Although photons in vacuum are massless particles that do not appreciably interact with each other, significant interactions appear in suitable nonlinear media, leading to hydrodynamic behaviours typical of quantum fluids. Here, we show the generation and manipulation of vortex–antivortex pairs in a coherent gas of strongly dressed photons (polaritons) flowing against an artificial potential barrier created and controlled by a light beam in a semiconductor microcavity. The optical control of the polariton flow allows us to reveal new quantum hydrodynamical phenomenologies such as the formation of vortex pairs upstream from the optical barrier, a case of ultrashort time excitation of the quantum flow, and the generation of vortices with counterflow trajectories. Additionally, we demonstrate how to permanently trap and store quantum vortices hydrodynamically generated in the wake of a defect. These observations are supported by time-dependent simulations based on the non-equilibrium Gross–Pitaevskii equation.

Although optical technology provides the best solution for the transmission of information, all-optical devices must satisfy several qualitative criteria to be used as logic elements. In particular, cascadability is difficult to obtain in optical systems, and it is assured only if the output of one stage is in the correct form to drive the input of the next stage. Excitonpolaritons, which are composite particles resulting from the strong coupling between excitons and photons, have recently demonstrated huge non-linearities and unique propagation properties. Here we show that polariton fluids moving in the plane of the microcavity can operate as input and output of an all-optical transistor, obtaining up to 19 times amplification and demonstrating the cascadability of the system. Moreover, the operation as an AND/OR gate is shown, validating the connectivity of multiple transistors in the microcavity plane and opening the way to the implementation of polariton integrated circuits.

Great control over size, shape and optical properties is now possible in colloidal Cd-based nanocrystals, which has paved the way for many fundamental studies and applications. One popular example of such class of nanocrystals is represented by CdSe(spherical core)/CdS(rod shell) nanorods. These can be nearly monodisperse in size and shape and have strong and stable photoluminescence that is tunable in the visible range (mainly by varying the size of the CdSe core). The corresponding Zn-based core/shell nanorods would be good candidates for tunable emission in the blue-UV region. However, while the synthesis of ZnS nanocrystals with elongated shapes has been demonstrated based on the oriented-attachment mechanism, elongated ZnS shells are difficult to fabricate because the more common cubic phase of ZnS has a highly symmetric crystal structure. We report here a procedure based on a sequence of two cation exchange reactions, namely, Cd2+>Cu+ and then Cu+>Zn2+, by which we transform colloidal CdSe(core)/CdS(shell) nanorods first into into Cu 2Se/Cu 2S nanorods, which are then converted into blue-UV fluorescent ZnSe(core)/ ZnS(shell) nanorods. The procedure transfers the morphological and structural information of the initial Cd-based nanorods to the Zn-based nanorods. Therefore, the final nanoparticles are made by a ZnSe dot embedded in a rod-shaped shell of wurtzite ZnS. Since in the starting Cd-based nanorods the size of the CdSe core and the length of the CdS shell can be well controlled, the same holds for the final Zn-based rods. In the second step of the exchange reaction (Cu+>Zn2+), a large excess of Zn2+ ions added over the Cu+ ions present in the Cu2Se/Cu2S nanorods is the key requisite to obtain bright, band-edge emission (with quantum yields approaching 15%) with narrow line widths (approaching 75 meV). In these ZnSe/ZnS nanorods, photogenerated carriers appear to be more confined in the core region compared to their parent CdSe/CdS nanorods.

