Search results for "time-dependent density functional theory"

showing 10 items of 59 documents

Ab Initio Simulation of Attosecond Transient Absorption Spectroscopy in Two-Dimensional Materials

2018

We extend the first-principles analysis of attosecond transient absorption spectroscopy to two-dimensional materials. As an example of two-dimensional materials, we apply the analysis to monolayer hexagonal boron nitride (h-BN) and compute its transient optical properties under intense few-cycle infrared laser pulses. Nonadiabatic features are observed in the computed transient absorption spectra. To elucidate the microscopic origin of these features, we analyze the electronic structure of h-BN with density functional theory and investigate the dynamics of specific energy bands with a simple two-band model. Finally, we find that laser-induced intraband transitions play a significant role in…

Materials scienceattosecond transient absorption spectroscopyAttosecondAb initioFOS: Physical sciences02 engineering and technologyElectronic structure01 natural sciencesMolecular physicslcsh:TechnologySettore FIS/03 - Fisica Della Materialcsh:Chemistry0103 physical sciencesUltrafast laser spectroscopyGeneral Materials Science010306 general physicsSpectroscopyInstrumentationlcsh:QH301-705.5Fluid Flow and Transfer ProcessesCondensed Matter - Materials Sciencelcsh:TProcess Chemistry and TechnologyGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)Time-dependent density functional theory021001 nanoscience & nanotechnologylcsh:QC1-999Computer Science Applicationstime-dependent density functional theoryfirst-principles simulationlcsh:Biology (General)lcsh:QD1-999lcsh:TA1-2040Density functional theoryTransient (oscillation)0210 nano-technologylcsh:Engineering (General). Civil engineering (General)lcsh:PhysicsOptics (physics.optics)Physics - OpticsApplied Sciences
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A TDDFT-based Study on the Proton-DNA Collision

2019

The interaction of heavy charged particles with DNA is of interest for several areas, from hadrontherapy to aero-space industry. In this paper, a TD-DFT study on the interaction of a 4 keV proton with an isolated DNA base pair was carried out. Ehrenfest dynamics was used to study the evolution of the system during and after the proton impact up to about 193 fs. This time was long enough to observe the dissociation of the target, which occurs between 80-100 fs. The effect of base pair linking to the DNA double helix was emulated by fixing the four O3' atoms responsible for the attachment. The base pair tends to dissociate into its main components, namely the phosphate groups, sugars and nitr…

Models MolecularBase pairFirst-principlesFOS: Physical sciences02 engineering and technology010402 general chemistry01 natural sciencesDissociation (chemistry)Settore FIS/03 - Fisica Della Materiachemistry.chemical_compoundFragmentationPhysics - Chemical PhysicsMaterials ChemistryPhysics - Biological PhysicsPhysical and Theoretical ChemistryBase PairingChemical Physics (physics.chem-ph)ChemistryTime-dependent density functional theoryDNA021001 nanoscience & nanotechnologyCollisionPhosphateCharged particle0104 chemical sciencesSurfaces Coatings and FilmsEnergy TransferBiological Physics (physics.bio-ph)Chemical physicsQuantum TheoryDensity functional theoryProtonsAtomic physics0210 nano-technologyDNADNA Damage
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Triggering dissymmetry in achiral dye molecules by chiral solvents: Circular dichroism experiments and DFT calculations

2011

The electronic circular dichroism spectra of achiral product “Lumogen F Red” (ROT-300) in four different chiral solvents are recorded at different temperatures. DFT calculations allow to identify two enantiomeric conformers for ROT-300. In vacuo they are equally populated; in chiral solvents one enantiomer prevails. Thermodynamic quantities involved in the chiral preference are derived. Chirality, 2011. © 2011 Wiley-Liss, Inc.

