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Selective CO(2) electrolysis to CO using isolated antimony alloyed copper

Renewable electricity-powered CO evolution from CO(2) emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO(2) reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high p...

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Autores principales: Li, Jiawei, Zeng, Hongliang, Dong, Xue, Ding, Yimin, Hu, Sunpei, Zhang, Runhao, Dai, Yizhou, Cui, Peixin, Xiao, Zhou, Zhao, Donghao, Zhou, Liujiang, Zheng, Tingting, Xiao, Jianping, Zeng, Jie, Xia, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860050/
https://www.ncbi.nlm.nih.gov/pubmed/36670129
http://dx.doi.org/10.1038/s41467-023-35960-z
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author Li, Jiawei
Zeng, Hongliang
Dong, Xue
Ding, Yimin
Hu, Sunpei
Zhang, Runhao
Dai, Yizhou
Cui, Peixin
Xiao, Zhou
Zhao, Donghao
Zhou, Liujiang
Zheng, Tingting
Xiao, Jianping
Zeng, Jie
Xia, Chuan
author_facet Li, Jiawei
Zeng, Hongliang
Dong, Xue
Ding, Yimin
Hu, Sunpei
Zhang, Runhao
Dai, Yizhou
Cui, Peixin
Xiao, Zhou
Zhao, Donghao
Zhou, Liujiang
Zheng, Tingting
Xiao, Jianping
Zeng, Jie
Xia, Chuan
author_sort Li, Jiawei
collection PubMed
description Renewable electricity-powered CO evolution from CO(2) emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO(2) reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high performance for CO(2)-to-CO. Cu is a potential catalyst to achieve CO(2) reduction to CO at the industrial scale, but the C-C coupling process on Cu significantly depletes CO* intermediates, thus limiting the CO evolution rate and producing many hydrocarbon and oxygenate mixtures. Herein, we tune the CO selectivity of Cu by alloying a second metal Sb into Cu, and report an antimony-copper single-atom alloy catalyst (Sb(1)Cu) of isolated Sb-Cu interfaces that catalyzes the efficient conversion of CO(2)-to-CO with a Faradaic efficiency over 95%. The partial current density reaches 452 mA cm(−2) with approximately 91% CO Faradaic efficiency, and negligible C(2+) products are observed. In situ spectroscopic measurements and theoretical simulations reason that the atomic Sb-Cu interface in Cu promotes CO(2) adsorption/activation and weakens the binding strength of CO*, which ends up with enhanced CO selectivity and production rates.
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spelling pubmed-98600502023-01-22 Selective CO(2) electrolysis to CO using isolated antimony alloyed copper Li, Jiawei Zeng, Hongliang Dong, Xue Ding, Yimin Hu, Sunpei Zhang, Runhao Dai, Yizhou Cui, Peixin Xiao, Zhou Zhao, Donghao Zhou, Liujiang Zheng, Tingting Xiao, Jianping Zeng, Jie Xia, Chuan Nat Commun Article Renewable electricity-powered CO evolution from CO(2) emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO(2) reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high performance for CO(2)-to-CO. Cu is a potential catalyst to achieve CO(2) reduction to CO at the industrial scale, but the C-C coupling process on Cu significantly depletes CO* intermediates, thus limiting the CO evolution rate and producing many hydrocarbon and oxygenate mixtures. Herein, we tune the CO selectivity of Cu by alloying a second metal Sb into Cu, and report an antimony-copper single-atom alloy catalyst (Sb(1)Cu) of isolated Sb-Cu interfaces that catalyzes the efficient conversion of CO(2)-to-CO with a Faradaic efficiency over 95%. The partial current density reaches 452 mA cm(−2) with approximately 91% CO Faradaic efficiency, and negligible C(2+) products are observed. In situ spectroscopic measurements and theoretical simulations reason that the atomic Sb-Cu interface in Cu promotes CO(2) adsorption/activation and weakens the binding strength of CO*, which ends up with enhanced CO selectivity and production rates. Nature Publishing Group UK 2023-01-20 /pmc/articles/PMC9860050/ /pubmed/36670129 http://dx.doi.org/10.1038/s41467-023-35960-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Jiawei
Zeng, Hongliang
Dong, Xue
Ding, Yimin
Hu, Sunpei
Zhang, Runhao
Dai, Yizhou
Cui, Peixin
Xiao, Zhou
Zhao, Donghao
Zhou, Liujiang
Zheng, Tingting
Xiao, Jianping
Zeng, Jie
Xia, Chuan
Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title_full Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title_fullStr Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title_full_unstemmed Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title_short Selective CO(2) electrolysis to CO using isolated antimony alloyed copper
title_sort selective co(2) electrolysis to co using isolated antimony alloyed copper
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860050/
https://www.ncbi.nlm.nih.gov/pubmed/36670129
http://dx.doi.org/10.1038/s41467-023-35960-z
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