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近临界温度下水超临界相的不同面貌:压力诱导的结构转变,从类气态流体到塑性晶体多晶型物

On the Different Faces of the Supercritical Phase of Water at a Near-Critical Temperature: Pressure-Induced Structural Transitions Ranging from a Gaslike Fluid to a Plastic Crystal Polymorph.

作者信息

Skarmoutsos Ioannis, Henao Andrés, Guardia Elvira, Samios Jannis

机构信息

Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, Vas. Constantinou 48, GR-116 35, Athens, Greece.

Dynamics of Condensed Matter and Center for Sustainable Systems Design, Department of Chemistry, University of Paderborn, Warburger Strasse 100, D-33098 Paderborn, Germany.

出版信息

J Phys Chem B. 2021 Sep 16;125(36):10260-10272. doi: 10.1021/acs.jpcb.1c05053. Epub 2021 Sep 7.

Abstract

The present study reports a systematic analysis of a wide variety of structural, thermodynamic, and dynamic properties of supercritical water along the near-critical isotherm of = 1.03 and up to extreme pressures, using molecular dynamics and Monte Carlo simulations. The methodology employed provides solid evidence about the existence of a structural transition from a liquidlike fluid to a compressed, tightly packed liquid, in the density and pressure region around 3.4ρ and 1.17 GPa, introducing an alternative approach to locate the crossing of the Frenkel line. Around 8.5 GPa another transition to a face-centered-cubic plastic crystal polymorph with density 5.178ρ is also observed, further confirmed by Gibbs free energy calculations using the two-phase thermodynamic model. The isobaric heat capacity maximum, closely related to the crossing of the Widom line, has also been observed around 0.8ρ, where the local density augmentation is also maximized. Another structural transition has been observed at 0.2ρ, related to the transformation of the fluid to a dilute gas at lower densities. These findings indicate that a near-critical isotherm can be divided into different domains where supercritical water exhibits distinct behavior, ranging from a gaslike one to a plastic crystal one.

摘要

本研究报告了一项系统分析,该分析利用分子动力学和蒙特卡洛模拟,研究了超临界水在 = 1.03 的近临界等温线以及直至极端压力下的各种结构、热力学和动力学性质。所采用的方法提供了确凿证据,证明在密度和压力约为 3.4ρ 和 1.17 GPa 的区域内,存在从类液态流体到压缩紧密液体的结构转变,引入了一种定位弗伦克尔线交叉点的替代方法。在约 8.5 GPa 处,还观察到向密度为 5.178ρ 的面心立方塑性晶体多晶型的另一种转变,使用两相热力学模型进行的吉布斯自由能计算进一步证实了这一点。与维德曼线交叉密切相关的等压热容最大值也在约 0.8ρ 处被观察到,此处局部密度增加也达到最大值。在 0.2ρ 处观察到另一种结构转变,这与流体在较低密度下转变为稀薄气体有关。这些发现表明,近临界等温线可分为不同区域,在这些区域中超临界水表现出不同行为,范围从类气态到塑性晶体态。

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