Abstract
Gold nanoparticles (partially below 5 nm in diameter) were successfully deposited on hexagonal and monoclinic WO3 supports by deposition–precipitation, which had been considered previously not feasible owing to the low isoelectronic point of WO3. The catalysts were characterized by TEM, SEM, N2-adsorption, XRD, and XPS. In CO oxidation m-WO3/Au showed better catalytic activity over 100 °C than h-WO3/Au. This was explained by that m-WO3 had higher surface OH coverage, resulting in larger Au nanoparticle loading and thus better catalytic activity.
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Acknowledgments
I. M. Szilágyi thanks for a János Bolyai Research Fellowship of the Hungarian Academy of Sciences and a Marie Curie Intra-European Fellowship (PIEF-GA-2009-235655). TÉT_10-1-2011-0045 and OTKA-PD-109129 Grants are gratefully acknowledged. Consultation with Dr. Ferenc Somodi (Institute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, USA) about the catalysis test results is acknowledged.
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Firkala, T., Fórizs, B., Drotár, E. et al. Influence of the Support Crystal Structure of WO3/Au Catalysts in CO Oxidation. Catal Lett 144, 831–836 (2014). https://doi.org/10.1007/s10562-014-1217-5
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DOI: https://doi.org/10.1007/s10562-014-1217-5