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Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports

The design and synthesis of robust sintering-resistant nanocatalysts for high-temperature oxidation reactions is ubiquitous in many industrial catalytic processes and still a big challenge in implementing nanostructured metal catalyst systems. Herein, we demonstrate a strategy for designing robust n...

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Autores principales: Yang, Xinwei, Li, Qing, Lu, Erjun, Wang, Zhiqiang, Gong, Xueqing, Yu, Zhiyang, Guo, Yun, Wang, Li, Guo, Yanglong, Zhan, Wangcheng, Zhang, Jinshui, Dai, Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453908/
https://www.ncbi.nlm.nih.gov/pubmed/30962455
http://dx.doi.org/10.1038/s41467-019-09662-4
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author Yang, Xinwei
Li, Qing
Lu, Erjun
Wang, Zhiqiang
Gong, Xueqing
Yu, Zhiyang
Guo, Yun
Wang, Li
Guo, Yanglong
Zhan, Wangcheng
Zhang, Jinshui
Dai, Sheng
author_facet Yang, Xinwei
Li, Qing
Lu, Erjun
Wang, Zhiqiang
Gong, Xueqing
Yu, Zhiyang
Guo, Yun
Wang, Li
Guo, Yanglong
Zhan, Wangcheng
Zhang, Jinshui
Dai, Sheng
author_sort Yang, Xinwei
collection PubMed
description The design and synthesis of robust sintering-resistant nanocatalysts for high-temperature oxidation reactions is ubiquitous in many industrial catalytic processes and still a big challenge in implementing nanostructured metal catalyst systems. Herein, we demonstrate a strategy for designing robust nanocatalysts through a sintering-resistant support via compartmentalization. Ultrafine palladium active phases can be highly dispersed and thermally stabilized by nanosheet-assembled γ-Al(2)O(3) (NA-Al(2)O(3)) architectures. The NA-Al(2)O(3) architectures with unique flowerlike morphologies not only efficiently suppress the lamellar aggregation and irreversible phase transformation of γ-Al(2)O(3) nanosheets at elevated temperatures to avoid the sintering and encapsulation of metal phases, but also exhibit significant structural advantages for heterogeneous reactions, such as fast mass transport and easy access to active sites. This is a facile stabilization strategy that can be further extended to improve the thermal stability of other Al(2)O(3)-supported nanocatalysts for industrial catalytic applications, in particular for those involving high-temperature reactions.
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spelling pubmed-64539082019-04-10 Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports Yang, Xinwei Li, Qing Lu, Erjun Wang, Zhiqiang Gong, Xueqing Yu, Zhiyang Guo, Yun Wang, Li Guo, Yanglong Zhan, Wangcheng Zhang, Jinshui Dai, Sheng Nat Commun Article The design and synthesis of robust sintering-resistant nanocatalysts for high-temperature oxidation reactions is ubiquitous in many industrial catalytic processes and still a big challenge in implementing nanostructured metal catalyst systems. Herein, we demonstrate a strategy for designing robust nanocatalysts through a sintering-resistant support via compartmentalization. Ultrafine palladium active phases can be highly dispersed and thermally stabilized by nanosheet-assembled γ-Al(2)O(3) (NA-Al(2)O(3)) architectures. The NA-Al(2)O(3) architectures with unique flowerlike morphologies not only efficiently suppress the lamellar aggregation and irreversible phase transformation of γ-Al(2)O(3) nanosheets at elevated temperatures to avoid the sintering and encapsulation of metal phases, but also exhibit significant structural advantages for heterogeneous reactions, such as fast mass transport and easy access to active sites. This is a facile stabilization strategy that can be further extended to improve the thermal stability of other Al(2)O(3)-supported nanocatalysts for industrial catalytic applications, in particular for those involving high-temperature reactions. Nature Publishing Group UK 2019-04-08 /pmc/articles/PMC6453908/ /pubmed/30962455 http://dx.doi.org/10.1038/s41467-019-09662-4 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
Yang, Xinwei
Li, Qing
Lu, Erjun
Wang, Zhiqiang
Gong, Xueqing
Yu, Zhiyang
Guo, Yun
Wang, Li
Guo, Yanglong
Zhan, Wangcheng
Zhang, Jinshui
Dai, Sheng
Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title_full Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title_fullStr Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title_full_unstemmed Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title_short Taming the stability of Pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
title_sort taming the stability of pd active phases through a compartmentalizing strategy toward nanostructured catalyst supports
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453908/
https://www.ncbi.nlm.nih.gov/pubmed/30962455
http://dx.doi.org/10.1038/s41467-019-09662-4
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