. T. Horvath, M. D. Johnson, L. Vaccaro, J. Coronas, C. W. Babbitt, X. Zhang, T. Pradeep and E. Drioli, Sustainable Nanoscale Engineering, 2020, 1–18 Search PubMed.
- T. Sang, C. J. Wallis, G. Hill and G. J. P. Britovsek, Eur. Polym. J., 2020, 136, 109873 Search PubMed.
- N. Saba, M. Jawaid, M. T. H. Sultan and O. Alothman, in Hybrid Polymer Composite Materials, eds. V. K. Thakur, M. K. Thakur and A. Pappu, Woodhead Publishing, 2017, doi: DOI:10.1016/B978-0-08-100785-3.00005-X, pp. 151–167.
- J. Han, H. Xu, G. T. Blazquez, S. H. K. Paleti, A. Sharma and D. Baran, Chem. Soc. Rev., 2024, 53(14), 7426–7454 Search PubMed.
- L. Mariani, B. Trivellato, M. Martini and E. Marafioti, J. Bus. Ethics, 2022, 180, 1075–1095 Search PubMed.
- J. C. Ince, M. Peerzada, L. D. Mathews, A. R. Pai, A. Al-qatatsheh, S. Abbasi, Y. Yin, N. Hameed, A. R. Duffy, A. K. Lau and N. V. Salim, Adv. Compos. Hybrid Mater., 2023, 6, 130 Search PubMed.
- S. Wacławek, M. Fijałkowski, P. Bardos, J. Kočí, S. Scholz, P. Hirsch, G. Domann and M. Černík, Ecol. Chem. Eng. S, 2022, 29, 447–462 Search PubMed.
- C. Shi, E. C. Quinn, W. T. Diment and E. Y. X. Chen, Chem. Rev., 2024, 124, 4393–4478 Search PubMed.
- J. Stejskal and J. Prokeš, Synth. Met., 2020, 264, 116373 Search PubMed.
- S. M. Aldosari, B. AlOtaibi, K. Alblalaihid, S. Aldoihi, K. A. AlOgab, S. S. Alsaleh, D. O. Alshamary, T. H. Alanazi, S. D. Aldrees and B. A. Alshammari, Polymers, 2024, 16, 1363 Search PubMed.
- P. Paraye and R. M. Sarviya, Polym-Plast. Tech. Mat., 2024, 63, 1474–1497 Search PubMed.
- P. Tan, H. Wang, F. Xiao, X. Lu, W. Shang, X. Deng, H. Song, Z. Xu, J. Cao, T. Gan, B. Wang and X. Zhou, Nat. Commun., 2022, 13(1), 358 Search PubMed.
- W. Huang, P.-H. Chien, K. R. McMillen, S. V. Patel, J. Tedesco, L. Zeng, S. Mukherjee, B. Wang, Y. Chen, G. Wang, Y. Wang, Y. Gao, M. J. Bedzyk, D. M. DeLongchamp, Y. Y. Hu, J. E. Medvedeva, T. J. Marks and A. Facchetti, Proc. Natl. Acad. Sci., 2020, 117, 18231–18239 Search PubMed.
- L. Alzoubi, A. A. A. Aljabali and M. M. Tambuwala, AAPS PharmSciTech, 2023, 24, 228 Search PubMed.
- K. Pal, A. A. A. Aljabali, S. Kralj, S. Thomas and F. Gomes de Souza, Chemosphere, 2021, 263, 128104 Search PubMed.
- G. Schottner, Chem. Mater., 2001, 13, 3422–3435 Search PubMed.
- B. Ben-Nissan and A. H. Choi, Nanomedicine, 2006, 1, 311–319 Search PubMed.
- W. Li, Z. Yang, W. Yang, H. Guo and C. Y. Tang, AIChE J., 2021, 68 Search PubMed.
- Y. Hamzat, A. A. A. Aljabali, M. El-Tanani and M. M. Tambuwala, Curr. Nanosci., 2025, 21, 404–422 Search PubMed.
- Z. Li, MATEC Web of Conferences, 2024, 404, 02006 Search PubMed.
