Document Type

Article

Publication Date

1-1-2017

Abstract

An unusual Fe-H bonding rather than conventional OH bonding is identified at Fe3O4 (001) surface. This abnormal behavior is associated with the oxygen vacancies which exist on the surface region but also penetrate deep into the bulk Fe3O4. In contrast, OH bonding becomes preferential as generally expected on an ozone processed surface, which has appreciably less oxygen vacancies. Such bonding site selective behavior, depending on oxygen vacancy concentrations, is further confirmed with DFT calculations. The results demonstrate an opportunity for tuning the chemical properties of oxide surfaces or oxide clusters.

Publication Source (Journal or Book title)

Surface Science

First Page

25

Last Page

30

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