Search results for "Density Functional Theory."

showing 10 items of 935 documents

Iron’s Wake: The Performance of Quantum Mechanical-Derived Versus General-Purpose Force Fields Tested on a Luminescent Iron Complex

2020

Recently synthetized iron complexes have achieved long-lived excited states and stabilities which are comparable, or even superior, to their ruthenium analogues, thus representing an eco-friendly and cheaper alternative to those materials based on rare metals. Most of computational tools which could help unravel the origin of this large efficiency rely on ab-initio methods which are not able, however, to capture the nanosecond time scale underlying these photophysical processes and the influence of their realistic environment. Therefore, it exists an urgent need of developing new low-cost, but still accurate enough, computational methodologies capable to deal with the steady-state and trans…

Work (thermodynamics)AcetonitrilesLuminescenceIronPharmaceutical ScienceMolecular Dynamics Simulation010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Molecular dynamicschemical environmentlcsh:Organic chemistry0103 physical sciencesDrug Discoverytime-dependent density functional theory.Statistical physicsPhysical and Theoretical ChemistryQuantumComputingMilieux_MISCELLANEOUSPhysics010304 chemical physicsSpectrum AnalysisScale (chemistry)Organic ChemistryTime-dependent density functional theoryNanosecond0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrytime-dependent density functional theoryiron complexChemistry (miscellaneous)Excited stateSolventsQuantum TheoryMolecular MedicineLuminescenceIron Compoundsforce field molecular dynamicsMolecules
researchProduct

Theoretical study of oligomeric alumatranes present in the chemistry of materials from micro to mesoporous molecular sieves and alumina composites

2008

Quantum chemical calculations using density functional theory have been carried out to investigate molecular precursors based on alumatranes which are one of the components with silatranes for the preparation of mesoporous aluminosilicate materials. In the same way, some oligomeric alumatranes of this study take part in chemical syntheses related to materials such as zeolites and alumina composite. Gas phase and solution equilibrium geometries of the alumatrane precursors were fully optimized at B3LYP level, modeling solvent effects using a self-consistent reaction field (SCRF). From these optimized geometries, calculations of the 1 H, 13 C and 27 Al NMR chemical shifts at GIAO/B3LYP/6-31G(…

Work (thermodynamics)Computational chemistryChemistryAluminosilicateChemical shiftDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsCondensed Matter PhysicsMass spectrometryMesoporous materialMolecular sieveBiochemistryJournal of Molecular Structure: THEOCHEM
researchProduct

Metallic subnanometer porous silicon: A theoretical prediction

2021

In the present work, T-Si, a silicon-based counterpart of T-carbon, has been designed with the aid of density functional theory (DFT) calculations. Its stability has been fully confirmed from energetic, mechanical, lattice dynamic, and thermodynamic aspects. Due to the space extrusion, the delocalized electrons on the ${\mathrm{Si}}_{4}$ tetrahedrons are squeezed onto the inter-tetrahedron $\mathrm{Si}\ensuremath{-}\mathrm{Si}$ bonds, which therefore leads T-Si to be metallic. Furthermore, the electronic conductivity of this new material has also been predicted and discussed in this work. This new silicon allotrope with a low density of $0.869\mathrm{g}/{\mathrm{cm}}^{3}$ can even floats on…

Work (thermodynamics)Materials scienceCondensed matter physicsSiliconLattice (group)chemistry.chemical_element02 engineering and technology021001 nanoscience & nanotechnologySpace (mathematics)Porous silicon01 natural sciencesDelocalized electronchemistry0103 physical sciencesTetrahedronDensity functional theory010306 general physics0210 nano-technologyPhysical Review B
researchProduct

Grand-canonical approach to density functional theory of electrocatalytic systems: Thermodynamics of solid-liquid interfaces at constant ion and elec…

2018

Properties of solid-liquid interfaces are of immense importance for electrocatalytic and electrochemical systems, but modeling such interfaces at the atomic level presents a serious challenge and approaches beyond standard methodologies are needed. An atomistic computational scheme needs to treat at least part of the system quantum mechanically to describe adsorption and reactions, while the entire system is in thermal equilibrium. The experimentally relevant macroscopic control variables are temperature, electrode potential, and the choice of the solvent and ions, and these need to be explicitly included in the computational model as well; this calls for a thermodynamic ensemble with fixed…

Work (thermodynamics)Materials scienceImplicit solvationGeneral Physics and AstronomyElectronDielectric010402 general chemistry01 natural sciencesELECTROCHEMISTRYthermodynamicsCHEMISTRY0103 physical sciencesWATERsolid-liquid interfacesStatistical physicsPhysical and Theoretical Chemistryrajapintailmiötta116QuantumAB-INITIOThermal equilibriumSELF-CONSISTENTta114010304 chemical physicstiheysfunktionaaliteoriaSIMULATIONS0104 chemical sciencesGrand canonical ensembleREDUCTIONCONTINUUMSOLVATIONSolvent modelsStandard electrode potentialtermodynamiikkakatalyysiDensity functional theoryElectronic densityAPPROXIMATIONElectrode potential
researchProduct

On the impact of side methyl groups on the structure and vibrational properties of β-carotenoids. The case of butadiene and isoprene

2021

Abstract Theoretical consideration about the impact of methyl groups on the structure and vibrational properties of β-carotenoids, using medium size molecules of trans-butadiene and trans-isoprene, are reported. Density functional theory (DFT) calculations with correlation-consistent and polarization-consistent basis sets were applied to trans-1,3-butadiene and trans-isoprene as the smallest building bricks of β-carotenoids. Their structure and harmonic vibrations were estimated in the complete basis set limit (CBS) using the non-linear least square fit. Optimized geometries and harmonic frequencies, obtained with B3LYP and BLYP density functionals and large basis sets, were favorably repro…

