Growing correlation length on cooling below the onset of caging in a simulated glass-forming liquid

被引:96
作者
Lacevic, N [1 ]
Starr, FW
Schroder, TB
Novikov, VN
Glotzer, SC
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[3] NIST, Ctr Theoret & Computat Mat Sci, Gaithersburg, MD 20899 USA
[4] NIST, Div Polymers, Gaithersburg, MD 20899 USA
[5] Johns Hopkins Univ, Dept Phys & Astron, Baltimore, MD 21210 USA
[6] Roskilde Univ, IMFUFA, DK-4000 Roskilde, Denmark
[7] Russian Acad Sci, Inst Automat & Electrometry, Novosibirsk 630090, Russia
来源
PHYSICAL REVIEW E | 2002年 / 66卷 / 03期
关键词
D O I
10.1103/PhysRevE.66.030101
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
We present a calculation of a fourth-order, time-dependent density correlation function that measures higher-order spatiotemporal correlations of the density of a liquid. From molecular dynamics simulations of a glass-forming Lennard-Jones liquid, we find that the characteristic length scale of this function has a maximum as a function of time which increases steadily beyond the characteristic length of the static pair correlation function g(r) in the temperature range approaching the mode coupling temperature from above. This length scale provides a measure of the spatially heterogeneous nature of the dynamics of the liquid in the alpha-relaxation regime.
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页数:4
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