Toward a Comprehensive Understanding of Photocatalysis: What Systematic Studies and Alcohol Surface Chemistry on TiO2(110) Have to Offer for Future Developments

被引:8
作者
Eder, Moritz [1 ,2 ]
Tschurl, Martin [1 ,2 ]
Heiz, Ueli [1 ,2 ]
机构
[1] Tech Univ Munich, TUM Sch Nat Sci, D-85748 Garching, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, D-85748 Garching, Germany
关键词
HYDROGEN-PRODUCTION; H-2; PRODUCTION; CORE/SHELL NANOPARTICLES; RUTILE TIO2(110); WATER; TIO2; METHANOL; SIZE; ADSORPTION; OXIDATION;
D O I
10.1021/acs.jpclett.3c00504
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
Heterogeneous photocatalyticsystems are usually described basedon electrochemistry, which the vast majority of interpretations andstrategies for optimizing photocatalysts rely on. Charge carrier dynamicsare usually in the spotlight, whereas the surface chemistry of thephotocatalyst is neglected. This is unjustified, because studies onalcohol photoreforming on metal-decorated rutile single crystals revealedthat the electrochemical reaction model is not generally applicable.Hence, many photocatalytic reactions may proceed in a different mannerand the thermal chemistry needs to be accounted for. The new mechanismis particularly relevant for reactions in gaseous environments inthe absence of solvated ionic species. Here, we compare both mechanismsand highlight their differences and consequences for photocatalysis.Based on alcohol photochemistry, we demonstrate the importance ofthermal reactions in photocatalytic mechanisms and the relevance ofsystematic studies in different environments for a holistic understandingof photocatalysis.
引用
收藏
页码:6193 / 6201
页数:9
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