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.

Density and spin dynamics of indirect excitons in asymmetric GaAs/AlGaAs coupled quantum wells is studied by time-resolved photoluminescence. Under electric bias applied in the growth direction the lifetime of indirect excitons formed by an electron in a wide and hole in a narrow quantum well reaches 12 ns, while the circular polarisation lifetime is about 5 ns. The structure is suited for further studies of dark indirect excitons by time-resolved pump-probe spectroscopy

spin fluctuations in atomic vapors and in semiconductors. As such it is quite attractive for probing non-perturbatively electrons or nuclear spins in atomic vapours or in semiconductors, particularly when the laser is detuned from optical resonances, an aspect which has triggered considerable interest to spin noise spectroscopy in recent years. The signal in spin noise spectroscopy can be considered as arising from intensity fluctuations due to the interference between the light scattered by Raman spin-flip excitations and the probe laser. This suggests that homodyne or heterodyne detection of spin noise by mixing of the Raman signal with a local oscillator is feasible, which we have demonstrated recently [1]. This opportunity is essential to spin noise spectroscopy because it allows us to increase its sensitivity and accessible frequency range.Homodyne and/or heterodyne detection of spin noise for scattered light directions different from that of the probe should give access to spatio-temporal spin correlations [2], and therefore could considerably extend the application range of spin noise spectroscopy. Here we demonstrate non-collinear homodyne detection of spin noise in n-doped CdTe epilayers. This allows us to exploit different scattering geometries based on spin-flip Raman selection rules. We are able to measure simultaneously different fluctuating spin components by homodyne mixing in different space directions, and also for different local oscillator polarizations. [1] S. Cronenberger and D. Scalbert, Review of Scientific Instruments 87, 093111 (2016).[2] G. G. Kozlov, I. I. Ryzhov, and V. S. Zapasskii, Phys. Rev. A 95, 043810 (2017).

In the recent years the spectroscopy of spin noise has won its spurs for spin dynamics related studies in semiconductors, largely because it exhibits several quite attractive features. Noticeably it enables almost perturbation-free detection of spontaneous electron spin fluctuations. In addition as the amplitude of spin noise grows when the size of the probed region is reduced, it is well adapted for spatially resolved studies. Also the spin noise spectrum is quite sensitive to internal effective fields, which allows to probe locally the existence of nuclear fields. Finally, the combination of spin noise spectroscopy and optical heterodyning has been demonstrated, which permits enhanced sensitivity and broadband detection, while keeping a high spectral resolution [1].In this poster we will present results obtained by heterodyne detection of spin noise in an n-doped CdTe epilayer with donor density n∼3×〖10〗^17cm-3. Thanks to the enhanced sensitivity gained by heterodyne detection we could detect the spin noise of electrons bound to neutral donors for probe powers as low as 5 µW. In these conditions we observe an extremely slow hopping rate W0 of electron spin between neighbouring donors, and extremely slow electron spin relaxation rate s (see Figure 1). The observed noise spectrum at zero field is characteristic of electron spin precession in the frozen nuclear field acting on the electrons bound to the donors and exhibits two components. A central lorentzian line corresponding to the electron spin component along the nuclear field, and two satellites gaussian lines corresponding to the spin precession in the nuclear field. We analyze our results in the framework of a theoretical model, which takes into account both the electron spin precession, and the hopping between donors, but slightly modified to take into account an eventual non-zero nuclear spin polarization [2]. In agreement with the theory we can see that the satellites merge with the central line as the hopping rate increases (at the highest probe power). Surprisingly W0 and s become quite small at the lowest probe power. We find that the electron spin relaxation time becomes longer than 1 µs in this regime.