Abstract

Surface-supported isolated atoms in single-atom catalysts (SACs) are usually stabilized by diverse defects. The fabrication of high-metal-loading and thermally stable SACs remains a formidable challenge due to the difficulty of creating high densities of underpinning stable defects. Here we report that isolated Pt atoms can be stabilized through a strong covalent metal-support interaction (CMSI) that is not associated with support defects, yielding a high-loading and thermally stable SAC by trapping either the already deposited Pt atoms or the PtO2 units vaporized from nanoparticles during high-temperature calcination. Experimental and computational modeling studies reveal that iron oxide reducibility is crucial to anchor isolated Pt atoms. The resulting high concentrations of single atoms enable specific activities far exceeding those of conventional nanoparticle catalysts. This non defect-stabilization strategy can be extended to non-reducible supports by simply doping with iron oxide, thus paving a new way for constructing high-loading SACs for diverse industrially important catalytic reactions.

Developing stable single-atom catalysts (SACs) with a high metal loading remains a challenge due to the difficulty of creating high densities of defects on support materials. Here the authors prepare Pt SACs with high Pt loadings by virtue of strong covalent metal-support interaction, rather than support defects.

Details

Title
Non defect-stabilized thermally stable single-atom catalyst
Author
Lang, Rui 1 ; Wei, Xi 2 ; Jin-Cheng, Liu 3   VIAFID ORCID Logo  ; Yi-Tao, Cui 4   VIAFID ORCID Logo  ; Li, Tianbo 5 ; Lee Adam Fraser 6   VIAFID ORCID Logo  ; Chen, Fang 1 ; Chen, Yang 5 ; Li, Lei 7 ; Li, Lin 1 ; Lin, Jian 1 ; Miao Shu 1 ; Liu, Xiaoyan 1 ; Ai-Qin, Wang 1 ; Wang, Xiaodong 1 ; Luo, Jun 2 ; Qiao Botao 8   VIAFID ORCID Logo  ; Li, Jun 9 ; Zhang, Tao 1 

 Dalian Institute of Chemical Physics, Chinese Academy of Sciences, State Key Laboratory of Catalysis, Dalian, China (GRID:grid.423905.9) (ISNI:0000 0004 1793 300X) 
 Tianjin University of Technology, Center for Electron Microscopy and Tianjin Key Lab of Advanced Functional Porous Materials, Institute for New Energy Materials, School of Materials, Tianjin, China (GRID:grid.265025.6) 
 Tsinghua University, Department of Chemistry & Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education, Beijing, China (GRID:grid.12527.33) (ISNI:0000 0001 0662 3178) 
 The University of Tokyo, Synchrotron Radiation Laboratory, Laser and Synchrotron Research Center (LASOR), The Institute for Solid State Physics, Hyogo, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X) 
 Dalian Institute of Chemical Physics, Chinese Academy of Sciences, State Key Laboratory of Catalysis, Dalian, China (GRID:grid.423905.9) (ISNI:0000 0004 1793 300X) ; University of Chinese Academy of Sciences, Beijing, China (GRID:grid.410726.6) (ISNI:0000 0004 1797 8419) 
 Royal Melbourne Institute of Technology University, School of Science, Melbourne, Australia (GRID:grid.1017.7) (ISNI:0000 0001 2163 3550) 
 Synchrotron Radiation Nanotechnology Center, University of Hyogo, Hyogo, Japan (GRID:grid.410726.6) 
 Dalian Institute of Chemical Physics, Chinese Academy of Sciences, State Key Laboratory of Catalysis, Dalian, China (GRID:grid.423905.9) (ISNI:0000 0004 1793 300X) ; Dalian National Laboratory for Clean Energy, Dalian, China (GRID:grid.410752.5) 
 Tsinghua University, Department of Chemistry & Key Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education, Beijing, China (GRID:grid.12527.33) (ISNI:0000 0001 0662 3178) ; Southern University of Science and Technology, Department of Chemistry, Shenzhen, China (GRID:grid.12527.33) 
Publication year
2019
Publication date
Jan 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1920305243
Copyright
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.