Colloidal rotation near the colloidal glass transition

被引:26
|
作者
Kim, Minsu [1 ]
Anthony, Stephen M. [2 ]
Bae, Sung Chul [3 ]
Granick, Steve [1 ,2 ,3 ]
机构
[1] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 135卷 / 05期
基金
美国国家科学基金会;
关键词
SPATIALLY HETEROGENEOUS DYNAMICS; MODULATED OPTICAL NANOPROBES; SUPERCOOLED LIQUIDS; RELAXATION; TERPHENYL; LENGTH;
D O I
10.1063/1.3623489
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We compare, using single-particle optical imaging, trajectories of rotation and translation for micron-sized spheres in index-matched colloidal suspensions near their glass transition. Rotational trajectories, while they show intermittent caged behavior associated with supercooled and glassy behavior, explore a sufficiently wider phase space such that in the averaged mean-square angular displacement there appears no plateau regime, but instead sub-Fickian angular diffusion that follows an apparent power law in time. We infer translation and rotation time constants, the former being the time to diffuse a particle diameter and the latter being the time to rotate a full revolution. Correlation between time constants increases with increasing volume fraction, but unlike the case for molecular glasses, the rotation time constant slows more weakly than the translation time. (c) 2011 American Institute of Physics. [doi:10.1063/1.3623489]
引用
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页数:4
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