Single-particle dynamics near the glass transition of a metallic glass

被引:12
|
作者
Lu, Y. J. [1 ]
Wang, W. H. [2 ]
机构
[1] Beijing Inst Technol, Sch Phys, Beijing 100081, Peoples R China
[2] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
LENNARD-JONES LIQUID; CU-ZR ALLOYS; FORMING LIQUIDS; STRUCTURAL RELAXATION; SUPERCOOLED LIQUIDS; MOLECULAR-DYNAMICS; TEMPERATURE; MOTION; DIFFUSION; POLYMERS;
D O I
10.1103/PhysRevE.94.062611
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
The single-particle dynamics of the glass-forming Cu50Zr50 alloy, from the supercooled liquid well above the glass-transition temperature, T-g to the glassy state, is studied by using the molecular dynamics simulations. When the liquid is cooled below 1.2 T-g, the dynamics heterogeneity characterized by the cage-jump motion becomes increasingly pronounced. The analyses based on the continuous time random walk method indicate that the liquid falls out of equilibrium in the present simulation time scale when it is cooled into the regime below 1.02 T-g. However, we find that the jump length and the jump rate do not display the non-equilibrium behaviors even in the glassy state below Tg, which allows us to study the intrinsic dynamic characteristics through Tg. The mean waiting time between two successive jumps has a rapid growth following the Vogel-Fulcher-Tammann law as the non-equilibrium regime is approached, in analogy with the temperature behaviors of transport properties for fragile supercooled liquids. In contrast, the jump rate maintains the Arrhenius decay and the jump length has even a weaker temperature dependence when the liquid is cooled into glassy state. We find that a pronounced enhancement of the spatial correlation of jumps occurs accompanied by the glass transition: the string-like cooperative jumps dominate the fast motion instead of the uncorrelated and individual jumps. Our work offers an insight into the equilibrium effect of the single-particle dynamics in glass transition.
引用
收藏
页数:9
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