Search results for "computational"

showing 10 items of 5884 documents

Simulations of the effect of the contact energy levels on a simple model of a hot carrier cell

2016

In the present work, the performance of a simplified model of a hot carrier cell is examined at different energy levels of carrier collection. Incident photons, Monte Carlo generated by employing the ASTM G173-03 data set, are accounted for individually as they interact with the cell. It is assumed that the carriers can be collected ultra-fast, thus avoiding considering hot carrier thermalisation effects. Although the model is preliminary and lacking some mechanisms of hot carrier cells, it has been demonstrated that the present approach to modelling hot carrier solar cells can be developed into fully working models. Some effects of the absorption energy levels in the valence band have been…

010302 applied physicsWork (thermodynamics)SIMPLE (dark matter experiment)PhotonMaterials sciencebusiness.industryMonte Carlo methodElectrical engineering02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesComputational physicsThermalisationEnergy absorbing0103 physical sciencesValence band0210 nano-technologybusinessEnergy (signal processing)2016 IEEE 43rd Photovoltaic Specialists Conference (PVSC)
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On the ‘expanded local mode’ approach applied to the methane molecule: isotopic substitution CH2D2←CH4

2011

On the basis of a compilation of the ‘expanded local mode’ model and the general isotopic substitution theory, sets of simple analytical relations between different spectroscopic parameters (harmonic frequencies, ωλ, anharmonic coefficients, x λμ, ro-vibrational coefficients, , different kinds of Fermi- and Coriolis-type interaction parameters) of the CH2D2 molecule are derived. All of them are expressed as simple functions of a few initial spectroscopic parameters of the mother, CH4, molecule. Test calculations with the derived isotopic relations show that, in spite of a total absence of initial information about the CH2D2 species, the numerical results of the calculations have a very good…

010304 chemical physicsBasis (linear algebra)ChemistrySubstitution (logic)AnharmonicityBiophysicsThermodynamics010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesComputational chemistryAb initio quantum chemistry methodsSimple (abstract algebra)Simple function0103 physical sciencesMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular BiologyFermi Gamma-ray Space TelescopeMolecular Physics
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On the N1-H and N3-H Bond Dissociation in Uracil by Low Energy Electrons: A CASSCF/CASPT2 Study.

2015

The dissociative electron-attachment (DEA) phenomena at the N1-H and N3-H bonds observed experimentally at low energies (<3 eV) in uracil are studied with the CASSCF/CASPT2 methodology. Two valence-bound π(-) and two dissociative σ(-) states of the uracil anionic species, together with the ground state of the neutral molecule, are proven to contribute to the shapes appearing in the experimental DEA cross sections. Conical intersections (CI) between the π(-) and σ(-) are established as the structures which activate the DEA processes. The N1-H and N3-H DEA mechanisms in uracil are described, and experimental observations are interpreted on the basis of two factors: (1) the relative energy of …

010304 chemical physicsChemistryHydrogen bondUracilElectronBond breaking010402 general chemistry01 natural sciencesDissociation (chemistry)0104 chemical sciencesComputer Science ApplicationsCrystallographychemistry.chemical_compoundLow energyComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryGround stateNeutral moleculeJournal of chemical theory and computation
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Quasi-RRHO approximation and DFT study for understanding the mechanism and kinetics of nitration reaction of benzonitrile with nitronium ion

2021

Abstract The nitration reaction of benzonitrile with nitronium cation, NO2+, has been studied within the Molecular Electron Density Theory at the MN15-L/aug-cc-pVTZ level of theory. For this electrophilic aromatic substitution (EAS) reaction, three regioisomeric reaction paths have been studied. Quasi-RRHO approximation was applied to consider the vibrational contribution to entropy and correct the Gibbs free energy profile of the reaction in the solvent phase. Benzonitrile is less nucleophilically activated than benzene due to the presence of the electron-withdrawing CN group the meta position is the more favorable reaction path of this EAS reaction. The analysis of ELF and AIM demonstrate…

010304 chemical physicsChemistryKineticsElectrophilic aromatic substitution010402 general chemistryCondensed Matter Physics01 natural sciencesBiochemistry0104 chemical sciencesGibbs free energychemistry.chemical_compoundBenzonitrilesymbols.namesakeMeta-Computational chemistryNitration0103 physical sciencessymbolsNitronium ionPhysical and Theoretical ChemistryBenzeneComputational and Theoretical Chemistry
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Unexpected Substituent Effects in the Iso-Heterocyclic Boulton-Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Stud…

2019

The kinetics of the iso-heterocyclic mononuclear rearrangement of some 3-aroylamino-5-methyl-1,2,4-ozadiazoles was carefully examined under largely variable acidic or alkaline conditions. This reaction may proceed via two different mechanistic pathways (an uncatalyzed and a base-catalyzed one), as accounted for also by the evaluation of the relevant activation parameters. Substituent effects, as quantified by means of the Hammett’s equation, appear relatively modest; however, they reveal some interesting anomalies, which enabled us to draw a very precise picture of the intimate reaction course.

