Universal Hydrodynamic Mechanisms for Crystallization in Active Colloidal Suspensions

Rajesh Singh and R. Adhikari
Phys. Rev. Lett. 117, 228002 – Published 23 November 2016
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Abstract

The lack of detailed balance in active colloidal suspensions allows dissipation to determine stationary states. Here we show that slow viscous flow produced by polar or apolar active colloids near plane walls mediates attractive hydrodynamic forces that drive crystallization. Hydrodynamically mediated torques tend to destabilize the crystal but stability can be regained through critical amounts of bottom heaviness or chiral activity. Numerical simulations show that crystallization is not nucleational, as in equilibrium, but is preceded by a spinodal-like instability. Harmonic excitations of the active crystal relax diffusively but the normal modes are distinct from an equilibrium colloidal crystal. The hydrodynamic mechanisms presented here are universal and rationalize recent experiments on the crystallization of active colloids.

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  • Received 17 June 2016

DOI:https://doi.org/10.1103/PhysRevLett.117.228002

© 2016 American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied PhysicsPolymers & Soft MatterStatistical Physics & Thermodynamics

Authors & Affiliations

Rajesh Singh* and R. Adhikari

  • The Institute of Mathematical Sciences-HBNI, CIT Campus, Chennai 600113, India

  • *rsingh@imsc.res.in
  • rjoy@imsc.res.in

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Issue

Vol. 117, Iss. 22 — 25 November 2016

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