Search results for "Atom"

showing 10 items of 31559 documents

Ion source research and development at University of Jyväskylä: Studies of different plasma processes and towards the higher beam intensities

2015

MonPS16; International audience; The long-term operation of high charge state electron cyclotron resonance ion sources fed withhigh microwave power has caused damage to the plasma chamber wall in several laboratories.Porosity, or a small hole, can be progressively created in the wall on a year time scale, which cancause a water leak from the cooling system into the plasma chamber vacuum. A burnout of theVENUS chamber is investigated. Information on the hole formation and on the necessary localhot electron power density is presented. Next, the hot electron flux to the wall is studied bymeans of simulations. First, the results of a simple model assuming that electrons are fullymagnetized and …

010302 applied physicsbeam intensityMaterials scienceta114ta213plasma diagnostics[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]Cyclotron resonanceElectronPlasma7. Clean energy01 natural sciencesElectron cyclotron resonanceIon source010305 fluids & plasmasIonBeamlinePhysics::Plasma Physics0103 physical scienceselectron cyclotron resonance ion sourcesPlasma diagnosticsAtomic physicsInstrumentation
researchProduct

Estimating ion confinement times from beam current transients in conventional and charge breeder ECRIS

2019

International audience; Cumulative ion confinement times are probed by measuring decaying ion current transients in pulsed material injection mode. The method is applied in a charge breeder and conventional ECRIS yielding mutually corroborative results. The cumulative confinement time estimates vary from approximately 2 ms–60 ms with a clear dependence on the ion charge-to-mass ratio—higher charges having longer residence times. The long cumulative confinement times are proposed as a partial explanation to recently observed unexpectedly high ion temperatures. The results are relevant for rare ion beam (RIB) production as the confinement time and the lifetime of stable isotopes can be used f…

010302 applied physicsplasma sourcesMaterials scienceplasma diagnosticsIon beamStable isotope ratio[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]Ion currentCharge (physics)plasmatekniikka7. Clean energy01 natural sciences010305 fluids & plasmasIonion sourcesplasma dischargesBreeder (animal)0103 physical sciencesAtomic physicsCurrent (fluid)InstrumentationBeam (structure)
researchProduct

Ab initio multi-reference perturbation theory calculations of the ground and low-lying electronic states of the KRb molecule

2016

The potential energy curves of the low-lying electronic states correlating up to the limit K(4p) + Rb(5s) of KRb molecule have been calculated using the multi-reference perturbation theory method at the CASSCF/ XMCQDPT2 level of theory without and with spin–orbit coupling. The calculated parameters of the ground X 1 R + state are in the best agreement among all previously performed ab initio calculations for the KRb molecule. The calculated vibrational intervals of the ground electronic term of the 39 K 85 Rb molecule describe the experiment with the accuracy within ±1 cm ?1 . The calculated intensities of the 2 1 R + (v 0 = 3, J 0 = 26) ? X 1 R + (v 00 = 0...24, J 00 = 25, 27) transitions …

010304 chemical physicsAb initiochemistry.chemical_elementOvertone bandSpin–orbit interactionCondensed Matter Physics01 natural sciencesBiochemistryMolecular physicsPotential energyDissociation (chemistry)Rubidiumsymbols.namesakeDipolechemistryFranck–Condon principle0103 physical sciences:ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Физика [ЭБ БГУ]Physics::Atomic and Molecular ClusterssymbolsPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physics010306 general physics
researchProduct

Carbonyl-functionalized quaterthiophenes: a study of the vibrational Raman and electronic absorption/emission properties guided by theoretical calcul…

2011

This work investigates the evolution of the molecular, vibrational, and optical properties within a family of carbonyl-functionalized quaterthiophenes: 5,5'''-diheptanoyl-2,2':5',2'':5'',2'''-quaterthiophene (1), 5,5'''-diperfluorohexylcarbonyl-2,2':5',2'':5'',2'''-quaterthiophene (2), and 2,7-[bis(5-perfluorohexylcarbonylthien-2-yl)]-4H-cyclopenta[2,1-b:3,4-b']-dithiophene-4-one (3). The analysis is performed by Raman and UV/Vis absorption/excitation/fluorescence spectroscopy in combination with density functional calculations. Theoretical calculations show that substitution with carbonyl groups and perfluorohexyl chains induces progressive quinoidization of the π-conjugated backbone in co…

