Search results for "ZA"

showing 10 items of 45515 documents

A Local Study of the Transport Mechanisms in MoS2 Layers for Magnetic Tunnel Junctions

2018

MoS2-based vertical spintronic devices have attracted an increasing interest thanks to theoretical predictions of large magnetoresistance signals. However, experimental performances are still far from expectations. Here, we carry out the local electrical characterization of thin MoS2 flakes in a Co/Al2O3/MoS2 structure through conductive tip AFM measurements. We show that thin MoS2 presents a metallic behavior with a strong lateral transport contribution that hinders the direct tunnelling through thin layers. Indeed, no resistance dependence is observed with the flake thickness. These findings reveal a spin depolarization source in the MoS2-based spin valves, thus pointing to possible solut…

010302 applied physics[PHYS]Physics [physics]Thin layersMaterials scienceCondensed matter physicsMagnetoresistanceSpintronics02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesLocal studyCharacterization (materials science)0103 physical sciencesGeneral Materials Science[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]0210 nano-technologyElectrical conductorQuantum tunnellingComputingMilieux_MISCELLANEOUSSpin-½
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Review of the PEA Method for Space Charge Measurements on HVDC Cables and Mini-Cables

2019

This review takes into account articles and standards published in recent years concerning the application of the Pulsed Electro Acoustic (PEA) method for space charge measurement on High Voltage Direct Current (HVDC) cables and mini-cables. Since the 80s, the PEA method has been implemented for space charge measurements on flat specimens in order to investigate space charge phenomena and to evaluate the ageing of dielectrics. In recent years, this technique has been adapted to cylindrical geometry. Several studies and experiments have been carried out on the use of the PEA method for full size cables and HVDC cable models. The experiments have been conducted using different arrangements of…

010302 applied physicspulsed Electroacoustic technique (PEA)Cylindrical geometryControl and Optimizationlcsh:TRenewable Energy Sustainability and the EnvironmentComputer science020209 energyEnergy Engineering and Power TechnologyMechanical engineering02 engineering and technologylcsh:Technology01 natural sciencesSpace chargeHVDC cablesSpace chargeSettore ING-IND/31 - ElettrotecnicaReliability (semiconductor)0103 physical sciences0202 electrical engineering electronic engineering information engineeringHigh-voltage direct currentElectrical and Electronic EngineeringEngineering (miscellaneous)Energy (miscellaneous)
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Laser-induced enhancement of tunneling in NHD2

2012

We apply and explore techniques aiming at enhancing the tunneling by laser fields, originally developed for a one-dimensional model, to a complete six-dimensional vibrational model of the inversion motion in NHD(2). The computational study is performed with the multi-configuration time-dependent Hartree method. Assuming an ideal three-dimensional alignment we obtain a driven tunneling time twenty times smaller than the natural one, in rather good agreement with an oversimplified three-state model. In the case of one-dimensional alignment, a linearly polarized field leads to a poor enhancement of the tunneling probability, after averaging over the rotation about the alignment axis, whereas a…

010304 chemical physicsChemistryLinear polarizationScanning tunneling spectroscopyGeneral Physics and AstronomyHartreeLaser01 natural scienceslaw.invention[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrylaw0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryPhysical and Theoretical ChemistryAtomic physics010306 general physicsTunneling timeQuantum tunnellingComputingMilieux_MISCELLANEOUS
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A QM/MM Approach Using the AMOEBA Polarizable Embedding: From Ground State Energies to Electronic Excitations

2016

International audience; A fully polarizable implementation of the hybrid Quantum Mechanics/Molecular Mechanics approach is presented, where the classical environment is described through the AMOEBA polarizable force field. A variational formalism, offering a self-consistent 1 relaxation of both the MM induced dipoles and the QM electronic density is used for ground state energies and extended to electronic excitations in the framework of Time-Dependent Density Functional Theory combined with a state specific response of the classical part. An application to the calculation of the solvatochromism of the pyridinium N-phenolate betaine dye used to define the solvent ET30 scale is presented. Th…

010304 chemical physicsChemistryPolarizable force fieldSolvatochromismQuantum Chemistry010402 general chemistryElementary chargeQM/MM01 natural sciences0104 chemical sciencesComputer Science Applications[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryQM/MMQM/MM; Polarisable embedding; Physical and Theoretical ChemistryPolarizabilityQuantum mechanics0103 physical sciencesPolarisable embeddingDensity functional theorypolarizable force field AMOEBAPhysical and Theoretical ChemistryGround stateExcitationElectronic densityJournal of Chemical Theory and Computation
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Dynamic Polarizability and Higher-Order Electric Properties of Fluorene, Carbazole, and Dibenzofuran

2019

Static electric properties, from the dipole moment to the second-hyperpolarizability tensor γ, of the 3-membered, isoelectronic ring molecules, fluorene (FL), carbazole (CR), and dibenzofuran (DBF), have been calculated at various levels of approximation. The electron correlation effects have been included at the coupled-cluster (CC) level, using CCSD and CC2 versions of the method. DFT calculations with the CAM-B3LYP functional have also been performed, and the results are compared to the CC values. The electric property-tailored Pol basis set and its more compact Z3Pol version have been employed in all static calculations. Differences between dipole polarizability values computed at the P…

010304 chemical physicsElectronic correlationChemistryCarbazoleFluorene010402 general chemistry01 natural sciencesMolecular physics0104 chemical scienceschemistry.chemical_compoundDipolePolarizabilityExcited state0103 physical sciencesPhysical and Theoretical ChemistryBasis setExcitationJournal of Physical Chemistry A
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Gas-Phase Synthesis of the Elusive Trisilicontetrahydride Species (Si3H4)

