No abstract

Chiral plasmonic nanostructures with tunable handedness-dependent absorption in the visible and infrared offer chiro-optical control at the nanoscale. Moreover, coupling them with emitting layers could lead to chiral nanosources, important for nanophotonic circuits. Here, we propose plasmonic elliptical nanohole arrays (ENHA) for circularly dependent near-infrared and visible emission. We first investigate broadband chiral behavior in an Au-ENHA embedded in glass by exciting it with plane waves. We then study the coupling of ENHA with a thin emitting layer embedded in glass; we focus on the emission wavelengths which provided high chirality in plane-wave simulations. Our novel simulation set-up monitors the chirality of the far-field emission by properly averaging a large set of homogeneously distributed, randomly oriented quantum sources. The intrinsic chirality of ENHA influences the circular polarization degree of the emitting layer. Finally, we study the emission dependence on the field distribution at the excitation wavelength. We demonstrate the chiral absorption and emission properties for Au-ENHA emitting in the near-infrared range, and for Ag-ENHA which is excited in green range and emits in the Lumogen Red range. The simple geometry of ENHA can be fabricated with low-cost nanosphere lithography and be covered with emission gel. We thus believe that this design can be of great importance for tunable chiral nanosources.

Chirality, the absence of mirror symmetry, governs behavior in most biologically important molecules, thus making the chiral recognition of great importance in the pharmaceutical and agrochemical industries, as well as medicine. Chiral molecules can be characterized by means of optical experiments based on chiro-optical excitation of molecules. Specifically, chiral absorptive materials differently absorb left- and right-circular polarized light, i.e., they possess circular dichroism (CD). Unfortunately, the natural CD of most molecules is very low and lies in the ultraviolet range. Fluorescence-detected CD is a fast and sensitive tool for investigation of chiral molecules which emit light; ultralow CD in absorption can be detected as the difference in emission. In this work, we perform fluorescence-detected CD on novel chiral amide compounds, designed specifically for visible green emission; we synthesize two enantiomeric fluorescent compounds using low-cost starting compounds and easy purification. We investigate different solutions of the enantiomers at different concentrations, and we show that the fluorescence of the intrinsically chiral compounds depends on the polarization state of the penetrating light, which is absorbed at 400 nm and emits across the green wavelength range. We believe that these compounds can be coupled with plasmonic nanostructures, which further shows promise in applications regarding chiral sensing or chiral emission.