Microscopic Insights into the Electrochemical Behavior of Nonaqueous Electrolytes in Electric Double-Layer Capacitors

被引:112
作者
Jiang, De-en [1 ]
Wu, Jianzhong [2 ]
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[2] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92521 USA
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; NANOPOROUS CARBON SUPERCAPACITORS; IONIC LIQUID; DIMER MODEL; PORE-SIZE; DIFFERENTIAL CAPACITANCE; SIMULATION; STORAGE;
D O I
10.1021/jz4002967
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electric double-layer capacitors (EDLCs) are electrical devices that store energy by adsorption of ionic species at the inner surface of porous electrodes. Compared with aqueous electrolytes, ionic liquid and organic electrolytes have the advantage of larger potential windows, making them attractive for the next generation of EDLCs with superior energy and power densities. The performance of both ionic liquid and organic electrolyte EDLCs hinges on the judicious selection of the electrode pore size and the electrolyte composition, which requires a comprehension of the charging behavior from a microscopic view. In this Perspective, we discuss predictions from the classical density functional theory (CDFT) on the dependence of the capacitance on the pore size for ionic liquid and organic electrolyte EDLCs. CDFT is applicable to electrodes with the pore size ranging from that below the ionic dimensionality to mesoscopic scales, thus unique for investigating the electrochemical behavior of the confined electrolytes for EDLC applications.
引用
收藏
页码:1260 / 1267
页数:8
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