Search results for "molecular dynamics"

showing 10 items of 1075 documents

Molecular dynamics of CH4/N2 mixtures on a flexible graphene layer: adsorption and selectivity case study

2019

We theoretically investigate graphene layers, proposing them as membranes of subnanometer size suitable for CH4/N2 separation and gas uptake. The observed potential energy surfaces, representing the intermolecular interactions within the CH4/N2 gaseous mixtures and between these and the graphene layers, have been formulated by adopting the so-called Improved Lennard-Jones (ILJ) potential, which is far more accurate than the traditional Lennard-Jones potential. Previously derived ILJ force fields are used to perform extensive molecular dynamics simulations on graphene's ability to separate and adsorb the CH4/N2 mixture. Furthermore, the intramolecular interactions within graphene were explic…

Materials scienceUNESCO::QUÍMICA02 engineering and technology010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]law.inventionlcsh:ChemistryMolecular dynamicsAdsorptionlawAb initio quantum chemistry methodsFlexibility (engineering)Grapheneab initio calculationsIntermolecular forceGeneral Chemistryflexible graphene021001 nanoscience & nanotechnologyPotential energymolecular dynamics0104 chemical scienceslcsh:QD1-999adsorptionChemical physicsIntramolecular forceab-initio potential0210 nano-technologyAb initio calculations; Ab-initio potential; Adsorption; Flexible graphene; Molecular dynamics
researchProduct

Nonlinear Structural Mechanics Based Modeling of Carbon Nanotube Deformation

2003

A nonlinear structural mechanics based approach for modeling the structure and the deformation of single-wall and multiwall carbon nanotubes (CNTs) is presented. Individual tubes are modeled using shell finite elements, where a specific pairing of elastic properties and mechanical thickness of the tube wall is identified to enable successful modeling with shell theory. The effects of van der Waals forces are simulated with special interaction elements. This new CNT modeling approach is verified by comparison with molecular dynamics simulations and high-resolution micrographs available in the literature. The mechanics of wrinkling of multiwall CNTs are studied, demonstrating the role of the …

Materials sciencecarbon nanotube numerical modelStructural mechanicsShell (structure)General Physics and AstronomyNanotechnologyCarbon nanotubeFinite element methodlaw.inventionSettore ING-IND/14 - Progettazione Meccanica E Costruzione Di MacchineCondensed Matter::Materials ScienceMolecular dynamicssymbols.namesakeBucklinglawPhysics::Atomic and Molecular ClusterssymbolsDeformation (engineering)van der Waals forceComposite materialPhysical Review Letters
researchProduct

Advanced approach to the local structure reconstruction and theory validation on the example of the W L 3 -edge extended x-ray absorption fine struct…

2018

The authors gratefully acknowledge the assistance of the ELETTRA XAFS beamline staff members during the EXAFS experiment No 20150303. This work has been carried out within the framework of the EUROfusion Consortium and has received funding from the Euratom research and training programme 2014-2018 under grant agreement No 633053. The views and opinions expressed herein do not necessarily reflect those of the European Commission.

Materials sciencechemistry.chemical_elementFOS: Physical sciences02 engineering and technologyEdge (geometry)Tungsten01 natural sciencesLocal structureTungstenCondensed Matter::Materials Science0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]General Materials Science010306 general physicsReverse Monte Carlo simulationsCondensed Matter - Materials ScienceExtended X-ray absorption fine structureMolecular dynamics simulationsMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyCondensed Matter PhysicsComputer Science ApplicationsComputational physicsEXAFSchemistryMechanics of MaterialsModeling and Simulation0210 nano-technologyModelling and Simulation in Materials Science and Engineering
researchProduct

Statics and dynamics of colloid-polymer mixtures near their critical point of phase separation: A computer simulation study of a continuous Asakura–O…

2008

We propose a new coarse-grained model for the description of liquid-vapor phase separation of colloid-polymer mixtures. The hard-sphere repulsion between colloids and between colloids and polymers, which is used in the well-known Asakura-Oosawa (AO) model, is replaced by Weeks-Chandler-Anderson potentials. Similarly, a soft potential of height comparable to thermal energy is used for the polymer-polymer interaction, rather than treating polymers as ideal gas particles. It is shown by grand-canonical Monte Carlo simulations that this model leads to a coexistence curve that almost coincides with that of the AO model and the Ising critical behavior of static quantities is reproduced. Then the …

