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离子液体中的表面分层:一项X射线反射率研究。

Surface layering in ionic liquids: an X-ray reflectivity study.

作者信息

Sloutskin Eli, Ocko Benjamin M, Tamam Lilach, Kuzmenko Ivan, Gog Thomas, Deutsch Moshe

机构信息

Department of Physics, Bar-Ilan University, Ramat-Gan 52900, Israel.

出版信息

J Am Chem Soc. 2005 Jun 1;127(21):7796-804. doi: 10.1021/ja0509679.

Abstract

The surface structure and thermodynamics of two ionic liquids, based on the 1-alkyl-3-methylimidazolium cations, were studied by X-ray reflectivity and surface tensiometry. A molecular layer of a density approximately 18% higher than that of the bulk is found to form at the free surface of these liquids. In common with surface layering in liquid metals and surface freezing in melts of organic chain molecules, this effect is induced by the lower dimensionality of the surface. The concentrations of the oppositely charged ions within the surface layer are determined by chemical substitution of the anion. The temperature-dependent surface tension measurements reveal a normal, negative-slope temperature dependence. The different possible molecular arrangements within the enhanced-density surface layer are discussed.

摘要

通过X射线反射率和表面张力测定法研究了两种基于1-烷基-3-甲基咪唑鎓阳离子的离子液体的表面结构和热力学。发现在这些液体的自由表面形成了一层密度比本体密度高约18%的分子层。与液态金属中的表面分层和有机链分子熔体中的表面冻结一样,这种效应是由表面较低的维度引起的。表面层中带相反电荷离子的浓度由阴离子的化学取代决定。随温度变化的表面张力测量显示出正常的负斜率温度依赖性。讨论了高密度表面层内不同可能的分子排列。

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