Early stages in the oxidation of ethanol at low index single crystal platinum electrodes

被引:223
作者
Xia, XH [1 ]
Liess, HD [1 ]
Iwasita, T [1 ]
机构
[1] Univ Bundeswehr Munchen, Inst Phys, D-85521 Neubiberg, Germany
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1997年 / 437卷 / 1-2期
关键词
D O I
10.1016/S0022-0728(97)00404-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Conventional electrochemical methods and in situ FTIR spectroscopy have been applied to study the early stages for adsorption and oxidation of ethanol at Pt(111), Pt(110), and Pt(100). Spectroscopic results show that the electrooxidation of ethanol on all three surfaces is characterised by the formation of acetaldehyde, acetic acid and carbon dioxide as soluble products. Linearly and bridge bonded CO are identified as adsorbed species. At Pt(110) other surface species containing CH and COH bonds are observed. In the hydrogen region of the Pt(100) surface, the interconversion between bridge and linearly bonded CO, turns out to be a common feature during the electrooxidation of small organic molecules. The important role played by adsorbed water is discussed. Adsorption of ethanol is the rate determining step. (C) 1997 Elsevier Science S.A.
引用
收藏
页码:233 / 240
页数:8
相关论文
共 23 条