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Surface Structure of TiO2 Rutile (011) Exposed to Liquid Water
Author(s) -
Jan Balajka,
Ulrich Aschauer,
Stijn F. L. Mertens,
Annabella Selloni,
Michael Schmid,
Ulrike Diebold
Publication year - 2017
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.7b09674
Subject(s) - overlayer , x ray photoelectron spectroscopy , scanning tunneling microscope , adsorption , density functional theory , rutile , low energy ion scattering , materials science , surface reconstruction , superstructure , analytical chemistry (journal) , crystallography , chemistry , nanotechnology , surface (topology) , computational chemistry , nuclear magnetic resonance , physics , geometry , organic chemistry , mathematics , chromatography , thermodynamics
The rutile TiO 2 (011) surface exhibits a (2 × 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 a (2 × 1) symmetry was observed containing two dissociated water molecules per unit cell. The two OH groups yield an apparent "c(2 × 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 × 1) surface. Investigation of possible adsorption structures and analysis of the domain boundaries in this structure provide strong evidence that the original (2 × 1) reconstruction is lifted. Unlike the (2 × 1) reconstruction, the (1 × 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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