X射线光电子能谱
单层
自组装单层膜
化学
密度泛函理论
图层(电子)
分子
亚稳态
结晶学
分析化学(期刊)
化学工程
计算化学
有机化学
生物化学
工程类
作者
Ahlam R. M. Alharbi,Tanglaw Roman,Abdulrahman S. Alotabi,Ingo Köper,Gunther G. Andersson
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-08-27
卷期号:40 (36): 18925-18941
标识
DOI:10.1021/acs.langmuir.4c01488
摘要
Self-assembled monolayers (SAMs), such as alkanethiols (AT), are widely used as functional coatings or interfaces between different materials. There is an assumption that the arrangement and alignment of the hydrocarbon chains in films made from carboxyl-terminated alkanethiols are similar to those made from alkanethiols. Here, the structure of the outermost layer and near-surface region of SAMs formed from carboxyl-terminated alkanethiols of various lengths has been analyzed. The chemical composition of the samples was measured using X-ray photoelectron spectroscopy (XPS) and angle-resolved XPS (AR-XPS), allowing the film thickness. Metastable induced photoelectron spectroscopy (MIES) as a surface analytical tool sensitive only for the outermost layer in conjunction with density functional theory (DFT) calculations provided insights into the composition of the topmost layer, showing that it consists mainly of the backbone of the SAM-forming molecules. Through combining AR-XPS concentration depth profiles and the measurement of the composition of the outermost layer, it can be shown that SAMs tend to favor a gauche orientation, enabling interactions between the functional groups.
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