Mechanism for electrochemical oxidation of highly oriented pyrolytic graphite in sulfuric acid solution

被引:65
作者
Choo, Hyun-Suk [1 ]
Kinumoto, Taro
Jeong, Soon-Ki
Iriyama, Yasutoshi
Abe, Takeshi
Ogumi, Zempachi
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Soonchunhyang Univ, Dept Chem Engn, Chungnam 336745, South Korea
关键词
D O I
10.1149/1.2767411
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In order to clarify the oxidation mechanism of carbon materials in polymer electrolyte fuel cells (PEFCs), electrochemical oxidation of highly oriented pyrolytic graphite (HOPG) was investigated in sulfuric acid solution at less than 1.0 V vs normal hydrogen electrode. Surface oxidation was accelerated at 1.0 V, whereas oxidation kinetics seemed to be slow at 0.6 V. In situ electrochemical atomic force microscopy clearly showed that hillock structure was developed with a formation of C-O bonding on the basal plane of HOPG in the early stage of the oxidation process. Hence, the hydrolysis reaction to produce alcohol and other functional groups was considered as the initiation reaction for electrochemical oxidation of HOPG. Accumulation of the surface strain by the formation of hillocks may lead to development of the oxidized layer. The oxidation kinetics of further process accompanied with an evolution of CO or CO2 could be slower than that of the hydrolysis reaction, which might be ascribed to the low electron conductivity of the oxidized HOPG surface. The mechanism for electrochemical oxidation of HOPG contributes an elucidation of carbon oxidation reactions in PEFCs. (c) 2007 The Electrochemical Society.
引用
收藏
页码:B1017 / B1023
页数:7
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