Materials sciencecritical pointsMonte Carlo methodFOS: Physical sciencesGeneral Physics and AstronomyThermodynamicsCondensed Matter - Soft Condensed MatterCritical point (mathematics)Molecular dynamicscolloidspolymer solutionsPhysical and Theoretical Chemistryliquid-vapour transformationsBinodalliquid mixturesLennard-Jones potentialMonte Carlo methodsDisordered Systems and Neural Networks (cond-mat.dis-nn)Statistical mechanicsCondensed Matter - Disordered Systems and Neural Networksself-diffusionIdeal gasliquid theoryCondensed Matter::Soft Condensed Mattermolecular dynamics methodLennard-Jones potentialSoft Condensed Matter (cond-mat.soft)Ising modelstatistical mechanicsphase separationThe Journal of Chemical Physics
researchProduct

Small angle neutron scattering on periodically deformed polymers

1984

Small angle neutron scattering from periodically deformed samples is a useful extension of the methods presently available for the study of molecular dynamics of polymers. In this paper we describe apparatus that has been used to produce large cyclic deformations at frequencies upto 10 Hz and the principles by which data is collected to give spectra corresponding to different states of strain of the sample. Some data on model polydimethylsiloxane networks is given as an illustration of the value of this technique.

Materials sciencedata collectionspectra02 engineering and technologysmall angle neutron scattering010402 general chemistry01 natural sciencescyclic deformationsSpectral linechemistry.chemical_compoundMolecular dynamicsOpticsmolecular reorientationpolymersneutron diffraction examination of materialschemistry.chemical_classificationPolydimethylsiloxanebusiness.industryPolymerpolydimethylsiloxane networks021001 nanoscience & nanotechnologySmall-angle neutron scatteringmolecular dynamics0104 chemical sciencesComputational physicschemistry[PHYS.HIST]Physics [physics]/Physics archivesBiological small-angle scattering0210 nano-technologybusinessperiodically deformed polymers
researchProduct

Surface Activity of Soft Polymer Colloids

2019

We investigate the behavior of polymer colloids at the interface between two immiscible liquids using molecular dynamics simulations. We study several colloid morphologies with various degrees of amphiphilicity, that is, purely solvophobic homogeneous and Janus particles and amphiphilic Janus and core-shell particles. Regardless of the specific morphology, the polymer colloids irreversibly anchor at the liquid-liquid interface, accompanied by a marked reduction of the interfacial tension, γ. Purely solvophobic particles lower γ because they reduce the interfacial area shared by the two immiscible liquids, whereas amphiphilic colloids have an additional enthalpic contribution. At the liquid-…

Materials sciencedigestive oral and skin physiologyJanus particles02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSurface tensionColloidMolecular dynamicsChemical physicsAmphiphileElectrochemistryParticleGeneral Materials ScienceJanus0210 nano-technologySolvophobicSpectroscopyLangmuir
researchProduct

Mesoscopic structural organization in fluorinated pyrrolidinium-based room temperature ionic liquids

2019

Abstract In this contribution the microscopic and mesoscopic structural organization in a series of fluorinated room temperature ionic liquids, based on N-methyl-N-alkylpyrrolidinium cations and on bis(perfluoroalkylsulfonyl)imide anions, is investigated, using a synergy of experimental (X-ray and neutron scattering) and computational (Molecular Dynamics) techniques. The proposed ionic liquids are of high interest as electrolyte media for lithium battery applications. Together with information on their good ion transport properties in conjunction with low viscosity, we also describe the existence of nm-scale spatial organization induced by the segregation of fluorous moieties into domains. …

