Search results for "time-dependent density functional theory"

showing 10 items of 59 documents

Fluorine-free blue-green emitters for light-emitting electrochemical cells

2014

Date of Acceptance: 29/05/2014 There is presently a lack of efficient and stable blue emitters for light-emitting electrochemical cells (LEECs), which limits the development of white light emitting systems for lighting. Cyclometalated iridium complexes as blue emitters tend to show low photoluminescence efficiency due to significant ligand-centred character of the radiative transition. The most common strategy to blue-shift the emission is to use fluorine substituents on the cyclometalating ligand, such as 2,4-difluorophenylpyridine, dFppy, which has been shown to decrease the stability of the emitter in operating devices. Herein we report a series of four new charged cyclometalated iridium…

PhotoluminescenceMaterials scienceLigandchemistry.chemical_elementGeneral ChemistryTime-dependent density functional theoryQD ChemistryPhotochemistryElectrochemistryElectrochemical cellchemistry.chemical_compoundchemistryPyridineMaterials ChemistryFluorineQDIridiumJ. Mater. Chem. C
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2015

In this work we review the mapping from densities to potentials in quantum mechanics, which is the basic building block of time-dependent density-functional theory and the Kohn-Sham construction. We first present detailed conditions such that a mapping from potentials to densities is defined by solving the time-dependent Schrodinger equation. We specifically discuss intricacies connected with the unboundedness of the Hamiltonian and derive the local-force equation. This equation is then used to set up an iterative sequence that determines a potential that generates a specified density via time propagation of an initial state. This fixed-point procedure needs the invertibility of a certain S…

Photon010304 chemical physicsTime-dependent density functional theoryCondensed Matter Physics01 natural sciencesSchrödinger equationsymbols.namesakeLattice (order)0103 physical sciencessymbolsApplied mathematicsGeneral Materials ScienceUniqueness010306 general physicsHamiltonian (quantum mechanics)MathematicsJournal of Physics: Condensed Matter
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Tailored pump-probe transient spectroscopy with time-dependent density-functional theory: controlling absorption spectra

2016

Recent advances in laser technology allow us to follow electronic motion at its natural time-scale with ultra-fast time resolution, leading the way towards attosecond physics experiments of extreme precision. In this work, we assess the use of tailored pumps in order to enhance (or reduce) some given features of the probe absorption (for example, absorption in the visible range of otherwise transparent samples). This type of manipulation of the system response could be helpful for its full characterization, since it would allow us to visualize transitions that are dark when using unshaped pulses. In order to investigate these possibilities, we perform first a theoretical analysis of the non…

Physics010304 chemical physicsSolid-state physicsAtomic Physics (physics.atom-ph)AttosecondQuantum dynamicsComplex systemFOS: Physical sciencesContext (language use)Time-dependent density functional theoryCondensed Matter Physics01 natural sciences7. Clean energySettore FIS/03 - Fisica Della MateriaPhysics - Atomic Physics3. Good healthElectronic Optical and Magnetic MaterialsCharacterization (materials science)Computational physicsCondensed Matter - Other Condensed Matter0103 physical sciences010306 general physicsAbsorption (electromagnetic radiation)Other Condensed Matter (cond-mat.other)Computational MethodsThe European Physical Journal B
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2021

Electronic circular dichroism (ECD) is a powerful spectroscopy method for investigating chiral properties at the molecular level. ECD calculations with the commonly used linear-response time-dependent density functional theory (LR-TDDFT) framework can be prohibitively costly for large systems. To alleviate this problem, we present here an ECD implementation within the projector augmented-wave method in a real-time-propagation TDDFT framework in the open-source GPAW code. Our implementation supports both local atomic basis sets and real-space finite-difference representations of wave functions. We benchmark our implementation against an existing LR-TDDFT implementation in GPAW for small chir…

PhysicsCircular dichroism010304 chemical physicsBasis (linear algebra)General Physics and AstronomyTime-dependent density functional theory010402 general chemistry01 natural sciences0104 chemical sciencesComputational physics0103 physical sciencesPhysics::Atomic and Molecular ClustersCluster (physics)Density functional theoryPhysical and Theoretical ChemistryWave functionSpectroscopyBasis setThe Journal of Chemical Physics
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Multicomponent density-functional theory for electrons and nuclei

2006

We present a general multi-component density functional theory in which electrons and nuclei are treated completely quantum mechanically, without the use of a Born-Oppenheimer approximation. The two fundamental quantities in terms of which our theory is formulated are the nuclear N-body density and the electron density expressed in coordinates referring to the nuclear framework. For these two densities coupled Kohn-Sham equations are derived and the electron-nuclear correlation functional is analyzed in detail. The formalism is tested on the hydrogen molecule $H_2$ and its positive ion $H_2^+$ using several approximations for the electron-nuclear correlation functional.

