Search results for "functional theory"

showing 10 items of 1012 documents

From determination of the fugacity coefficients to estimation of hydrogen storage capacity: A convenient theoretical method

2015

Abstract The equation of state (EOS) from virial expansion (VE) is used in this work to pave the way for determining the fugacity coefficients of the hydrogen fluid at arbitrary temperature and pressure. The fugacity coefficients from our VE method have more physical meanings than the empirical values. In this way, the hydrogen storage capacity of a novel material model can be estimated by using few density functional theory (DFT) calculations with the aid of a continuum model. The efficient continuum model can provide a more accurate estimation of the hydrogen storage capacity than the pure DFT calculations. Furthermore, the expensive grand canonical ensemble (μNT) simulations combining wi…

HydrogenRenewable Energy Sustainability and the EnvironmentChemistryEnergy Engineering and Power TechnologyThermodynamicschemistry.chemical_elementCondensed Matter PhysicsHydrogen storageGrand canonical ensembleFuel TechnologyTemperature and pressureVirial expansionDensity functional theoryFugacityBilayer grapheneInternational Journal of Hydrogen Energy
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A computational and conceptual DFT study on the mechanism of hydrogen activation by novel frustrated Lewis pairs.

2015

A computational and conceptual density functional theory (DFT) study on the mechanism of molecular hydrogen activation by a set of three frustrated Lewis pairs (FLPs) was performed at the ωB97X-D/6-311G(d,p) level of theory. A reduced model and other two prototypes derived from experimental data, based on the donor nitrogen and acceptor boron atoms, were used. Analysis based on the energy results, geometries and the global electron density transfer at the TSs made it possible to obtain some interesting conclusions: (i) despite the well-known very low reactivity of molecular hydrogen, the catalytic effectiveness of the three FLPs produces reactions with almost unappreciable activation energi…

HydrogenSubstituentGeneral Physics and Astronomychemistry.chemical_elementAcceptorFrustrated Lewis pairCatalysischemistry.chemical_compoundAcetylenechemistryComputational chemistryReactivity (chemistry)Density functional theoryPhysical and Theoretical ChemistryPhysical chemistry chemical physics : PCCP
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Anharmonicity modeling in hydrogen bonded solvent dimers

2021

Abstract Harmonic and anharmonic frequencies of dimers and mixed dimers of water, methanol and benzene were computed and the results were critically analysed to investigate the anharmonicity of the normal mode vibrations within density functional theory (DFT) with empirically included Grimme correction for dispersion (D3). From several options, the B3LYP-D3/6-31++G* level of theory was selected as a good compromise between accuracy and calculation speed, suitable for future modeling of larger solvent clusters. The obtained raw harmonic and anharmonic second-order perturbation theory of vibrational frequencies (VPT2) were additionally scaled using a two-range procedure (below and above 2000 …

Hydrogenchemistry.chemical_element02 engineering and technology010402 general chemistryDFT01 natural sciencesMolecular physicsQuality (physics)Normal modePhysics::Atomic and Molecular ClustersMaterials ChemistryVPT2Physics::Chemical PhysicsPhysical and Theoretical ChemistryPerturbation theorySpectroscopyPhysicsAnharmonicity021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFrequency scaling0104 chemical sciencesElectronic Optical and Magnetic MaterialsVibrationchemistrySolvent dimersHarmonicH-BondingDensity functional theoryAnharmonic vibrational frequencies0210 nano-technologyJournal of Molecular Liquids
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Correlating Schiff Moments in the Light Actinides with Octupole Moments

2018

We show that the measured intrinsic octupole moments of $^{220}$Rn, $^{224}$Ra, and $^{226}$Ra constrain the intrinsic Schiff moments of $^{225}$Ra$^{221}$Rn, $^{223}$Rn, $^{223}$Fr, $^{225}$Ra, and $^{229}$Pa. The result is a dramatically reduced uncertainty in intrinsic Schiff moments. Direct measurements of octupole moments in odd nuclei will reduce the uncertainty even more. The only significant source of nuclear-physics error in the laboratory Schiff moments will then be the intrinsic matrix elements of the time-reversal non-invariant interaction produced by CP-violating fundamental physics. Those matrix elements are also correlated with octupole moments, but with a larger systematic u…

