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Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene

Use of multi-metallic catalysts to enhance reactions is an interesting research area, which has attracted much attention. In this work, we carried out the first work to prepare trimetallic electrocatalysts by a one-step co-electrodeposition process. A series of Cu–X–Y (X and Y denote different metal...

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Autores principales: Jia, Shuaiqiang, Zhu, Qinggong, Wu, Haihong, Han, Shitao, Chu, Mengen, Zhai, Jianxin, Xing, Xueqing, Xia, Wei, He, Mingyuan, Han, Buxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241956/
https://www.ncbi.nlm.nih.gov/pubmed/35872807
http://dx.doi.org/10.1039/d1sc06964k
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author Jia, Shuaiqiang
Zhu, Qinggong
Wu, Haihong
Han, Shitao
Chu, Mengen
Zhai, Jianxin
Xing, Xueqing
Xia, Wei
He, Mingyuan
Han, Buxing
author_facet Jia, Shuaiqiang
Zhu, Qinggong
Wu, Haihong
Han, Shitao
Chu, Mengen
Zhai, Jianxin
Xing, Xueqing
Xia, Wei
He, Mingyuan
Han, Buxing
author_sort Jia, Shuaiqiang
collection PubMed
description Use of multi-metallic catalysts to enhance reactions is an interesting research area, which has attracted much attention. In this work, we carried out the first work to prepare trimetallic electrocatalysts by a one-step co-electrodeposition process. A series of Cu–X–Y (X and Y denote different metals) catalysts were fabricated using this method. It was found that Cu(10)La(1)Cs(1) (the content ratio of Cu(2+), La(3+), and Cs(+) in the electrolyte is 10 : 1 : 1 in the deposition process), which had an elemental composition of Cu(10)La(0.16)Cs(0.14) in the catalyst, formed a composite structure on three dimensional (3D) carbon paper (CP), which showed outstanding performance for CO(2) electroreduction reaction (CO(2)RR) to produce ethylene (C(2)H(4)). The faradaic efficiency (FE) of C(2)H(4) could reach 56.9% with a current density of 37.4 mA cm(−2) in an H-type cell, and the partial current density of C(2)H(4) was among the highest ones up to date, including those over the catalysts consisting of Cu and noble metals. Moreover, the FE of C(2+) products (C(2)H(4), ethanol, and propanol) over the Cu(10)La(1)Cs(1) catalyst in a flow cell reached 70.5% with a high current density of 486 mA cm(−2). Experimental and theoretical studies suggested that the doping of La and Cs into Cu could efficiently enhance the reaction efficiency via a combination of different effects, such as defects, change of electronic structure, and enhanced charge transfer rate. This work provides a simple method to prepare multi-metallic catalysts and demonstrates a successful example for highly efficient CO(2)RR using non-noble metals.
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spelling pubmed-92419562022-07-22 Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene Jia, Shuaiqiang Zhu, Qinggong Wu, Haihong Han, Shitao Chu, Mengen Zhai, Jianxin Xing, Xueqing Xia, Wei He, Mingyuan Han, Buxing Chem Sci Chemistry Use of multi-metallic catalysts to enhance reactions is an interesting research area, which has attracted much attention. In this work, we carried out the first work to prepare trimetallic electrocatalysts by a one-step co-electrodeposition process. A series of Cu–X–Y (X and Y denote different metals) catalysts were fabricated using this method. It was found that Cu(10)La(1)Cs(1) (the content ratio of Cu(2+), La(3+), and Cs(+) in the electrolyte is 10 : 1 : 1 in the deposition process), which had an elemental composition of Cu(10)La(0.16)Cs(0.14) in the catalyst, formed a composite structure on three dimensional (3D) carbon paper (CP), which showed outstanding performance for CO(2) electroreduction reaction (CO(2)RR) to produce ethylene (C(2)H(4)). The faradaic efficiency (FE) of C(2)H(4) could reach 56.9% with a current density of 37.4 mA cm(−2) in an H-type cell, and the partial current density of C(2)H(4) was among the highest ones up to date, including those over the catalysts consisting of Cu and noble metals. Moreover, the FE of C(2+) products (C(2)H(4), ethanol, and propanol) over the Cu(10)La(1)Cs(1) catalyst in a flow cell reached 70.5% with a high current density of 486 mA cm(−2). Experimental and theoretical studies suggested that the doping of La and Cs into Cu could efficiently enhance the reaction efficiency via a combination of different effects, such as defects, change of electronic structure, and enhanced charge transfer rate. This work provides a simple method to prepare multi-metallic catalysts and demonstrates a successful example for highly efficient CO(2)RR using non-noble metals. The Royal Society of Chemistry 2022-06-10 /pmc/articles/PMC9241956/ /pubmed/35872807 http://dx.doi.org/10.1039/d1sc06964k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Jia, Shuaiqiang
Zhu, Qinggong
Wu, Haihong
Han, Shitao
Chu, Mengen
Zhai, Jianxin
Xing, Xueqing
Xia, Wei
He, Mingyuan
Han, Buxing
Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title_full Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title_fullStr Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title_full_unstemmed Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title_short Preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient CO(2) reduction to ethylene
title_sort preparation of trimetallic electrocatalysts by one-step co-electrodeposition and efficient co(2) reduction to ethylene
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241956/
https://www.ncbi.nlm.nih.gov/pubmed/35872807
http://dx.doi.org/10.1039/d1sc06964k
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