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author:

Xiong, H. (Xiong, H..) [1] | Lin, S. (Lin, S..) [2] | Goetze, J. (Goetze, J..) [3] | Pletcher, P. (Pletcher, P..) [4] | Guo, H. (Guo, H..) [5] | Kovarik, L. (Kovarik, L..) [6] | Artyushkova, K. (Artyushkova, K..) [7] | Weckhuysen, B.M. (Weckhuysen, B.M..) [8] | Datye, A.K. (Datye, A.K..) [9]

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Scopus

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. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Keyword:

catalyst regeneration; ceria; light alkane dehydrogenation; single atoms; subnanometer Pt–Sn catalysis

Community:

  • [ 1 ] [Xiong, H.]Department of Chemical & Biological Engineering and Center for Microengineered Materials, University of New Mexico, Albuquerque, NM 87131, United States
  • [ 2 ] [Lin, S.]Research Institute of Photocatalysis, State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University, Fuzhou, 350002, China
  • [ 3 ] [Goetze, J.]Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, Utrecht, 3584 CG, Netherlands
  • [ 4 ] [Pletcher, P.]Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, Utrecht, 3584 CG, Netherlands
  • [ 5 ] [Guo, H.]Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, NM 87131, United States
  • [ 6 ] [Kovarik, L.]Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA 99352, United States
  • [ 7 ] [Artyushkova, K.]Department of Chemical & Biological Engineering and Center for Microengineered Materials, University of New Mexico, Albuquerque, NM 87131, United States
  • [ 8 ] [Weckhuysen, B.M.]Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, Utrecht, 3584 CG, Netherlands
  • [ 9 ] [Datye, A.K.]Department of Chemical & Biological Engineering and Center for Microengineered Materials, University of New Mexico, Albuquerque, NM 87131, United States

Reprint 's Address:

  • [Lin, S.]Research Institute of Photocatalysis, State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou UniversityChina

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Source :

Angewandte Chemie - International Edition

ISSN: 1433-7851

Year: 2017

Issue: 31

Volume: 56

Page: 8986-8991

1 2 . 1 0 2

JCR@2017

1 6 . 1 0 0

JCR@2023

ESI HC Threshold:226

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 289

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 5

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