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Strong metal-support interactions between palladium and iron oxide and their effect on CO oxidation

MPS-Authors
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Naumann d'Alnoncourt,  Raoul
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Friedrich,  Matthias
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Kunkes,  Edward L.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Rosenthal,  Dirk
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Zhang,  Bing Sen
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Shao,  Lidong
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
College of Environmental and Chemical Engineering, Shanghai University of Electric Power;

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Schuster,  Manfred Erwin
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21347

Behrens,  Malte
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Universität Duisburg-Essen, Fakultät für Chemie;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Naumann d'Alnoncourt, R., Friedrich, M., Kunkes, E. L., Rosenthal, D., Girgsdies, F., Zhang, B. S., et al. (2014). Strong metal-support interactions between palladium and iron oxide and their effect on CO oxidation. Journal of Catalysis, 317, 220-228. doi:10.1016/j.jcat.2014.06.019.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0019-E447-A
Abstract
Pd/FeOx catalysts were prepared by co-precipitation and characterized before and after reduction using X-ray powder diffraction, thermal analysis, CO chemisorption, electron microscopy, and X-ray photoelectron spectroscopy.
Results give evidence for the encapsulation of palladium particles by iron oxide after reduction at high temperatures (523 K). Oxidation of carbon monoxide was applied as test reaction to characterize catalyst samples in different
states. Strong metal-–support interactions significantly enhance catalytic activity for oxidation of carbon monoxide. However, this state is not stable under the applied reaction conditions. Catalyst deactivation occurs in two ways: (1)
via changes in the oxidation state of iron species and (2) due to sintering of palladium particles