In situ XRD and IR optical measurements demonstrate the coexistence of M₁ and R phases during the SMT transition of VO₂ thin films.

Electromagnetically induced transparency (EIT) is a pump-induced narrowband transparency window within an absorption line of the probe beam spectrum in an atomic system. In this paper we propose a way to bring together the all-dielectric metamaterials to have EIT-like effects and to optically tune the response by hybridizing them with a layer of a phase change material. We propose a design of the metamaterial based on Si nanoresonators that can support an EIT-like resonant response. On the top of the resonators we consider a thin layer of a chalcogenide phase change material, which we will use to tune the optical response. Our choice is Ge₂Sb₂Te₅ (GST), since it has two stable phases at room temperature, namely amorphous and crystalline, between which it can be switched quickly, nonvolatively and reversibly, sustaining a large number of switching cycles. They differ in optical properties, while still having moderately low losses in telecom range. Since such dielectric resonators do not have non-radiative losses of metals around 1550nm, they can lead to a high-Q factor of the EIT-like response in this range. Firstly, we optimize the starting structure so that it gives an EIT-like response at 1550 nm when the GST layer is in the amorphous state. Our starting design uses glass as a substrate, but we also consider implementation in SOI technology. If we then switch the thin layer of GST to its crystalline phase, which has higher losses, the EIT-like response is red shifted, providing around 10:1 contrast at 1550nm. This reversible tuning can be done with an ns visible pulsed laser. We discuss the results of the simulation of the dielectric metasurface for different configurations and the tuning possibility.

Chirality conferral is fundamental for understanding the origin of life, and it is of direct importance for synthesizing new pharmaceuticals in the face of growing antibiotic resistance. Human-made, self-assembling nanostructures replicate the biological chirality conferral processes utilizing covalent and non-covalent bonds. However, chirality conferral from one form of matter to another via electromagnetic fields is more subtle and less explored. Here we report chirality conferral between gold nanohelices and achiral molecules (crystal violet). This conferral enables the experimental observation of a physical effect predicted in 1979—hyper-Raman optical activity. To benefit from Fermi’s golden rule, the chirality conferral system was designed as doubly resonant, with the nanohelices and molecules resonating at the fundamental frequency and at the second-harmonic, respectively. We provide a theoretical framework for our results that expands the original mathematical formalism to include surface-enhanced hyper-Raman scattering and the chirality conferral process. Our results demonstrate that field-driven chirality conferral mechanisms are opening up entire fields of research, as exemplified by the discovery of a physical phenomenon.

Semiconductor nanostructures hybridized with metals have been known to offer new opportunities in nonlinear optics, plasmonics, lasing, biosensors; among them GaAs‐based nanowires (NWs) hybridized with gold can offer new functionalities, as chiral sensing and light manipulation, as well as circular polarization sources. This study investigates GaAs–AlGaAs–GaAs NWs fabricated by self‐catalyzed growth on Si substrates, and partially covered with gold, thus inducing the symmetry breaking and a potential chiral response. Three different samples are investigated, each of them with a different morphology, as the length and the overall diameter ranging from 4.6 to 5.19 µm and from 138 up to 165 nm, respectively. The samples are first characterized by measuring the absorption spectra by using a scattering‐free photoacoustic (PA) technique. Then, the circular dichroism (CD) is investigated by measuring PA absorption for circularly polarized light under different incident angles at 532 and 980 nm. An efficient CD is found for proper configurations, and results are in good agreement with extrinsic chiral theory predictions and numerical simulations. It is therefore proven that these samples exhibit chiral behavior, and can be further optimized. Moreover, PA technique can be used as an extremely sensitive and efficient technique to characterize their “extrinsic” chirality.

Nowadays, nanophotonics aims towards low-cost chip-scale devices that can tailor electromagnetic properties, one of which is the control of circular polarization at the nanoscale. Here, we demonstrate the chiral properties of metasurfaces produced by means of nanosphere lithography combined with tilted metal deposition. We apply the photo-acoustic technique to characterize the circular dichroism (CD) at 633 nm of polystyrene nanospheres covered by three different metals: Au- and Cr-covered samples show extrinsic chiral behavior, while the Ag-covered sample shows CD at normal incidence, characteristic of intrinsic chirality. As the experimental data are in good agreement with numerical predictions, we believe that such design can be optimized to get efficient circularly polarized detection at the nanoscale.

III–V semiconductors nanowires (NW) have recently attracted a significant interest for their potential application in the development of high efficiency, highly-integrated photonic devices and in particular for the possibility to integrate direct bandgap materials with silicon-based devices. Here we report the absorbance properties of GaAs-AlGaAs-GaAs core-shell-supershell NWs using photo-acoustic spectroscopy (PAS) measurements in the spectral range from 300 nm to 1100 nm wavelengths. The NWs were fabricated by self-catalyzed growth on Si substrates and their dimensions (length ~5 μm, diameter ~140–150 nm) allow for the coupling of the incident light to the guided modes in near-infrared (IR) part of the spectrum. This coupling results in resonant absorption peaks in the visible and near IR clearly evidenced by PAS. The analysis reveal broadening of the resonant absorption peaks arising from the NW size distribution and the interaction with other NWs. The results show that the PAS technique, directly providing scattering independent absorption spectra, is a very useful tool for the characterization and investigation of vertical NWs as well as for the design of NW ensembles for photonic applications, such as Si-integrated light sources, solar cells, and wavelength dependent photodetectors.