A popular principle in designing chemical micromachines is to take advantage of asymmetric chemical reactions such as the catalytic decomposition of H2O2. Contrary to intuition, we use Janus micromotors half-coated with platinum (Pt) or catalase as an example to show that this ingredient is not sufficient in powering a micromotor into self-propulsion. In particular, by annealing a thin Pt film on a SiO2 microsphere, the resulting microsphere half-decorated with discrete Pt nanoparticles swims ∼80% more slowly than its unannealed counterpart in H2O2, even though they both catalytically produce comparable amounts of oxygen. Similarly, SiO2 microspheres half-functionalized with the enzyme catalase show negligible self-propulsion despite high catalytic activity toward decomposing H2O2. In addition to highlighting how surface morphology of a catalytic cap enables/disables a chemical micromotor, this study offers a refreshed perspective in understanding how chemistry powers nano- and microscopic objects (or not): our results are consistent with a self-electrophoresis mechanism that emphasizes the electrochemical decomposition of H2O2 over nonelectrochemical pathways. More broadly, our finding is a critical piece of the puzzle in understanding and designing nano- and micromachines, in developing capable model systems of active colloids, and in relating enzymes to active matter.

Spatiotemporal coordination of a nanorobot ensemble is critical for their operation in complex environments, such as tissue removal or drug delivery. Current strategies of achieving this task, however, rely heavily on sophisticated, external manipulation. We here present an alternative, biomimetic strategy by which oscillating Ag Janus micromotors spontaneously synchronize their dynamics as chemically coupled oscillators. By quantitatively tracking the kinetics at both an individual and cluster level, we find that synchronization emerges as the oscillating entities are increasingly coupled as they approach each other. In addition, the synchronized beating of a cluster of these oscillating colloids was found to be dominated by substrate electroosmosis, revealed with the help of an acoustic trapping technique. This quantitative, systematic study of synchronizing micromotors could facilitate the design of biomimetic nanorobots that spontaneously communicate and organize at micro- and nanoscales. It also serves as a model system for nonlinear active matter.

Traveling waves are common in biological and synthetic systems, including the recent discovery that silver (Ag) colloids form traveling motion waves in H 2 O 2 and under light. Here, we show that this colloidal motion wave is a heterogeneous excitable system. The Ag colloids generate traveling chemical waves via reaction-diffusion, and either self-propel through self-diffusiophoresis (“ballistic waves”) or are advected by diffusio-osmotic flows from gradients of neutral molecules (“swarming waves”). Key results include the experimental observation of traveling waves of OH − with pH-sensitive fluorescent dyes and a Rogers-McCulloch model that qualitatively and quantitatively reproduces the key features of colloidal waves. These results are a step forward in elucidating the Ag-H 2 O 2 -light oscillatory system at individual and collective levels. In addition, they pave the way for using colloidal waves either as a platform for studying nonlinear phenomena, or as a tool for colloidal transport and for information transmission in microrobot ensembles.