Optically Driven Janus Microengine with Full Orbital Motion Control.

Microengines have shown promise for a variety of applications in nanotechnology, microfluidics, and nanomedicine, including targeted drug delivery, microscale pumping, and environmental remediation. However, achieving precise control over their dynamics remains a significant challenge. In this study, we introduce a microengine that exploits both optical and thermal effects to achieve a high degree of controllability. We find that in the presence of a strongly focused light beam, a gold-silica Janus particle becomes confined at the stationary point where the optical and thermal forces balance. By using circularly polarized light, we can transfer angular momentum to the particle, breaking the symmetry between the two forces and resulting in a tangential force that drives directed orbital motion. We can simultaneously control the velocity and direction of rotation of the particle changing the ellipticity of the incoming light beam while tuning the radius of the orbit with laser power. Our experimental results are validated using a geometrical optics phenomenological model that considers the optical force, the absorption of optical power, and the resulting heating of the particle. The demonstrated enhanced flexibility in the control of microengines opens up new possibilities for their utilization in a wide range of applications, including microscale transport, sensing, and actuation.

Ordering of binary colloidal crystals by random potentials.

Structural defects are ubiquitous in condensed matter, and not always a nuisance. For example, they underlie phenomena such as Anderson localization and hyperuniformity, and they are now being exploited to engineer novel materials. Here, we show experimentally that the density of structural defects in a 2D binary colloidal crystal can be engineered with a random potential. We generate the random potential using an optical speckle pattern, whose induced forces act strongly on one species of particles (strong particles) and weakly on the other (weak particles). Thus, the strong particles are more attracted to the randomly distributed local minima of the optical potential, leaving a trail of defects in the crystalline structure of the colloidal crystal. While, as expected, the crystalline ordering initially decreases with an increasing fraction of strong particles, the crystalline order is surprisingly recovered for sufficiently large fractions. We confirm our experimental results with particle-based simulations, which permit us to elucidate how this non-monotonic behavior results from the competition between the particle-potential and particle-particle interactions.

Clustering of Janus particles in an optical potential driven by hydrodynamic fluxes.

Self-organisation is driven by the interactions between the individual components of a system mediated by the environment, and is one of the most important strategies used by many biological systems to develop complex and functional structures. Furthermore, biologically-inspired self-organisation offers opportunities to develop the next generation of materials and devices for electronics, photonics and nanotechnology. In this work, we demonstrate experimentally that a system of Janus particles (silica microspheres half-coated with gold) aggregates into clusters in the presence of a Gaussian optical potential and disaggregates when the optical potential is switched off. We show that the underlying mechanism is the existence of a hydrodynamic flow induced by a temperature gradient generated by the light absorption at the metallic patches on the Janus particles. We also perform simulations, which agree well with the experiments and whose results permit us to clarify the underlying mechanism. The possibility of hydrodynamic-flux-induced reversible clustering may have applications in the fields of drug delivery, cargo transport, bioremediation and biopatterning.

Electro- and photosensitive azopolymer for alignment of liquid crystals.

We report an electro- and photosensitive metal containing polymer material for alignment of liquid crystals (LCs). Irradiation with polarized light and/or application of dc-field result in an anisotropy of the polymer and formation of an easy orientation axes of a LC on the polymer surface. The light-induced anisotropy of the polymer and the LC anchoring on the polymer surface can be controlled by the low dc-field at room temperature.

Formation of liquid-crystal cholesteric pitch in the centimeter range.

The formation of a macroscopic cholesteric spiral in a nematic liquid crystal (LC) doped with chiral molecules is studied. Measurements of the orientation of the disclination line formed in a LC θ-cell manufactured with one substrate having linear in-plane alignment and the opposing substrate having circular alignment showed the formation of a uniform macroscopic cholesteric spiral with a pitch length of centimeters. We found a linear dependence of the reciprocal pitch p(-1) on the concentration c in a wide range of p, extending from micrometers up to several centimeters. It suggests that the pitch of a spiral in a nematic LC doped with chiral dopants results from a long-range orientation owing to short-range chiral interactions in the vicinity of the chiral additive.