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在吉帕斯卡范围内水中的平动和转动扩散。

Translational and rotational diffusion in water in the Gigapascal range.

机构信息

IMPMC, CNRS-UMR 7590, Université Pierre & Marie Curie, 75252 Paris, France and Ecole Polytech Fed Lausanne, Inst Condensed Matter Phys, EPSL, CH-1015 Lausanne, Switzerland.

出版信息

Phys Rev Lett. 2013 Nov 1;111(18):185901. doi: 10.1103/PhysRevLett.111.185901. Epub 2013 Oct 28.

Abstract

First measurements of the self-dynamics of liquid water in the GPa range are reported. The GPa range has here become accessible through a new setup for the Paris-Edinburgh press specially conceived for quasielastic neutron scattering studies. A direct measurement of both the translational and rotational diffusion coefficients of water along the 400 K isotherm up to 3 GPa, corresponding to the melting point of ice VII, is provided and compared with molecular dynamics simulations. The translational diffusion is observed to strongly decrease with pressure, though its variation slows down for pressures higher than 1 GPa and decouples from that of the shear viscosity. The rotational diffusion turns out to be insensitive to pressure. Through comparison with structural data and molecular dynamics simulations, we show that this is a consequence of the rigidity of the first neighbors shell and of the invariance of the number of hydrogen bonds of a water molecule under high pressure. These results show the inadequacy of the Stokes-Einstein-Debye equations to predict the self-diffusive behavior of water at high temperature and high pressure, and challenge the usual description of hot dense water behaving as a simple liquid.

摘要

首次在 GPa 范围内测量了液态水的自扩散。通过专门设计用于准弹性中子散射研究的巴黎-爱丁堡压力机的新设置,使 GPa 范围内的测量成为可能。沿着 400 K 等焓线直至 3 GPa 的温度直接测量了水的平移和旋转扩散系数,并与分子动力学模拟进行了比较。观察到平移扩散随压力强烈减小,尽管在高于 1 GPa 的压力下其变化速度减慢,并与剪切粘度的变化解耦。旋转扩散对压力不敏感。通过与结构数据和分子动力学模拟的比较,我们表明这是由于第一近邻壳的刚性以及高压下水分子氢键数量不变的结果。这些结果表明,Stokes-Einstein-Debye 方程不足以预测高温高压下水的自扩散行为,并挑战了将高温高密度水描述为简单液体的常用方法。

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