Minimal mechanism for flocking in phoretically interacting active particles
Arvin Gopal Subramaniam, Sagarika Adhikary, Rajesh Singh
TL;DR
This work identifies a minimal, deterministic mechanism for global polar order in phoretically interacting active particles, arising purely from chemo-repulsive torques and short-range excluded-volume repulsion to produce Chemorepulsive Liquid Flocks (CLF); adding long-range translational repulsion yields Chemorepulsive Crystalline Flocks (CCF). The authors develop a pair-collision sliding criterion, quantify density- and translation-dependent phase boundaries via dimensionless groups Λ_r and Λ_t, and supplement particle simulations with a continuum hydrodynamic stability analysis that reproduces the observed transition lines. They show distinct structural signatures in CLF versus CCF through pair correlations and hexatic order, and demonstrate robustness to long-range attractive translational interactions. The findings reveal a purely dynamical route to global polar order without explicit alignment, with potential implications for migrating cells and phoretic colloids in experimental settings.
Abstract
Coherent collective motion is a widely observed phenomenon in active matter systems. Here, we report a flocking transition mechanism in a system of chemically interacting active colloidal particles sustained purely by chemo-repulsive torques at low to medium densities. The basic requirements to maintain the global polar order are excluded volume repulsions and long-ranged repulsive torques. This mechanism requires that the time scale individual colloids move a unit length to be dominant with respect to the time they deterministically respond to chemical gradients, or equivalently, pair colloids sliding together a minimal unit length before deterministically rotating away from each other. Switching on the translational repulsive forces renders the flock a crystalline structure. Furthermore, liquid flocks are observed for a range of chemo-attractive inter-particle forces. Various properties of these two distinct flocking phases are contrasted and discussed. We complement these results with stability analysis of a hydrodynamic model, which admits the transition corresponding to destabilization of the flocking state observed in particle-based simulations.
