High-performance Flexible Energy Research Articles

High-Conductivity and Ultrastretchable Self-Healing Hydrogels for Flexible Zinc-Ion Batteries.

Aqueous zinc-ion batteries are promising candidates for flexible energy storage devices due to their safety, economic efficiency, and environmental friendliness. However, the uncontrollable dendrite growth and side reactions at the zinc anode hinder their commercial application. Herein, we designed and synthesized a dual network self-healing hydrogel electrolyte with zwitterionic groups (PAM-PAAS-QCS), which can be used for the large deformations of flexible devices due to its excellent stretchability (ε = 5100%). The incorporation of zwitterionic groups into the PAM-PAAS-QCS hydrogel electrolyte endows it with high ionic conductivity (33.61 mS/cm), a wide electrochemical stability window, and the ability to suppress zinc dendrite formation and side reactions. Besides, the Zn//Zn symmetric cell with PAM-PAAS-QCS can stably plate and strip zinc for 1500 h at 0.5 mA/cm2, and the Zn//Polyaniline full cell retains 82.4% of its capacity after 1500 cycles at 1 A/g. Additionally, flexible batteries based on both the original and self-healed PAM-PAAS-QCS hydrogel electrolytes demonstrate good cycling stability and stable charge-discharge performance under various bending conditions. This self-healing hydrogel electrolyte with excellent stretchability and high ionic conductivity is expected to pave the way for the development of high-performance flexible energy storage and wearable devices.

CuO nanoparticles embedded in laser-induced graphene for flexible planar micro-supercapacitors

Utilizing predefined electrode geometries, laser direct writing technology is employed to intricately inscribe flexible polyimide (PI) films, thereby inducing porous graphene patterned electrodes for flexible planar micro-supercapacitors (MSCs), which greatly facilitates the integration of MSCs into functional devices for power supply. Nevertheless, prevailing challenges confront current flexible MSCs relying on laser-induced graphene (LIG), including the constrained electrochemical functionality of pure LIG electrodes and the uneven incorporation of heterogeneous constituents within LIG electrodes. In light of these challenges, this study delves into the fundamental mechanism underlying the formation of polyimide (PI) films and introduces an innovative approach to uniformly integrate CuO nanoparticles into the poly (acrylic acid) (PAA) precursor solution. The subsequent imidization process culminates in the synthesis of a CuO-embedded PI film. The research progresses to the fabrication of shape-controllable CuO/LIG patterned electrodes utilizing a precision laser direct writing technique, and the subsequent construction of flexible planar MSCs. Harnessing the synergistic interactions between the dual components within the electrode, the resulting MSC possesses an impressive areal capacitance of 6.45 mF·cm-2, coupled with an energy density of 0.896 mWh·cm-2 and a power density of 0.081 mW·cm-2, thus illustrating the potential of this innovative material integration for high-performance flexible energy storage implementations.

Facile assembly of flexible, stretchable and attachable symmetric microsupercapacitors with wide working voltage windows and favorable durability

With the increasing development of intelligent robots and wearable electronics, the demand for high-performance flexible energy storage devices is drastically increasing. In this study, flexible symmetric microsupercapacitors (MSCs) that could operate in a wide working voltage window were developed by combining laser-direct-writing graphene (LG) electrodes with a phosphoric acid-nonionic surfactant liquid crystal (PA-NI LC) gel electrolyte. To increase the flexibility and enhance the conformal ability of the MSC devices to anisotropic surfaces, after the interdigitated LG formed on the polyimide (PI) film surface, the devices were further transferred onto a flexible, stretchable and transparent polydimethylsiloxane (PDMS) substrate; this substrate displayed favorable flexibility and mechanical characteristics in the bending test. Furthermore, the electrochemical performances of the symmetric MSCs with various electrode widths (300, 400, 500 and 600 μm) were evaluated. The findings revealed that symmetric MSC devices could operate in a large voltage range (0–1.5 V); additionally, the device with a 300 μm electrode width (MSC-300) exhibited the largest areal capacitance of 2.3 mF cm−2 at 0.07 mA cm−2 and an areal (volumetric) energy density of 0.72 μWh cm−2 (0.36 mWh cm−3) at 55.07 μW cm−2 (27.54 mW cm−3), along with favorable mechanical and cycling stability. After charging for ~20 s, two MSC-300 devices connected in series could supply energy to a calculator to operate for ~130 s, showing its practical application potential as an energy storage device. Moreover, the device displayed favorable reversibility, stability and durability. After 12 months of aging in air at room temperature, its electrochemical performance was not altered, and after charging-discharging measurements for 5000 cycles at 0.07 mA cm−2, ~93.6% of the areal capacitance was still retained; these results demonstrated its practical long-term application potential as an energy storage device.

