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Electron Irradiation-Induced Local Surface Reconstruction to the (1 × 1) Domain on the Anatase TiO2(001)-(1 × 4)
Junjie Shi1, Zhan Shi2, Zongfang Wu3
1State Key Laboratory of Precision and Intelligent Chemistry, iChEM, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes and Department of Chemical Physics, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.
None:
In this study, we use low-energy electron diffraction, X-ray photoelectron spectroscopy, temperature-programmed desorption, and density functional theory calculations to unveil that low-energy electron irradiation (140.8 eV) induces local reconstruction of the irradiated area on the anatase TiO2(001)-(1 × 4) surface to the (1 × 1) domain, accompanied by the formation of Ti3+ species in the subsurface region and subsurface oxygen vacancies/surface hydroxyl groups, whereas the unirradiated regions retain the (1 × 4) periodicity. The low-energy electrons locally stimulate desorption of oxygen from the anatase TiO2(001)-(1 × 4) surface probably via interatomic Auger processes, creating surface oxygen vacancies with associated Ti3+ species that consequently trigger the local (1 × 4) → (1 × 1) surface reconstruction. Such a local surface reconstruction process is facilitated by surface hydroxyl groups. The created surface oxygen vacancies and Ti3+ species tend to migrate into the bulk, leading to a recovery of the (1 × 4) surface structure. The anatase TiO2(001)-(1 × 1) domain provides reactive Ti5c surface sites with a much larger density than the reactive Ti4c surface sites on the corresponding anatase TiO2(001)-(1 × 4) surface. These results demonstrate the sensitivity of TiO2 surface structures to the surface reduction, which commonly occurs for TiO2-involved (photo/electro)catalysts.
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