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Thermally Stable and Regenerable Platinum-Tin Clusters for Propane Dehydrogenation Prepared by Atom Trapping on Ceria

  • Haifeng Xiong
  • , Sen Lin
  • , Joris Goetze
  • , Paul Pletcher
  • , Hua Guo
  • , Libor Kovarik
  • , Kateryna Artyushkova
  • , Bert M. Weckhuysen
  • , Abhaya K. Datye
    • Department of Chemical & Biological Engineering and Center for Microengineered Materials; University of New Mexico; Albuquerque NM 87131 USA
    • Research Institute of Photocatalysis; State Key Laboratory of Photocatalysis on Energy and Environment; Fuzhou University; Fuzhou 350002 China
    • Department of Chemistry and Chemical Biology; University of New Mexico; Albuquerque NM 87131 USA
    • Environmental Molecular Sciences Laboratory; Pacific Northwest National Laboratory; Richland WA 99352 USA

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    Ceria (CeO2) supports are unique in their ability to trap ionic platinum (Pt), providing exceptional stability for isolated single atoms of Pt. The reactivity and stability of single-atom Pt species was explored for the industrially important light alkane dehydrogenation reaction. The single-atom Pt/CeO2 catalysts are stable during propane dehydrogenation, but are not selective for propylene. DFT calculations show strong adsorption of the olefin produced, leading to further unwanted reactions. In contrast, when tin (Sn) is added to CeO2, the single-atom Pt catalyst undergoes an activation phase where it transforms into Pt–Sn clusters under reaction conditions. Formation of small Pt–Sn clusters allows the catalyst to achieve high selectivity towards propylene because of facile desorption of the product. The CeO2-supported Pt–Sn clusters are very stable, even during extended reaction at 680 °C. Coke formation is almost completely suppressed by adding water vapor to the feed. Furthermore, upon oxidation the Pt–Sn clusters readily revert to the atomically dispersed species on CeO2, making Pt–Sn/CeO2 a fully regenerable catalyst.
    Original languageEnglish
    Pages (from-to)8986-8991
    JournalAngewandte Chemie-International Edition
    Volume56
    Issue number31
    DOIs
    Publication statusPublished - 24 Jul 2017

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