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Complementarity between high-energy photoelectron and L-edge spectroscopy for probing the electronic structure of 5d transition metal catalysts
Stockholm University, Faculty of Science, Department of Physics.
Stockholm University, Faculty of Science, Department of Physics.
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2010 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 12, no 21, 5694-5700 p.Article in journal (Refereed) Published
Abstract [en]

We demonstrate the successful use of hard X-ray photoelectron spectroscopy (HAXPES) for selectively probing the platinum partial d-density of states (DOS) in a Pt-Cu nanoparticle catalyst which shows activity superior to pure Pt towards the oxygen-reduction reaction (ORR). The information about occupied Pt d-band states was complemented by Pt L-2-edge X-ray absorption near-edge spectroscopy (XANES), which probes unoccupied valence states. We found a significant electronic perturbation of the Pt projected d-DOS which was narrowed and shifted to higher binding energy compared to pure platinum. The effect of this electronic structure perturbation on the chemical properties of the nanoparticle surface is discussed in terms of the d-band model. We have thereby demonstrated that the combination of L-edge spectroscopy and HAXPES allows for an experimental derivation of the valence electronic structure in an element-specific way for 5d metal catalysts.

Place, publisher, year, edition, pages
2010. Vol. 12, no 21, 5694-5700 p.
National Category
Natural Sciences
URN: urn:nbn:se:su:diva-50319DOI: 10.1039/b926414kISI: 000277926500019OAI: diva2:380730
authorCount :11Available from: 2010-12-22 Created: 2010-12-22 Last updated: 2010-12-22Bibliographically approved

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Ljungberg, MathiasWikfeldt, Kjartan T.Pettersson, Lars G. M.Nilsson, Anders
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