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- W4313260151 abstract "Electrochemical CO2 reduction reactions can lead to high value-added chemical and materials production while helping decrease anthropogenic CO2 emissions. Copper metal clusters can reduce CO2 to more than thirty different hydrocarbons and oxygenates yet they lack the required selectivity. We present a computational characterization of the role of nano-structuring and alloying in Cu-based catalysts on the activity and selectivity of CO2 reduction to generate the following one-carbon products: carbon monoxide (CO), formic acid (HCOOH), formaldehyde (H2C=O), methanol (CH3OH) and methane (CH4). The structures and energetics were determined for the adsorption, activation, and conversion of CO2 on monometallic and bimetallic (decorated and core@shell) 55-atom Cu-based clusters. The dopant metals considered were Ag, Cd, Pd, Pt, and Zn, located at different coordination sites. The relative binding strength of the intermediates were used to identify the optimal catalyst for the selective CO2 conversion to one-carbon products. It was discovered that single atom Cd or Zn doping is optimal for the conversion of CO2 to CO. The core@shell models with Ag, Pd and Pt provided higher selectivity for formic acid and formaldehyde. The Cu-Pt and Cu-Pd showed lowest overpotential for methane formation." @default.
- W4313260151 created "2023-01-06" @default.
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- W4313260151 date "2022-12-24" @default.
- W4313260151 modified "2023-10-04" @default.
- W4313260151 title "Optimal Icosahedral Copper-Based Bimetallic Clusters for the Selective Electrocatalytic CO2 Conversion to One Carbon Products" @default.
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- W4313260151 doi "https://doi.org/10.3390/nano13010087" @default.
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