Preferential adsorption followed by spontaneous desorption of 1-octadecanol at a solution/graphite interface

被引:3
|
作者
Takajo, Daisuke [1 ]
Inaba, Akira [1 ]
Isoda, Seiji [2 ]
机构
[1] Osaka Univ, Res Ctr Struct Thermodynam, Grad Sch Sci, Osaka 5600043, Japan
[2] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
关键词
Adsorption; Desorption; Hydrogen bonding; Scanning tunneling microscopy; Liquid-solid interface; Graphite; SCANNING TUNNELING MICROSCOPE; SELF-ASSEMBLED MONOLAYERS; CRYSTALLINE-STRUCTURES; 2-DIMENSIONAL CRYSTALS; SUBMONOLAYER COVERAGES; GRAPHITE; LIQUID; ALKANES; MOLECULES; DYNAMICS;
D O I
10.1016/j.tsf.2010.09.038
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The dynamical behavior of adsorption/desorption of 1-octadecanol on graphite was investigated by scanning tunneling microscopy under the existence of 3-imino-4,5,6,7-tetrachloroisoindolin-1-one (ITCH) in a 1-phenyloctane solution. The monolayer of 1-octadecanol was first formed preferentially, as it was the rich component, with many domains at the solution/graphite interface. The molecules at the domain boundaries were then spontaneously replaced by the ITCH molecules, keeping the hydrogen bonding of the OH head groups of 1-octadecanol. The driving force of this replacement can be explained by the difference in heats of adsorption per unit area between those two molecules. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1371 / 1374
页数:4
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