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(Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting
Earth-abundant and efficient bifunctional electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are highly significant for renewable energy systems. However, the performance of existing electrocatalysts is usually restricted by the low electroic conductivity...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013453/ https://www.ncbi.nlm.nih.gov/pubmed/29930378 http://dx.doi.org/10.1038/s41598-018-27477-z |
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author | Xu, Peiman Li, Jingwei Luo, Jiaxian Wei, Licheng Zhang, Dawei Zhou, Dan Xu, Weiming Yuan, Dingsheng |
author_facet | Xu, Peiman Li, Jingwei Luo, Jiaxian Wei, Licheng Zhang, Dawei Zhou, Dan Xu, Weiming Yuan, Dingsheng |
author_sort | Xu, Peiman |
collection | PubMed |
description | Earth-abundant and efficient bifunctional electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are highly significant for renewable energy systems. However, the performance of existing electrocatalysts is usually restricted by the low electroic conductivity and the limited amount of exposed active sites. In this work, (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam have been prepared by a sulfuration of FeNi layered double hydroxide spheres grown on Ni foam. Benefiting from the unique tubular sphere architecture, the rich inner defects and the enhanced electron interactions between Fe, Ni and S, this electrocatalyst shows low overpotential of 48 mV for HER at 10 mA cm(−2) in 1.0 mol L(−1) KOH solution, which is one of the lowest value of non-previous electrocatalyts for HER in alkaline electrolyte. Furthermore, assembled this versatile electrode as an alkaline electrolyzer for overall water splitting, a current density of 10 mA cm(−2) is achieved at a low cell voltage of 1.56 V, and reach up to 30 mA cm(−2) only at an operating cell voltage of 1.65 V. |
format | Online Article Text |
id | pubmed-6013453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60134532018-06-27 (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting Xu, Peiman Li, Jingwei Luo, Jiaxian Wei, Licheng Zhang, Dawei Zhou, Dan Xu, Weiming Yuan, Dingsheng Sci Rep Article Earth-abundant and efficient bifunctional electrocatalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are highly significant for renewable energy systems. However, the performance of existing electrocatalysts is usually restricted by the low electroic conductivity and the limited amount of exposed active sites. In this work, (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam have been prepared by a sulfuration of FeNi layered double hydroxide spheres grown on Ni foam. Benefiting from the unique tubular sphere architecture, the rich inner defects and the enhanced electron interactions between Fe, Ni and S, this electrocatalyst shows low overpotential of 48 mV for HER at 10 mA cm(−2) in 1.0 mol L(−1) KOH solution, which is one of the lowest value of non-previous electrocatalyts for HER in alkaline electrolyte. Furthermore, assembled this versatile electrode as an alkaline electrolyzer for overall water splitting, a current density of 10 mA cm(−2) is achieved at a low cell voltage of 1.56 V, and reach up to 30 mA cm(−2) only at an operating cell voltage of 1.65 V. Nature Publishing Group UK 2018-06-21 /pmc/articles/PMC6013453/ /pubmed/29930378 http://dx.doi.org/10.1038/s41598-018-27477-z Text en © The Author(s) 2018 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 Xu, Peiman Li, Jingwei Luo, Jiaxian Wei, Licheng Zhang, Dawei Zhou, Dan Xu, Weiming Yuan, Dingsheng (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title | (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title_full | (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title_fullStr | (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title_full_unstemmed | (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title_short | (Fe(0.2)Ni(0.8))(0.96)S tubular spheres supported on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
title_sort | (fe(0.2)ni(0.8))(0.96)s tubular spheres supported on ni foam as an efficient bifunctional electrocatalyst for overall water splitting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013453/ https://www.ncbi.nlm.nih.gov/pubmed/29930378 http://dx.doi.org/10.1038/s41598-018-27477-z |
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