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Mechanism of the OH Radical Generation in Photocatalysis with TiO2 of Different Crystalline Types

Zhang, Jie, Nosaka, Yoshio·2014·The Journal of Physical Chemistry C

Abstract

The difference in the OH radical generation through photocatalytic reaction with distinct crystalline types of TiO 2 in aqueous suspension was explored by means of a fluorescence probe method. By employing two kinds of probe molecules with different adsorptivities, that is, coumarin and coumarin-3-carboxylic acid, we could detect OH radicals located near the TiO 2 surface and those in the bulk solution individually. The amount of the OH radicals near the TiO 2 surface was much larger than that in the solution, which diffused from the TiO 2 surface to the bulk solution. Rutile TiO 2 produced a much smaller amount of OH radicals as compared to anatase and anatase-contained TiO 2 . On the addition of H 2 O 2, the OH radical generation for pure anatase TiO 2 decreased but increased for rutile and rutile-contained TiO 2 . This difference could be explained as follows: at the surface of anatase TiO 2, trapped holes become adsorbed OH radicals, while at the rutile surface, Ti-peroxo (Ti-OO-Ti) produced by the combination of two trapped holes which correspond to the adsorbed H 2 O 2, could work as a catalyst for the OH radical generation from water.

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Metadata

Authors
Zhang, J., & Nosaka, Y.
Venue
The Journal of Physical Chemistry C
Published
2014-05-07
Volume
118
Issue
20
Pages
10824-10832
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W2318043664
Cited by
396
References
25
FWCI
7.64
Type
journal article
Language
en
Open access
closed

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