The role of topological defects in the two-stage melting and elastic behavior of active Brownian particles

Abstract

We find that crystalline states of repulsive active Brownian particles at high activity melt into a hexatic state but this transition is not driven by an unbinding of bound dislocation pairs as suggested by the Kosterlitz-Thouless-Halperin-Nelson-Young (KTHNY) theory. Upon reducing the density, the crystalline state melts into a high-density hexatic state devoid of any defects. Decreasing the density further, the dislocations proliferate and introduce plasticity in the system, nevertheless maintaining the hexatic state, but eventually melting into a fluid state. Remarkably, the elastic constants of active solids are equal to those of their passive counterparts, as the swim contribution to the stress tensor is negligible in the solid state. The sole effect of activity is that the stable solid regime shifts to higher densities. Furthermore, discontinuities in the elastic constants as a function of density correspond to changes in the defect concentrations rather than to the solid-hexatic transition.

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• Extreme Spontaneous Deformations of Active Crystals
• Defects Superdiffusion and Unbinding in a 2D XY Model of Self-Driven Rotors
• Dynamic Overlap Concentration Scale of Active Colloids
• Active control of transport through nanopores