Water-COOH Composite Structure with Enhanced Hydrophobicity Formed by Water Molecules Embedded into Carboxyl-Terminated Self-Assembled Monolayers

被引:48
|
作者
Guo, Pan [1 ,2 ,3 ]
Tu, Yusong [1 ,4 ]
Yang, Jinrong [1 ,2 ,3 ]
Wang, Chunlei [1 ,2 ]
Sheng, Nan [1 ,2 ]
Fang, Haiping [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Div Interfacial Water, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Yangzhou Univ, Coll Phys Sci & Technol, Yangzhou 225009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
CHEMICAL FORCE MICROSCOPY; ORGANIC-SURFACES; DYNAMICS SIMULATIONS; PROTEIN ADSORPTION; QUANTUM-MECHANICS; SILICON SURFACES; ACID MONOLAYERS; CELL-ADHESION; GOLD SURFACES; LIQUID WATER;
D O I
10.1103/PhysRevLett.115.186101
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
By combining molecular dynamics simulations and quantum mechanics calculations, we show the formation of a composite structure composed of embedded water molecules and the COOH matrix on carboxyl-terminated self-assembled monolayers (COOH SAMs) with appropriate packing densities. This composite structure with an integrated hydrogen bond network inside reduces the hydrogen bonds with the water above. This explains the seeming contradiction on the stability of the surface water on COOH SAMs observed in experiments. The existence of the composite structure at appropriate packing densities results in the two-step distribution of contact angles of water droplets on COOH SAMs, around 0 degrees and 35 degrees, which compares favorably to the experimental measurements of contact angles collected from forty research articles over the past 25 years. These findings provide a molecular-level understanding of water on surfaces (including surfaces on biomolecules) with hydrophilic functional groups.
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页数:6
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