Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/126167
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Type: Journal article
Title: Electrochemical reduction of CO₂ to ethane through stabilization of an ethoxy intermediate
Other Titles: Electrochemical reduction of CO(2) to ethane through stabilization of an ethoxy intermediate
Author: Vasileff, A.
Zhu, Y.
Zhi, X.
Zhao, Y.
Ge, L.
Chen, H.M.
Zheng, Y.
Qiao, S.
Citation: Angewandte Chemie International Edition, 2020; 59(44):19649-19653
Publisher: Wiley
Issue Date: 2020
ISSN: 1433-7851
1521-3773
Statement of
Responsibility: 
Anthony Vasileff, Yanping Zhu, Xing Zhi, Yongqiang Zhao, Lei Ge ... Yao Zheng, Shi‐Zhang Qiao
Abstract: Electrochemical conversion of CO2 to ethane is seldom observed because of the generally higher selectivity towards methane, ethylene, and ethanol. Consequently, little experimental evidence for its reaction mechanism exists and thus remains largely unknown. Here, by combining electrochemistry with in-situ X-ray absorption fine structure and in-situ Raman techniques, we study iodide-derived copper (ID-Cu) and oxide-derived copper (OD-Cu) systems to obtain a deeper understanding of the CO2 to ethane mechanism. With trace iodine species on the surface and positively charged Cu species, production of ethane is significantly more favored on ID-Cu compared to OD-Cu, with higher selectivity and faster kinetics. For the first time, it is experimentally found that the formation of ethane follows the same pathway to ethylene and ethanol, and better stabilization of the late stage ethoxy intermediate can steer the reaction to ethane over ethanol.
Keywords: CO2 reduction; Copper catalysts; In-situ Spectroscopy; Raman; XAFS
Rights: © 2020 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim.
RMID: 1000019634
DOI: 10.1002/anie.202004846
Grant ID: http://purl.org/au-research/grants/arc/FL170100154
http://purl.org/au-research/grants/arc/DP160104866
http://purl.org/au-research/grants/arc/DP170104464
Appears in Collections:Chemistry publications

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