Electrochemical Behavior of Nanoporous Gold/Polypyrrole Supercapacitor under Deformation

Due to the high demand of wearable electronics, flexible supercapacitors have been extensively developed in recent years. Yet, the effect of deformation in the interior electrode material suffered in practical applications on the performance received less attention. Here, we study the electrochemical behavior of macroscopic nanoporous gold/polypyrrole (NPG/PPy) in situ under compression deformation. Dealloying-driven NPG, a network constructed by bi-continuous nano-scaled ligaments and pores, can serve as a compression-tolerant substrate for PPy supercapacitor material. The electrochemical capacitance of NPG/PPy subjected to compression deformation is revealed to decrease at the scan rates and discharge current densities applied in this work. At the same time, the charge transfer resistance of NPG/PPy is found to increase. This electrochemical behavior is due to the locally reduced mass transport of electrolyte caused by the formation of new connections between the neighboring ligaments under the application of compression loads. The fundamental understanding of the effect of deformation on the performance of energy storage materials revealed in this study paves the way for their practical application in wearable devices.


Introduction
In order to meet the growing demand for green energy, high-performance energystorage and conversion devices, such as batteries, electrochemical supercapacitors (ESCs), and fuel cells have been extensively explored [1]. Among them, ESCs are expected to bridge the gap between conventional electrolytic capacitors featuring high-power density but low-energy density and batteries characterized by high-energy density yet low-power density and short lifetime. According to the charge storage mechanisms, the ESCs are sorted into electrochemical double-layer capacitors (EDLCs) where energy is stored via charge carriers adsorption/desorption in the double layer at electrode/electrolyte interface [2,3] and pseudocapacitors, which effectuate charge storage by means of redox reactions at the surface [4,5]. Thus, pseudocapacitors are expected to possess higher energy density and larger capacitance than EDLCs.
Transition-metal oxides/hydroxides, such as RuO 2 [6], MnO 2 [7], and Ni(OH) 2 [8], and conductive polymers (CPs), such as polyaniline (PANI) [5,9] and polypyrrole (PPy) [5,10] are most commonly used as electrode materials for pseudocapacitors. Amongst diverse reference electrode (RE, 0.515 V vs. standard hydrogen electrode, SHE). A constant potential of 0.75 V (vs. pseudo Ag/AgCl) was applied to deplete Ag out of Au 25 Ag 75 cylinders until the current dropped below 10 µA. Ag content was further reduced below 2 at.% (as seen in Figure S5 in Supplementary Materials) through 15 cycle potential sweeps between −0.5 and 1.0 V (vs. pseudo Ag/AgCl) at a scan rate of 5 mV s −1 in 1 M HClO 4 (70%, Suprapur, Merck & Co., USA). The dealloyed samples were rinsed with ultrapure water (18.2 MΩ·cm, Siemens Ultra Clear TWF UV TM) and ethanol at least three times to remove residual acid and metal ions. NPG microstructure was coarsened by annealing at 300 • C for 30 min in the air (IRF 10, behr Labor Technik Gmbh, Germany). NPG/PPy hybrid materials were fabricated by electropolymerizing pyrrole monomers on NPG. Prior to electropolymerization, pyrrole monomer liquid (98%, Sigma-Aldrich Chemie GmbH, Germany) was purified by flowing through Si particles (0.063-0.200 mm particle size, Sigma-Aldrich Chemie GmbH, Germany). Electropolymerization was conducted in a one-chamber electrochemical cell under the protection of Ar at RT. Annealed NPG, Pt mesh, and Ag/AgCl (filled with saturated KCl, Metrohm AG, Switzerland), respectively, working as WE, CE, and RE were placed in Acetonitrile solvent containing 0.3 M LiClO 4 , 0.3 M purified pyrrole, and 2 vol.% H 2 O. In this work, pulse electropolymerization was employed to obtain homogeneous PPy coating throughout the mm-scaled specimens [10]. In one typical electropolymerization cycle, a 0.8 V potential was applied for 1 s then the potential was switched off for 60 s to allow the pyrrole monomers to diffuse into NPG inner pores for the subsequent electropolymerization cycle. By adjusting pulse cycles, NPG/PPy hybrid materials with PPy coating thickness ranging from 0 to 30 nm were fabricated. The NPG/PPy hybrid materials were rinsed with ultrapure water and ethanol and dried in a fume hood.

