Search results for "density-functional theory"

showing 10 items of 26 documents

Hot-Carrier Generation in Plasmonic Nanoparticles: The Importance of Atomic Structure

2020

Metal nanoparticles are attractive for plasmon-enhanced generation of hot carriers, which may be harnessed in photochemical reactions. In this work, we analyze the coherent femtosecond dynamics of photon absorption, plasmon formation, and subsequent hot-carrier generation through plasmon dephasing using first-principles simulations. We predict the energetic and spatial hot-carrier distributions in small metal nanoparticles and show that the distribution of hot electrons is very sensitive to the local structure. Our results show that surface sites exhibit enhanced hot-electron generation in comparison to the bulk of the nanoparticle. While the details of the distribution depend on particle s…

Materials scienceDephasingAtom and Molecular Physics and OpticsFOS: Physical sciencesGeneral Physics and AstronomyNanoparticlePhysics::Optics02 engineering and technology010402 general chemistry01 natural sciencesAtomic unitsArticleplasmon dephasingPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials ScienceAbsorption (electromagnetic radiation)Plasmonatomic-scaleatomic scaleChemical Physics (physics.chem-ph)Plasmonic nanoparticlesCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicslocalized surface plasmonGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)plasmon decay021001 nanoscience & nanotechnologyCondensed Matter Physicstime-dependent density-functional theory0104 chemical sciencespintaplasmonitplasmonittime-dependent density functional theoryChemical physicsFemtosecondnanohiukkasetAstrophysics::Earth and Planetary Astrophysicshot carriers0210 nano-technologyhot electronsLocalized surface plasmon
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Plasmon Excitations in Mixed Metallic Nanoarrays

2019

Features of the surface plasmon from macroscopic materials emerge in molecular systems, but differentiating collective excitations from single-particle excitations in molecular systems remains elusive. The rich interactions between single-particle electron-hole and collective electron excitations produce phenomena related to the chemical physics aspects within the atomic array. We study the plasmonic properties of atomic arrays of noble (Au, Ag, and Cu) and transition-metal (Pd, Pt) homonuclear chains using time-dependent density functional theory and their Kohn-Sham transition contributions. The response to the electromagnetic radiation is related to both the geometry-dependent confinement…

Materials scienceGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyElectronoptiset ominaisuudet01 natural sciencesMolecular physicsElectromagnetic radiationHomonuclear moleculeplasmonicsnanorakenteet0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Physics::Atomic and Molecular Clusterstransition contribution mapsGeneral Materials ScienceSurface plasmon resonance010306 general physicsPlasmonCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicsta114Surface plasmontiheysfunktionaaliteoriaGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)molecular plasmonics021001 nanoscience & nanotechnologytime-dependent density-functional theorytime-dependent density functional theorycollective excitationQuasiparticleDensity functional theory0210 nano-technology
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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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Theoretical Study of the Charge Transfer Exciton Binding Energy in Semiconductor Materials for Polymer:Fullerene-Based Bulk Heterojunction Solar Cells

2019

Recent efforts and progress in polymer solar cell research have boosted the photovoltaic efficiency of the technology. This efficiency depends not only on the device architecture but also on the material properties. Thus, insight into the design of novel semiconductor materials is vital for the advancement of the field. This paper looks from a theoretical viewpoint into two of the factors for the design of semiconductor materials with applications to bulk heterojunction solar cells: the charge transfer exciton binding energy and the nanoscale arrangement of donor and acceptor molecules in blend systems. Being aware that the exciton dissociation of local excitons in charge transfer states in…

ORGANIC SEMICONDUCTORSOrganic solar cellExcitonBinding energyCHEMICAL-STRUCTURE010402 general chemistry01 natural sciences7. Clean energyENERGETICSPolymer solar cellArticleDENSITY-FUNCTIONAL THEORY0103 physical sciencesSTRATEGYPhysical and Theoretical Chemistry010304 chemical physicsChemistryGAPHeterojunctionAcceptor0104 chemical sciencesP3HT/PCBMOrganic semiconductorSTATESChemical physicsExcited stateSEPARATIONMORPHOLOGYThe Journal of Physical Chemistry. a
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Photochemistry of 1,2,4-oxadiazoles. A DFT study on photoinduced competitive rearrangements of 3-amino- and 3-N-methylamino-5-perfluoroalkyl-1,2,4-ox…

