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  Adsorption energetics of CO on supported Pd nanoparticles as a function of particle size by single crystal microcalorimetry

Flores Camacho, J. M., Fischer-Wolfarth, J.-H., Peter, M., Campbell, C. T., Schauermann, S., & Freund, H.-J. (2011). Adsorption energetics of CO on supported Pd nanoparticles as a function of particle size by single crystal microcalorimetry. Physical Chemistry Chemical Physics, 13(37), 16800-16810. doi:10.1039/c1cp21677e.

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 Creators:
Flores Camacho, Jose Manuel1, Author           
Fischer-Wolfarth, Jan-Henrik 1, Author           
Peter, Matthias1, Author           
Campbell, Charles T.2, Author
Schauermann, Swetlana1, Author           
Freund, Hans-Joachim1, Author           
Affiliations:
1Chemical Physics, Fritz Haber Institute, Max Planck Society, Berlin, DE, ou_24022              
2Department of Chemistry, University of Washington, Seattle, WA 98195-1700, USA, ou_persistent22              

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 Abstract: The heat of adsorption and sticking probability of CO on well-defined Pd nanoparticles were measured as a function of particle size using single crystal adsorption microcalorimetry. Pd particles of different average sizes ranging from 120 to 4900 atoms per particle (or from 1.8 to 8 nm) and Pd(111) were used that were supported on a model in situ grown Fe3O4/Pt(111) oxide film. To precisely quantify the adsorption energies, the reflectivities of the investigated model surfaces were measured as a function of the thickness of the Fe3O4 oxide layer and the amount of deposited Pd. A substantial decrease of the binding energy of CO was found with decreasing particle size. Initial heat of adsorption obtained on the virtually adsorbate-free surface was observed to be reduced by about 20–40 kJ mol-1 on the smallest 1.8 nm sized Pd particles as compared to the larger Pd clusters and the extended Pd(111) single crystal surface. This effect is discussed in terms of the size-dependent properties of the Pd nanoparticles. The CO adsorption kinetics indicates a strong enhancement of the adsorbate flux onto the metal particles due to a capture zone effect, which involves trapping of adsorbates on the support and diffusion to metal clusters. The CO adsorption rate was found to be enhanced by a factor of 8 for the smallest 1.8 nm sized particles and by 1.4 for the particles of 7–8 nm size.

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Language(s): eng - English
 Dates: 2011-05-242011-08-052011-08-112011-10-07
 Publication Status: Issued
 Pages: 11
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/c1cp21677e
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Title: Physical Chemistry Chemical Physics
Source Genre: Journal
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Publ. Info: Cambridge [England] : Royal Society of Chemistry
Pages: - Volume / Issue: 13 (37) Sequence Number: - Start / End Page: 16800 - 16810 Identifier: ISSN: 1463-9076
CoNE: https://pure.mpg.de/cone/journals/resource/954925272413_1