The nucleation of two kinds of crystalline nanoparticles, zinc sulfide (ZnS), and cadmium sulfide (CdS), is achieved directly into specific sites of polymer matrices after their irradiation with UV laser pulses. The starting samples consist of polymers doped with precursors of Zn or Cd thiolate that are proved to decompose after the absorption of UV light, resulting into the nanoparticles formation. The growth of the crystalline nanostructures is followed throughout the irradiation of the samples with successive incident pulses, by different methods, such as transmission electron microscopy, atomic force microscopy, confocal microscopy, and X-ray diffraction. Special attention is paid to the difference of the formation pathways of the two kinds of nanoparticles studied, because the Cd thiolate precursor exhibits much higher absorption efficiency than the Zn thiolate one, at the applied UV wavelength. Indeed, CdS nanoparticles become evident after the very first incident UV pulses, whereas the formation of ZnS nanocrystals requires rather prolonged irradiation, always through a macroscopically nondestructive procedure for the polymer matrix

We investigate the cross interactions in a two-component polariton quantum fluid coherently driven by two independent pumping lasers tuned at different energies and momenta. We show that both the hysteresis cycles and the on-off threshold of one polariton signal can be entirely controlled by a second polariton fluid. Furthermore, we study the ultrafast switching dynamics of a driven polariton state, demonstrating the ability to control the polariton population with an external laser pulse, in less than a few picoseconds. © 2012 American Physical Society.

Three fluorenone-derived two-photon fluorescent probes (TK) targeting the lysosomes (TK-Lyso) and mitochondria (TK-Mito1 and TK-Mito2) were synthesized by introducing different diphenylamine moieties into the fluorenone core. The TK dyes showed high biocompatibility and long-term retention, low cytotoxicity, large Stokes shift and good fluorescence quantum yield. The results of the present work disclose a class of organic dyes with potential wide applications as specific and efficient probes for lysosomes and mitochondria in the study of various biological processes.

The nanoscaling of metamaterial structures represents a technological challenge toward their application in the optical frequency range. In this work we demonstrate tailored chiro-optical effects in plasmonic nanohelices, by a fabrication process providing a nanometer scale control on geometrical features, that leads to a fine tuning of operation band even in the visible range. Helicoidal 3D nanostructures have been prototyped by a bottom-up approach based on focused ion and electron beam induced deposition, investigating resolution limits, growth control and 3D proximity effects as a function of the interactions between writing beam and deposition environment. The fabricated arrays show chiro-optical properties at the optical frequencies and extremely high operation bandwidth tailoring dependent on the dimensional features of these 3D nanostructures: with the focused ion beam we obtained a broadband polarization selection of about 600 nm and maximum dissymmetry factor up to 40% in the near-infrared region, while with the reduced dimensions obtained by the focused electron beam a highly selective dichroic band shifted toward shorter wavelengths is obtained, with a maximum dissymmetry factor up to 26% in the visible range. A detailed finite difference time domain model highlighted the role of geometrical and compositional parameters on the optical response of fabricated nanohelices, in good agreement with experimental results.

We report on photoconduction and optical properties of aligned assemblies of core-shell CdSe/CdS nanorods prepared by a seeded growth approach. We fabricate oriented layers of nanorods by drop casting the nanorods from a solution on substrates with prepatterned, micrometer-spaced electrodes and obtain nanorod alignment due to the coffee stain effect. The photoconductivity of the nanorod layers can be improved significantly by an annealing process under vacuum conditions. The spectral response of the photocurrent shows distinct features that can be assigned to the electronic level structure of the core-shell nanorods and that relate well to the spectra obtained by absorption measurements. We study assemblies of nanorods oriented parallel and perpendicular to the applied electric field by the combined use of photocurrent and photoluminescence spectroscopy. We obtain consistent results which show that charge carrier separation and transport are more efficient for nanorods oriented parallel to the electric field. We also investigate the light polarization sensitivity of the photocurrent for the oriented nanorod layers and observe higher conductivity in the case of perpendicular polarization with respect to the long axis of the nanorods.

