Abstract
At the single-particle level, the main difference between active colloids and passive ones is the time scale over which the motion crosses over from ballistic to diffusive regime. In both cases, friction coefficients or equivalently diffusion coefficients determine this time scale. For instance, the motion of a passive colloid of 1m radius is diffusive when observed over lag times longer than a microsecond, once the direction of its momentum has been randomized by collisions with solvent molecules. At the macroscopic scale these collisions are accounted for by the translational friction coefficient. For an active colloid the effective diffusive behavior observed over lag times larger than few seconds results from the randomization of the direction of self-propulsion by rotational diffusion. In this thesis we investigated the motion of an active Janus colloid trapped at air-water interface. Spherical catalytic Janus colloids have been prepared through the deposition of platinum metal at the surface of silica particles. Immersion depth of the Janus colloid as well as their orientation with respect to the water surface, has been characterized and interpreted in terms of the non-uniform wetting properties of the Janus particles. The motion of the active Janus colloids in the presence of various concentration of hydrogen peroxide H2O2 as fuel was characterized by video microscopy and the trajectories analyzed through the mean square displacement and the velocity autocorrelation function. The types of trajectories, directional and circular ones that we observed in our experiments, revealed the effective force and torque induced by the catalytic decomposition of H2O2. At the water surface, active colloids perform more persistent directional motions as compared to the motions performed in the bulk. This has been interpreted as due to the loss of degrees of freedom resulting from the confinement at interface and also to the partial wetting conditions that possibly bring new contributions to the rotational friction at interface.