Electrochemical approach to evaluate the mechanism of photocatalytic water splitting on oxide photocatalysts

被引:61
作者
Matsumoto, Y
Unal, U
Tanaka, N
Kudo, A
Kato, H
机构
[1] Kumamoto Univ, Fac Engn, Dept Appl Chem, Kumamoto, Kumamoto 8608555, Japan
[2] Sci Univ Tokyo, Fac Sci, Shinjuku Ku, Tokyo 1628601, Japan
基金
日本科学技术振兴机构;
关键词
photochemistry; water splitting; reverse reactions; TiO2; oxide photocatalyst; water photolysis; oxide films; semiconductor/solution interface; doping;
D O I
10.1016/j.jssc.2004.08.001
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Photoelectrochemical measurements of TiO2, NaTaO3, and Cr or Sb doped TiO2 and SrTiO3 photocatalysts were carried out in H, and 0, saturated electrolytes in order to evaluate the reverse reactions during water photolysis. The poor activity of TiO2 as a result of reverse photoreactions of O-2 reduction and H-2 oxidation was revealed with the respective high cathodic and anodic photocurrents. The rise in the photocurrents at NaTaO3 after La doping was in harmony with the doping-induced increase in the photocatalytic activity. NiO loading suppresses the O-2 photoreverse reactions, which declines photocatalytic activity, and/or promotes the photo-oxidation of water, because the O-2 photo-reduction current was scarcely observed near the flatband potential. Photocurrents of O-2 reduction and H-2 oxidation were observed under visible light for the Cr and Sb doped SrTiO3 and TiO2, respectively. These phenomena are in harmony with the previous reports on the photocatalysts examined with sacrificial reagents. (C) 2004 Elsevier Inc. All rights reserved.
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页码:4205 / 4212
页数:8
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