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We present the state of the art in the realization of a new spectrometer especially designed for high resolution and high-contrast scattering experiments in the ultra-violet (UV) spectral region. Different scattering techniques, employing neutrons, X-rays or visible light are compared with each other for transferred energies and momenta. The importance of high-resolution measurements in the UV range is stressed with particular attention devoted to the study of disordered materials. [ABSTRACT FROM AUTHOR]

The presence of a fast-sound mode in the microscopic dynamics of the rare-gas mixture He-Ne, predicted by theoretical studies and molecular-dynamics simulations, was demonstrated by an inelastic neutron scattering experiment. In order to study the transition between the fast and the normal acoustic modes in the hydrodynamic regime, k values lower by about one order of magnitude than in the usual experiments have to be probed. We describe here the results of the first neutron Brillouin scattering experiment performed with this purpose on the same system already investigated at larger k. The results of both experiments, together with those of a new molecular-dynamics simulation, provide a complete and consistent description, still missing so far, of the onset of fast-sound propagation in a binary mixture. [ABSTRACT FROM AUTHOR]

We show that an exact solution of the generalized Langevin equation (GLE) for the autocorrelations of a many-body classical system can be given in an exponential functionality (EF) form. As a consequence, the power spectrum of the correlation has a Lorentzian functionality, i.e., is represented by an infinite sum of Lorentzian functions corresponding to the eigenmodes of the considered correlation. By means of the simple derivation of the GLE by M. H. Lee [Phys. Rev. B 26, 2547 (1982)], we also show that, in practical cases of interest to experimental spectroscopies, possible approximations of the EF are related to a reduction of the relevant dynamical variables via a restriction of the dimensions of the orthogonalized space onto which the dynamics of the system is projected., (© 2012 American Physical Society)

Five models for the site-site intermolecular pair interactions of methane are compared in some detail and used to investigate both structural and dynamical properties of the dense liquid deuteromethane by means of molecular dynamics (MD) simulations. The orientational distribution probabilities of molecular pairs are carefully analyzed for each anisotropic potential model. We propose a revision of existing classification methods used to group the innumerable relative orientations of methane-methane pairs into six basic geometries. With this new approach, our results for the probability of the six basic categories as a function of the intermolecular distance are different from the ones present in the literature, where the role of the angular spread on the anisotropic interaction energy is not taken in full consideration and certain configurations with no significant change in the pair-potential are assigned to different categories. The analysis of the static orientational correlations in liquid methane and the prevalence of certain configurations in different ranges guide the subsequent discussion of the MD model-dependent results for the dynamic structure factor. Comparison with our inelastic neutron scattering results for liquid CD(4) at the nanometer and picosecond space and time scales allows us to confirm the full adequacy of the Tsuzuki, Uchimaru and Tanabe model of 1998 with respect to more recent potentials., (© 2011 American Institute of Physics)

Molecular-dynamics calculations of the translational dynamic structure factor in liquid CO2 and CD4 are analyzed by means of the generalized Langevin equation for the intermediate scattering function in the second-order memory function approximation. We give a rigorous general relation among the decay times of the memory and the lifetimes of the modes of the density-density correlation function. The comparison of the various characteristic times among them and with the collision time, carried out as a function of the wave vector, reveals strong relationships between the memory relaxation and the density-density correlation modes, some of which have purely "collisional" and other "collective" character. We show that essential information about the life time of structural properties in a molecular liquid at nanometer dimensions can be obtained if the time behavior of the correlation function is considered in addition to that of the memory function.

Anisotropic interactions of liquid CD4 are studied in detail by comparison of inelastic neutron Brillouin scattering data with molecular dynamics simulations using up to four different models of the methane site-site potential. We demonstrate that the experimental dynamic structure factor S(Q,omega) acts as a highly discriminating quantity for possible interaction schemes. In particular, the Q evolution of the spectra enables a selective probing of the short- and medium-range features of the anisotropic potentials. We show that the preferential configuration of methane dimers at liquid densities can thus be discerned by analyzing the orientation-dependent model potential curves, in light of the experimental and simulation results.

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.

