2016/01/01 by Soree Kim, Sang-Won Park, YounJoon Jung
Chemical Engineering · Materials Science · Physics and Astronomy · #Block Copolymer Self-Assembly #Charge (physics) #Crossover #Ionic bonding #Ionic liquid #Ionic liquids properties and applications #Length scale #Material Dynamics and Properties #Molecular dynamics #Scale (ratio) #Supercooling #cond-mat.soft
paper · pdf · doi:10.1039/c5cp07368e
published as Physical Chemistry Chemical Physics 2016,18, 6486-6497
openalex publication_date 2016/01/01 · arxiv created 2016/03/09 · arxiv updated 2016/03/10 · openalex created_date 2016/06/24 · openalex updated_date 2026/08/05
We numerically investigate the dynamic heterogeneity and its length scale found in coarse-grained ionic liquid model systems. In our ionic liquid model systems, cations are modeled as dimers with a positive charge, while anions are modeled as monomers with a negative charge, respectively. To study the effect of the charge distributions on the cations, two ionic liquid models with different charge distributions are used and the model with a neutral charge is also considered as a counterpart. To reveal the heterogeneous dynamics in the model systems, we examine spatial distributions of displacement and time distributions of exchange and persistence times. All the models show a significant increase of the dynamic heterogeneity as the temperature is lowered. The dynamic heterogeneity is quantified via the well-known four-point susceptibility, χ4(t), which measures the fluctuations of a time correlation function. The dynamic correlation length is calculated by fitting the dynamic structure factor, S4(k,t), with the Ornstein-Zernike form at the time scale at which the dynamic heterogeneity reaches the maximum value. The obtained time and length scales exhibit a power law relation at the low temperatures, similar to various supercooled liquid models. In particular, the charged model systems show unusual crossover behaviors which are not observed in the uncharged model system. We ascribe the crossover behavior to the enhanced cage effect caused by charges on the particles.