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Temperature dependence of water-water and ion-water correlations in bulk water and electrolyte solutions probed by femtosecond elastic second harmonic scattering

机译:水 - 水和离子水相关在散装水和电解质溶液中的温度依赖性由飞秒弹性第二谐波散射探测

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The temperature dependence of the femtosecond elastic second harmonic scattering (fs-ESHS) response of bulk light and heavy water and their electrolyte solutions is presented. We observe clear temperature dependent changes in the hydrogen (H)-bond network of water that show a decrease in the orientational order of water with increasing temperature. Although D2O has a more structured H-bond network (giving rise to more fs-ESHS intensity), the relative temperature dependence is larger in H2O. The changes are interpreted in terms of the symmetry of H-bonds and are indicators of nuclear quantum effects. Increasing the temperature in electrolyte solutions decreases the influence of the total electrostatic field from ions on the water-water correlations, as expected from Debye-Huckel theory, since the Debye length becomes longer. The effects are, however, 1.9 times (6.3 times) larger than those predicted for H2O (D2O). Since fs-ESHS responses can be computed from known molecular coordinates, our observations provide a unique opportunity to refine quantum mechanical models of water. (c) 2018 Author(s).
机译:提出了散装光和重水的飞秒弹性二次谐波散射(FS-ESHS)响应及其电解质溶液的温度依赖性。我们观察到氢气(H) - 跨网络的透明温度依赖性变化,其水显示出较大温度的尺寸序列的降低。尽管D2O具有更具结构化的H键网络(引起更多FS-ESHS强度),但H2O中相对温度依赖性更大。根据H-CONDS的对称性解释变化,并且是核量子效应的指标。增加电解质溶液中的温度降低了离子对水 - 水相关的总静电场的影响,因为德英的长度变长。然而,效果大于对H2O(D2O)预测的1.9倍(6.3倍)。由于FS-ESHSS响应可以从已知的分子坐标计算,因此我们的观察结果提供了一种优化水机械模型的独特机会。 (c)2018年作者。

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