Oxygen vacancies and defect electronic states on the SnO2(110)-1×1 surface

David F. Cox, Teresa B. Fryberger, and Steve Semancik
Phys. Rev. B 38, 2072 – Published 15 July 1988
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Abstract

The SnO2(110)-1×1 surface, a surface which is structurally similar to the more studied TiO2(110) surface, has been found to be an ideal system of study for the identification and characterization of surface oxygen vacancies. Heating a well-oxidized, nearly perfect (110) surface in UHV removes large amounts of surface lattice oxygen. Ion-scattering spectroscopy (ISS) and ultraviolet photoelectron spectroscopy (UPS) have shown conclusively that defect electronic states which appear low in the band gap for annealing temperatures less than 800 K arise from ‘‘bridging’’ oxygen vacancies [i.e., from the removal of oxygen anions from the terminal layer of an ideal, rutile-structure (110) surface]. UPS and four-point conductivity measurements indicate that heating at 800 K or above causes the formation of a second type of surface defect. It is argued that this second defect is an ‘‘in-plane’’ oxygen vacancy [i.e., the result of removing an oxygen anion from what is normally the second, tin-containing, atomic plane of an ideal (110) surface]. The in-plane oxygen vacancy is characterized by occupied states higher in the band gap which extend to the Fermi level.

  • Received 6 January 1988

DOI:https://doi.org/10.1103/PhysRevB.38.2072

©1988 American Physical Society

Authors & Affiliations

David F. Cox, Teresa B. Fryberger, and Steve Semancik

  • Chemical Process Metrology Division, National Bureau of Standards, Gaithersburg, Maryland 20899

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Vol. 38, Iss. 3 — 15 July 1988

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