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TIP4P/2005 水在高压下的相图。

Phase Diagram of TIP4P/2005 Water at High Pressure.

机构信息

Graduate School of Natural Science and Technology and ‡Research Institute for Interdisciplinary Science, Okayama University , Okayama 700-8530, Japan.

出版信息

Langmuir. 2017 Oct 24;33(42):11561-11569. doi: 10.1021/acs.langmuir.7b01764. Epub 2017 Aug 24.

Abstract

We report a new ice phase that forms spontaneously at the interface between ice VII and liquid water in molecular dynamics simulations of TIP4P/2005 water. The new phase is structurally quite similar to an ice phase originally found to be a precursor in the course of the homogeneous nucleation of ice VII in liquid water. A part of the water molecules in these ice phases can rotate easily because the number of hydrogen bonds in them is less than four, and thus they can be regarded as partial plastic phases. A rough estimate suggests that these phases are thermodynamically more stable than either ice VI or ice VII for 3 GPa < P < 18 GPa at T = 300 K. Although the partial plastic phases would be metastable states at any point in the phase diagram of real water, they might be realized experimentally with the aid of dopants and/or solid surfaces.

摘要

我们在 TIP4P/2005 水的分子动力学模拟中报告了一种在冰 VII 和液态水界面上自发形成的新冰相。该新相在结构上与在液态水中冰 VII 均匀成核过程中最初发现的冰相非常相似。这些冰相中部分水分子由于氢键数量少于四个,因此可以轻松旋转,因此它们可以被视为部分塑料相。粗略估计表明,在 T = 300 K 时,3 GPa < P < 18 GPa 的范围内,这些相在热力学上比冰 VI 或冰 VII 更稳定。尽管在实际水的相图的任何一点上,这些部分塑性相都将是亚稳状态,但它们可能在掺杂剂和/或固体表面的帮助下在实验中实现。

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