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Catalysis Letters

, Volume 125, Issue 1–2, pp 160–167 | Cite as

Structure-activity Relation of Fe2O3–CeO2 Composite Catalysts in CO Oxidation

  • Huizhi Bao
  • Xin Chen
  • Jun Fang
  • Zhiquan Jiang
  • Weixin HuangEmail author
Article
First Online:

Abstract

A series of Fe2O3–CeO2 composite catalysts were synthesized by coprecipitation and characterized by X-ray diffraction (XRD), BET surface area measurement, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). Their catalytic activities in CO oxidation were also tested. The Fe2O3–CeO2 composites with an Fe molar percentage below 0.3 form solid solutions with the CeO2 cubic fluorite structure, in which the doped Fe3+ initially substitutes Ce4+ in fluorite cubic CeO2, but then mostly locate in the interstitial sites after a critical concentration of doped Fe3+. With an Fe molar percentage between 0.3 and 0.95, the Fe2O3–CeO2 composites are mixed oxides of the cubic fluorite CeO2 solid solution and the hematite Fe2O3. XPS results indicate that CeO2 is enriched in the surface region of Fe2O3–CeO2 composites. The Fe2O3–CeO2 composites have much higher catalytic activities in CO oxidation than the individual pure CeO2 and Fe2O3, and the Fe0.1Ce0.9 composite shows the best catalytic performance. The structure-activity relation of the Fe2O3–CeO2 composites in CO oxidation is discussed in terms of the formation of solid solution and surface oxygen vacancies. Our results demonstrate a proportional relation between the catalytic activity of cubic CeO2-like solid solutions and their density of oxygen vacancies, which directly proves the formation of oxygen vacancies as the key step in CO oxidation over oxide catalysts.

Keywords

Structure-activity relation CeO2 Fe2O3 Oxide solid solution CO oxidation 
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Notes

Acknowledgments

This work was financially supported by National Natural Science Foundation of China (grant 20503027), the “Hundred Talent Program” of Chinese Academy of Sciences, the MOE program for PCSIRT (IRT0756), and the MPG-CAS partner group.

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Copyright information

© Springer Science+Business Media, LLC 2008

Authors and Affiliations

  • Huizhi Bao
    • 1
  • Xin Chen
    • 1
  • Jun Fang
    • 1
  • Zhiquan Jiang
    • 1
  • Weixin Huang
    • 1
    Email author
  1. 1.Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemical PhysicsUniversity of Science and Technology of ChinaHefeiChina

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