Li‐ion hybrid capacitors (LIHCs), consisting of an energy‐type redox anode and a power‐type double‐layer cathode, are attracting significant attention due to the good combination with the advantages of conventional Li‐ion batteries and supercapacitors. However, most anodes are battery‐like materials with the sluggish kinetics of Li‐ion storage, which seriously restrict the energy storage of LIHCs at the high charge/discharge rates. Herein, vanadium nitride (VN) nanowire is demonstated to have obvious pseudocapacitive characteristic of Li‐ion storage and can get further gains in energy storage through a 3D porous architecture with the assistance of conductive reduced graphene oxide (RGO). The as‐prepared 3D VN–RGO composite exhibits the large Li‐ion storage capacity and fast charge/discharge rate within a wide working widow from 0.01–3 V (vs Li/Li+), which could potentially boost the operating potential and the energy and power densities of LIHCs. By employing such 3D VN–RGO composite and porous carbon nanorods with a high surface area of 3343 m2 g−1 as the anode and cathode, respectively, a novel LIHCs is fabricated with an ultrahigh energy density of 162 Wh kg−1 at 200 W kg−1, which also remains 64 Wh kg−1 even at a high power density of 10 kW kg−1.

There is currently a strong demand for energy storage devices which are cheap, light weight, flexible, and possess high power and energy densities to meet the various requirements of modern gadgets. Herein, we prepare a flexible and easily processed electrode via a simple ''brush-coating and drying'' process using everyday cotton cloth as the platform and a stable graphene oxide (GO) suspension as the ink. After such a simple manufacturing operation followed by annealing at 300 C in argon atmosphere, the as-obtained graphene sheets (GNSs)-cotton cloth (CC) composite fabric exhibits good electrical conductivity, outstanding flexibility, and strong adhesion between GNSs and cotton fibers. Using this GNSs-CC composite fabric as the electrode material and pure CC as the separator, a homemade supercapacitor was fabricated. The supercapacitor shows the specific capacitance of 81.7 F g À1 (two-electrode system) in aqueous electrolyte, which is one of the highest values for GNSs-based supercapacitors. Moreover, the supercapacitor also exhibits satisfactory capacitance in ionic-liquid/ organic electrolyte. An all-fabric supercapacitor was also fabricated using pure CC as separator and GNSs-CC composite fabric as electrode and current collector. Such a conductive GNSs-CC composite fabric may provide new design opportunities for wearable electronics and energy storage applications.

Business costs and energy/environmental concerns have increased interested in biomass materials for production of activated carbons, especially as electrode materials for supercapacitors or as solid-state adsorbents in CO₂ adsorption area. In this paper, waste celtuce leaves were used to prepare porous carbon by air-drying, pyrolysis at 600 °C in argon, followed by KOH activation. The as-prepared porous carbon have a very high specific surface area of 3404 m²/g and a large pore volume of 1.88 cm³/g. As an electroactive material, the porous carbon exhibits good capacitive performance in KOH aqueous electrolyte, with the specific capacitances of 421 and 273 F/g in three and two-electrode systems, respectively. As a solid-state adsorbent, the porous carbon has an excellent CO₂ adsorption capacity at ambient pressures of up to 6.04 and 4.36 mmol/g at 0 and 25 °C, respectively. With simple production process, excellent recyclability and regeneration stability, the porous carbon that was derived from celtuce leaves is among the most promising materials for high-performance supercapacitors and CO₂ capture.

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