Oxidation of carbon monoxide on poly-oriented and single-crystalline platinum electrodes over a wide range of pH

被引:49
作者
Gisbert, Ruben [1 ,2 ]
Garcia, Gonzalo [1 ,3 ]
Koper, Marc T. M. [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
[2] Univ Alicante, Inst Electroquim, E-03080 Alicante, Spain
[3] Univ La Laguna, Fac Quim, Dept Quim Fis, Tenerife 38071, Spain
关键词
Carbon monoxide oxidation; Platinum; pH; Carbonate; Phosphate; CO ADLAYER OXIDATION; MONOLAYER OXIDATION; ALKALINE MEDIA; ADSORBED CO; ELECTROOXIDATION; MECHANISM; METHANOL; PT(111); CATALYSTS; KINETICS;
D O I
10.1016/j.electacta.2010.11.032
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The oxidative stripping of pre-adsorbed carbon monoxide has been studied on poly-oriented platinum, and on Pt(1 1 1), Pt(1 0 0) and Pt(1 1 0) single-crystal electrodes in phosphate buffer solutions as a function of pH, both stripping voltammetry and chronoamperometry. It was found that the stripping peak potential has a tendency to decrease as a function of pH until a pH of ca. 10-11, which is ascribed to a weaker adsorption of phosphate on platinum with increasing pH. Above a pH of ca. 11, the stripping peak appears to stay constant or increase, depending on the surface structure. We hypothesize that this may be due to the fact that above a pH of ca. 10-11, the main product of carbon monoxide oxidation is carbonate, which may be block active sites on the surface. By comparison with the stripping on the single-crystalline Pt, the stripping voltammetry on the poly-oriented Pt electrode appears as a convolution of the oxidation on the different facets. A similar conclusion is drawn for the chronoamperometry experiments, and it is suggested that this may be the main reason for the asymmetrical transients observed on the poly-oriented Pt electrodes, as well as on other strongly heterogeneous Pt electrodes that have been studied in the literature. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2443 / 2449
页数:7
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