Daewhan
Kim
,
Youngjoo
Park
and
Min Sang
Kwon
*
Department of Material Science and Engineering, Research Institute of Advanced Materials, Seoul National University, Seoul 08826, Republic of Korea. E-mail: minsang@snu.ac.kr
First published on 28th May 2025
Electronic waste (e-waste) is one of the fastest-growing waste streams, largely due to surging demand for devices like smartphones, tablets, and laptops. While e-waste contains valuable resources, its disposal also involves hazardous components that threaten human health and the environment. A critical barrier to effective recycling is the adhesives used in device assembly, which complicate disassembly and reduce material recovery. Recent research has explored diverse residue-free and efficient debonding methods. Notably, irreversible photo-debondable adhesives show particular promise by enabling precise, controlled, and on-demand release without damaging sensitive components. Moving forward, developing adhesives that incorporate both debonding capabilities and degradability will be essential for achieving efficient, sustainable recycling and minimizing the environmental impact of e-waste.
Given these concerns, to minimize the generation of e-waste, two primary approaches can be considered (Fig. 1). When an entire electronic device is no longer functional, valuable materials such as metals and plastics can be extracted from its components for recycling. Alternatively, if only a specific component is defective or malfunctioning, that faulty unit can be selectively removed and replaced, enabling the reusing of the remaining functional components. While recycling contributes to reducing e-waste, reusing functional components offers an additional advantage by lowering production costs in the industry, thereby providing both environmental and economic benefits. Thus, the development of efficient recycling and reusing strategies for electronic devices has become a critical challenge in modern society, reflecting both sustainability and economic viability. One of the primary obstacles in these strategies is the difficulty of component separation due to the use of adhesives in device assembly.5 As a first step, devices must be manually disassembled without causing damage to the intricate electronic structures, allowing for the recovery and reuse of functional components while discarding malfunctioning or defective parts. In this process, achieving clean and efficient disassembly from the substrate through appropriate external stimuli is essential. Advancements in such disassembly techniques can significantly mitigate the environmental and health impacts of e-waste while also contributing to environmental, social, and governance (ESG) goals. Furthermore, from a practical perspective, reusing layers and enabling the recycling of high-value materials contribute to reducing production costs, improving resource efficiency, and ultimately enhancing the economic viability of the process.6 As industries increasingly prioritize cost-effective and scalable solutions, these technologies are becoming not only environmentally beneficial but also economically indispensable.
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| Fig. 1 The recycling and reusing process of electronic devices and the future direction approach for sustainable adhesives using debonding strategies. | ||
To address this challenge, extensive research has been conducted on adhesive removal for electronic device disassembly. In particular, numerous studies have explored practical methods for removing adhesives used in bonding single-layer components, such as printed circuit boards (PCBs), with transesterification reactions at temperatures exceeding 140 °C.13 However, research on practical adhesive debonding strategies specifically aimed at disassembling multi-layer structures into individual layers remains significantly limited.11 Unlike single-layer systems, multi-layer electronic devices, such as display modules, lithium-ion batteries, and solar cells, which consist of multiple functional layers require precise separation methods. Display modules use adhesives to assemble components such as polarizers, color filters, organic light-emitting diode (OLED) layers, and thin film transistor (TFT) layers. Similarly, lithium-ion battery packs employ adhesives for cell-to-cell bonding, thermal runaway protection, compression pads, electrical insulation, and pack sealing. These layers exhibit significant thermal sensitivity; for example, color filters and OLED dyes may undergo thermal bleaching at temperatures exceeding approximately 100 °C,14,15 while excessive heat also introduces explosion risks in lithium-ion batteries.16 This thermal constraint severely limits the applicability of conventional high-temperature adhesive removal techniques, emphasizing the urgent need for on-demand debonding strategies to alternative recycling and reusing tailored specifically for multi-layer systems.