Polymethylene trisulfide/reduced graphene oxide nanocomposite electrodes: Deciphering microstructure/electrochemistry relationship

Flexible polysulfide electrodes can play a crucial role in the future development of wearable energy storage devices. Understanding the electrochemical energy storage mechanism in these electrodes can guide the engineering of polysulfides and their composites to design high-performance flexible energy storage devices. Polymethylene trisulfide (PMTS) and PMTS/reduced graphene oxide (rGO) nanocomposites, synthesized via in-situ interfacial polymerization, are introduced as active materials for developing high-performance electrodes. The fundamental scientific objective of this study is to uncover the correlation between the microstructural properties of linear polysulfides and the electrochemical behavior of low molecular weight intermediate polysulfide species. Based on microstructural studies, Coulomb interactions between rGO and PMTS macromolecules dictate PMTS chain confinements. Such molecular confinements affect the glass transition temperature and the crystallinity of PMTS, hence controlling the electrochemistry of electrodes. A high specific capacity of 366 mAh/g (5 μA) is reached using the flexible PMTS/0.5 wt% rGO nanocomposite electrode in Li-PMTS cells. The suggested mechanism for the anodic and cathodic polarizations in Li-PMTS cells is based on the formation of low molecular weight sulfide polymeric species. Therefore, the crystallinity and moveability of polymeric chains are introduced as structural features of polysulfide electrodes that can be utilized to improve the performance of energy storage systems based on these active materials.

High-performance piezoelectric energy harvesting in amorphous perovskite thin films deposited directly on a plastic substrate

Most reported thin-film piezoelectric energy harvesters have been based on cantilever-type crystalline ferroelectric oxide thin films deposited on rigid substrates, which utilize vibrational input sources. Herein, we introduce flexible amorphous thin-film energy harvesters based on perovskite CaCu3Ti4O12 (CCTO) thin films on a plastic substrate for highly competitive electromechanical energy harvesting. The room-temperature sputtering of CCTO thin films enable the use of plastic substrates to secure reliable flexibility, which has not been available thus far. Surprisingly, the resultant amorphous nature of the films results in an output voltage and power density of ~38.7 V and ~2.8 × 106 μW cm−3, respectively, which break the previously reported record for typical polycrystalline ferroelectric oxide thin-film cantilevers. The origin of this excellent electromechanical energy conversion is systematically explored as being related to the localized permanent dipoles of TiO6 octahedra and lowered dielectric constant in the amorphous state, depending on the stoichiometry and defect states. This is the leading example of a high-performance flexible piezoelectric energy harvester based on perovskite oxides not requiring a complex process for transferring films onto a plastic substrate.

