Search results for "physics.chem-ph"

showing 10 items of 359 documents

Experimental IR study and ab initio modelling of ethylene adsorption in a MFI - type host zeolite.

2009

International audience; Different ab initio methods and experimental results are used to investigate the effect of the adsorption of one ethylene molecule on silicalite-1, a MFI type zeolite. We used simplified models to simulate a portion of a straight or sinusoidal channel of silicalite-1 at a quantum level. The calculated absorption spectra of the models are qualitatively in good agreement with the experimental FTIR spectrum of silicalite-1. Additionally we simulate the FTIR spectrum of the isolated ethylene molecule and that of an ethylene molecule in interaction with the above-mentioned zeolite models. Results are discussed depending on the method and specific basis set and compared wi…

Ethylene010304 chemical physicsAbsorption spectroscopyChemistryBiophysicsAb initio010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesMolecular dynamicschemistry.chemical_compound[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]AdsorptionComputational chemistry0103 physical sciencesPhysical SciencesPhysical chemistryMolecule[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryZeoliteMolecular BiologyBasis setComputingMilieux_MISCELLANEOUS
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Determination of transport and kinetic properties in self-propagating high-temperature synthesis

2007

International audience; Exothermic reactions in solid powders are analyzed using the usual macroscopic modeling based on the heat transfer equation coupled to an Arrhenius type of dynamics. This problem have important applications in the synthesis of intermetallics and ceramic materials which occur when a high temperature reaction wave propagates throughout the system. Understanding the mechanism of such processes are thus crucial in mastering real laboratory experiments. We first analyze the model, both theoretically and numerically, for a set of representative parameters. We then use traditional data analyses procedures to estimate from the temperature profiles the same set of representat…

Exothermic reactionChemical substanceIntermetallics[ PHYS.COND.CM-MS ] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Self-propagating high-temperature synthesisThermodynamics02 engineering and technologyActivation energy010402 general chemistryKinetic energy01 natural sciencessymbols.namesakePowder metallurgyMaterials ChemistryThermal analysisThermal analysisArrhenius equationChemistryMechanical EngineeringMetals and AlloysMechanicsComputer simulation021001 nanoscience & nanotechnology0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Mechanics of MaterialsHeat transfer[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]symbols[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Solid-state reactions0210 nano-technologyJournal of Alloys and Compounds
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Combustion synthesis of MoSi2 and MoSi2–Mo5Si3 composites: Multilayer modeling and control of the microstructure

2010

International audience; In this work, we present a multilayer modeling for the formation of molybdenum silicides in the exothermic reaction between Mo and Si under the influence of a temperature pulse. The heating rate can either be a well-controlled ramp or be generated spontaneously by the propagation of a combustion synthesis front. The model addresses the specific situation above the melting point of silicon and describes the solid–liquid reaction taking place in a single representative particle of molybdenum surrounded by the melt of silicon. We obtain a set of kinetic equations for the propagation of the interfaces between the different layers (Mo/Mo5Si3 and Mo5Si3/MoSi2) in the solid…

Exothermic reactionMaterials scienceSiliconSelf-propagating high-temperature synthesischemistry.chemical_element02 engineering and technologyCombustion01 natural sciences7. Clean energy[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Powder metallurgy0103 physical sciencesMolybdenum silicidesMaterials ChemistryComposite material010302 applied physicsMechanical EngineeringModelingMetals and Alloys021001 nanoscience & nanotechnologyMicrostructure[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]KineticsSolid–liquid reactionschemistryMechanics of MaterialsMolybdenumMelting pointParticle[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologySelf-propagating high-temperature synthesisJournal of Alloys and Compounds
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Study of the reactive dynamics of nanometric metallic multilayers using Molecular Dynamics: the Al−Ni system

2012

A molecular dynamics study of a layered Ni-Al-Ni system is developed using an embedded atom method potential. The specific geometry is designed to model a Ni-Al nanometric metallic multilayer. The system is initially thermalized at the fixed temperature of 600 K. We first observe the interdiffusion of Ni and Al at the interfaces, which is followed by the spontaneous phase formation of B2-NiAl in the Al layer. The solid-state reaction is associated with a rapid system's heating which further enhances the diffusion processes. NiAl phase is organized in small regions separated by grain boundaries. This study confirms the hypothesis of a layer-by-layer development of the new phase. For longer t…

