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Bio-inspired hydrophobicity promotes CO2 reduction on a Cu surface

The aqueous electrocatalytic reduction of CO 2 into alcohol and hydrocarbon fuels presents a sustainable route towards energy-rich chemical feedstocks. Cu is the only material able to catalyse the substantial formation of multicarbon products (C 2 /C 3 ), but competing proton reduction to hydrogen i...

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Bibliographic Details
Published in:Nature materials 2019-11, Vol.18 (11), p.1222-1227
Main Authors: Wakerley, David, Lamaison, Sarah, Ozanam, François, Menguy, Nicolas, Mercier, Dimitri, Marcus, Philippe, Fontecave, Marc, Mougel, Victor
Format: Article
Language:English
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Summary:The aqueous electrocatalytic reduction of CO 2 into alcohol and hydrocarbon fuels presents a sustainable route towards energy-rich chemical feedstocks. Cu is the only material able to catalyse the substantial formation of multicarbon products (C 2 /C 3 ), but competing proton reduction to hydrogen is an ever-present drain on selectivity. Here, a superhydrophobic surface was generated by 1-octadecanethiol treatment of hierarchically structured Cu dendrites, inspired by the structure of gas-trapping cuticles on subaquatic spiders. The hydrophobic electrode attained a 56% Faradaic efficiency for ethylene and 17% for ethanol production at neutral pH, compared to 9% and 4% on a hydrophilic, wettable equivalent. These observations are assigned to trapped gases at the hydrophobic Cu surface, which increase the concentration of CO 2 at the electrode–solution interface and consequently increase CO 2 reduction selectivity. Hydrophobicity is thus proposed as a governing factor in CO 2 reduction selectivity and can help explain trends seen on previously reported electrocatalysts. Aqueous electrocatalytic reduction of CO 2 into alcohol and hydrocarbon fuels is a sustainable route towards energy-rich chemical feedstocks. A superhydrophobic surface of hierarchically structured Cu dendrites exhibits a significant increase in CO 2 reduction selectivity.
ISSN:1476-1122
1476-4660
DOI:10.1038/s41563-019-0445-x