电化学
氧化还原
表面粗糙度
吸附
选择性
氧合物
化学
氢
电流密度
法拉第效率
分析化学(期刊)
化学工程
表面光洁度
电极
无机化学
催化作用
材料科学
复合材料
冶金
物理化学
有机化学
物理
工程类
量子力学
作者
Kun Jiang,Yufeng Huang,Guosong Zeng,Francesca M. Toma,William A. Goddard,Alexis T. Bell
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-03-19
卷期号:5 (4): 1206-1214
被引量:241
标识
DOI:10.1021/acsenergylett.0c00482
摘要
We have investigated the role of surface roughening on the CO2 reduction reaction (CO2RR) over Cu. The activity and product selectivity of Cu surfaces roughened by plasma pretreatment in Ar, O2, or N2 were compared with that of electrochemically polished Cu samples. Differences in total and product current densities, the ratio of current densities for HER (the hydrogen evolution reaction) to CO2RR, and the ratio of current densities for C2+ to C1 products depend on the electrochemically active surface and are nearly independent of plasma composition. Theoretical analysis of an electropolished and roughened Cu surface reveals a higher fraction of undercoordinated Cu sites on the roughened surface, sites that bind CO preferentially. Roughened surfaces also contain square sites similar to those on a Cu(100) surface but with neighboring step sites, which adsorb OC–COH, a precursor to C2+ products. These findings explain the increases in the formation of oxygenates and hydrocarbons relative to CO and the ratio of oxygenates to hydrocarbons observed with increasing surface roughness.
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