2016

The bimolecular gas-phase reaction of ground-state atomic silicon (Si; 3P) with disilane (Si2H6; 1A1g) was explored under single-collision conditions in a crossed molecular beam machine at a collision energy of 21 kJ mol–1. Combined with electronic structure calculations, the results suggest the formation of Si3H4 isomer(s) along with molecular hydrogen via indirect scattering dynamics through Si3H6 collision complex(es) and intersystem crossing from the triplet to the singlet surface. The nonadiabatic reaction dynamics can synthesize the energetically accessible singlet Si3H4 isomers in overall exoergic reaction(s) (−93 ± 21 kJ mol–1). All reasonable reaction products are either cyclic or …

010304 chemical physicsElectronic structure010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesChemical DynamicsCrossed molecular beamchemistry.chemical_compoundIntersystem crossingchemistryReaction dynamics0103 physical sciencesGeneral Materials ScienceSinglet stateDisilanePhysical and Theoretical ChemistryIsomerizationThe Journal of Physical Chemistry Letters
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Approximate treatment of higher excitations in coupled-cluster theory. II. Extension to general single-determinant reference functions and improved a…

2008

The theory and implementation of approximate coupled-cluster (CC), in particular approximate CC singles, doubles, triples, and quadruples methods, are discussed for general single-determinant reference functions. While the extension of iterative approximate models to the non-Hartree-Fock case is straightforward, the generalization of perturbative approaches is not trivial. In contrast to the corresponding perturbative triples methods, there are additional terms required for non-Hartree-Fock reference functions, and there are several possibilities to derive approximations to these terms. As it turns out impossible to develop an approach that is consistent with the canonical Hartree-Fock-base…

010304 chemical physicsGeneralizationHartree–Fock methodGeneral Physics and AstronomyContrast (statistics)Extension (predicate logic)010402 general chemistry01 natural sciences0104 chemical sciencesCoupled clusterComputational chemistry0103 physical sciencesApplied mathematicsPerturbation theory (quantum mechanics)Physical and Theoretical ChemistryMathematicsThe Journal of Chemical Physics
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pKa at Quartz/Electrolyte Interfaces.

2016

Acidity of silanol sites at the crystalline quartz/aqueous electrolyte (NaCl, NaI, KCl) interfaces are calculated from ab initio molecular dynamics simulations. pKa’s are found to follow a combination of the cationic and anionic Hofmeister series in the order pKa(neat solution) < pKa(NaCl) < pKa(NaI) < pKa(KCl), in agreement with experimental measurements. Rationalization of this ranking is achieved in terms of the microscopic local solvation of the protonated silanols and their conjugated bases, the silanolates SiO–. The change in the pKa is the result of both water destructuring by alkali halides, as well as of the specific cation/SiO– interaction, depending on the electrolyte. M…

010304 chemical physicsHofmeister series[SDV]Life Sciences [q-bio]Inorganic chemistrySolvationCationic polymerizationHalideProtonation02 engineering and technologyElectrolyte021001 nanoscience & nanotechnologyAlkali metal01 natural sciencesSilanolchemistry.chemical_compoundchemistry0103 physical sciencesGeneral Materials Science[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical Chemistry0210 nano-technologyThe journal of physical chemistry letters
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Inelastic neutron scattering study of proton dynamics in Ca(OH)2 at 20 K

1995

Abstract Inelastic neutron scattering (INS) spectra of Ca(OH) 2 at 20 K are presented from 30 to 4000 cm −1 for a powder sample, from 30 to 12000 cm −1 for an oriented single-crystal. INS band splitting due to the lattice density-of-states is observed. Polarization effects reveal the orientation of atomic displacements for each mode and a new band assignment scheme is proposed. For the single-crystal, the v OH mode and overtones are observed. This oscillator shows only moderate anharmonicity. Spectrum simulation reveals that INS spectral intensities are not consistent with simple normal coordinates and harmonic force-fields for Ca(OH) 2 entities. A new dynamical model is proposed, including…

010304 chemical physicsInfraredChemistryAnharmonicityGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnologyPolarization (waves)01 natural sciencesMolecular physicsSpectral lineInelastic neutron scatteringsymbols.namesakeCrystallographyLattice (order)0103 physical sciencessymbolsNormal coordinates[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technologyRaman spectroscopyComputingMilieux_MISCELLANEOUS
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Pressure‐induced widths and shifts for the ν3 band of methane

1994

International audience; Widths and shifts of methane lines perturbed by nitrogen are calculated using a complex-valued implementation of Robert-Bonamy (RB) theory. The static intermolecular potential is described as a sum of electrostatic forces and Lennard-Jones (6-12) atom-atom terms, using literature values for all physical parameters. Vibrational dependence of the isotropic potential is obtained from the polarizability of methane assuming a dispersion interaction. The repulsive part of the Lennard-Jones accounts for the greatest part of widths, while dispersion interactions are largely responsible for shifts. Although the average error between calculated and observed linewidths (up to J…

010304 chemical physicsMathematical modelAbsorption spectroscopyIntermolecular forceIsotropyGeneral Physics and Astronomy7. Clean energy01 natural sciencesMethane010309 opticschemistry.chemical_compoundLennard-Jones potentialchemistryPolarizability0103 physical sciencesDispersion (optics)Physics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsThe Journal of Chemical Physics
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