Search results for "molecular dynamics"

showing 10 items of 1075 documents

Structural features of selected protic ionic liquids based on a super-strong base

2019

Protic ionic liquids (PIL) were prepared from a super-strong base 1,7-diazabicyclo[5.4.0]undec-7-ene (DBU) and super-strong acids, trifluoromethane sulfonic acid (TfOH), and (trifluoromethanesulfonyl)-(nonafluorobutylsulfonyl)imide, (IM14H), ([DBUH][TfO] and [DBUH][IM14], respectively; the latter for the first time) and their chemical and physical properties and structural features have been explored using a synergy of experimental and computational tools. The short range order in neat DBU, as well as the long range structural correlations induced by charge correlation and hydrogen bonding interactions in the ionic liquids, have been explored under ambient conditions, where these compounds …

Materials scienceBase (chemistry)XRDGeneral Physics and Astronomy02 engineering and technologySulfonic acid010402 general chemistry01 natural scienceschemistry.chemical_compoundx-ray scatteringIonic liqids; structure; XRD; MDstructurePhysical and Theoretical ChemistryImideionic liquidchemistry.chemical_classificationIonic liqidsHydrogen bondMDneutron scattering021001 nanoscience & nanotechnologysegregationmolecular dynamics0104 chemical scienceschemistryIonic liquidShort range orderPhysical chemistryproticIonic Liquids Structure Protic Solvent Classical MD0210 nano-technologyProtic solvent
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Modeling the Interaction of Carbon Monoxide with Flexible Graphene: From Coupled Cluster Calculations to Molecular-Dynamics Simulations

2018

The interaction of CO with graphene was studied at different theoretical levels. Quantum-mechanical calculations on finite graphene models with the use of coronene for coupled cluster calculations and circumcoronene for B97D calculations showed that there was no preferential site for adsorption and that the most important factor was the orientation of CO relative to graphene. The parallel orientation was preferred, with binding energies around 9 kJ mol-1 at the CCSD(T) and B97D levels, which was in good agreement with experimental findings. From a large number of CO-circumcoronene and CO-CO interactions, computed at different distances and randomly generated orientations, parameters were fi…

Materials scienceBinding energy02 engineering and technologyMolecular dynamics010402 general chemistry01 natural scienceslaw.inventionMolecular dynamicschemistry.chemical_compoundAdsorptionlawAtomic and Molecular PhysicsAdsorption; Density functional calculations; Graphene; Interaction energies; Molecular dynamics; Atomic and Molecular Physics and Optics; Physical and Theoretical ChemistryInteraction energiesPhysical and Theoretical ChemistryCanonical ensembleGraphene021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsCoronene0104 chemical sciencesDensity functional calculationsCoupled clusterchemistryChemical physicsIntramolecular forceAdsorptionGrapheneand Optics0210 nano-technologyChemPhysChem
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Effect of melting on ionization potential of sodium clusters

2003

The effect of melting transition on the ionization potential has been studied for sodium clusters with 40, 55, 142, and 147 atoms, using ab initio and classical molecular dynamics. Classical and ab initio simulations were performed to determine the ionization potential of Na142 and Na147 for solid, partly melted, and liquid structures. The results reveal no correlation between the vertical ionization potential and the degree of surface disorder, melting, or the total energy of the cluster obtained with the ab initio method. However, in the case of 40 and 55 atom clusters, the ionization potential seems to decrease when the cluster melts.

Materials scienceBinding energyAb initioMolar ionization energies of the elementsAtomic and Molecular Physics and OpticsMolecular dynamicsChemical physicsAb initio quantum chemistry methodsIonizationPhysics::Atomic and Molecular ClustersCluster (physics)Physics::Atomic PhysicsAtomic physicsIonization energyThe European Physical Journal D - Atomic, Molecular and Optical Physics
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Proteins in amorphous saccharide matrices: Structural and dynamical insights on bioprotection

2013

Bioprotection by sugars, and in particular trehalose peculiarity, is a relevant topic due to the implications in several fields. The underlying mechanisms are not yet clearly elucidated, and remain the focus of current investigations. Here we revisit data obtained at our lab on binary sugar/water and ternary protein/sugar/water systems, in wide ranges of water content and temperature, in the light of the current literature. The data here discussed come from complementary techniques (Infrared Spectroscopy, Molecular Dynamics simulations, Small Angle X-ray Scattering and Calorimetry), which provided a consistent description of the bioprotection by sugars from the atomistic to the macroscopic …

Materials scienceBiophysicsComplex systemOligosaccharidesInfrared spectroscopyCalorimetryMolecular Dynamics SimulationMolecular dynamicsMatrix (mathematics)X-Ray DiffractionScattering Small AngleSpectroscopy Fourier Transform InfraredGeneral Materials ScienceSpectroscopytrehalosesaccharidemyoglobin spectroscopy simulationschemistry.chemical_classificationProtein StabilitySmall-angle X-ray scatteringBiomoleculeTemperatureProteinsWaterSurfaces and InterfacesGeneral ChemistrySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)chemistryChemical physicsBiophysicsTernary operationBiotechnology
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Water orientation and hydrogen-bond structure at the fluorite/water interface

2016

AbstractWater in contact with mineral interfaces is important for a variety of different processes. Here, we present a combined theoretical/experimental study which provides a quantitative, molecular-level understanding of the ubiquitous and important CaF2/water interface. Our results show that, at low pH, the surface is positively charged, causing a substantial degree of water ordering. The surface charge originates primarily from the dissolution of fluoride ions, rather than from adsorption of protons to the surface. At high pH we observe the presence of Ca-OH species pointing into the water. These OH groups interact remarkably weakly with the surrounding water and are responsible for the…