Models MolecularCircular dichroismMolecular ConformationPhotochemistryCatalysisAnalytical ChemistryProchiralityComputational chemistryDrug Discoverycircular dichroism (CD)time-dependent density functional theory (TDDFT)MoleculeColoring AgentsConformational isomerismSpectroscopySettore CHIM/02 - Chimica FisicaPharmacologyChemistryCircular DichroismOrganic ChemistryStereoisomerismCircular dichroism spectradye molecules solvent effectSolventsQuantum TheoryEnantiomerChirality (chemistry)Chirality
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Integrated experimental and computational spectroscopy study on the protonation of the α-nitronyl nitroxide radical unit

2011

The stability of the α-nitronyl nitroxide radical unit under acidic conditions is investigated by an integrated experimental UV/Vis spectroscopy and TDDFT study. In the field of molecular magnetism, α-nitronyl nitroxide radicals are important as purely organic spin carriers due to their synthetic versatility. Here, the existence of an intermediate of the protonated α-nitronyl nitroxide radical unit is demonstrated for the first time and a proposed disproportionation reaction is confirmed.

Models MolecularNitroxide mediated radical polymerizationFree RadicalsChemistryMagnetismSpectrum AnalysisRadicalMolecular ConformationGeneral Physics and AstronomyDisproportionationProtonationTime-dependent density functional theoryPhotochemistryCyclic N-OxidesQuantum TheoryProtonsPhysical and Theoretical ChemistrySpectroscopySpin (physics)Phys. Chem. Chem. Phys.
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Quantum Chemical Parametrization and Spectroscopic Characterization of the Frenkel Exciton Hamiltonian for a J-Aggregate Forming Perylene Bisimide Dye

2012

Quantum chemical and quantum dynamical calculations are performed for a bay-substituted perylene bisimide dye up to its hexameric aggregate. The aggregate structure is determined by employing the self-consistent charge density functional tight-binding (SCC-DFTB) approach including dispersion corrections. It is characterized by a stabilization via two chains of hydrogen bonds facilitated by amide functionalities. Focusing on the central embedded dimer, the Coulomb coupling for this J-aggregate is determined by means of the time-dependent density functional theory (TDDFT) to be -514 cm(-1). Exciton vibrational coupling is treated within the shifted oscillator model from which five strongly co…

Molecular StructureAbsorption spectroscopyChemistryExcitonCharge densityTime-dependent density functional theoryImideschemistry.chemical_compoundQuantum TheoryDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsRotational–vibrational couplingPeryleneJ-aggregatePeryleneFluorescent DyesThe Journal of Physical Chemistry A
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Ag44(SeR)30: A Hollow Cage Silver Cluster with Selenolate Protection.

2015

Selenolate protected, stable and atomically precise, hollow silver cluster was synthesized using solid state as well as solution state routes. The optical absorption spectrum shows multiple and sharp features similar to the thiolated Ag44 cluster, Ag44(SR)30 whose experimental structure was reported recently. High-resolution electrospray ionization mass spectrometry (HRESI MS) shows well-defined molecular ion features with two, three, and four ions with isotopic resolution, due to Ag44(SePh) 30. Additional characterization with diverse tools confirmed the composition. The closed-shell 18 electron superatom electronic structure, analogous to Ag44(SR)30 stabilizes the dodecahedral cage with a…

Nano-moleculesElectronic structureAbsorption spectroscopyMass spectrometryChemistryElectrospray ionizationPolyatomic ionSuperatomAnalytical chemistryElectronic structureTime-dependent density functional theoryselenolateMALDI-MSSuperatomsCrystallographyTDDFTOptical materialsCluster (physics)Silver clusterGeneral Materials ScienceDensity functional theoryPhysical and Theoretical ChemistryESI MSThe journal of physical chemistry letters
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Plasmon-Induced Direct Hot-Carrier Transfer at Metal-Acceptor Interfaces.

