Hybrid plasmonic nanoemitters based on the combination of quantum dot emitters (QD) and plasmonic nanoantennas open up new perspectives in the control of light. However, precise positioning of any active medium at the nanoscale constitutes a challenge. Here, we report on the optimal overlap of antenna's near-field and active medium whose spatial distribution is controlled via a plasmon-triggered 2-photon polymerization of a photosensitive formulation containing QDs. Au nanoparticles of various geometries are considered. The response of these hybrid nano-emitters is shown to be highly sensitive to the light polarization. Different light emission states are evidenced by photoluminescence measurements. These states correspond to polarization-sensitive nanoscale overlap between the exciting local field and the active medium distribution. The decrease of the QD concentration within the monomer formulation allows trapping of a single quantum dot in the vicinity of the Au particle. The latter objects show polarization-dependent switching in the single-photon regime.

The objective of this study is to report a case of severe hypocalcemia secondary to hypoparathyroidism in a pregnant woman. We report a case of a 45-year-old woman who presented for tonico-clonic seizure in the third trimester of gestation. She was diagnosed with idiopathic hypoparathyroidism for the first time during pregnancy. She was successfully treated with calcium and calcitriol in the rest of her pregnancy with resolution of symptoms but her infant was born with hypercalcemia and secondary hyperparathyroidism due to the late maternal presentation. To the best of our knowledge, hypoparathyroidism is a disorder rarely observed during pregnancy, resulting in most cases from surgical thyroidectomy.

The integration of nanoparticles (NPs) into photonic devices and plasmonic sensors requires selective patterning of these NPs with fine control of their size, shape and spatial positioning. In this article, we report on a general strategy to pattern different types of NPs. This strategy involves the functionalization of photopolymers before their patterning by two-photon laser writing to fabricate micro-and nanostructures that selectively attract colloidal 2 NPs with suitable ligands, allowing their precise immobilization and organization even within complex 3D structures. Monolayers of NPs without aggregations are obtained and the surface density of NPs on the polymer surface can be controlled by changing either the time of immersion in the colloidal solution or the type of amine molecule chemically grafted on the polymer surface. Different types of NPs (gold, silver, polystyrene, iron oxide, colloidal quantum dots and nanodiamonds) of different sizes are introduced showing a potential towards nanophotonic applications. To validate the great potential of our method, we successfully demonstrate the integration of quantum dots within a gold nanocube with high spatial resolution and nanometer precision. The promise of this hybrid nano-source of light (plasmonic/polymer/QDs) as optical nanoswitch is illustrated through photoluminescence measurements under polarized exciting light.

A major challenge towards nanophotonics is the integration of nanoemitters on optical chips. Combining the optical properties of nanoemitters with the benefits of integration and scalability of integrated optics is still a major issue to overcome. In this work, we demonstrate the integration of nanoemitters positioned in a controlled manner onto a substrate and onto an optical ion-exchanged glass waveguide via direct laser writing based on two-photon polymerization. Our nanoemitters are colloidal CdSe/ZnS quantum dots (QDs) embedded in polymeric nanostructures. By varying the laser parameters during the patterning process, we make size-controlled QD-polymer nanostructures that were systematically characterized using optical and structural methods. Structures as small as 17 nm in height were fabricated. The well-controlled QD-polymer nanostructure systems were then successfully integrated onto a new photonic platform for nanophotonics made of an ion-exchanged waveguide. We show that our QDs maintain their light emitting quality after integration as verified by photoluminescence (PL) measurements. Ultimately, QD emission coupled to our waveguides is detected through a home-built fiber-edge coupling PL measurement setup. Our results show the potential for future integration of nanoemitters onto complex photonic chips.

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Gold nanocubes with tunable size and interparticle gap were produced by altering the spin-coating speed of PMMA/gold precursor dispersion on silicon substrate. Then, their optical properties were provided by spectroscopic ellipsometry measurements.

We present a general strategy for incorporating metallic precursors into ring-like nanostructures. The method is promising for the fabrication of multifunctional materials.

Three-dimensional (3D) photoluminescent crypto-images can be created by nanopatterning quantum dots (QDs) within a polymeric micro-object. A UV-sensitive photoresist, doped with (CdSe)ZnS core−shell QDs, is employed to fabricate fluorescent devices, by two-photon polymerization direct laser writing (TPP-DLW). In this work, we report on the expulsion of the majority of QDs from the irradiated area, caused by the crosslinking of the monomers, determining their accumulation on the photopolymer surface. At the same time, QDs get excited and trigger a surrounding thermal polymerization, leading to a variation of the spatial resolution of the fabricated structures. By opportunely combining these physical phenomena, it is possible to control the local density of QDs with nanometric resolution and, as a consequence, to tune the local photoemission of the fabricated polymeric structure. A photopolymer doped with five different concentrations of (CdSe)ZnS core−shell QDs is analyzed and tested. We define the best conditions to create nanostructures containing only few QDs to be integrated in optical devices, as well as to create 3D photoluminescent micro crypto-images. By TPP-DLW and one-photon lithography, a 3D fluorescent design can be concealed inside a polymeric microstructure that is swiftly fabricated using a photoresist. An example of a 3D crypto-image is shown to illustrate the technique.