Exothermic reactionNialMaterials scienceDiffusionmultilayersIntermetallicnanometric metallic multilayersNanotechnology02 engineering and technology01 natural sciencesinterfacesMolecular dynamicsPhase (matter)0103 physical sciencesGeneral Materials Scienceintermetallics010306 general physicscomputer.programming_languageRadiationnanoscale effects[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsMicrostructuremolecular dynamics[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Chemical physics[ CHIM.MATE ] Chemical Sciences/Material chemistryGrain boundary[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologycomputer
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Extension of the MIRS computer package for the modeling of molecular spectra : from effective to full ab initio ro-vibrational hamiltonians in irredu…

2012

The MIRS software for the modeling of ro-vibrational spectra of polyatomic molecules was considerably extended and improved. The original version (Nikitin, et al. JQSRT, 2003, pp. 239--249) was especially designed for separate or simultaneous treatments of complex band systems of polyatomic molecules. It was set up in the frame of effective polyad models by using algorithms based on advanced group theory algebra to take full account of symmetry properties. It has been successfully used for predictions and data fitting (positions and intensities) of numerous spectra of symmetric and spherical top molecules within the vibration extrapolation scheme. The new version offers more advanced possib…

ExtrapolationAb initioFOS: Physical sciences02 engineering and technologyPoint group01 natural scienceshigh-resolution infrared spectroscopyTheoretical physicsAb initio quantum chemistry methodsPhysics - Chemical PhysicsQuantum mechanics0103 physical sciencesMolecular symmetrypolyadsSpectroscopycomputational spectroscopyChemical Physics (physics.chem-ph)Physics[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Radiation010304 chemical physicsab initio calculationseffective hamiltoniansRotational–vibrational spectroscopy021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Opticsmolecular symmetryPhysics - Atmospheric and Oceanic Physicsvibration-rotation spectroscopy[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Atmospheric and Oceanic Physics (physics.ao-ph)Curve fittingirreducible tensors0210 nano-technologyGroup theory
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Visualizing coherent molecular rotation in a gaseous medium

2021

Inducing and controlling the ultrafast molecular rotational dynamics using shaped laser fields is essential in numerous applications. Several approaches exist that allow following the coherent molecular motion in real-time, including Coulomb explosion-based techniques and recovering molecular orientation from the angular distribution of high harmonics. We theoretically consider a non-intrusive optical scheme for visualizing the rotational dynamics in an anisotropic molecular gas. The proposed method allows determining the instantaneous orientation of the principal optical axes of the gas. The method is based on probing the sample using ultra-short circularly polarized laser pulses and recor…

FOS: Physical sciences01 natural sciences7. Clean energyWaveplatelaw.invention010309 opticslawPhysics - Chemical PhysicsOrientation (geometry)0103 physical sciences010306 general physicsComputingMilieux_MISCELLANEOUSPhysics[PHYS]Physics [physics]Chemical Physics (physics.chem-ph)[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Coulomb explosionLaserPulse (physics)Computational physicsVortexHarmonics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Ultrashort pulsePhysics - OpticsOptics (physics.optics)
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Towards nonlocal density functionals by explicit modelling of the exchange-correlation hole in inhomogeneous systems

2013

We put forward new approach for the development of a non-local density functional by a direct modeling of the shape of exchange-correlation (xc) hole in inhomogeneous systems. The functional is aimed at giving an accurate xc-energy and an accurate corresponding xc-potential even in difficult near-degeneracy situations such as molecular bond breaking. In particular we demand that: (1) the xc hole properly contains -1 electron, (2) the xc-potential has the asymptotic -1/r behavior outside finite systems and (3) the xc-potential has the correct step structure related to the derivative discontinuities of the xc-energy functional. None of the currently existing functionals satisfies all these re…

