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A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution
The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology require...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647847/ https://www.ncbi.nlm.nih.gov/pubmed/26365764 http://dx.doi.org/10.1038/ncomms9304 |
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author | Hod, Idan Deria, Pravas Bury, Wojciech Mondloch, Joseph E. Kung, Chung-Wei So, Monica Sampson, Matthew D. Peters, Aaron W. Kubiak, Cliff P. Farha, Omar K. Hupp, Joseph T. |
author_facet | Hod, Idan Deria, Pravas Bury, Wojciech Mondloch, Joseph E. Kung, Chung-Wei So, Monica Sampson, Matthew D. Peters, Aaron W. Kubiak, Cliff P. Farha, Omar K. Hupp, Joseph T. |
author_sort | Hod, Idan |
collection | PubMed |
description | The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm(−2). Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst. |
format | Online Article Text |
id | pubmed-4647847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46478472015-12-01 A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution Hod, Idan Deria, Pravas Bury, Wojciech Mondloch, Joseph E. Kung, Chung-Wei So, Monica Sampson, Matthew D. Peters, Aaron W. Kubiak, Cliff P. Farha, Omar K. Hupp, Joseph T. Nat Commun Article The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm(−2). Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst. Nature Pub. Group 2015-09-14 /pmc/articles/PMC4647847/ /pubmed/26365764 http://dx.doi.org/10.1038/ncomms9304 Text en Copyright © 2015, 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 Hod, Idan Deria, Pravas Bury, Wojciech Mondloch, Joseph E. Kung, Chung-Wei So, Monica Sampson, Matthew D. Peters, Aaron W. Kubiak, Cliff P. Farha, Omar K. Hupp, Joseph T. A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title | A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title_full | A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title_fullStr | A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title_full_unstemmed | A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title_short | A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
title_sort | porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647847/ https://www.ncbi.nlm.nih.gov/pubmed/26365764 http://dx.doi.org/10.1038/ncomms9304 |
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