Emergence Of Directional Rotation In Optothermally Activated Colloidal System

TL;DR

This paper experimentally shows how directional rotation can emerge in optothermally activated colloidal systems, controlled by particle positioning and optical intensity, without using light's angular momentum.

Contribution

It introduces a novel mechanism for inducing and controlling rotational dynamics in colloids via localized optothermal effects, without relying on light's angular momentum.

Findings

Rotation direction can be controlled by colloid positioning.

Angular velocity depends on optical intensity and particle size.

Rotational dynamics arise from asymmetric temperature distribution.

Abstract

We experimentally demonstrate the emergence of directional rotation in thermally active-passive colloidal structures under optical confinement. The observed handedness of rotation of the structure can be controlled by changing the relative position of the constituent colloids. We show that the angular velocity of rotation is sensitive to the intensity of the incident optical fields and the size of the constituent colloidal entities. The emergence of rotational dynamics can be understood in the context of asymmetric temperature distribution in the system and the relative location of the active colloid, which creates a local imbalance of optothermal torques to the confined system. Our work demonstrates how localized optothermal fields lead to directional rotational dynamics without explicitly utilizing spin or orbital angular momentum of light. We envisage that our results will have implications in realizing Brownian engines, and can directly relate to rotational dynamics in biological and ecological systems.