PhysicsCondensed Matter - Materials ScienceElectron density010304 chemical physicsOrbital-free density functional theoryNuclear TheoryMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronTime-dependent density functional theory01 natural sciences7. Clean energyMolecular physicsAtomic and Molecular Physics and OpticsHybrid functionalQuantum mechanics0103 physical sciencesPhysics::Atomic and Molecular ClustersDensity functional theoryPhysics::Chemical PhysicsLocal-density approximation010306 general physicsElectronic densityPhysical Review A
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Aharonov-Bohm effect in many-electron quantum rings

2010

The Aharonov-Bohm effect is investigated in two-dimensional, single-terminal quantum rings in magnetic fields by using time-dependent density-functional theory. We find multiple transport loops leading to the oscillation periods of $h/(en)$, where $n$ is the number of loops. We show that the Aharonov-Bohm oscillations are relatively weakly affected by the electron-electron interactions, whereas the ring width has a strong effect on the characteristics of the oscillations. Our results propose that in those experimental semiconductor quantum-ring devices that show clear Aharonov-Bohm oscillations the electron current is dominated by a few states along narrow conduction channels.

PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsbusiness.industryOscillationFOS: Physical sciencesQuantum PhysicsTime-dependent density functional theoryElectronCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsMagnetic fieldCondensed Matter - Strongly Correlated Electronssymbols.namesakeSemiconductorQuantum dotQuantum mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)symbolsbusinessAharonov–Bohm effectQuantumPhysical Review B
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Comparative study of many-body perturbation theory and time-dependent density functional theory in the out-of-equilibrium Anderson model

2011

We study time-dependent electron transport through an Anderson model. The electronic interactions on the impurity site are included via the self-energy approximations at Hartree-Fock (HF), second Born (2B), GW, and T-matrix levels as well as within a time-dependent density functional (TDDFT) scheme based on the adiabatic Bethe-ansatz local density approximation (ABALDA) for the exchange-correlation potential. The Anderson model is driven out of equilibrium by applying a bias to the leads, and its nonequilibrium dynamics is determined by real-time propagation. The time-dependent currents and densities are compared to benchmark results obtained with the time-dependent density matrix renormali…

PhysicsCondensed Matter - Mesoscale and Nanoscale Physicsta114Non-equilibrium thermodynamicsFOS: Physical sciences02 engineering and technologyTime-dependent density functional theory021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMany bodySettore FIS/03 - Fisica della MateriaElectronic Optical and Magnetic MaterialsCondensed Matter - Other Condensed MatterQuantum mechanicsQuantum electrodynamics0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Local-density approximationPerturbation theory010306 general physics0210 nano-technologyAdiabatic processAnderson impurity modelOther Condensed Matter (cond-mat.other)
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Generation and Evolution of Spin-, Valley-, and Layer-Polarized Excited Carriers in Inversion-Symmetric WSe2

2016

We report the spin-selective optical excitation of carriers in inversion-symmetric bulk samples of the transition metal dichalcogenide (TMDC) ${\mathrm{WSe}}_{2}$. Employing time- and angle-resolved photoelectron spectroscopy (trARPES) and complementary time-dependent density functional theory (TDDFT), we observe spin-, valley-, and layer-polarized excited state populations upon excitation with circularly polarized pump pulses, followed by ultrafast ($l100\text{ }\text{ }\mathrm{fs}$) scattering of carriers towards the global minimum of the conduction band. TDDFT reveals the character of the conduction band, into which electrons are initially excited, to be two-dimensional and localized wit…

PhysicsCondensed matter physicsSpintronicsScatteringGeneral Physics and AstronomyHeterojunction02 engineering and technologyTime-dependent density functional theoryElectron021001 nanoscience & nanotechnology01 natural sciencesExcited state0103 physical sciencesDensity functional theory010306 general physics0210 nano-technologyExcitationPhysical Review Letters
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Continuity equation and local gauge invariance for the N3LO nuclear energy density functionals

2011

Background: The next-to-next-to-next-to-leading order (N3LO) nuclear energy density functional extends the standard Skyrme functional with new terms depending on higher-order derivatives of densities, introduced to gain better precision in the nuclear many-body calculations. A thorough study of the transformation properties of the functional with respect to different symmetries is required, as a step preliminary to the adjustment of the coupling constants. Purpose: Determine to which extent the presence of higher-order derivatives in the functional can be compatible with the continuity equation. In particular, to study the relations between the validity of the continuity equation and invari…

PhysicsDensity matrixNuclear and High Energy PhysicsNuclear Theoryta114IsovectorOrbital-free density functional theoryRunge–Gross theoremFOS: Physical sciencesTime-dependent density functional theoryNuclear Theory (nucl-th)Continuity equationQuantum mechanicsDensity functional theoryGauge theoryMathematical physicsPhysical Review C
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Quantum dots in magnetic fields: Unrestricted symmetries in the current spin-density functional formalism

1999

We apply the current spin-density functional formalism (CSDFT) of Vignale and Rasolt to two-dimensional quantum dots in magnetic fields. Avoiding any spatial symmetry restrictions of the solutions, we find that a broken rotational symmetry of the electronic charge density can occur in high magnetic fields.

PhysicsFormalism (philosophy of mathematics)Condensed matter physicsQuantum dotQuantum mechanicsHomogeneous spaceRotational symmetryTime-dependent density functional theoryElectronic charge densitySpin densityAtomic and Molecular Physics and OpticsMagnetic fieldThe European Physical Journal D
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