Density depletion at solid-liquid interfaces: A neutron reflectivity study

被引:98
作者
Maccarini, M.
Steitz, R.
Himmelhaus, M.
Fick, J.
Tatur, S.
Wolff, M.
Grunze, M.
Janecek, J.
Netz, R. R.
机构
[1] Heidelberg Univ, Inst Angewandte Phys Chem, D-69120 Heidelberg, Germany
[2] FZK, Inst Nukl Entsorgung, D-76021 Karlsruhe, Germany
[3] Hahn Meitner Inst Berlin GmbH, D-14109 Berlin, Germany
[4] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[5] Univ Montreal, Ctr Rech, CHUM Hotel Dieu, Montreal, PQ, Canada
[6] Ruhr Univ Bochum, Lehrstuhl Festkorperphys, D-4630 Bochum, Germany
[7] Tech Univ Munich, Dept Phys, D-85748 Garching, Germany
关键词
D O I
10.1021/la061943y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Neutron reflectivity experiments conducted on self-assembled monolayers (SAMs) against polar (water) and nonpolar (organic) liquid phases reveal further evidence for a density reduction at hydrophobic-hydrophilic interfaces. The density depletion is found at the interface between hydrophobic dodecanethiol (C12) and hexadecanethiol (C16) SAMs and water and also between hydrophilic SAMs (C12/C11OH) and nonpolar fluids. The results show that the density deficit of a fluid in the boundary layer is not unique to aqueous solid-liquid interfaces but is more general and correlated with the affinity of the liquid to the solid surface. In water the variation of pH has only minor influence, while different electrolytes taken from the Hofmeister series seem to increase the depletion. On hydrophobic SAMs an increase in density depletion with temperature was observed, in agreement with Monte Carlo simulations performed on corresponding model systems. The increase in the water density depletion layer is governed by two effects: the surface energy difference between water and the substrate and the chemical potential of the aqueous phase.
引用
收藏
页码:598 / 608
页数:11
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