Templating one-dimensional water chains on the alkali halide surface

被引:0
|
作者
Yoon, Cheolhwan [1 ]
Han, Huijun [1 ]
Kim, Yohan [1 ]
Shin, Hyung-Joon [1 ,2 ]
机构
[1] Ulsan Natl Inst Sci & Technol UNIST, Dept Mat Sci & Engn, Ulsan 44919, South Korea
[2] Inst Basic Sci IBS, Ctr Multidimens Carbon Mat, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
Scanning tunneling microscopy (STM); Density functional theory (DFT); 1-D water chain; Hydrogen bond; HELIUM ATOM SCATTERING; ADSORPTION; DISSOCIATION; DIFFUSION; MGO(100); CRYSTAL; STATE;
D O I
10.1016/j.apsusc.2025.162507
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding the adsorption structure of water is regarded as a first step in exploring its reaction with specific surfaces. The surface geometry and its components considerably influence both the adsorption energy and the structure of water adsorption. In this study, we report the unusual adsorption structure of water molecules on a KCl(100) film by means of low-temperature scanning tunneling microscopy (LT-STM). Rather than forming a closed-loop hydrogen bond network, water molecules align into a one-dimensional chain on the film. The lateral positioning of individual water molecules, manipulated in a row, successfully recreated the single-molecule-thick chain. Introducing an additional water molecule extended the chain by the K-Cl distance. The creation of the one-dimensional water chain is influenced not only by the large lattice parameter of KCl but also by the weak interactions between the surface and the water molecules.
引用
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页数:7
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