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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(...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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