INTRINSIC REFLECTION ASYMMETRYPARAMETRIZATIONnuclear many-body theoryODDNuclear TheoryNUCLEInuclear density functional theorySKYRME INTERACTIONFOS: Physical sciencesRA-225114 Physical sciencesnuclear structure and decays3100Nuclear Theory (nucl-th)FORCESydinfysiikkanuclear tests of fundamental interactions
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Water and carbon oxides on monoclinic zirconia: experimental and computational insights

2014

Zirconium oxide (ZrO2, zirconia) is an interesting catalytic material to be used in biomass conversion, e.g., gasification and reforming. In this work, we show that reducing and hydrating pretreatments affect the surface sites on monoclinic zirconia. The multitechnique approach comprises temperature-programmed surface reactions (TPSR) under CO and CO2 at 100-550 °C, in situ DRIFTS investigations of the surface species and density functional theory (DFT) calculations. The key findings of the work are: (1) formates are formed either directly from gas-phase CO on terminal surface hydroxyls or via the linear CO surface species that are found exclusively on the reduced zirconia without water tre…

In situWork (thermodynamics)ChemistryInorganic chemistryta220General Physics and AstronomyCatalysisCarbon oxideDensity functional theoryCubic zirconiaWater treatmentPhysical and Theoretical Chemistryta216ta215ta116Monoclinic crystal systemPhysical Chemistry Chemical Physics
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NMR Spectroscopic Characterization and DFT Calculations of Zirconium(IV)-3,3′-Br2–BINOLate and Related Complexes Used in an Enantioselective Friedel–…

2012

Experimental and theoretical studies on the structure of several complexes based on (R)-3,3'-Br-2-BINOL ligand and group (IV) metals used as catalysts in an enantioselective Friedel-Crafts alkylation of indoles with alpha,beta-unsaturated ketones have been carried out. NMR spectroscopic studies of these catalysts have been performed, which suggested that at room temperature the catalysts would form a monomeric structure in the case of Ti-IV and a dimeric structure in the cases of Zr-IV and Hf-IV. Density functional theory (DFT) calculations clearly corroborate the conclusions of these experimental spectroscopic studies. The dimeric structure with a doubly bridged motif [Zr-2(IV)(mu-(R)-3,3'…

Indole testIndolesMagnetic Resonance SpectroscopyAlkylationMolecular StructureStereochemistryLigandOrganic ChemistryEnantioselective synthesisStereoisomerismNaphtholsKetonesAlkylationMedicinal chemistryCatalysischemistry.chemical_compoundMonomerchemistryFISICA APLICADADensity functional theoryZirconiumFriedel–Crafts reactionThe Journal of Organic Chemistry
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Selectivity in Propene Dehydrogenation on Pt and Pt3Sn Surfaces from First Principles

2013

Propene can be produced via dehydrogenation of propane on Pt-based catalysts; however, the catalysts are plagued by low selectivity toward propene and high coke formation. The selectivity can be improved and the coke formation reduced by alloying Pt with Sn. The alloying is known to weaken the binding of propene, which in part explains the improved performance. We conducted density functional theory calculations to study the dehydrogenation of propene on flat and stepped Pt and Pt3Sn surfaces. The steps on Pt dehydrogenate propene readily, whereas, on Pt3Sn, the steps are inert because they are decorated with Sn. Our results indicate that the high selectivity and low coking on the Pt–Sn cat…

InertChemistryInorganic chemistryGeneral ChemistryCokeCatalysisCatalysisPropenechemistry.chemical_compoundPropaneDensity functional theoryDehydrogenationSelectivityta116ACS Catalysis
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Regional Susceptibility in VCD Spectra to Dynamic Molecular Motions

