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水和其他玻璃形成液体中动态交叉现象的证据:实验、分子动力学模拟与理论

Evidence of dynamic crossover phenomena in water and other glass-forming liquids: experiments, MD simulations and theory.

作者信息

Chen S H, Zhang Y, Lagi M, Chong S H, Baglioni P, Mallamace F

机构信息

Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

J Phys Condens Matter. 2009 Dec 16;21(50):504102. doi: 10.1088/0953-8984/21/50/504102. Epub 2009 Nov 23.

Abstract

In a recent quasi-elastic neutron scattering experiment on water confined in a Portland cement paste, we find that this 3D confined water shows a dynamic crossover phenomenon at T(L) = 227 ± 5 K. The DSC heat-flow scan upon cooling and an independent measurement of specific heat at constant pressure of confined water in silica gel show a prominent peak at the same temperature. We show in this paper that this type of behavior is common to many other glassy liquids, which also show the crossover temperature in coincidence with the temperature of a small specific heat peak. We also demonstrate with MD simulations that the dynamic crossover phenomenon in confined water is an intrinsic property of bulk water, and is not due to the confinement effect. Recently, an extended version of the mode coupling theory (MCT) including the hopping effect was developed. This theory shows that, instead of a structural arrest transition at T(C) predicted by the idealized MCT, a fragile-to-strong dynamic crossover phenomenon takes place instead at T(C), confirming both the experimental and the numerical results. The coherent and incoherent α relaxation times can be scaled with the calculated viscosity, showing the same crossover phenomenon. We thus demonstrated with experiments, simulations and theory that a genuine change of dynamical behavior of both water and many glassy liquids happens at the crossover temperature T(L), which is 10-30% higher than the calorimetric glass transition temperature T(g).

摘要

在最近一项针对波特兰水泥浆体中受限水的准弹性中子散射实验中,我们发现这种三维受限水在T(L)=227±5 K时呈现出动态转变现象。冷却时的DSC热流扫描以及对硅胶中受限水的恒压比热的独立测量在相同温度下显示出一个显著的峰值。我们在本文中表明,这种行为在许多其他玻璃态液体中很常见,它们也在与小比热峰温度一致的温度下出现转变。我们还通过分子动力学模拟证明,受限水中的动态转变现象是 bulk 水的固有特性,并非由限制效应导致。最近,发展了一种包括跳跃效应的扩展版模式耦合理论(MCT)。该理论表明,在T(C)处发生的不是理想化MCT预测的结构冻结转变,而是从脆弱到强烈的动态转变现象,这证实了实验和数值结果。相干和非相干α弛豫时间可以用计算出的粘度进行标度,呈现出相同的转变现象。因此,我们通过实验、模拟和理论证明,水和许多玻璃态液体的动力学行为在转变温度T(L)处发生了真正的变化,该温度比量热玻璃化转变温度T(g)高10 - 30%。

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