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首页> 外文期刊>The Journal of Chemical Physics >Structure and dynamics of water in nanoscopic spheres and tubes
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Structure and dynamics of water in nanoscopic spheres and tubes

机译:纳米球和管中水的结构和动力学

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We study the reorientation dynamics of liquid water confined in nanometer-sized reverse micelles of spherical and cylindrical shape. The size and shape of the micelles are characterized in detail using small-angle x-ray scattering, and the reorientation dynamics of the water within the micelles is investigated using GHz dielectric relaxation spectroscopy and polarization-resolved infrared pump-probe spectroscopy on the OD-stretch mode of dilute HDO:H2O mixtures. We find that the GHz dielectric response of both the spherical and cylindrical reverse micelles can be well described as a sum of contributions from the surfactant, the water at the inner surface of the reversed micelles, and the water in the core of the micelles. The Debye relaxation time of the core water increases from the bulk value tau(H2O) of 8.2 +/- 0.1 ps for the largest reverse micelles with a radius of 3.2 nm to 16.0 +/- 0.4 ps for the smallest micelles with a radius of 0.7 nm. For the nano-spheres the dielectric response of the water is approximately similar to 6 times smaller than expected from the water volume fraction and the bulk dielectric relaxation of water. We find that the dielectric response of nano-spheres is more attenuated than that of nano-tubes of identical composition (water-surfactant ratio), whereas the reorientation dynamics of the water hydroxyl groups is identical for the two geometries. We attribute the attenuation of the dielectric response compared to bulk water to a local anti-parallel ordering of the molecular dipole moments. The difference in attenuation between nano-spheres and nano-cylinders indicates that the anti-parallel ordering of the water dipoles is more pronounced upon spherical than upon cylindrical nanoconfinement. (C) 2014 AIP Publishing LLC.
机译:我们研究了球形和圆柱形的纳米反胶束中的液态水的重新定向动力学。使用小角度X射线散射详细描述了胶束的大小和形状,并使用OD-上的GHz介电弛豫光谱和偏振分辨红外泵浦光谱研究了胶束中水的重新定向动力学。稀释的HDO:H2O混合物的拉伸模式。我们发现球形和圆柱形反胶束的GHz介电响应都可以很好地描述为表面活性剂,反胶束内表面的水和胶束核心中的水贡献的总和。核心水的德拜弛豫时间从半径为3.2 nm的最大反胶束的总值tau(H2O)的8.2 +/- 0.1 ps增加到半径为0.2 nm的最小胶束的16.0 +/- 0.4 ps 0.7纳米对于纳米球,水的介电响应大约比水的体积分数和水的整体介电弛豫所预期的小约6倍。我们发现,纳米球的介电响应比相同组成(水表面活性剂比率)的纳米管的介电响应更弱,而在两个几何结构中,水羟基的重新定向动力学是相同的。我们将与大量水相比的介电响应衰减归因于分子偶极矩的局部反平行排序。纳米球和纳米圆柱体之间的衰减差异表明,水偶极子的反平行排序在球形时要比在圆柱纳米约束时更明显。 (C)2014 AIP Publishing LLC。

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