Probing the Equilibrium Dynamics of Colloidal Hard Spheres above the Mode-Coupling Glass Transition

被引:300
作者
Brambilla, G. [1 ,2 ]
El Masri, D. [1 ,2 ]
Pierno, M. [1 ,2 ]
Berthier, L. [1 ,2 ]
Cipelletti, L. [1 ,2 ]
Petekidis, G. [3 ]
Schofield, A. B. [4 ]
机构
[1] Univ Montpellier 2, Lab Colloides Verres & Nanomat, UMR 5587, F-34095 Montpellier, France
[2] CNRS, F-34095 Montpellier, France
[3] Univ Crete, IESL FORTH & Dept Mat Sci & Technol, GR-71110 Iraklion, Greece
[4] Univ Edinburgh, Sch Phys & Astron, Edinburgh EH9 3JZ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
SCATTERING FUNCTION; SUSPENSIONS; PARTICLES; LIQUIDS; SPECTROSCOPY; STATE;
D O I
10.1103/PhysRevLett.102.085703
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We use dynamic light scattering and computer simulations to study equilibrium dynamics and dynamic heterogeneity in concentrated suspensions of colloidal hard spheres. Our study covers an unprecedented density range and spans seven decades in structural relaxation time, tau(alpha), including equilibrium measurements above phi(c), the location of the glass transition deduced from fitting our data to mode-coupling theory. Instead of falling out of equilibrium, the system remains ergodic above phi(c) and enters a new dynamical regime where tau(alpha) increases with a functional form that was not anticipated by previous experiments, while the amplitude of dynamic heterogeneity grows slower than a power law with tau(alpha), as found in molecular glass formers close to the glass transition.
引用
收藏
页数:4
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