Hydrogenation of Pt/TiO2{101} nanobelts: a driving force for the improvement of methanol catalysis

被引:20
|
作者
Liu, Feila [1 ]
Xiao, Peng [1 ,2 ]
Tian, Wei Quan [1 ]
Zhou, Ming [1 ]
Li, Yanhong [2 ]
Cui, Xun [1 ]
Zhang, Yunhuai [1 ]
Zhou, Xin [3 ]
机构
[1] Chongqing Univ, Coll Chem & Chem Engn, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Coll Phys, Chongqing 400044, Peoples R China
[3] Harbin Inst Technol, Acad Fundamental & Interdisciplinary Sci, Inst Theoret & Simulat Chem, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
TIO2 NANOTUBE ARRAYS; PT-RU; CRYSTAL FACES; ELECTROOXIDATION; SURFACE; ADSORPTION; RUTILE; OXIDE; PHOTOCATALYSIS; ABSORPTION;
D O I
10.1039/c5cp05018a
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
Single-crystalline anatase TiO2 nanobelts with a dominant surface of the {101} facet were hydrogenated and used as substrates of platinum for methanol oxidation reaction (MOR). The hydrogenated TiO2 anatase{101} supporting Pt exhibits a 228% increase of current density for methanol oxidation compared with the same system without hydrogenation under dark conditions. The synergetic interactions of hydrogenated anatase{101} with the Pt cluster were investigated through first principles calculations, and found that the hydrogenation shifts the conduction band minimum to the Fermi level of pristine TiO2, and reduces the activation barrier for methanol dissociation considerably. Thus, this work provides an experimental and theoretical basis for developing non-carbon substrates with high electro-catalytic activity toward MOR.
引用
收藏
页码:28626 / 28634
页数:9
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