Search results for "physics.atm-clus"

showing 10 items of 38 documents

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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Efficient and accurate modeling of electron photoemission in nanostructures with TDDFT

2017

We derive and extend the time-dependent surface-flux method introduced in [L. Tao, A. Scrinzi, New J. Phys. 14, 013021 (2012)] within a time-dependent density-functional theory (TDDFT) formalism and use it to calculate photoelectron spectra and angular distributions of atoms and molecules when excited by laser pulses. We present other, existing computational TDDFT methods that are suitable for the calculation of electron emission in compact spatial regions, and compare their results. We illustrate the performance of the new method by simulating strong-field ionization of C60 fullerene and discuss final state effects in the orbital reconstruction of planar organic molecules.

FullereneFOS: Physical sciences02 engineering and technologyElectron01 natural sciences7. Clean energySettore FIS/03 - Fisica Della MateriaSpectral linelaw.inventionlawPhysics - Chemical PhysicsIonization0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular Clusters010306 general physicsChemical Physics (physics.chem-ph)PhysicsAtoms in moleculesTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter PhysicsLaserElectronic Optical and Magnetic MaterialsExcited stateAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technologyComputational Methods
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Isomer effects in fragmentation of Polycyclic Aromatic Hydrocarbons

2015

We have observed significant differences in the fragmentation patterns of isomeric Polycyclic Aromatic Hydrocarbon (PAH) cations following collisions with helium atoms at center-of-mass energies around 100 eV. This is in contrast to the situation at other collision energies or in photo-absorption experiments where isomeric effects are very weak and where the lowest-energy dissociation channels (H- and C2H2-loss) domihate in statistical fragmentation processes. In the 100 eV range, non-statistical fragmentation also competes and is uniquely linked to losses of single carbon atoms (CHx-losses). We find that such CHx-losses are correlated with the ionic ground state energy within a given group…

IONSCollision-induced dissociationIonic bondingPolycyclic aromatic hydrocarbonPhotochemistryANTHRACENE01 natural sciencesDissociation (chemistry)IsomersMOLECULESchemistry.chemical_compoundFragmentation (mass spectrometry)Fragmentation0103 physical sciencesMoleculeCollisionsTANDEM MASS-SPECTROMETRYPolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryCOLLISION-INDUCED DISSOCIATION010303 astronomy & astrophysicsInstrumentationSpectroscopyNon-statistical fragmentationchemistry.chemical_classificationAnthracenePolycyclic Aromatic Hydrocarbons PAHs[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]010401 analytical chemistryCondensed Matter Physics0104 chemical sciencesDIFFERENTIATIONchemistryIONIZATIONCATIONSGROWTH[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Ground stateC14H10International Journal of Mass Spectrometry
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Photoelectron spectra of aluminum cluster anions: Temperature effects and ab initio simulations

1999

Photoelectron (PES) spectra from aluminum cluster anions (from 12 to 15 atoms) at various temperature regimes, were studied using ab-initio molecular dynamics simulations and experimentally. The calculated PES spectra, obtained via shifting of the simulated electronic densities of states by the self-consistently determined values of the asymptotic exchange-correlation potential, agree well with the measured ones, allowing reliable structural assignments and theoretical estimation of the clusters' temperatures.

Materials scienceAb initiochemistry.chemical_elementFOS: Physical sciencesMolecular physicsSpectral lineAb initio molecular dynamicsX-ray photoelectron spectroscopychemistryAluminiumCluster (physics)Physics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersAtomic physicsPhysics::Chemical PhysicsAtomic and Molecular Clusters (physics.atm-clus)Temperature coefficient
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Mg impurity in helium droplets.

2011

Within the diffusion Monte Carlo approach, we have determined the structure of isotopically pure and mixed helium droplets doped with one magnesium atom. For pure 4He clusters, our results confirm those of M. Mella et al. [J. Chem. Phys. 123, 054328 (2005)] that the impurity experiences a transition from a surface to a bulk location as the number of helium atoms in the droplet increases. Contrarily, for pure 3He clusters Mg resides in the bulk of the droplet due to the smaller surface tension of this isotope. Results for mixed droplets are presented. We have also obtained the absorption spectrum of Mg around the 3s3p 1P_1 <-- 3s2 1S_0 transition.

