4.7 Article

Improving the energy density of quasi-solid-state supercapacitors by assembling two redox-active gel electrolytes

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 41, 期 13, 页码 5725-5732

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2016.02.052

关键词

Supercapacitor; Gel polymer electrolyte; Redox additive; VOSO4; Na2MoO4

资金

  1. National Natural Science Foundation of China [U1205112, 21301060, 61306077]
  2. Promotion Program for Young and Middle-aged Teacher in Science and Technology Research of Huaqiao University [ZQN-PY106]
  3. Program for New Century Excellent Talents in Fujian Province University [2014FJ-NCET-ZR02]
  4. Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry

向作者/读者索取更多资源

Redox additives of VOSO4 and Na2MoO4 were respectively added into two polyvinyl alcohol (PVA)-H2SO4 gels to form two gel polymer electrolytes (GPEs). These two redox-active GPEs were separated by a Nafion 117 membrane and assembled with a pair of activated carbon electrodes to construct quasi-solid-state supercapacitors, in which PVA-H2SO4-VOSO4 and PVA-H2SO4-Na2MoO4 GPEs worked on the sides of the negative and positive electrodes of the supercapacitor, respectively. Cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy techniques were used to evaluate the electrochemical performances of the supercapacitor with optimized PVA-H2SO4-VOSO4 and PVA-H2SO4-Na2MoO4 GPEs. After the introduction of VOSO4 and Na2MoO4, the specific capacitance and energy density of the supercapacitor with PVA H2SO4 VO-SO4 vertical bar PVA-H2SO4-Na2MoO4 GPEs can reach 543.4 F g(-1) and 17.9 Wh kg(-1), respectively, which are about four times those of the supercapacitor with a PVA-H2SO4 GPE. The enhanced energy storage is attributed to the reversible Faradaic reactions related to VOSO4 and Na2MoO4 in the corresponding gel polymer electrolytes. In addition, the supercapacitor shows good cyclic durability. Copyright (C) 2016, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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