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固液界面处的密度耗尽:一项中子反射率研究。

Density depletion at solid-liquid interfaces: a neutron reflectivity study.

作者信息

Maccarini M, Steitz R, Himmelhaus M, Fick J, Tatur S, Wolff M, Grunze M, Janecek J, Netz R R

机构信息

Institut für Angewandte Physikalische Chemie, Ruprecht Karls Universität Heidelberg, Im Neuenheimer Feld 253, D-69120, Heidelberg, Germany.

出版信息

Langmuir. 2007 Jan 16;23(2):598-608. doi: 10.1021/la061943y.

Abstract

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.

摘要

对自组装单分子层(SAMs)与极性(水)和非极性(有机)液相进行的中子反射率实验,进一步揭示了疏水 - 亲水界面处密度降低的证据。在疏水的十二烷硫醇(C12)和十六烷硫醇(C16)自组装单分子层与水之间的界面,以及亲水自组装单分子层(C12/C11OH)与非极性流体之间的界面,均发现了密度损耗。结果表明,边界层中流体的密度亏缺并非水相固 - 液界面所特有,而是更为普遍,且与液体对固体表面的亲和力相关。在水中,pH值的变化影响较小,而取自霍夫迈斯特序列的不同电解质似乎会增加密度损耗。在疏水自组装单分子层上,观察到密度损耗随温度升高,这与对相应模型系统进行的蒙特卡罗模拟结果一致。水密度损耗层的增加受两种效应控制:水与基底之间的表面能差以及水相的化学势。

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