Characterizations and Instruments
The microstructure and composition of NPG and NPG/PPy specimens were characterized by a scanning electron microscope (SEM, Zeiss Supra VP55) coupled with energy dispersive spectroscopy (EDS). All electrochemical experiments were carried out with an Autolab PGSTAT302N potentiostat (Metrohm).

Electrochemical Measurements
The electrochemical properties of NPG/PPy hybrid materials and NPG were inspected in a three-electrode system in situ under uniaxial compression. The compressive deformations were carried out with a mechanical device (Zwick/Roell Z010) and all samples were successively deformed to 0%, 2.5%, 7.5%, and 15%, respectively. Under each specific deformation, cyclic voltammograms (CV) and galvanostatic charge-discharge (GCD) curves were recorded in a potential range of 0∼0.8 V at various scan rates and current densities. The electrochemical impedance spectroscopy (EIS) was performed at frequencies from 0.01 to 100 kHz with a sinusoidal potential amplitude of 10 mV, which superimposed to a DC formal potential of 0.5 V and 0.4 V, the middle potential in CV, for bare NPG and NPG/PPy hybrid materials, respectively. All electrochemical measurements were performed in the 0.1 M HClO 4 (70%, Suprapur, Merck) at RT using the explored specimen, pseudo Ag/AgCl, and carbon cloth as WE, RE, and CE, respectively.
In this work, all potentials were normalized to SHE unless otherwise stated. Figure 1 illustrates the microstructure of as-prepared bare NPG and NPG/PPy hybrid materials. NPG is characterized by a 3D bicontinuous network constructed by nanoscaled ligaments and pores, as shown in Figure 1a. The mean ligament size of NPG is L = 150 ± 40 nm (based on averaging over 30 measurements). It well matches the characteristic size (156 nm) predicted by g/α V [34], with the volume specific surface area of α V ∼ 80 cm 2 /mm 3 , which was obtained based on the capacitance ratio method ( Figure S2) [35,36] and the geometry constant of g = 4. Among the ligaments are the pores that have a comparable feature size with the surrounding ligaments, providing pathways for electrolyte flux for the electrochemical process. Figure 1b depicts NPG ligaments coated by a uniform PPy layer. The inset of Figure 1b displays one representative strut at a higher magnification clearly illustrating the thin PPy layer with a thickness of t PPy = 11 ± 2 nm (simplified as NPG/PPy(10 nm) herein and after), which corresponds to an electrodeposition charge density of q A = 3.3 mC/cm 2 [18]. The small thickness around 10 nm was intentionally chosen to remain the ligament and pore sizes as much as similar to those of bare NPG. On the other hand, a PPy layer of t PPy = 29 ± 3 nm (NPG/PPy(30 nm), q A = 10 mC/cm 2 ) was elaborately electrodeposited, as shown in Figure 1c. The pores between the enlarged ligaments in NPG/PPy(30 nm) are much smaller than those in NPG/PPy(10 nm), however, they still remain open. NPG and NPG/PPy specimens are intrinsically strong to sustain a large load of 40 MPa ( Figure S3). The microstructure characteristic, e.g., porosity, can be elaborately adjusted simply by deforming, predestining them for model materials to study the electrochemical behavior under deformation. Figure 1d-f show the microstructure of bare NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm) after deformation of 15%, respectively. It can be seen that after deformation, new connections (alternatively called "bridging" [26]) are formed between neighboring ligaments, as marked by the red ellipses in the figures. As seen from SEM micrographs, more connections are formed in the deformed NPG/PPy(30 nm) in comparison with bare NPG and NPG/PPy(10 nm), which illustrates a fairly similar amount of new connections after compression. Figure 2 shows the cyclic voltammogram (CV) of NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm) under different deformations as well as their corresponding specific capacitance, C m . In order to avoid the hydrogen evolution ( Figure S4 in SI) and the over-oxidation of PPy [37,38], NPG/PPy hybrid materials were explored in a potential of 0∼0.8 V while bare NPG was explored in a potential range of 0.2∼0.8 V. Non-deformed NPG/PPy hybrid materials and bare NPG display quasi-rectangular current response in the investigated potential range, as shown in Figure 2a. The magnitude of current density, j m , follows NPG/PPy(10 nm) > NPG/PPy (30 nm) NPG. Under a deformation of 15%, NPG shows an identical current response to that obtained under zero deformation. Yet, distorted current profiles are revealed in the cases of 15%-deformed NPG/PPy hybrid materials, as shown in Figure 2a. Figure 2b presents the CV curves of NPG/PPy(10 nm) under the studied deformations. All current responses (at engineering strains of 2.5%, 7.5%, and 15%) feature a malformed rectangular shape and are comparable in magnitudes.

