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Strong Influence of Coadsorbate Interaction on CO Desorption Dynamics on Ru(0001) Probed by Ultrafast X-Ray Spectroscopy and Ab Initio Simulations
Stockholm University, Faculty of Science, Department of Physics.
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2015 (English)In: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 114, no 15, 156101Article in journal (Refereed) Published
Abstract [en]

We show that coadsorbed oxygen atoms have a dramatic influence on the CO desorption dynamics from Ru(0001). In contrast to the precursor-mediated desorption mechanism on Ru(0001), the presence of surface oxygen modifies the electronic structure of Ru atoms such that CO desorption occurs predominantly via the direct pathway. This phenomenon is directly observed in an ultrafast pump-probe experiment using a soft x-ray free-electron laser to monitor the dynamic evolution of the valence electronic structure of the surface species. This is supported with the potential of mean force along the CO desorption path obtained from density-functional theory calculations. Charge density distribution and frozen-orbital analysis suggest that the oxygen-induced reduction of the Pauli repulsion, and consequent increase of the dative interaction between the CO 5 sigma and the charged Ru atom, is the electronic origin of the distinct desorption dynamics. Ab initio molecular dynamics simulations of CO desorption from Ru(0001) and oxygen-coadsorbed Ru(0001) provide further insights into the surface bond-breaking process.

Place, publisher, year, edition, pages
2015. Vol. 114, no 15, 156101
National Category
Physical Sciences
URN: urn:nbn:se:su:diva-117452DOI: 10.1103/PhysRevLett.114.156101ISI: 000352990700006PubMedID: 25933322OAI: diva2:812553


Available from: 2015-05-19 Created: 2015-05-19 Last updated: 2015-05-19Bibliographically approved

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Öberg, HenrikGladh, JörgenSellberg, Jonas A.Östrom, HenrikPettersson, Lars G. M.Nilsson, Anders
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