Search results for "electrons"

showing 10 items of 1325 documents

Complete-active-space second-order perturbation theory (CASPT2//CASSCF) study of the dissociative electron attachment in canonical DNA nucleobases ca…

2015

Low-energy (0-3 eV) ballistic electrons originated during the irradiation of biological material can interact with DNA/RNA nucleobases yielding transient-anion species which undergo decompositions. Since the discovery that these reactions can eventually lead to strand breaking of the DNA chains, great efforts have been dedicated to their study. The main fragmentation at the 0-3 eV energy range is the ejection of a hydrogen atom from the specific nitrogen positions. In the present study, the methodological approach introduced in a previous work on uracil [I. González-Ramírez et al., J. Chem. Theory Comput. 8, 2769-2776 (2012)] is employed to study the DNA canonical nucleobases fragmentations…

Valence (chemistry)GuaninePyrimidineGuanineAdenineDNA BreaksGeneral Physics and AstronomyElectronsHydrogen atomDNAMolecular physicsIonNucleobaseThyminechemistry.chemical_compoundCytosinechemistryThermodynamicsComplete active spacePhysical and Theoretical ChemistryAtomic physicsUracilThymineHydrogenThe Journal of chemical physics
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Electronic Transitions in Tetrathiafulvalene and Its Radical Cation:  A Theoretical Contribution

2001

The low-lying electronic states of tetrathiafulvalene (TTF) and its radical cation (TTF+) have been studied using the multistate extension of a multiconfigurational second-order perturbation method (MS−CASPT2). The minimum-energy equilibrium geometries optimized at the CASSCF level have a boatlike conformation for the neutral molecule, with no significant barrier toward planarity. A more aromatic planar structure is, however, found for the ionic system. For TTF, the calculations of the vertical excitation energies comprise valence singlet and triplet states as well as the lowest members of the Rydberg series converging to the first ionization limit. Valence doublet states have been consider…

Valence (chemistry)Ionic bondingMolecular physicschemistry.chemical_compoundsymbols.namesakechemistryRadical ionComputational chemistryIonizationPhysics::Atomic and Molecular ClustersRydberg formulasymbolsCondensed Matter::Strongly Correlated ElectronsSinglet statePhysical and Theoretical ChemistryIonization energyTetrathiafulvaleneThe Journal of Physical Chemistry A
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Spin-resolved low-energy and hard x-ray photoelectron spectroscopy of off-stoichiometric Co2MnSi Heusler thin films exhibiting a record TMR

2015

Half-metallic Co2MnSi-based Heusler compounds have attracted attention because they yield very high tunnelling magnetoresistance (TMR) ratios. Record TMR ratios of 1995% (at 4.2 K) are obtained from off-stoichiometric Co2MnSi-based magnetic tunnel junctions. This work reports on a combination of band structure calculations and spin-resolved and photon-polarisation-dependent photoelectron spectroscopy for off-stoichiometric Heusler thin films with the composition Co2Mn1.30Si0.84. Co and Mn are probed by magnetic dichroism in angle-resolved photoelectron spectroscopy at the 2p core level. In contrast to the delocalised Co 3d states, a pronounced localisation of the Mn 3d states is deduced fro…

Valence (chemistry)Materials scienceAcoustics and UltrasonicsCondensed matter physicsMagnetoresistanceFermi energyDichroismPhoton energyCondensed Matter PhysicsLinear dichroismSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceX-ray photoelectron spectroscopyCondensed Matter::Strongly Correlated ElectronsElectronic band structureJournal of Physics D: Applied Physics
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Coexistence of metamagnetism and slow relaxation of magnetization in ammonium hexafluoridorhenate.

2020

The (NH4)2[ReF6] (1) salt was studied by X-ray diffraction, Raman spectroscopy, theoretical calculations, and magnetic measurements. 1 crystallizes in the trigonal space group Pm1 (Re–F = 1.958(5) A). In the Raman spectrum of 1, splitting of the observed peaks was observed and correlated to the valence frequencies of vibration of the [ReF6]2− anion. The study of the magnetic properties of 1, through DC and AC magnetic susceptibility measurements, reveals the coexistence of metamagnetism and slow relaxation of magnetization at low temperature, which is unusual in the molecular systems based on the paramagnetic 5d metal ions reported so far.

