Surface composition of magnetron sputtered Pt-Co thin film catalyst for proton exchange membrane fuel cells

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TitreSurface composition of magnetron sputtered Pt-Co thin film catalyst for proton exchange membrane fuel cells
Type de publicationJournal Article
Year of Publication2016
AuteursVorokhta M, Khalakhan I, Vaclavu M, Kovacs G, Kozlov SM, Kus P, Skala T, Tsud N, Lavkova J, Potin V, Matolinova I, Neyman KM, Matolin V
JournalAPPLIED SURFACE SCIENCE
Volume365
Pagination245-251
Date PublishedMAR 1
Type of ArticleArticle
ISSN0169-4332
Mots-clésDensity functional theory (DFT) methods, Magnetron sputtering, Pt-Co alloy, Thin film catalyst, XPS
Résumé

Recently we have tested a magnetron sputtered Pt-Co catalyst in a hydrogen-fed proton exchange membrane fuel cell and showed its high catalytic activity for the oxygen reduction reaction. Here we present further investigation of the magnetron sputtered Pt-Co thin film catalyst by both experimental and theoretical methods. Scanning electron microscopy and transmission electron microscopy experiments confirmed the nanostructured character of the catalyst. The surface composition of as-deposited and annealed at 773 K Pt-Co films was investigated by surface analysis techniques, such as synchrotron radiation photoelectron spectroscopy and X-ray photoelectron spectroscopy. Modeling based on density functional theory showed that the surface of 6 nm large 1:1 Pt-Co nanoparticles is almost exclusively composed of Pt atoms (>90%) at typical operation conditions and the Co content does not exceed 20% at 773 K, in agreement with the experimental characterization of such films annealed in vacuum. According to experiment, the density of valence states of surface atoms in Pt-Co nanostructures is shifted by 0.3 eV to higher energies, which can be associated with their higher activity in the oxygen reduction reaction. The changes in electronic structure caused by alloying are also reflected in the measured Pt 4f, Co 3p and Co 2p photoelectron peak binding energies. (C) 2016 Elsevier B.V. All rights reserved.

DOI10.1016/j.apsusc.2016.01.004