Project description:Carbon-based supercapacitors have aroused ever-increasing attention in the energy storage field due to high conductivity, chemical stability, and large surface area of the investigated carbon active materials. Herein, eucalyptus-derived nitrogen/oxygen doped hierarchical porous carbons (NHPCs) are prepared by the synergistic action of the ZnCl2 activation and the NH4Cl blowing. They feature superiorities such as high specific surface area, rational porosity, and sufficient N/O doping. These excellent physicochemical characteristics endow them excellent electrochemical performances in supercapacitors: 359 F g-1 at 0.5 A g-1 in a three-electrode system and 234 F g-1 at 0.5 A g-1 in a two-electrode system, and a high energy density of 48 Wh kg-1 at a power density of 750 W kg-1 accompanied by high durability of 92% capacitance retention through 10,000 cycles test at a high current density of 10 A g-1 in an organic electrolyte. This low-cost and facile strategy provides a novel route to transform biomass into high value-added electrode materials in energy storage fields.
Project description:Activated carbons (ACs) for supercapacitors were synthesized from Eucommia ulmoides Oliver (EUO) wood by H3PO4 with systemic activation processes. The target structure of ACs could be prepared by adjusting the technological parameters. As the H3PO4 concentration was 25%, the mass ratio of feedstocks to activator was 1:4, the activation time was 6 h, and the activation temperature was 400 °C, the obtained AC revealed a high specific surface area (2033.87 m2·g-1) and well-developed mesoporous (the rate of mesoporous was 96.4%) with the best economic feasibility. Besides, it possessed excellent electrochemical performance: the maximum specific capacitance reached up to 252 F·g-1, the charging and discharging period was 3098.2 s at 0.2 A·g-1, and the retention rate of specific capacitance reached 92.3% after 10,000 cycles. This low temperature and convenience technology provide a valuable reference for synthesizing the EUO-based ACs, making high-value utilization on the EUO branches, and owning a broad application prospect in supercapacitors.
Project description:Biomass-derived activated carbon materials with hierarchically nanoporous structures containing nitrogen functionalities show excellent electrochemical performances and are explored extensively in energy storage and conversion applications. Here, we report the electrochemical supercapacitance performances of the nitrogen-doped activated carbon materials with an ultrahigh surface area prepared by the potassium hydroxide (KOH) activation of the Nelumbo nucifera (Lotus) seed in an aqueous electrolyte solution (1 M sulfuric acid: H2SO4) in a three-electrode cell. The specific surface areas and pore volumes of Lotus-seed-derived carbon materials carbonized at a different temperatures, from 600 to 1000 °C, are found in the range of 1059.6 to 2489.6 m2 g-1 and 0.819 to 2.384 cm3 g-1, respectively. The carbons are amorphous materials with a partial graphitic structure with a maximum of 3.28 atom% nitrogen content and possess hierarchically micro- and mesoporous structures. The supercapacitor electrode prepared from the best sample showed excellent electrical double-layer capacitor performance, and the electrode achieved a high specific capacitance of ca. 379.2 F g-1 at 1 A g-1 current density. Additionally, the electrode shows a high rate performance, sustaining 65.9% capacitance retention at a high current density of 50 A g-1, followed by an extraordinary long cycle life without any capacitance loss after 10,000 subsequent charging/discharging cycles. The electrochemical results demonstrate that Nelumbo nucifera seed-derived hierarchically porous carbon with nitrogen functionality would have a significant probability as an electrical double-layer capacitor electrode material for the high-performance supercapacitor applications.
Project description:N/S co-doped porous carbon spheres (NSPCSs) were prepared by a simple ultrasonic spray pyrolysis (USP) using the mixed solution of coal oxide and l-cysteine, and without a subsequent activation process. The surface properties of carbon materials have been successfully modified by the concurrent incorporation of N and S. So the capacitive performance of NSPCSs was greatly enhanced. It is used as a supercapacitor electrode to achieve a high specific capacitance of 308 F g-1 at a current density of 1 A g-1 and 90.2% capacitance retention even after 10 000 cycles at 5 A g-1. These numerical results show that the supercapacitors based on coal-based carbon materials have great potential in high performance electrochemical energy storage.
Project description:In this paper, NiSb/NiTe/Ni composites were smoothly developed via the microwave method for supercapacitors. The synthesis of NiSb/NiTe crystals was revealed by X-ray photoelectron spectroscopy and X-ray diffraction. The analytic results of scanning electron microscopy and energy dispersive spectroscopy uncover the microscopic morphology as well as the constituent elements of the composites. Self-supported NiSb/NiTe is a supercapacitor cathode that combines high capacitance with excellent cycling stability. The obtained composite electrode displayed remarkable electrochemical properties, presenting a special capacitance of 1870 F g-1 (1 A g-1) and 81.5% of the original capacity through 30,000 times (10 A g-1) of the charging/discharging process. Further, an asymmetric supercapacitor was prepared employing NiSb/NiTe as a cathode and activated carbon as an anode. NiSb/NiTe//AC exhibited a high energy density of 224.6 uW h cm-2 with a power density of 750 μW cm-2 and provided a favorable cycling stability of 83% after 10,000 cycles.
