Surface Chemistry and Interfacial Charge-Transfer Mechanisms in Photoinduced Oxygen Exchange at O2-TiO2 Interfaces

被引:26
|
作者
Felipe Montoya, Juan [2 ]
Peral, Jose [2 ]
Salvador, Pedro [1 ]
机构
[1] Univ Illes Balears, Dept Ciencies Matemat & Informat, Palma De Mallorca 07071, Spain
[2] Univ Autonoma Barcelona, Dept Quim, Cerdanyola Del Valles 08193, Spain
关键词
adsorbed water; electron transfer; oxygen exchange; surface chemistry; titanium dioxide; HETEROGENEOUS PHOTOCATALYTIC OXIDATION; ISOTOPIC EXCHANGE; AQUEOUS-SOLUTIONS; TIO2; O-2; ELECTRON; PHOTOOXIDATION; DIOXIDE; CYANIDE; LIGHT;
D O I
10.1002/cphc.201000611
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
Experimental results obtained over the last three decades on photoinduced oxygen isotopic exchange (POIE) of TiO2 oxygen atoms with those of adsorbed water molecules and gaseous O-2 are analyzed in the light of recent information from the literature on the interaction of water and O-2 species with the TiO2 surface (obtained by application of surface spectroscopy techniques in combination with high-resolution scanning tunnelling microscopy). The analysis emphasizes the singular role that bridging oxygen ions and bridging oxygen vacancies play in TiO2 surface chemistry and interfacial electron transfer at the gas phase-TiO2 interface in the absence and presence of water. The observed competition between POIE and the photo-oxidation (PO) of organic compounds is analyzed in terms of the recently developed direct-indirect (D-I) kinetic model for heterogeneous photocatalysis (D. Monllor-Satoca et al., Catal. Today, 2007, 129, 247, and references therein).
引用
收藏
页码:901 / 907
页数:7
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