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Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution

It is essential to precisely develop low-cost and sustainable electrocatalysts for the hydrogen evolution reaction. Herein, we explore a robust and controllable hydrothermal approach to synthesize defect-rich MoS(2) nanoflakes on exfoliated MoS(2) and WS(2). Such well-designed hetero-structural hybr...

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Autores principales: Gao, Guanhui, Xie, Xiaobin, Kang, Shendong, Lei, Yanhua, Trampert, Achim, Cai, Lintao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065390/
https://www.ncbi.nlm.nih.gov/pubmed/35514720
http://dx.doi.org/10.1039/c9ra02673h
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author Gao, Guanhui
Xie, Xiaobin
Kang, Shendong
Lei, Yanhua
Trampert, Achim
Cai, Lintao
author_facet Gao, Guanhui
Xie, Xiaobin
Kang, Shendong
Lei, Yanhua
Trampert, Achim
Cai, Lintao
author_sort Gao, Guanhui
collection PubMed
description It is essential to precisely develop low-cost and sustainable electrocatalysts for the hydrogen evolution reaction. Herein, we explore a robust and controllable hydrothermal approach to synthesize defect-rich MoS(2) nanoflakes on exfoliated MoS(2) and WS(2). Such well-designed hetero-structural hybrids of MoS(2)/exfoliated MoS(2) and MoS(2)/exfoliated WS(2) exhibit dramatically promoted electrochemical activity and high stability. The as-grown MoS(2) nanoflakes hybridized on exfoliated MoS(2) and WS(2) generate abundant active edge sites (rich in basal defects) and unsaturated sulfur atoms, resulting in highly enhanced electrocatalytic performance. This is expected to pave the way towards a significant improvement in transition metal dichalcogenide heterostructures as electrocatalysts.
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spelling pubmed-90653902022-05-04 Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution Gao, Guanhui Xie, Xiaobin Kang, Shendong Lei, Yanhua Trampert, Achim Cai, Lintao RSC Adv Chemistry It is essential to precisely develop low-cost and sustainable electrocatalysts for the hydrogen evolution reaction. Herein, we explore a robust and controllable hydrothermal approach to synthesize defect-rich MoS(2) nanoflakes on exfoliated MoS(2) and WS(2). Such well-designed hetero-structural hybrids of MoS(2)/exfoliated MoS(2) and MoS(2)/exfoliated WS(2) exhibit dramatically promoted electrochemical activity and high stability. The as-grown MoS(2) nanoflakes hybridized on exfoliated MoS(2) and WS(2) generate abundant active edge sites (rich in basal defects) and unsaturated sulfur atoms, resulting in highly enhanced electrocatalytic performance. This is expected to pave the way towards a significant improvement in transition metal dichalcogenide heterostructures as electrocatalysts. The Royal Society of Chemistry 2019-06-25 /pmc/articles/PMC9065390/ /pubmed/35514720 http://dx.doi.org/10.1039/c9ra02673h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Gao, Guanhui
Xie, Xiaobin
Kang, Shendong
Lei, Yanhua
Trampert, Achim
Cai, Lintao
Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title_full Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title_fullStr Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title_full_unstemmed Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title_short Toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
title_sort toward heterostructured transition metal hybrids with highly promoted electrochemical hydrogen evolution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065390/
https://www.ncbi.nlm.nih.gov/pubmed/35514720
http://dx.doi.org/10.1039/c9ra02673h
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