Computer simulation study of surface wave dynamics at the crystal-melt interface

被引:26
|
作者
Benet, Jorge [1 ]
MacDowell, Luis G. [1 ]
Sanz, Eduardo [1 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Fis, E-28040 Madrid, Spain
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 141卷 / 03期
关键词
HOMOGENEOUS ICE NUCLEATION; MOLECULAR-DYNAMICS; FREE-ENERGY; POLYMER-SOLUTIONS; CAPILLARY; FLUCTUATIONS; GROWTH; MODES; WATER; CROSSOVER;
D O I
10.1063/1.4886806
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We study, by means of computer simulations, the crystal-melt interface of three different systems: hard-spheres, Lennard Jones, and the TIP4P/2005 water model. In particular, we focus on the dynamics of surface waves. We observe that the processes involved in the relaxation of surface waves are characterized by distinct time scales: a slow one related to the continuous recrystallization and melting, that is governed by capillary forces; and a fast one which we suggest to be due to a combination of processes that quickly cause small perturbations to the shape of the interface (e. g., Rayleigh waves, subdiffusion, or attachment/detachment of particles to/from the crystal). The relaxation of surface waves becomes dominated by the slow process as the wavelength increases. Moreover, we see that the slow relaxation is not influenced by the details of the microscopic dynamics. In a time scale characteristic for the diffusion of the liquid phase, the relaxation dynamics of the crystal-melt interface of water is around one order of magnitude slower than that of Lennard Jones or hard spheres, which we ascribe to the presence of orientational degrees of freedom in the water molecule. Finally, we estimate the rate of crystal growth from our analysis of the capillary wave dynamics and compare it with previous simulation studies and with experiments for the case of water. (C) 2014 AIP Publishing LLC.
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页数:14
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