The physics of the colloidal glass transition

被引:472
作者
Hunter, Gary L. [1 ]
Weeks, Eric R. [1 ]
机构
[1] Emory Univ, Dept Phys, Math & Sci Ctr, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
HARD-SPHERE COLLOIDS; MODE-COUPLING-THEORY; DYNAMIC LIGHT-SCATTERING; SPATIALLY HETEROGENEOUS DYNAMICS; DIFFUSING-WAVE SPECTROSCOPY; DIGITAL VIDEO MICROSCOPY; FLUCTUATION-DISSIPATION RELATION; DENSITY CORRELATION-FUNCTION; COMPRESSED EMULSION SYSTEM; LENNARD-JONES MIXTURE;
D O I
10.1088/0034-4885/75/6/066501
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
As one increases the concentration of a colloidal suspension, the system exhibits a dramatic increase in viscosity. Beyond a certain concentration, the system is said to be a colloidal glass; structurally, the system resembles a liquid, yet motions within the suspension are slow enough that it can be considered essentially frozen. For several decades, colloids have served as a valuable model system for understanding the glass transition in molecular systems. The spatial and temporal scales involved allow these systems to be studied by a wide variety of experimental techniques. The focus of this review is the current state of understanding of the colloidal glass transition, with an emphasis on experimental observations. A brief introduction is given to important experimental techniques used to study the glass transition in colloids. We describe features of colloidal systems near and in glassy states, including increases in viscosity and relaxation times, dynamical heterogeneity and ageing, among others. We also compare and contrast the glass transition in colloids to that in molecular liquids. Other glassy systems are briefly discussed, as well as recently developed synthesis techniques that will keep these systems rich with interesting physics for years to come.
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页数:30
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