Correlation between capacitances of porous carbons in acidic and aprotic EDLC electrolytes

被引:86
作者
Centeno, T. A.
Hahn, M.
Fernandez, J. A.
Kotz, R.
Stoeckli, F.
机构
[1] Univ Neuchatel, IMT Chim Surfaces, CH-2009 Neuchatel, Switzerland
[2] CSIC, Inst Nacl Carbon, E-33080 Oviedo, Spain
[3] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
关键词
supercapacitor; double-layer; carbon; porosity; chemical groups;
D O I
10.1016/j.elecom.2007.01.031
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A study based on a total of 41 nanoporous carbons shows that there exists a good correlation between the limiting gravimetric capacitances Co at low current densities j (1 mA cm(-2)) measured in aprotic (1 M (C2H5)(4)NBF4 in acetonitrile) and in acidic (2 M aqueous H2SO4) electrolytes. The comparison of the surface-related capacitances (F m(-2)) of well characterized samples with the amount of thermodesorbed CO suggests a strong contribution of CO generating surface groups to charge storage in the acidic electrolyte, but a negligible contribution in the aprotic medium. It also appears that the decrease of the capacitance with current density is similar in both electrolytes. This confirms that the average micropore width and the CO2 generating surface groups are the main factors which limit the ionic mobility in both electrolytes. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1242 / 1246
页数:5
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