Materials sciencefluorinated02 engineering and technologyElectrolyteNeutron scattering010402 general chemistrymicroscopic01 natural sciencesionic liquidschemistry.chemical_compoundMolecular dynamicsSettore CHIM/02Materials ChemistrymesoscopicPhysics::Chemical PhysicsPhysical and Theoretical ChemistryImideSpectroscopyMesoscopic physicsStructural organizationscatteringionic liquids; fluorinated; microscopic; mesoscopic; scattering; simulation021001 nanoscience & nanotechnologyCondensed Matter PhysicssimulationAtomic and Molecular Physics and OpticsLithium battery0104 chemical sciencesElectronic Optical and Magnetic MaterialschemistryChemical physicsOthersIonic liquidionic liquids structural organization0210 nano-technology
researchProduct

Communication: anion-specific response of mesoscopic organization in ionic liquids upon pressurization

2018

One of the outstanding features of ionic liquids is their inherently hierarchical structural organization at mesoscopic spatial scales. Recently experimental and computational studies showed the fading of this feature when pressurising. Here we use simulations to show that this effect is not general: appropriate anion choice leads to an obstinate resistance against pressurization. Published by AIP Publishing.

Materials scienceneutron x-raycomputational studiesGeneral Physics and Astronomy010402 general chemistrystructural scale01 natural sciencesIonionic liquidsPhysics and Astronomy (all)chemistry.chemical_compoundCabin pressurizationSettore CHIM/02Mesoscopic spatial scalesionic liquidspressurisationmolecular dynamics0103 physical sciencesFadingPhysical and Theoretical Chemistrystructural organization; ionic liquids; structural scale; computational studies; mesoscopic organizationMesoscopic physicsStructural organization010304 chemical physicsstructural organization0104 chemical scienceschemistryChemical physicsFeature (computer vision)mesoscopic organizationIonic liquid
researchProduct

H2 Transformations on Graphene Supported Palladium Cluster: DFT-MD Simulations and NEB Calculations

2020

Molecular dynamics simulations based on density functional theory were employed to investigate the fate of a hydrogen molecule shot with different kinetic energy toward a hydrogenated palladium cluster anchored on the vacant site of a defective graphene sheet. Hits resulting in H2 adsorption occur until the cluster is fully saturated. The influence of H content over Pd with respect to atomic hydrogen spillover onto graphene was investigated. Calculated energy barriers of ca. 1.6 eV for H-spillover suggest that the investigated Pd/graphene system is a good candidate for hydrogen storage.

Materials sciencespilloverhydrogen reactionchemistry.chemical_elementsupported metal catalysts02 engineering and technology010402 general chemistryKinetic energylcsh:Chemical technology01 natural sciencesDFTCatalysislaw.inventionlcsh:ChemistryMolecular dynamicsHydrogen storagelawCluster (physics)lcsh:TP1-1185Physical and Theoretical Chemistryhydrogenation elementary eventsGraphene021001 nanoscience & nanotechnology0104 chemical scienceschemistrylcsh:QD1-999Chemical physicsDensity functional theoryHydrogen spillover0210 nano-technologyPalladiumCatalysts
researchProduct

Limits of stability in supported graphene nanoribbons subject to bending

2016

Graphene nanoribbons are prone to in-plane bending even when supported on flat substrates. However, the amount of bending that ribbons can stably withstand remains poorly known. Here, by using molecular dynamics simulations, we study the stability limits of 0.5-1.9 nm wide armchair and zigzag graphene nanoribbons subject to bending. We observe that the limits for maximum stable curvatures are below ~10 deg/nm, in case the bending is externally forced and the limit is caused by buckling instability. Furthermore, it turns out that the limits for maximum stable curvatures are also below ~10 deg/nm, in case the bending is not forced and the limit arises only from the corrugated potential energy…

Materials sciencestability limitsFOS: Physical sciencesNanotechnology02 engineering and technologyLimits of stability01 natural sciencesPotential energy landscapeMolecular dynamicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesElasticity (economics)010306 general physicsta114Condensed Matter - Mesoscale and Nanoscale PhysicsCondensed matter physicsmolecular dynamics simulationsBuckling instabilitybending021001 nanoscience & nanotechnologyZigzagPure bending0210 nano-technologyGraphene nanoribbonsgraphene nanoribbonsPhysical Review B
researchProduct