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Needle-like CoO nanowires have been successfully synthesized by a facile hydrothermal process on an electrospun carbon nanofibers substrate. The as-prepared sample mesoporous CoO nanowires aligned vertically on the surface of carbon nanofibers and cross-linked with each other, producing loosely porous nanostructures. These hybrid composite electrodes exhibit a high specific capacitance of 1068.3 F g−1 at a scan rate of 5 mV s−1 and a good rate capability of 613.7 F g−1 at a scan rate of 60 mV s−1 in a three-electrode cell. The CoO NWs@CNF//CNT@CNF asymmetric device exhibits remarkable cycling stability and delivers a capacitance of 79.3 F/g with a capacitance retention of 92.1 % after 10,000 cycles. The asymmetric device delivers a high energy density of 37 Wh kg−1 with a power density of 0.8 kW kg−1 and a high power density of 16 kW kg−1 with an energy density of 23 Wh kg−1. This study demonstrated a promising strategy to enhance the electrochemical performance of flexible supercapacitors. [ABSTRACT FROM AUTHOR]

Different modifications of woven carbon fiber (WCF) based on carbon aerogel (CAG), copper oxide nanoparticles (CuO-NPs), and lignin (LIG) has been tested and used to study their effect on the fabrication and performance of a flexible supercapacitor. New symmetric flexible supercapacitors (SFSCs) were fabricated using different separators. According to the electrochemical results, the device fabricated using CAG and woven glass fiber (WGF) in a sandwich type configuration CAG/WGF/CAG embedded in H3PO4/PVA exhibited the best performance (1.4 F/g, 0.961 W/kg, 0.161 Wh/kg). A proof of concept based on a LED powered on and a bending test was done, and the capacitor demonstrated excellent electrochemical values even during and after bending. The new device was able to recover 96.12% of its capacitance when returned to its original unbent position. The manufacturing process was critical, as the fibers or layers must be completely embedded in the gel electrolyte to function effectively. A double flexible supercapacitor connected in parallel was fabricated and it showed higher stability, in the same voltage window, yielding 311 mF/cm2 of areal capacitance. [ABSTRACT FROM AUTHOR]

The ever-growing interest in wearable electronic devices has unleashed a strong demand for sustainable and flexible power sources that are represented by the combination of flexible energy harvesting with storage devices/technologies. Triboelectric nanogenerators (TENG), which harvest mechanical energy and charge their matching supercapacitors (SCs), may form a distributed power system with flexibility to tap their potential applications in powering wearable electronic devices. This review aims to cover the recent progress in the integration of TENG with flexible SC in terms of operation principle, material selection, device configuration and power management, with an accent on the application scenario in flexible wearable electronics. Further, the current shortcomings, challenges and new prospects for future developments in the emerging field of integrated flexible TENG-SCs for self-powered wearable electronics are discussed. [ABSTRACT FROM AUTHOR]

In this study, an ionogel electrolyte (PAIM-X) consisting of 1-vinyl-3-methylimidazole bis (trifluoromethyl sulfonyl) imide ([VMIM][TFSI]), Polyacrylamide (PAAm), and MXene were prepared. The conductivity of PAIM-X and integral area of the voltammetric curve of the supercapacitor (PAIMSC) were improved by adding MXene. The addition of [VMIM][TFSI] enhanced the conductivity and applicable temperature of the ionogel electrolyte. At 90 °C, the conductivity of PAIM-4 can reach 36.4 mS/cm. In addition, spherical polyaniline with good electrochemical properties was synthesized and coated on graphite paper as an active substance. An all-solid-state supercapacitor was composed of PAIM-4, polyaniline electrode with 1.2 V potential window, pseudo-capacitors and high quality capacitors. The solvent 1-ethyl-3-methylimidazolium bis (trifluoromethyl sulfonyl imide) ([EMIM][TFSI]) and methanesulfonic acid (MSA) were introduced into the ionogel to promote the redox reaction of polyaniline (PANI). The mass specific capacitance of PAIMSC was 204.6 F/g and its energy density could reach 40.92 Wh/kg, which shows great potential for practical application at high temperature. The device had good rate performance and cycle performance, and its capacitance retention rate was still 91.56% after 10,000 cycles. In addition, the supercapacitor can work within the temperature range of −20 °C to 90 °C. These excellent electrochemical properties indicate that PAAm/IL/Mxene-X has broad application space and prospect. [ABSTRACT FROM AUTHOR]