2006

The photoinduced competitive rearrangements of 5-perfluoroalkyl-3-amino(N-alkylamino)-1,2,4-oxadia- zoles have been investigated by DFT calculations and UV-vis spectroscopy. The observed product selectivity depends on the number of hydrogen atoms present in the amino moiety and involves two or three possible routes: (i) ring contraction-ring expansion (RCRE), (ii) internal-cyclization isomerization (ICI), or (iii) C(3)-N(2) migration-nucleophilic attack-cyclization (MNAC). UV absorption and fluorescence spectra of the reactants, and vertical excitation energy values, calculated by time dependent DFT, support the involvement of a neutral singlet excited state in the photoexcitation process. …

PhotochemistryUltraviolet RaysFluorescence spectrometryReaction intermediatePhotochemistryDENSITY-FUNCTIONAL THEORYSinglet stateHUMAN 5-HT1B RECEPTORBASIS-SETSOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructureChemistryOrganic ChemistryEXPEDIENT ROUTETautomerTransition statePhotoexcitationMOLECULAR-ORBITAL METHODSModels ChemicalLUORINATED HETEROCYCLIC-COMPOUNDSAROMATICITY INDEXExcited state5-MEMBERED HETEROCYCLESEXCITATION-ENERGIESIsomerization
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On the lower bound on the exchange-correlation energy in two dimensions

2010

We study the properties of the lower bound on the exchange-correlation energy in two dimensions. First we review the derivation of the bound and show how it can be written in a simple density-functional form. This form allows an explicit determination of the prefactor of the bound and testing its tightness. Next we focus on finite two-dimensional systems and examine how their distance from the bound depends on the system geometry. The results for the high-density limit suggest that a finite system that comes as close as possible to the ultimate bound on the exchange-correlation energy has circular geometry and a weak confining potential with a negative curvature. Fil: Räsänen, Esa. Universi…

PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsStrongly Correlated Electrons (cond-mat.str-el)Mathematical analysisFOS: Physical sciences//purl.org/becyt/ford/1.3 [https]Condensed Matter PhysicsCurvatureUpper and lower boundsAtomic and Molecular Physics and OpticsQUANTUM DOTElectronic Optical and Magnetic MaterialsDENSITY-FUNCTIONAL THEORYLIEB-OXFORD BOUND//purl.org/becyt/ford/1 [https]Condensed Matter - Strongly Correlated ElectronsSimple (abstract algebra)Quantum mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Density functional theoryLimit (mathematics)Focus (optics)Gravitational binding energyEnergy (signal processing)
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Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning

2015

Halogen bonding, a noncovalent interaction possessing several unique features compared to the more familiar hydrogen bonding, is emerging as a powerful tool in functional materials design. Herein, we unambiguously show that one of these characteristic features, namely high directionality, renders halogen bonding the interaction of choice when developing azobenzene-containing supramolecular polymers for light-induced surface patterning. The study is conducted by using an extensive library of azobenzene molecules that differ only in terms of the bond-donor unit. We introduce a new tetrafluorophenol-containing azobenzene photoswitch capable of forming strong hydrogen bonds, and show that an io…

RELIEF GRATINGSDENSITY-FUNCTIONAL THEORY CALCULATIONSMaterials sciencePHOTOINDUCED BIREFRINGENCE116 Chemical sciencesta221Supramolecular chemistryPhotochemistrysupramolecular chemistryDENSITY-FUNCTIONAL THEORYchemistry.chemical_compoundMaterials ChemistryMoleculeTHERMAL-ISOMERIZATIONPOLARIZATION DEPENDENCECO-CRYSTALSLIQUID-CRYSTAL ORDERta218chemistry.chemical_classificationta214Halogen bondta114PhotoswitchHydrogen bondPolymers Halogen Bonding Supramolecular Chemistry Photoresponsive AzobenzeneGeneral Chemistryhydrogen bondingPOLYMER-AZOBENZENE COMPLEXESSupramolecular polymersSOLID-STATEchemistryAzobenzeneHALOGEN BONDINGHalogenlight-induced surface patterningSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTONIC APPLICATIONSPOLYMER-AZOBENZENE COMPLEXES; DENSITY-FUNCTIONAL THEORY; LIQUID-CRYSTAL ORDER; RELIEF GRATINGS; SOLID-STATE; PHOTOINDUCED BIREFRINGENCE; POLARIZATION DEPENDENCE; THERMAL-ISOMERIZATION; PHOTONIC APPLICATIONS; CO-CRYSTALSJournal of Materials Chemistry C
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A many-body approach to transport in quantum systems : From the transient regime to the stationary state

