Search results for "DENSITY FUNCTIONAL THEORY"

showing 10 items of 981 documents

On the nature of parr functions to predict the most reactive sites along organic polar reactions

2013

Abstract Very recently, local electrophilic and nucleophilic “Parr functions” were empirically introduced (L.R. Domingo, P. Perez, J.A. Saez RSC Adv. 3 (2013) 1486) in order to properly characterize the most reactive sites along polar chemical reactions. This Letter reports a theoretical advance to the new methodology by identifying these quantities with key Fukui descriptors of the spin-polarized density functional theory . Given such framework properly incorporates the treatment of both charge-transfer and spin-polarization, this finding provides a significant insight and substantial step forward within the field of a chemical reactivity theory based on the conceptual framework of density…

Field (physics)ChemistryComputational chemistryGeneral Physics and AstronomyPolarDensity functional theoryStatistical physicsPhysical and Theoretical ChemistryChemical reactionTheory based
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Quantum chemistry of the excited state: 2005 overview

2005

The present contribution contains an overview of quantum-chemical methods and strategies to compute and interpret spectroscopic and photochemical phenomena in molecular systems. The state of the art for the quantum chemistry of the excited state is reviewed, focusing in the advantages and disadvantages of the most commonly employed computational methods, from the single configurational procedures like CI-Singles (CIS), propagator approaches, and Coupled-Cluster (CC) techniques, to the more sophisticated multiconfigurational treatments, with particular emphasis on perturbation theory, the CASPT2 approach. Also, a short summary on the performance, lights, and shadows of the popular TDDFT meth…

Field (physics)ChemistryPropagatorTime-dependent density functional theoryMolecular systemsCondensed Matter PhysicsBiochemistryQuantum chemistryQuantum mechanicsExcited statePotential energy surfaceStatistical physicsPhysical and Theoretical ChemistryPerturbation theoryJournal of Molecular Structure: THEOCHEM
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Ab initio simulation of (Ba,Sr)TiO3 and (Ba,Ca)TiO3 perovskite solid solutions

2019

This research was supported by the ERA-NET HarvEnPiez project. Many thanks to R. Dovesi, M.M. Kržmanc and D. Gryaznov for fruitful discussions.

First-principles computationAb initio:NATURAL SCIENCES:Physics [Research Subject Categories]Density functional theory (DFT)Perovskite solid solutionLead-free piezoelectric
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Survival of Floquet–Bloch States in the Presence of Scattering

2021

Floquet theory has spawned many exciting possibilities for electronic structure control with light, with enormous potential for future applications. The experimental demonstration in solids, however, remains largely unrealized. In particular, the influence of scattering on the formation of Floquet-Bloch states remains poorly understood. Here we combine time- and angle-resolved photoemission spectroscopy with time-dependent density functional theory and a two-level model with relaxation to investigate the survival of Floquet-Bloch states in the presence of scattering. We find that Floquet-Bloch states will be destroyed if scattering-activated by electronic excitations-prevents the Bloch elec…

Floquet theoryLetterField (physics)BioengineeringElectrons02 engineering and technologyElectronElectronic structureSettore FIS/03 - Fisica Della Materiadriven two-level system with dissipationGeneral Materials ScienceFloquet−Bloch statesPhysicsScatteringMechanical EngineeringRelaxation (NMR)General ChemistryTime-dependent density functional theorydissipation021001 nanoscience & nanotechnologyCondensed Matter Physicstime and angle-resolved photoemission spectroscopy3. Good healthFloquet-Bloch statestime-dependent density functional theoryFloquetBloch statesQuantum electrodynamicsddc:660Density functional theory0210 nano-technologytime- and angle-resolved photoemission spectroscopyNano Letters
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Interaction-induced spin polarization in quantum dots.

2010

The electronic states of lateral many electron quantum dots in high magnetic fields are analyzed in terms of energy and spin. In a regime with two Landau levels in the dot, several Coulomb blockade peaks are measured. A zig-zag pattern is found as it is known from the Fock-Darwin spectrum. However, only data from Landau level 0 show the typical spin-induced bimodality, whereas features from Landau level 1 cannot be explained with the Fock-Darwin picture. Instead, by including the interaction effects within spin-density-functional theory a good agreement between experiment and theory is obtained. The absence of bimodality on Landau level 1 is found to be due to strong spin polarization.

