Quorum sensing of light-activated colloids in nematic liquid crystals

TL;DR

This study introduces a novel experimental platform where light-activated colloids in nematic liquid crystals exhibit adaptive, quorum-sensing behaviors, enabling the creation of life-like, self-regulating materials through simple liquid crystal and colloid properties.

Contribution

The paper demonstrates how colloids can switch motion modes and adapt their motility based on crowding, revealing a new self-propulsion mechanism and quorum-sensing interactions in liquid crystal environments.

Findings

Colloids switch from directed to Brownian motion depending on anchoring.

Many-body dynamics show clustering via quorum sensing.

Active Brownian particle model describes single colloid motion under certain conditions.

Abstract

Motile living organisms routinely probe their surroundings to adapt in ever-evolving environments. Although synthetic microswimmers offer surrogates for self-propelled living entities, they often lack the complex feedback mechanisms that enable organisms to adapt. In this work, we present an experimental platform in which light-activated colloids dispersed in a nematic liquid crystal can (i) switch from directed to active Brownian motion depending on the nematic anchoring and (ii) mechanically adjust their motility in response to crowding, effectively enforcing quorum-sensing interactions. Both features are caused by a distinctive self-propulsion mechanism as unveiled through experiments, simulations, and theory. We characterize the dynamics of a single colloid and demonstrate that its motion is captured by an active Brownian particle model if the nematic anchoring is homeotropic, and by directed self-propulsion along the nematic director if the anchoring is planar. Next, we investigate the many-body dynamics, showing that it undergoes a clustering phase separation through effective quorum-sensing interactions. Our work suggests how to create adaptive materials with life-like capabilities using readily accessible properties of liquid crystals and colloids without explicitly engineering any of the needed mechano-chemical feedbacks.