Research and development of double layer P-doped laser induced graphene thin film electrode for flexible micro-supercapacitor applications

Laser-induced graphene (LIG) has garnered significant attention for its cost-effectiveness and high efficiency in fabricating flexible micro-energy storage devices. In this study, we devised a simple method to fabricate double layer P-doped LIG electrodes through repetitive laser induction technology for high-performance flexible energy storage applications. Instead of utilizing commercial polyimide (PI) thin film, we optimized the formation process of P-doped PI thin film and achieved a highly flexible double layer P-doped LIG thin film electrode with a uniformly porous structure and the high porosity through repeated laser induction processes. Experimental results demonstrated that the developed double layer P-doped LIG thin film electrode exhibits high porosity, high specific areal capacitance of 180 mF cm−2, and high energy density of 0.025 mWh cm−2. Furthermore, an all-solid-state micro-supercapacitor utilizing hydrogel electrolyte was assembled, demonstrating a high areal capacitance of 62 mF cm−2 and excellent cycling stability with 95% capacitance retention after 6000 charging/discharging cycles. Moreover, the developed all-solid-state micro-supercapacitor successfully powered a light-emitting diode, showcasing its significant potential for practical energy storage applications.

Conformal Engineering of Both Electrodes Toward High-Performance Flexible Quasi-Solid-State Zn-Ion Micro-Supercapacitors.

The severe Zn-dendrite growth and insufficient carbon-based cathode performance are two critical issues that hinder the practical applications of flexible Zn-ion micro-ssupercapacitors (FZCs). Herein, a self-adaptive electrode design concept of the synchronous improvement on both the cathode and anode is proposed to enhance the overall performance of FZCs. Polypyrrole doped with anti-expansion graphene oxide and acrylamide (PPy/GO-AM) on the cathode side can exhibit remarkable electrochemical performance, including decent capacitance and cycling stability, as well as exceptional mechanical properties. Meanwhile, a robust protective polymeric layer containing reduced graphene oxide and polyacrylamide is self-assembled onto the Zn surface (rGO/PAM@Zn) at the anode side, by which the "tip effect" of Zn small protuberance can be effectively alleviated, the Zn-ion distribution homogenized, and dendrite growth restricted. Benefiting from these advantages, the FZCs deliver an excellent specific capacitance of 125mFcm-2 (125Fcm-3) at 1mAcm-2, along with a maximum energy density of 44.4µWhcm-2, and outstanding long-term durability with 90.3% capacitance remained after 5000 cycles. This conformal electrode design strategy is believed to enlighten the practical design of high-performance in-plane flexible Zn-based electrochemical energy storage devices (EESDs) by simultaneously tackling the challenges faced by Zn anodes and capacitance-type cathodes.

Development of novel paper-based supercapacitor electrode material by combining copper-cellulose fibers with polyaniline

Along with the developing of flexible electronics, there is a strong interest in high performance flexible energy storage materials. As natural carbohydrate polymer, cellulose fibers have potential applications in the area due to their biodegradability and flexibility. However, their conductive and electrochemical properties are impossible to meet the demands of practical applications. In this study, cellulose fibers were combined with polyaniline to develop novel paper-based supercapacitor electrode material. Cellulose fibers were firstly coordinated to Cu(II) and subsequently involved in polymerization of polyaniline. Not only the mass loading of polyaniline was significantly increased, but also an impressive area specific capacitance (2767 mF/cm2 at 1 mA/cm2) was achieved. The developed strategy is efficient, environmentally friendly, and has implications for the development of cellulosic paper-based advanced functional materials.

Dendrite-free zinc anode enabled by zwitterionic organic hydrogel electrolytes for high-voltage zinc-ion hybrid capacitors

Aqueous zinc-ion hybrid supercapacitors (ZIHC) have been widely researched due to their inherent high safety, low cost, and high power. However, the low operating voltage of aqueous electrolytes, H2O-induced side reactions, and intractable dendrites severely compromise the energy output and durability of ZIHC. Herein, a freeze-tolerant zwitterionic organic hydrogel electrolyte (PSAMOHE) was constructed for high-voltage flexible ZIHC. The hydrogen bonding between ethylene glycol and water inhibited the formation of ice crystals, preventing the electrolyte from freezing at −40 °C. Concurrently, the hydrophilic PSAMOHE mitigated harmful side reactions and achieved a wide electrochemical stability window (2.2 V) by anchoring water molecules. In addition to exhibiting exceptional interface adhesion and mechanical adaptability, PSAMOHE with charged functional groups effectively facilitated ion migration, diminished the desolvation energy barrier of hydrated Zn2+, and induced uniform Zn deposition. By combining these advantages, the assembled flexible ZIHC exhibited a battery-level specific capacity of 269.1 mAh/g (at 0.5 A/g), impressive environmental adaptability, and excellent mechanical adaptability. Impressively, the ZIHC maintained 89.5 % of the initial capacity and obtained a dendrite-free Zn anode after 14,000 cycles of charge and discharge. This study provides valuable insights into the exploration of hydrogel electrolyte engineering for high-performance zinc-based flexible energy storage devices.

