We have studied effects of surface oxygen vacancies on electronic states of TiO2(110), TiO2(001) and SrTiO3(001) surfaces by means of angle-resolved photoemission spectroscopy. The surface oxygen vacancy induces a state at ~leV below the Fermi level in the bulk band gap. In the angleresolved photoem
Effect of surface oxygen vacancies on electronic states of reduced SrTiO3(110) surface
β Scribed by Y. Aiura; H. Bando; T. Maruyama; Y. Nishihara; Y. Haruyama; S. Kodaira; T. Komeda; Y. Sakisaka; H. Kato
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 316 KB
- Volume
- 235-240
- Category
- Article
- ISSN
- 0921-4534
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β¦ Synopsis
The electronic structure of reduced SrTiO3(ll0) surface prepared by annealing in ultrahigh vacuum (UHV), has been studied using photoemission spectroscopy (PES) and scanning tunneling microscopy/spectroscopy (STM/STS). In the PES spectra of reduced SrTiO3(ll0) surface after annealing in UHV at 8(AJ~C, a clear metallic state with a sharp Fermi cut-off and a broad state centered at .-.1.1eV below the Fermi level are observed in the band gap region. A Ti3p->3d resonance enhancement is occurred for the metallic state, but not for the ~l.leV state. On the other hand, after the sample was anneNed in UHV at 1000*C, it has been shown that the metallic state becomes drastically weak, and that only the ~l.leV state is seen in the band gap region. Thereafter, the ~l.leV state exhibits a clear Ti3p->3d resonance enhancement. Tlle difference in the spectral feature of these band gap states is directly related to the surface geometric structural change.
π SIMILAR VOLUMES
The stability of oxygen anions and the hydrogen abstraction from Ε½ . methane on a reduced SnO 110 crystal surface have been studied theoretically using a 2 point-charge model. The geometric and electronic structures for the present molecules are calculated by means of a hybrid HartreeαFockrdensity f