In the present work, with the intent of exploring the out-of-equilibrium polymerization of active patchy particles in linear chains, we study a suspension of active bivalent Brownian particles (ABBPs). At all studied temperatures and densities, ABBPs self-assemble in aggregating chains, as opposed to the uniformly space-distributed chains observed in the corresponding passive systems. The main effect of activity, other than inducing chain aggregation, is to reduce the chain length and favour alignment of the propulsion vectors in the bonding process. At low activities, attraction dominates over activity in the bonding process, leading self-assembly to occur randomly regardless of the particle orientations. Interestingly, we find that at the lowest temperature, as density increases, chains aggregate forming a novel state: MISP, i.e., Motility-Induced Spirals, where spirals are characterised by a finite angular velocity. On the contrary, at the highest temperature, density and activity, chains aggregate forming a different novel state (a spinning crystalline cluster) characterised by a compact and hexagonal ordered structure, both translating and rotating. The rotation arises from an effective torque generated by the presence of competing domains where particles self-propel in the same direction.
Self-assembly of active bifunctional Brownian particles / Landi, Caterina; Russo, John; Sciortino, Francesco; Valeriani, Chantal. - In: SOFT MATTER. - ISSN 1744-683X. - (2024). [10.1039/d4sm00805g]
Self-assembly of active bifunctional Brownian particles
Russo, John;Sciortino, Francesco;Valeriani, Chantal
2024
Abstract
In the present work, with the intent of exploring the out-of-equilibrium polymerization of active patchy particles in linear chains, we study a suspension of active bivalent Brownian particles (ABBPs). At all studied temperatures and densities, ABBPs self-assemble in aggregating chains, as opposed to the uniformly space-distributed chains observed in the corresponding passive systems. The main effect of activity, other than inducing chain aggregation, is to reduce the chain length and favour alignment of the propulsion vectors in the bonding process. At low activities, attraction dominates over activity in the bonding process, leading self-assembly to occur randomly regardless of the particle orientations. Interestingly, we find that at the lowest temperature, as density increases, chains aggregate forming a novel state: MISP, i.e., Motility-Induced Spirals, where spirals are characterised by a finite angular velocity. On the contrary, at the highest temperature, density and activity, chains aggregate forming a different novel state (a spinning crystalline cluster) characterised by a compact and hexagonal ordered structure, both translating and rotating. The rotation arises from an effective torque generated by the presence of competing domains where particles self-propel in the same direction.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.