Processing routes and characterization methods commonly used in carbon nanotubes research require agood dispersion of nanotubes in liquid media. In particular, single walled carbon nanotubes (SWNT) mustbe dispersed, preferably as individuals in order to tap their full potential in optical applications [1]. Onesensitive probe of dispersion is photoluminescence (PL), since it is quenched as long as semiconductingSWNT are bundled with metallic ones. However, the detailed interpretation of the mechanismsresponsible for PL and the relation between PL intensity and dispersion state are still a matter ofcontroversy [2].
In this work, we present new insights on the near infrared photoluminescence of aqueous suspensions ofSWNT stabilized by bile salts surfactants. In one hand, the dispersion of the nanotubes is probed byabsorption spectroscopy, where the absorption coefficient shows high sensitivity to nanotube exfoliation.On the other hand, we revisit the interpretation of the NIR-PL spectra, and we discuss the differentphysical mechanisms responsible of the PL, i.e. Direct Excitonic Transitions (DET), Exciton-PhononCoupling (EPC), and Exciton Energy Transfer (EET) between nanotubes [3-7]. Finally, we discuss thekinetics of PL as a function of sonication time and debundling/exfoliation of SWNT (Figure 1).
References
[1] S. M. Bachilo, et al. Science, 298 (2002). pp 2361-2366.
[2] V.C Moore, et al. Nano letters, 3 (2003). pp 1379-1382.
[3] T. Ando, J. Phys. Soc. Jpn, 66(4) (1997). pp. 1066-1073.
[4] J. Maultzsch, et al. PRB, 72(24) (2005). pp. 241402.
[5] F. Wang, et al. Science, 308(5723) 2005. pp. 838-841.
[6] S. Chou, et al. PRL, 94(12) (2005), pp. 127402.
[7] P. Tan, et al. PRL, 99(13) (2007) pp. 137402.

We investigate the dynamics of freely expanding liquid sheets prepared with fluids with different rheological properties, (i) viscous fluids with a zero-shear viscosity $\eta_0$ in the range $(1-1000) \, \mathrm{mPa.s}$ and (ii) viscoelastic Maxwell fluids whose elastic modulus, $G_0$, characteristic relaxation time, $\tau$, and zero-shear viscosity, $\eta_0=G_0 \tau$, can be tuned over several orders of magnitude. The sheets are produced by impacting a drop of fluid on a small cylindrical solid target. For viscoelastic fluids, we show that, when $\tau$ is shorter than the typical lifetime of the sheet ($\sim 10$ ms), the dynamics of the sheet is similar to that of Newtonian viscous liquids with equal zero-shear viscosity. In that case, for little viscous samples ($\eta_0 <\sim 30$ mPa.s), the maximal expansion of the sheet, $d_{\rm{max}}$, is independent of $\eta_0$, whereas for more viscous samples, $d_{\rm{max}}$ decreases as $\eta_0$ increases. We provide a simple model to account for the dependence of the maximal expansion of the sheet with the viscosity that is based on an energy balance between inertia, surface tension and viscous shear dissipation on the solid target, and which accounts well for our experimental data. By contrast, when $\tau$ is longer than the typical lifetime of the sheet, the behavior drastically differs. The sheet expansion is strongly enhanced as compared to that of viscous samples with comparable zero-shear viscosity, but is heterogeneous with the occurrence of cracks, revealing the elastic nature of the viscoelastic fluid.

This paper presents a survey of soft modes and their relationship to structural phase transitions. After introducing the concept of a soft mode, the origin of softening is considered from a lattice-dynamical point. The Landau theory approach to structural transitions is then discussed, followed by a generalization of the soft-mode concept through the use of the dynamic order-parameter susceptibility. The hyper-Raman spectra in the cubic phase of (Ba0.8Sr0.2)Ti-0.95(Zn1/3Nb2/3)(0.05)O-3 are studied with special emphasis on the lowest-frequency phonon mode. The spectral structure is found to change above the Curie temperature (303-873 K). Soft modes were put forward by Cochran and Anderson about 50 years ago as an explanation of structural phase transitions. Extending Landau's theory of phase transitions, their prediction was that the square of the frequency of the soft mode was proportional omega(0)(T)= C root T-T-C where T-c is the transition temperature.

We report on measurements in large quantum Hall devices, made of high-quality graphene grown by propane/hydrogen chemical vapor deposition on SiC. These devices, having all the properties of an ideal quantum electrical resistance standard, surpass state-of-the-art GaAs/AlGaAs devices by considerable margins in their operational conditions. The Hall resistance can be found accurately quantized within one part in 10(9) over a 10-T range of magnetic fields with a lower bound at 3.5 T, temperatures as high as 10 K, or currents as high as 0.5 mA. This simplification sets the superiority of graphene for accessible and low-cost primary resistance standards.

Research is in progress to incorporate nuclear waste in new matrices with high structural stability, resistance to thermal shock, and high chemical durability. Interactions with water are important for materials used as a containment matrix for the radio nuclides. It is indispensable to improve their chemical durability to limit the possible release of radioactive chemical species, if the glass structure is attacked by corrosion. By associating high structural stability and high chemical durability, silica glass optimizes the properties of a suitable host matrix. According to an easy sintering stage, nanoporous glasses such as xerogels, aerogels, and composite gels are alternative ways to synthesize silica glass at relatively low temperatures (approximate to 1,000-1,200 degrees C). Nuclear wastes exist as aqueous salt solutions and we propose using the open pore structure of the nanoporous glass to enable migration of the solution throughout the solid volume. The loaded material is then sintered, thereby trapping the radioactive chemical species. The structure of the sintered materials (glass ceramics) is that of nanocomposites: actinide phases (similar to 100 nm) embedded in a vitreous silica matrix. Our results showed a large improvement in the chemical durability of glass ceramic over conventional nuclear glass.