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Operando XANES Reveals the Chemical State of Iron-Oxide Monolayers During Low-Temperature CO Oxidation
Malmö University, Faculty of Technology and Society (TS), Department of Materials Science and Applied Mathematics (MTM).ORCID iD: 0000-0003-1280-6821
Malmö University, Faculty of Technology and Society (TS), Department of Materials Science and Applied Mathematics (MTM).ORCID iD: 0000-0002-4691-1606
Chalmers University of Technology, Department of Chemical Physics, SWEDEN.
University of Oregon, Department of Chemistry and Biochemistry and the Oregon Center for Electrochemistry, UNITED STATES OF AMERICA.
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2025 (English)In: ChemPhysChem, ISSN 1439-4235, E-ISSN 1439-7641, Vol. 26, no 2, article id e202400835Article in journal (Refereed) Published
Abstract [en]

We have used grazing incidence X-ray absorption near edge spectroscopy (XANES) to investigate the behavior of monolayer FeOx films on Pt(111) under near ambient pressure CO oxidation conditions with a total gas pressure of 1 bar. Spectra indicate reversible changes during oxidation and reduction by O2 and CO at 150ºC, attributed to a transformation between FeO bilayer and FeO2 trilayer phases. The trilayer phase is also reduced upon heating in CO+O2, consistent with a Mars-van-Krevelen type mechanism for CO oxidation. At higher temperatures, the monolayer film dewets the surface, resulting in a loss of the observed reducibility. A similar iron oxide film prepared on Au(111) shows little sign of reduction or oxidation under the same conditions. The results highlight the unique properties of monolayer FeO and the importance of the Pt support in this reaction. The study furthermore demonstrates the power of grazing-incidence XAFS for in situ studies of these model catalysts under realistic conditions.

Place, publisher, year, edition, pages
John Wiley & Sons, 2025. Vol. 26, no 2, article id e202400835
Keywords [en]
Heterogeneous catalysis, Thin Films, XANES, iron oxide, operando
National Category
Condensed Matter Physics
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URN: urn:nbn:se:mau:diva-71719DOI: 10.1002/cphc.202400835ISI: 001358845900001PubMedID: 39403857Scopus ID: 2-s2.0-85209646728OAI: oai:DiVA.org:mau-71719DiVA, id: diva2:1907459
Available from: 2024-10-22 Created: 2024-10-22 Last updated: 2025-02-07Bibliographically approved

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Gajdek, DoroteaWallander, Harald J.Merte, Lindsay Richard

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