Improving the capacitance of hydrogel-based supercapacitors by pre-depositing a zwitterionic 3,4-ethylenedioxythiophene

Polymer hydrogel electrolytes show great advantages in the flexible electronic applications of supercapacitors, but the poor interfaces between electrode and electrolyte are limiting their energy and power densities. In this work, by taking the well-developed pair of poly(vinyl alcohol)/H2SO4 gel electrolyte and graphene film electrode as a prototype, after electrochemically depositing a functional monomer of zwitterionic 3,4-ethylenedioxythiophene (EDOTSB) onto the graphene film electrodes, the specific capacitance of supercapacitors receives a 2.5-fold increase up to 248 mF cm−2 (346 F g−1). By comparing with other pendent groups on EDOT, the decisive role of the zwitterionic group is demonstrated. Attributed to the strong hydration ability of the zwitterion group, the deposition of EDOTSB effectively improves the hydrophilicity of graphene film electrodes, so that the interfacial affinity between the electrode and hydrogel electrolyte is greatly promoted. On the one hand, the EIS measurements certify that the charge-transfer resistance is largely reduced. On the other hand, tests with electrochemical quartz crystal microbalance demonstrate that the interior of graphene film is highly accessible for EDOTSB, thereby enlarging the accessible surface area on the electrode and accelerating the electrolyte infilling process. Furthermore, the general comparison with the liquid electrolyte counterpart is also discussed. This developed method is highly universalizable and can find applications in different electrode/electrolyte supercapacitors and other high-performance flexible energy storage devices.

Highly efficient utilization of polypyrrole enabled by dispersed buckypaper tape for high-performance flexible energy storage

This work develops a facile anodic treatment process to prepare dispersed buckypaper tape for the highly efficient utilization of polypyrrole towards durable flexible energy storage.

A flexible supercapacitor with high energy density and wide range of temperature tolerance using a high-concentration aqueous gel electrolyte

As the demand for a wide range of wearable devices increases, extensive effort is devoted to developing high-performance flexible energy storage devices such as batteries and supercapacitors. Of particular interest, flexible supercapacitors using aqueous electrolytes have high application potential owing to their many advantages including low cost, harmlessness to the human, and environmental safety compared to others using electrolytes such as ionic liquids and organic electrolytes. However, poor temperature tolerance and narrow operation voltage window have hindered the practical application of aqueous supercapacitors. In this study, we report on a wide temperature-tolerant flexible aqueous supercapacitor featuring high electrochemical performance designed by a deliberate selection of electrode materials and electrolytes. As a flexible electrode, three-dimensional microporous graphene foam coated with conducting polymer Polypyrrole (PPy) is used to enhance capacitance up -to 90.0 F/g by increasing the surface area and inducing the pseudo-capacitance of PPy. As a gel-type electrolyte, a high-concentration NaClO4 is mixed with Polyvinyl alcohol to enlarge the voltage window to 1.8 V and a stable temperature range from -25 to 80°C, even under repetitive bending deformation. The fabricated supercapacitor exhibits a superior energy density of 37.4 Wh kg−1 and maintains 92.0% of initial capacitance at room temperature after three repeated cycles of cooling/heating across a wide temperature range over 100°C. This work suggests a high potential application of the fabricated supercapacitor as an eco-friendly and stable energy storage system for powering diverse wearable devices under various conditions.

