FT-IR study of the reaction mechanisms for photocatalytic reduction of NO with CO promoted by various single-site photocatalysts

被引:8
作者
Toyao, Takashi [1 ]
Morishima, Jun [1 ]
Saito, Masakazu [1 ]
Horiuchi, Yu [1 ]
Kamegawa, Takashi [2 ]
Martra, Gianmario [3 ]
Coluccia, Salvatore [3 ]
Matsuoka, Masaya [1 ]
Anpo, Masakazu [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Naka Ku, Sakai, Osaka 5998531, Japan
[2] Osaka Univ, Grad Sch Engn, Div Mat & Mfg Sci, Suita, Osaka 5650817, Japan
[3] Univ Turin, Dipartimento Chim IFM, I-10125 Turin, Italy
关键词
Single-site photocatalyst; Photocatalytic reduction; Nitrogen oxide; Carbon monoxide; VISIBLE-LIGHT; CHROMIUM-OXIDE; NITRIC-OXIDE; THIN-FILMS; SILICA; TIO2; OXIDATION; CATALYSTS; VANADIUM; ZEOLITE;
D O I
10.1016/j.jcat.2012.12.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic reduction of NO with CO has been carried out using various single-site photocatalysts under UV-light irradiation. The single-site photocatalysts prepared by incorporating transition metal oxides within SiO2 (M/Sio(2): M=Mo, V, and Cr) display different photocatalytic activities. Mo/SiO2 promotes photocatalytic reduction of NO with CO efficiently to produce N-2 via the intermediate N2O. V/SiO2 was observed to promote the reaction that leads to selective production of N2O that does not undergo subsequent reduction to form N-2. When Cr/SiO2 is used as the photocatalyst, reduction of NO does not take place. The results of Fourier transform infrared investigations reveal that differences in photocatalytic activities are due to different reactivity of reactants-adsorbed transition metal oxides in M/SiO2 and, consequently, the reaction mechanisms for the photocatalytic reduction of NO with CO over M/SiO2 are proposed. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:232 / 239
页数:8
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