Cyclic Voltammetry
N P G N P G / P P y ( 1 0 n m ) N P G / P P y ( 3 0 n m ) The electrochemical behavior was examined at various scan rates, v. The CV curves of non-deformed NPG/PPy(10 nm) are representatively displayed in Figure 2c. It is seen that the j m increases with v, and the quasi-rectangular profile is well maintained until 20 mV s −1 , beyond which, the CV curves deviate from the rectangular shape. The specific capacitance based on the CV results is plotted in Figure 2d. As seen in the figure, at all studied scan rates, NPG/PPy(10 nm) shows higher specific capacitance than NPG/PPy(30 nm), whereas, NPG exhibits the lowest ones. Specifically, the C m value decreases from ∼500 F g −1 to ∼150 F g −1 for NPG/PPy(10 nm) and from ∼400 F g −1 to ∼30 F g −1 for NPG/PPy(30 nm) with increasing scan rate from 5 mV s −1 to 100 mV s −1 . The C m value of NPG is independent of the scan rates at a magnitude of ∼0.6 F g −1 (Figure 2d). It has also been observed that C m decreases with deformation. In the case of NPG/PPy(10 nm), C m values at various deformations are well distinguished at all studied scan rates, especially at v > 50 mV s −1 (as indicated by the black arrow). Moreover, C m values of NPG are also impacted by deformation, as marked by the red ellipse.

Galvanostatic Charge-Discharge
Galvanostatic charge-discharge (GCD) is an effective way to evaluate the specific capacitance of active materials. Figure 3a displays the charging-discharging curves of NPG/PPy(10 nm) and NPG/PPy(30 nm) at current density j m = 0.5 A g −1 under various deformations (please refer to Figure S5 in SI for GCD results of bare NPG). NPG/PPy(30 nm) exhibited linear and symmetric GCD curves, whereas, NPG/PPy(10 nm) showed plateaus at the end of the discharging process. Moreover, larger potential drops were observed in NPG/PPy(30 nm) in comparison with those in NPG/PPy(10 nm). However, the magnitude of the potential drop of individual specimen was unvaried, even at larger deformations. The charging and discharging (specifically of the linear part) time of the non-deformed specimens were longer than those obtained under deformations, where the GCD curves nearly overlap. Figure 3b displays the GCD curves of non-deformed NPG/PPy(10 nm) at various current density of j m = 0.5∼22.5 A g −1 . The plateau in the discharging curve at j m = 0.5 A g −1 was absent at larger current densities. However, pronounced potential drops were recognized as the current density increased. Specific capacitance values were evaluated from the GCD curves and displayed in Figure 3c. It is evident that C m values of both NPG/PPy hybrid materials decline with deformation at all studied current densities, as indicated by the black arrows. C m of both NPG/PPy hybrid materials decreases with j m until j m = 2.5 A g −1 . At this j m valu,e C m stabilized at about 260 F g −1 , as marked by the orange rectangular in Figure 3c. In the case of non-deformed NPG/PPy(10 nm), C m remains invariant up to 15 A g −1 , beyond which, C m gradually decreased. Yet, when NPG/PPy(10 nm) was deformed, a steady decrease of C m was initiated at a smaller current density of j m = 12.5 A g −1 . It is noted that C m of NPG/PPy(30 nm) abruptly dropped at j m = 7.5 A g −1 even the specimen was at a pristine state. The cycling performances of NPG/PPy hybrid materials were examined under strain values of 0% and 15%. Current densities in the orange rectangular area (Figure 3c) were elaborately chosen to attain comparable C m for each specimen. The results are compiled in Figure 3d. It is found that C m obtained under a deformation of 15% are smaller than those of 0% for both NPG/PPy(10 nm) and NPG/PPy(30 nm) at all explored current densities over the studied cycles. Moreover, for a given specimen, comparable C m values were obtained at different j m values under the same deformation except in the cases of 15%-deformed NPG/PPy(30 nm). C m values at the beginning and end of the cycling course are summarized in Table 1. One can find that in comparison with the non-deformed specimens, the durability of 15%-deformed ones was substantially impaired. Table 1. Specific capacitance, C m , of NPG/PPy hybrid materials at the beginning and end of GCD cycling under various deformations and current densities. The data in the table are in agreement with the data points shown in Figure 3d.

