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The Role of Grain Boundary Sites for the Oxidation of Copper Catalysts during the CO Oxidation Reaction

Nilsson, Sara, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
El Berch, John N. (author)
University of Pittsburgh
Albinsson, David, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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Fritzsche, Joachim, 1977 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Mpourmpakis, Giannis (author)
University of Pittsburgh
Langhammer, Christoph, 1978 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2023
2023
English.
In: ACS Nano. - 1936-086X .- 1936-0851. ; 17:20, s. 20284-20298
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The oxidation of transition metal surfaces is a process that takes place readily at ambient conditions and that, depending on the specific catalytic reaction at hand, can either boost or hamper activity and selectivity. Cu catalysts are no exception in this respect since they exhibit different oxidation states for which contradicting activities have been reported, as, for example, in the catalytic oxidation of CO. Here, we investigate the impact of low-coordination sites on nanofabricated Cu nanoparticles with engineered grain boundaries on the oxidation of the Cu surface under CO oxidation reaction conditions. Combining multiplexed in situ single particle plasmonic nanoimaging, ex situ transmission electron microscopy imaging, and density functional theory calculations reveals a distinct dependence of particle oxidation rate on grain boundary density. Additionally, we found that the oxide predominantly nucleates at grain boundary-surface intersections, which leads to nonuniform oxide growth that suppresses Kirkendall-void formation. The oxide nucleation rate on Cu metal catalysts was revealed to be an interplay of surface coordination and CO oxidation behavior, with low coordination favoring Cu oxidation and high coordination favoring CO oxidation. These findings explain the observed single particle-specific onset of Cu oxidation as being the consequence of the individual particle grain structure and provide an explanation for widely distributed activity states of particles in catalyst bed ensembles.

Subject headings

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)
NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

Keyword

CO oxidation
plasmonic nanoimaging
DFT
single particle
copper nanoparticles
grain boundary sites
surfaceoxidation

Publication and Content Type

art (subject category)
ref (subject category)

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