Valence (chemistry)Materials scienceCondensed matter physicsGeneral Chemical EngineeringRelaxation (NMR)General ChemistryMagnetic susceptibilityIonMagnetizationParamagnetismsymbols.namesakesymbolsCondensed Matter::Strongly Correlated ElectronsRaman spectroscopyMetamagnetismRSC advances
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Modelling electric field control of the spin state in the mixed-valence polyoxometalate [GeV14O40]8−

2013

International audience; : The two-electron reduced mixed-valence polyoxometalate [GeV14O40](8-) presents an unusual paramagnetic behaviour as a consequence of the partial trapping of these electrons. The effect of applying an electric field is that of inducing antiferromagnetic coupling between the two delocalized electronic spins.

Valence (chemistry)SpinsSpin statesCondensed matter physicsChemistryMetals and Alloys02 engineering and technologyGeneral ChemistryElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDelocalized electronParamagnetismElectric fieldPolyoxometalateMaterials ChemistryCeramics and CompositesCondensed Matter::Strongly Correlated Electrons[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyChemical Communications
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The lineshape of the electronic spectrum of the green fluorescent protein chromophore, part I: gas phase.

2014

The vibronic spectra of the green fluorescent protein chromophore analogues p-hydroxybenzylidene-2,3-dimethylimidazolinone (HBDI) and 3,5-tert-butyl-HBDI (35Bu) are similar in the vacuum, but very different in water or ethanol. To understand this difference, we have computed the vibrationally resolved solution spectra of these chromophores, using the polarizable continuum model (PCM) to account for solvent effects on the (harmonic) potential energy surfaces (PES). In agreement with experiment, we found that the vibrational progression increases with the polarity of the solvent, but we could neither reproduce the broadening, nor the large difference between the absorption spectra of HBDI and…

Vibrational spectroscopyComputational chemistrygenetic structuresAbsorption spectroscopySpectrophotometry InfraredPopulationGreen Fluorescent ProteinsAnalytical chemistryElectronsPolarizable continuum modelMolecular physicsAbsorptionMolecular dynamicsBenzyl CompoundsVibronic spectroscopyGreen fluorescent proteinPhysical and Theoretical ChemistryeducationImidazolinesta116education.field_of_studyChemistryTemperatureChromophoreChromophoresPotential energyAtomic and Molecular Physics and OpticsQuantum TheoryThermodynamicsGasesSolvent effectsChemphyschem : a European journal of chemical physics and physical chemistry
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Quantum wire with periodic serial structure

1991

Electron wave motion in a quantum wire with periodic structure is treated by direct solution of the Schr\"odinger equation as a mode-matching problem. Our method is particularly useful for a wire consisting of several distinct units, where the total transfer matrix for wave propagation is just the product of those for its basic units. It is generally applicable to any linearly connected serial device, and it can be implemented on a small computer. The one-dimensional mesoscopic crystal recently considered by Ulloa, Casta\~no, and Kirczenow [Phys. Rev. B 41, 12 350 (1990)] is discussed with our method, and is shown to be a strictly one-dimensional problem. Electron motion in the multiple-stu…

Wave propagationThin filmsDispersió (Física nuclear)Schrödinger equationElectronTransport d'electronsSchrödinger equationsymbols.namesakeOpticsQuantum mechanicsPel·lícules finesPhysicsMesoscopic physicsFenòmens mesoscòpics (Física)business.industryQuantum wireElectron transportNanostructured materialsTransfer matrixElectronic transportProduct (mathematics)Scattering (Physics)Equació de SchrödingersymbolsMesoscopic phenomena (Physics)Fundamental Resolution EquationMaterials nanoestructuratsbusinessTeoria del transport
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Electronic transport in molecular junctions : The generalized Kadanoff–Baym ansatz with initial contact and correlations

