Zongyuan
Jiang‡
a,
Shaohui
Li‡
b,
Yining
Chen
b,
Jingwei
Chen
c,
Cong
Wei
*b and
Qun
Xu
*ab
aHenan Institute of Advanced Technology, Zhengzhou University, Zhengzhou, 450001, P. R. China. E-mail: Qunxu@zzu.edu.cn
bSchool of Materials Science and Engineering, Zhengzhou University, Zhengzhou, 450001, P. R. China. E-mail: weicong@zzu.edu.cn
cSchool of Materials Science and Engineering, Ocean University of China, Qingdao, 266100, P. R. China
First published on 23rd June 2023
Manganese sulfide (MnS) has gained significant attention as a high capacity and durable anode material for sodium-ion batteries (SIBs) due to its high theoretical capacity and decent redox reversibility. However, sluggish Na+ diffusion and significant volume variation during charge/discharge cycles limited its rate capability and cycling stability. Here, a new MnS/CoS heterojunction embedded in S-doped carbon (MnS/CoS@C) is designed through sulfurization of a bimetallic metal–organic framework (MOF). The synergistic effect of heterojunction design and carbon framework encapsulation integrates several benefits, including facilitating ion/electron transport, alleviating volume variation, and preventing the agglomeration of metal sulfide nanoparticles. Therefore, the MnS/CoS@C composite manifests remarkable rate capability (526.1 mA h g−1 at 0.1 A g−1 and 273.7 mA h g−1 at 10 A g−1) and stable long-term cycle life (214.8 mA h g−1 after 1000 cycles at 5 A g−1). Meanwhile, the sodium storage mechanism is examined using in situ electrochemical impedance spectroscopy (EIS), ex situ X-ray diffraction (XRD) and ex situ X-ray photoelectron spectroscopy (XPS). Coupled with a carbon nanosheet cathode, a prototype sodium-ion capacitor (SIC) has been fabricated. The SIC can achieve a high energy density of 120.7 W h kg−1 and a maximum power density of 12250 W kg−1, demonstrating the high application potential of the composite for sodium-ion based energy storage systems.
Transition metal sulfides (TMSs) have garnered widespread attention as novel anode materials in SIBs because of their high theoretical capacity, controllable morphologies/nanostructures, relatively weak M–S bonding strength and unique electrochemical properties.9 Until now, numerous metal sulfides (MxSy = Fe, Co, Ni, Cu, Mn, etc.) have been explored as anodes for SIBs and great progress has been achieved.10–12 Among them, manganese sulfide (MnS) has been extensively explored as an SIB anode candidate owing to its high theoretical specific capacity (616 mA h g−1) and suitable electrochemical reaction platform. However, they still suffer from severe volume change, intrinsic poor conductivity and the polysulfide shuttle effect, resulting in inferior rate capacity and inadequate cycle life.13 To circumvent these problems, numerous strategies have been adopted from other rechargeable batteries. (1) Constructing micro/nanostructures with interior space, which can efficiently accelerate ion/electron migration and alleviate volume changes; (2) forming composites with conductive heteroatom (such as S, N, and P) doped carbonous materials, which can promote charge transport, maintain structural integrity, and impede the dissolution of polysulfides.8,14–19 So far, most of the work has focused on the two perspectives mentioned above, with the aim of promoting the diffusion kinetics. As expected, significant progress has been made in recent years on MnS-based anode materials, but the comprehensive properties are still unsatisfactory. In addition, little research has been done on regulating the internal crystal structure of MnS materials to further enhance the ionic/electronic transport kinetics.
Recently, binary metal sulfides with heterojunction structures have caught many researchers’ attention owing to their significant advantages in sodium storage, such as WS2−x/ZnS@C,20 Sb2S3@FeS221 hollow nanorods and SnS2/Co3S4 hollow nanocubes.22 The interface between different components could induce an internal electric field and increase the number of active sites, resulting in improved electrochemical properties.11,23–25 Nonetheless, the passivation of the interfacial reaction and the dissolution of polysulfide intermediates still retard the reaction kinetics during the repeated sodiation/desodiation process. In addition, the scrupulous and accurate design of highly integrated and uniformly distributed heterostructure electrodes remains a challenge that needs to be resolved.
