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Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis
Development of cost-effective electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is key to enabling advanced electrochemical energy conversion technologies. Here, a novel nitrogen-doped metal-carbon hybrid (NiCo/CN) with a unique 3D hierarchical structure, consi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856206/ https://www.ncbi.nlm.nih.gov/pubmed/31788468 http://dx.doi.org/10.3389/fchem.2019.00747 |
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author | Zhou, Yu Zhang, Yan Xu, Xianzhen Zhao, Shenlong Guo, Ziyi Wu, Kuang-Hsu Tan, Chunhui Wang, Zonghua |
author_facet | Zhou, Yu Zhang, Yan Xu, Xianzhen Zhao, Shenlong Guo, Ziyi Wu, Kuang-Hsu Tan, Chunhui Wang, Zonghua |
author_sort | Zhou, Yu |
collection | PubMed |
description | Development of cost-effective electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is key to enabling advanced electrochemical energy conversion technologies. Here, a novel nitrogen-doped metal-carbon hybrid (NiCo/CN) with a unique 3D hierarchical structure, consisting of uniformly distributed bimetallic nanoparticles encapsulated by partially graphitized N-doped carbon shells, is fabricated by a one-step pyrolysis of a nanoscale metal-organic framework as precursor, which exhibits excellent activity for both ORR and OER. The surface chemical changes on the carbon hybrid probed by X-ray photoelectron spectroscopy (XPS) reveal the presence of favorable electronic interaction at the metal-nitrogen-carbon interface. Remarkably, the NiCo/CN catalyst prepared at high temperature (800°C) manifests a comparable performance to a commercial Pt/C catalyst for the ORR, but also superior stability, path selectivity and methanol tolerance. On the other hand, the E(onset) (1.48 V vs. reversible hydrogen electrode) and [Formula: see text] of NiCo/CN-800 for OER is very close to the state-of-the-art noble catalyst RuO(2) (E(onset) = 1.46 and [Formula: see text]) along with superior stability over 20 h of operation. The excellent catalytic property is attributable to the unique nanostructure, high porosity and the constructive synergistic effects of the elements M, N, and C. |
format | Online Article Text |
id | pubmed-6856206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68562062019-11-29 Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis Zhou, Yu Zhang, Yan Xu, Xianzhen Zhao, Shenlong Guo, Ziyi Wu, Kuang-Hsu Tan, Chunhui Wang, Zonghua Front Chem Chemistry Development of cost-effective electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is key to enabling advanced electrochemical energy conversion technologies. Here, a novel nitrogen-doped metal-carbon hybrid (NiCo/CN) with a unique 3D hierarchical structure, consisting of uniformly distributed bimetallic nanoparticles encapsulated by partially graphitized N-doped carbon shells, is fabricated by a one-step pyrolysis of a nanoscale metal-organic framework as precursor, which exhibits excellent activity for both ORR and OER. The surface chemical changes on the carbon hybrid probed by X-ray photoelectron spectroscopy (XPS) reveal the presence of favorable electronic interaction at the metal-nitrogen-carbon interface. Remarkably, the NiCo/CN catalyst prepared at high temperature (800°C) manifests a comparable performance to a commercial Pt/C catalyst for the ORR, but also superior stability, path selectivity and methanol tolerance. On the other hand, the E(onset) (1.48 V vs. reversible hydrogen electrode) and [Formula: see text] of NiCo/CN-800 for OER is very close to the state-of-the-art noble catalyst RuO(2) (E(onset) = 1.46 and [Formula: see text]) along with superior stability over 20 h of operation. The excellent catalytic property is attributable to the unique nanostructure, high porosity and the constructive synergistic effects of the elements M, N, and C. Frontiers Media S.A. 2019-11-08 /pmc/articles/PMC6856206/ /pubmed/31788468 http://dx.doi.org/10.3389/fchem.2019.00747 Text en Copyright © 2019 Zhou, Zhang, Xu, Zhao, Guo, Wu, Tan and Wang. 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 Zhou, Yu Zhang, Yan Xu, Xianzhen Zhao, Shenlong Guo, Ziyi Wu, Kuang-Hsu Tan, Chunhui Wang, Zonghua Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title | Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title_full | Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title_fullStr | Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title_full_unstemmed | Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title_short | Bimetallic Metal-Organic Framework Derived Metal-Carbon Hybrid for Efficient Reversible Oxygen Electrocatalysis |
title_sort | bimetallic metal-organic framework derived metal-carbon hybrid for efficient reversible oxygen electrocatalysis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856206/ https://www.ncbi.nlm.nih.gov/pubmed/31788468 http://dx.doi.org/10.3389/fchem.2019.00747 |
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