- A. Khalfallah and C. Leitão, Machines, 2024, 12, 815 Search PubMed.
- M. De Keersmaecker, A. W. Lang, A. M. Österholm and J. R. Reynolds, ACS Appl. Mater. Interfaces, 2018, 10, 31568–31579 Search PubMed.
- E. L. Howard, A. M. Osterholm, D. E. Shen, L. P. Panchumarti, C. Pinheiro and J. R. Reynolds, ACS Appl. Mater. Interfaces, 2021, 13, 16732–16743 Search PubMed.
- T. M. Swager, Macromolecules, 2017, 50, 4867–4886 Search PubMed.
- T. Nezakati, A. Seifalian, A. Tan and A. M. Seifalian, Chem. Rev., 2018, 118, 6766–6843 Search PubMed.
- S. Meer, A. Kausar and T. Iqbal, Polym.-Plast. Technol. Eng., 2016, 55, 1416–1440 Search PubMed.
- I. Botiz, S. Astilean and N. Stingelin, Polym. Int., 2016, 65, 157–163 Search PubMed.
- N. Stingelin, Semiconducting Polymers: Controlled Synthesis and Microstructure, 2016, 21, p. 187 Search PubMed.
- Y. Li, F. Zhu, E. Liu, H. Ouyang, W. Lu, H. Gu, J. Ren, W. Peng, H. Hou and Y. He, Adv. Compos. Hybrid Mater., 2024, 7, 147 Search PubMed.
- S. N. A. Safri, M. T. H. Sultan, M. Jawaid and K. Jayakrishna, Composites, Part B, 2018, 133, 112–121 Search PubMed.
- P. Jagadeesh, S. M. Rangappa and S. Siengchin, Adv. Ind. Eng. Polym. Res., 2024, 7, 122–143 Search PubMed.
- E. O. Pyzer-Knapp, J. W. Pitera, P. W. J. Staar, S. Takeda, T. Laino, D. P. Sanders, J. Sexton, J. R. Smith and A. Curioni, npj Comput. Mater., 2022, 8, 84 Search PubMed.
- B. Anasori and Y. Gogotsi, Graphene 2D Mater., 2022, 7, 75–79 Search PubMed.
- Y. Huang, C. Wu, J. Chen and J. Tang, Angew. Chem., Int. Ed., 2024, 63, e202313885 Search PubMed.
- D. Pochan and O. Scherman, Chem. Rev., 2021, 121, 13699–13700 Search PubMed.
- P. Baskaran and M. Rajasekar, RSC Adv., 2024, 14, 21706–21744 Search PubMed.
- Y. Hong, Z. Lin, Y. Yang, T. Jiang, J. Shang and Z. Luo, Int. J. Mol. Sci., 2022, 23, 4578 Search PubMed.
- E. Mikinka and M. Siwak, J. Mater. Sci.: Mater. Electron., 2021, 32, 24585–24643 Search PubMed.
- A. Yusuf, A. Sodiq, A. Giwa, J. Eke, O. Pikuda, G. De Luca, J. L. Di Salvo and S. Chakraborty, J. Cleaner Prod., 2020, 266, 121867 Search PubMed.
- M. M. Mariani, I. Machado, V. Magrelli and Y. K. Dwivedi, Technovation, 2023, 122, 102623 Search PubMed.
- R. Singh, S. Dogra, S. Dixit, N. I. Vatin, R. Bhardwaj, A. K. Sundramoorthy, H. C. S. Perera, S. P. Patole, R. K. Mishra and S. Arya, Hybrid Adv., 2024, 5, 100176 Search PubMed.
- F. Nie and D. Yan, Nat. Commun., 2024, 15, 5519 Search PubMed.
- Kenry and B. Liu, Biomacromolecules, 2018, 19(6), 1783–1803 Search PubMed.
- X. Gao, Y. Chen, Y. Wang, L. Zhao, X. Zhao, J. Du, H. Wu and A. Chen, Nano-Micro Lett., 2024, 16, 237 Search PubMed.
- X. Guo, Nat. Mater., 2020, 19, 921 Search PubMed.
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