Scalable fabrication of textile-based planar-structured supercapacitors with excellent capacitive performance

The researchers have been engaged in the development of textile-based high-performance flexible energy storage devices. The conventional fabrics are transformed into electrode composites by uniformly depositing polypyrrole (PPy) coating onto them using a simple interfacial solution polymerization method. The traditional textiles encompass cellulose fabrics such as cotton and ramie, protein fabrics like silk and wool, as well as chemical fiber fabric including polyester, polyamide, and acrylon. The PPy can be effectively coated onto the surface of cellulose fibers and penetrate into their interior, resulting in significantly higher loading capacity on cotton and ramie fabrics compared to other types of fibers. The two fabric electrodes (cotton@PPy and ramie@PPy) have better capacitive properties, especially the areal capacitance of ramie@PPy reaches 2836 mF cm−2. The PPy-coated fabric is precisely divided into standardized interdigital electrodes of consistent dimensions through the utilization of laser cutting techniques. The fabrication of a planar supercapacitor can be achieved through the straightforward assembly of two interdigital electrodes. The planar supercapacitor based on ramie@PPy shows a maximum energy density of 8.21 μWh cm−2 at power density of 0.20 mW cm−2. After undergoing 5000 cycles, the device demonstrates a remarkable ability to retain 90 % of its initial capacitance. The assembled supercapacitors exhibit exceptional flexibility and practicality, enabling power supply to electronic devices when connected in series. The fabric-based flexible supercapacitor can be easily mass-produced, making it a promising candidate for flexible energy storage devices.

Boosting the Lithium Storage Properties of a Flexible Li4Ti5O12/Graphene Fiber Anode via a 3D Printing Assembly Strategy

Traditional lithium-ion batteries cannot meet the high flexibility and bendability requirements of modern flexible electronic devices due to the limitations of the electrode material. Therefore, the development of high-performance flexible energy storage devices is of great significance for promoting flexible electronics. In recent years, one-dimensional flexible fiber lithium-ion batteries have been rapidly developed due to their advantages of high flexibility and bendability. However, it remains highly challenging to realize 1D flexible fiber lithium-ion batteries with excellent electrochemical properties and good mechanical performance. In this work, a reduced graphene oxide-based printing ink is proposed for the fabrication of flexible Li4Ti5O12/graphene fiber electrodes using a 3D printing assembly strategy. It is noteworthy that the green reducing agent vitamin C was used to reduce the graphene oxide in one step, which improved the conductivity of the fiber electrode. Furthermore, a 3D conductive network was constructed inside the fiber electrodes due to the high specific surface area of the reduced graphene oxide, which enhanced the electronic conductivity and ion mobility. The fiber electrode not only exhibits good mechanical performance, but also has excellent electrochemical properties. Equally importantly, the method is simple and efficient, and the working environment is flexible. It can precisely control the shape, size and structure of the one-dimensional fiber flexible electrode, which is of great significance for the development of future flexible electronic devices.

High-performance flexible energy storage: Decorating wrinkled MXene with in situ grown Cu2O nanoparticles

The precise design and fabrication of electrode materials is important for the development of high-performance flexible supercapacitors. Cu2O/MXene film electrodes with an interconnected conductive network structure are prepared in this work by in situ growth of Cu2O nanoparticles in a Ti3C2Tx dispersion, followed by alkali induction and vacuum filtration. The interconnected crimpled Ti3C2Tx structure produced by alkali induction not only works as the self-supported conductive network of the thin film electrode but also demonstrates sufficient open pores and high surface area, which can promote electrolyte penetration and increase active sites for energy storage. The synergy between Cu2O nanoparticles and the crimpled Ti3C2Tx framework leads to good structural stability and electrochemical performance. The results show that the Cu2O/MXene electrode exhibits a high specific area capacitance of 1518 mF cm−2 in 1 M LiCl electrolyte. In addition, the all-solid-state flexible supercapacitor fabricated with the Cu2O/MXene electrode exhibits excellent cyclic stability and flexibility; the capacity retains 94.3% after 10,000 charge and discharge cycles, and the energy storage performance remains stable after 50 mechanical bending cycles.

