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Coverage-dependent adsorption and desorption of oxygen on Pd(100)
Author(s) -
Angela den Dunnen,
Leon Jacobse,
Sandra Wiegman,
Otto T. Berg,
Ludo B. F. Juurlink
Publication year - 2016
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.4953541
Subject(s) - overlayer , desorption , dissociation (chemistry) , adsorption , nucleation , molecular beam , oxygen , kinetic energy , thermal desorption , chemistry , thermal desorption spectroscopy , chemical physics , activation energy , analytical chemistry (journal) , materials science , molecule , physics , organic chemistry , quantum mechanics , chromatography
We have studied the adsorption and desorption of O2 on Pd(100) by supersonic molecular beam techniques and thermal desorption spectroscopy. Adsorption measurements on the bare surface confirm that O2 initially dissociates for all kinetic energies between 56 and 380 meV and surface temperatures between 100 and 600 K via a direct mechanism. At and below 150 K, continued adsorption leads to a combined O/O2 overlayer. Dissociation of molecularly bound O2 during a subsequent temperature ramp leads to unexpected high atomic oxygen coverages, which are also obtained at high incident energy and high surface temperature. At intermediate temperatures and energies, these high final coverages are not obtained. Our results show that kinetic energy of the gas phase reactant and reaction energy dissipated during O2 dissociation on the cold surface both enable activated nucleation of high-coverage surface structures. We suggest that excitation of local substrate phonons may play a crucial role in oxygen dissociation at any coverage.

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