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Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting

It is extremely meaningful to develop cheap, highly efficient, and stable bifunctional electrocatalysts for both hydrogen and oxygen evolution reactions (HER and OER) to promote large-scale application of water splitting technology. Herein, we reported the preparation of CoS(2) nanoparticles support...

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Autores principales: Zhang, Wei, Ma, Xiaoya, Zhong, Cheng, Ma, Tianyi, Deng, Yida, Hu, Wenbin, Han, Xiaopeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258795/
https://www.ncbi.nlm.nih.gov/pubmed/30519558
http://dx.doi.org/10.3389/fchem.2018.00569
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author Zhang, Wei
Ma, Xiaoya
Zhong, Cheng
Ma, Tianyi
Deng, Yida
Hu, Wenbin
Han, Xiaopeng
author_facet Zhang, Wei
Ma, Xiaoya
Zhong, Cheng
Ma, Tianyi
Deng, Yida
Hu, Wenbin
Han, Xiaopeng
author_sort Zhang, Wei
collection PubMed
description It is extremely meaningful to develop cheap, highly efficient, and stable bifunctional electrocatalysts for both hydrogen and oxygen evolution reactions (HER and OER) to promote large-scale application of water splitting technology. Herein, we reported the preparation of CoS(2) nanoparticles supported on nitrogen-doped graphene (CoS(2)@N-GN) by one-step hydrothermal method and the enhanced electrochemical efficacy for catalyzing hydrogen and oxygen in water electrolysis. The CoS(2)@N-GN composites are composed of nitrogen-doped graphene and CoS(2) nanocrystals with the average size of 73.5 nm. Benefitting from the improved electronic transfer and synergistic effect, the as-prepared CoS(2)@N-GN exhibits remarkable OER and HER performance in 1.0 M KOH, with overpotentials of 243 mV for OER and 204 mV for HER at 10 mA cm(−2), and the corresponding Tafel slopes of 51.8 and 108 mV dec(−1), respectively. Otherwise, the CoS(2)@N-GN hybrid also presents superior long-term catalytic durability. Moreover, an alkaline water splitting device assembled by CoS(2)@N-GN as both anode and cathode can achieve a low cell voltage of 1.53 V at 60 °C with a high faraday efficiency of 100% for overall water splitting. The tremendously enhanced electrochemical behaviors arise from favorable factors including small sized, homogenously dispersed novel CoS(2) nanocrystals and coupling interaction with the underlying conductive nitrogen-doped graphene, which would provide insight into the rational design of transition metal chalcogenides for highly efficient and durable hydrogen and oxygen-involved electrocatalysis.
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spelling pubmed-62587952018-12-05 Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting Zhang, Wei Ma, Xiaoya Zhong, Cheng Ma, Tianyi Deng, Yida Hu, Wenbin Han, Xiaopeng Front Chem Chemistry It is extremely meaningful to develop cheap, highly efficient, and stable bifunctional electrocatalysts for both hydrogen and oxygen evolution reactions (HER and OER) to promote large-scale application of water splitting technology. Herein, we reported the preparation of CoS(2) nanoparticles supported on nitrogen-doped graphene (CoS(2)@N-GN) by one-step hydrothermal method and the enhanced electrochemical efficacy for catalyzing hydrogen and oxygen in water electrolysis. The CoS(2)@N-GN composites are composed of nitrogen-doped graphene and CoS(2) nanocrystals with the average size of 73.5 nm. Benefitting from the improved electronic transfer and synergistic effect, the as-prepared CoS(2)@N-GN exhibits remarkable OER and HER performance in 1.0 M KOH, with overpotentials of 243 mV for OER and 204 mV for HER at 10 mA cm(−2), and the corresponding Tafel slopes of 51.8 and 108 mV dec(−1), respectively. Otherwise, the CoS(2)@N-GN hybrid also presents superior long-term catalytic durability. Moreover, an alkaline water splitting device assembled by CoS(2)@N-GN as both anode and cathode can achieve a low cell voltage of 1.53 V at 60 °C with a high faraday efficiency of 100% for overall water splitting. The tremendously enhanced electrochemical behaviors arise from favorable factors including small sized, homogenously dispersed novel CoS(2) nanocrystals and coupling interaction with the underlying conductive nitrogen-doped graphene, which would provide insight into the rational design of transition metal chalcogenides for highly efficient and durable hydrogen and oxygen-involved electrocatalysis. Frontiers Media S.A. 2018-11-21 /pmc/articles/PMC6258795/ /pubmed/30519558 http://dx.doi.org/10.3389/fchem.2018.00569 Text en Copyright © 2018 Zhang, Ma, Zhong, Ma, Deng, Hu and Han. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Zhang, Wei
Ma, Xiaoya
Zhong, Cheng
Ma, Tianyi
Deng, Yida
Hu, Wenbin
Han, Xiaopeng
Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title_full Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title_fullStr Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title_full_unstemmed Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title_short Pyrite-Type CoS(2) Nanoparticles Supported on Nitrogen-Doped Graphene for Enhanced Water Splitting
title_sort pyrite-type cos(2) nanoparticles supported on nitrogen-doped graphene for enhanced water splitting
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258795/
https://www.ncbi.nlm.nih.gov/pubmed/30519558
http://dx.doi.org/10.3389/fchem.2018.00569
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