Glass-Like Phonon Dynamics and Thermal Transport in a GeTe Nano-Composite at Low Temperature.

In this work, the experimental evidence of glass-like phonon dynamics and thermal conductivity in a nanocomposite made of GeTe and amorphous carbon is reported, which is of interest for microelectronics, and specifically phase change memories. It is shown that, the total thermal conductivity is reduced by a factor of three at room temperature with respect to pure GeTe, due to the reduction of both electronic and phononic contributions. This latter, similarly to glasses, is small and weakly increasing with temperature between 100 and 300 K, indicating a mostly diffusive thermal transport and reaching a value of 0.86(7) Wm-1K-1 at room temperature. A thorough investigation of the nanocomposite's phonon dynamics reveals the appearance of an excess intensity in the low energy vibrational density of states, reminiscent of the Boson peak in glasses. These features can be understood in terms of an enhanced phonon scattering at the interfaces, due to the presence of elastic heterogeneities, at wavelengths in the 2-20 nm range. The findings confirm recent simulation results on crystalline/amorphous nanocomposites and open new perspectives in phonon and thermal engineering through the direct manipulation of elastic heterogeneities.

Localization of propagative phonons in a perfectly crystalline solid.

Perfectly crystalline solids are excellent heat conductors. Prominent counterexamples are intermetallic clathrates, guest-host systems with a high potential for thermoelectric applications due to their ultralow thermal conductivities. Our combined experimental and theoretical investigation of the lattice dynamics of a particularly simple binary representative, Ba(8)Si(46), identifies the mechanism responsible for the reduction of lattice thermal conductivity intrinsic to the perfect crystal structure. Above a critical wave vector, the purely harmonic guest-host interaction leads to a drastic transfer of spectral weight to the guest atoms, corresponding to a localization of the propagative phonons.

Mesophilic anaerobic digestion of several types of spent livestock bedding in a batch leach-bed reactor: substrate characterization and process performance.

Spent animal bedding is a valuable resource for green energy production in rural areas. The properties of six types of spent bedding collected from deep-litter stables, housing either sheeps, goats, horses or cows, were compared and their anaerobic digestion in a batch Leach-Bed Reactor (LBR) was assessed. Spent horse bedding, when compared to all the other types, appeared to differ the most due to a greater amount of straw added to the litter and a more frequent litter change. Total solids content appeared to vary significantly from one bedding type to another, with consequent impact on the methane produced from the raw substrate. However, all the types of spent bedding had similar VS/TS (82.3-88.9)%, a C/N well-suited to anaerobic digestion (20-28, except that of the horse, 42) and their BMPs were in a narrow range (192-239NmLCH4/gVS). The anaerobic digestion in each LBR was stable and the pH always remained higher than 6.6 regardless of the type of bedding. In contrast to all the other substrates, spent goat bedding showed a stronger acidification resulting in a methane production lag phase. Finally, spent bedding of different origins reached, on average, (89±11)% of their BMP after 60days of operation. This means that this waste is well-suited for treatment in LBRs and that this is a promising process to recover energy from dry agricultural waste.

High pressure study of Li-doped fullerides, Li(x)C60 (x = 4,12), by x-ray diffraction and Raman spectroscopy.

In this article we study the alkali metal-intercalated 2D polymeric Li4C60 and the monomeric Li12C60 under pressure up to 40 GPa at room temperature, using x-ray diffraction and Raman spectroscopy. Li4C60 undergoes several transitions in the studied pressure range. At pressures lower than 8 GPa, we observed changes in both diffraction patterns and Raman scattering spectra, probably due to the displacement of Li atoms. At 8 GPa another structural and electronic transition occurs. We observe an enhancement of background and a broadening of diffraction peaks. Raman modes weaken and broaden considerably. An important structural transition occurs at around 16 GPa, in which new Raman bands exhibit features similar to those of a reported 3D C60 polymeric structure. The XRD data shows a collapse in volume with the simultaneous formation of amorphous material. The cell parameters deviate from their early pressure evolution and become less compressible. The high pressure study of highly doped monomeric Li12C60 shows that its structural integrity is retained up to 13 GPa, with increasing pressure-induced structural distortion and disorder. Above 13 GPa, Li12C60 transforms to a highly disordered state.