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Enhanced multi-carbon alcohol electroproduction from CO via modulated hydrogen adsorption
Multi-carbon alcohols such as ethanol are valued as fuels in view of their high energy density and ready transport. Unfortunately, the selectivity toward alcohols in CO(2)/CO electroreduction is diminished by ethylene production, especially when operating at high current densities (>100 mA cm(−2)...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378828/ https://www.ncbi.nlm.nih.gov/pubmed/32703956 http://dx.doi.org/10.1038/s41467-020-17499-5 |
Sumario: | Multi-carbon alcohols such as ethanol are valued as fuels in view of their high energy density and ready transport. Unfortunately, the selectivity toward alcohols in CO(2)/CO electroreduction is diminished by ethylene production, especially when operating at high current densities (>100 mA cm(−2)). Here we report a metal doping approach to tune the adsorption of hydrogen at the copper surface and thereby promote alcohol production. Using density functional theory calculations, we screen a suite of transition metal dopants and find that incorporating Pd in Cu moderates hydrogen adsorption and assists the hydrogenation of C(2) intermediates, providing a means to favour alcohol production and suppress ethylene. We synthesize a Pd-doped Cu catalyst that achieves a Faradaic efficiency of 40% toward alcohols and a partial current density of 277 mA cm(−2) from CO electroreduction. The activity exceeds that of prior reports by a factor of 2. |
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