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Embedded-cluster study of hydrogen interaction with an oxygen vacancy at the magnesium oxide surface
Unita INFM Torino, I-10125 Turin, Italy.
Unita INFM Torino, I-10125 Turin, Italy.
Unita INFM Torino, I-10125 Turin, Italy.
Linköping University, Department of Physics, Chemistry and Biology, Chemistry. Linköping University, The Institute of Technology.ORCID iD: 0000-0002-5341-2637
1999 (English)In: JOURNAL OF PHYSICAL CHEMISTRY B, ISSN 1089-5647, Vol. 103, no 19, 3872-3876 p.Article in journal (Refereed) Published
Abstract [en]

An embedded-cluster Hartree−Fock approximation is adopted for simulating the formation of Fs(H) color centers at the (001) surface of magnesium oxide. This process is assumed to take place in two steps at an isolated surface anion vacancy:  first, a hydrogen molecule is adsorbed dissociatively at the defect; second, following UV irradiation, a neutral hydrogen atom is removed and an electron remains trapped at the vacancy with a hydroxyl group nearby. According to the present calculations, the activation energy for the dissociation is appreciable (about 25 kcal/mol) and the products (a proton bound to a low-coordinated oxygen and a hydride ion above the vacancy) are considerably less stable than the reactants. The excitation of the adsorbed species owing to the UV irradiation is simulated by considering a singlet−triplet transition of the hydride−vacancy complex, which then dissociates into an H atom and a trapped lone electron. The electronic structure and the EPR parameters of the resulting paramagnetic state are explored. The theoretical results agree in many respects with the experimental data as concerns one of the forms of heterolitically dissociated hydrogen which are found at the defective MgO surface. However, from the viewpoint of the energetics, this model is untenable because that species is known to form irreversibly at room temperature with low activation energy.

Place, publisher, year, edition, pages
1999. Vol. 103, no 19, 3872-3876 p.
National Category
Physical Chemistry
URN: urn:nbn:se:liu:diva-115217DOI: 10.1021/jp990117dISI: 000080552500011OAI: diva2:794261
Available from: 2015-03-10 Created: 2015-03-10 Last updated: 2015-03-26

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