Materials scienceChemical physics[SDV]Life Sciences [q-bio]FOS: Physical sciences02 engineering and technologyElectronic structureMolecular dynamics010402 general chemistry01 natural sciencesArticleSpectral lineIonchemistry.chemical_compoundAdsorptionPhysics - Chemical PhysicsSurface chargeDissolutionChemical Physics (physics.chem-ph)MultidisciplinaryHydrogen bond021001 nanoscience & nanotechnologySurface spectroscopy0104 chemical sciencesGeochemistrychemistryChemical physics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyFluorideScientific Reports
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Piezoelectric coefficients by molecular dynamics simulations in the constant stress ensemble: A case study of quartz

2006

Piezoelectric (strain) coefficients dij of quartz are calculated in terms of molecular dynamics as a function of pressure and temperature. We review the necessary formulas for the computation of electromechanical materials coefficients obtained at constant stress and temperature, and discuss how to overcome complications of the definition of polarization variations due to fluctuating box geometries. A method is employed suppressing significantly stochastic fluctuations of the estimators for piezoelectric coefficients. A recently suggested force field for the simulation of SiO2 reproduces available experimental data quite accurately. Predictions are made for the pressure dependence of dij of…

Materials scienceComputationGeneral Physics and AstronomyEstimatorMechanicsPolarization (waves)PiezoelectricityForce field (chemistry)Condensed Matter::Materials ScienceMolecular dynamicsHardware and ArchitectureConstant stressStatistical physicsQuartzComputer Physics Communications
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Nucleus-driven crystallization of amorphous Ge2Sb2Te5: A density functional study

2012

Early stages of nucleus-driven crystallization of the prototype phase change material Ge${}_{2}$Sb${}_{2}$Te${}_{5}$ have been studied by density functional/molecular dynamics simulations for amorphous samples (460 and 648 atoms) at 500, 600, and 700 K. All systems assumed a fixed cubic seed of 58 atoms and 6 vacancies. Crystallization occurs within 600 ps for the 460-atom system at 600 and 700 K, and signs of crystallization (nucleus growth, percolation) are present in the others. Crystallization is accompanied by an increase in the number of ``$ABAB$ squares'' ($A$: Ge, Sb, $B$: Te), and atoms of all elements move significantly. There is no evidence of cavity movement to the crystal-glass…

Materials scienceCondensed Matter PhysicsPhase-change materialElectronic Optical and Magnetic Materialslaw.inventionAmorphous solidMolecular dynamicsmedicine.anatomical_structureChemical physicslawPercolationmedicineCrystallizationNucleusPhysical Review B
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Chain Motion in an Unentangled Polyethylene Melt: A Critical Test of the Rouse Model by Molecular Dynamics Simulations and Neutron Spin Echo Spectros…

1998

We have investigated the dynamic structure factor for single-chain relaxation in a polyethylene melt by means of molecular dynamics simulations and neutron spin echo spectroscopy. After accounting for a 20% difference in the chain self-diffusion coefficient between simulation and experiment we find a perfect quantitative agreement of the intermediate dynamic structure factor over the whole range of momentum transfer studied. Based on this quantitative agreement one can test the experimental results for deviations from standard Rouse behavior reported so far for only computer simulations of polymer melt dynamics.

Materials scienceCondensed matter physicsDynamic structure factorMomentum transferDynamics (mechanics)Relaxation (NMR)General Physics and AstronomyPolyethyleneMolecular physicsNeutron spin echoCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicschemistrySpectroscopyPhysical Review Letters
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Amorphous silica between confining walls and under shear: a computer simulation study

2002

Molecular dynamics computer simulations are used to investigate a silica melt confined between walls at equilibrium and in a steady-state Poisseuille flow. The walls consist of point particles forming a rigid face-centered cubic lattice and the interaction of the walls with the melt atoms is modelled such that the wall particles have only a weak bonding to those in the melt, i.e. much weaker than the covalent bonding of a Si-O unit. We observe a pronounced layering of the melt near the walls. This layering, as seen in the total density profile, has a very irregular character which can be attributed to a preferred orientational ordering of SiO4 tetrahedra near the wall. On intermediate lengt…

Materials scienceCondensed matter physicsStatistical Mechanics (cond-mat.stat-mech)Shear viscosityGeneral Physics and AstronomyFOS: Physical sciencesSlip (materials science)Disordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Disordered Systems and Neural NetworksPhysics::Fluid DynamicsMolecular dynamicsLattice (order)TetrahedronPhysical and Theoretical ChemistryLayeringAmorphous silicaCondensed Matter - Statistical Mechanics
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Oxidation of nanocrystalline aluminum by variable charge molecular dynamics

2010

International audience; We investigate the oxidation of nanocrystalline aluminum surfaces using molecular dynamics (MD) simulations with the variable charge model that allows charge dynamically transfer among atoms. The interaction potential between atoms is described by the electrostatic plus (Es+) potential model, which is composed of an embedded atom method potential and an electrostatic term. The simulations were performed from 300 to 750K on polycrystalline samples with a mean grain size of 5 nanometers. We mainly focused on the effect of the temperature parameter on the oxidation kinetic. The results show that, beyond a first linear regime, the kinetics follow a direct logarithmic law…

Materials scienceDiffusionOxideA. metals A. oxides A. thin films D. diffusion D. microstructure02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences7. Clean energyNanocrystalline materialGrain sizeMolecular dynamicsCrystallinitychemistry.chemical_compoundCondensed Matter::Materials SciencechemistryChemical physics0103 physical sciencesAtomGeneral Materials ScienceThin film010306 general physics0210 nano-technology
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