Balajka Jan, Aschauer Ulrich, Mertens Stijn F L, Selloni Annabella, Schmid Michael, Diebold Ulrike
Institute of Applied Physics, TU Wien, Wiedner Hauptstraße 8-10/134, 1040 Vienna, Austria.
Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012, Bern, Switzerland.
J Phys Chem C Nanomater Interfaces. 2017 Nov 30;121(47):26424-26431. doi: 10.1021/acs.jpcc.7b09674. Epub 2017 Oct 31.
The rutile TiO(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.
当在超高真空(UHV)中通过标准技术制备时,金红石TiO(011)表面呈现出(2×1)重构。在此我们报告,在室温下将该表面暴露于液态水时会发生结构重组。实验在一个专门的超高真空系统中进行,该系统配备了用于在超高真空和液体环境之间直接且清洁地转移样品的装置。暴露于液态水后,观察到一个具有(2×1)对称性的覆盖层,每个晶胞包含两个解离的水分子。这两个OH基团在扫描隧道显微镜(STM)图像中产生明显的“c(2×1)”对称性。基于STM分析和密度泛函理论(DFT)计算,该覆盖层归因于未重构的(1×1)表面顶部的解离水。对该结构中可能的吸附结构的研究以及对畴边界的分析提供了有力证据,表明原始的(2×1)重构被解除。与(2×1)重构不同,(1×1)表面具有合适的吸附位点密度和对称性。基于X射线光电子能谱(XPS)和低能He离子散射(LEIS)测量,排除了污染物诱导结构重组的可能性。