Herein, an octahedral structure of MnS/CoS heterojunctions homogeneously encapsulated in S-doped carbon (denoted as MnS/CoS@C) was precisely designed by using Mn- and Co-based bimetallic metal–organic frameworks (MOFs) as starting materials. The formed S-doped carbon shell derived from organic ligands can mitigate the volume variation, inhibit the aggregation of MnS/CoS nanoparticles caused by Na+ insertion/extraction, and improve the kinetics of ion/electron migration,26 while the heterojunction of MnS and CoS could generate internal built-in electric fields that greatly enhance the interfacial reaction kinetics and ion/electron migration. Benefiting from its hierarchical structure, the as-produced MnS/CoS@C composite can yield an ultrahigh initial capacity (526.1 mA h g−1 at 0.1 A g−1), excellent rate performance (273.7 mA h g−1 at 10 A g−1) and cycling durability (84.7% capacity retention after 1000 cycles). The electrochemical Na+ storage behavior of MnS/CoS@C was also characterized by in situ EIS, ex situ XRD and ex situ XPS. In addition, a prototype sodium-ion capacitor (SIC) composed of the MnS/CoS@C anode and the N-doped carbon nanosheet (NC) cathode can demonstrate a remarkable energy density of 120.7 W h kg−1 and a superior high-power density of 12250 W kg−1.
The transmission electron microscopy (TEM) image of MnS/CoS@C11 further proved that all the metal sulfide nanoparticles are homogeneously dispersed in the carbon framework (Fig. 1e and S5a†). The carbon framework can not only enhance the ionic conductivity of the composite but can also prevent the aggregation of the nanoparticles and buffer the volume changes during discharge/charge cycles. In addition, the typical high-resolution TEM image (Fig. 1f) shows that the MnS and CoS components are in close contact with the interface, confirming the presence of abundant and robust MnS/CoS heterostructures. The lattice fringes of 0.30 and 0.19 nm are in good agreement with the (111) crystal plane of MnS and the (102) crystal plane of CoS, respectively. As shown in Fig. S5b,† the selected area electron diffraction (SAED) pattern (Fig. S5b†) clearly presents the (100) and (201) planes from CoS and the (220) and (200) planes from MnS. These results demonstrate the formation of the MnS/CoS heterostructure in the carbon matrix, which can induce an internal built-in-electric field, thus boosting the ion/electron transport and promoting the interfacial reaction. The elemental mappings of C, Mn, Co, and S in the MnS/CoS@C11 composite are shown in Fig. 1g. Obviously, all the elements are homogeneously distributed throughout the octahedral structure of the carbon skeleton, which is beneficial for improving the utilization of CoS and MnS, boosting the sodium storage performance. In addition, based on thermogravimetric analysis (TGA) curves, the carbon contents in MnS@C, MnS/CoS@C11 and CoS@C composites are calculated to be 23.5%, 7.8% and 5.3%, respectively (Fig. S6†).
As demonstrated in Fig. 2a–e, the surface chemistry and elemental valence states of MnS/CoS@C11 were examined using XPS analysis. The full XPS spectrum depicted in Fig. 2a demonstrates the presence of Mn, Co, S, and C elements, agreeing with the EDX mapping result. The C 1s spectrum shown in Fig. 2b reveals peaks corresponding to CC/C–C, C
S, and C
O bonding at 284.8, 286.2, and 289.3 eV, respectively. The existence of sulfur- and oxygen-related bonds indicates that a small amount of sulfur- and oxygen-rich groups is present on the carbon matrix surface. In the Mn 2p spectra (Fig. 2c), the obvious peaks at 653.4 and 641.6 eV are associated with Mn 2p1/2 and Mn 2p3/2, respectively. The minor peak appearing at 664.3 eV is associated with the formation of a C–S–Mn bond between MnS and the carbon skeleton. The formation of the C–S–Mn bond can not only enhance the structural stability, but can also accelerate the charge migration between MnS and the carbon matrix. In the Co 2p spectra (Fig. 2d), the peaks at 781.2 and 797.4 eV can be associated with Co 2p3/2 and Co 2p1/2 of Co2+, while the peaks at 778.8 and 797.7 eV can be related to Co 2p3/2 and Co 2p1/2 of Co3+. In addition, the peaks sited at 785.2 and 802.8 eV are assigned to two satellite peaks of Co 2p. For the S 2p spectrum (Fig. 2e), the peaks at 163.8 and 165.2 eV can be associated with the C–S–C bond, demonstrating that the S atoms are doped into the carbon framework during sulfurization. The peaks present at 162.1 and 