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C: Surfaces, Interfaces, Porous Materials, and Catalysis
Effect of Structural Evolution of Gold Species Supported on Ceria in Catalyzing CO Oxidation Xiu-Ling Wang, Xin-Pu Fu, Wei-Wei Wang, Chao Ma, Rui Si, and Chun-Jiang Jia J. Phys. Chem. C, Just Accepted Manuscript • DOI: 10.1021/acs.jpcc.9b00096 • Publication Date (Web): 13 Mar 2019 Downloaded from http://pubs.acs.org on March 13, 2019
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The Journal of Physical Chemistry
Effect of Structural Evolution of Gold Species Supported on Ceria in Catalyzing CO Oxidation Xiu-Ling Wang1, Xin-Pu Fu1, Wei-Wei Wang1, Chao Ma3,*, Rui Si2,*, Chun-Jiang Jia1,* 1
Key Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated
Materials, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, People’s Republic of China. 2
Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese
Academy of Sciences, Shanghai 201204, People’s Republic of China. 3
College of Materials Science and Engineering, Hunan University, Changsha 410082, People’s
Republic of China. * Corresponding author:
[email protected];
[email protected];
[email protected] ACS Paragon Plus Environment
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ABSTRACT: The intrinsic reactivity of atomically dispersed gold catalysts for low-temperature (L-T) CO oxidation remains an elusive issue. Here two kinds of atomically dispersed gold with different loadings supported on nano-ceria prepared via a deposition precipitation (DP) method were evaluated as catalysts for L-T CO oxidation. Much distinct differences in catalyzing CO oxidation behaviors were exhibited on the two kinds of gold catalysts. These weakly anchored gold species in 1% Au/CeO2 (1 wt% gold loading) catalyst revealed increasing reactivity under the reaction condition, while these strongly anchored ones in 0.5% Au/CeO2 (0.5 wt% gold loading) catalyst were inactive. For 1% Au/CeO2 catalyst, in-situ diffuse reflectance infrared spectroscopy (DRIFTS) proved the gold species transformation from Aun+ (1 ≤ n < 3) to Auδ+ (0 < δ
