Abstract

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)Ox (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 (Pd1@HEFO) sublattice by forming stable Pd–O–M bonds (M = Ce/Zr/La). Compared to the traditional support stabilized catalysts such as Pd@CeO2, Pd1@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.

Fabricating intrinsically stable single-atom catalysts (SACs) on traditional supports remains a formidable challenge in catalysis. Here, the authors propose a new strategy to construct a sintering-resistant Pd SAC on a novel equimolar high-entropy fluorite oxide.

Details

Title
Entropy-stabilized single-atom Pd catalysts via high-entropy fluorite oxide supports
Author
Xu, Haidi 1   VIAFID ORCID Logo  ; Zhang, Zihao 2 ; Liu Jixing 3 ; Do-Thanh Chi-Linh 3   VIAFID ORCID Logo  ; Chen, Hao 3 ; Xu Shuhao 4 ; Lin Qinjing 4 ; Jiao Yi 5 ; Wang, Jianli 4 ; Wang, Yun 6   VIAFID ORCID Logo  ; Chen Yaoqiang 7   VIAFID ORCID Logo  ; Dai Sheng 2   VIAFID ORCID Logo 

 Sichuan University, Institute of New Energy and Low-Carbon Technology, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581); Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, USA (GRID:grid.135519.a) (ISNI:0000 0004 0446 2659); University of Tennessee, Department of Chemistry, Joint Institute for Advanced Materials, Knoxville, USA (GRID:grid.411461.7) (ISNI:0000 0001 2315 1184) 
 Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, USA (GRID:grid.135519.a) (ISNI:0000 0004 0446 2659); University of Tennessee, Department of Chemistry, Joint Institute for Advanced Materials, Knoxville, USA (GRID:grid.411461.7) (ISNI:0000 0001 2315 1184) 
 University of Tennessee, Department of Chemistry, Joint Institute for Advanced Materials, Knoxville, USA (GRID:grid.411461.7) (ISNI:0000 0001 2315 1184) 
 Sichuan University, College of Chemistry, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581) 
 Sichuan University, Institute of New Energy and Low-Carbon Technology, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581) 
 Sinocat Environmental Technology Co. Ltd., Chengdu, China (GRID:grid.13291.38) 
 Sichuan University, Institute of New Energy and Low-Carbon Technology, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581); Sichuan University, College of Chemistry, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2430817739
Copyright
© This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.