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Identification of a Catalytically Highly Active Surface Phase for CO Oxidation over PtRh Nanoparticles under Operando Reaction Conditions

Hejral, U. LU ; Franz, D. ; Volkov, S. ; Francoual, S. ; Strempfer, J. and Stierle, A. (2018) In Physical Review Letters 120(12).
Abstract

Pt-Rh alloy nanoparticles on oxide supports are widely employed in heterogeneous catalysis with applications ranging from automotive exhaust control to energy conversion. To improve catalyst performance, an atomic-scale correlation of the nanoparticle surface structure with its catalytic activity under industrially relevant operando conditions is essential. Here, we present x-ray diffraction data sensitive to the nanoparticle surface structure combined with in situ mass spectrometry during near ambient pressure CO oxidation. We identify the formation of ultrathin surface oxides by detecting x-ray diffraction signals from particular nanoparticle facets and correlate their evolution with the sample's enhanced catalytic activity. Our... (More)

Pt-Rh alloy nanoparticles on oxide supports are widely employed in heterogeneous catalysis with applications ranging from automotive exhaust control to energy conversion. To improve catalyst performance, an atomic-scale correlation of the nanoparticle surface structure with its catalytic activity under industrially relevant operando conditions is essential. Here, we present x-ray diffraction data sensitive to the nanoparticle surface structure combined with in situ mass spectrometry during near ambient pressure CO oxidation. We identify the formation of ultrathin surface oxides by detecting x-ray diffraction signals from particular nanoparticle facets and correlate their evolution with the sample's enhanced catalytic activity. Our approach opens the door for an in-depth characterization of well-defined, oxide-supported nanoparticle based catalysts under operando conditions with unprecedented atomic-scale resolution.

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author
; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Physical Review Letters
volume
120
issue
12
article number
126101
publisher
American Physical Society
external identifiers
  • pmid:29694082
  • scopus:85044435476
ISSN
0031-9007
DOI
10.1103/PhysRevLett.120.126101
language
English
LU publication?
yes
id
96ba6724-fd94-45ee-8532-d4a3a6da0d1c
date added to LUP
2018-05-22 12:37:07
date last changed
2024-04-15 07:01:01
@article{96ba6724-fd94-45ee-8532-d4a3a6da0d1c,
  abstract     = {{<p>Pt-Rh alloy nanoparticles on oxide supports are widely employed in heterogeneous catalysis with applications ranging from automotive exhaust control to energy conversion. To improve catalyst performance, an atomic-scale correlation of the nanoparticle surface structure with its catalytic activity under industrially relevant operando conditions is essential. Here, we present x-ray diffraction data sensitive to the nanoparticle surface structure combined with in situ mass spectrometry during near ambient pressure CO oxidation. We identify the formation of ultrathin surface oxides by detecting x-ray diffraction signals from particular nanoparticle facets and correlate their evolution with the sample's enhanced catalytic activity. Our approach opens the door for an in-depth characterization of well-defined, oxide-supported nanoparticle based catalysts under operando conditions with unprecedented atomic-scale resolution.</p>}},
  author       = {{Hejral, U. and Franz, D. and Volkov, S. and Francoual, S. and Strempfer, J. and Stierle, A.}},
  issn         = {{0031-9007}},
  language     = {{eng}},
  month        = {{03}},
  number       = {{12}},
  publisher    = {{American Physical Society}},
  series       = {{Physical Review Letters}},
  title        = {{Identification of a Catalytically Highly Active Surface Phase for CO Oxidation over PtRh Nanoparticles under Operando Reaction Conditions}},
  url          = {{http://dx.doi.org/10.1103/PhysRevLett.120.126101}},
  doi          = {{10.1103/PhysRevLett.120.126101}},
  volume       = {{120}},
  year         = {{2018}},
}