The aqueous electrocatalytic reduction of CO2 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 (C2/C3), 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 CO2 at the electrode–solution interface and consequently increase CO2 reduction selectivity. Hydrophobicity is thus proposed as a governing factor in CO2 reduction selectivity and can help explain trends seen on previously reported electrocatalysts.
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Raw data used in preparation of this manuscript is available to download at https://doi.org/10.7910/DVN/DSPZHE.
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V.M. acknowledges financial support from CNRS-Cellule Energie and Fondation of Collège de France for the acquisition of the GC equipment. D.W. was supported by an Idex PSL grant (ANR-10-IDEX-001-02 PSL), the Fondation du Collège de France and the Marie Curie PRESTIGE Fellowship programme. S.L. was funded by the Corps des Ponts, des Eaux et des Forêts. X-ray diffraction measurements were carried out by G. Rousse at the Collège de France. SEM images were collected by D. Montero at the Institut des Matériaux de Paris and F. Pillier at the Laboratoire Interfaces et Systèmes Electrochimiques. BET measurements were carried by J. Blanchard at the Laboratoire de Réactivité de Surface at Sorbonne Université.
Authors declare no competing interests.
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