Collective dynamics of chemo-mechanical colloidal chains with active tips

Abstract

We report a study of the emergent dynamics arising in two-dimensional suspensions of semi-flexible chains whose tip is chemically active, generating a phoretic field. By varying the chain length (number of monomers per chain $N_{pc}$), the area fraction $\varphi$, and the sign of the phoretic coupling $J_0$, we map out a rich non-equilibrium phase diagram in the presence of phoretic interactions. For repulsive phoretic interactions ($J_0>0$) between the chains, we find that short chains ($N_{pc}=2$) develop a transient chaotic flow state that crosses over at long times to a global polar flock with super-diffusive mean-squared displacement and long-ranged velocity correlations. Surprisingly, we find this state to have suppressed density fluctuations, indicating the emergence of hyperuniformity. At intermediate chain lengths ($N_{pc}\sim 4$-$8$), the repulsive chemical field drives chaotic mesoscale flows -- a dry route to active turbulence -- without the need for hydrodynamic interactions or steric alignment interactions. For attractive phoretic interactions ($J_0<0$), chains self-organise into hedgehog-like micellar aggregates with heads forming the core and flexible tails radiating outward, in structural analogy with amphiphile micellisation but driven entirely by non-equilibrium self-propulsion. A coarse-grained theory of a tip-emitting active rod predicts the onset of the flocking of dimers, though overestimates the presence of polar order for longer chains. Our results establish phoretic tip activity as a minimal, experimentally realisable mechanism for a spectrum of collective states hitherto attributed to hydrodynamic interactions or steric alignment.