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The high frequency dynamics of liquid iodine has been investigated by deep inelastic x-ray scattering at exchanged wave-vectors (q) ranging from 2.5 to 15 Å-1. The experimental data have been analyzed in the frame of the Sachs-Teller theory of the molecular spectrum while accounting for final state corrections to the lineshape. The performed data analysis carries insights on physical quantities as relevant as the mean rototranslational kinetic energy and the mean square Laplacian of the intermolecular potential. In both cases the measured values are consistent with corresponding theoretical expectations. [ABSTRACT FROM AUTHOR]

We measured the dynamic structure factor of the liquid and glassy phases of the LiCl–6H2O solution by means of inelastic scattering of radiation in the visible, UV, and x-ray range, between 1 GHz and 10 THz, and by means of photon-correlation spectroscopy, between 0.01 Hz and 20 kHz. The measurements were performed in the temperature range between 353 and 80 K. Our data show that a single-relaxation process exists at high temperature, which has features similar to those of the single relaxation of pure water. Upon cooling the system below ∼220 K, this single mode starts to differentiate two processes, a structural (α-) and a secondary (β-) relaxation. As the temperature is decreased, the β-relaxation is the vanishing continuation of the single, high-temperature process, while the onset of the α-relaxation occurs at the expense of the β-process. [ABSTRACT FROM AUTHOR]

We discuss the microscopic dynamics and structure of liquid hydrogen and deuterium, as probed by inelastic x-ray scattering measurements. Samples are kept in corresponding thermodynamic conditions, at which classical systems are expected to exhibit the same dynamic and static responses. On the contrary, we observe clear differences revealing the onset of quantum deviations, both in the broadening of inelastic excitations and in the position of the first sharp diffraction peak. These features are discussed, compared to path-integral Monte Carlo simulations, and finally associated with the different de Broglie wavelengths of the two isotopes. [ABSTRACT FROM AUTHOR]

The high frequency behavior of the dynamic structure factor, S(Q,ω), of liquid and supercritical neon is investigated by inelastic x-ray scattering at different temperatures and pressure. The spectral evolution is described in terms of a single-relaxation-time viscoelastic model. The occurrence of a positive dispersion in the sound velocity is clearly visible in both investigated thermodynamic phases. The anomalies in the dispersive behavior deeply reduce at the higher temperatures, probably, as a consequence of important changes in the first shell interactions. More generally, the atomic dynamics is dominated by a relaxation process whose time scale is in the range of fast microscopic degrees of freedom (approx. 10[sup -13] s), and whose strength and typical time scale stay constant over all the explored liquid and supercritical regions. © 2001 American Institute of Physics. [ABSTRACT FROM AUTHOR]

We measured the dynamic structure factor of the liquid and glassy phases of the LiCl-6H(2)O solution by means of inelastic scattering of radiation in the visible, UV, and x-ray range, between 1 GHz and 10 THz, and by means of photon-correlation spectroscopy, between 0.01 Hz and 20 kHz. The measurements were performed in the temperature range between 353 and 80 K. Our data show that a single-relaxation process exists at high temperature, which has features similar to those of the single relaxation of pure water. Upon cooling the system below approximately 220 K, this single mode starts to differentiate two processes, a structural (alpha-) and a secondary (beta-) relaxation. As the temperature is decreased, the beta-relaxation is the vanishing continuation of the single, high-temperature process, while the onset of the alpha-relaxation occurs at the expense of the beta-process.