Theory of non-linear susceptibility and correlation length in glasses and liquids

被引:162
作者
Donati, C
Franz, S
Glotzer, SC
Parisi, G
机构
[1] Abdus Salam Int Ctr Theoret Phys, I-34100 Trieste, Italy
[2] NIST, Ctr Theoret & Computat Mat Sci, Gaithersburg, MD 20899 USA
[3] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[5] Univ Roma La Sapienza, I-00185 Rome, Italy
关键词
D O I
10.1016/S0022-3093(02)01461-8
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Within the framework of the effective potential theory of the structural glass transition, we calculate for the p-spin model and for a hard sphere liquid in the hypernetted chain approximation a static non-linear susceptibility related to a four-point density correlation function, and show that it diverges in mean field with exponent gamma = 1/2 as the critical temperature T-c is approached from below. When T-c is approached from above, we calculate for the p-spin model a time dependent non-linear susceptibility and show that there is a characteristic time where this susceptibility has a maximum, and that this time grows with decreasing T. This susceptibility diverges as T-c is approached from above, and has key features in common with a generalized susceptibility related to particle displacements, previously introduced to measure correlated particle motion in simulations of glass-forming liquids. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:215 / 224
页数:10
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