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The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring

Single-site catalysts feature high catalytic activity but their facile construction and durable utilization are highly challenging. Herein, we report a simple impregnation-adsorption method to construct platinum single-site catalysts by synergic micropore trapping and nitrogen anchoring on hierarchi...

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Autores principales: Zhang, Zhiqi, Chen, Yugang, Zhou, Liqi, Chen, Chi, Han, Zhen, Zhang, Bingsen, Wu, Qiang, Yang, Lijun, Du, Lingyu, Bu, Yongfeng, Wang, Peng, Wang, Xizhang, Yang, Hui, Hu, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458126/
https://www.ncbi.nlm.nih.gov/pubmed/30971769
http://dx.doi.org/10.1038/s41467-019-09596-x
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author Zhang, Zhiqi
Chen, Yugang
Zhou, Liqi
Chen, Chi
Han, Zhen
Zhang, Bingsen
Wu, Qiang
Yang, Lijun
Du, Lingyu
Bu, Yongfeng
Wang, Peng
Wang, Xizhang
Yang, Hui
Hu, Zheng
author_facet Zhang, Zhiqi
Chen, Yugang
Zhou, Liqi
Chen, Chi
Han, Zhen
Zhang, Bingsen
Wu, Qiang
Yang, Lijun
Du, Lingyu
Bu, Yongfeng
Wang, Peng
Wang, Xizhang
Yang, Hui
Hu, Zheng
author_sort Zhang, Zhiqi
collection PubMed
description Single-site catalysts feature high catalytic activity but their facile construction and durable utilization are highly challenging. Herein, we report a simple impregnation-adsorption method to construct platinum single-site catalysts by synergic micropore trapping and nitrogen anchoring on hierarchical nitrogen-doped carbon nanocages. The optimal catalyst exhibits a record-high electrocatalytic hydrogen evolution performance with low overpotential, high mass activity and long stability, much superior to the platinum-based catalysts to date. Theoretical simulations and experiments reveal that the micropores with edge-nitrogen-dopants favor the formation of isolated platinum atoms by the micropore trapping and nitrogen anchoring of [PtCl(6)](2-), followed by the spontaneous dechlorination. The platinum-nitrogen bonds are more stable than the platinum-carbon ones in the presence of adsorbed hydrogen atoms, leading to the superior hydrogen evolution stability of platinum single-atoms on nitrogen-doped carbon. This method has been successfully applied to construct the single-site catalysts of other precious metals such as palladium, gold and iridium.
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spelling pubmed-64581262019-04-12 The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring Zhang, Zhiqi Chen, Yugang Zhou, Liqi Chen, Chi Han, Zhen Zhang, Bingsen Wu, Qiang Yang, Lijun Du, Lingyu Bu, Yongfeng Wang, Peng Wang, Xizhang Yang, Hui Hu, Zheng Nat Commun Article Single-site catalysts feature high catalytic activity but their facile construction and durable utilization are highly challenging. Herein, we report a simple impregnation-adsorption method to construct platinum single-site catalysts by synergic micropore trapping and nitrogen anchoring on hierarchical nitrogen-doped carbon nanocages. The optimal catalyst exhibits a record-high electrocatalytic hydrogen evolution performance with low overpotential, high mass activity and long stability, much superior to the platinum-based catalysts to date. Theoretical simulations and experiments reveal that the micropores with edge-nitrogen-dopants favor the formation of isolated platinum atoms by the micropore trapping and nitrogen anchoring of [PtCl(6)](2-), followed by the spontaneous dechlorination. The platinum-nitrogen bonds are more stable than the platinum-carbon ones in the presence of adsorbed hydrogen atoms, leading to the superior hydrogen evolution stability of platinum single-atoms on nitrogen-doped carbon. This method has been successfully applied to construct the single-site catalysts of other precious metals such as palladium, gold and iridium. Nature Publishing Group UK 2019-04-10 /pmc/articles/PMC6458126/ /pubmed/30971769 http://dx.doi.org/10.1038/s41467-019-09596-x Text en © The Author(s) 2019 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
Zhang, Zhiqi
Chen, Yugang
Zhou, Liqi
Chen, Chi
Han, Zhen
Zhang, Bingsen
Wu, Qiang
Yang, Lijun
Du, Lingyu
Bu, Yongfeng
Wang, Peng
Wang, Xizhang
Yang, Hui
Hu, Zheng
The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title_full The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title_fullStr The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title_full_unstemmed The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title_short The simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
title_sort simplest construction of single-site catalysts by the synergism of micropore trapping and nitrogen anchoring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458126/
https://www.ncbi.nlm.nih.gov/pubmed/30971769
http://dx.doi.org/10.1038/s41467-019-09596-x
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