To overcome these challenges, fundamental research is required to develop effective and easily removable adhesives that facilitate efficient disassembly. As part of these efforts, various on-demand debonding systems have been proposed (Fig. 2). These systems enable precise, stimulus-activated separation from the substrate, allowing disassembly to occur only when necessary. Such on-demand responsiveness is a key advantage over traditional methods, offering tailored performance in complex multi-layer devices and minimizing damage to reusable components. To ensure that this on-demand functionality remains effective in extended-use strategies, debondable adhesives should be validated through comprehensive environmental stability testing that reflects realistic and long-term operational conditions. Currently, reported stimuli include thermal, photocuring, magnetic, and electric triggers, which offer potential solutions to the limitations of conventional removal methods. By integrating these techniques, more efficient and environmentally friendly disassembly processes can be developed, providing a strategic direction for sustainable electronic waste management.
For hydrogen bonding modulation, adhesives are formulated with low critical solution temperature (LCST) monomers to enable temperature-responsive adhesion. For instance, adhesives incorporating N-isopropylacrylamide (NIPAAM) exhibit enhanced inter- and intramolecular hydrogen bonding at 80 °C, reducing substrate interaction.17 To lower the debonding temperature, poly(N-vinyl caprolactam) (PVCL)–poly(ethylene glycol) (PEG) blends are applied to undergo phase transition at a lower temperature of 50 °C, resulting adhesion reduction.18 However, this study demonstrates that the reduction in adhesion is limited, and cohesive failure may leave residues, restricting their applicability in disassembly.
Research has also been conducted on dynamic covalent bonding to modify the adhesive network and reduce adhesion. Dynamic covalently bonded adhesives fabricated using polyglutaramide and polysuccinamide undergo cleavage of dicarboxamide linkages at temperatures above 200 °C, resulting in their conversion into cyclic imides and amines. This process leads to a reduction in network crosslinking density and changes in chain mobility, ultimately causing a decrease in adhesion. Although the dynamic covalent bonds are reversible and allow re-adhesion upon cooling, the need for extremely high temperatures remains a significant limitation.19 Similarly, hot-melt thermoplastic polyurethane adhesives exhibited oxime-carbamate dynamic crosslinking around 100 °C, affecting lap shear strength.20 Additionally, adhesives with ladder-like poly(silsesquioxanes) and alkyl crosslinkers demonstrated switchable adhesion via Diels–Alder reaction between 90 °C and 135 °C.21 Although these approaches are customizable, the high activation temperatures may damage sensitive functional layers. As such, developing thermally responsive adhesive with lower activation thresholds is an ongoing focus, particularly to align with on-demand debonding objectives that require both material safety and operational efficiency.
One approach involves preparing PSA by incorporating diacrylate oligomers, obtained through acrylate functionalization of thermally cured polyurethane end groups, together with a photoinitiator, to induce additional crosslinking under UV irradiation and reduce adhesion strength.26,27 Another method involves post-modification of polyacrylates with glycidyl methacrylate (GMA) and acrylic acid to achieve crosslinking.28 While these methods allow for crosslinking density control by adjusting the substitution ratio, they require mixing different polymers or additional post-modification processing steps, presenting limitations.
To address these challenges, monomers containing UV-responsive sites are copolymerized to develop reversible and irreversible photo-debondable adhesives. In the reversible method, phase transition behaviors are induced by varying wavelengths of UV irradiation. A commonly employed strategy involves the incorporation of azobenzene groups, which facilitate phase transitions from solid to liquid through cis–trans isomerization. However, their applicability in optical devices is limited due to inherent color constraints.29 In contrast, reversible photodimerization using anthracene30 or coumarin monomers31 enables adhesion control via switching between 254 nm and 365 nm light. For irreversible methods, benzophenone monomers are used in the Norrish type II reaction to create optically clear adhesives, allowing for residue-free substrate reuse in foldable displays.22 Other UV-responsive sites, such as azide32 or alkoxyphenyacyl groups,33 have also been applied to PSA for adhesion reduction under UV stimuli.
