The curious case of CO2 dissociation on Cu(110)

被引:3
|
作者
Singh, Saurabh Kumar [1 ]
Shirhatti, Pranav R. [1 ]
机构
[1] Tata Inst Fundamental Res Hyderabad, 36-P Gopanpally, Hyderabad 500046, Telangana, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 160卷 / 02期
关键词
METHANOL SYNTHESIS; ADSORPTION DYNAMICS; OXYGEN-ADSORPTION; CH4; DISSOCIATION; CARBON-DIOXIDE; SURFACE; ACTIVATION; N-2; CHEMISORPTION; MECHANISM;
D O I
10.1063/5.0176642
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
Dissociation of CO2 on copper surfaces is an important model system for understanding the elementary steps in catalytic conversion of CO2 to methanol. Using molecular beam-surface scattering methods, we measure the initial dissociation probabilities (S-0) of CO2 on a flat, clean Cu(110) surface under ultrahigh vacuum conditions. The observed S-0 ranges from 3.9 x 10(-4) to 1.8 x 10(-2) at incidence energies of 0.64-1.59 eV. By extrapolating the trend observed in the incidence energy dependence of S-0, we estimate the lower limit of the dissociation barrier on terrace sites to be around 2 eV. We discuss these results in the context of what is known from previous studies on this system using different experiments and theoretical/computational methods. These findings are anticipated to be valuable for correctly understanding the elementary steps in CO2 dissociation on Cu surfaces.
引用
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页数:9
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