Electrochemical Impedance Spectroscopy
The electrochemical properties of NPG and NPG/PPy hybrid materials were also explored by electrochemical impedance spectroscopy (EIS). Figure 4a-c plot the Nyquist diagrams of bare NPG and NPG/PPy hybrid materials under various deformations. It has been shown that all of the curves consist of a distinct semicircle at high frequencies and a straight line at lower frequencies. The negligibly small discrepancies in the interceptions between Nyquist curves and real part-axes demonstrate that the bulk electrolyte resistance and any contact resistance keep unchanged under deformation for all the investigated specimens. This is also evidenced by the fitting parameter R 0 shown in Table 2. Yet, the radius was observed to increase with deformation. Despite the disturbances, the lower frequency region shows (quasi-) straight lines, which shift positively with deformation.   Capacitance contributes to both the real and imaginary parts of the impedance. However, the influence of the capacitance on the real part is negligible in a broad frequency range while it is decisive of the imaginary part. Accordingly, the imaginary part of the impedance is in focus as shown in Figure 4d-f. The frequency-dependent capacitance was calculated from the imaginary part of the impedance as [39]: where f , Z , and m represent frequency, imaginary part of the impedance, and mass of active material addressed in the following part. As can be seen in Figure 4, C m − f curves of bare NPG and NPG/PPy hybrid materials showed common features and are divided into three parts : (1) The part at high frequency range (larger than 100 Hz), where the capacitance seems to be frequency independent and contributes negligibly at various compression strain values. (2) The part at the frequency range of 100 Hz∼0.1 Hz, where the capacitance increases linearly along with the decreasing frequency. In this part, the capacitance value of NPG/PPy hybrids improved compared with that of bare NPG, which is consistent with CV and GCD results. Moreover, the capacitance values slightly decrease at increasing deformation and a given frequency value. (3) The part at the low frequency range (lower than 0.1 Hz), where the capacitance nearly approaches the saturation. Despite some disturbances in NPG/PPy hybrid materials, the dependence of capacitance on the deformation is similar to that observed for the middle frequency range.

Discussion
The present work studies the in situ electrochemical behavior of NPG/PPy hybrid materials subjected to compressive deformations in a range from 0% to 15%. The discussion starts with the current responses of non-deformed NPG and NPG/PPy. Despite the similar rectangular profiles, NPG and NPG/PPy store charges in different ways. In the explored potential window, anions (ClO 4 − in this work) are electrostatically adsorbed onto the gold ligament surface, following the capacitive charging mechanism [2,40,41]. On the other hand, anions migrate into the PPy matrix to maintain the charge neutrality when PPy is oxidized, which is the characteristic of the pseudocapacitive charging mechanism [41][42][43]. The electrochemical responses were normalized to the weight of the active material, m. Since the surface atoms take up a high percentage of the overall atoms in nano-scaled objects [44], m is equal to m NPG for the bare NPG. Yet, when NPG is coated by a second active material, say, MnO 2 and PPy, the current response mainly originates from the reactions between active material matrix and bulk solution, whereas the electrosorption at NPG/MnO 2 and the NPG/PPy interface is negligibly small [45,46]. To this end, m = m PPy for NPG/PPy hybrid materials. In this work, m NPG is one order of magnitude higher than m PPy . Moreover, it has been shown that more charge carriers participate in the pseudocapacitive charging process compared to those in the double layer process [47,48]. Therefore, NPG/PPy hybrid materials yield a much higher specific current density, j m (Figure 2a), and specific capacitance, C m (Figure 2d), compared with bare NPG. The resulting current responses ( Figure S7) and m PPy synergetically determine higher C m and j m for NPG/PPy(10 nm) compared to those of NPG/PPy(30 nm). The same phenomenon has also been revealed in the literature [17,27,29], where the lower C m values of materials with thicker deposited layers are ascribed to the smaller surface area exposed to the electrolyte and only partial PPy take part in the reactions. A similar phenomenon was also observed in the GCD results, where NPG/PPy(10 nm) processed a higher C m in comparison with NPG/PPy(30 nm) (Figure 3c).
