317 research outputs found
Cage rattling does not correlate with the local geometry in molecular liquids
Molecular-dynamics simulations of a liquid of short linear molecules have
been performed to investigate the correlation between the particle dynamics in
the cage of the neighbors and the local geometry. The latter is characterized
in terms of the size and the asphericity of the Voronoi polyhedra. The
correlation is found to be poor. In particular, in spite of the different
Voronoi volume around the end and the inner monomers of a molecule, all the
monomers exhibit coinciding displacement distribution when they are caged (as
well as at longer times during the structural relaxation). It is concluded that
the fast dynamics during the cage trapping is a non-local collective process
involving monomers beyond the nearest neighbours.Comment: 15 pages, 6 figure
Non-local cooperative atomic motions that govern dissipation in amorphous tantala unveiled by dynamical mechanical spectroscopy
The mechanisms governing mechanical dissipation in amorphous tantala are studied at microscopic scale via Molecular Dynamics simulations, namely by mechanical spectroscopy in a wide range of temperature and frequency. We find that dissipation is associated with irreversible atomic rearrangements with a sharp cooperative character, involving tens to hundreds of atoms arranged in spatially extended clusters of polyhedra. Remarkably, at low temperature we observe an excess of plastically rearranging oxygen atoms which correlates with the experimental peak in the macroscopic mechanical losses. A detailed structural analysis reveals preferential connections of the irreversibly rearranging polyhedra, corresponding to edge and face sharing. These results might lead to microscopically informed design rules for reducing mechanical losses in relevant materials for structural, optical, and sensing applications
Competition of the connectivity with the local and the global order in polymer melts and crystals
The competition between the connectivity and the local or global order in
model fully-flexible chain molecules is investigated by molecular-dynamics
simulations. States with both missing (melts) and high (crystal) global order
are considered. Local order is characterized within the first coordination
shell (FCS) of a tagged monomer and found to be lower than in atomic systems in
both melt and crystal. The role played by the bonds linking the tagged monomer
to FCS monomers (radial bonds), and the bonds linking two FCS monomers (shell
bonds) is investigated. The detailed analysis in terms of Steinhardt's
orientation order parameters Q_l (l = 2 - 10) reveals that increasing the
number of shell bonds decreases the FCS order in both melt and crystal.
Differently, the FCS arrangements organize the radial bonds. Even if the
molecular chains are fully flexible, the distribution of the angle formed by
adjacent radial bonds exhibits sharp contributions at the characteristic angles
{\theta} = 70{\deg}, 122{\deg}, 180{\deg}. The fractions of adjacent radial
bonds with {\theta} = 122{\deg}, 180{\deg} are enhanced by the global order of
the crystal, whereas the fraction with 70{\deg} < {\theta} < 110{\deg} is
nearly unaffected by the crystallization. Kink defects, i.e. large lateral
displacements of the chains, are evidenced in the crystalline state.Comment: J. Chem. Phys. in pres
Coincident correlation between vibrational dynamics and primary relaxation of polymers with strong or weak johari-goldstein relaxation
The correlation between the vibrational dynamics, as sensed by the Debye-Waller factor, and the primary relaxation in the presence of secondary Johari-Goldstein (JG) relaxation, has been investigated through molecular dynamics simulations. Two melts of polymer chains with different bond length, resulting in rather different strength of the JG relaxation are studied. We focus on the bond-orientation correlation function, exhibiting higher JG sensitivity with respect to alternatives provided by torsional autocorrelation function and intermediate scattering function. We find that, even if changing the bond length alters both the strength and the relaxation time of the JG relaxation, it leaves unaffected the correlation between the vibrational dynamics and the primary relaxation. The finding is in harmony with previous studies reporting that numerical models not showing secondary relaxations exhibit striking agreement with experimental data of polymers also where the presence of JG relaxation is known
Weak links between fast mobility and local structure in molecular and atomic liquids
We investigate by molecular-dynamics simulations, the fast mobility-the rattling amplitude of the particles temporarily trapped by the cage of the neighbors-in mildly supercooled states of dense molecular (linear trimers) and atomic (binary mixtures) liquids. The mixture particles interact by the Lennard-Jones potential. The non-bonded particles of the molecular system are coupled by the more general Mie potential with variable repulsive and attractive exponents in a range which is a characteristic of small n-alkanes and n-alcohols. Possible links between the fast mobility and the geometry of the cage (size and shape) are searched. The correlations on a per-particle basis are rather weak. Instead, if one groups either the particles in fast-mobility subsets or the cages in geometric subsets, the increase of the fast mobility with both the size and the asphericity of the cage is revealed. The observed correlations are weak and differ in states with equal relaxation time. Local forces between a tagged particle and the first-neighbour shell do not correlate with the fast mobility in the molecular liquid. It is concluded that the cage geometry alone is unable to provide a microscopic interpretation of the known, universal link between the fast mobility and the slow structural relaxation. We suggest that the particle fast dynamics is affected by regions beyond the first neighbours, thus supporting the presence of collective, extended fast modes
The kinetic fragility of liquids as manifestation of the elastic softening
We show that the fragility , the steepness of the viscosity and relaxation
time close to the vitrification, increases with the degree of elastic
softening, i.e. the decrease of the elastic modulus with increasing
temperature, in universal way. This provides a novel connection between the
thermodynamics, via the modulus, and the kinetics. The finding is evidenced by
numerical simulations and comparison with the experimental data of glassformers
with widely different fragilities (), leading to a
fragility-independent elastic master curve extending over eighteen decades in
viscosity and relaxation time. The master curve is accounted for by a cavity
model pointing out the roles of both the available free volume and the cage
softness. A major implication of our findings is that ultraslow relaxations,
hardly characterised experimentally, become predictable by linear elasticity.
As an example, the viscosity of supercooled silica is derived over about
fifteen decades with no adjustable parameters.Comment: 7 pages, 6 figures; Added new results, improved the theoretical
sectio
Collective Excitations and Thermodynamics of Disordered State: New Insights into an Old Problem
K.T. is grateful to EPSRC and V.V.B. to RFBR for financial
suppor
Quantum Backaction on kg-Scale Mirrors: Observation of Radiation Pressure Noise in the Advanced Virgo Detector
The quantum radiation pressure and the quantum shot noise in laser-interferometric gravitational wave detectors constitute a macroscopic manifestation of the Heisenberg inequality. If quantum shot noise can be easily observed, the observation of quantum radiation pressure noise has been elusive, so far, due to the technical noise competing with quantum effects. Here, we discuss the evidence of quantum radiation pressure noise in the Advanced Virgo gravitational wave detector. In our experiment, we inject squeezed vacuum states of light into the interferometer in order to manipulate the quantum backaction on the 42 kg mirrors and observe the corresponding quantum noise driven displacement at frequencies between 30 and 70 Hz. The experimental data, obtained in various interferometer configurations, is tested against the Advanced Virgo detector quantum noise model which confirmed the measured magnitude of quantum radiation pressure noise
Advanced Virgo Plus: Future Perspectives
While completing the commissioning phase to prepare the Virgo interferometer for the next joint Observation Run (O4), the Virgo collaboration is also finalizing the design of the next upgrades to the detector to be employed in the following Observation Run (O5). The major upgrade will concern decreasing the thermal noise limit, which will imply using very large test masses and increased laser beam size. But this will not be the only upgrade to be implemented in the break between the O4 and O5 observation runs to increase the Virgo detector strain sensitivity. The paper will cover the challenges linked to this upgrade and implications on the detector's reach and observational potential, reflecting the talk given at 12th Cosmic Ray International Seminar - CRIS 2022 held in September 2022 in Napoli
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