It is well-known that micro- and nanoparticles can move by phoretic effects in response to externally imposed gradients of scalar quantities such as chemical concentration or electric potential. A class of active colloids can propel themselves through aqueous media by generating local gradients of concentration and electrical potential via surface reactions. Phoretic active colloids can be controlled using external stimuli and can mimic collective behaviors exhibited by many biological swimmers. Low–Reynolds number physicochemical hydrodynamics imposes unique challenges and constraints that must be understood for the practical potential of active colloids to be realized. Here, we review the rich physics underlying the operation of phoretic active colloids, describe their interactions and collective behaviors, and discuss promising directions for future research.

Mitchell originally proposed that an asymmetric ion flux across an organism's membrane could generate electric fields that drive locomotion. Although this locomotion mechanism was later rejected for some species of bacteria, engineered Janus particles have been realized that can swim due to ion fluxes generated by asymmetric electrochemical reactions. Here we present governing equations, scaling analyses and numerical simulations that describe the motion of bimetallic rod-shaped motors in hydrogen peroxide solutions due to reaction-induced charge auto-electrophoresis. The coupled Poisson–Nernst–Planck–Stokes equations are numerically solved using Frumkin-corrected Butler–Volmer equations to represent electrochemical reactions at the rod surface. Our simulations show strong agreement with the scaling analysis and experiments. The analysis shows that electrokinetic locomotion results from electro-osmotic fluid slip around the nanomotor surface. The electroviscous flow is driven by electrical body forces which are generated from a coupling of a reaction-induced dipolar charge density distribution and the electric field it creates. The magnitude of the electroviscous velocity increases quadratically with the surface reaction rate for an uncharged motor, and linearly when the motor supports a finite surface charge.

Bimetallic rod-shaped nanomotors swim autonomously in hydrogen peroxide solutions. Here, we present a scaling analysis, computational simulations, and experimental data that show that the nanomotor locomotion is driven by fluid slip around the nanomotor surface due to electrical body forces. The body forces are generated by a coupling of charge density and electric fields induced by electrochemical reactions occurring on the nanomotor surface. We describe the dependence of nanomotor motion on the nanomotor surface potential and reaction-driven flux.

Catalytic bimetallic nanomotors can swim at 100 body lengths per second as well as pick up, haul, and release micrometer-scale cargo. The electrokinetic locomotion of bimetallic nanomotors is driven by the electrocatalytic decomposition of hydrogen peroxide. The motors are typically fabricated by electrodeposition-based template synthesis techniques that result in heterogeneous samples and require specialized knowledge of electrochemistry, a three-electrode potentiostat setup, cyanide-based chemistry, and porous membranes. This paper presents a rapid and facile method for fabrication of spherical bimetallic motors that only requires access to metal deposition equipment and commercially available microspheres. The resulting spherical motors swim at speeds comparable to rod-shaped motors with the same dimensions and composition. The spherical motors' velocity increases with fuel concentration and decreasing diameter.

This review article provides practical, experimentally relevant details on six common types of active colloids useful for soft matter research.