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金(111)表面上硫醇盐和氟化硫醇盐的表面偶极子和功函数

Surface dipoles and work functions of alkylthiolates and fluorinated alkylthiolates on Au(111).

作者信息

Rusu Paul C, Brocks Geert

机构信息

Faculty of Science and Technology and MESA+ Institute for Nanotechnology,University of Twente, P. O. Box 217, 7500 AE Enschede, The Netherlands.

出版信息

J Phys Chem B. 2006 Nov 16;110(45):22628-34. doi: 10.1021/jp0642847.

Abstract

We study the dipole formation at the surface formed by -CH(3) and -CF(3) terminated short-chain alkylthiolate monolayers on Au(111). In particular, we monitor the change in work function upon chemisorption using density functional theory calculations. We separate the surface dipole into two contributions, resulting from the gold-adsorbate interaction and the intrinsic dipole of the adsorbate layer, respectively. The two contributions turn out to be approximately additive. Adsorbate dipoles are defined by calculating dipole densities of free-standing molecular monolayers. The gold-adsorbate interaction is, to a good degree, determined by the Au-S bond only. This bond is nearly apolar and its contribution to the surface dipole is relatively small. The surface dipole of the self-assembled monolayer is then dominated by the intrinsic dipole of the thiolate molecules. Alkylthiolates increase the work function of Au(111), whereas fluorinated alkylthiolates decrease it.

摘要

我们研究了在Au(111)上由-CH(3)和-CF(3)端基的短链烷基硫醇盐单层形成的表面上的偶极子形成。特别是,我们使用密度泛函理论计算监测化学吸附时功函数的变化。我们将表面偶极子分为两个部分,分别由金-吸附质相互作用和吸附质层的固有偶极子产生。结果表明这两个部分大致是相加的。通过计算独立分子单层的偶极子密度来定义吸附质偶极子。金-吸附质相互作用在很大程度上仅由Au-S键决定。该键几乎是非极性的,其对表面偶极子的贡献相对较小。然后,自组装单层的表面偶极子由硫醇盐分子的固有偶极子主导。烷基硫醇盐增加Au(111)的功函数,而氟化烷基硫醇盐则降低它。

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