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      Identifying pseudocapacitance of Fe2O3 in an ionic liquid and its application in asymmetric supercapacitors

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          Abstract

          We identify the pseudocapacitive behaviour of Fe 2O 3 in an ionic liquid electrolyte, and build high-performance asymmetric supercapacitors by utilizing such pseudocapacitance.

          Abstract

          Pseudocapacitance is commonly associated with surface or near-surface reversible redox reactions, as observed with transition metal oxides in alkaline aqueous electrolytes. Here, we demonstrate that pseudocapacitive behavior of Fe 2O 3 can occur in a 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF 4) ionic liquid (IL), and it is closely related to the chemical state variation between Fe 3+ and Fe 2+ on the surface of a Fe 2O 3 electrode during the charging/discharging process. By taking advantage of such pseudocapacitance, we prepared a promising electrode material, i.e., graphene nanosheet-supported Fe 2O 3 nanoparticles (denoted as Fe 2O 3@GNS), and then built high-performance asymmetric supercapacitors (ASs) using Fe 2O 3@GNS as the battery-type electrode material, commercial activated carbon (AC)/or activated polyaniline-derived carbon nanorods (denoted as APDC) as the capacitor-type electrode material, and EMIMBF 4 IL as the electrolyte. The as-made ASs are able to work reversibly in a full operation voltage region of 0–4 V and exhibit very high energy density. Especially, the AS of Fe 2O 3@GNS//APDC achieves an extremely high energy density of 177 W h kg −1 and shows a superior combination of high energy and power density (the energy density still remains 62.4 W h kg −1 even at a high power density of 8 kW kg −1).

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          Most cited references39

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          Anomalous increase in carbon capacitance at pore sizes less than 1 nanometer.

          Carbon supercapacitors, which are energy storage devices that use ion adsorption on the surface of highly porous materials to store charge, have numerous advantages over other power-source technologies, but could realize further gains if their electrodes were properly optimized. Studying the effect of the pore size on capacitance could potentially improve performance by maximizing the electrode surface area accessible to electrolyte ions, but until recently, no studies had addressed the lower size limit of accessible pores. Using carbide-derived carbon, we generated pores with average sizes from 0.6 to 2.25 nanometer and studied double-layer capacitance in an organic electrolyte. The results challenge the long-held axiom that pores smaller than the size of solvated electrolyte ions are incapable of contributing to charge storage.
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            Carbon properties and their role in supercapacitors

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              Carbon materials for chemical capacitive energy storage.

              Carbon materials have attracted intense interests as electrode materials for electrochemical capacitors, because of their high surface area, electrical conductivity, chemical stability and low cost. Activated carbons produced by different activation processes from various precursors are the most widely used electrodes. Recently, with the rapid growth of nanotechnology, nanostructured electrode materials, such as carbon nanotubes and template-synthesized porous carbons have been developed. Their unique electrical properties and well controlled pore sizes and structures facilitate fast ion and electron transportation. In order to further improve the power and energy densities of the capacitors, carbon-based composites combining electrical double layer capacitors (EDLC)-capacitance and pseudo-capacitance have been explored. They show not only enhanced capacitance, but as well good cyclability. In this review, recent progresses on carbon-based electrode materials are summarized, including activated carbons, carbon nanotubes, and template-synthesized porous carbons, in particular mesoporous carbons. Their advantages and disadvantages as electrochemical capacitors are discussed. At the end of this review, the future trends of electrochemical capacitors with high energy and power are proposed. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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                Author and article information

                Journal
                JMCAET
                J. Mater. Chem. A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2014
                2014
                : 2
                : 35
                : 14550-14556
                Article
                10.1039/C4TA02026J
                6a04d780-1365-49bf-b460-e83036e50023
                © 2014
                History

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