161.0 eV are from the Mn–S bond, while the peaks at 162.6 eV and 161.6 eV are ascribed to the Co–S bond. XPS analysis results reveal that S has been incorporated into the carbon matrix, which can create a variety of defect structures that enhance the sodium storage performance. Combined with the C–S–Mn bond formed between MnS and the carbon skeleton and the heterostructure of MnS and CoS, the MnS/CoS@C11 composite is expected to exhibit exceptional electrochemical properties. Fig. 2f shows the Raman spectra of MnS@C, MnS/CoS@C and CoS@C11, respectively. Two broad peaks of D (disordered domain) and G (graphitic structure) bands can be detected at around 1347 and 1584 cm−1, respectively. According to the fitting results, the D/G intensity ratios of MnS@C, MnS/CoS@C11 and CoS@C are 1.23, 1.30 and 1.69, respectively. Compared with MnS@C and CoS@C, MnS/CoS@C11 has an appropriate amount of defects, which can offer moderate active sites for sodium storage.30
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Fig. 2 (a) XPS survey of the MnS/CoS@C11 composite. High-resolution XPS spectra of (b) C 1s, (c) Mn 2p, (d) Co 2p and (e) S 2p of MnS/CoS@C11. (f) Raman spectra of MnS@C, MnS/CoS@C and CoS@C samples. |
The electrochemical characteristics of the MnS/CoS@C11 composite and control samples (MnS@C, MnS/CoS@C31, MnS/CoS@C32 and CoS@C) were used as anode materials and evaluated in SIB half-cells. As illustrated in Fig. 3a, the cyclic voltammetry (CV) profiles of the MnS/CoS@C11 composite for the initial three cycles were recorded at a speed of 0.2 mV s−1 with a potential range from 0.01 to 3 V (vs. Na+/Na). Two distinct reduction peaks appeared at 0.8 and 0.4 V during the initial sodiation, which later disappeared in the subsequent cycles, corresponding to the electrolyte decomposition and solid electrolyte interface (SEI) formation. The double peaks that appeared at 1.72 V and 2.14 V during the oxidation process might be attributed to the conversion reactions from metallic elements and Na2S to MnS and CoS. The CV profiles for the later cycles are nearly superimposed, indicating the occurrence of a reversible conversion on the MnS/CoS@C11 electrode. As depicted in Fig. S7,† the CV profiles of MnS@C and CoS@C electrodes are also tested for comparison. Fig. 3b demonstrates the galvanostatic charge/discharge (GCD) profiles of the MnS/CoS@C11 electrode at a current of 0.1 A g−1 in the 1st, 2nd, and 10th cycles. Obviously, the potential plateaus correspond well to the peak positions in the CV profiles. The GCD profiles of MnS@C, MnS/CoS@C31, MnS/CoS@C32 and CoS@C are also tested and displayed in Fig. S8.† Moreover, the subsequent cycles overlap well with the second one, demonstrating the excellent cycling performance of the material. The typical GCD profiles of MnS/CoS@C11 at various current densities have been tested and displayed in Fig. 3c. All the profiles show a similar shape, demonstrating excellent cycling stability. The initial discharge/charge specific capacities of the MnS@CoS@11 electrode are 792 and 529.3 mA h g−1, which are equivalent to an initial coulombic efficiency (ICE) of 66.8%. The low ICE could be attributed to the electrolyte decomposition and SEI formation in the first cycle.25,31 It is noteworthy that the coulombic efficiency was nearly 100% in the subsequent cycles, which should be ascribed to the highly reversible Na+ insertion/extraction process. Moreover, the fast Na+ storage performance of the MnS/CoS@C11 electrode was proved by the rate capability tests (Fig. 3d), and the relevant GCD profiles at various current densities are presented in Fig. 3c. The sodium storage capacities of the MnS/CoS@C11 electrode at current densities of 0.1, 0.5, 1.0, 2.0, 5.0, 8.0 and 10.0 A g−1 were 526.1, 498.7, 464.3, 428.6, 383.2, 316.4 and 273.7 mA h g−1, respectively. When the current density was returned to 0.1 A g−1, the capacity was restored to 520.1 mA h g−1, manifesting superior structural stability and excellent reversibility for fast sodiation/desodiation. These values are higher than those of MnS@C (224.3 mA h g−1), MnS/CoS@C31 (316.7 mA h g−1), MnS/CoS@C32 (422.2 mA h g−1) and CoS@C (432.5 mA h g−1). The GCD profiles of MnS@C, MnS/CoS@C31, MnS/CoS@C32 and CoS@C with different current densities are also characterized and displayed in Fig. S9.