Thermodynamic approach to the double layer capacity of a Pt(111) electrode in perchloric acid solutions

被引:73
|
作者
Garcia-Araez, Nuria
Climent, Victor
Herrero, Enrique
Feliu, Juan M.
Lipkowski, Jacek
机构
[1] Univ Alicante, Inst Electroquim, E-03080 Alicante, Spain
[2] Univ Guelph, Dept Chem, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
platinum single crystal electrode; Pt(111); double layer; differential capacity; potential of zero charge;
D O I
10.1016/j.electacta.2005.10.043
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A thermodynamic method based on the work done by Frumkin and Petrii [A.N. Frumkin, O.A. Petrii, Electrochim. Acta 20 (1975) 347], to calculate the so-called double layer capacity for a Pt(111) electrode is proposed. The analysis requires careful measurement of the total charge density versus potential curves for a series of solutions with composition (0.1 - x) M KClO4 + xM HClO4. A method in which the total charge densities are determined by integration of cyclic voltammograms recorded in solutions with or without chloride is described. Following this procedure the double layer capacity curves were calculated. The double layer capacity curves displayed three peaks that were tentatively assigned to the solvent reorientation, onset of OH adsorption and completion of the OH adlayer. In the hydrogen adsorption region, the double layer capacity values were 14 +/- 5 mu F/cm(2), in good agreement with previous estimates reported in the literature by using other approaches. (c) 2005 Elsevier Ltd. All rights reserved.
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页码:3787 / 3793
页数:7
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