2022

We review one of the most versatile theoretical approaches to the study of time-dependent correlated quantum transport in nano-systems: the non-equilibrium Green's function (NEGF) formalism. Within this formalism, one can treat, on the same footing, inter-particle interactions, external drives and/or perturbations, and coupling to baths with a (piece-wise) continuum set of degrees of freedom. After a historical overview on the theory of transport in quantum systems, we present a modern introduction of the NEGF approach to quantum transport. We discuss the inclusion of inter-particle interactions using diagrammatic techniques, and the use of the so-called embedding and inbedding techniques w…

Statistics and ProbabilityTIME-DEPENDENT TRANSPORTKADANOFF-BAYM EQUATIONSGeneral Physics and AstronomyFOS: Physical sciencesnon-equilibrium Green's functionGREENS-FUNCTIONDENSITY-FUNCTIONAL THEORYCondensed Matter - Strongly Correlated ElectronsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)COHERENT TRANSPORTSINGLE-MOLECULEkvanttifysiikkamany-body correlationMathematical Physicsquantum transportMEAN-FIELD THEORYChemical Physics (physics.chem-ph)Quantum PhysicsANDERSON-HOLSTEIN MODELCondensed Matter - Mesoscale and Nanoscale PhysicsStrongly Correlated Electrons (cond-mat.str-el)Statistical and Nonlinear PhysicsCHARGE MIGRATIONModeling and Simulationnon-equilibrium Green’s functionQuantum Physics (quant-ph)SHOT-NOISE
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Excited State N−H Tautomer Selectivity in the Singlet Energy Transfer of a Zinc(II)-Porphyrin-Truxene-Corrole Assembly

2017

International audience; An original corrole-containing polyad for S-1 energy transfer, in which one zinc(II)-porphyrin donor is linked to two free-base corrole acceptors by a truxene linker, is reported. This polyad exhibits a rapid zinc(II)-porphyrin*free-base corrole transfer (4.83x10(10)s(-1); 298K), even faster than the tautomerization in the excited state processes taking advantage of the good electronic communication provided by the truxene bridge. Importantly, the energy transfer process shows approximately 3-fold selectivity for one corrole N-H tautomer over the other even at low temperature (77K). This selectivity is due to the difference in the J-integral being effective in both t…

chemistry.chemical_elementDexter energy transferZinccore-modified corroles010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesmain-group elements[ CHIM ] Chemical SciencesCatalysisfree-base corroleschemistry.chemical_compoundmolecular-orbital methods[CHIM]Chemical SciencesSinglet stateCorrolecorrolesdensity-functional theoryvalence basis-setsphotophysical propertiestautomerization010405 organic chemistrytruxenesensitized solar-cellsOrganic ChemistryGeneral ChemistryTautomerPorphyrin0104 chemical scienceschemistrymesosubstituted corrolesExcited stateFRETextended basis-setsSelectivityLinker
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Metal Dependence on the Bidirectionality and Reversibility of the Singlet Energy Transfer in Artificial Special Pair-Containing Dyads

2017

International audience; The demetalation of a precursor dyad, 3, built upon a zinc(II)-containing artificial special pair and free-base antenna, leads to a new dyad, 4, for singlet energy transfer composed of cofacial free-base porphyrins (acceptor), [Fb](2) bridged by a 1,4-C6H4 group to a free-base antenna (donor), [Fb]. This dyad exhibits the general structure [M](2)-C6H4-[Fb], where [M](2) = [Fh](2), and completes a series reported earlier, where [M](2) = [Mg](2) (2) and [Zn](2) (3). The latter dyads exhibit a bidirectional energy-transfer process at 298 K for 2 and at 77 K for 3. Interestingly, a very scarce case of cycling process is observed for the zinc-containing dyad at 298 K. The…

cofacial bisporphyrin dyadsStereochemistryEnergy transferchemistry.chemical_elementZinc[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesphotoinduced electron-transferInorganic ChemistryMetalmolecular-orbital methodsMolecular orbitalSinglet statePhysical and Theoretical Chemistryphotosynthetic reaction-centerdensity-functional theoryvalence basis-setsbase hybrid diporphyrins010405 organic chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryResonance (chemistry)Acceptor0104 chemical sciencesCrystallographychemistrylight-harvesting systemsvisual_artpolarizable continuum modelvisual_art.visual_art_mediumDensity functional theoryextended basis-sets
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