Origin of CO promoted methanol oxidation in alkaline media catalyzed by gold: A first-principle investigation

被引:3
|
作者
Lv, Cun-Qin [1 ]
Liu, Jian-Hong [1 ]
Wang, He [2 ,3 ]
Wang, Gui-Chang [2 ,3 ]
机构
[1] Shanxi Datong Univ, Coll Chem & Chem Engn, Datong 037009, Shanxi Province, Peoples R China
[2] Nankai Univ, Dept Chem, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
[3] Nankai Univ, Tianjin Key Lab & Mol Based Mat Chem, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
基金
山西省青年科学基金; 中国国家自然科学基金;
关键词
Methanol oxidation; Au(111); Alkaline media; CO promotion effect; DFT calculations; DENSITY-FUNCTIONAL THEORY; FUEL-CELL CATHODE; OXYGEN REDUCTION; ADSORPTION; SURFACES; MODEL; DISSOCIATION; BASICITY; AU(111); CYCLES;
D O I
10.1016/j.catcom.2014.11.013
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
We performed density functional theory calculations to investigate the kinetics of methanol oxidation into formic acid catalyzed by Au(111) with and without CO in alkaline media. The calculation results show that the surface with pre-adsorbed molecular CO reduces the adsorption energy of possible species. The pre-adsorbed CO species promotes almost every step of methanol oxidation both thermochemically and kinetically, which agrees well with the experimental observation. This finding may be associated with the relatively strong basicity of OH species in the presence of adsorbed CO species, thereby enhancing their ability to strip the H atoms. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 64
页数:5
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