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Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells
Alkaline polymer electrolyte fuel cells are a class of fuel cells that enable the use of non-precious metal catalysts, particularly for the oxygen reduction reaction at the cathode. While there have been alternative materials exhibiting Pt-comparable activity in alkaline solutions, to the best of ou...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447550/ https://www.ncbi.nlm.nih.gov/pubmed/30944328 http://dx.doi.org/10.1038/s41467-019-09503-4 |
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author | Wang, Ying Yang, Yao Jia, Shuangfeng Wang, Xiaoming Lyu, Kangjie Peng, Yanqiu Zheng, He Wei, Xing Ren, Huan Xiao, Li Wang, Jianbo Muller, David A. Abruña, Héctor D. Hwang, Bing Joe Lu, Juntao Zhuang, Lin |
author_facet | Wang, Ying Yang, Yao Jia, Shuangfeng Wang, Xiaoming Lyu, Kangjie Peng, Yanqiu Zheng, He Wei, Xing Ren, Huan Xiao, Li Wang, Jianbo Muller, David A. Abruña, Héctor D. Hwang, Bing Joe Lu, Juntao Zhuang, Lin |
author_sort | Wang, Ying |
collection | PubMed |
description | Alkaline polymer electrolyte fuel cells are a class of fuel cells that enable the use of non-precious metal catalysts, particularly for the oxygen reduction reaction at the cathode. While there have been alternative materials exhibiting Pt-comparable activity in alkaline solutions, to the best of our knowledge none have outperformed Pt in fuel-cell tests. Here we report a Mn-Co spinel cathode that can deliver greater power, at high current densities, than a Pt cathode. The power density of the cell employing the Mn-Co cathode reaches 1.1 W cm(−2) at 2.5 A cm(−2) at 60 (o)C. Moreover, this catalyst outperforms Pt at low humidity. In-depth characterization reveals that the remarkable performance originates from synergistic effects where the Mn sites bind O(2) and the Co sites activate H(2)O, so as to facilitate the proton-coupled electron transfer processes. Such an electrocatalytic synergy is pivotal to the high-rate oxygen reduction, particularly under water depletion/low humidity conditions. |
format | Online Article Text |
id | pubmed-6447550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64475502019-04-05 Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells Wang, Ying Yang, Yao Jia, Shuangfeng Wang, Xiaoming Lyu, Kangjie Peng, Yanqiu Zheng, He Wei, Xing Ren, Huan Xiao, Li Wang, Jianbo Muller, David A. Abruña, Héctor D. Hwang, Bing Joe Lu, Juntao Zhuang, Lin Nat Commun Article Alkaline polymer electrolyte fuel cells are a class of fuel cells that enable the use of non-precious metal catalysts, particularly for the oxygen reduction reaction at the cathode. While there have been alternative materials exhibiting Pt-comparable activity in alkaline solutions, to the best of our knowledge none have outperformed Pt in fuel-cell tests. Here we report a Mn-Co spinel cathode that can deliver greater power, at high current densities, than a Pt cathode. The power density of the cell employing the Mn-Co cathode reaches 1.1 W cm(−2) at 2.5 A cm(−2) at 60 (o)C. Moreover, this catalyst outperforms Pt at low humidity. In-depth characterization reveals that the remarkable performance originates from synergistic effects where the Mn sites bind O(2) and the Co sites activate H(2)O, so as to facilitate the proton-coupled electron transfer processes. Such an electrocatalytic synergy is pivotal to the high-rate oxygen reduction, particularly under water depletion/low humidity conditions. Nature Publishing Group UK 2019-04-03 /pmc/articles/PMC6447550/ /pubmed/30944328 http://dx.doi.org/10.1038/s41467-019-09503-4 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Wang, Ying Yang, Yao Jia, Shuangfeng Wang, Xiaoming Lyu, Kangjie Peng, Yanqiu Zheng, He Wei, Xing Ren, Huan Xiao, Li Wang, Jianbo Muller, David A. Abruña, Héctor D. Hwang, Bing Joe Lu, Juntao Zhuang, Lin Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title | Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title_full | Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title_fullStr | Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title_full_unstemmed | Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title_short | Synergistic Mn-Co catalyst outperforms Pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
title_sort | synergistic mn-co catalyst outperforms pt on high-rate oxygen reduction for alkaline polymer electrolyte fuel cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447550/ https://www.ncbi.nlm.nih.gov/pubmed/30944328 http://dx.doi.org/10.1038/s41467-019-09503-4 |
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