In situ electrochemical dilatometry of carbide-derived carbons

被引:75
作者
Hantel, M. M. [1 ]
Presser, V. [2 ,3 ]
Koetz, R. [1 ]
Gogotsi, Y. [2 ,3 ]
机构
[1] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
[2] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[3] Drexel Univ, AJ Drexel Nanotechnol Inst, Philadelphia, PA 19104 USA
基金
瑞士国家科学基金会;
关键词
Electrochemical dilatometry; Carbide-derived carbons; Supercapacitors; ADSORPTION; ELECTRODES;
D O I
10.1016/j.elecom.2011.08.039
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The long life durability and extraordinary stability of supercapacitors are ascribed to the common concept that the charge storage is purely based on double-layer charging. Therefore the ideal supercapacitor electrode should be free of charge induced microscopic structural changes. However, recent in-situ investigations on different carbon materials for supercapacitor electrodes have shown that the charge and discharge is accompanied by dimensional changes of the electrode up to several percent. This work studies the influence of the pore size on the expansion behavior of carbon electrodes derived from titanium carbide-derived carbons with an average pore size between 5 and 8 angstrom. Using tetraethylammonium tetrafluoroborate in acetonitrile, the swelling of the electrodes was measured by in situ dilatometry. The experiments revealed an increased expansion on the negatively charged electrode for pores below 6 angstrom, which could be described with pore swelling. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1221 / 1224
页数:4
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