Flexible supercapacitors can be ideal flexible power sources for wearable electronics due to their ultra-high power density and high cycle life. In daily applications, wearable devices will inevitably cause damage or short circuit during bending, stretching, and compression. Therefore, it is necessary to develop proper energy storage devices to meet the requirements of various wearable electronic devices. Herein, Poly(vinyl alcohol) linked various content of phytic acid (PVA-PAx) hydrogels are synthesized with high transparency and high toughness by a one-step freeze-thaw method. The effects of different raw material ratios and agents on the ionic conductivity and mechanical properties of the hydrogel electrolyte are investigated. The PVA-PA21% with 2 M H2SO4 solution (PVA-PA21%-2 M H2SO4) shows a high ionic conductivity of 62.75 mS cm−1. Based on this, flexible supercapacitors fabricated with PVA-PA21%-2 M H2SO4 hydrogel present a high specific capacitance at 1 A g−1 after bending at 90° (64.8 F g−1) and for 30 times (67.3 F g−1), respectively. Moreover, the device shows energy densities of 13.5 Wh kg−1 and 14.0 Wh kg−1 at a power density of 300 W kg−1 after bending at 90° and for 30 times during 10,000 cycles. It provides inspiration for the design and development of electrolytes for related energy electrochemical devices. [ABSTRACT FROM AUTHOR]

Smart hydrogels with high electrical conductivity, which can be a real source of power while also collecting and storing the diverse sources of energy with ultrahigh stretchability, strong self-healability, low-temperature tolerance, and excellent mechanical properties, are great value for tailored wearable cloths. Considerable effort has been dedicated in both scientific and technological developments of electroconductive hydrogels for supercapacitor applications in the past few decades. The key to realize those functionalities depends on the processing of hydrogels with desirable electrochemical properties. The various hydrogel materials with such properties are now emerging and investigated by various scholars. The last decade has witnessed the development of high-performance supercapacitors using hydrogels. Here, in this review, the current status of different hydrogels for the production of flexible supercapacitors has been discussed. The electrochemical properties such as capacitance, energy density and cycling ability has been given attention. Diverse hydrogels, with their composites such as carbon-based hydrogels, cellulose-based hydrogels, conductive-polymer-based hydrogels and other hydrogels with excellent electromechanical properties are summarized. One could argue that hydrogels have played a central, starring role for the assembly of flexible supercapacitors for energy storage applications. This work stresses the importance of producing flexible supercapacitors for wearable clothing applications and the current challenges of hydrogel-based supercapacitors. The results of the review depicted that hydrogels are the next materials for the production of the flexible supercapacitor in a more sustainable way. [ABSTRACT FROM AUTHOR]

Flexible supercapacitors (FSCs) are limited in flexible electronics applications due to their low energy density. Therefore, developing electrode materials with high energy density, high electrochemical activity, and remarkable flexibility is challenging. Herein, we designed nitrogen-doped porous MXene (N-MXene), using melamine-formaldehyde (MF) microspheres as a template and nitrogen source. We combined it with an electrospinning process to produce a highly flexible nitrogen-doped porous MXene nanofiber (N-MXene-F) as a self-supporting electrode material and assembled it into a symmetrical supercapacitor (SSC). On the one hand, the interconnected mesh structure allows the electrolyte to penetrate the porous network to fully infiltrate the material surface, shortening the ion transport channels; on the other hand, the uniform nitrogen doping enhances the pseudocapacitive performance. As a result, the as-assembled SSC exhibited excellent electrochemical performance and excellent long-term durability, achieving an energy density of 12.78 Wh kg−1 at a power density of 1080 W kg−1, with long-term cycling stability up to 5000 cycles. This work demonstrates the impact of structural design and atomic doping on the electrochemical performance of MXene and opens up an exciting possibility for the fabrication of highly FSCs. [ABSTRACT FROM AUTHOR]

The increasing demands for portable, intelligent, and wearable electronics have significantly promoted the development of flexible supercapacitors (SCs) with features such as a long lifespan, a high degree of flexibility, and safety. MXenes, a class of unique two-dimensional materials with excellent physical and chemical properties, have been extensively studied as electrode materials for SCs. However, there is little literature that systematically summarizes MXene-based flexible SCs according to different flexible electrode construction methods. Recent progress in flexible electrode fabrication and its application to SCs is reviewed according to different flexible electrode construction methods based on MXenes and their composite electrodes, with or without substrate support. The fabrication methods of flexible electrodes, electrochemical performance, and the related influencing factors of MXene-based flexible SCs are summarized and discussed in detail. In addition, the future possibilities of flexible SCs based on MXene are explored and presented. [ABSTRACT FROM AUTHOR]