010304 chemical physicsChemistryKineticsSubstituent124-oxadiazoleSettore CHIM/06 - Chimica OrganicaMononuclear Heterocyclic Rearrangement010402 general chemistry01 natural sciences0104 chemical sciencesKineticschemistry.chemical_compoundSubstituent effectComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryReaction mechanismThe journal of physical chemistry. A
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Origin of Enzymatic Kinetic Isotope Effects in Human Purine Nucleoside Phosphorylase

2017

Here we report a study of the effect of heavy isotope labeling on the reaction catalyzed by human purine nucleoside phosphorylase (hPNP) to elucidate the origin of its catalytic effect and of the enzymatic kinetic isotope effect (EKIE). Using quantum mechanical and molecular mechanical (QM/MM) molecular dynamics (MD) simulations, we study the mechanism of the hPNP enzyme and the dynamic effects by means of the calculation of the recrossing transmission coefficient. A free energy surface (FES), as a function of both a chemical and an environmental coordinate, is obtained to show the role of the environment on the chemical reaction. Analysis of reactive and nonreactive trajectories allows us …

010304 chemical physicsChemistryPurine nucleoside phosphorylasevariational transition state theoryGeneral Chemistry010402 general chemistryenzyme catalysis01 natural sciencesChemical reactionCatalysis0104 chemical sciencesEnzyme catalysisCatalysisSolventMolecular dynamicsComputational chemistryenzymatic kinetic isotope effect0103 physical sciencesKinetic isotope effectMoleculeQM/MM methodsprotein motionsACS Catalysis
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A quantum dynamics study of the benzopyran ring opening guided by laser pulses

2014

Abstract The ring-opening photoisomerization of benzopyran, which occurs via a photochemical route involving a conical intersection, has been studied with quantum dynamics calculations using the multi-configuration time-dependent Hartree method (MCTDH). We introduce a mechanistic strategy to control the conversion of benzopyran to merocyanine with laser pulses. We use a six-dimensional model developed in a previous work for the potential energy surfaces (PES) based on an extension of the vibronic-coupling Hamiltonian model (diabatization method by ansatz), which depends on the most active degrees of freedom. The main objective of these quantum dynamics simulations is to provide a set of str…

010304 chemical physicsChemistryQuantum dynamicsDegrees of freedom (physics and chemistry)General Physics and AstronomyHartreeConical intersection010402 general chemistry01 natural sciencesPotential energyMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeStark effectComputational chemistry0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysical and Theoretical ChemistryGround stateAdiabatic processComputingMilieux_MISCELLANEOUS
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Force probe simulations of a reversibly rebinding system: Impact of pulling device stiffness.

2017

We present a detailed study of the parameter dependence of force probe molecular dynamics (FPMD) simulations. Using a well studied calix[4]arene catenane dimer as a model system, we systematically vary the pulling velocity and the stiffness of the applied external potential. This allows us to investigate how the results of pulling simulations operating in the constant velocity mode (force-ramp mode) depend on the details of the simulation setup. The system studied has the further advantage of showing reversible rebinding meaning that we can monitor the opening and the rebinding transition. Many models designed to extract kinetic information from rupture force distributions work in the limit…

010304 chemical physicsChemistryWork (physics)General Physics and AstronomyEnergy landscapeStiffnessMechanics010402 general chemistryKinetic energy01 natural sciences0104 chemical sciencesMolecular dynamicsSpring (device)Computational chemistry0103 physical sciencesJumpmedicinePhysical and Theoretical Chemistrymedicine.symptomConstant (mathematics)The Journal of chemical physics
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Spin-orbit ZORA and four-component Dirac-Coulomb estimation of relativistic corrections to isotropic nuclear shieldings and chemical shifts of noble …

2015

Hartree-Fock and density functional theory with the hybrid B3LYP and general gradient KT2 exchange-correlation functionals were used for nonrelativistic and relativistic nuclear magnetic shielding calculations of helium, neon, argon, krypton, and xenon dimers and free atoms. Relativistic corrections were calculated with the scalar and spin-orbit zeroth-order regular approximation Hamiltonian in combination with the large Slater-type basis set QZ4P as well as with the four-component Dirac-Coulomb Hamiltonian using Dyall's acv4z basis sets. The relativistic corrections to the nuclear magnetic shieldings and chemical shifts are combined with nonrelativistic coupled cluster singles and doubles …

010304 chemical physicsElectronic correlationChemical shiftNuclear TheoryKryptonchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesComputational Mathematicssymbols.namesakeNeonCoupled clusterchemistry0103 physical sciencesPhysics::Atomic and Molecular ClusterssymbolsDensity functional theoryAtomic physicsHamiltonian (quantum mechanics)Basis setJournal of Computational Chemistry
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Approximate treatment of higher excitations in coupled-cluster theory. II. Extension to general single-determinant reference functions and improved a…

2008

The theory and implementation of approximate coupled-cluster (CC), in particular approximate CC singles, doubles, triples, and quadruples methods, are discussed for general single-determinant reference functions. While the extension of iterative approximate models to the non-Hartree-Fock case is straightforward, the generalization of perturbative approaches is not trivial. In contrast to the corresponding perturbative triples methods, there are additional terms required for non-Hartree-Fock reference functions, and there are several possibilities to derive approximations to these terms. As it turns out impossible to develop an approach that is consistent with the canonical Hartree-Fock-base…

010304 chemical physicsGeneralizationHartree–Fock methodGeneral Physics and AstronomyContrast (statistics)Extension (predicate logic)010402 general chemistry01 natural sciences0104 chemical sciencesCoupled clusterComputational chemistry0103 physical sciencesApplied mathematicsPerturbation theory (quantum mechanics)Physical and Theoretical ChemistryMathematicsThe Journal of Chemical Physics
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