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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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Published in: | Nature materials 2019-11, Vol.18 (11), p.1222-1227 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/s41563-019-0445-x |