FOS: Physical sciences02 engineering and technologyElectronClassification of discontinuities01 natural sciencesDFTCondensed Matter - Strongly Correlated ElectronsAtomic orbitalQuantum mechanicsPhysics - Chemical Physics0103 physical sciencesPhysics - Atomic and Molecular ClustersSDG 7 - Affordable and Clean Energy010306 general physicsEnergy functionalChemical Physics (physics.chem-ph)PhysicsQuantum Physics/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyStrongly Correlated Electrons (cond-mat.str-el)ta114theoretical nanoscienceFunction (mathematics)021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsCondensed Matter - Other Condensed MatterDensity functional theorySum rule in quantum mechanicsLocal-density approximationAtomic and Molecular Clusters (physics.atm-clus)Quantum Physics (quant-ph)0210 nano-technologyOther Condensed Matter (cond-mat.other)Physical Review A
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Point Group Symmetry Analysis of the Electronic Structure of Bare and Protected Metal Nanocrystals

2018

The electronic structures of a variety of experimentally identified gold and silver nanoclusters from 20 to 246 atoms, either unprotected or protected by several types of ligands, are characterized by using point group specific symmetry analysis. The delocalized electron states around the HOMO-LUMO energy gap, originating from the metal s-electrons in the cluster core, show symmetry characteristics according to the point group that describes best the atomic arrangement of the core. This indicates strong effects of the lattice structure and overall shape of the metal core to the electronic structure, which cannot be captured by the conventional analysis based on identification of spherical a…

FOS: Physical sciences02 engineering and technologyElectronic structureCrystal structure010402 general chemistry01 natural sciencesMolecular physicsArticleNanoclustersDelocalized electronnanocrystalsPhysics - Chemical PhysicsMolecular symmetryPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersPhysical and Theoretical Chemistryta116Chemical Physics (physics.chem-ph)ta114ChemistrySuperatomSpherical harmonicsComputational Physics (physics.comp-ph)021001 nanoscience & nanotechnologySymmetry (physics)0104 chemical sciencesnanohiukkasetAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technologyPhysics - Computational Physics
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Spontaneous emission of a sodium Rydberg atom close to an optical nanofibre

2019

International audience; We report on numerical calculations of the spontaneous emission rate of a Rydberg-excited sodium atom in the vicinity of an optical nanobre. In particular, we study how this rate varies with the distance of the atom to the bre, the bre's radius, the symmetry s or p of the Rydberg state as well as its principal quantum number. We nd that a fraction of the spontaneously emitted light can be captured and guided along the bre. This suggests that such a setup could be used for networking atomic ensembles, manipulated in a collective way due to the Rydberg blockade phenomenon.

FOS: Physical sciences02 engineering and technologyoptical nanofibres01 natural sciencessymbols.namesake020210 optoelectronics & photonics[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]0103 physical sciencesAtomPrincipal quantum number0202 electrical engineering electronic engineering information engineeringSpontaneous emissionPhysics::Atomic Physics010306 general physicsPhysicsQuantum Physics[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Spontaneous emission ratesRadiusCondensed Matter Physicsspontaneous emission ratesAtomic and Molecular Physics and OpticsSymmetry (physics)Optical nanobresRydberg atomRydberg formulasymbols[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsRydberg stateQuantum Physics (quant-ph)Rydberg atoms
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Génération de supercontinuum infrarouge et enjeux de vieillissement au sein de fibres optiques à coeur suspendu hautement non linéaires en verre de c…

2014

The work reported in this thesis deals with the fabrication of suspended core chalcogenide microstructured optical fibers (MOFs) for supercontinuum generation (SCG) beyond 6 μm. In this context, As2S3-based suspended-core MOFs were fabricated under vacuum, and loss threshold of 1-2 dB/m at 2.9µm were systematically registered. In addition, MOFs were designed with core diameter ranging from 1.5 to 3.5µm, allowing therefore to control the MOF's dispersive properties and to shift corresponding zero dispersion wavelength to 2.0-2.5 µm range. SCG experiments were performed by pumping the fabricated MOFs in their anomalous dispersion regime by means of tunable femtosecond laser source. Simultaneo…

Fibres de chalcogénuresGénération supercontinuum[CHIM.MATE] Chemical Sciences/Material chemistryConception et fabrication des fibres optiquesFibres optiques microstructuréesInfrarouge proche et infrarouge moyenNon linéarités optiqueVieillissementChalcogenide fibersDurabilité[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]
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