Mixing of longitudinal and transverse dynamics in liquid water

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16 Νοε 2013 (πριν από 3 χρόνια και 6 μήνες)

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Mixing of longitudinal and transverse dynamics in liquid water
The investigation of large wavevector excitations in liquid water has been a challenging task since
the pioneering computational and experimental studies on its dynamic structure factor, S(Q,). These
works revealed the existence of acoustic-like excitations propagating with a speed, = 3300 m/s,
corresponding to a value more than twice the hydrodynamic sound uo
~ 1500 m/s. Many
subsequent works studied this issue by molecular dynamics (MD), inelastic neutron-scattering (INS),
and inelastic X-ray-scattering (IXS). The high-frequency picture emerging from S(Q,) of H
O can
be summarised as follows: i) The acoustic-like mode propagates with in the 4 to 14 nm
Q range.
ii) For Q larger than 4 nm
, there is a second, weakly dispersing mode with an energy of ~ 5 meV.
iii) Both modes involve the motion of the molecular centre of mass. iv) At Q = 4 nm
the energy of
the two modes becomes comparable, and in the 1 to 4 nm
Q region only one mode is observed; the
sound velocity of this mode changes decreasing Q from towards
. This picture indicates the
existence of two branches, one strongly- and the other weakly-dispersing with Q. The first one is
identified as the sound branch with a bend up in the region below Q = 4 nm
. The second one, on the
basis of MD and of INS and IXS results on ice crystals can be related to a localised motion
reminiscent of the transverse dynamics in the crystal and to the bending motion between three
hydrogen-bonded water molecules. The most important point, however, is not yet settled: is the
physical mechanism responsible for the bending of the sound branch and for the observation of a
second mode at Q larger than 4 nm
a feature common to a large class of liquids or is it specific to
We performed a numerical MD investigation on the symmetry character of the modes observed in
liquid water. The MD results in the Q range of the IXS and INS experiments show the existence of
two different dynamic regimes. In the small Q limit, Q < 2 ~ nm
, the dynamics is liquid-like: there
are pure longitudinal modes propagating with =
, and the transverse dynamics is relaxational-like.
In the opposite limit, at Q larger than 4 ~ nm
, the dynamics is solid-like: there are two modes with
ies close to the lon
itudinal and transverse
honon branches in ice. Here, however, contrar
ice, both modes have a large mixing of longitudinal and transverse symmetry. A propagating
transverse dynamics starts to appear in the same intermediate Q region where the longitudinal branch
acquires a transverse component, and its sound velocity changes from
to . The transition
between the two regimes is found in the Q - region corresponding to the lengthscale and lifetime o

local order in liquid water. Therefore, these results link the anomalies in the high frequency
collective dynamics of liquid water to relaxation processes originating from locally ordered
molecular assemblies. Moreover, the analysis of the longitudinal and transverse current spectra
calculated by MD simulations gives a coherent picture of the previous experimental and MD results
on the high frequency dynamics of liquid water, and shows that these dynamics can be described
within the same framework used for other molecular liquids.
M. Sampoli (a), G. Ruocco (b), F. Sette (c), Phys. Rev. Lett. 79, 1678 (1997)
(a) Universita di Firenze and INFM, Firenze (Italy)
(b) Universita di L'Aquila and INFM, L'Aquila (Italy)
(c) ESRF