Materials scienceAbsorption spectroscopyMagnesiumDopingAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementFísicaFOS: Physical sciencesSurface tensionCondensed Matter - Other Condensed MatterchemistryImpurityAtomPhysics::Atomic and Molecular ClustersDiffusion Monte CarloPhysics::Atomic PhysicsPhysics - Atomic and Molecular ClustersPhysical and Theoretical ChemistryAtomic and Molecular Clusters (physics.atm-clus)HeliumOther Condensed Matter (cond-mat.other)The Journal of chemical physics
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Femtosecond laser pulse shaping for enhanced ionization

2009

El pdf del artículo es la versión post-print: arXiv:0906.1938v1

Materials scienceFOS: Physical sciencesGeneral Physics and Astronomy01 natural sciencesFluence010305 fluids & plasmaslaw.inventionSchrödinger equationsymbols.namesakelawIonization0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersPhysics::Atomic PhysicsIrradiation010306 general physicsRange (particle radiation)Computational Physics (physics.comp-ph)LaserPulse (physics)FemtosecondsymbolsAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)Physics - Computational PhysicsEPL (Europhysics Letters)
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Determination of accurate rest frequencies and hyperfine structure parameters of cyanobutadiyne, HC5N

2020

Very accurate transition frequencies of HC$_5$N were determined between 5.3 and 21.4 GHz with a Fourier transform microwave spectrometer. The molecules were generated by passing a mixture of HC$_3$N and C$_2$H$_2$ highly diluted in neon through a discharge valve followed by supersonic expansion into the Fabry-Perot cavity of the spectrometer. The accuracies of the data permitted us to improve the experimental $^{14}$N nuclear quadrupole coupling parameter considerably and the first experimental determination of the $^{14}$N nuclear spin-rotation parameter. The transition frequencies are also well suited to determine in astronomical observations the local speed of rest velocities in molecula…

Nuclear TheoryFOS: Physical scienceschemistry.chemical_element010402 general chemistry01 natural sciencesNeonsymbols.namesakePhysics - Chemical Physics0103 physical sciencesPhysics - Atomic and Molecular ClustersPhysical and Theoretical ChemistryInstrumentation and Methods for Astrophysics (astro-ph.IM)Hyperfine structureSpectroscopyChemical Physics (physics.chem-ph)CouplingPhysics010304 chemical physicsSpectrometerAstrophysics - Astrophysics of GalaxiesAtomic and Molecular Physics and Optics0104 chemical sciencesFourier transformchemistryCoupling parameterAstrophysics of Galaxies (astro-ph.GA)QuadrupolesymbolsRotational spectroscopyAtomic physicsAstrophysics - Instrumentation and Methods for AstrophysicsAtomic and Molecular Clusters (physics.atm-clus)Journal of Molecular Spectroscopy
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Long-distance spin-transport across the Morin phase transition up to room temperature in ultra-low damping single crystals of the antiferromagnet α-F…

2020

Antiferromagnetic materials can host spin-waves with polarizations ranging from circular to linear depending on their magnetic anisotropies. Until now, only easy-axis anisotropy antiferromagnets with circularly polarized spin-waves were reported to carry spin-information over long distances of micrometers. In this article, we report long-distance spin-transport in the easy-plane canted antiferromagnetic phase of hematite and at room temperature, where the linearly polarized magnons are not intuitively expected to carry spin. We demonstrate that the spin-transport signal decreases continuously through the easy-axis to easy-plane Morin transition, and persists in the easy-plane phase through …

Phase transition530 PhysicsScienceDephasingGeneral Physics and Astronomy02 engineering and technology01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyArticleMagnetic properties and materialsElectronic and spintronic devices0103 physical sciencesAntiferromagnetism010306 general physicsAnisotropyPhysicsMultidisciplinaryMorin transitionCondensed matter physicsCondensed Matter - Mesoscale and Nanoscale PhysicsMagnonQ[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]General ChemistrySpintronics021001 nanoscience & nanotechnology530 PhysikFerromagnetismMagnetic dampingCondensed Matter::Strongly Correlated Electrons0210 nano-technologyNature Communications
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Excitation levels and magic numbers of small parahydrogen clusters (N⩽40)

2008

The excitation energies of parahydrogen clusters have been systematically calculated by the diffusion Monte Carlo technique in steps of one molecule from 3 to 40 molecules. These clusters possess a very rich spectra, with angular momentum excitations arriving up to L=13 for the heavier ones. No regular pattern can be guessed in terms of the angular momenta and the size of the cluster. Clusters with N=13 and 36 are characterized by a peak in the chemical potential and a large energy gap of the first excited level, which indicate the magical character of these clusters. From the calculated excitation energies the partition function has been obtained, thus allowing for an estimate of thermal e…

PhysicsAngular momentumPartition function (statistical mechanics)Excited statesFOS: Physical sciencesGeneral Physics and AstronomyMonte Carlo methodsSpin isomers of hydrogenMolecular physicsSpectral lineUNESCO::FÍSICA::Química físicaEnergy gapMolecular clustersExcited stateChemical potential ; Energy gap ; Excited states ; Molecular clusters ; Monte Carlo methodsCluster (physics)Diffusion Monte CarloPhysics - Atomic and Molecular ClustersPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Atomic and Molecular Clusters (physics.atm-clus)Chemical potentialExcitationThe Journal of Chemical Physics
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