Search results for "density functionals"

showing 10 items of 20 documents

Landau parameters for energy density functionals generated by local finite-range pseudopotentials

2017

In Landau theory of Fermi liquids, the particle-hole interaction near the Fermi energy in different spin-isospin channels is probed in terms of an expansion over the Legendre polynomials. This provides a useful and efficient way to constrain properties of nuclear energy density functionals in symmetric nuclear matter and finite nuclei. In this study, we present general expressions for Landau parameters corresponding to a two-body central local regularized pseudopotential. We also show results obtained for two recently adjusted NLO and N$^2$LO parametrizations. Such pseudopotentials will be used to determine mean-field and beyond-mean-field properties of paired nuclei across the entire nucle…

Nuclear and High Energy PhysicsNuclear Theory[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]HARTREE-FOCK CALCULATIONSNuclear Theoryregularized pseudopotentialsFOS: Physical sciencesFinite range114 Physical sciences7. Clean energy01 natural sciencesenergy density functionalsNuclear Theory (nucl-th)PseudopotentialLandau parametersQuantum mechanics0103 physical sciencesNuclear Experiment010306 general physicsLegendre polynomialsNUCLEAR-MATTERPhysics010308 nuclear & particles physicsFermi energyNuclear matterLandau theoryEnergy densityFermi Gamma-ray Space TelescopeJournal of Physics G: Nuclear and Particle Physics
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Nonlocal energy density functionals for pairing and beyond-mean-field calculations

2017

We propose to use two-body regularized finite-range pseudopotential to generate nuclear energy density functional (EDF) in both particle-hole and particle-particle channels, which makes it free from self-interaction and self-pairing, and also free from singularities when used beyond mean field. We derive a sequence of pseudopotentials regularized up to next-to-leading order (NLO) and next-to-next-to-leading order (N2LO), which fairly well describe infinite-nuclear-matter properties and finite open-shell paired and/or deformed nuclei. Since pure two-body pseudopotentials cannot generate sufficiently large effective mass, the obtained solutions constitute a preliminary step towards future imp…

Nuclear and High Energy PhysicsNuclear Theory[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]regularized pseudopotentialsFOS: Physical sciences114 Physical sciences01 natural sciences7. Clean energyenergy density functionalsPseudopotentialNuclear Theory (nucl-th)Effective mass (solid-state physics)0103 physical sciencesEQUATIONStatistical physics010306 general physicsPhysicsNUCLEIEnergy density functional010308 nuclear & particles physicsMean field theoryPairingEnergy densitynuclear pairingGravitational singularityFORCES
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Properties of nuclei in the nobelium region studied within the covariant, Skyrme, and Gogny energy density functionals

2015

We calculate properties of the ground and excited states of nuclei in the nobelium region for proton and neutron numbers of 92 <= Z <= 104 and 144 <= N <= 156, respectively. We use three different energy-density-functional (EDF) approaches, based on covariant, Skyrme, and Gogny functionals, each within two different parameter sets. A comparative analysis of the results obtained for odd-even mass staggerings, quasiparticle spectra, and moments of inertia allows us to identify single-particle and shell effects that are characteristic to these different models and to illustrate possible systematic uncertainties related to using the EDF modelling

Nuclear and High Energy Physics[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]ProtonNuclear TheoryNuclear Theorychemistry.chemical_elementFOS: Physical sciences7. Clean energySpectral lineMoments of inertiaNuclear physicsNuclear Theory (nucl-th)NeutronCovariant transformationHeavy and superheavy nucleiPhysicsta114Odd–even mass staggeringMoment of inertiachemistryExcited stateQuasiparticleNobeliumQuasiparticle excitationsNuclear energy density functionalsNuclear masses
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Spectroscopic Properties of Nuclear Skyrme Energy Density Functionals

2014

We address the question of how to improve the agreement between theoretical nuclear single-particle energies (SPEs) and experiment. Empirically, in doubly magic nuclei, the SPEs can be deduced from spectroscopic properties of odd nuclei that have one more, or one less neutron or proton. Theoretically, bare SPEs, before being confronted with experiment, must be corrected for the effects of the particle-vibration-coupling (PVC). In the present work, we determine the PVC corrections in a fully self-consistent way. Then, we adjust the SPEs, with PVC corrections included, to empirical data. In this way, the agreement with experiment, on average, improves; nevertheless, large discrepancies still …

PhysicsEmpirical dataNuclear Theoryta114FOS: Physical sciencesGeneral Physics and Astronomyenergy density functionals3. Good healthNuclear Theory (nucl-th)Nuclear physicsnuclear skyrmeEnergy densityNeutronspectroscopic propertiesNuclear theoryPhysical review letters
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Mean-Field Calculation Based on Proton-Neutron Mixed Energy Density Functionals

2015

We have performed calculations based on the Skyrme energy density functional (EDF) that includes arbitrary mixing between protons and neutrons. In this framework, single-particle states are generalized as mixtures of proton and neutron components. The model assumes that the Skyrme EDF is invariant under the rotation in isospin space and the Coulomb force is the only source of the isospin symmetry breaking. To control the isospin of the system, we employ the isocranking method, which is analogous to the standard cranking approach used for describing high-spin states. Here, we present results of the isocranking calculations performed for the isobaric analog states in A = 40 and A = 54 nuclei.

