Force measurements between semifluorinated thiolate self-assembled monolayers: Long-range hydrophobic interactions and surface charge

被引:14
作者
Ederth, T
Tamada, K
Claesson, PM
Valiokas, R
Colorado, R
Graupe, M
Shmakova, OE
Lee, TR
机构
[1] Royal Inst Technol, Dept Chem, SE-10044 Stockholm, Sweden
[2] Inst Surface Chem, SE-11486 Stockholm, Sweden
[3] Natl Inst Mat & Chem Res, NIMC, Tsukuba, Ibaraki 3058565, Japan
[4] Linkoping Univ, Dept Phys & Measurement Technol, SE-58183 Linkoping, Sweden
[5] Univ Houston, Dept Chem, Houston, TX 77204 USA
基金
美国国家科学基金会;
关键词
self-assembled monolayers; flourocarbons; interfacial charge; surface forces; hydrophobic interaction; ion adsorption;
D O I
10.1006/jcis.2000.7318
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
Long-range interactions between self-assembled monolayers (SAMs) of semifluorinated alkanethiols have been studied by direct force measurements in water and aqueous NaCl solutions. SAMs prepared from three different thiols, with identical fluorinated head groups but varying hydrocarbon spacer lengths, were investigated: CF3(CF2)(9)(CH2)(x)SH, where x = 2, 11, or 17. Force measurements show that the interactions in water and electrolyte solutions are composed of both double-layer interactions emerging from what appears to be charges adsorbed onto the surfaces and long-range "hydrophobic" attractions, in excess of the expected van der Waals forces. The three investigated thiols produce similar results in force measurements, though the contact angles with water are slightly different, The "hydrophobic" attraction has the form of step-like attractive discontinuities in the force profiles at separations ranging from 20 to 40 nm, caused by bridging of microscopic bubbles residing at the surfaces, The shape or range of these discontinuities are not significantly affected by replacement of the water with either 1 mM or 1 M NaCl solutions. The origin of the charges causing the electrostatic double-layer interaction is unclear, but some possible causes are discussed. (C) 2001 Academic Press.
引用
收藏
页码:391 / 397
页数:7
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