| Literature DB >> 33231928 |
Dazhong Zhong1,2, Zhi-Jian Zhao1, Qiang Zhao2, Dongfang Cheng1, Bin Liu1, Gong Zhang1, Wanyu Deng1, Hao Dong1, Lei Zhang1, Jingkun Li1, Jinping Li2, Jinlong Gong1,3.
Abstract
Copper can efficiently electro-catalyze carbon dioxide reduction to C2+ products (C2 H4 , C2 H5 OH, n-propanol). However, the correlation between the activity and active sites remains ambiguous, impeding further improvements in their performance. The facet effect of copper crystals to promote CO adsorption and C-C coupling and consequently yield a superior selectivity for C2+ products is described. We achieve a high Faradaic efficiency (FE) of 87 % and a large partial current density of 217 mA cm-2 toward C2+ products on Cu(OH)2 -D at only -0.54 V versus the reversible hydrogen electrode in a flow-cell electrolyzer. With further coupled to a Si solar cell, record-high solar conversion efficiencies of 4.47 % and 6.4 % are achieved for C2 H4 and C2+ products, respectively. This study provides an in-depth understanding of the selective formation of C2+ products on Cu and paves the way for the practical application of electrocatalytic or solar-driven CO2 reduction.Entities:
Keywords: C2+ products; CO2 reduction; copper; facets; solar-driven conversion
Year: 2021 PMID: 33231928 DOI: 10.1002/anie.202015159
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336