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Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution
Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal s...
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/PMC6823491/ https://www.ncbi.nlm.nih.gov/pubmed/31672970 http://dx.doi.org/10.1038/s41467-019-12851-w |
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author | Yan, Qiang-Qiang Wu, Dao-Xiong Chu, Sheng-Qi Chen, Zhi-Qin Lin, Yue Chen, Ming-Xi Zhang, Jing Wu, Xiao-Jun Liang, Hai-Wei |
author_facet | Yan, Qiang-Qiang Wu, Dao-Xiong Chu, Sheng-Qi Chen, Zhi-Qin Lin, Yue Chen, Ming-Xi Zhang, Jing Wu, Xiao-Jun Liang, Hai-Wei |
author_sort | Yan, Qiang-Qiang |
collection | PubMed |
description | Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm(−2) and a high mass activity of 26.1 A mg(−1) at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts. |
format | Online Article Text |
id | pubmed-6823491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68234912019-11-04 Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution Yan, Qiang-Qiang Wu, Dao-Xiong Chu, Sheng-Qi Chen, Zhi-Qin Lin, Yue Chen, Ming-Xi Zhang, Jing Wu, Xiao-Jun Liang, Hai-Wei Nat Commun Article Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm(−2) and a high mass activity of 26.1 A mg(−1) at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts. Nature Publishing Group UK 2019-10-31 /pmc/articles/PMC6823491/ /pubmed/31672970 http://dx.doi.org/10.1038/s41467-019-12851-w 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 Yan, Qiang-Qiang Wu, Dao-Xiong Chu, Sheng-Qi Chen, Zhi-Qin Lin, Yue Chen, Ming-Xi Zhang, Jing Wu, Xiao-Jun Liang, Hai-Wei Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title | Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title_full | Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title_fullStr | Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title_full_unstemmed | Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title_short | Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
title_sort | reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823491/ https://www.ncbi.nlm.nih.gov/pubmed/31672970 http://dx.doi.org/10.1038/s41467-019-12851-w |
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