The high-frequency collective dynamics of molten potassium has been investigated by inelastic x-ray scattering, disclosing an energy/momentum transfer region unreachable by previous inelastic neutron scattering (INS) experiments. We find that a two-step relaxation scenario, similar to that found in other liquid metals, applies to liquid potassium. In particular, we show how the sound velocity determined by INS experiments, exceeding the hydrodynamic value by approximately 30%, is the higher limit of a speedup, located in the momentum region 1 < Q < 3 nm(-1), which marks the departure from the isothermal value. We point out how this phenomenology is the consequence of a microscopic relaxation process that, in turn, can be traced back to the presence of "instantaneous" disorder, rather than to the crossover from a liquid to solidlike response., (Copyright 2004 American Institute of Physics)

The density response of supercooled glycerol to an impulsive stimulated thermal grating (q=0.63 microm(-1)) has been studied in the temperature range (T=200-340 K) where the structure rearrangement (alpha relaxation) and the thermal diffusion occur on the same time scale. A strong interaction between the two modes occurs giving rise to a dip in the T dependence of the apparent thermal conductivity and a flattening of the apparent alpha-relaxation time upon cooling. A nonequilibrium thermodynamic model for the long time response has been developed. The model is capable to reproduce the experimental data and to explain the observed phenomenology.

Molecular dynamics (MD) results for the dynamic structure of a He(0.77)Ne(0.23) gas mixture at two densities (15.8 and 36.1 nm(-3)) show a clear crossover from hydrodynamic modes to distinct excitations for the two species. The higher density dispension curve neatly shows high- and low-frequency branches setting on with a rather localized transition. The lower density results agree very well with existing neutron scattering data and, in particular, display hydrodynamic behavior up to k approximately 2 nm(-1), in contrast with the conclusions of previous simulation studies. A smooth transition to fast sound is shown to take place for 2

The dynamics of the fragile glass-forming orthoterphenyl have been investigated by transient grating experiments with an heterodyne detection technique. We measured the relaxation processes of this glass former over more than six decades in time with an excellent signal-to-noise ratio. Acoustic, structural, and thermal relaxations have been clearly identified in a time-frequency window not covered by previous spectroscopic studies and their characteristic dynamic parameters have been measured as a function of temperature and wave vector. A detailed comparison with the density response function, calculated on the basis of generalized hydrodynamic model, has been worked out.

We present a molecular dynamics study of the collective dynamics of a model for the fragile glass former orthoterphenyl. In this model, introduced by Mossa, Di Leonardo, Ruocco, and Sampoli [Phys. Rev. E 62, 612 (2000)], the intramolecular interaction among the three rigid phenyl rings is described by a set of force constants whose value has been fixed in order to obtain a realistic isolated molecule spectrum. The interaction between different molecules is described by a Lennard Jones site-site potential. We study the behavior of the coherent scattering functions F(t)(q,t), considering the density fluctuations of both molecular and phenyl-ring centers of mass; moreover we directly simulate the neutron scattering spectra taking into account both the contributions due to carbon and hydrogens atoms. We compare our results with the main predictions of the mode-coupling theory and with the available coherent neutron scattering experimental data.

We present a realistic model of the fragile glass-former orthoterphenyl and the results of extensive molecular dynamics simulations in which we investigated its basic static and dynamic properties. In this model the internal molecular interactions between the three rigid phenyl rings are described by a set of force constants, including harmonic and anharmonic terms; the interactions among different molecules are described by Lennard-Jones site-site potentials. Self-diffusion properties are discussed in detail together with the temperature and momentum dependencies of the self-intermediate scattering function. The simulation data are compared with existing experimental results and with the main predictions of the mode-coupling theory.

A relaxation process, with the associated phenomenology of sound attenuation and sound velocity dispersion, is found in a simulated harmonic Lennard-Jones glass. We propose to identify this process with the so-called microscopic (or, instantaneous) relaxation process observed in real glasses and supercooled liquids. A model based on the memory function approach accounts for the observation and allows one to relate to each other (1) the characteristic time and strength of this process, (2) the low frequency limit of the dynamic structure factor of the glass, and (3) the high frequency sound attenuation coefficient, with its observed quadratic dependence on the momentum transfer.