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MD simulations of charged binary mixtures reveal a generic relation between high- and low-temperature behavior

机译:带电二元混合物的MD模拟显示高温和低温性能之间的通用关系

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Experimental studies of the glassy slowdown in molecular liquids indicate that the high-temperature activation energy E-infinity of glass-forming liquids is directly related to their glass transition temperature T-g. To further investigate such a possible relation between high- and low-temperature dynamics in glass-forming liquids, we analyze the glassy dynamics of binary mixtures using molecular dynamics simulations. We consider a binary mixture of charged Lennard-Jones particles and vary the partial charges of the particles and, thus, the high-temperature activation energy and the glass transition temperature of the system. Based on previous results, we introduce a phenomenological model describing relaxation times over the whole temperature regime from high temperatures to temperatures well inside the supercooled regime. By investigating the dynamics of both particle species on molecular and diffusive length scales along isochoric and isobaric pathways, we find a quadratic charge dependence of both E-infinity and T-g, resulting in an approximately constant ratio of both quantities independent of the underlying observable, the thermodynamic ensemble, and the particle species, and this result is robust against the actual definition of T-g. This generic relation between the activation energy and the glass transition temperature indicates that high-temperature dynamics and the glassy slowdown are related phenomena, and the knowledge of E-infinity may allow us to approximately predict T-g.
机译:对分子液体中玻璃态减速的实验研究表明,玻璃形成液体的高温活化能E无穷大与其玻璃化转变温度T-g直接相关。为了进一步研究玻璃形成液体中高温和低温动力学之间的这种可能关系,我们使用分子动力学模拟来分析二元混合物的玻璃态动力学。我们考虑了带电Lennard Jones粒子的二元混合物,改变了粒子的部分电荷,从而改变了系统的高温活化能和玻璃化转变温度。基于之前的结果,我们引入了一个唯象模型,描述了从高温到过冷区内部温度的整个温度区的弛豫时间。通过沿等容和等压路径在分子和扩散长度尺度上研究这两种粒子的动力学,我们发现E无穷大和T-g的二次电荷依赖性,导致这两个量的比例近似恒定,与潜在的可观测量、热力学系综和粒子种类无关,这一结果对T-g的实际定义是可靠的。活化能和玻璃化转变温度之间的一般关系表明,高温动力学和玻璃化减速是相关的现象,对E无穷大的了解可能使我们能够大致预测T-g。

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  • 来源
    《The Journal of Chemical Physics》 |2021年第2期|共9页
  • 作者单位

    Tech Univ Darmstadt Inst Phys Kondensierter Materie Hochschulstr 8 D-64289 Darmstadt Germany;

    Tech Univ Darmstadt Inst Phys Kondensierter Materie Hochschulstr 6 D-64289 Darmstadt Germany;

    Tech Univ Darmstadt Inst Phys Kondensierter Materie Hochschulstr 8 D-64289 Darmstadt Germany;

    Tech Univ Darmstadt Inst Phys Kondensierter Materie Hochschulstr 6 D-64289 Darmstadt Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
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