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Phase-change materials (PCMs) are the cornerstone for the development of reconfigurable and programmable photonic devices. Sb2S3 has been recently proposed as an interesting PCM due to its low-losses in the visible and near-IR. Here, we report the use of imaging polarimetry and spectroscopic ellipsometry to reveal and directly measure the optical properties of Sb2S3 both in crystalline and amorphous states obtained upon crystallization by annealing in the air of chemical bath deposited amorphous Sb2S3. The Mueller Matrix polarimetric analysis reveals the strong anisotropy of the Sb2S3 crystallites which crystallize in radial spherulitic domains in contrast to the optical isotropy of the amorphous films. A refractive index contrast of Δn = 0.5 is demonstrated while maintaining low-losses at telecommunications C-band, i.e., λ = 1550 nm.

Low-loss dielectric nanomaterials are being extensively studied as novel platforms for enhanced light-matter interactions. Dielectric materials are more versatile than metals when nanostructured as they are able to generate simultaneously electric- and magnetic-type resonances. This unique property gives rise to a wide gamut of new phenomena not observed in metal nanostructures such as directional scattering conditions or enhanced optical chirality density. Traditionally studied dielectrics such as Si, Ge or GaP have an operating range constrained to the infrared and/or the visible range. Tuning their resonances up to the UV, where many biological samples of interest exhibit their absorption bands, is not possible due to their increased optical losses via heat generation. Herein, we report a quantitative survey on the UV optical performance of 20 different dielectric nanostructured materials for UV surface light-matter interaction based applications. The near-field intensity and optical chirality density averaged over the surface of the nanoparticles together with the heat generation are studied as figures of merit for this comparative analysis.

Discrete dipole approximation (DDA) is a computational method broadly used to solve light scattering problems. In this work, we propose an extension of DDA that we call Chiral-DDA (CDDA), to study light-chiral matter interactions with the capability of describing the underlying physics behind. Here, CDDA is used to solve and analyze the interaction of a nanoantenna (either metallic or dielectric) with a chiral molecule located in its near field at different positions. Our method allowed to relate near field interactions with far field spectral response of the system, elucidating the role that the nanoantenna electric and magnetic polarizabilities play in the coupling with a chiral molecule. In general, this is not straightforward with other methods. We believe that CDDA has the potential to help researchers revealing some of the still unclear mechanisms responsible for the chiral signal enhancements induced by nanoantennas.

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