Work (thermodynamics)Materials scienceIsopreneMolecular modelIR/Raman spectroscopySpectrum Analysis RamanDFTVibrationMolecular physicsAnalytical Chemistrychemistry.chemical_compoundHemiterpenesSpectroscopy Fourier Transform InfraredButadienesMoleculeBasis setIsopreneButadieneBasis (linear algebra)General MedicineFunction (mathematics)Carotenoidschemistryβ-CarotenoidsQuantum TheoryDensity functional theoryMolecular structureFood ScienceFood Chemistry
researchProduct

Ab initio molecular dynamics studies of Au38(SR)24 isomers under heating

2019

Despite the great success in achieving monodispersity for a great number of monolayer-protected clusters, to date little is known about the dynamics of these ultra-small metal systems, their decomposition mechanisms, and the energy that separates their structural isomers. In this work, we use density functional theory (DFT) to calculate and compare the ground state energy and the Born-Oppenheimer molecular dynamics of two well-known Au 38 (SCH 2 CH 2 Ph) 24 nanocluster isomers. The aim is to shed light on the energy difference between the two clusters isomers and analyze their decomposition mechanisms triggered by high temperatures. The results demonstrate that the energy that separates the…

Work (thermodynamics)Materials scienceOptical physics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesmolecular dynamicsAtomic and Molecular Physics and Optics0104 chemical sciencesMolecular dynamicsChemical physicsStructural isomerCluster (physics)molekyylidynamiikkananohiukkasetDensity functional theory0210 nano-technologyGround stateOrder of magnitudeThe European Physical Journal D
researchProduct

Structural, energetic and kinetic database of catalytic reactions: Benzyl alcohol to benzaldehyde oxidation on MnOx clusters

2021

Abstract Data here reported are connected with the research article “Benzyl Alcohol to Benzaldehyde Oxidation on MnO x Clusters: Unraveling Atomistic Features” Gueci et al. [1] . This work described and discussed structural and energetic results, calculated by Density Functional Theory (DFT). In order to get kinetic information, DFT results were refined by an original approach, which will be shortly described in the following article. The crossed analysis of experimental and computational energetic and kinetic data allowed to (i) reconstruct the complicated lattice that connects the primary and secondary mechanisms of the reaction and (ii) identify alternative process pathways capable of by…

Work (thermodynamics)Science (General)MultidisciplinaryMaterials scienceMnOx Oxidative–dehydrogenation Deactivation Remediation DFT Reaction kineticMnOxComputer applications to medicine. Medical informaticsKineticsDeactivationReaction kineticR858-859.7RemediationAlternative processHeterogeneous catalysisDFTCatalysisBenzaldehydeQ1-390chemistry.chemical_compoundchemistryBenzyl alcoholComputational chemistryDensity functional theoryOxidative–dehydrogenationSettore CHIM/02 - Chimica FisicaData in Brief
researchProduct

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
researchProduct

cis-[(η5-C5H5)Fe(η1-CO)(μ-CO)]2, the poor relative between cis and trans tautomers. A theoretical study of the gas-phase Fe L3-edge and C and O K-edg…

2021

The relative stability of trans-[(η5-C5H5)Fe(η1-CO)(μ-CO)]2 (trans-I) and cis-I tautomers in a vacuum and in solvents with different dielectric constants (e) has been investigated by exploiting density functional theory (DFT). Theoretical results indicate that, in agreement with experimental evidence, trans-I is more stable than cis-I in a vacuum (∼1.5 kcal mol−1; e = 1), while the opposite is true in media with e > 7. Differently from solution, DFT outcomes pertaining to the vapor-phase cis-I ⇆ trans-I equilibrium at T = 368 K, the temperature at which the Fe L2,3-edges and the C and O K-edge X-ray absorption spectroscopy (XAS) data of I have been recorded, ultimately indicate the trans-I …

X-ray absorption spectroscopyMaterials scienceK-edgeAbsorption spectroscopyGeneral Physics and AstronomyPhysical chemistryDensity functional theoryDielectricPhysical and Theoretical ChemistryTautomerSpectral lineCis–trans isomerismPhysical Chemistry Chemical Physics
researchProduct

Y:BaZrO3 Perovskite Compounds I: DFT Study on the Unprotonated and Protonated Local Structures

2011

Y-doped BaZrO(3) derivatives were studied by density functional theory (DFT) to investigate the local arrangements of the octahedral sites in Pm3m cubic frameworks. Single- and double substitution of zirconium by yttrium were considered, including in the presence of a nearby oxygen vacancy. Although the structural symmetry of undoped barium zirconate was not modified after yttrium doping, the presence of yttrium induced several differences in the oxygen sites around it, according to the local geometrical arrangement of yttrium in the host matrix. As an example, the differences between such oxygen sites were shown in the presence of a proton. In this case, different stabilization energies ch…

ZirconiumProtonChemistryProtonic conductionOrganic ChemistryInorganic chemistrychemistry.chemical_elementProtonationyttrium-doped barium zirconateGeneral ChemistryYttriumSiestaBiochemistryDFTCondensed Matter::Materials ScienceCrystallographyOctahedronSettore CHIM/03 - Chimica Generale E InorganicaDensity functional theoryfuel-cellOrder of magnitudeperovskitePerovskite (structure)
researchProduct