In-situ surface-enhanced Raman spectroscopic investigation on ethanol electrooxidation in different media

被引:5
|
作者
Zhong Qi-Ling [1 ]
Zhang Bing
Ding Yue-Min
Liu Yue-Long
Rao Gui-Shi
Wang Guo-Fu
Ren Bin
Tian Zhong-Qun
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Peoples R China
[2] Tianjin Univ, Sch Sci, Tianjin 300072, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Fujian Province, Peoples R China
关键词
ethanol oxidation; roughened platinum electrode; alkaline medium; in-situ SERS;
D O I
10.3866/PKU.WHXB20070923
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical voltametric methods and in-situ electrochemical surface-enhanced Raman spectroscopy (SERS) were used to investigate the electrooxidation behavior of ethanol in different media on a roughened platinum electrode. It was found that ethanol could dissociate spontaneously to produce strongly adsorbed intermediate, CO, in acidic, neutral, and alkaline media on the roughened platinum electrode. The complete oxidation potential of COad on the roughened platinum electrode was negatively shifted about 0.300 V in the alkaline medium (0.20 V) compared with that in the acidic and neutral media (0.50 V). The positive oxidation peak potential of ethanol was negatively shifted about 0.85 V in the alkaline medium (-0.20 V) than that in the acidic medium (0.65 V). By comparing the oxidation current and the peak potential, it was found that the electrocatalytic activity of roughened platinum electrode for ethanol and CO oxidation in the alkaline medium was higher than in acidic and neutral media. The results suggested that ethanol was oxidized to CO2 on the roughened platinum electrode via parallel reaction mechanism in acidic, neutral or alkaline media.
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页码:1432 / 1436
页数:5
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