Search results for "Calculation"

showing 10 items of 594 documents

Data quality monitors of vertex detectors at the start of the Belle II experiment

2019

The Belle II experiment features a substantial upgrade of the Belle detector and will operate at the SuperKEKB energy-asymmetric e+e− collider at KEK in Tsukuba, Japan. The accelerator completed its first phase of commissioning in 2016, and the Belle II detector saw its first electron-positron collisions in April 2018. Belle II features a newly designed silicon vertex detector based on double-sided strip layers and DEPFET pixel layers. A subset of the vertex detector was operated in 2018 to determine background conditions (Phase 2 operation). The collaboration completed full detector installation in January 2019, and the experiment started full data taking. This paper will report on the fin…

Physics::Instrumentation and DetectorsQC1-999vertex detectorBELLEquality: monitoring01 natural sciences7. Clean energyprogrammingSilicon vertex detectorlaw.inventionNuclear physicssemiconductor detector: pixellaw0103 physical sciencesQuality monitoring[INFO]Computer Science [cs][PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]010306 general physicsCollidernumerical calculationsdetector: designactivity reportPhysics010308 nuclear & particles physicsPhysicsDetectorUpgradeFull dataData qualityPhysics::Accelerator Physicssemiconductor detector: microstripHigh Energy Physics::ExperimentupgradeVertex detectormonitoring: on-lineperformance
researchProduct

Polarizability and optical rotation calculated from the approximate coupled cluster singles and doubles CC2 linear response theory using cholesky dec…

2004

A new implementation of the approximate coupled cluster singles and doubles CC2 linear response model using Cholesky decomposition of the two-electron integrals is presented. Significantly reducing storage demands and computational effort without sacrificing accuracy compared to the conventional model, the algorithm is well suited for large-scale applications. Extensive basis set convergence studies are presented for the static and frequency-dependent electric dipole polarizability of benzene and C60, and for the optical rotation of CNOFH2 and (−)-trans-cyclooctene (TCO). The origin-dependence of the optical rotation is calculated and shown to persist for CC2 even at basis set convergence. …

PolarisabilityChemistryUNESCO::FÍSICAGeneral Physics and AstronomyComputational physicsDipolePhysics and Astronomy (all)Coupled clusterCoupled cluster calculationsFullerene compoundsOptical rotation ; Coupled cluster calculations ; Organic compounds ; Polarisability ; Fullerene compoundsComputational chemistryPolarizability:FÍSICA [UNESCO]Convergence (routing)Organic compoundsOptical rotationPhysical and Theoretical ChemistryLinear response theoryOptical rotationBasis setCholesky decomposition
researchProduct

Novel meso-substituted porphyrins: Synthesis, characterization and photocatalytic activity of their TiO2-based composites

2009

Abstract Two series of novel meso-substituted porphyrins, namely 5,10,15,20-tetra[4-(3-phenoxy)-propoxy]phenyl porphyrin, the structural analogue 5,10,15,20-tetra[2-(3-phenoxy)-propoxy]phenyl porphyrin and their Co(II) Cu(II) and Zn(II) complexes were synthesized. The compounds were characterized using various spectroscopic techniques and their molecular structure was proposed based on density functional theory calculations. The diverse properties of the porphyrin derivatives result from the different stereochemistry of the particular substituents at the meso site on the macrocycle and are controlled also by the coordinated metal. The 1H NMR spectrum of the free-base porphyrin showed a comp…

PorphyrinsMetalloporphyrinsProcess Chemistry and TechnologyGeneral Chemical EngineeringPhotosensitizerDFT calculationsPhotochemistryPorphyrinMetalchemistry.chemical_compoundchemistryvisual_artPhotodegradationPolymer chemistryvisual_art.visual_art_mediumProton NMRPhotocatalysisTiO2MoleculePhotosensitizerDensity functional theoryPhotodegradationporphyrinphotocatalysisDyes and Pigments
researchProduct

Use of a running coupling in the NLO calculation of forward hadron production

2018

We address and solve a puzzle raised by a recent calculation [1] of the cross-section for particle production in proton-nucleus collisions to next-to-leading order: the numerical results show an un- reasonably large dependence upon the choice of a prescription for the QCD running coupling, which spoils the predictive power of the calculation. Specifically, the results obtained with a prescription formulated in the transverse coordinate space differ by one to two orders of magnitude from those obtained with a prescription in momentum space. We show that this discrepancy is an artefact of the interplay between the asymptotic freedom of QCD and the Fourier transform from coordinate space to mo…

