Decoupling of rotation and translation at the colloidal glass transition

被引:0
|
作者
Geiger, John [1 ]
Grimm, Niklas [2 ]
Fuchs, Matthias [2 ]
Zumbusch, Andreas [1 ]
机构
[1] Univ Konstanz, Fachbereich Chem, D-78457 Constance, Germany
[2] Univ Konstanz, Fachbereich Phys, D-78457 Constance, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2024年 / 161卷 / 01期
关键词
ROUGH SPHERE FLUID; HARD-SPHERE; MOLECULAR-DYNAMICS; DIFFUSION; PARTICLE; LIQUIDS; SIMULATIONS; SUSPENSIONS; RELAXATION;
D O I
10.1063/5.0205459
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
In dense particle systems, the coupling of rotation and translation motion becomes intricate. Here, we report the results of confocal fluorescence microscopy where simultaneous recording of translational and rotational particle trajectories from a bidisperse colloidal dispersion is achieved by spiking the samples with rotational probe particles. The latter consist of colloidal particles containing two fluorescently labeled cores suited for tracking the particle's orientation. A comparison of the experimental data with event driven Brownian simulations gives insights into the system's structure and dynamics close to the glass transition and sheds new light onto the translation-rotation coupling. The data show that with increasing volume fractions, translational dynamics slows down drastically, whereas rotational dynamics changes very little. We find convincing agreement between simulation and experiments, even though the simulations neglect far-field hydrodynamic interactions. An additional analysis of the glass transition following mode coupling theory works well for the structural dynamics but indicates a decoupling of the diffusion of the smaller particle species. Shear stress correlations do not decorrelate in the simulated glass states and are not affected by rotational motion.
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页数:10
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