†Fig. 3e shows the rate capability comparison of the MnS/CoS@C11 electrode with other reported MnS-based and CoS-based anodes.14,32–40 Evidently, the MnS/CoS@C11 electrode possesses superiority in both capacity and rate capability. As depicted in Fig. 3f, the cycling performances of MnS@C, MnS/CoS@C31, MnS/CoS@C32, MnS/CoS@C11 and CoS@C electrodes at 1 A g−1 were evaluated. This shows that MnS/CoS@C11 has the best cycling stability and capacity performance. Furthermore, the long-term cycling performance of the MnS/CoS@C11 anode at a high current of 5 A g−1 was evaluated and demonstrated in Fig. 3g. Impressively, the MnS/CoS@C11 electrode can maintain a high capacity of 214.8 mA h g−1 after 1000 cycles, equivalent to 84.7% capacity retention, showing excellent cycling durability. The nanostructure of the MnS/CoS@C11 electrode after long-term cycling was characterized by SEM. As observed in Fig. S10,† the octahedral structure of MnS/CoS@C11 can still be preserved.
To further investigate the high-rate performance of MnS/CoS@C11, the CV profiles of MnS@C, MnS/CoS@C11 and CoS@C electrodes were recorded at different scan rates ranging from 0.2 to 2 mV s−1 (Fig. 4a and Fig. S11†). As displayed in Fig. 4a, these CV profiles of the MnS/CoS@C11 electrode exhibited similar shapes with slight peak separations, indicating minimal polarization and fast Na+ mitigation at high rates. As previously reported, the correlation between the measured peak current (i) and the scan rate (ν) conforms to the following equation:41
i = aνb. | (1) |
Configurable parameters a and b are involved in this equation, and the b value has the potential to assess the sodium storage performance. Specifically, b = 0.5 indicates battery-like behavior, while b = 1 demonstrates capacitor-like behavior.34,42 For the MnS/CoS@C11 electrode, the b values of anodic and cathodic peaks were 0.91, 0.87, 0.91, 0.89, 0.87, and 0.82 (Fig. 4b), respectively, manifesting that the sodium storage kinetics of MnS@CoS@C11 is dominated by the capacitive-like behavior.39 The b values of MnS@C and CoS@C electrodes are also calculated and shown in Fig. S12† for comparison. Additionally, the contribution ratio of the capacitive current at a given CV curve can be determined using the following formula:43
i(V) = k1 + k2ν1/2. | (2) |
In the above equation, i (mA) and ν (mV s−1) represent the current at a particular potential (V) and sweep rate, respectively. The parameters k1 and k2 correspond to the fitting of capacitance and diffusion-controlled contributions. As displayed in Fig. 4c, MnS/CoS@C11 exhibited contribution ratios of 70.5%, 73.6%, 77.3%, 81.6%, and 85.4% at sweep rates of 0.2, 0.5, 0.7, 1, and 2 mV s−1, respectively. These values are larger than those obtained from the MnS@C and CoS@C electrodes, implying faster Na+ transport in the MnS/CoS@C11 electrode. Obviously, the MnS/CoS@C11 electrode exhibits a higher capacitive contribution value than MnS@C and CoS@C electrodes due to the formation of MnS/CoS heterojunctions, which are expected to elevate the charge transfer and accelerate the interfacial reaction. For example, Fig. 4d depicts that 81.6% of the total capacity of the MnS/CoS@C11 electrode comes from the capacitive-controlled contribution at a sweep rate of 1 mV s−1. Hence, the remarkable rate capability of the MnS/CoS@11 electrode could be promoted by the high capacitive contribution.9
As illustrated in Fig. 4e, the electrochemical impedance spectroscopy (EIS) plots of MnS@C, MnS/CoS@C and CoS@C electrodes were recorded after three cycles. The Nyquist plots exhibit a consistent pattern, characterized by a semicircle at high frequencies and a straight line at low frequencies. Apparently, compared to MnS/C and CoS/C electrodes, the MnS/CoS@C11 electrode has a smaller semicircle, indicating the lowest charge transfer resistance, which can be ascribed to the internal built-in electric field formed at the MnS and CoS contact interface, which can accelerate the charge mitigation and interfacial reaction kinetics. The Na+ diffusion coefficients could be studied using the Warburg factor (σ) related to the low frequency linear drift slope in eqn (3).44
Z′ = Re + Rct + σwω−1/2 | (3) |
As shown in Fig. 4f, Z′–ω−1/2 curves show that the MnS/CoS@C11 electrode has the lowest slope (55.9), indicating that the Na+ diffusion coefficients of the MnS/CoS@C11 electrode are higher than those of the MnS@C and CoS@C electrodes. The fast Na+ diffusion rate is attributed to the heterojunction between MnS and CoS that can greatly promote the ion mitigation and conductivity of the electrode materials.
