TY - JOUR
T1 - Effects of the structure of the Rh3+modifier on photocatalytic performances of an Rh3+/TiO2photocatalyst under irradiation of visible light
AU - Kitano, Sho
AU - Sadakiyo, Masaaki
AU - Kato, Kenichi
AU - Yamauchi, Miho
AU - Asakura, Hiroyuki
AU - Tanaka, Tsunehiro
AU - Hashimoto, Keiji
AU - Kominami, Hiroshi
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - For a rhodium ion-modified TiO2(Rh3+/TiO2) photocatalyst responding to visible light, control of the structure of the Rh3+modifier and effects of the structures of the Rh3+modifier on photocatalytic activities were examined. A TiO2support was pre-calcined to maintain crystallinity and specific surface area during post-calcination, and the structure of the Rh3+modifier for Rh3+/TiO2was changed by post-calcination without causing changes in the crystallinity and specific surface area of the TiO2support. In mineralization of acetone under irradiation of visible light, the photocatalytic activities of the post-calcined Rh3+/TiO2showed a volcano-like tendency as a function of post-calcination temperature. The results of this study showed that an atomically isolated structure of the Rh3+modifier was preferable for high activities and that aggregation of the Rh species led to a decrease in the activities.
AB - For a rhodium ion-modified TiO2(Rh3+/TiO2) photocatalyst responding to visible light, control of the structure of the Rh3+modifier and effects of the structures of the Rh3+modifier on photocatalytic activities were examined. A TiO2support was pre-calcined to maintain crystallinity and specific surface area during post-calcination, and the structure of the Rh3+modifier for Rh3+/TiO2was changed by post-calcination without causing changes in the crystallinity and specific surface area of the TiO2support. In mineralization of acetone under irradiation of visible light, the photocatalytic activities of the post-calcined Rh3+/TiO2showed a volcano-like tendency as a function of post-calcination temperature. The results of this study showed that an atomically isolated structure of the Rh3+modifier was preferable for high activities and that aggregation of the Rh species led to a decrease in the activities.
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U2 - 10.1016/j.apcatb.2016.12.047
DO - 10.1016/j.apcatb.2016.12.047
M3 - Article
AN - SCOPUS:85007354799
SN - 0926-3373
VL - 205
SP - 340
EP - 346
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -