Excitons in wide nitride Quantum Wells (QWs) are naturally indirect due to the strong internal electric field: within such excitons the electron and the hole are spatially separated, resulting in strong dipole moments and long radiative lifetimes. These properties offer the possibility to explore the collective exitonic phases with complex phase diagrams predicted theoretically in the temperature-density-dipole moment parameter space. Here we study 8 nm-wide GaN/(AlGa)N QWs presenting 1MV/cm built-in electric field in the growth direction, microsecond-long radiative lifetimes, 8 meV exciton emission linewidth and 100 µm transport lengths at cryogenic temperatures. To address the quasi-equilibrium properties of the strongly dipolar excitons (i.e. whose electric dipoles are twice as long as their Bohr radii d = 2aB), we confine them in the QW’s plane using electrostatic traps with a semi-transparent Schottly electrode. These traps consist in semitransparent electrodes deposited on the sample’s surface. We make micro-photoluminescence (µPL) measurements (less than 1µm- resolution) upon point-like optical excitation. We thus obtain the spectrally resolved information on the emission of the excitons as a function of power and density. Our experiments demonstrate an efficient trapping of excitons in the plane of the QW, with a trapping potential of an order of 50 meV. We demonstrate that it is possible to uniformly fill areas up to hundreds of microns in length with excitons and/or electron hole pairs in the QW’s plane. At T=4K, the emission from these areas exhibits a peculiar behavior. At low densities, such that there is no measurable screening of the built-in electric field, the emission from the trap is weak and spatially homogeneous. However, for weak built-in electric field screenings (as low as 10 meV, ~1011 cm-2 pair density), the PL brightens up and becomes spatially inhomogeneous – droplet like. We tentatively interpret this fragmentation as the coexistence of the gas and liquid phases of the excitons. As expected, the fragmented character of the emission disappears when either power and/or temperature is further increased, due to either exciton heating (gas phase), ionization or dissociation (Mott transition). Our results suggest that excitons in GaN QWs are promising candidates for the study of collective phenomena in cold dipolar bosonic systems. The advantages of the nitrides over arsenides include both higher critical temperatures for the onset of collective phenomena, and the ability to increase the dipolarity of systems based on their small exciton Bohr radius.

We investigate both entanglement and energy transport properties for two-level systems in the vicinity of a photonic topological insulator (PTI) interface, which supports a nonreciprocal (unidirectional), scattering-immune and topologically-protected surface plasmon polariton in the bandgap of the bulk material. Moreover, we demonstrate that despite the presence of considerable imperfections at the interface of the PTI, the efficiency of the SPP-assisted energy transport is almost unaffected by discontinuities. We also show that the SPP properties allow energy transport over considerably much larger distances then in the reciprocal case, and we point out a particularly simple way to tune the transport. Finally, we analyze the specific case of a two-emitter-chain and unveil the origin of the efficiency amplification. The efficiency amplification and the practical advantages highlighted in this work might be particularly useful in the development of new devices intended to manage energy at the atomic scale, e.g. in quantum technologies.

Some countries with rich textile industries are nowadays facing water quality issues as a consequence of impacting dye pollution. In addition to their inherent toxicity, dyes induce modification in water acidity or salinity which has harmful consequences on the photosynthesis of aquatic plants. As dye are hardly biodegradable, water treatment is necessary to get ride of them [1], and adsorption treatment appears as a good candidate with efficient low-cost adsorbents, such as clays [2]. As a matter of fact, lamellar materials are widely used for sorbtion of ions and molecules harmful for health and environment. In order to gain in efficiency in the use of such materials, it is essential to get a deeper understanding of the retention mechanisms at the interface solid/liquid. In this work, anionic clays, namely layered double hydroxides (LDH) have been chosen as model compounds in order to study sorption mechanism. The presence of charged layer induce strong anionic exchange capacity in these materials, moreover their composition and structual parameters are easily controled through mastered synthesis process [3]. This study work has been focused on the the mechanisms that can lead to the capture of polluting molecules. Several model dyes have been chosen (MethylOrange - MO, Carmen Indigo - CI et Orange G - OG) for their charge, symmetry and hydrophobicity. Parameters such as the solution concentration and the activity of the solvant, playing with the nature of ions, have also been explored.The work presented here rely on vibrational spectroscopies (Infrared and Raman spectroscopies) sensitive to the intermolecular interaction of the dye with its environment particularly at the interface solid/dye. In parallel, X-Ray Diffraction probes the structural modification in the clay during sorption.The experimental results interpreted though the help of simulations (Monte-Carlo, DFT), lead a fine description of ions sorption at the interfaces with these models lamellar materials.

Bridged silsesquioxane nanomaterials exhibit original mechanical properties thanks to the association of non-covalent and covalent interactions. Thanks to in situ high pressure spectroscopic studies, achieved in diamond anvil cells, the mechanical behavior of these materials was followed as a function of pressure. Figure 1: Schematic representation of bottom-up structuring in organic-inorganic hybrid silica through self-assembling process Vibrational studies on organic models coupled to ab-initio simulations show that H bond response to pressure is strengthening. In hybrid materials the H bond shows its ability to absorb the mechanical constrains by the modulation of H bond interactions. We thus show that the rigidity yielded by the inorganic polymerization is counterbalanced by the presence of the intermolecular H bond network. The hybrid materials have therefore a reversible behavior, thanks to h bonds behaving as molecular springs. For higher pressure ranges inorganic network start to be strongly impacted in a dominant way so that an irreversible loss of long range order within the organic network is observed.In a second time, the influence of the nature of the organic substructure (thiourea versus urea link, aryl versus aliphatic core) on this spring behavior is discussed.