期刊
ACS CATALYSIS
卷 8, 期 2, 页码 1490-1499出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b03477
关键词
artificial photosynthesis; DFT; electrocatalysis; mechanisms; ethanol; ethylene
资金
- Office of Science of the U.S. Department of Energy [DE-SC00004993, DE-AC02-05CH11231]
On the basis of constraints from reported experimental observations and density functional theory simulations, we propose a mechanism for the reduction of CO2 to C-2 products on copper electrodes. To model the effects of an applied potential bias on the reactions, calculations are carried out with a variable, fractional number of electrons on the unit cell, which is optimized so that the Fermi level matches the actual chemical potential of electrons (i.e., the applied bias); an implicit electrolyte model allows for compensation of the surface charge so that neutrality is maintained in the overall simulation cell. Our mechanism explains the presence of the seven C-2 species that have been detected in the reaction, as well as other notable experimental observations. Furthermore, our results shed light on the difference in activities toward C-2 products between the (100) and (111) facets of copper. We compare our methodologies and findings with those in other recent mechanistic studies of the copper-catalyzed CO2 reduction reaction.
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