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Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules
It is desirable to design nonprecious metal nanocatalysts with high stability and catalytic performance for fine chemicals production. Here, a method is reported for the preparation of cobalt metal and cobalt oxide cores confined within nanoporous nitrogen‐doped hollow carbon capsules. Core–shell st...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865004/ https://www.ncbi.nlm.nih.gov/pubmed/31763134 http://dx.doi.org/10.1002/advs.201900807 |
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author | Tian, Hao Liu, Xiaoyan Dong, Liubing Ren, Xiaomin Liu, Hao Price, Cameron Alexander Hurd Li, Ying Wang, Guoxiu Yang, Qihua Liu, Jian |
author_facet | Tian, Hao Liu, Xiaoyan Dong, Liubing Ren, Xiaomin Liu, Hao Price, Cameron Alexander Hurd Li, Ying Wang, Guoxiu Yang, Qihua Liu, Jian |
author_sort | Tian, Hao |
collection | PubMed |
description | It is desirable to design nonprecious metal nanocatalysts with high stability and catalytic performance for fine chemicals production. Here, a method is reported for the preparation of cobalt metal and cobalt oxide cores confined within nanoporous nitrogen‐doped hollow carbon capsules. Core–shell structured Zn/Co‐ZIF@polymer materials are fabricated through a facile coating polymer strategy on the surface of zeolitic imidazolate frameworks (ZIF). A series of hollow carbon capsules with cobalt metal and cobalt oxide are derived from a facile confined pyrolysis of Zn/Co‐ZIF@polymer. The hollow Co‐CoOx@N‐C capsules can prevent sintering and agglomeration of the cobalt nanoparticles and the nanoporous shell allows for efficient mass transport. The specific surface area and Co particle size are optimized through finely tuning the original Zn content in ZIF particles, thus enhancing overall catalytic activity. The yolk–shell structured Zn(4)Co(1)O(x)@carbon hollow capsules are shown to be a highly active and selective catalyst (selectivity >99%) for hydrogenation of nitrobenzene to aniline. Furthermore, Zn(4)Co(1)O(x)@carbon hollow particles show superior catalytic stability, and no deactivation after 8 cycles of reaction. The hollow Co‐CoOx@N‐C capsules may shed light on a green and sustainable catalytic process for fine chemicals production. |
format | Online Article Text |
id | pubmed-6865004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68650042019-11-22 Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules Tian, Hao Liu, Xiaoyan Dong, Liubing Ren, Xiaomin Liu, Hao Price, Cameron Alexander Hurd Li, Ying Wang, Guoxiu Yang, Qihua Liu, Jian Adv Sci (Weinh) Full Papers It is desirable to design nonprecious metal nanocatalysts with high stability and catalytic performance for fine chemicals production. Here, a method is reported for the preparation of cobalt metal and cobalt oxide cores confined within nanoporous nitrogen‐doped hollow carbon capsules. Core–shell structured Zn/Co‐ZIF@polymer materials are fabricated through a facile coating polymer strategy on the surface of zeolitic imidazolate frameworks (ZIF). A series of hollow carbon capsules with cobalt metal and cobalt oxide are derived from a facile confined pyrolysis of Zn/Co‐ZIF@polymer. The hollow Co‐CoOx@N‐C capsules can prevent sintering and agglomeration of the cobalt nanoparticles and the nanoporous shell allows for efficient mass transport. The specific surface area and Co particle size are optimized through finely tuning the original Zn content in ZIF particles, thus enhancing overall catalytic activity. The yolk–shell structured Zn(4)Co(1)O(x)@carbon hollow capsules are shown to be a highly active and selective catalyst (selectivity >99%) for hydrogenation of nitrobenzene to aniline. Furthermore, Zn(4)Co(1)O(x)@carbon hollow particles show superior catalytic stability, and no deactivation after 8 cycles of reaction. The hollow Co‐CoOx@N‐C capsules may shed light on a green and sustainable catalytic process for fine chemicals production. John Wiley and Sons Inc. 2019-09-03 /pmc/articles/PMC6865004/ /pubmed/31763134 http://dx.doi.org/10.1002/advs.201900807 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Tian, Hao Liu, Xiaoyan Dong, Liubing Ren, Xiaomin Liu, Hao Price, Cameron Alexander Hurd Li, Ying Wang, Guoxiu Yang, Qihua Liu, Jian Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title | Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title_full | Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title_fullStr | Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title_full_unstemmed | Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title_short | Enhanced Hydrogenation Performance over Hollow Structured Co‐CoOx@N‐C Capsules |
title_sort | enhanced hydrogenation performance over hollow structured co‐coox@n‐c capsules |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865004/ https://www.ncbi.nlm.nih.gov/pubmed/31763134 http://dx.doi.org/10.1002/advs.201900807 |
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