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The active motion of phoretic colloids leads them to accumulate at boundaries and interfaces. Such an excess accumulation, with respect to their passive counterparts, makes the dynamics of phoretic colloids particularly sensitive to the presence of boundaries and pave new routes to externally control their single particle as well as collective behavior. Here we review some recent theoretical results about the dynamics of phoretic colloids close to and adsorbed at fluid interfaces in particular highlighting similarities and differences with respect to solid-fluid interfaces.
The dynamics of active colloids is very sensitive to the presence of boundaries and interfaces which therefore can be used to control their motion. Here we analyze the dynamics of active colloids adsorbed at a fluid-fluid interface. By using a mesosc
We explore the interfacial instability that results when a Newtonian fluid (a glycerol-water mixture, inner fluid) displaces a viscoelastic fluid (a dense cornstarch suspension, outer fluid) in a radial Hele-Shaw cell. As the ratio of viscosities of
Artificial phoretic particles swim using self-generated gradients in chemical species (self-diffusiophoresis) or charges and currents (self-electrophoresis). These particles can be used to study the physics of collective motion in active matter and m
We report experiments that show rapid crystallization of colloids tethered to an oil-water interface in response to laser illumination. This light-induced transition is due to a combination of long-ranged thermophoretic pumping and local optical bind
Microfluidic devices manufactured from soft polymeric materials have emerged as a paradigm for cheap, disposable and easy-to-prototype fluidic platforms for integrating chemical and biological assays and analyses. The interplay between the flow force