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IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media
A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192761/ https://www.ncbi.nlm.nih.gov/pubmed/34112770 http://dx.doi.org/10.1038/s41467-021-23907-1 |
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author | Li, Rui Wang, Haiyun Hu, Fei Chan, K. C. Liu, Xiongjun Lu, Zhaoping Wang, Jing Li, Zhibin Zeng, Longjiao Li, Yuanyuan Wu, Xiaojun Xiong, Yujie |
author_facet | Li, Rui Wang, Haiyun Hu, Fei Chan, K. C. Liu, Xiongjun Lu, Zhaoping Wang, Jing Li, Zhibin Zeng, Longjiao Li, Yuanyuan Wu, Xiaojun Xiong, Yujie |
author_sort | Li, Rui |
collection | PubMed |
description | A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(−2) at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm(−2) at least 800 h with a negligible degradation rate of ~4 μV h(−1). Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO(2))(n) clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO(2) clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers. |
format | Online Article Text |
id | pubmed-8192761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81927612021-06-17 IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media Li, Rui Wang, Haiyun Hu, Fei Chan, K. C. Liu, Xiongjun Lu, Zhaoping Wang, Jing Li, Zhibin Zeng, Longjiao Li, Yuanyuan Wu, Xiaojun Xiong, Yujie Nat Commun Article A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(−2) at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm(−2) at least 800 h with a negligible degradation rate of ~4 μV h(−1). Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO(2))(n) clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO(2) clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers. Nature Publishing Group UK 2021-06-10 /pmc/articles/PMC8192761/ /pubmed/34112770 http://dx.doi.org/10.1038/s41467-021-23907-1 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 Li, Rui Wang, Haiyun Hu, Fei Chan, K. C. Liu, Xiongjun Lu, Zhaoping Wang, Jing Li, Zhibin Zeng, Longjiao Li, Yuanyuan Wu, Xiaojun Xiong, Yujie IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title | IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title_full | IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title_fullStr | IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title_full_unstemmed | IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title_short | IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media |
title_sort | irw nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 a cm(−2) in acidic media |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192761/ https://www.ncbi.nlm.nih.gov/pubmed/34112770 http://dx.doi.org/10.1038/s41467-021-23907-1 |
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