Position and momentum spaceQCD EVOLUTION01 natural sciencesAsymptotic freedomquantum chromodynamics: correctionhard scatteringHigh Energy Physics - Phenomenology (hep-ph)coupling constant: energy dependencestrong interaction: coupling constantEQUATIONkvanttifysiikkaComputingMilieux_MISCELLANEOUSPhysicsQuantum chromodynamicsQUARKhigher-order: 1nuclear physicssddc:12.39.StHigh Energy Physics - Phenomenology12.38.Bxsymbolsydinfysiikkahadron: forward productionFOS: Physical sciences114 Physical sciencesRENORMALIZATION-GROUP12.38.Cysymbols.namesakeCross section (physics)Theoretical physicsquantum chromodynamics0103 physical sciencessirontarelativistic heavy-ion collisionCoordinate spacenumerical calculations010306 general physicsp nucleus: scatteringcorrection: higher-orderCouplingta114010308 nuclear & particles physics25.75.-qCOLOR GLASS CONDENSATENONLINEAR GLUON EVOLUTIONRenormalization groupFourier transformasymptotic freedom[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph][ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]Physical Review D
researchProduct

Phase behaviour of Ag2CrO4 under compression: Structural, vibrational, and optical properties

2013

We have performed an experimental study of the crystal structure, lattice dynamics, and optical properties of silver chromate (Ag2CrO4) at ambient temperature and high pressures. In particular, the crystal structure, Raman-active phonons, and electronic band gap have been accurately determined. When the initial orthorhombic Pnma Ag2CrO4 structure (phase I) is compressed up to 4.5 GPa, a previously undetected phase (phase II) has been observed with a 0.95% volume collapse. The structure of phase II can be indexed to a similar orthorhombic cell as phase I, and the transition can be considered to be an isostructural transition. This collapse is mainly due to the drastic contraction of the a ax…

Potassium chromatePhase transitionCrystal structureSilver chromateAntifluoriteCondensed Matter::Materials Sciencesymbols.namesakechemistry.chemical_compoundX-Ray DiffractionCondensed Matter::SuperconductivityPhase (matter)Physical and Theoretical ChemistryIsostructuralTotal-Energy calculationsHigh-pressuresRamanCondensed matter physicsChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyGeneral EnergyCrystal-structureAugmented-wave methodFISICA APLICADAX-ray crystallographySilver cromateTransitionsymbolsCondensed Matter::Strongly Correlated ElectronsOrthorhombic crystal systemRaman spectroscopy
researchProduct

Computation of conical intersections by using perturbation techniques

2005

Multiconfigurational second-order perturbation theory, both in its single-state multiconfigurational second-order perturbation theory (CASPT2) and multistate (MS-CASPT2) formulations, is used to search for minima on the crossing seams between different potential energy hypersurfaces of electronic states in several molecular systems. The performance of the procedures is tested and discussed, focusing on the problem of the nonorthogonality of the single-state perturbative solutions. In different cases the obtained structures and energy differences are compared with available complete active space self-consistent field and multireference configuration interaction solutions. Calculations on dif…

Potential Energy SurfacesConfiguration Interactions ; Perturbation Theory ; Potential Energy Surfaces ; Molecular Electronic States ; SCF Calculations ; Lithium Compounds ; Organic Compounds ; Wave FunctionsOrganic CompoundsChemistryComputationUNESCO::FÍSICAConfiguration InteractionsGeneral Physics and AstronomyMultireference configuration interactionConical surfaceSCF CalculationsPotential energyWave FunctionsMaxima and minima:FÍSICA [UNESCO]Molecular Electronic StatesQuantum mechanicsPerturbation TheoryLithium CompoundsStatistical physicsComplete active spacePerturbation theory (quantum mechanics)Physical and Theoretical ChemistryWave functionThe Journal of Chemical Physics
researchProduct

Rovibrational structure of the Ar–CO complex based on a novel three-dimensional ab initio potential

2002

The first three-dimensional ab initio intermolecular potential energy surface of the Ar–CO van der Waals complex is calculated using the coupled cluster singles and doubles including connected triples model and the augmented correlation-consistent polarized valence quadruple zeta (aug-cc-pVQZ) basis set extended with a (3s3p2d1f1g) set of midbond functions. The three-dimensional surface is averaged over the three lowest vibrational states of CO. Rovibrational energies are calculated up to 50 cm−1 above the ground state, thus enabling comprehensive comparison between theory and available experimental data as well as providing detailed guidance for future spectroscopic investigations of highe…

Potential Energy SurfacesCoupled Cluster CalculationsAb initioGeneral Physics and AstronomyPhysics and Astronomy (all)symbols.namesakeAb initio quantum chemistry methodsQuasimoleculesPhysics::Atomic and Molecular ClustersVibrational StatesPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryArgon:FÍSICA::Química física [UNESCO]Rotational-Vibrational StatesBasis setValence (chemistry)ChemistryRotational–vibrational spectroscopyCarbon CompoundsUNESCO::FÍSICA::Química físicaCoupled clustersymbolsArgon ; Carbon Compounds ; Quasimolecules ; Rotational-Vibrational States ; Potential Energy Surfaces ; Ab Initio Calculations ; Intermolecular Mechanics ; Coupled Cluster Calculations ; Vibrational StatesIntermolecular Mechanicsvan der Waals forceAtomic physicsGround stateAb Initio Calculations
researchProduct