The galvanostatic intermittent titration technique (GITT) was employed to evaluate the Na+ diffusion coefficients (DNa+) during the discharge/charge process. The DNa+ of MnS@C, CoS@C, and MnS/CoS@C11 electrodes can be calculated using the following formula:45
![]() | (4) |
The obtained outcomes that correspond to the aforementioned calculations are demonstrated in Fig. 4g and h. Obviously, the DNa+ values of the MnS/CoS@C11 electrode are higher than those of the MnS@C and CoS@C electrodes. The enhanced ionic transport should be ascribed to the internal built-in electric field formed between MnS and CoS, which significantly accelerates the interfacial reaction kinetics and ion/electron migration.
To further gain insight into the underlying sodium storage behavior of MnS/CoS@C11, in situ EIS and ex situ XRD and XPS were performed. As depicted in Fig. 5a, the Nyquist plots at different potentials were collected and displayed as a 3D image. The intersection with the x-axis at a low frequency represents the solid-state Na+ diffusion resistance (Rs), while the two semicircles at the high frequency are attributed to the charge transfer resistance (Rct) and second-phase impedance (Rf). The impedance changes during the sodiation/desodiation cycle can reflect the electrochemical process to a certain extent. As shown in Fig. 5b, during the discharge/charge process, Rs remains almost unchanged (from 7.1 Ω to 6.8 Ω), indicating that the electrode structure is very stable. In the first sodiation process (from 3.0 V to 0.6 V), the Nyquist plot consists of a semicircle and a diagonal line, demonstrating a single-phase sodium storage behavior. Meanwhile, the Rct value exhibits a slight decrease, indicating facile charge transfer. However, during the sodiation/desodiation process from 0.6 V to 0.01 V and 0.01 V to 0.6 V, the Nyquist plot gradually separates into two semicircles and one diagonal line, displaying a multiphase electrochemical process. In this cycle, the initial Rct value remains stable (from 9.4 Ω to 9.5 Ω). Meanwhile, a new Rf value first increases from 13.9 Ω to 20.1 Ω (from 0.6 V to 0.01 V) and then decreases to 16.9 Ω (from 0.01 V to 0.6 V); these variations demonstrate that the composite mainly undergoes conversion reactions in the low potential range. Significant structural evolution and compositional variations occur at a low potential, resulting in a sluggish ion/electron transfer rate. When charged back from 0.6 to 3.0 V, the Nyquist plots recover to their original shape, manifesting a similar single-phase sodium storage behavior as the initial. Overall, in the first discharge/charge process, the MnS/CoS@C11 electrode suffers from two different impedance variation steps, with the main structural variation occurring at a low potential (below 0.6 V). The corresponding minor changes in the resistance values indicate that the electrochemical reaction is highly reversible.15
As shown in Fig. 5c–g, ex situ XRD and ex situ XPS were characterized under selected potentials. The structural evolution of the MnS/CoS@C11 electrode during Na+ insertion/extraction was determined (Fig. 5d). For the original sample, diffraction peaks belonging to MnS and CoS were detected. In the following discharge process, the peak intensities of MnS and CoS gradually decreased. Meanwhile, diffraction peaks from Mn, Co, NaS2, and Na2S gradually appeared. As continuously discharged to 0.01 V, the peaks of MnS and CoS vanished, while the peaks of Mn, Co, NaS2, and Na2S became dominant. Moreover, in the reversed charging process, the peaks of Mn, Co, NaS2, and Na2S became progressively weaker. Subsequently, the minor peaks of MnS and CoS can be observed again, demonstrating that the electrochemical reaction between the MnS/CoS heterostructure and Na+ is reversible.16
