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Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports
Single-atom catalysts (SACs) have attracted considerable attention in the catalysis community. However, fabricating intrinsically stable SACs on traditional supports (N-doped carbon, metal oxides, etc.) remains a formidable challenge, especially under high-temperature conditions. Here, we report a n...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413391/ https://www.ncbi.nlm.nih.gov/pubmed/32764539 http://dx.doi.org/10.1038/s41467-020-17738-9 |
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author | Xu, Haidi Zhang, Zihao Liu, Jixing Do-Thanh, Chi-Linh Chen, Hao Xu, Shuhao Lin, Qinjing Jiao, Yi Wang, Jianli Wang, Yun Chen, Yaoqiang Dai, Sheng |
author_facet | Xu, Haidi Zhang, Zihao Liu, Jixing Do-Thanh, Chi-Linh Chen, Hao Xu, Shuhao Lin, Qinjing Jiao, Yi Wang, Jianli Wang, Yun Chen, Yaoqiang Dai, Sheng |
author_sort | Xu, Haidi |
collection | PubMed |
description | Single-atom catalysts (SACs) have attracted considerable attention in the catalysis community. However, fabricating intrinsically stable SACs on traditional supports (N-doped carbon, metal oxides, etc.) remains a formidable challenge, especially under high-temperature conditions. Here, we report a novel entropy-driven strategy to stabilize Pd single-atom on the high-entropy fluorite oxides (CeZrHfTiLa)O(x) (HEFO) as the support by a combination of mechanical milling with calcination at 900 °C. Characterization results reveal that single Pd atoms are incorporated into HEFO (Pd(1)@HEFO) sublattice by forming stable Pd–O–M bonds (M = Ce/Zr/La). Compared to the traditional support stabilized catalysts such as Pd@CeO(2), Pd(1)@HEFO affords the improved reducibility of lattice oxygen and the existence of stable Pd–O–M species, thus exhibiting not only higher low-temperature CO oxidation activity but also outstanding resistance to thermal and hydrothermal degradation. This work therefore exemplifies the superiority of high-entropy materials for the preparation of SACs. |
format | Online Article Text |
id | pubmed-7413391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74133912020-08-17 Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports Xu, Haidi Zhang, Zihao Liu, Jixing Do-Thanh, Chi-Linh Chen, Hao Xu, Shuhao Lin, Qinjing Jiao, Yi Wang, Jianli Wang, Yun Chen, Yaoqiang Dai, Sheng Nat Commun Article Single-atom catalysts (SACs) have attracted considerable attention in the catalysis community. However, fabricating intrinsically stable SACs on traditional supports (N-doped carbon, metal oxides, etc.) remains a formidable challenge, especially under high-temperature conditions. Here, we report a novel entropy-driven strategy to stabilize Pd single-atom on the high-entropy fluorite oxides (CeZrHfTiLa)O(x) (HEFO) as the support by a combination of mechanical milling with calcination at 900 °C. Characterization results reveal that single Pd atoms are incorporated into HEFO (Pd(1)@HEFO) sublattice by forming stable Pd–O–M bonds (M = Ce/Zr/La). Compared to the traditional support stabilized catalysts such as Pd@CeO(2), Pd(1)@HEFO affords the improved reducibility of lattice oxygen and the existence of stable Pd–O–M species, thus exhibiting not only higher low-temperature CO oxidation activity but also outstanding resistance to thermal and hydrothermal degradation. This work therefore exemplifies the superiority of high-entropy materials for the preparation of SACs. Nature Publishing Group UK 2020-08-06 /pmc/articles/PMC7413391/ /pubmed/32764539 http://dx.doi.org/10.1038/s41467-020-17738-9 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 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 Xu, Haidi Zhang, Zihao Liu, Jixing Do-Thanh, Chi-Linh Chen, Hao Xu, Shuhao Lin, Qinjing Jiao, Yi Wang, Jianli Wang, Yun Chen, Yaoqiang Dai, Sheng Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title | Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title_full | Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title_fullStr | Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title_full_unstemmed | Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title_short | Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports |
title_sort | entropy-stabilized single-atom pd catalysts via high-entropy fluorite oxide supports |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413391/ https://www.ncbi.nlm.nih.gov/pubmed/32764539 http://dx.doi.org/10.1038/s41467-020-17738-9 |
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