Search results for "molecular dynamics"

showing 10 items of 1075 documents

Molecular mode-coupling theory for supercooled liquids: application to water.

1999

We present mode-coupling equations for the description of the slow dynamics observed in supercooled molecular liquids close to the glass transition. The mode-coupling theory (MCT) originally formulated to study the slow relaxation in simple atomic liquids, and then extended to the analysis of liquids composed by linear molecules, is here generalized to systems of arbitrarily shaped, rigid molecules. We compare the predictions of the theory for the $q$-vector dependence of the molecular nonergodicity parameters, calculated by solving numerically the molecular MCT equations in two different approximation schemes, with ``exact'' results calculated from a molecular dynamics simulation of superc…

PhysicsStatistical Mechanics (cond-mat.stat-mech)ThermodynamicsFOS: Physical sciencesLinear molecular geometryCondensed Matter - Soft Condensed MatterCondensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterMolecular dynamicsMode couplingRelaxation (physics)MoleculeSoft Condensed Matter (cond-mat.soft)Statistical physicsPhysics::Chemical PhysicsSupercoolingGlass transitionCondensed Matter - Statistical MechanicsPhysical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics
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Sum Frequency Generation Spectra from Velocity–Velocity Correlation Functions

2017

We developed an expression for the calculation of the sum frequency generation spectra (SFG) of water interfaces that is based on the projection of the atomic velocities on the local normal modes. Our approach permits one to obtain the SFG signal from suitable velocity-velocity correlation functions, reducing the computational cost to that of the accumulation of a molecular dynamics trajectory, and therefore cutting the overhead costs associated with the explicit calculation of the dipole moment and polarizability tensor. Our method permits to interpret the peaks in the spectrum in terms of local modes, also including the bending region. The results for the water-air interface, obtained usi…

PhysicsSum-frequency generation010304 chemical physicsAnalytical chemistryPhase (waves)010402 general chemistry01 natural sciencesProjection (linear algebra)Spectral line0104 chemical sciencesComputational physicsMoment (mathematics)Molecular dynamicsDipoleNormal mode0103 physical sciencesGeneral Materials SciencePhysical and Theoretical ChemistryThe Journal of Physical Chemistry Letters
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Simple Microscopic Theory of Amontons' Laws for Static Friction

2001

A microscopic theory for the ubiquitous phenomenon of static friction is presented. Interactions between two surfaces are modeled by an energy penalty that increases exponentially with the degree of surface overlap. The resulting static friction is proportional to load, in accordance with Amontons' laws. However the friction coefficient between bare surfaces vanishes as the area of individual contacts grows, except in the rare case of commensurate surfaces. An area independent friction coefficient is obtained for any surface geometry when an adsorbed layer of mobile atoms is introduced between the surfaces. The predictions from our simple analytic model are confirmed by atomistically detail…

PhysicsSurface (mathematics)Condensed Matter - Materials ScienceAnalytic modelMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and Astronomy02 engineering and technologyCondensed Matter - Soft Condensed Matter021001 nanoscience & nanotechnology53001 natural sciencesStatic frictionMolecular dynamicsClassical mechanicsSimple (abstract algebra)Law0103 physical sciencesRare caseSoft Condensed Matter (cond-mat.soft)Surface geometryMicroscopic theory010306 general physics0210 nano-technology
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Simulation of surface-controlled phase separation in slit pores: Diffusive Ginzburg-Landau kinetics versus Molecular Dynamics

2008

The phase separation kinetics of binary fluids in constrained geometry is a challenge for computer simulation, since nontrivial structure formation occurs extending from the atomic scale up to mesoscopic scales, and a very large range of time needs to be considered. One line of attack to this problem is to try nevertheless standard Molecular Dynamics (MD), another approach is to coarse-grain the model to apply a time-dependent nonlinear Ginzburg–Landau equation that is numerically integrated. For a symmetric binary mixture confined between two parallel walls that prefer one species, both approaches are applied and compared to each other. There occurs a nontrivial interplay between the forma…

PhysicsSurface (mathematics)Mesoscopic physicswettingStructure formationComponent (thermodynamics)domain growthGeneral Physics and AstronomyMechanicsAtomic unitssurface-directed spinodal decompositionNonlinear systemMolecular dynamicstime-dependent Ginzburg–Landau equationHardware and ArchitectureStatistical physicsbinary Lennard–Jones mixtureLine (formation)
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Memory expansion for diffusion coefficients

1998

We present a memory expansion for macroscopic transport coefficients such as the collective and tracer diffusion coefficients ${D}_{C}$ and ${D}_{T},$ respectively. The successive terms in this expansion for ${D}_{C}$ describe rapidly decaying memory effects of the center-of-mass motion, leading to fast convergence when evaluated numerically. For ${D}_{T},$ one obtains an expansion of similar form that contains terms describing memory effects in single-particle motion. As an example we evaluate ${D}_{C}$ and ${D}_{T}$ for three strongly interacting surface systems through Monte Carlo simulations, and for a simple model diffusion system via molecular dynamics calculations. We show that the n…

PhysicsSurface (mathematics)SpeedupNumerical analysisPhysicsMonte Carlo methodmacroscopic transport coefficients02 engineering and technology021001 nanoscience & nanotechnologysurface systems01 natural sciencesMonte Carlo simulationsMolecular dynamics0103 physical sciencesConvergence (routing)numerical methodsDiffusion (business)010306 general physics0210 nano-technologyOrder of magnitudeMathematical physicsmemory expansions
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Quantifying Artifacts in Ewald Simulations of Inhomogeneous Systems with a Net Charge

