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Abstract Microswimmers are self‐propelled particles that navigate fluid environments, offering significant potential for applications in environmental pollutant decomposition, biosensing, and targeted drug delivery. Their performance relies on engineered catalytic surfaces. Gold nanoclusters (AuNCs), with atomically precise structures, tunable optical properties, and high surface area‐to‐volume ratio, provide a new optimal catalyst for enhancing microswimmer propulsion. Unlike bulk gold or nanoparticles, AuNCs may deliver tunable photocatalytic activity and increased catalytic specificity, making them ideal co‐catalysts for hybrid microswimmers. For the first time, this study combines AuNCs with TiO₂/Cr₂O₃Janus microswimmers, combining the unique properties of both materials. This hybrid system capitalizes on the tuned optical properties of AuNCs and their role as co‐catalysts with TiO₂, driving enhanced photocatalytic performance under ultraviolet (UV) excitation. Using motion analysis, it is shown that the AuNC‐microswimmers exhibit significantly greater propulsion and mean squared displacement (MSD) as compared to controls. These findings suggest that the integration of nanoclusters with semiconductor materials enables state of the art, light‐switchable microswimmers. These AuNC‐microswimmer systems may thus offer new opportunities for environmental catalysis and other applications, providing precise control over catalytic and motile behaviors at the microscale. 

Self-propelling, light-activated colloidal particles can be actuated in water alone. Here we study the effect of adding different amounts of a gold/palladium alloy to titanium dioxide-based, active colloids. We observe a correlation between alloy-thickness and the average speed of the particles, and we discover an intermediate thickness leads to the highest activity for this system. We argue that a non-continuous thin-film of the co-catalyst improves the efficiency of water-splitting at the surface of the particles, and in-turn, the performance of “fuel-free” self-propulsion. 

Abstract It is demonstrated how the strength of activation for photocatalytic, self‐propelled colloids can be enhanced with a constant, uniform magnetic field. When exposed to ultraviolet light and hydrogen peroxide, the titanium dioxide‐based colloids become actively propelled. Due to the iron oxide core, a uniform field oriented perpendicular to the surface where motion takes place causes the asymmetrically shaped particles to rotate, which consequently leads to an increase in activity. The field‐dependent dynamics of self‐propulsion is quantified, and a qualitative description of how this effect arises is proposed. Since the application of the field is easily reversible, modulating the field on‐and‐off serves as a de facto “switch” that controls particle behavior. 

Abstract Active colloidal microcrystallites capable of generating flow patterns around or through their porous network are introduced, which in combination with “free microspheres,” create self‐assembled active clusters with multiple moving parts. Fluid flow draws microspheres within a microcrystallite's local environment toward—and aggregate at—the edge of the microcrystallite, where the previously translational movement transitions to continuous spinning. These experiments show that the spinning frequency decreases with an increase in diameter and that when the center of mass of a spinning particle is shifted off‐center—here Janus spheres—a time‐varying angular frequency is observed. Weight‐anisotropy also leads to a particularly intriguing phenomenon, which manifests as the spontaneous realignment of the rotational axis to a preferential direction; this effect is attributed to a gravitropic self‐correcting mechanism. Thus, the dynamics of the self‐assembled active structure remains stable over long time periods, despite being subjected to significant noise, for example, Brownian forces.