144 research outputs found
Density fluctuations and single-particle dynamics in liquid lithium
The single-particle and collective dynamical properties of liquid lithium
have been evaluated at several thermodynamic states near the triple point. This
is performed within the framework of mode-coupling theory, using a
self-consistent scheme which, starting from the known static structure of the
liquid, allows the theoretical calculation of several dynamical properties.
Special attention is devoted to several aspects of the single-particle
dynamics, which are discussed as a function of the thermodynamic state. The
results are compared with those of Molecular Dynamics simulations and other
theoretical approaches.Comment: 31 pages (in preprint format), 14 figures. Submitted to Phys. Rev.
Evidence of two viscous relaxation processes in the collective dynamics of liquid lithium
New inelastic X-ray scattering experiments have been performed on liquid
lithium in a wide wavevector range. With respect to the previous measurements,
the instrumental resolution, improved up to 1.5 meV, allows to accurately
investigate the dynamical processes determining the observed shape of the the
dynamic structure factor, . A detailed analysis of the lineshapes
shows the co-existence of relaxation processes with both a slow and a fast
characteristic timescales, and therefore that pictures of the relaxation
mechanisms based on a simple viscoelastic model must be abandoned.Comment: 5 pages, 4 .PS figure
Inelastic X-ray scattering study of the collective dynamics in liquid sodium
Inelastic X-ray scattering data have been collected for liquid sodium at
T=390 K, i.e. slightly above the melting point. Owing to the very high
instrumental resolution, pushed up to 1.5 meV, it has been possible to
determine accurately the dynamic structure factor, , in a wide
wavevector range, nm, and to investigate on the dynamical
processes underlying the collective dynamics. A detailed analysis of the
lineshape of , similarly to other liquid metals, reveals the
co-existence of two different relaxation processes with slow and fast
characteristic timescales respectively. The present data lead to the conclusion
that: i) the picture of the relaxation mechanism based on a simple viscoelastic
model fails; ii) although the comparison with other liquid metals reveals
similar behavior, the data do not exhibit an exact scaling law as the principle
of corresponding state would predict.Comment: RevTex, 7 pages, 6 eps figures. Accepted by Phys. Rev.
Collective dynamics of liquid aluminum probed by Inelastic X-ray Scattering
An inelastic X-ray scattering experiment has been performed in liquid
aluminum with the purpose of studying the collective excitations at wavevectors
below the first sharp diffraction peak. The high instrumental resolution (up to
1.5 meV) allows an accurate investigation of the dynamical processes in this
liquid metal on the basis of a generalized hydrodynamics framework. The
outcoming results confirm the presence of a viscosity relaxation scenario ruled
by a two timescale mechanism, as recently found in liquid lithium.Comment: 8 pages, 7 figure
Evidence of short time dynamical correlations in simple liquids
We report a molecular dynamics (MD) study of the collective dynamics of a
simple monatomic liquid -interacting through a two body potential that mimics
that of lithium- across the liquid-glass transition. In the glassy phase we
find evidences of a fast relaxation process similar to that recently found in
Lennard-Jones glasses. The origin of this process is ascribed to the
topological disorder, i.e. to the dephasing of the different momentum
Fourier components of the actual normal modes of vibration of the disordered
structure. More important, we find that the fast relaxation persists in the
liquid phase with almost no temperature dependence of its characteristic
parameters (strength and relaxation time). We conclude, therefore, that in the
liquid phase well above the melting point, at variance with the usual
assumption of {\it un-correlated} binary collisions, the short time particles
motion is strongly {\it correlated} and can be described via a normal mode
expansion of the atomic dynamics.Comment: 7 pages, 7 .eps figs. To appear in Phys. Rev.
Creating a low-dimensional quantum gas using dark states in an inelastic evanescent-wave mirror
We discuss an experimental scheme to create a low-dimensional gas of
ultracold atoms, based on inelastic bouncing on an evanescent-wave mirror.
Close to the turning point of the mirror, the atoms are transferred into an
optical dipole trap. This scheme can compress the phase-space density and can
ultimately yield an optically-driven atom laser. An important issue is the
suppression of photon scattering due to ``cross-talk'' between the mirror
potential and the trapping potential. We propose that for alkali atoms the
photon scattering rate can be suppressed by several orders of magnitude if the
atoms are decoupled from the evanescent-wave light. We discuss how such dark
states can be achieved by making use of circularly-polarized evanescent waves.Comment: 8 pages, 4 figure
Quantum-state control in optical lattices
We study the means to prepare and coherently manipulate atomic wave packets
in optical lattices, with particular emphasis on alkali atoms in the
far-detuned limit. We derive a general, basis independent expression for the
lattice operator, and show that its off-diagonal elements can be tailored to
couple the vibrational manifolds of separate magnetic sublevels. Using these
couplings one can evolve the state of a trapped atom in a quantum coherent
fashion, and prepare pure quantum states by resolved-sideband Raman cooling. We
explore the use of atoms bound in optical lattices to study quantum tunneling
and the generation of macroscopic superposition states in a double-well
potential. Far-off-resonance optical potentials lend themselves particularly
well to reservoir engineering via well controlled fluctuations in the
potential, making the atom/lattice system attractive for the study of
decoherence and the connection between classical and quantum physics.Comment: 35 pages including 8 figures. To appear in Phys. Rev. A. March 199
Dynamical properties of liquid Al near melting. An orbital-free molecular dynamics study
The static and dynamic structure of liquid Al is studied using the orbital
free ab-initio molecular dynamics method. Two thermodynamic states along the
coexistence line are considered, namely T = 943 K and 1323 K for which X-ray
and neutron scattering data are available. A new kinetic energy functional,
which fulfills a number of physically relevant conditions is employed, along
with a local first principles pseudopotential. In addition to a comparison with
experiment, we also compare our ab-initio results with those obtained from
conventional molecular dynamics simulations using effective interionic pair
potentials derived from second order pseudopotential perturbation theory.Comment: 15 pages, 12 figures, 2 tables, submitted to PR
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