2018

Experimental and theoretical studies of the vibrational circular dichroism (VCD) spectrum of 3-methyl-1-(methyldiphenlsilyl)-1-phenylbutan-1-ol, whose absolute configuration is key to elucidating the Brook rearrangement of tertiary benzylic α-hydroxylsilanes, are presented. It is found that the entire OH-bending region in this spectrum—a region that provides important marker bands—cannot be reproduced at all by standard theoretical approaches even though other regions are well described. Using a novel approach to disentangle contributions to the rotational strength of these bands, internal coordinates are identified that critically influence the appearance of this part of the spectrum. We s…

Infrared spectroscopy02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsSpectral lineForce field (chemistry)COUPLED OSCILLATOR MECHANISMconformations analysisMolecular motionIMPLEMENTATIONPhysical and Theoretical Chemistrydensity functional theoryPhysicsconfiguration determinationVIBRATIONAL CIRCULAR-DICHROISMOLD CONCEPTAbsolute configurationCORRELATION-ENERGYBrook rearrangement021001 nanoscience & nanotechnologyvibrational circular dichroismAtomic and Molecular Physics and Opticsvibrational spectroscopy0104 chemical sciencesMODELLARGE-AMPLITUDE MOTIONSVibrational circular dichroismFORCE-FIELDDensity functional theory0210 nano-technologyAPPROXIMATIONChemphyschem
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Vibrational Sum Frequency Generation Spectroscopy of the Water Liquid–Vapor Interface from Density Functional Theory-Based Molecular Dynamics Simulat…

2013

International audience; The vibrational sum frequency generation (VSFG) spectrum of the water liquid-vapor (LV) interface is calculated using density functional theory-based molecular dynamics simulations. The real and imaginary parts of the spectrum are in good agreement with the experimental data, and we provide an assignment of the SFG bands according to the dipole orientation of the interfacial water molecules. We use an instantaneous definition of the surface, which is more adapted to the study of interfacial phenomena than the Gibbs dividing surface. By calculating the vibrational (infrared, Raman) properties for interfaces of varying thickness, we show that the bulk spectra signature…

InfraredBulk spectra02 engineering and technologyMolecular dynamicsVibrational sum-frequency generations010402 general chemistry01 natural sciencesMolecular physicsSpectral lineInterfacial phenomenaLiquid-vapor interfaceMolecular dynamicssymbols.namesakeDipole orientationComputational chemistryGeneral Materials SciencePhysical and Theoretical ChemistryDividing surfacesDensity functionalsSum-frequency generationMolecular dynamics simulationsChemistryInterfacial water moleculesThin layers021001 nanoscience & nanotechnologyLiquid-vapor0104 chemical sciencesDipoleImaginary partsDensity functional theoryVaporssymbolsDensity functional theory[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyRaman spectroscopyVarying thicknessSum frequency generation spectroscopyThe Journal of Physical Chemistry Letters
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Spectroscopic and theoretical study of push-pull chromophores containing thiophene-based quinonoid structures as electron spacers

2003

Donor−acceptor chromophores containing three different types of thiophene-based electron spacers and the same donor (1,3-dithiol-2-ylidene) and acceptor (dicyanomethylene) end groups have been investigated by infrared and vis-near-IR absorption spectroscopies with the aim of elucidating the ability of the heteroquinonoid spacers as electron transmitters. Density functional theory calculations have been carried out, both within the standard and the time-dependent formalisms, to assign the most relevant electronic and infrared features of these chromophores and to assess useful information about their molecular structures. Both theoretical calculations and vibrational spectra demonstrate the …

InfraredElectronChromophorePhotochemistryAcceptorSurfaces Coatings and Filmschemistry.chemical_compoundchemistryIntramolecular forceMaterials ChemistryThiopheneDensity functional theoryPhysical and Theoretical ChemistryGround state
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