Exciton-polaritons, composite particles resulting from the strong coupling between excitons and photons, have shown the capability to undergo condensation into a macroscopically coherent quantum state, demonstrating strong non-linearities and unique propagation properties. These strongly-coupled light-matter particles are promising candidates for the realization of semiconductor all-optical devices with fast time response and small energy consumption. Recently, quantum fluids of polaritons have been used to demonstrate the possibility to implement optical functionalities as spin switches, transistors or memories, but also to provide a channel for the transmission of information inside integrated circuits. In this context, the possibility to extend the range of light-matter interaction up to room temperature becomes of crucial importance. One of the most intriguing promises is to use organic Frenkel excitons, which, thanks to their huge oscillator strength, not only sustain the polariton picture at room temperature, but also bring the system into the unexplored regime of ultra-strong coupling. The combination of these materials with ad-hoc designed structures may allow the control of the propagation properties of polaritons, paving the way towards their implementation of the polariton functionalities in actual devices for opto-electronic applications.

Exciton-polaritons in semiconductors are quasi-particles which have recently shown the capability to undergo phase transition into a coherent hybrid state of light and matter. The observation of such quasi-particles in organic microcavities has attracted increasing attention for their characteristic of reaching condensation at room temperature. In this work, the emission properties of organic polaritons are demonstrated not to depend on the overlap between the absorption and emission states of the molecule and that the emission dynamics are modified in the strong coupling regime, showing a significant enhancement of the photoluminescence intensity as compared to the bare dye. This paves the way to the investigation of molecules with large absorption coefficients but poor emission efficiencies for the realization of polariton condensates and organic electrically injected lasers by exploiting strong exciton-photon coupling regimes.

In this work, we experimentally investigate the chiro-optical properties of 3D metallic helical systems at optical frequencies. Both single and triple-nanowire geometries have been studied. In particular, we found that in single-helical nanostructures, the enhancement of chiro-optical effects achievable by geometrical design is limited, especially with respect to the operation wavelength and the circular polarization conversion purity. Conversely, in the triple-helical nanowire configuration, the dominant interaction is the coupling among the intertwined coaxial helices which is driven by a symmetric spatial arrangement. Consequently, a general improvement in the g-factor, extinction ratio and signal-to-noise-ratio is achieved in a broad spectral range. Moreover, while in single-helical nanowires a mixed linear and circular birefringence results in an optical activity strongly dependent on the sample orientation and wavelength, in the triple-helical nanowire configuration, the obtained purely circular birefringence leads to a large optical activity up to 8°, independent of the sample angle, and extending in a broad band of 500 nm in the visible range. These results demonstrate a strong correlation between the configurational internal interactions and the chiral feature designation, which can be effectively exploited for nanoscale chiral device engineering.

We have investigated the optical properties ofcolloidal seed-grown CdSe (seed)/CdTe (arms) nanotetrapodsboth experimentally and computationally. The tetrapods exhibita type-II transition arising from electrons localized in the CdSeseed region and holes delocalized in the CdTe arms, along witha residual type-I recombination in long-arm tetrapods.Experimentsand theory helped to identify the origin of both types oftransitions and their size dependence. In particular, timeresolvedexperiments performed at 10 K evidenced a sizedependent,long living type-II radiative emission arising fromthe peculiar electron-hole wave function localization. Temperature-dependent photoluminescence (PL) studies indicate that, at high temperature (>150 K), the main process limiting the PLquantum efficiency of the type-I PL is thermal escape of the charge carriers through efficient exciton-optical phonon coupling. Thetype-II PL instead is limited both by thermal escape and by the promotion of electrons from the conduction band of the seed regionto that of the arms, occurring at T > 200 K.

A model for realistic InAs quantum dot composition profile is proposed and analyzed, consisting of a double region scheme with an In-rich internal core and an In-poor external shell, in order to mimic the atomic scale phenomena such as In-Ga intermixing and In segregation during the growth and overgrowth with GaAs. The parameters of the proposed model are derived by reproducing the experimentally measured polarization data. Further understanding is developed by analyzing the strain fields which suggests that the two-composition model indeed results in lower strain energies than the commonly applied uniform composition model.