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Cited by 393

The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.

Efficient Electrocatalytic CO2 Reduction to C2+ Alcohols at Defect-Site-Rich Cu Surface

Open access
Gu, Zhengxiang, Shen, Hao, Chen, Zheng, Yang, Yaoyue, Yang, Chao, Ji, Yali, Wang, Yuhang, Zhu, Chan, Liu, Junlang, Li, Jun, Sham, Tsun-Kong, Xu, Xin, Zheng, Gengfeng·2021·Joule

Abstract

Summary Electrochemical CO2 reduction is a promising approach for upgrading excessive CO2 into value-added chemicals, while the exquisite control of the catalyst atomic structures to obtain high C2+ alcohol selectivity has remained challenging due to the intrinsically favored ethylene pathways at Cu surface. Herein, we demonstrate a rational strategy to achieve ∼70% faradaic efficiency toward C2+ alcohols. We utilized a CO-rich environment to construct Cu catalysts with stepped sites that enabled high surface coverages of ∗CO intermediates and the bridge-bound ∗CO adsorption, which allowed to trigger CO2 reduction pathways toward the formation alcohols. Using this defect-site-rich Cu catalyst, we achieved C2+ alcohols with partial current densities of > 100 mA·cm−2 in both a flow-cell electrolyzer and a membrane electrode assembly (MEA) electrolyzer. A stable alcohol faradaic efficiency of ∼60% was also obtained, with ∼500 mg C2+ alcohol production per cm2 catalyst during a continuous 30-h operation.

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Metadata

Authors
Gu, Z., Shen, H., Chen, Z., Yang, Y., Yang, C., Ji, Y., Wang, Y., Zhu, C., Liu, J., Li, J., Sham, T.-K., Xu, X., & Zheng, G.
Venue
Joule
Publisher
Elsevier BV
Published
2021-02
Volume
5
Issue
2
Pages
429-440
ISSN
2542-4351 (ISSN-L)
OpenAlex
W3120105118
Cited by
393
References
14
FWCI
11.58
Type
journal article
Language
en
Open access
bronze

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Gu, Z., Shen, H., Chen, Z., Yang, Y., Yang, C., Ji, Y., Wang, Y., Zhu, C., Liu, J., Li, J., Sham, T.-K., Xu, X., & Zheng, G. (2021). Efficient Electrocatalytic CO2 Reduction to C2+ Alcohols at Defect-Site-Rich Cu Surface. Joule. https://doi.org/10.1016/j.joule.2020.12.011

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