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一种新型氧化还原电解液电化学电容器体系
引用本文:李强,李开喜,孙国华,范慧,谷建宇.一种新型氧化还原电解液电化学电容器体系[J].物理化学学报,2006,22(12):1445-1450.
作者姓名:李强  李开喜  孙国华  范慧  谷建宇
作者单位:(Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, P. R. China; Graduate School of the Chinese Academy of Sciences, Beijing 100049, P. R. China)
基金项目:国家自然科学基金(50272070)资助项目
摘    要:以含有Fe3+/Fe2+离子对的H2SO4溶液为电解液, 以多孔炭做电极材料, 就Fe3+/Fe2+离子对在多孔炭纳米孔隙中的电化学行为及准电容效应进行了探讨. 循环伏安测试结果表明, Fe3+/Fe2+离子对在多孔炭电极纳米孔隙中发生了可逆的电化学反应. 恒流充放电结果发现, 加入Fe3+/Fe2+使得充放曲线出现对称的充放电平台, 有效地提高了电化学电容器(EC)的电能存储容量, 其单电极比电容最高达174 mAh•g−1, 比单纯的H2SO4电解液的比电容高109 mAh•g−1, 且有着良好的循环稳定性. 根据实验现象及结果, 探讨了Fe3+/Fe2+离子对在EC电极上的充放电机理, 并提出了一种新的概念——氧化还原电解液电化学电容器.

关 键 词:电化学电容器  法拉第准电容  多孔炭  Fe3+/Fe2+离子对  电吸附  
收稿时间:2006-05-19
修稿时间:2006-06-28

A New Kind of Redox Electrolyte Electrochemical Capacitor System
LI Qiang,LI Kai-Xi,SUN Guo-Hua,FAN Hui,GU Jian-Yu.A New Kind of Redox Electrolyte Electrochemical Capacitor System[J].Acta Physico-Chimica Sinica,2006,22(12):1445-1450.
Authors:LI Qiang  LI Kai-Xi  SUN Guo-Hua  FAN Hui  GU Jian-Yu
Institution:(Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, P. R. China; Graduate School of the Chinese Academy of Sciences, Beijing 100049, P. R. China)
Abstract:The electrochemical characteristics and pseudocapacitive effects of Fe3+/Fe2+ ion pair were investigated in an electrochemical capacitor (EC) system using porous carbon as electrode material and with H2SO4 solution containing Fe3+/Fe2+ ion pair as electrolyte. The cyclic voltammetric results indicated that highly reversible electrochemical redox reactions of Fe3+/Fe2+ ion pair occurred within the nano-pore structures of the porous carbon electrodes. Symmetrical charge/discharge cycles were achieved due to the existence of Fe3+/Fe2+ ion pair, which effectively improved the capacity of the electrochemical capacitor system. Apart from its excellent cyclic stability, the specific capacitance of the single electrode system reached 174 mAh•g−1, which is 109 mAh•g−1 higher than that obtained for H2SO4 as the electrolyte. The charge/discharge mechanism of Fe3+/Fe2+ ion pair in the EC systems was discussed and a new type of redox electrolyte electrochemical capacitor was suggested.
Keywords:Electrochemical capacitor  Faradic pseudocapacitance  Porous carbon  Fe3 /Fe2  ion pair  Electrosorption
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