2021

The generalized Kadanoff-Baym ansatz (GKBA) offers a computationally inexpensive approach to simulate out-of-equilibrium quantum systems within the framework of nonequilibrium Green's functions. For finite systems the limitation of neglecting initial correlations in the conventional GKBA approach has recently been overcome [Phys. Rev. B 98, 115148 (2018)]. However, in the context of quantum transport the contacted nature of the initial state, i.e., a junction connected to bulk leads, requires a further extension of the GKBA approach. In this work, we lay down a GKBA scheme which includes initial correlations in a partition-free setting. In practice, this means that the equilibration of the …

Work (thermodynamics)116 Chemical sciencesGeneral Physics and AstronomyNon-equilibrium thermodynamicsFOS: Physical sciencesContext (language use)Electron010402 general chemistry01 natural sciences114 Physical sciencesCondensed Matter - Strongly Correlated ElectronsPhysics - Chemical Physics0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Statistical physicsPhysical and Theoretical ChemistrykvanttifysiikkaQuantumAnsatzPhysicsChemical Physics (physics.chem-ph)Settore FIS/03Condensed Matter - Mesoscale and Nanoscale Physics010304 chemical physicsStrongly Correlated Electrons (cond-mat.str-el)State (functional analysis)0104 chemical sciencesEmbedding
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Molecular polarizability of Scn, Cn and endohedral Scn@Cm clusters

2002

The interacting induced dipoles polarization model implemented in the program POLAR is used for the calculation of the molecular dipole-dipole polarizability . The method is tested with Sc1-Sc7, Sc12, Sc17, Sc74, C, C12, C60, C70, C82-fullerene, Sc@C60, Sc@C82, Sc2@C82, Sc3@C82, C1-C6, C10, C13, C16, C19, C22, C24, C42, C54, C84 and C96-graphite clusters. The polarizability is an important quantity for the identification of clusters with different numbers of atoms and even for the separation of isomers. The results for the polarizability are of the same order of magnitude as reference calculations performed with another program based on the same formulation. The bulk limit for the polarizab…

Work (thermodynamics)Materials scienceBioengineeringMolecular physicsPolarizabilityPhysics::Atomic and Molecular ClustersCluster (physics)Experimental workGeneral Materials SciencePhysics::Atomic PhysicsElectrical and Electronic EngineeringChemistryMechanical EngineeringDangling bondGeneral ChemistryCondensed Matter PhysicsPolarization (waves)Atomic and Molecular Physics and OpticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyDipoleMechanics of MaterialsPolarCondensed Matter::Strongly Correlated ElectronsAtomic physicsOrder of magnitudeNanotechnology
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Ferromagnetic kinetic exchange interaction in magnetic insulators

2020

The superexchange theory predicts dominant antiferromagnetic kinetic interaction when the orbitals accommodating magnetic electrons are covalently bonded through diamagnetic bridging atoms/groups. Here we show that explicit consideration of magnetic and (leading) bridging orbitals, together with the electron transfer between the former, reveals a strong ferromagnetic kinetic exchange contribution. First principle calculations show that it is comparable in strength with antiferromagnetic superexchange in a number of magnetic materials with diamagnetic metal bridges. In particular, it is responsible for a very large ferromagnetic coupling ($-10$ meV) between the iron ions in a Fe$^{3+}$-Co$^{…

Work (thermodynamics)magneettiset ominaisuudetMaterials scienceelectronic-structurePhysics MultidisciplinaryFOS: Physical sciencesmagnetic couplingelektronitmagneettikentätKinetic energyteoriatORBITAL PHYSICSCondensed Matter - Strongly Correlated ElectronsCondensed Matter::Materials ScienceANTIFERROMAGNETISMHUBBARD-MODELPhysics - Chemical PhysicsSUPEREXCHANGE INTERACTIONSdensity functional theoryChemical Physics (physics.chem-ph)Condensed Matter - Materials SciencecomplexesScience & TechnologyStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsCRYSTALmagnetic insulatorsPhysicsSUPERCONDUCTIVITYExchange interactionMaterials Science (cond-mat.mtrl-sci)transitionORDERhubbard-modelsuperexchange interactionsWannier function methodsELECTRONIC-STRUCTUREFerromagnetismPhysical SciencesCondensed Matter::Strongly Correlated ElectronsCOMPLEXESTRANSITION
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