The availability of active material is also influenced by the kinetics of electrolyte transport. The current density increases with scan rates (Figure 2c), indicating excellent electronic conductivity of the NPG/PPy [49]. However, the deviation of the CV curve from a rectangular shape (Figure 2c) and the drop of C m at the faster scan rates (Figure 2d) observed for both NPG/PPy specimens suggest the dominant role of mass transport in the NPG/PPy/electrolyte system [50,51]. On the other hand, the linear I − v relationship ( Figure S2b) and the fairly unvaried C m over studied scan rates (inset in Figure 2d) manifest the adsorption-controlled process in the NPG/electrolyte system. In the case of GCD, when the discharging current density increases, the incremental IR drops (Figures 3b and S6) and the degressive C m (Figures 3c and S5c) demonstrate insufficient active material involved in the reaction, especially, for NPG/PPy. Till now, it has been clarified that the electrochemical performance of NPG and NPG/PPy under zero deformation, where the microstructure is kept unchanged (neglecting the electrochemical process-induced expansion and contraction with amplitudes of ∼10 −4 [18,52]), is substantially determined by the amount of involved active material, which is closely associated with the kinetics of the electrolyte in the confined microstructure. Below, the impact of the compressive deformation-induced microstructure change on the mass transport and the accompanying electrochemical behavior are discussed.
For bare NPG, comparable CV curves (inset in Figure 2a) and GCD curves ( Figure S5a) were obtained under deformations of 0% and 15%. This demonstrates that the capacitive charging and adsorption processes in NPG/electrolyte are negligibly impacted in the deformed microstructure. In the case of NPG/PPy hybrid materials, however, the CV curves under deformation of 15% deviate from those of 0%. Moreover, despite the CV curves obtained under 2.5%∼15% being similar, the corresponding C m values were observed to decrease with deformation (Figure 2d), indicating that the pseudocapacitive charging and mass transport are substantially influenced in the compacted specimens. Besides, the descending C m values evaluated from GCD results under the ascending deformations (Figure 3c) also verify the aforementioned findings.
As is widely acknowledged, semi-circles at a high frequency regime in the Nyquist plots reflect the charge transfer resistance between the electrode and solution. The semicircle in the bare NPG can be ascribed to the oxidation of residual Ag at the applied potential of 0.5 V [53,54]. For the NPG/PPy hybrid materials, it can be ascribed to the ion transfer at the PPy/solution boundary. The larger R ct obtained from EIS data indicate larger charge transfer resistance and slower mass transfer kinetics. It is also reported that the decreased availability of active material for electrolyte impregnation will induce larger impedance [55], implying the significant role of deformation-caused microstructure change on the properties of electrode material. The behavior of the interface in the oxidized state in both specimens was similar. Towards the high and medium frequencies, the role of diffusion-like and charge transfer steps increases with the deformation, which also explain the current response reduction under different deformation in the CV tests. The overall current output comprises surface-controlled (capacitive) and diffusioncontrolled components. According to the peak current (i) in CV curves at various scan rates (v), they can be identified via the following equation [56,57]: where a and b are adjustable parameters. The slope of log(i) vs. log(v) plot gives b. Pure capacitive dominated processes and diffusion dominated processes are characterized by a b of 1 and 0.5, respectively. When b lies between 0.5 and 1, a mixed capacitive-diffusion controlled process is identified. At a given potential (V), the two contributions can be distinguished according to the following equation [56,57]: where k 1 v and k 2 v 1/2 respectively represent surface capacitive current and diffusion-limited current. This equation can also be rearranged to: to this end, k 1 and k 2 can be evaluated from the slope and intercept from i(V)/v 1/2 vs. the v 1/2 plot, respectively. Figure 5a presents the linear regressions of log(j m ) vs. log(v), yielding b = 0.98 (R 2 = 0.998), b = 0.90 (R 2 = 0.998), and b = 0.70 (R 2 = 0.996) for non-deformed NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm), respectively. This suggests a nearly pure capacitive process in bare NPG and mixed capacitive-diffusion dominated processes in NPG/PPy specimens (Figure 5b). Under deformation of 15%, a comparable b value (0.98, R 2 = 0.999) was obtained for NPG, implying that the surface capacitive process is free from deformation and the influence of surface area loss caused by the gold ligaments contact (see discussion below) on the capacitance of bare NPG can be neglected. On the other hand, smaller slopes of b = 0.88 (R 2 = 0.993) and b = 0.67 (R 2 = 0.990) are estimated respectively for 15%-deformed NPG/PPy(10 nm) and NPG/PPy(30 nm), leading to an improved contribution of diffusion process under deformation (Figure 5c).
