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加热和压力诱导非晶态和六方冰的转变:使用 TIP4P/2005 模型的计算机模拟研究。

Heating- and pressure-induced transformations in amorphous and hexagonal ice: A computer simulation study using the TIP4P/2005 model.

机构信息

Department of Physics, Brooklyn College of the City University of New York, Brooklyn, New York 11210, USA.

出版信息

J Chem Phys. 2017 Aug 21;147(7):074505. doi: 10.1063/1.4998747.

Abstract

We characterize the phase behavior of glassy water by performing extensive out-of-equilibrium molecular dynamics simulations using the TIP4P/2005 water model. Specifically, we study (i) the pressure-induced transformations between low-density (LDA) and high-density amorphous ice (HDA), (ii) the pressure-induced amorphization (PIA) of hexagonal ice (I), (iii) the heating-induced LDA-to-HDA transformation at high pressures, (iv) the heating-induced HDA-to-LDA transformation at low and negative pressures, (v) the glass transition temperatures of LDA and HDA as a function of pressure, and (vi) the limit of stability of LDA upon isobaric heating and isothermal decompression (at negative pressures). These transformations are studied systematically, over a wide range of temperatures and pressures, allowing us to construct a P-T phase diagram for glassy TIP4P/2005 water. Our results are in qualitative agreement with experimental observations and with the P-T phase diagram obtained for glassy ST2 water that exhibits a liquid-liquid phase transition and critical point. We also discuss the mechanism for PIA of ice I and show that this is a two-step process where first, the hydrogen-bond network (HBN) is distorted and then the HBN abruptly collapses. Remarkably, the collapse of the HB in ice I occurs when the average molecular orientations order, a measure of the tetrahedrality of the HBN, is of the same order as in LDA, suggesting a common mechanism for the LDA-to-HDA and I-to-HDA transformations.

摘要

我们通过使用 TIP4P/2005 水模型进行广泛的非平衡分子动力学模拟来描绘玻璃态水的相行为。具体来说,我们研究了(i)低密度(LDA)和高密度非晶冰(HDA)之间的压力诱导转变,(ii)六方冰(I)的压力诱导非晶化(PIA),(iii)在高压下加热诱导的 LDA 到 HDA 转变,(iv)在低和负压力下加热诱导的 HDA 到 LDA 转变,(v)LDA 和 HDA 的玻璃化转变温度作为压力的函数,以及(vi)在等压加热和等温减压(在负压力下)时 LDA 的稳定性极限。这些转变在广泛的温度和压力范围内进行了系统研究,使我们能够构建玻璃态 TIP4P/2005 水的 P-T 相图。我们的结果与实验观察结果和获得的玻璃态 ST2 水的 P-T 相图定性一致,ST2 水表现出液相-液相转变和临界点。我们还讨论了冰 I 的 PIA 机制,并表明这是一个两步过程,首先是氢键网络(HBN)被扭曲,然后 HBN 突然崩溃。值得注意的是,冰 I 中 HB 的崩溃发生在平均分子取向有序时,这是 HBN 的四面体度的度量,与 LDA 中的有序度相同,这表明 LDA 到 HDA 和 I 到 HDA 转变的共同机制。

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