Fast and slow crystal growth kinetics in glass-forming melts

被引:100
作者
Orava, J.
Greer, A. L. [1 ]
机构
[1] Tohoku Univ, WPI AIMR, Aoba Ku, 2-1-1 Katahira, Sendai, Miyagi 9808577, Japan
关键词
PHASE-CHANGE MATERIALS; LIQUID-METALS; VISCOSITY; CRYSTALLIZATION; SOLIDIFICATION; TEMPERATURE; NUCLEATION; TRANSITION; DIFFUSION; SELENIUM;
D O I
10.1063/1.4880959
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
Published values of crystal growth rates are compared for supercooled glass-forming liquids undergoing congruent freezing at a planar crystal-liquid interface. For the purposes of comparison pure metals are considered to be glass-forming systems, using data from molecular-dynamics simulations. For each system, the growth rate has a maximum value U-max at a temperature T-max that lies between the glass-transition temperature T-g and the melting temperature T-m. A classification is suggested, based on the lability (specifically, the propensity for fast crystallization), of the liquid. High-lability systems show "fast" growth characterized by a high U-max, a low T-max/T-m, and a very broad peak in U vs. T/T-m. In contrast, systems showing "slow" growth have a low Umax, a high T-max/T-m, and a sharp peak in U vs. T/T-m. Despite the difference of more than 11 orders of magnitude in U-max seen in pure metals and in silica, the range of glass-forming systems surveyed fit into a common pattern in which the lability increases with lower reduced glass-transition temperature (T-g/T-m) and higher fragility of the liquid. A single parameter, a linear combination of T-g/T-m and fragility, can show a good correlation with U-max. For all the systems, growth at Umax is coupled to the atomic/molecular mobility in the liquid. It is found that, across the diversity of glass-forming systems, T-max/T-g = 1.48 +/- 0.15. (C) 2014 AIP Publishing LLC.
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页数:10
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