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Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster
Although the hydrogen evolution reaction (HER) is one of the fastest electrocatalytic reactions, modern polymer electrolyte membrane (PEM) electrolysers require larger platinum loadings (∼0.5–1.0 mg cm(−2)) than those in PEM fuel cell anodes and cathodes altogether (∼0.5 mg cm(−2)). Thus, catalyst o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792955/ https://www.ncbi.nlm.nih.gov/pubmed/26960565 http://dx.doi.org/10.1038/ncomms10990 |
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author | Tymoczko, Jakub Calle-Vallejo, Federico Schuhmann, Wolfgang Bandarenka, Aliaksandr S. |
author_facet | Tymoczko, Jakub Calle-Vallejo, Federico Schuhmann, Wolfgang Bandarenka, Aliaksandr S. |
author_sort | Tymoczko, Jakub |
collection | PubMed |
description | Although the hydrogen evolution reaction (HER) is one of the fastest electrocatalytic reactions, modern polymer electrolyte membrane (PEM) electrolysers require larger platinum loadings (∼0.5–1.0 mg cm(−2)) than those in PEM fuel cell anodes and cathodes altogether (∼0.5 mg cm(−2)). Thus, catalyst optimization would help in substantially reducing the costs for hydrogen production using this technology. Here we show that the activity of platinum(111) electrodes towards HER is significantly enhanced with just monolayer amounts of copper. Positioning copper atoms into the subsurface layer of platinum weakens the surface binding of adsorbed H-intermediates and provides a twofold activity increase, surpassing the highest specific HER activities reported for acidic media under similar conditions, to the best of our knowledge. These improvements are rationalized using a simple model based on structure-sensitive hydrogen adsorption at platinum and copper-modified platinum surfaces. This model also solves a long-lasting puzzle in electrocatalysis, namely why polycrystalline platinum electrodes are more active than platinum(111) for the HER. |
format | Online Article Text |
id | pubmed-4792955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47929552016-03-21 Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster Tymoczko, Jakub Calle-Vallejo, Federico Schuhmann, Wolfgang Bandarenka, Aliaksandr S. Nat Commun Article Although the hydrogen evolution reaction (HER) is one of the fastest electrocatalytic reactions, modern polymer electrolyte membrane (PEM) electrolysers require larger platinum loadings (∼0.5–1.0 mg cm(−2)) than those in PEM fuel cell anodes and cathodes altogether (∼0.5 mg cm(−2)). Thus, catalyst optimization would help in substantially reducing the costs for hydrogen production using this technology. Here we show that the activity of platinum(111) electrodes towards HER is significantly enhanced with just monolayer amounts of copper. Positioning copper atoms into the subsurface layer of platinum weakens the surface binding of adsorbed H-intermediates and provides a twofold activity increase, surpassing the highest specific HER activities reported for acidic media under similar conditions, to the best of our knowledge. These improvements are rationalized using a simple model based on structure-sensitive hydrogen adsorption at platinum and copper-modified platinum surfaces. This model also solves a long-lasting puzzle in electrocatalysis, namely why polycrystalline platinum electrodes are more active than platinum(111) for the HER. Nature Publishing Group 2016-03-10 /pmc/articles/PMC4792955/ /pubmed/26960565 http://dx.doi.org/10.1038/ncomms10990 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tymoczko, Jakub Calle-Vallejo, Federico Schuhmann, Wolfgang Bandarenka, Aliaksandr S. Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title | Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title_full | Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title_fullStr | Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title_full_unstemmed | Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title_short | Making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
title_sort | making the hydrogen evolution reaction in polymer electrolyte membrane electrolysers even faster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792955/ https://www.ncbi.nlm.nih.gov/pubmed/26960565 http://dx.doi.org/10.1038/ncomms10990 |
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