4.8 Article

Shape-dependent interplay between oxygen vacancies and Ag-CeO2 interaction in Ag/CeO2 catalysts and their influence on the catalytic activity

Journal

JOURNAL OF CATALYSIS
Volume 293, Issue -, Pages 195-204

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2012.06.025

Keywords

Ag/CeO2 catalysts; CO oxidation; Active structure; Metal-support interaction; Oxygen vacancy; Shape dependence

Funding

  1. National Natural Science Foundation of China [21173204, J1030412]
  2. National Basic Research Program of China
  3. Fundamental Research Funds for the Central Universities
  4. MPG-CAS partner group program

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Ag/CeO2 catalysts employing CeO2 nanocubes (c-CeO2) and nanorods (r-CeO2) as the support were prepared by conventional incipient wetness impregnation followed by calcination at 500 degrees C in air. Their structures have been characterized in detail and their catalytic activities in CO oxidation have also been tested. c-CeO2 and r-CeO2 nanocrystals exhibit different concentrations and structures of oxygen vacancies. The silver-r-CeO2 interaction is stronger than the silver-c-CeO2 interaction. Fine Ag nanoparticles form in 1%-Ag/c-CeO2 and grow in size in 3%-Ag/c-CeO2; however, positively charged Ag-n(+) clusters dominate in 1%-Ag/r-CeO2, and fine Ag nanoparticles dominate in 3%-Ag/r-CeO2. Supported Ag nanoparticles are much more capable of creating oxygen vacancies in CeO2 than supported positively charged Ag-n(+) clusters. More oxygen vacancies form in Ag/c-CeO2 than in Ag/r-CeO2. The average charge density of oxygen vacancies and the ratio between large oxygen vacancy clusters and small vacancies in CeO2 nanocrystals are enhanced when loaded with positively charged Ag-n(+) clusters but reduced when loaded with Ag nanoparticles. Ag nanoparticles greatly promote the reduction and catalytic activity in CO oxidation of CeO2 nanocrystals but positively charged Ag-n(+) clusters do not. These results demonstrate the concept that the interplay between oxygen vacancies and Ag-CeO2 interaction controls the structures of silver and CeO2 in Ag/CeO2 catalysts and thus their surface reactivity and catalytic activity, deepening the fundamental understanding of metal/CeO2 catalysts. These results also reveal that the interplay between oxygen vacancies and Ag-CeO2 interaction in Ag/CeO2 catalysts depends on the shape of CeO2 support, opening up a new strategy for the design of efficient and economic metal/CeO2 catalysts by engineering the shape of CeO2 support. (C) 2012 Elsevier Inc. All rights reserved.

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