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A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide
Rational design and controlled synthesis of hybrid structures comprising multiple components with distinctive functionalities are an intriguing and challenging approach to materials development for important energy applications like electrocatalytic hydrogen production, where there is a great need f...
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/PMC4762894/ https://www.ncbi.nlm.nih.gov/pubmed/26892437 http://dx.doi.org/10.1038/ncomms10771 |
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author | Liu, Wen Hu, Enyuan Jiang, Hong Xiang, Yingjie Weng, Zhe Li, Min Fan, Qi Yu, Xiqian Altman, Eric I. Wang, Hailiang |
author_facet | Liu, Wen Hu, Enyuan Jiang, Hong Xiang, Yingjie Weng, Zhe Li, Min Fan, Qi Yu, Xiqian Altman, Eric I. Wang, Hailiang |
author_sort | Liu, Wen |
collection | PubMed |
description | Rational design and controlled synthesis of hybrid structures comprising multiple components with distinctive functionalities are an intriguing and challenging approach to materials development for important energy applications like electrocatalytic hydrogen production, where there is a great need for cost effective, active and durable catalyst materials to replace the precious platinum. Here we report a structure design and sequential synthesis of a highly active and stable hydrogen evolution electrocatalyst material based on pyrite-structured cobalt phosphosulfide nanoparticles grown on carbon nanotubes. The three synthetic steps in turn render electrical conductivity, catalytic activity and stability to the material. The hybrid material exhibits superior activity for hydrogen evolution, achieving current densities of 10 mA cm(−2) and 100 mA cm(−2) at overpotentials of 48 mV and 109 mV, respectively. Phosphorus substitution is crucial for the chemical stability and catalytic durability of the material, the molecular origins of which are uncovered by X-ray absorption spectroscopy and computational simulation. |
format | Online Article Text |
id | pubmed-4762894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47628942016-03-04 A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide Liu, Wen Hu, Enyuan Jiang, Hong Xiang, Yingjie Weng, Zhe Li, Min Fan, Qi Yu, Xiqian Altman, Eric I. Wang, Hailiang Nat Commun Article Rational design and controlled synthesis of hybrid structures comprising multiple components with distinctive functionalities are an intriguing and challenging approach to materials development for important energy applications like electrocatalytic hydrogen production, where there is a great need for cost effective, active and durable catalyst materials to replace the precious platinum. Here we report a structure design and sequential synthesis of a highly active and stable hydrogen evolution electrocatalyst material based on pyrite-structured cobalt phosphosulfide nanoparticles grown on carbon nanotubes. The three synthetic steps in turn render electrical conductivity, catalytic activity and stability to the material. The hybrid material exhibits superior activity for hydrogen evolution, achieving current densities of 10 mA cm(−2) and 100 mA cm(−2) at overpotentials of 48 mV and 109 mV, respectively. Phosphorus substitution is crucial for the chemical stability and catalytic durability of the material, the molecular origins of which are uncovered by X-ray absorption spectroscopy and computational simulation. Nature Publishing Group 2016-02-19 /pmc/articles/PMC4762894/ /pubmed/26892437 http://dx.doi.org/10.1038/ncomms10771 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 Liu, Wen Hu, Enyuan Jiang, Hong Xiang, Yingjie Weng, Zhe Li, Min Fan, Qi Yu, Xiqian Altman, Eric I. Wang, Hailiang A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title | A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title_full | A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title_fullStr | A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title_full_unstemmed | A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title_short | A highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
title_sort | highly active and stable hydrogen evolution catalyst based on pyrite-structured cobalt phosphosulfide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762894/ https://www.ncbi.nlm.nih.gov/pubmed/26892437 http://dx.doi.org/10.1038/ncomms10771 |
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