2014

Ewald summation, which has become the de facto standard for computing electrostatic interactions in biomolecular simulations, formally requires that the simulation box is neutral. For non-neutral systems the Ewald algorithm implicitly introduces a uniform background charge distribution that e ectively neutralizes the simulation box. Because a uniform distribution of counter charges typically deviates from the spatial distribution of counterions in real systems, artifacts may arise, in particular in systems with an inhomogeneous dielectric constant. Here we derive an analytical expression for the e ect of using an implicit background charge instead of explicit counterions, on the chemical po…

PhysicsUniform distribution (continuous)010304 chemical physicsCharge densityCharge (physics)02 engineering and technologyDielectricEwald simulations021001 nanoscience & nanotechnologyElectrostatics01 natural sciencesEwald summationComputer Science ApplicationsMolecular dynamicsinhomogeneous systems0103 physical sciencesStatistical physicsPhysical and Theoretical ChemistryTest particle0210 nano-technologyta116SimulationJournal of Chemical Theory and Computation
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Temperature dependence of dynamic, tunnelling and kinetic isotope effects in formate dehydrogenase

2018

The origin of the catalytic power of enzymes has been a question of debate for a long time. In this regard, the possible contribution of protein dynamics in enzymatic catalysis has become one of the most controversial topics. In the present work, the hydride transfer step in the formate dehydrogenase (FDH EC 1.2.1.2) enzyme is studied by means of molecular dynamic (MD) simulations with quantum mechanics/molecular mechanics (QM/MM) potentials in order to explore any correlation between dynamics, tunnelling effects and the rate constant. The temperature dependence of the kinetic isotope effects (KIEs), which is one of the few tests that can be studied by experiments and simulations to shed li…

PhysicsWork (thermodynamics)010405 organic chemistryTemperatureGeneral Physics and Astronomy010402 general chemistryKinetic energyFormate Dehydrogenases01 natural sciences0104 chemical sciencesReaction coordinateKineticsMolecular dynamicsReaction rate constantIsotopesChemical physicsKinetic isotope effectPhysical and Theoretical ChemistryQuantumQuantum tunnellingPhysical Chemistry Chemical Physics
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Linear-scaling self-consistent field theory based molecular dynamics: application to C60buckyballs colliding with graphite

2018

In this work, we investigate the collision of a C fullerene with graphite using large-scale molecular dynamics simulations, where the interatomic forces are computed ‘on-the-fly’ by means of self-c...

PhysicsWork (thermodynamics)Fullerene010304 chemical physicsCondensed Matter::OtherGeneral Chemical EngineeringGeneral ChemistryCondensed Matter PhysicsCollision01 natural sciencesLangevin equationCondensed Matter::Materials ScienceMolecular dynamicsClassical mechanicsModeling and Simulation0103 physical sciencesPhysics::Atomic and Molecular ClustersLinear scaleGeneral Materials ScienceField theory (psychology)Graphite010306 general physicsInformation SystemsMolecular Simulation
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LATTICE–BOLTZMANN SIMULATION OF DENSE NANOFLOWS: A COMPARISON WITH MOLECULAR DYNAMICS AND NAVIER–STOKES SOLUTIONS

2007

In a recent work, a dense fluid flow across a nanoscopic thin plate was simulated by means of Molecular Dynamics (MD) and Lattice Boltzmann (LB) methods. It was found that in order to recover quantitative agreement with MD results, the LB simulation must be pushed down to sub–nanoscopic scales, i.e. fractions of the range of molecular interactions. In this work, we point out that in this sub–nanoscopic regime, the LB method works outside the hydrodynamic limit at the level of a single cell spacing. A quantitative comparison with the Navier–Stokes (NS) solution shows however that LB and NS results are quite similar, thereby indicating that, apart for a small region past the plate, this nano…

PhysicsWork (thermodynamics)Range (particle radiation)Lattice Boltzmann methodsGeneral Physics and AstronomyStatistical and Nonlinear PhysicsMechanicsComputer Science ApplicationsLattice boltzmann simulationMolecular dynamicsClassical mechanicsComputational Theory and MathematicsFluid dynamicsNavier stokesNanoscopic scaleMathematical PhysicsInternational Journal of Modern Physics C
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Rotational echoes as a tool for investigating ultrafast collisional dynamics of molecules

2019

We show that recently discovered rotational echoes of molecules provide an efficient tool for studying collisional molecular dynamics in high-pressure gases. Our study demonstrates that rotational echoes enable the observation of extremely fast collisional dissipation, at timescales of the order of a few picoseconds, and possibly shorter. The decay of the rotational alignment echoes in ${\mathrm{CO}}_{2}$ gas and ${\mathrm{CO}}_{2}\text{\ensuremath{-}}\mathrm{He}$ mixture up to 50 bar was studied experimentally, delivering collision rates that are in good agreement with the theoretical expectations. The suggested measurement protocol may be used in other high-density media, and potentially …

Physics[PHYS]Physics [physics][PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics][PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Dynamics (mechanics)[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]General Physics and AstronomyOrder (ring theory)Dissipation01 natural sciencesMolecular dynamicsPicosecond0103 physical sciencesMoleculeAtomic physics010306 general physicsUltrashort pulseBar (unit)
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