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      Sodium Ion Capacitor Using Pseudocapacitive Layered Ferric Vanadate Nanosheets Cathode

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          Summary

          Sodium ion capacitors (SICs) are designed to deliver both high energy and power densities at low cost. Electric double-layer capacitive cathodes are typically used in these devices, but they lead to very limited capacity. Herein, we apply a pseudocapacitive layered ferric vanadate (Fe-V-O) as cathode to construct non-aqueous SICs with both high energy and power densities. The Fe-V-O nanosheets cathode displays remarkable rate capability and cycling stability. The pseudocapacitive sodium storage mechanism of Fe-V-O, with over 83% of total capacity from capacitive contribution, is confirmed by kinetics analysis and ex situ characterizations. The capacitive-adsorption mechanism of hard carbon (HC) anode is demonstrated, and it delivers excellent rate capability. Based on as-synthesized materials, the assembled HC//Fe-V-O SIC delivers a maximum energy density of 194 Wh kg −1 and power density of 3,942 W kg −1. Our work highlights the advantages of pseudocapacitive cathodes for achieving both high energy and power densities in sodium storage devices.

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          Highlights

          • Pseudocapacitive cathode is applied to construct a high-energy sodium ion capacitor

          • Layered ferric vanadate cathode displays pseudocapacitive sodium storage behavior

          • Ferric vanadate cathode delivers remarkable rate capability and cycling stability

          • Hard carbon anode exhibits capacitive adsorption mechanism and high-rate performance

          Abstract

          Electrochemical Energy Storage; Energy Materials; Nanoelectrochemistry

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          Most cited references49

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          Research development on sodium-ion batteries.

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            Pseudocapacitive oxide materials for high-rate electrochemical energy storage

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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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                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                26 July 2018
                31 August 2018
                26 July 2018
                : 6
                : 212-221
                Affiliations
                [1 ]State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China
                [2 ]Department of Materials Science and Engineering, University of California Los Angeles, Los Angeles, CA 90095, USA
                [3 ]Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
                Author notes
                []Corresponding author anqinyou86@ 123456whut.edu.cn
                [∗∗ ]Corresponding author mlq518@ 123456whut.edu.cn
                [4]

                Lead Contact

                Article
                S2589-0042(18)30108-1
                10.1016/j.isci.2018.07.020
                6137391
                2a3ddb4f-f81a-4e96-8c17-676efbc540b6
                © 2018 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 1 March 2018
                : 9 July 2018
                : 23 July 2018
                Categories
                Article

                electrochemical energy storage,energy materials,nanoelectrochemistry

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