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.

Spin noise spectroscopy is a new very promising technique for non-perturbative measurement of spin dynamics in semiconductors.I will show how the homodyne and heterodyne detection of spin noise allows us to extend the possibilities of spin noise. These possibilities we be illustrated with our recent results on q-selective detection of spin noise, and on nuclear spin thermometry.

A novel and simple method for the measurement of cloud point temperatures of solutions is presented. Cloud point determination , which is currently used to establish the phase diagrams of protein solutions, is indicative of proteins interactions and constitutes a useful tool for food products engineering. We describe a novel experimental setup that allows screening of a large number of physical-chemical conditions in one measurement and the determination of cloud point temperatures both above and below ambient temperature. We use a simple method to avoid solvent evaporation and condensation, so that the setup can be used for solutions prepared with a volatile solvent. We present the operating parameter range and the precision of the measurement. The optical properties of the system are calibrated with solutions of known transmittance, and the determination of cloud point temperatures is validated on a standard non-ionic surfactant solution. Finally, we demonstrate the efficiency of the method by determining the phase diagram of a wheat protein extract, soluble in a water/ethanol mixture. Complemented with differential scanning calorimetry measurements, the liquid-liquid phase transition can be determined up to a protein concentration of 250 g/L, a range inaccessible with conventional methods for this protein extract.

The paper will discuss the possibility for light spectroscopies, e.g. Brillouin Light Scat- tering or Raman Scattering, to locally monitor the densification of amorphous silica. It is indeed well-known that silica significantly densifies under high stresses, either elastically as for example during a high-pressure experiment in a diamond-anvil cell below about 10 GPa or plastically above that limit. Further, this elastic limit strongly depends on the temperature. Irradiation-induced density changes are also observed using ultra-short laser pulses, neutrons or other particles. All these different routes lead to substantial structural modifications which in turn alter the response of silica to light spectroscopy in a complex manner.

High-pressure Brillouin [1] and polarized Raman spectra [2] of vitreous silica are measured up to 8 GPa in diamond-anvil cell at room temperature. On one hand, Brillouin frequencies show that the well-known anomalous maximum in the pressure dependence of the compressibility is suppressed by He incorporation into the silica network. This shows that the elastic anomaly relates to the collapse of the largest interstitial voids in the structure. On the other hand, the combined use of either a nonpenetrating pressurizing medium-argon-or a penetrating one-helium and Neon, allows one to separate density from stress effects on the Raman frequencies.[1]C. Weigel, A. Polian, M. Kint, B. Ruffl ́e, M. Foret, and R. Vacher, Phys. Rev. Lett. 109, 245504 , 2012[2]C. Weigel, M. Foret, B. Hehlen, M. Kint, S. Cl ́ement, A. Polian, R. Vacher, and B. Ruffl ́e, Phys. Rev. B 93, 224303 , 2016