High mass loading paper-based electrode material with cellulose fibers under coordination of zirconium oxyhydroxide nanoparticles and sulfosalicylic acid

With the rapid expansion of the flexible electronics market, it is critical to develop high-performance flexible energy storage electrode materials. Cellulose fibers, which are sustainable, low cost, and flexible, fully meet the requirements of flexible electrode materials, but they are electrically insulating and cause a decrease in energy density. In this study, high-performance paper-based flexible electrode materials (PANI:SSA/Zr-CFs) were prepared with cellulose fibers and polyaniline. A high mass loading of polyaniline was wrapped on zirconia hydroxide-modified cellulose fibers under metal-organic acid coordination through a facile in situ chemical polymerization process. The increase in mass loading of PANI on cellulose fibers not only improves the electrical conductivity but also enhances the area-specific capacitance of the flexible electrodes. The results of electrochemical tests show that the area specific capacitance of the PANI:SSA/Zr-CFs electrode is 4181 mF/cm2 at 1 mA/cm2, which is more than two times higher than that of the electrode with PANI on pristine CFs. This work provides a new strategy for the design and manufacture of high-performance flexible electronic electrodes based on cellulose fibers.

Rational designed Cu-MOF@1D carbon nanofibers as free-standing and flexible electrode for robust electrochemical energy storage

The present study reported the performance of free-standing carbon nanofibers decorated with copper-metal-organic frameworks (Cu-MOFs). A green electrospinning technique was utilized to obtain nanofiber sheets that were carbonized and activated to produce activated carbon nanofiber sheets (ACNFs). These ACNFs consist of inherent oxygen functionalities of the lignin that can aid the growth of MOF structure on it in a single step, which motivated us to do this work. Cu-MOF particles were in-situ grown over the surface of ACNFs using a hydrothermal-assisted technique. The developed materials were characterized using FESEM, Raman Spectroscopy and BET analysis in order to identify morphological, porosity, and surface area transformations. Along with these, Cyclic Voltammetry (CV), Electrochemical Impedance Spectroscopy (EIS), and Galvanostatic Charge-Discharge (GCD) studies were performed to compare the electrochemical performance of the Cu-MOF, ACNF, and Cu-MOF@ACNF as electrode materials for supercapacitors. Among three electrodes, the Cu-MOF@ACNF sheet reveals a higher specific capacitance of 303.2 F/g compared to ACNF (203.3 F/g) and Cu-MOF (68.2 F/g) at the same current density of 1 A/g. Based on the higher performance of Cu-MOF@ACNF two types of symmetrical devices, i.e., aqueous (using electrolyte-impregnated filter paper) and solid-state devices (using a polymeric gel electrolyte), were fabricated. The all-solid-state supercapacitor device was found to feature high flexibility, stand-alone characteristics, and excellent performance as an electrode with a working potential window of 0–2.0 V. The device demonstrates a high energy density of 78.71 Wh/kg and a power density of 1050.0 W/kg, along with high coulombic efficiency (99.8 %) after 10,000 cycles. The achieved performance is superior to many published reports, revealing that the developed composite materials hold prospect for applications in green and high-performance flexible energy storage devices.

