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

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [1];  [2];  [2]
  1. Faculty of Engineering, Department of Applied Chemistry, Kumamoto University, Kurokami 2-39-1, Kumamoto-shi, Kumamoto-ken, 860-8555 (Japan)
  2. Faculty of Science, Science University of Tokyo, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601 (Japan)
Photoelectrochemical measurements of TiO{sub 2}, NaTaO{sub 3}, and Cr or Sb doped TiO{sub 2} and SrTiO{sub 3} photocatalysts were carried out in H{sub 2} and O{sub 2} saturated electrolytes in order to evaluate the reverse reactions during water photolysis. The poor activity of TiO{sub 2} as a result of reverse photoreactions of O{sub 2} reduction and H{sub 2} oxidation was revealed with the respective high cathodic and anodic photocurrents. The rise in the photocurrents at NaTaO{sub 3} after La doping was in harmony with the doping-induced increase in the photocatalytic activity. NiO loading suppresses the O{sub 2} photoreverse reactions, which declines photocatalytic activity, and/or promotes the photo-oxidation of water, because the O{sub 2} photo-reduction current was scarcely observed near the flatband potential. Photocurrents of O{sub 2} reduction and H{sub 2} oxidation were observed under visible light for the Cr and Sb doped SrTiO{sub 3} and TiO{sub 2}, respectively. These phenomena are in harmony with the previous reports on the photocatalysts examined with sacrificial reagents.
OSTI ID:
20658199
Journal Information:
Journal of Solid State Chemistry, Journal Name: Journal of Solid State Chemistry Journal Issue: 11 Vol. 177; ISSN 0022-4596; ISSN JSSCBI
Country of Publication:
United States
Language:
English