In this study, α-MnO2 and Fe2O3 nanomaterials are prepared on a carbon fiber modified with carbon nanotubes to produce the nonbinder core–shell positive (α-MnO2@CNTs/CC) and negative (Fe2O3@CNTs/CC) electrodes that can be operated in a wide voltage window in ultrafast asymmetrical flexible supercapacitors. MnO2 and Fe2O3 have attracted wide research interests as electrode materials in energy storage applications because of the abundant natural resources, high theoretical specific capacities, environmental friendliness, and low cost. The electrochemical performance of each electrode is assessed in 1 M Na2SO4 and the energy storage properties of the supercapacitors consisting of the two composite electrodes are determined in Na2SO4 and EMImBF4 electrolytes in the 2 V and 4 V windows. The 2 V supercapacitor can withstand a large scanning rate of 5000 mV S−1 without obvious changes in the cyclic voltammetry (CV) curves, besides showing a maximum energy density of 57.29 Wh kg−1 at a power density of 833.35 W kg−1. Furthermore, the supercapacitor retains 87.06% of the capacity after 20,000 galvanostatic charging and discharging (GCD) cycles. The 4 V flexible supercapacitor shows a discharging time of 1260 s and specific capacitance of 124.8 F g−1 at a current of 0.5 mA and retains 87.77% of the initial specific capacitance after 5000 GCD cycles. The mechanical robustness and practicality are demonstrated by physical bending and the powering of LED arrays. In addition, the contributions of the active materials to the capacitive properties and the underlying mechanisms are explored and discussed [ABSTRACT FROM AUTHOR]

Electrode materials for electrochemical capacitors or supercapacitors (SCs) are widely studied, as they are needed for the development of energy storage devices in electrical vehicles and flexible electronics. In the current work, a self-supported paper of reduced graphene oxide (rGO) with polycarbonate (PC) (as rGO-PC composite) was prepared by simple vacuum filtration and low-temperature annealing. rGO-PC as a freestanding single electrode was studied in a three-electrode system and presented a capacitive energy storage mechanism. To fabricate SCs based on rGO-PC, flexible polyethylene terephthalate (PET) with layers of both Cu tape (Cu tape) and carbon tape (C tape) (PET/Cu/C), as well as PET covered by graphene ink (PET/GrI), were used as supports. Fabricated flexible symmetric SCs have shown similar behavior with a higher areal capacitance value than that on PET/Cu/C substrate. [ABSTRACT FROM AUTHOR]

Graphene fiber-based supercapacitors are known as the potential energy resources for wearable/flexible electronics. However, increasing their specific capacitance and energy density remains a significant challenge. This paper indicates a double layer capacitance of the graphene nanosheets accompanied by pseudocapacitive behavior of the polyaniline to prepare composite fibers with high capacitive response. The polyaniline/graphene composite fibers (PANI/GFs) were synthesized by the self-assembled strategy and chemical reduction by HI. The wrinkle architecture of graphene nanosheets and uniform dispersion of the polyaniline are beneficial to increase the internal electroactive sites and provide a stable structure for the composite fibers. The constructed fiber-shaped supercapacitors with solid-state electrolyte deliver an excellent areal specific capacitance of 370.2 mF cm−2 and an outstanding areal energy density of 12.9 μW h cm−2. The current work reveals the attractive potential of the as-synthesized composite fibers for constructing fiber-shaped supercapacitors with distinguished electrochemical performance, which can be applied in future flexible electronics. [ABSTRACT FROM AUTHOR]

With the development of wearable and flexible electronic devices, there is an increasing demand for new types of flexible energy storage power supplies. The flexible supercapacitor has the advantages of fast charging and discharging, high power density, long cycle life, good flexibility, and bendability. Therefore, it exhibits great potential for use in flexible electronics. In flexible supercapacitors, graphene materials are often used as electrode materials due to the advantages of their high specific surface area, high conductivity, good mechanical properties, etc. In this review, the classification of flexible electrodes and some common flexible substrates are firstly summarized. Secondly, we introduced the advantages and disadvantages of five graphene-based materials used in flexible supercapacitors, including graphene quantum dots (GQDs), graphene fibers (GFbs), graphene films (GFs), graphene hydrogels (GHs), and graphene aerogels (GAs). Then, we summarized the latest developments in the application of five graphene-based materials for flexible electrodes. Finally, the defects and outlooks of GQDs, GFbs, GFs, GHs, and GAs used in flexible electrodes are given. [ABSTRACT FROM AUTHOR]

The development of polymer-based devices has attracted much attention due to their miniaturization, flexibility, lightweight and sustainable power sources with high efficiency in the field of wearable/portable electronics, and energy system. In this work, we proposed a polyvinylidene fluoride (PVDF)-based composite matrix for both energy harvesting and energy storage applications. The physicochemical characterizations, such as X-ray diffraction, laser Raman, and field-emission scanning electron microscopy (FE-SEM) analyses, were performed for the electrospun PVDF/sodium niobate and PVDF/reduced graphene oxide composite film. The electrospun PVDF/sodium niobate nanofibrous mat has been utilized for the energy harvester which shows an open circuit voltage of 40 V (peak to peak) at an applied compressive force of 40 N. The PVDF/reduced graphene oxide composite film acts as the electrode for the symmetric supercapacitor (SSC) device fabrication and investigated for their supercapacitive properties. Finally, the self-charging system has been assembled using PVDF/sodium niobate (energy harvester), and PVDF/reduced graphene oxide SSC (energy storage) and the self-charging capability is investigated. The proposed self-charging system can create a pathway for the all-polymer based composite high-performance self-charging system. [ABSTRACT FROM AUTHOR]