If citing, it is advised that you check and use the publisher's definitive version for pagination, volume/issue, and date of publication details. And where the final published version is provided on the Research Portal, if citing you are again advised to check the publisher's website for any subsequent corrections.
It is well known that spin angular momentum of light, and therefore that of photons, is directly related to their circular polarization. Naturally, for totally unpolarized light, polarization is undefined and the spin vanishes. However, for nonparaxial light, the recently discovered transverse spin component, orthogonal to the main propagation direction, is largely independent of the polarization state of the wave.Here we demonstrate, both theoretically and experimentally, that this transverse spin survives even in nonparaxial fields (e.g., tightly focused or evanescent) generated from a totally unpolarized light source. This counterintuitive phenomenon is closely related to the fundamental difference between the degrees of polarization for 2D paraxial and 3D nonparaxial fields. Our results open an avenue for studies of spinrelated phenomena and optical manipulation using unpolarized light.
The spin angular momentum of light plays an important role in nonlinear interactions in optical systems with rotational symmetries. Here, the existence of the nonlinear geometric Berry phase is demonstrated in the four‐wave mixing process and applied to spin‐controlled nonlinear light generation from plasmonic metasurfaces. The polarization state of four‐wave mixing from the ultrathin metasurfaces, comprising gold meta‐atoms with four‐fold rotational symmetry, can be controlled by manipulating the spin of the excitation beams. The mutual orientation of the meta‐atoms in the metasurface influences the intensity of four‐wave mixing via the geometric phase effects. These findings provide novel solutions for designing metasurfaces for spin‐controlled nonlinear optical processes with inbuilt all‐optical switching.
While free electrons in metals respond to ultrafast excitation with refractive index changes on femtosecond time scales, typical relaxation mechanisms occur over several picoseconds, governed by electron-phonon energy exchange rates. Here, we propose tailoring these intrinsic rates by engineering a non-uniform electron temperature distribution through nanostructuring, thus, introducing an additional electron temperature relaxation channel. We experimentally demonstrate a sub-300 fs switching time due to the wavelength dependence of the induced hot electron distribution in the nanostructure. The speed of switching is determined by the rate of redistribution of the inhomogeneous electron temperature and not just the rate of heat exchange between electrons and phonons. This effect depends on both the spatial overlap between control and signal fields in the metamaterial and hot-electron diffusion effects. Thus, switching rates can be controlled in nanostructured systems by designing geometrical parameters and selecting wavelengths, which determine the control and signal mode distributions.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.