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Anomalous segregation dynamics of self-propelled particles

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 Added by Enys Mones
 Publication date 2014
  fields Physics
and research's language is English




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A number of novel experimental and theoretical results have recently been obtained on active soft matter, demonstrating the various interesting universal and anomalous features of this kind of driven systems. Here we consider a fundamental but still unexplored aspect of the patterns arising in the system of actively moving units, i.e., their segregation taking place when two kinds of them with different adhesive properties are present. The process of segregation is studied by a model made of self-propelled particles such that the particles have a tendency to adhere only to those which are of the same kind. The calculations corresponding to the related differential equations can be made in parallel, thus a powerful GPU card allows large scale simulations. We find that the segregation kinetics is very different from the non-driven counterparts and is described by the new scaling exponents $zsimeq 1$ and $zsimeq 0.8$ for the 1:1 and the non-equal ratio of the two constituents, respectively. Our results are in agreement with a recent observation of segregating tissue cells emph{in vitro}.



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We study the glassy dynamics taking place in dense assemblies of athermal active particles that are driven solely by a nonequilibrium self-propulsion mechanism. Active forces are modeled as an Ornstein-Uhlenbeck stochastic process, characterized by a persistence time and an effective temperature, and particles interact via a Lennard-Jones potential that yields well-studied glassy behavior in the Brownian limit, obtained as the persistence time vanishes. By increasing the persistence time, the system departs more strongly from thermal equilibrium and we provide a comprehensive numerical analysis of the structure and dynamics of the resulting active fluid. Finite persistence times profoundly affect the static structure of the fluid and give rise to nonequilibrium velocity correlations that are absent in thermal systems. Despite these nonequilibrium features, for any value of the persistence time we observe a nonequilibrium glass transition as the effective temperature is decreased. Surprisingly, increasing departure from thermal equilibrium is found to promote (rather than suppress) the glassy dynamics. Overall, our results suggest that with increasing persistence time, microscopic properties of the active fluid change quantitatively, but the broad features of the nonequilibrium glassy dynamics observed with decreasing the effective temperature remain qualitatively similar to those of thermal glass-formers.
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