Search results for "Hamiltonian"

showing 10 items of 662 documents

Dependence of two-proton radioactivity on nuclear pairing models

2017

Sensitivity of two-proton emitting decay to nuclear pairing correlation is discussed within a time-dependent three-body model. We focus on the $^6$Be nucleus assuming $\alpha + p + p$ configuration, and its decay process is described as a time-evolution of the three-body resonance state. For a proton-proton subsystem, a schematic density-dependent contact (SDDC) pairing model is employed. From the time-dependent calculation, we observed the exponential decay rule of a two-proton emission. It is shown that the density dependence does not play a major role in determining the decay width, which can be controlled only by the asymptotic strength of the pairing interaction. This asymptotic pairin…

Light nucleusNuclear TheoryNuclear TheoryFOS: Physical sciences01 natural sciences114 Physical sciencesDECAYSNuclear Theory (nucl-th)symbols.namesakeENERGY-LEVELSLIMITS0103 physical sciencesmedicineExponential decayNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentNuclear ExperimentPhysicsta114010308 nuclear & particles physicsQUASI-STATIONARY STATEproton emissionTime evolutionwidthsnuclear forcesScattering lengthDRIP-LINEmedicine.anatomical_structureLIGHT-NUCLEIDensity distributionPairing3-BODY SYSTEMfew-body systemssymbolslifetimesAtomic physicsHamiltonian (quantum mechanics)Nucleus
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Chaotic Scattering in the Gaussian Potential

1995

It is well known that general classical Hamiltonian dynamical systems have as a rule chaotic behaviour. By such a term one usually understands a sensitive dependence on initial conditions which manifests itself in the topology of phase space. For the most studied case of bounded motions this behaviour is detected, for example, by analysing the Poincare surfaces of section and by calculating Lyapunov characteristic exponents. The question then naturally arises of what are the effects of this complexity on the unbounded motions, i.e., on scattering phenomena. The signature of chaotic dynamics in these scattering regions of phase space has been the object of several papers appeared mainly in t…

Lyapunov functionPhysicssymbols.namesakeClassical mechanicsDynamical systems theoryBounded functionChaotic scatteringPhase spacesymbolsChaoticCovariant Hamiltonian field theoryHamiltonian (quantum mechanics)
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Isomorphous replacement of MII ions in MII–GdIII dimers (MII = CuII, MnII, NiII, CoII, ZnII): magnetic studies of the products

2011

Complexes [M(II)Gd(III){pyCO(OEt)pyC(OH)(OEt)py}₃](ClO₄)₂·EtOH [M(II) = Cu(II) (1), Mn(II) (2), Ni(II) (3), Co(II) (4) and Zn(II) (5)] crystallize in the monoclinic Cc space group and contain one hexacoordinate M(II) ion and one enneacoordinate Gd(III) ion, bridged by three {pyCO(OEt)pyC(OH)(OEt)py}⁻ ligands. Magnetic susceptibility measurements indicate a ferromagnetic interaction for 1 and antiferromagnetic interactions for 2-4. Using the Ĥ = -JŜ(Gd(III))Ŝ(M(II)) spin Hamiltonian formalism, fits to the magnetic susceptibility data yielded J values of +0.32 cm⁻¹ for 1, -1.7 cm⁻¹ for 2, and -0.22 cm⁻¹ for 3. In complex 4, the orbital contributions of Co(II) precluded the determination of th…

ManganeseChemistryStereochemistryMolecular ConformationHexacoordinateSpin hamiltonianGadoliniumCobaltCrystallography X-RayMagnetic susceptibilityInductive couplingIonInorganic ChemistryMagneticsZincCrystallographyFerromagnetismCoordination ComplexesMetalsNickelAntiferromagnetismDimerizationCopperMonoclinic crystal systemDalton Transactions
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High-Resolution Stimulated Raman Spectroscopy of Methane 13CD4 in the Pentad Region

1988

Abstract We present the first Raman spectrum of 13CD4 recorded at room temperature in the pentad region by inverse Raman spectroscopy, thus including the ν1 (A1), 2ν2 (A1), 2ν4 (A1), and ν2 + ν4(F1 + F2) Q branches. It is noteworthy that the overtone bands 2ν2 and 2ν4 are observed for the first time in a methane-like molecule by a coherent Raman process. The wide frequency range investigated, covering 45 cm−1 in three parts, contains more than 300 lines with uncertainty less than 10−3 cm−1 in most cases. These Raman data are combined with high-resolution infrared data in a weighted least-squares fit of the vibration-rotation constants of the pentad, thanks to a relevant partially reduced ef…

Materials science010304 chemical physicsInfraredOvertone02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsAtomic and Molecular Physics and Opticssymbols.namesakeNuclear magnetic resonance0103 physical sciencessymbolsCoherent anti-Stokes Raman spectroscopyPhysical and Theoretical Chemistry0210 nano-technologySpectroscopyHamiltonian (quantum mechanics)Raman spectroscopySpectroscopyRaman scatteringOrder of magnitude
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Hybrid Particle-Field Molecular Dynamics Simulations of Charged Amphiphiles in an Aqueous Environment.