Study of the benzene⋅N2 intermolecular potential-energy surface

2003

The intermolecular potential-energy surface pertaining to the interaction between benzene and N2 is investigated theoretically and experimentally. Accurate intermolecular interaction energies are evaluated for the benzene–N2 van der Waals complex using the coupled cluster singles and doubles including connected triples [CCSD(T)] method and the aug-cc-pVDZ basis set extended with a set of 3s3p2d1f1g midbond functions. After fitting the energies to an analytic function, the intermolecular Schrödinger equation is solved to yield energies, rotational constants, and Raman-scattering coefficients for the lowest intermolecular levels of several benzene–N2 isotopomers. Experimentally, intermolecula…

Potential Energy SurfacesCoupled Cluster CalculationsNitrogenBinding energyGeneral Physics and AstronomyPotential Energy Functionssymbols.namesakePhysics and Astronomy (all)IsomerismQuasimoleculesRotational IsomerismPhysics::Atomic and Molecular ClustersQuantum-mechanical explanation of intermolecular interactionsRotational StatesPhysical and Theoretical ChemistryPhysics::Chemical Physics:FÍSICA::Química física [UNESCO]Basis setSchrodinger EquationChemistryOrganic CompoundsIsotope EffectsIntermolecular forceStimulated Raman ScatteringUNESCO::FÍSICA::Química físicaCoupled clustersymbolsAtomic physicsvan der Waals forceOrganic Compounds ; Nitrogen ; Quasimolecules ; Potential Energy Surfaces ; Potential Energy Functions ; Coupled Cluster Calculations ; Rotational States ; Isomerism ; Isotope Effects ; Stimulated Raman Scattering ; Rotational Isomerism ; Schrodinger EquationRaman spectroscopyRaman scattering
researchProduct

Computational and experimental investigation of intermolecular states and forces in the benzene-helium van der Waals complex

2003

A study of the intermolecular potential-energy surface (IPS) and the intermolecular states of the perprotonated and perdeuterated benzene–He complex is reported. From a fit to ab initio data computed within the coupled cluster singles and doubles including connected triples model for 280 interaction geometries, an analytic IPS including two- to four-body atom–atom terms is obtained. This IPS, and two other Lennard-Jones atom–atom surfaces from the literature, are each employed in dynamically exact (within the rigid-monomer approximation) calculations of J = 0 intermolecular states of the isotopomers. Rotational constants and Raman-scattering coefficients for intermolecular vibrational trans…

Potential Energy SurfacesCoupled Cluster CalculationsRaman SpectraHelium Neutral AtomsOrganic Compounds ; Helium Neutral Atoms ; Intermolecular Mechanics ; Quasimolecules ; Potential Energy Surfaces ; Ab Initio Calculations ; Coupled Cluster Calculations ; Lennard-Jones Potential ; Isotope Effects ; Isomerism ; Rotational States ; Raman SpectraAb initioGeneral Physics and AstronomyIsotopomerssymbols.namesakePhysics and Astronomy (all)IsomerismAb initio quantum chemistry methodsQuasimoleculesKinetic isotope effectPhysics::Atomic and Molecular ClustersRotational StatesPhysics::Atomic PhysicsLennard-Jones PotentialPhysics::Chemical PhysicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]ChemistryOrganic CompoundsIsotope EffectsIntermolecular forceUNESCO::FÍSICA::Química físicaCoupled clusterLennard-Jones potentialsymbolsIntermolecular MechanicsAtomic physicsvan der Waals forceAb Initio Calculations
researchProduct

Multiconfigurational second-order perturbation study of the decomposition of the radical anion of nitromethane

2004

The doublet potential energy surfaces involved in the decomposition of the nitromethane radical anion (CH(3)NO(2) (-)) have been studied by using the multistate extension of the multiconfigurational second-order perturbation method (MS-CASPT2) in conjunction with large atomic natural orbital-type basis sets. A very low energy barrier is found for the decomposition reaction: CH(3)NO(2) (-)--[CH(3)NO(2)](-)--CH(3)+NO(2) (-). No evidence has been obtained on the existence of an isomerization channel leading to the initial formation of the methylnitrite anion (CH(3)ONO(-)) which, in a subsequent reaction, would yield nitric oxide (NO). In contrast, it is suggested that NO is formed through the …

Potential Energy SurfacesNitromethaneOrganic CompoundsGeneral Physics and AstronomyOrganic Compounds ; Negative Ions ; Potential Energy Surfaces ; Dissociation ; Ion-Molecule Reactions ; Perturbation Theory ; Density Functional Theory ; SCF CalculationsSCF CalculationsPotential energyDissociation (chemistry)UNESCO::FÍSICA::Química físicaIonIon-Molecule Reactionschemistry.chemical_compoundchemistryComputational chemistryPerturbation TheoryNegative IonsDensity functional theorySymmetry breakingPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]IsomerizationDissociationDensity Functional TheoryChemical decompositionThe Journal of Chemical Physics
researchProduct