The debonding mechanism of electrically debondable adhesives has been explored in only a limited number of studies. One such study reported that incorporating organic salts or ionic liquids enables ion migration toward the electrode interfaces under applied voltage, where interfacial electrodelamination occurs via carbene-induced degradation and hydrogen gas evolution at the cathode, and metal oxidation accompanied by metal ion migration at the anode.36 These systems provide effective functionality at low temperatures and can be applied to various adhesives, such as acrylate, epoxy, and urethane, through the incorporation of ionic liquids.37 Utilizing this strategy, the adhesive can be applied not only for mounting and dismounting components in high-speed aircraft but has also been practically demonstrated to enable the separation of aluminum-shelled battery cells in electric vehicles and smartphone battery cells within a few seconds. However, they necessitate a metal substrate to conduct current, making them unsuitable for adhesion to materials such as PET or glass. Both magnetic and electrical debonding strategies show significant potential for enhancing packing density and resolution, making them particularly effective for micro- and nanoscale transfer processes in silicon wafers, but limited in electronic devices.
Among the debonding strategies introduced above, thermal and photo stimuli have been the most extensively studied due to their feasibility for practical applications. However, thermal stimuli pose challenges due to their limited precise on/off control, as chemical reactions may occur outside the targeted temperature range. To pass stability tests under high temperature (60 °C or more and 105 °C or less) conditions, debonding should not occur at excessively low temperatures.7 However, activation above 100 °C risks thermal degradation, narrow debonding temperature range is less suitable for achieving a realistic on-demand debonding operation.14
Given these challenges, photo-debondable adhesives emerge as one of the most promising on-demand system, offering precise and rapid adhesion control with wide wavelength selectivity. Here, ensuring that the overall irradiation dosage remains within a controlled range is sufficient to prevent degradation of sensitive layers. Thus, this capability enables the development of reusable adhesives, facilitating multiple attachment and detachment cycles, but dust and impurities introduced during reattachment can cause defects, generating malfunction of recycled electronics. Given that adhesive costs constitute extremely minor fraction of electronic device production, adopting irreversible photo-debondable adhesives with single-use, on-demand separation provides both economic and technical advantages. From a practical standpoint, photo-debonding allows for significant reduction in adhesion within seconds and offers controllability in terms of irradiation area, location, and on/off switching. These advantages make it one of the most favorable options in terms of both process efficiency and economic viability.
However, its applicability remains limited by the requirement that at least one of the bonded substrates must be optically transparent to allow light transmission to the adhesive layer. In cases where light cannot sufficiently reach the adhesive due to the non-transmissive materials, alternative debonding stimuli must be employed. Additionally, achieving rapid debonding typically requires high-intensity UV irradiation, which can pose a risk of damaging adjacent components, particularly those sensitive to UV exposure. Therefore, considering both economic and practical constraints, on-demand debonding strategies that enable selective, rapid, and clean separation under mild and broadly applicable stimuli should be continuously researched.
In addition to enabling efficient disassembly, addressing the environmental impact of adhesive waste itself is critical for achieving true sustainability. Debonded adhesives composed of C–C backbones are inherently non-degradable, which contributes to environmental pollution. Therefore, beyond recycling electronic devices, it is essential to incorporate pathways for adhesive degradation, monomer recycling, and upcycling to achieve ultimate sustainability. Improper disposal of adhesives may lead to the formation of “stickies,” which can contaminate paper and plastic recycling streams and cause machinery fouling during processing. To promote recyclability and degradability across different adhesive systems, various approaches have been investigated, including backbone modification for acrylic adhesives,43 vitrimer-based dynamic bonding for epoxy adhesives,44 and chemical recycling via aminolysis and acidolysis for polyurethane adhesives.45 Integrating these recycling and degradation strategies into debondable adhesive systems will be essential for future progress. Ultimately, future studies should focus on developing adhesive systems that combine efficient debonding with controlled degradation capabilities, advancing environmentally responsible adhesive technologies.
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