Project description:Supercapacitors (SCs) due to their high energy density, fast charge storage and energy transfer, long charge discharge curves and low costs are very attractive for designing new generation of energy storage devices. In this work we present a simple and scalable synthetic approach to engineer ternary composite as electrode material based on combination of graphene with doped metal oxides (iron oxide) and conductive polymer (polypyrrole) with aims to achieve supercapacitors with very high gravimetric and areal capacitances. In the first step a binary composite with graphene mixed with doped iron oxide (rGO/MeFe2O4) (Me = Mn, Ni) was synthesized using new single step process with NaOH acting as a coprecipitation and GO reducing agent. This rGO/MnFe2O4 composite electrode showed gravimetric capacitance of 147 Fg-1 and areal capacitance of 232 mFcm-2 at scan rate of 5 mVs-1. In the final step a conductive polypyrrole was included to prepare a ternary composite graphene/metal doped iron oxide/polypyrrole (rGO/MnFe2O4/Ppy) electrode. Ternary composite electrode showed significantly improved gravimetric capacitance and areal capacitance of 232 Fg-1 and 395 mFcm-2 respectively indicating synergistic impact of Ppy additives. The method is promising to fabricate advanced electrode materials for high performing supercapacitors combining graphene, doped iron oxide and conductive polymers.
Project description:A three-dimensional bi-continuous nanoporous gold (NPG)/nickel foam is developed though the electrodeposition of a gold-tin alloy on Ni foam and subsequent chemical dealloying of tin. The newly-designed 3D metal structure is used to anchor MnO2 nanosheets for high-performance supercapacitors. The formed ternary composite electrodes exhibit significantly-enhanced capacitance performance, rate capability, and excellent cycling stability. A specific capacitance of 442?Fg-1 is achieved at a scan rate of 5?mV?s-1 and a relatively high mass loading of 865??g?cm-2. After 2500 cycles, only a 1% decay is found at a scan rate of 50?mV?s-1. A high power density of 3513?W?kg-1 and an energy density of 25.73?Wh?kg-1 are realized for potential energy storage devices. The results demonstrate that the NPG/nickel foam hybrid structure significantly improves the dispersibility of MnO2 and makes it promising for practical energy storage applications.
Project description:Ni foam is an extensively used current collector and substrate in investigations of electrochemically active materials such as supercapacitors and electrocatalysts for oxygen and hydrogen evolution reactions. This material is relatively cheap, porous, and conductive and has a large specific surface area, all of which make it a good substrate. We investigated Ni-Mg ferrites and NiMn2O4 as active materials for electrochemical energy storage. These materials, when loaded on Ni foam, gave promising capacitance values: 172 F/g (at 2 mV/s) for NiMn2O4 in 6 M KOH and 242 F/g (at 2 mV/s) for MgFe2O4 in 3 M KOH. Nevertheless, during the authors' work, many experimental problems occurred. Inconsistencies in the results directed further investigation towards measuring the capacitance of the active materials using GCE and platinum electrodes as substrates to discover if Ni foam was the culprit of the inconsistencies. When non-nickel substrates were used, both NiMn2O4 and MgFe2O4 showed reduced capacitance. Experimental problems associated with the utilization of Ni foam as a substrate for active materials in supercapacitor electrodes are discussed here, combined with other problems already addressed in the scientific literature.
Project description:In the energy storage field, an electrode material must possess both good ionic and electronic conductivities to perform well, especially when high power is needed. In this context, the development of composite electrode materials combining an electrochemically active and good ionic conductor phase with an electronic conductor appears as a perfectly adapted approach to generate a synergetic effect and optimize the energy storage performance. In this work, three layered MnO2 phases with various morphologies (veils, nanoplatelets and microplatelets) were combined with electronic conductor cobalt oxyhydroxides with different platelet sizes (∼20 nm vs. 70 nm wide), to synthesize 6 different composites by exfoliation and restacking processes. The influence of precursors' morphology on the distribution of the Mn and Co objects within the composites was carefully investigated and correlated with the electrochemical performance of the final restacked material. Overall, the best performing restacked composite was obtained by combining MnO2 possessing a veil morphology with the smallest cobalt oxyhydroxide nanoplatelets, leading to the most homogeneous distribution of the Mn and Co objects at the nanoscale. More generally, the aim of this work is to understand how the size and morphology of the precursor building blocks influence their distribution homogeneity within the final composite and to find the most compatible building blocks to reach a homogeneous distribution at the nanoscale.