The increased diffusion-controlled effect is related to the intrinsic microstructure change of the material under compression. Higher electrochemical performance has been reported in nanoporous materials with hierarchical microstructure due to the improved diffusion of electrolyte in large pores [58][59][60][61]. In the context of nanoporous metal with monolithic-scale pore distribution, the mass transport should be different from that in hierarchical nanoporous materials. An important figure of merit to characterize the effect of microstructure of a porous electrode on its effective transport is tortuosity, τ [62,63]. In terms of geometrics, τ is the fraction of the shortest pathway for the electrolyte to flow through the porous structure and the Euclidean distance between the start and end points of this pathway. According to the Bruggeman equation, the tortuosity-microstructure relationship is described as [63,64]: where is the porosity. Taking the porosity of NPG of ∼ 0.7 and PPy film density of ρ PPy = 1.5 g/cm 3 [65,66], τ was estimated to be 1.08, 1.10, and 1.17 for NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm), respectively. As has been reported, the change in Poisson's ratio of nanoporous gold with ligament size of 120∼180 nm, which embraces the ligament size in the present work, was smaller than 0.025 when the NPG was compressed up to 20% [67]. In other words, such a small transverse deformation mainly led to the densification of NPG in the loading axis under compression, giving rise to a smaller and, consequently, a larger τ. Under a deformation of 15%, τ of NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm) increased to 1.13, 1.15, and 1.22, respectively. Tortuosity has also been reported to be related to the diffusion coefficient [63,68,69]: where D bulk and D eff represent bulk diffusion coefficient and effective diffusion coefficient, respectively. To this end, D eff has been revealed to decrease by ∼21% in all 15%-deformed NPG and NPG/PPy hybrid materials. The limited mass transport might be attributed to the microstructure change under deformation. Simulations of compression of random networks demonstrates that the struts along the load tend to be bended, while the ones perpendicular to the load will be stretched [70]. Given this, the adjacent ligaments in the deformed network are anticipated to encounter each other, as indicated by the red ovals in the SEM images (Figure 1d-f), giving rise to a larger amount of connections. With increasing compressing of the specimen, its connectivity density will increase and result in a more complex network. Finally, this leads to a restrained mass transport.

Conclusions
This work explores the electrochemical behavior of the NPG/PPy supercapacitor under various compression deformation states. The macroscopic specimen, synthesized by dealloying and electropolymerization, consists of billions of nano-scaled ligaments and pores. The unique bi-continuous network provides numerous pathways for electrolyte and active sites, meanwhile exhibiting considerable ability against the external load, predestining NPG/PPy as a promising model material to study the electrochemical performance under compressive deformation. Electrochemical measurements of bare NPG, NPG/PPy(10 nm), and NPG/PPy(30 nm) were carried out in situ under different compression strains in the range of 0 to 15%, respectively. NPG/PPy(10 nm) possesses larger specific capacitance, C m , as compared with NPG/PPy(30 nm) and bare NPG. The C m is found to decrease with deformation at studied scan rates and discharging current densities for all explored specimens. NPG/PPy hybrid materials show high stability with 70% capacitance retained after 4000 cycles. Moreover, the charge transfer resistance, R ct , increases with deformation. This electrochemical behavior of NPG/PPy is due to the locally reduced mass transport of electrolyte caused by the formation of new connections between the neighboring ligaments under the application of compression loads. The fundamental understanding of the effect of deformation on the performance of energy storage materials revealed in this study paves the way for their practical application in wearable devices.

Institutional Review Board Statement: Not applicable
Data Availability Statement: The data presented in this study are available on request from the corresponding author.