期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 124, 期 17, 页码 9385-9393出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.0c01304
关键词
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资金
- National Science Foundation [ACI-1532235, ACI-1532236, CHE1556041]
- University of Colorado Boulder
- Colorado State University
A first-principles study of the ethanol decomposition mechanism on Cu(111) is presented with a focus on the selectivity of acetaldehyde production controlled through the addition of molecular water in the reaction network. We include a pathway-switching bimolecular mechanism in which water and a substrate species undergo a double hydrogen exchange reaction, which alters the decomposition pathway of ethanol. The mechanistic study is performed on a portion of the ethanol decomposition network consisting of eight hydrogen abstraction reactions, adsorption of ethanol, desorption of acetaldehyde, and addition of two water-catalyzed pathway-switching reactions. The reaction rates are determined with density functional theory (DFT) and transition-state theory (TST). We use a recently developed technique, the sum over histories representation SOHR, to describe the chemical pathways of ethanol decomposition. The addition of the water pathway-switching mechanism shows an increase of acetaldehyde production, which closely follows experimental results.
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