Manipulating Reaction Rates of Metal-Oxide Heterogeneous Catalysts via Semiconductor Heterojunctions

被引:4
作者
Nandakumar, Navaneetha K. [1 ,2 ]
Seebauer, Edmund G. [1 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Maxim Integrated, Dallas, TX 75254 USA
基金
美国国家科学基金会;
关键词
POLYCRYSTALLINE ANATASE TIO2; V2O5; SINGLE-CRYSTALS; THIN-FILMS; METHANOL OXIDATION; CARRIER CONCENTRATION; ELECTRICAL-PROPERTIES; VANADIUM-OXIDES; SURFACE; SUPPORT; MICROSTRUCTURE;
D O I
10.1021/acs.jpcc.8b00712
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
Heterojunctions of metal oxide semiconductors enable the manipulation of surface chemistry for heterogeneous catalysts or sensors without introducing dopants and their attendant complications. If one of the semiconductors is sufficiently thin, charge exchange between the two semiconductors leads to charge buildup at the free surface. The excess charge influences the Lewis acid-base character of the surface and propagates into properties such as catalytic activity. Although the available literature offers evidence for such effects, published work does not outline a quantitative framework that links heterojunction behavior to catalytic activity. The present work develops and demonstrates such a framework for the oxidation of methanol to formaldehyde with a heterojunction of thin polycrystalline V2O5 grown on polycrystalline anatase TiO2. The framework accurately reproduces activity changes by a factor of 20 in response to V2O5 thickness and TiO2 donor concentration.
引用
收藏
页码:16655 / 16663
页数:9
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