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Anisotropic macromolecules exposed to non-equilibrium (active) noise are very common in biological systems, and an accurate understanding of their anisotropic dynamics is therefore crucial. Here, we experimentally investigate the dynamics of isolated chains assembled from magnetic microparticles at a liquid-air interface and moving in an active bath consisting of motile E. coli bacteria. We investigate both the internal chain dynamics and the anisotropic center-of-mass dynamics through particle tracking. We find that both the internal and center-of-mass dynamics are greatly enhanced compared to the passive case, i.e., a system without bacteria, and that the center-of-mass diffusion coefficient $D$ features a non-monotonic dependence as a function of the chain length. Furthermore, our results show that the relationship between the components of $D$ parallel and perpendicular with respect to the direction of the applied magnetic field is preserved in the active bath compared to the passive case, with a higher diffusion in the parallel direction, in contrast to previous findings in the literature. We argue that this qualitative difference is due to subtle differences in the experimental geometry and conditions and the relative roles played by long-range hydrodynamic interactions and short-range collisions.

Based on a microscopic approach, we propose a Lagrangian for the combined system of a rotating dielectric nanoparticle above a plane surface in the presence of electromagnetic vacuum fluctuations. In the framework of canonical quantization, the electromagnetic vacuum field is quantized in the presence of dielectric fields describing the nanoparticle and a semi-infinite dielectric with planar interface. The radiative heat power absorbed by the rotating nanoparticle is obtained and the result is in agreement with previous results when the the rotational frequency of the nanoparticle is zero or much smaller than the relaxation frequency of the dielectrics. The well known near field effect is reexamined and discussed in terms of the rotational frequency. The radiative heat power absorbed by the nanoparticle for well-known peak frequencies, is plotted in terms of the rotational frequency showing an interesting effect resembling a phase transition around a critical frequency, determined by the relaxation frequency of the dielectrics.

We demonstrate that a single sub-wavelength nanoaperture in a metallic thin film can be used to achieve dynamic optical trapping and control of a single dielectric nanowire. A nanoaperture can trap a nanowire, control its orientation when illuminated by a linearly-polarized incident field, and also rotate the nanowire when illuminated by a circularly-polarized incident field. Compared to other designs, this approach has the advantages of a low-power driving field entailing low heating and photodamage., Comment: 5 pages, 4 figures