Fock-Darwin spectrumSpin polarizationSpin-density-functional theoryQuantum DotGeneral Physics and AstronomyFOS: Physical sciencesElectronSpin dynamicsShubnikov–de Haas effectMesoscale and Nanoscale Physics (cond-mat.mes-hall)Electronic statesSemiconductor quantum dotsddc:530Landau levelsSpin-½PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsCondensed matter physicsSpin polarizationCoulomb blockadeHigh magnetic fieldsLandau quantizationCondensed Matter::Mesoscopic Systems and Quantum Hall EffectMagnetic fieldQuantum dotMagnetic fieldsDensity functional theoryDewey Decimal Classification::500 | Naturwissenschaften::530 | PhysikInteraction effectPhysical review letters
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Density functional theory calculations on magnetic properties of actinide compounds

2010

We have performed a detailed analysis of the magnetic (collinear and noncollinear) order and atomic and the electron structures of UO2, PuO2 and UN on the basis of density functional theory with the Hubbard electron correlation correction (DFT+U). We have shown that the 3-k magnetic structure of UO2 is the lowest in energy for the Hubbard parameter value of U=4.6 eV (and J=0.5 eV) consistent with experiments when Dudarev's formalism is used. In contrast to UO2, UN and PuO2 show no trend for a distortion towards rhombohedral structure and, thus, no complex 3-k magnetic structure is to be anticipated in these materials.

Formalism (philosophy of mathematics)Condensed Matter - Materials ScienceMaterials scienceElectronic correlationMagnetic structureCondensed matter physicsGeneral Physics and AstronomyDensity functional theoryActinideTrigonal crystal systemElectronPhysical and Theoretical ChemistryPhysics - Computational Physics
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Redox potentials and acidity constants from density functional theory based molecular dynamics.

2014

CONSPECTUS: All-atom methods treat solute and solvent at the same level of electronic structure theory and statistical mechanics. All-atom computation of acidity constants (pKa) and redox potentials is still a challenge. In this Account, we review such a method combining density functional theory based molecular dynamics (DFTMD) and free energy perturbation (FEP) methods. The key computational tool is a FEP based method for reversible insertion of a proton or electron in a periodic DFTMD model system. The free energy of insertion (work function) is computed by thermodynamic integration of vertical energy gaps obtained from total energy differences. The problem of the loss of a physical refe…

Free energy perturbationMolecular dynamicsStandard hydrogen electrodeChemistryPeriodic boundary conditionsThermodynamicsThermodynamic integrationPhysical chemistryDensity functional theoryGeneral MedicineGeneral ChemistryElectronic structureIonization energyAccounts of chemical research
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Bending Carbon Nanoforms for Supramolecular Recognition: A Topological Study on Hemifullerene-Based Aggregates

2018

International audience; Buckybowls have risen as appealing fullerene fragment derivatives. Their intrinsic curvature has been exploited in the generation of host–guest supramolecular assemblies, not only through concave–convex complementarity but also through less-known concave–concave staggered arrangements. Whereas the stabilization of bowl-in-bowl dispositions has been ascribed to efficient π–π forces together with favorable dipole–dipole interactions, a detailed analysis on the forces guiding the formation of the staggered arrangements is missing so far. Herein, we present a thorough theoretical characterization of bowl-in-bowl vs staggered hemifullerene-based homodimers and heterodimer…

Fullerene010405 organic chemistryChemistrySupramolecular chemistrychemistry.chemical_elementBending010402 general chemistry01 natural sciences0104 chemical sciencesCharacterization (materials science)Chemical bondChemical physicsMoleculeDensity functional theory[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryCarbonThe Journal of Physical Chemistry A
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Complexation and Electronic Communication between Corannulene-Based Buckybowls and a Curved Truxene-TTF Donor

2017

Abstract: The association behavior of an electron-donating, bowl-shaped, truxene-based tetrathiafulvalene (truxTTF) with two corannulene-based fullerene fragments, C32H12 and C38H14, is investigated in several solvents. Formation of 1:1 complexes is followed by absorption titrations and complemented by density functional theory (DFT) calculations. The binding constants are in the range logKa=2.9–3.5. DFT calculations reveal that the most stable arrangement is the conformation in which the 1,3-dithiole ring of truxTTF is placed inside the concave cavity of the corannulene derivative. This arrangement is confirmed experimentally by NMR measurements, and implies that a combination of p–p and C…

Fullerene010405 organic chemistryOrganic ChemistrySupramolecular chemistryQuímica orgánicaGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis3. Good health0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundCrystallographychemistryCorannuleneUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)Tetrathiafulvalene
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From small to medium and beyond: a pragmatic approach in predicting properties of Ne containing structures

2013

In this study, we outlined a pragmatic approach for structural studies leading to better understanding of polycarbon structures using 21Ne as a nuclear magnetic resonance (NMR) probe. 21Ne NMR parameters of a single neon atom and its dimer were predicted at the CCSD(T) level in combination with large basis sets. At a lower level of theory, an interaction of neon atom with 1,3-cyclopentadiene ring and with five- and six-membered rings in carbazole was studied using the restricted Hartree–Fock (RHF) and density functional theory (DFT) combined with smaller basis sets. The RHF and DFT modelling of neon interaction with nanosized objects were performed on cyclacenes and selected fullerenes.

Fullerene21Ne NMRDimerBiophysicschemistry.chemical_elementRing (chemistry)Molecular physicsDFTNeonchemistry.chemical_compoundComputational chemistrycarbazoleAtomPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular Biologydispersion interactionsBasis (linear algebra)CarbazolefullerenesCondensed Matter PhysicschemistryDensity functional theorycyclacenesMolecular Physics
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