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Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer

Efficient and selective CO(2) electroreduction into chemical fuels promises to alleviate environmental pollution and energy crisis, but it relies on catalysts with controllable product selectivity and reaction path. Here, by means of first-principles calculations, we identify six ferroelectric catal...

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Autores principales: Ju, Lin, Tan, Xin, Mao, Xin, Gu, Yuantong, Smith, Sean, Du, Aijun, Chen, Zhongfang, Chen, Changfeng, Kou, Liangzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390745/
https://www.ncbi.nlm.nih.gov/pubmed/34446718
http://dx.doi.org/10.1038/s41467-021-25426-5
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author Ju, Lin
Tan, Xin
Mao, Xin
Gu, Yuantong
Smith, Sean
Du, Aijun
Chen, Zhongfang
Chen, Changfeng
Kou, Liangzhi
author_facet Ju, Lin
Tan, Xin
Mao, Xin
Gu, Yuantong
Smith, Sean
Du, Aijun
Chen, Zhongfang
Chen, Changfeng
Kou, Liangzhi
author_sort Ju, Lin
collection PubMed
description Efficient and selective CO(2) electroreduction into chemical fuels promises to alleviate environmental pollution and energy crisis, but it relies on catalysts with controllable product selectivity and reaction path. Here, by means of first-principles calculations, we identify six ferroelectric catalysts comprising transition-metal atoms anchored on In(2)Se(3) monolayer, whose catalytic performance can be controlled by ferroelectric switching based on adjusted d-band center and occupation of supported metal atoms. The polarization dependent activation allows effective control of the limiting potential of CO(2) reduction on TM@In(2)Se(3) (TM = Ni, Pd, Rh, Nb, and Re) as well as the reaction paths and final products on Nb@In(2)Se(3) and Re@In(2)Se(3). Interestingly, the ferroelectric switching can even reactivate the stuck catalytic CO(2) reduction on Zr@In(2)Se(3). The fairly low limiting potential and the unique ferroelectric controllable CO(2) catalytic performance on atomically dispersed transition-metals on In(2)Se(3) clearly distinguish them from traditional single atom catalysts, and open an avenue toward improving catalytic activity and selectivity for efficient and controllable electrochemical CO(2) reduction reaction.
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spelling pubmed-83907452021-09-22 Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer Ju, Lin Tan, Xin Mao, Xin Gu, Yuantong Smith, Sean Du, Aijun Chen, Zhongfang Chen, Changfeng Kou, Liangzhi Nat Commun Article Efficient and selective CO(2) electroreduction into chemical fuels promises to alleviate environmental pollution and energy crisis, but it relies on catalysts with controllable product selectivity and reaction path. Here, by means of first-principles calculations, we identify six ferroelectric catalysts comprising transition-metal atoms anchored on In(2)Se(3) monolayer, whose catalytic performance can be controlled by ferroelectric switching based on adjusted d-band center and occupation of supported metal atoms. The polarization dependent activation allows effective control of the limiting potential of CO(2) reduction on TM@In(2)Se(3) (TM = Ni, Pd, Rh, Nb, and Re) as well as the reaction paths and final products on Nb@In(2)Se(3) and Re@In(2)Se(3). Interestingly, the ferroelectric switching can even reactivate the stuck catalytic CO(2) reduction on Zr@In(2)Se(3). The fairly low limiting potential and the unique ferroelectric controllable CO(2) catalytic performance on atomically dispersed transition-metals on In(2)Se(3) clearly distinguish them from traditional single atom catalysts, and open an avenue toward improving catalytic activity and selectivity for efficient and controllable electrochemical CO(2) reduction reaction. Nature Publishing Group UK 2021-08-26 /pmc/articles/PMC8390745/ /pubmed/34446718 http://dx.doi.org/10.1038/s41467-021-25426-5 Text en © The Author(s) 2021 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
Ju, Lin
Tan, Xin
Mao, Xin
Gu, Yuantong
Smith, Sean
Du, Aijun
Chen, Zhongfang
Chen, Changfeng
Kou, Liangzhi
Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title_full Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title_fullStr Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title_full_unstemmed Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title_short Controllable CO(2) electrocatalytic reduction via ferroelectric switching on single atom anchored In(2)Se(3) monolayer
title_sort controllable co(2) electrocatalytic reduction via ferroelectric switching on single atom anchored in(2)se(3) monolayer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390745/
https://www.ncbi.nlm.nih.gov/pubmed/34446718
http://dx.doi.org/10.1038/s41467-021-25426-5
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