Utilizing hybrid faradaic mechanism via catalytic and surface interactions for high-performance flexible energy storage system

Improving the capacitance and energy density is a significant challenge while developing practical and flexible energy storage system (ESS). Redox mediators (RMs), as redox-active electrolyte additives, can provide additional energy storing capability via electrochemical faradaic contribution on electrodes for high-performance flexible ESSs. Particularly, determining effective material combinations between electrodes and RMs is essential for maximizing surface faradaic redox reactions for energy-storage performance. In this study, an electrode-RM system comprising heterostructured hybrid (carbon fiber (CF)/MnO2) faradaic electrodes and iodine RMs (I-RMs) in a redox-active electrolyte is investigated. The CF/MnO2 with the I-RMs (CF/MnO2-I) induces dominant catalytic faradaic interaction with the I-RMs, significantly enhancing the surface faradaic kinetics and increasing the overall energy-storage performance. The CF/MnO2-I ESSs show a 12.6-fold (or higher) increased volumetric energy density of 793.81 mWh L−1 at a current of 10 µA relative to ESSs using CF/MnO2 without I-RMs (CF/MnO2). Moreover, the CF/MnO2-I retains 93.1% of its initial capacitance after 10,000 cycles, validating the excellent cyclability. Finally, the flexibility of the ESSs is tested at different bending angles (180° to 0°), demonstrating its feasibility for flexible and high-wear environments. Therefore, CF/MnO2 electrodes present a practical material combination for high-performance flexible energy-storage devices owing to the catalytic faradaic interaction with I-RMs.

Aestivum-inspired photothermal 3D-MXene-unity membrane-aerogel for flexible supercapacitor with solar enhanced performance

Designing high gravimetric capacitance, flexible, and functional structural electrodes based on 2D nanomaterials is crucial for wearable electronics, however, it is still limited by serious restacking problems and uncontrollable assembly processes. Herein, inspired by a specialized network of rigidity-flexible integration in aestivum, an effective half-dry 2D-1D-2D pre-assembly combined with an “ice templating” strategy was proposed to construct a novel 3D-MXene-unity membrane-aerogel for the desirable supercapacitor substrate with energy harvesting capacity, addressing the incompatible contradiction between electrochemical properties and desirable mechanical strength. With cellulose nanofiber serving as a 1D structural modifier as well as black-phosphorus nanosheets applied as a 2D restacking reliever and electron-conductive network jointer, the multi-leveled mimicked topology facilitated the configured complexity of the membrane-aerogel can be achieved to be utilized in multifunctional composite electrodes. The resulting super-flexible and net-shaped 3D-MXene-unity membrane-aerogel showed low-tortuosity topology, superior electron-conductive network (870 S/cm), outstanding mechanical strength (53.2 MPa), and favorable electrochemical property (215 F/g), hardly achieved in a single system. Because of the synergistic photo-thermal capability from MXene and BP, assembled supercapacitors can harvest energy from sunlight and result in a 196% enhancement in capacitance. This work would lay a significant foundation for the construction of high-performance flexible energy storage devices.

FeV LDH Coated on Sandpaper as an Electrode Material for High-Performance Flexible Energy Storage Devices

Recently, considerable research efforts to achieve advanced design of promising electroactive materials as well as unique structures in supercapacitor electrodes have been explored for high-performance energy storage systems. We suggest the development of novel electroactive materials with an enlarged surface area for sandpaper materials. Based on the inherent micro-structured morphologies of the sandpaper substrate, nano-structured Fe-V electroactive material can be coated on it by facile electrochemical deposition technique. A hierarchically designed electroactive surface is covered with FeV-layered double hydroxide (LDH) nano-flakes on Ni-sputtered sandpaper as a unique structural and compositional material. The successful growth of FeV-LDH is clearly revealed by surface analysis techniques. Further, electrochemical studies of the suggested electrodes are carried out to optimize the Fe-V composition as well as the grit number of the sandpaper substrate. Herein, optimized Fe0.75V0.25 LDHs coated on #15000 grit Ni-sputtered sandpaper are developed as advanced battery-type electrodes. Finally, along with the negative electrode of activated carbon and the FeV-LDH electrode, it is utilized for hybrid supercapacitor (HSC) assembly. The fabricated flexible HSC device indicates high energy and power density by showing excellent rate capability. This study is a remarkable approach to improving the electrochemical performance of energy storage devices using facile synthesis.