The reduction reaction of selenate ions in an aqueous solution by TiO2 phot
ocatalyst is investigated. The conduction band of TiO2 is much more positiv
e than the standard redox potential of the reduction reaction of selenium t
o selenide. However, the selenate ions are reduced to hydrogen selenide via
amorphous selenium, by the TiO2 photocatalyst. After all selenate ions and
selenite ions are reduced to amorphous selenium, no chemicals in the solut
ion can capture the electrons from the TiO2 photocatalyst. Under this condi
tion, photogenerated electrons accumulate in the TiO2 particles, and they r
aise the conduction band of the TiO2. All the experimental results can be e
xplained by this mechanism. (C) 2000 The Electrochemical Society. All right
s reserved.