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Electrochemical deposition as a universal route for fabricating single-atom catalysts
Single-atom catalysts (SACs) exhibit intriguing catalytic performance owing to their maximized atom utilizations and unique electronic structures. However, the reported strategies for synthesizing SACs generally have special requirements for either the anchored metals or the supports. Herein, we rep...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058015/ https://www.ncbi.nlm.nih.gov/pubmed/32139683 http://dx.doi.org/10.1038/s41467-020-14917-6 |
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author | Zhang, Zhirong Feng, Chen Liu, Chunxiao Zuo, Ming Qin, Lang Yan, Xupeng Xing, Yulin Li, Hongliang Si, Rui Zhou, Shiming Zeng, Jie |
author_facet | Zhang, Zhirong Feng, Chen Liu, Chunxiao Zuo, Ming Qin, Lang Yan, Xupeng Xing, Yulin Li, Hongliang Si, Rui Zhou, Shiming Zeng, Jie |
author_sort | Zhang, Zhirong |
collection | PubMed |
description | Single-atom catalysts (SACs) exhibit intriguing catalytic performance owing to their maximized atom utilizations and unique electronic structures. However, the reported strategies for synthesizing SACs generally have special requirements for either the anchored metals or the supports. Herein, we report a universal approach of electrochemical deposition that is applicable to a wide range of metals and supports for the fabrication of SACs. The depositions were conducted on both cathode and anode, where the different redox reactions endowed the SACs with distinct electronic states. The SACs from cathodic deposition exhibited high activities towards hydrogen evolution reaction, while those from anodic deposition were highly active towards oxygen evolution reaction. When cathodically- and anodically-deposited Ir single atoms on Co(0.8)Fe(0.2)Se(2)@Ni foam were integrated into a two-electrode cell for overall water splitting, a voltage of 1.39 V was required at 10 mA cm(−2) in alkaline electrolyte. |
format | Online Article Text |
id | pubmed-7058015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70580152020-03-06 Electrochemical deposition as a universal route for fabricating single-atom catalysts Zhang, Zhirong Feng, Chen Liu, Chunxiao Zuo, Ming Qin, Lang Yan, Xupeng Xing, Yulin Li, Hongliang Si, Rui Zhou, Shiming Zeng, Jie Nat Commun Article Single-atom catalysts (SACs) exhibit intriguing catalytic performance owing to their maximized atom utilizations and unique electronic structures. However, the reported strategies for synthesizing SACs generally have special requirements for either the anchored metals or the supports. Herein, we report a universal approach of electrochemical deposition that is applicable to a wide range of metals and supports for the fabrication of SACs. The depositions were conducted on both cathode and anode, where the different redox reactions endowed the SACs with distinct electronic states. The SACs from cathodic deposition exhibited high activities towards hydrogen evolution reaction, while those from anodic deposition were highly active towards oxygen evolution reaction. When cathodically- and anodically-deposited Ir single atoms on Co(0.8)Fe(0.2)Se(2)@Ni foam were integrated into a two-electrode cell for overall water splitting, a voltage of 1.39 V was required at 10 mA cm(−2) in alkaline electrolyte. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7058015/ /pubmed/32139683 http://dx.doi.org/10.1038/s41467-020-14917-6 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Zhirong Feng, Chen Liu, Chunxiao Zuo, Ming Qin, Lang Yan, Xupeng Xing, Yulin Li, Hongliang Si, Rui Zhou, Shiming Zeng, Jie Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title | Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title_full | Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title_fullStr | Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title_full_unstemmed | Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title_short | Electrochemical deposition as a universal route for fabricating single-atom catalysts |
title_sort | electrochemical deposition as a universal route for fabricating single-atom catalysts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058015/ https://www.ncbi.nlm.nih.gov/pubmed/32139683 http://dx.doi.org/10.1038/s41467-020-14917-6 |
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