Emergent Synchronization and Defect Dynamics in Confined Chiral Active Suspensions

TL;DR

This study demonstrates that hydrodynamic interactions alone can induce self-organization, synchronization, and defect dynamics in confined chiral active suspensions, revealing a purely hydrodynamic pathway to complex collective behavior.

Contribution

The paper uncovers a new hydrodynamic mechanism for spontaneous synchronization and defect formation in chiral active matter without relying on explicit alignment or interparticle forces.

Findings

Hydrodynamic coupling drives self-assembly into dimers and hexatic lattices.

Synchronization occurs through hydrodynamic repulsion, tunable by Reynolds number.

Defect formation leads to long-range concentration gradients and vortex dynamics.

Abstract

Hydrodynamic interactions can generate rich emergent structures in active matter systems. Using large-scale hydrodynamic simulations, we demonstrate that hydrodynamic coupling alone can drive spontaneous self-organization across a hierarchy of spatial and temporal scales in confined suspensions of torque-driven particles at moderate Reynolds numbers. Spinners first self-assemble into dimers, which crystallize into a hexatic lattice and subsequently undergo a collective tilting instability. The resulting tilted dimers rotate and synchronize through hydrodynamic repulsion, which can be tuned by the Reynolds number. Upon synchronization, the polar director develops splay and bend deformations and nucleates topological defects with charges of $\pm1$. These defects induce long-wavelength concentration gradients and drive crystal vortex dynamics spanning hundreds of particle diameters. Our results reveal a purely hydrodynamic route to synchronization and defect-mediated dynamics in chiral active matter, without explicit alignment rules or interparticle forces.