Physicsta114Proton010308 nuclear & particles physicsNuclear TheoryInvariant (physics)01 natural sciencesenergy density functionalsCoulomb's lawNuclear physicssymbols.namesakeMean field theoryproton-neutron mixingisobaric analog statesQuantum electrodynamicsIsospin0103 physical sciencessymbolsIsobaric processNeutronSymmetry breakingNuclear Experiment010306 general physicsProceedings of the Conference on Advances in Radioactive Isotope Science (ARIS2014)
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Large Conductance Switching in a Single-Molecule Device through Room Temperature Spin-Dependent Transport

2016

Controlling the spin of electrons in nanoscale electronic devices is one of the most promising topics aiming at developing devices with rapid and high density information storage capabilities. The interface magnetism or spinterface resulting from the interaction between a magnetic molecule and a metal surface, or vice versa, has become a key ingredient in creating nanoscale molecular devices with novel functionalities. Here, we present a single-molecule wire that displays large (>10000%) conductance switching by controlling the spin-dependent transport under ambient conditions (room temperature in a liquid cell). The molecular wire is built by trapping individual spin crossover Fe-II comple…

SpinterfaceMagnetoresistanceMagnetismIronBioengineering02 engineering and technologyLigands010402 general chemistry01 natural sciencesMolecular wireSpin-crossover complexesSpin crossoverNanotechnologyGeneral Materials ScienceDensity functionalsSpin orbit couplingSTM break-junctionCondensed matter physicsNanotecnologiaMagnetoresistanceChemistryMechanical EngineeringTeoria del funcional de densitatConductanceGeneral ChemistrySpin–orbit interaction021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesDensity functional calculationsLligandsSingle-molecule junctionsFerromagnetismChemical physicsElectrode0210 nano-technologyFerroNano Letters
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Katalizatory i proces koordynacyjnej polimeryzacji etylenu - eksperyment i teoria

2004

Badania eksperymentalne i teoretyczne koordynacyjnej polimeryzacji etylenu przeprowadzono wobec katalizatorów otrzymanych z prekursorów - kompleksów halogenków Ti, Zr, Hf, V z organicznymi zasadami Lewisa, nośnika magnezowego [MgCl2(THF)2] i związków glinoorganicznych. Określono zależnosć pomiędzy rodzajem halogenków w prekursorze a aktywnością katalizatora wanadowego. Ustalono profile energetyczne reakcji insercji i terminacji (beta-eliminacji) oraz przeniesienia atomu wodoru beta. Obliczone wartości barier insercji, a także energii wiązania etylenu do centrum aktywnego dobrze korelują z wynikami polimeryzacji. Stwierdzono występowanie w centrach aktywnych oddziaływań agostycznych, które o…

energetic profilesHfkompleksy halogenków TiZrHf i Vreakcja terminacjikoordynacyjna polimeryzacja etylenuprofil energetycznycatalytic activitynośnik magnezowyreakcja insercjimagnesium supportV halidesdensity functionals method (DFT)aktywność katalitycznaoxygen-donor ligandsinsertion and termination reactionspolimeryzacja etylenucoordination polymerization of ethylenecomplexes of Tiligandy tlen-donorowePolimery
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Higher-order energy density functionals in nuclear self-consistent theory

2011

In this thesis consisting of two publications and an overview part, a study of two aspects of energy density functionals has been performed. Firstly, we have linked the next-to-next-to-next-to-leading order nuclear energy density functional to a zero-range pseudopotential that includes all possible terms up to sixth order in derivatives. Within the Hartree-Fock approximation, the quasi-local nuclear Energy Density Functional (EDF) has been calculated as the average energy obtained from the pseudopotential. The direct reference of the EDF to the pseudopotential acts as a constraint that allows for expressing the isovector coupling constants functional in terms of the isoscalar ones, or vice …

pseudopotentialsydinenergianuclear energy density functionalscontinuity equationbioceramics
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Structure and dynamics in liquid bismuth and Bin clusters: A density functional study

2014

Density functional/molecular dynamics simulations with more than 500 atoms have been performed on liquid bismuth at 573, 773, 923, and 1023 K and on neutral Bi clusters with up to 14 atoms. There are similar structural patterns (coordination numbers, bond angles, and ring patterns) in the liquid and the clusters, with significant differences from the rhombohedral crystalline form. We study the details of the structure (structure factor, pair, and cavity distribution functions) and dynamical properties (vibration frequencies, diffusion constants, power spectra), and compare with experimental results where available. While the three short covalent bonds typical to pnictogens are characteristi…

vibration frequencyCoordination numberGeneral Physics and Astronomychemistry.chemical_element02 engineering and technology01 natural sciencesMolecular physicsBinBismuthMolecular dynamics0103 physical sciencesAtomPhysical and Theoretical Chemistry010306 general physicsconcentration variationspin-orbit couplingsta114021001 nanoscience & nanotechnologybismuth distribution functionsdynamical propertiesMolecular geometrychemistrydensity functionalsddc:540structure and dynamicsDensity functional theoryAtomic physics0210 nano-technologyStructure factordensity-functional studycoordination numberJournal of chemical physics
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Conformational investigation of alpha,beta-dehydropeptides. IX. N-Acetyl-(E)-alpha,beta-methylamide: stereoelectronic properties from infrared and th…

1998

The Fourier transform infrared spectra of Ac-(E)-deltaAbu-NHMe were analyzed to determine the predominant solution conformation(s) of this (E)-alpha,beta-dehydropeptide-related compound and the electron density perturbation in its amide groups. The measurements were performed in dichloromethane and acetonitrile in the region of mode vs (N-H), amide I, amide II and vs (C(alpha)=Cbeta). The equilibrium geometrical parameters, calculated by a method based on the density functional theory with the B3LYP functional and the 6-31G* basis set, were used to support spectroscopic interpretation and gain some deeper insight into the molecule. The experimental and theoretical data were compared with th…

β-dehydroamino acidsFTIR spectroscopyα(E)-αMolecular orbital methodAmidic resonanceC5 hydrogen bondβ- dehydrobutyrineC5 conformationSolution peptide conformationDensity functionalsJOURNAL OF PEPTIDE RESEARCH
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