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Research Article

Catalysis under shell: Improved CO oxidation reaction confined in Pt@h-BN core–shell nanoreactors

Mengmeng Sun1Qiang Fu1( )Lijun Gao1,2Yanping Zheng3Yangyang Li3Mingshu Chen3Xinhe Bao1
State Key Laboratory of CatalysisiChEMDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian116023China
Department of Chemical PhysicsUniversity of Science and Technology of ChinaHefei230026China
State Key Laboratory of Physical Chemistry of Solid SurfacesDepartment of ChemistryXiamen UniversityXiamen361005China
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Abstract

Core–shell nanostructures consisting of active metal cores and protective shells often exhibit enhanced catalytic performance, in which reactants can access a small part of the core surfaces through the pores in the shells. In this study, we show that Pt nanoparticles (NPs) can be embedded into few-layer hexagonal boron nitride (h-BN) overlayers, forming Pt@h-BN core–shell nanocatalysts. The h-BN shells not only protect the Pt NPs under harsh conditions but also allow gaseous molecules such as CO and O2 to access a large part of the Pt surfaces through a facile intercalation process. As a result, the Pt@h-BN nanostructures act as nanoreactors, and CO oxidation reactions with improved activity, selectivity, and stability occur at the core–shell interfaces. The confinement effect exerted by the h-BN shells promotes the Pt-catalyzed reactions. Our work suggests that two-dimensional shells can function as robust but flexible covers on nanocatalyst surfaces and tune the surface reactivity.

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Nano Research
Pages 1403-1412
Cite this article:
Sun M, Fu Q, Gao L, et al. Catalysis under shell: Improved CO oxidation reaction confined in Pt@h-BN core–shell nanoreactors. Nano Research, 2017, 10(4): 1403-1412. https://doi.org/10.1007/s12274-017-1512-8
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Received: 07 January 2017
Revised: 25 January 2017
Accepted: 03 February 2017
Published: 17 March 2017
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2017
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