This result can be confirmed by the ex situ XPS characterization. Fig. 5e and f show the Mn 2p and Co 2p spectra in different states, respectively. When the potential gradually decreased to 0.01 V, new peaks assigned to Mn0 and Co0 appeared at 649.5 and 778.8 eV, respectively, which are ascribed to the electrochemical reaction between Na+ and the MnS/CoS heterostructure. Subsequently, in the S 2p spectra (Fig. 5g), a new Na–S compound peak appeared at 162.7 eV. These results manifest the conversion reaction of the MnS/CoS heterostructure during sodiation. In the subsequent charging process, the peaks of Mn0 (649.5 eV), Co0 (778.8 eV) and Na–S compounds (162.7 eV) weakened, but the MnS and CoS peaks are strengthened. When the battery is charged to 3.0 V, the peaks belonging to Mn0 and Co0 fully disappear, while the peaks of MnS and CoS almost recover to their pristine position. The ex situ XPS results showed that the conversion reaction between the MnS/CoS heterostructure is highly reversible, agreeing well with the ex situ XRD result.
To showcase the practical application of MnS/CoS@C11 heterostructures as anode materials, a prototype sodium-ion capacitor (SIC) was constructed. As shown in Fig. 6a, the SIC consists of a MnS/CoS@C11 based battery-type anode and a N-doped carbon nanosheet (NC) based capacitive-type cathode, which is denoted as MnS/CoS@C11//NC. The NC cathode was prepared according to our previous report. The electrochemical properties of the NC cathode were tested and are demonstrated in Fig. S13,† which can yield a high capacity of 71.1 mA h g−1 at 1 A g−1 and maintain 67.2 mA h g−1 at 10 A g−1. To achieve the maximum electrochemical performance, the mass ratio of NC to MnS/CoS@C11 was controlled to 2.5:
1. The voltage range was adjusted to 0–3.5 V based on the CV curves of various materials to prevent potential electrolyte decomposition and side reactions (Fig. S14†). Fig. 6c depicts the CV profiles of SIC at various sweep rates. As the sweep rate increases, the CV profiles maintain their initial shape without obvious deformation, demonstrating excellent reversibility and rate capability. The slight deviation from the conventional symmetric supercapacitor observed in the CV curves provides evidence for the amalgamation of two distinct charge storage mechanisms in the anode and cathode. Similarly, the GCD curves shown in Fig. 6c also demonstrate a minor deviation from the triangular shape, confirming the coexistence of faradaic and non-faradaic reactions again. The energy density and power density of the SIC were calculated based on the GCD profiles; the SIC can deliver a maximum energy density of 120.7 W h kg−1 at a power of 87.5 W kg−1. Even at an ultra-high power of 12
250 W kg−1, the SIC can still provide an energy density of 29.2 W h kg−1, showing its excellent rate capability. To demonstrate the practical applications of the SIC, a humidity/temperature sensor can be powered by a charged SIC (Fig. S15†). These results are comparable to or even better than most previously reported SICs (Fig. 6d), such as Na2Ti2O5−x//rGO/AC (51 W h kg−1), SnO2/G//CNT (103 W h kg−1), Fe6%–CoS2/rGO//PSC (110 W h kg−1), MoS2–C//PDPC (111.4 W h kg−1), MoS2/CoS2–RGO//CC (115 W h kg−1), Nb2O5//PSC NICs (43.2 W h kg−1), AC//VS4–CNT (100 W h kg−1), and TiS2@Cpvp//AC (98 W h kg−1).42,46–52 In addition, the MnS/CoS@C11//NC SIC also delivers remarkable cycling stability, maintaining 85% of the initial capacity with almost 100% CE after 2000 cycles at 1 A g−1, showing great potential application in high-power energy storage systems.
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3nr01618h |
‡ These two authors contributed equally to this work. |
This journal is © The Royal Society of Chemistry 2023 |