Ethanol photocatalysis on rutile TiO2(110): the role of defects and water

被引:45
作者
Walenta, Constantin A.
Kollmannsberger, Sebastian L.
Kiermaier, Josef
Winbauer, Andreas
Tschurl, Martin
Heiz, Ueli [1 ]
机构
[1] Tech Univ Munich, Dept Chem, Chair Phys Chem, D-85748 Garching, Germany
关键词
SURFACE SCIENCE; SINGLE-CRYSTAL; METHANOL PHOTOCHEMISTRY; HYDROGEN-PRODUCTION; ALIPHATIC-ALCOHOLS; TIO2; OXYGEN; PHOTOOXIDATION; DISSOCIATION; DEHYDROGENATION;
D O I
10.1039/c5cp03550c
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
In this work we present a stoichiometric reaction mechanism for the photocatalytic ethanol oxidation on TiO2(110). The reaction products are analyzed either under reaction conditions or after irradiation at lower temperatures. Water is identified as a quantitative by-product, which resides in a defect site. These water molecules cause a blocking of the defect sites which results in poisoning of the catalyst. By different preparation techniques of the TiO2(110) surface, the role of surface defects is further elucidated and the role of molecular oxygen is investigated. Based on the investigation, a complete photochemical reaction mechanism is given, which provides insights into general photon driven oxidation mechanisms on TiO2.
引用
收藏
页码:22809 / 22814
页数:6
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