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Catalyst synthesis under CO2 electroreduction favours faceting and promotes renewable fuels electrosynthesis

Authors :
Cao-Thang Dinh
Andrew H. Proppe
Fengwang Li
Edward H. Sargent
Mingchuan Luo
Ziyun Wang
Yuhang Wang
Yanwei Lum
Andrew Johnston
Golam Kibria
Tao Tao Zhuang
Ali Seifitokaldani
Shana O. Kelley
Petar Todorović
Mengxia Liu
Adnan Ozden
Jun Li
David Sinton
Hua Zhou
Christine M. Gabardo
Yi Xu
Christopher McCallum
Chih Shan Tan
Source :
Nature Catalysis. 3:98-106
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

The electrosynthesis of C2+ hydrocarbons from CO2 has attracted recent attention in light of the relatively high market price per unit energy input. Today’s low selectivities and stabilities towards C2+ products at high current densities curtail system energy efficiency, which limits their prospects for economic competitiveness. Here we present a materials processing strategy based on in situ electrodeposition of copper under CO2 reduction conditions that preferentially expose and maintain Cu(100) facets, which favour the formation of C2+ products. We observe capping of facets during catalyst synthesis and achieve control over faceting to obtain a 70% increase in the ratio of Cu(100) facets to total facet area. We report a 90% Faradaic efficiency for C2+ products at a partial current density of 520 mA cm−2 and a full-cell C2+ power conversion efficiency of 37%. We achieve nearly constant C2H4 selectivity over 65 h operation at 350 mA cm−2 in a membrane electrode assembly electrolyser. Electrocatalytic reduction of CO2 to multicarbon products is useful for producing high-value chemicals and fuels. Here the authors present a strategy that is based on the in situ electrodeposition of copper under CO2 reduction conditions that preferentially expose and maintain Cu(100) facets, which favour the formation of C2+ products.

Details

ISSN :
25201158
Volume :
3
Database :
OpenAIRE
Journal :
Nature Catalysis
Accession number :
edsair.doi...........6b62ee53f3fdbb2a2e03a5de68c5799e
Full Text :
https://doi.org/10.1038/s41929-019-0397-1