2019

Plasmon-induced hot-carrier transfer from a metal nanostructure to an acceptor is known to occur via two key mechanisms: (i) indirect transfer, where the hot carriers are produced in the metal nanostructure and subsequently transferred to the acceptor, and (ii) direct transfer, where the plasmons decay by directly exciting carriers from the metal to the acceptor. Unfortunately, an atomic-level understanding of the direct-transfer process, especially with regard to its quantification, remains elusive even though it is estimated to be more efficient compared to the indirect-transfer process. This is due to experimental challenges in separating direct from indirect transfer as both processes o…

NanostructureMaterials scienceprobabilityta221General Physics and Astronomyhot holes02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionMetalnanorakenteetpuolijohteetlawTransfer (computing)General Materials SciencePlasmonta114nanoelektroniikkatiheysfunktionaaliteoriaGeneral Engineeringplasmon decayTime-dependent density functional theory021001 nanoscience & nanotechnologyLaserAcceptortime-dependent density-functional theory0104 chemical sciencesdirect transferChemical physicsvisual_artFemtosecondvisual_art.visual_art_mediumtodennäköisyys0210 nano-technologyhot electronsACS nano
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Time-Dependent Density Functional Theory Calculations of N- and S-Doped TiO2 Nanotube for Water-Splitting Applications

2021

This research was funded by the Latvian Council of Science grant LZP-2018/2-0083. Institute of Solid State Physics, University of Latvia, as the Center of Excellence, has received funding from the European Union?s Horizon 2020 Framework Program H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under Grant Agreement No. 739508, project CAMART2.

NanotubeAnataseMaterials scienceAbsorption spectroscopyabsorption spectraGeneral Chemical Engineering02 engineering and technology7. Clean energy01 natural sciencesTiO2 nanotubeCondensed Matter::Materials Science0103 physical sciencesTime-dependent density functional theoryPhysics::Atomic and Molecular Clusterstransition contribution mapsGeneral Materials ScienceTransition contribution maps010306 general physicsQD1-999TiO<sub>2</sub> nanotubeDopantphotocatalystDopingAbsorption spectraPhotocatalystTime-dependent density functional theory021001 nanoscience & nanotechnologyChemistrytime-dependent density functional theoryChemical physics:NATURAL SCIENCES [Research Subject Categories]Water splittingDensity functional theory0210 nano-technologyNanomaterials
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Comparative quantum chemistry study of the F-center in lanthanum trifluoride

2020

Abstract In this study we report the results of first principle quantum chemical modeling of electronic structure and spatial configuration of LaF3 crystal containing the F-center. Theoretical predictions of atomic and electronic properties of LaF3 are given by means of density functional theory. From our modeling we predict that the F-center placed at fluorine ion position between the lanthanum planes at tysonite LaF3 is the most energetically stable. In order to interpret the structure of the optical absorption spectrum of X-irradiated LaF3 we performed calculations of excited and transition states of the F-center within the embedded cluster formalism using time dependent density function…

Nuclear and High Energy PhysicsMaterials scienceAbsorption spectroscopy02 engineering and technologyElectronic structureTime-dependent density functional theory010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesQuantum chemistry0104 chemical scienceschemistry.chemical_compoundchemistryAb initio quantum chemistry methodsExcited stateLanthanum trifluorideDensity functional theoryAtomic physics0210 nano-technologyInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Ultrastrong Coupling of a Single Molecule to a Plasmonic Nanocavity: A First-Principles Study

2022

| openaire: EC/H2020/838996/EU//RealNanoPlasmon Funding Information: We acknowledge financial support from the Swedish Research Council (VR Miljö, Grant No: 2016-06059), the Knut and Alice Wallenberg Foundation (Grant No: 2019.0140), the Polish National Science Center (projects 2019/34/E/ST3/00359 and 2019/35/B/ST5/02477). T.P.R. acknowledges support from the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie Grant Agreement No. 838996 and support from the Academy of Finland under the Grant No. 332429. T.J.A. acknowledges support from the Project HPC-EUROPA3 (INFRAIA-2016-1-730897), with the support of the EC Research Innovation Action under the H…

Other Physics TopicsexcitonsAtom and Molecular Physics and OpticstiheysfunktionaaliteoriaCondensed Matter PhysicsAtomic and Molecular Physics and OpticsplasmonicsElectronic Optical and Magnetic Materialstime-dependent density functional theorynanorakenteetfotoniikkaplasmoniikkastrong couplingnanophotonicsElectrical and Electronic EngineeringBiotechnology
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