Setvin Martin, Daniel Benjamin, Aschauer Ulrich, Hou Weiyi, Li Ye-Fei, Schmid Michael, Selloni Annabella, Diebold Ulrike
Institute of Applied Physics, Vienna University of Technology, Wiedner Hauptstrasse 8-10/134, 1040 Wien, Austria.
Phys Chem Chem Phys. 2014 Oct 21;16(39):21524-30. doi: 10.1039/c4cp03212h. Epub 2014 Sep 4.
While Scanning Tunneling Microscopy (STM) has evolved as an ideal tool to study surface chemistry at the atomic scale, the identification of adsorbed species is often not straightforward. This paper describes a way to reliably identify H2O, CO and O2 on the TiO2 anatase (101) surface with STM. These molecules are of a key importance in the surface chemistry of this and many other (photo-) catalytic materials. They exhibit a wide variety of contrasts in STM images, depending on the tip condition. With clean, metallic tips the molecules appear very similar, i.e., as bright, dimer-like features located in the proximity of surface Ti5c atoms. However, each species exhibits a specific response to the electric field applied by the STM tip. It is shown that this tip-adsorbate interaction can be used to reliably ascertain the identity of such species. The tip-adsorbate interactions, together with comparison of experimental and calculated STM images, are used to analyse and revisit the assignments of molecular adsorbed species reported in recent studies.
虽然扫描隧道显微镜(STM)已发展成为在原子尺度上研究表面化学的理想工具,但吸附物种的识别往往并非易事。本文描述了一种利用STM可靠地识别TiO₂锐钛矿(101)表面上的H₂O、CO和O₂的方法。这些分子在这种以及许多其他(光)催化材料的表面化学中至关重要。它们在STM图像中表现出各种各样的对比度,这取决于针尖条件。使用干净的金属针尖时,这些分子看起来非常相似,即呈现为位于表面Ti₅c原子附近的明亮的、二聚体状特征。然而,每种物种对STM针尖施加的电场都表现出特定的响应。结果表明,这种针尖 - 吸附质相互作用可用于可靠地确定此类物种的身份。针尖 - 吸附质相互作用,以及实验和计算得到的STM图像的比较,被用于分析和重新审视近期研究中报道的分子吸附物种的归属。