2018

We develop and test specific coarse-grained models for charged amphiphilic systems such as palmitoyloleoylphosphatidylglycerol (POPG) lipid bilayer and sodium dodecyl sulfate (SDS) surfactant in an aqueous environment, to verify the ability of the hybrid particle-field method to provide a realistic description of polyelectrolytes. According to the hybrid approach, the intramolecular interactions are treated by a standard molecular Hamiltonian, and the nonelectrostatic intermolecular forces are described by density fields. Electrostatics is introduced as an additional external field obtained by a modified particle-mesh Ewald procedure, as recently proposed [Zhu et al. Phys. Chem. Chem. Phys.…

Materials scienceAqueous solution010304 chemical physicsIntermolecular force010402 general chemistryElectrostatics01 natural sciencesPolyelectrolyte0104 chemical sciencesComputer Science ApplicationsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicschemistryChemical physicsIntramolecular force0103 physical sciencesMolecular HamiltonianPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySodium dodecyl sulfateJournal of chemical theory and computation
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Tight-Binding study of the electronic and magnetic properties of an L1_0 ordered FeCu alloy

1997

We have calculated the electronic structure of the tetragonal L1$_0$ ordered FeCu by solving self-consistently a tight-binding Hamiltonian for s, p and d electrons. We have found by total energy calculation that this structure is ferromagnetic. In addition, we have determined that the equilibrium ratio between the interlayer and the intralayer lattice parameters is 0.947.

Materials scienceCondensed matter physicsAlloyCondensed Matter (cond-mat)General Physics and AstronomyFOS: Physical sciencesElectronElectronic structureCondensed Matterengineering.materialsymbols.namesakeTetragonal crystal systemCondensed Matter::Materials ScienceTight bindingFerromagnetismLattice (order)Condensed Matter::SuperconductivitysymbolsengineeringCondensed Matter::Strongly Correlated ElectronsHamiltonian (quantum mechanics)
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Monte Carlo Simulations of Body Centered Cubic Alloys

1994

We illustrate the use of Monte Carlo simulations in the study of order-disorder phenomena in metallic alloys by presenting detailed work on a fairly realistic lattice model for iron aluminum. The model has been constructed based on recent measurements of effective interaction parameters and includes a description of the magnetism of iron within a Heisenberg Hamiltonian. We show that it reproduces the bulk phase diagram in a qualitatively correct way. Then internal antiphase boundaries and free surfaces in the (100)-direction are studied. An interfacial roughening transition is predicted as well as critical broadening of the profiles as the bulk approaches a second order transition. Nonstoec…

Materials scienceCondensed matter physicsMagnetismMonte Carlo methodchemistry.chemical_elementCubic crystal systemMetallic alloysymbols.namesakechemistrySurface fieldAluminiumsymbolsHamiltonian (quantum mechanics)Phase diagram
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Electronic structure of poly(p-(disilanylene)phenylene)

1996

Abstract We present the geometrical and electronic structures of several isomers of poly(p-(disilanylene)phenylene), The structural analysis, performed at the 3-21G* level, shows that the isomers with the phenylene group perpendicular to the silicon backbone are the more stable conformations, displaying almost the same energy. The electronic properties, as obtained from the valence-effective Hamiltonian (VEH) band structure calculations, strongly depend on the disposition of the phenylene group into the polymeric backbone. The VEH predicts a wide and asymmetric absorption band in excellent agreement with UV experimental data.

Materials scienceSiliconMechanical EngineeringMetals and Alloyschemistry.chemical_elementElectronic structureCondensed Matter PhysicsElectronic Optical and Magnetic Materialssymbols.namesakeCrystallographychemistryMechanics of MaterialsAbsorption bandPhenylenePolymer chemistryPhysics::Atomic and Molecular ClustersMaterials ChemistrysymbolsElectronic band structureHamiltonian (quantum mechanics)Electronic propertiesSynthetic Metals
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Infrared spectroscopy of ruthenium tetroxide and high-resolution analysis of the ν3 band

2015

Abstract RuO 4 is a heavy tetrahedral molecule which has practical uses for several industrial fields. Due to its chemical toxicity and the radiological impact of its 103 and 106 isotopologues, the possible remote sensing of this compound in the atmosphere has renewed interest in its spectroscopic properties. New, higher resolution FTIR spectra have been recorded at room temperature, using an isotopic pure sample of 102 RuO 4 and a sample with all stable isotopes present in natural abundance. We reinvestigate here the strong ν 3 stretching fundamental region and perform new assignments and effective Hamiltonian parameter fits for the five main isotopologues ( 99 RuO 4 , 100 RuO 4 , 101 RuO …

Materials scienceStable isotope ratioAnalytical chemistryTetrahedral molecular geometryInfrared spectroscopyAtomic and Molecular Physics and OpticsSpectral lineRuthenium tetroxidesymbols.namesakechemistry.chemical_compoundNuclear magnetic resonancechemistryIsotopic shiftsymbolsIsotopologuePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)SpectroscopyJournal of Molecular Spectroscopy
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Evolution of the electronic properties of graded poly(thienylene vinylene)-poly(pyrrylene vinylene) mixed copolymers

1993

Abstract We present a valence effective Hamiltonian (VEH) theoretical investigation of the evolution of the electronic properties of poly(thienylene vinylene)-poly(pyrrylene vinylene) mixed copolymers as a function of the unit cell content on the basis of ab initio 3–21G∗ and 3–21G optimized geometries. As a consequence of the strong localization of the LUCO both electron affinity and bandgap deviate from a linear dependence, and only the ionization potential presents the expected values.

Materials scienceValence (chemistry)Band gapMechanical EngineeringMetals and AlloysAb initioCondensed Matter PhysicsElectronic Optical and Magnetic Materialssymbols.namesakeMechanics of MaterialsComputational chemistryMaterials ChemistrysymbolsCopolymerPhysical chemistryIonization energyHamiltonian (quantum mechanics)Electronic propertiesSynthetic Metals
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