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Hollow Pt/CeO2 nanocatalysts pretreated with pulsed steam for enhanced CO oxidation performance

•Hollow Pt/CeO2H catalysts were fabricated for the oxidation of CO.•Pulsed steam treatment enhanced the catalytic activity of Pt/CeO2H for CO oxidation.•The oxygen vacancy of Pt/CeO2H can be improved by the pulsed steam treatment.•The valence state of pt was significantly controlled by the pulsed st...

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Bibliographic Details
Published in:Molecular catalysis 2025-02, Vol.572, Article 114720
Main Authors: Huang, Mingzhen, He, Jinxin, Xu, Kaiji, Cai, Dongren, Zhan, Guowu
Format: Article
Language:English
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Summary:•Hollow Pt/CeO2H catalysts were fabricated for the oxidation of CO.•Pulsed steam treatment enhanced the catalytic activity of Pt/CeO2H for CO oxidation.•The oxygen vacancy of Pt/CeO2H can be improved by the pulsed steam treatment.•The valence state of pt was significantly controlled by the pulsed steam treatment.•Pt/CeO2H exhibited the weaker CO adsorption to prevent the CO poisoning effect. The supported Pt/CeO2 catalysts are widely used for the catalytic oxidation of CO at ambient conditions. Herein, we reported a new strategy for modifying the interaction between Pt and CeO2 support via pulsed steam treatment, which significantly optimized the catalytic performance of Pt/CeO2 for CO oxidation. Specifically, the hollow CeO2 nanospheres were prepared by using carbon spheres as sacrificial templates and then subjected to pulsed steam treatment at 150 °C for different times to obtain the CeO2-xH support (x means the time of pulsed steam treatment, min). It was found that the complete oxidation of CO can be achieved at 90 °C over the Pt/CeO2–50H sample, which was much lower than that (130 °C) on Pt/CeO2 without pulsed steam treatment. The XPS and in-situ DRIFTS characterizations were conducted to reveal the high performance of the Pt/CeO2–50H catalyst for CO oxidation. It was found that the valence state of Pt significantly controlled by pulsed steam treatment was critical to the catalytic activity, whereby the presence of two types of active sites (Pt0-CO and Ptδ+-CO) over Pt/CeO2–50H greatly promoted the combination of adsorbed CO and O2 to generate CO2. Accordingly, this study provides a facile method to regulate the Pt valence state by pulsed steam treatment for CeO2 support, which is critical to the CO oxidation activity. [Display omitted]
ISSN:2468-8231
2468-8231
DOI:10.1016/j.mcat.2024.114720