4.6 Article

Surface Structure of TiO2 Rutile (011) Exposed to Liquid Water

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 121, Issue 47, Pages 26424-26431

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.7b09674

Keywords

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Funding

  1. European Research Council [OxideSurfaces ERC-2011-ADG_20110209]
  2. Austrian Science Fund FWF [Z 250-N27]
  3. Austrian Science Fund FWF (Doctoral College) [Solids4Fun W1243-N16]
  4. SNF [PP00P2_157615]
  5. DoE-BES, Division of Chemical Sciences, Geosciences and Biosciences [DE-FG02-12ER16286]
  6. Austrian Science Fund (FWF) [W1243] Funding Source: Austrian Science Fund (FWF)

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The rutile TiO2(011) surface exhibits a (2 x 1) reconstruction when prepared by standard techniques in ultrahigh vacuum (UHV). Here we report that a restructuring occurs upon exposing the surface to liquid water at room temperature. The experiment was performed in a dedicated UHV system, equipped for direct and clean transfer of samples between UHV and liquid environment. After exposure to liquid water, an overlayer with (2 x 1) symmetry was observed containing two dissociated water molecules per unit cell. The two OH groups yield an apparent c(2 x 1) symmetry in scanning tunneling microscopy (STM) images. On the basis of STM analysis and density functional theory (DFT) calculations, this overlayer is attributed to dissociated water on top of the unreconstructed (1 x 1) surface. Investigation of possible adsorption structures and analysis of the domain boundaries in this structure provide strong evidence that the original (2 x 1) reconstruction is lifted. Unlike the (2 x 1) reconstruction, the (1 x 1) surface has an appropriate density and symmetry of adsorption sites. The possibility of contaminant-induced restructuring was excluded based on X-ray photoelectron spectroscopy (XPS) and low-energy He+ ion scattering (LEIS) measurements.

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