Suppressed Activation Energy for Interfacial Charge Transfer of a Prussian Blue Analog Thin Film Electrode with Hydrated Ions (Li+, Na+, and Mg2+)

被引:144
|
作者
Mizuno, Yoshifumi [1 ,2 ]
Okubo, Masashi [1 ]
Hosono, Eiji [1 ]
Kudo, Tetsuichi [1 ]
Zhou, Haoshen [1 ]
Oh-ishi, Katsuyoshi [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058568, Japan
[2] Chuo Univ, Dept Appl Chem, Bunkyo Ku, Tokyo 1128551, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2013年 / 117卷 / 21期
关键词
COORDINATION POLYMER ELECTRODE; HEXACYANOFERRATE FILM; BATTERY ELECTRODES; MAGNETISM; STORAGE;
D O I
10.1021/jp311616s
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
Interfacial charge transfer is one of the most important fundamental steps in the charge and discharge processes of intercalation compounds for rechargeable batteries. In this study, temperature-dependent electrochemical impedance spectroscopy was carried out to clarify the origin of the high power output of aqueous batteries with Prussian blue analog electrodes. The activation energy for the interfacial charge transfer, E-a, was estimated from the temperature dependence of the interfacial charge transfer resistance. The E-a values with Li+ and Na+ aqueous electrolytes were considerably smaller than those with organic electrolytes. The small E-a values with aqueous electrolytes could result from the fact that the Coulombic repulsion at the interface is largely suppressed by the screening effect of hydration.
引用
收藏
页码:10877 / 10882
页数:6
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