Issue 37, 2011

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

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.

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

Article information

Article type
Paper
Submitted
24 May 2011
Accepted
05 Aug 2011
First published
22 Aug 2011

Phys. Chem. Chem. Phys., 2011,13, 16800-16810

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

J. M. Flores-Camacho, J.-H. Fischer-Wolfarth, M. Peter, C. T. Campbell, S. Schauermann and H.-J. Freund, Phys. Chem. Chem. Phys., 2011, 13, 16800 DOI: 10.1039/C1CP21677E

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