Carbon dioxide electroreduction to C2 products over copper-cuprous oxide derived from electrosynthesized copper complex

Efficient electroreduction of carbon dioxide to multicarbon products in aqueous solution is of great importance and challenging. Unfortunately, the low efficiency of the production of C 2 products limits implementation at scale. Here, we report reduction of carbon dioxide to C 2 products (acetic aci...

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Published in:Nature communications Vol. 10; no. 1; pp. 1 - 11
Main Authors: Zhu, Qinggong, Sun, Xiaofu, Yang, Dexin, Ma, Jun, Kang, Xinchen, Zheng, Lirong, Zhang, Jing, Wu, Zhonghua, Han, Buxing
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 26-08-2019
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Summary:Efficient electroreduction of carbon dioxide to multicarbon products in aqueous solution is of great importance and challenging. Unfortunately, the low efficiency of the production of C 2 products limits implementation at scale. Here, we report reduction of carbon dioxide to C 2 products (acetic acid and ethanol) over a 3D dendritic copper-cuprous oxide composite fabricated by in situ reduction of an electrodeposited copper complex. In potassium chloride aqueous electrolyte, the applied potential was as low as −0.4 V vs reversible hydrogen electrode, the overpotential is only 0.53 V (for acetic acid) and 0.48 V (for ethanol) with high C 2 Faradaic efficiency of 80% and a current density of 11.5 mA cm −2 . The outstanding performance of the electrode for producing the C 2 products results mainly from near zero contacting resistance between the electrocatalysts and copper substrate, abundant exposed active sites in the 3D dendritic structure and suitable copper(I)/copper(0) ratio of the electrocatalysts. Electrocatalytic reduction of carbon dioxide is attractive for obtaining multicarbon products, but conversion efficiency is low. Here the authors use copper complex materials for electrochemical reduction of carbon dioxide to ethanol and acetic acid with high efficiencies and activities.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-11599-7