Dutta Suman, Chakrabarti J
S. N. Bose National Centre for Basic Sciences, Blcok-JD, Sector-III, Salt Lake, Kolkata 700 106, India.
Phys Chem Chem Phys. 2020 Aug 21;22(31):17731-17737. doi: 10.1039/d0cp02703k. Epub 2020 Aug 3.
Here we study the characteristic length scales in an aqueous suspension of a symmetric oppositely charged colloid subjected to a uniform electric field by Brownian dynamics simulations. We consider the in-plane structure in the presence of a sufficiently strong electric field where the like charges in the system form macroscopic lanes. We construct spatial correlation functions characterizing the structural order and that of particles of different mobilities in the plane transverse to the electric field at a given time. We call these functions equal time density correlation functions (ETDCFs). The ETDCFs between particles of different charges, irrespective of mobilities, are the structural ETDCFs, while those between particles of different mobilities are the dynamic ETDCFs. We extract the characteristic length of correlation by fitting the envelopes of the ETDCFs to exponential dependences. We find that the correlation length scales of the structural ETDCFs and the dynamic ETDCFs of the slow particles increase with time in a concurrent manner. This suggests that the clustering of particles tends to build up dynamically correlated slow particles in the plane transverse to the lanes. The ETDCFs can be measured for colloidal systems by directly following the particle motion by video-microscopy and may be useful to understand the patterns out of equilibrium.
在此,我们通过布朗动力学模拟研究了在均匀电场作用下对称的带相反电荷胶体的水悬浮液中的特征长度尺度。我们考虑在足够强的电场存在下的面内结构,此时系统中的同种电荷形成宏观通道。我们构建了空间相关函数,以表征给定时间在垂直于电场的平面内的结构有序性以及不同迁移率粒子的结构有序性。我们将这些函数称为等时密度相关函数(ETDCF)。不同电荷粒子之间的ETDCF,无论迁移率如何,都是结构ETDCF,而不同迁移率粒子之间的ETDCF则是动态ETDCF。我们通过将ETDCF的包络拟合为指数依赖关系来提取相关特征长度。我们发现,结构ETDCF和慢速粒子的动态ETDCF的相关长度尺度随时间同时增加。这表明粒子的聚集倾向于在垂直于通道的平面内动态构建相关的慢速粒子。通过视频显微镜直接跟踪粒子运动,可以测量胶体系统的ETDCF,这对于理解非平衡态模式可能是有用的。