010304 chemical physicsAbsorption spectroscopyChemistryTime-dependent density functional theory010402 general chemistryResonance (chemistry)Photochemistry01 natural sciencesAtomic and Molecular Physics and OpticsFluorescence spectroscopyMolecular electronic transition0104 chemical sciencesCrystallographysymbols.namesakeUltraviolet visible spectroscopy0103 physical sciencesBathochromic shiftsymbolsPhysical and Theoretical ChemistryRaman spectroscopyChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct

Structural, electronic and energetic effects in heterocyclic fluorene derivatives fused with a fulvene unit

2019

Abstract A set of 36 heterocyclic (B, N and O) fluorene (C) derivatives fused in nine ways with fulvene ring have been analyzed by means of different local aromaticity criteria. Molecular geometry of analyzed compounds were optimized at B3LYP/6-311++G(2d,2p) level of theory. The evaluation of the local aromaticity has been carried out through the use of the geometry-based harmonic oscillator model of aromaticity (HOMA) and the magnetism-based zz‐component of the nucleus independent chemical shifts calculated 1 A above the ring center (NICS1zz) indices as well as one aromaticity index derived from the Quantum Theory Atoms in Molecules (QTAIM), i.e. the para-delocalization index (PDI). Additi…

010304 chemical physicsChemical shiftAtoms in moleculesHeterocyclic fluorene derivativesHOMO-LUMO energy gapsAromaticityFluoreneFulvene010402 general chemistryCondensed Matter PhysicsKinetic energyRing (chemistry)01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundCrystallographyMolecular geometrychemistry0103 physical sciencesPhysical and Theoretical ChemistryFulveneAromaticity indexesComputational and Theoretical Chemistry
researchProduct

Coupled-Cluster study of ‘no-pair’ bonding in the tetrahedral Cu4 cluster

2011

Abstract Ab initio Coupled-Cluster calculations with single and double excitations and perturbative correction to the triple, CCSD(T), have been carried out for the high-spin electronic state, ( 5 A 2 ) , of the copper cluster Cu 4 in its tetrahedral arrangement. Like alkali metals clusters, tetrahedral Cu 4 presents a bound quintet state, i.e., a situation where all the valence electrons are unpaired. This rather exotic wavefunction, also known as no-pair bonding state, is examined in detail. The influence of the basis set is also analyzed, as well as the importance of the core correlation and the effect of the basis-set superposition errors.

010304 chemical physicsChemistryAb initioGeneral Physics and Astronomy010402 general chemistryAlkali metal01 natural sciences0104 chemical sciencesCoupled cluster0103 physical sciencesPhysics::Atomic and Molecular ClustersCluster (physics)Tetrahedron[CHIM]Chemical SciencesPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsValence electronWave functionBasis setChemical Physics Letters
researchProduct

Towards highly accurate ab initio thermochemistry of larger systems: benzene.

2011

The high accuracy extrapolated ab initio thermochemistry (HEAT) protocol is applied to compute the total atomization energy (TAE) and the heat of formation of benzene. Large-scale coupled-cluster calculations with more than 1500 basis functions and 42 correlated electrons as well as zero-point energies based on full cubic and (semi)diagonal quartic force fields obtained with the coupled-cluster singles and doubles with perturbative treatment of the triples method and atomic natural orbital (ANO) triple- and quadruple-zeta basis sets are presented. The performance of modifications to the HEAT scheme and the scaling properties of its contributions with respect to the system size are investiga…

010304 chemical physicsChemistryAb initioGeneral Physics and AstronomyBasis function010402 general chemistry01 natural sciences7. Clean energyStandard enthalpy of formation0104 chemical sciencesChemical thermodynamicsAb initio quantum chemistry methodsQuartic function0103 physical sciencesThermochemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsScalingThe Journal of chemical physics
researchProduct

Theoretical investigation of the potential energy surface of the van der Waals complex CH4-N-2

2009

International audience; The interaction potential energy surface of the van der Waals CH4-N-2 complex has been calculated for a broad range of intermolecular separations and configurations in the approximation of rigid interacting molecules at the CCSD(T) and MP2 levels of theory using the correlation consistent aug-cc-pVTZ basis set. The BSSE correction was taken into account for all the calculations. The most stable configurations of the complex were found. Binding energies were calculated in the CBS limit with accounting for the molecular deformations. The harmonic and anharmonic fundamental vibrational frequencies and rotational constants for the ground and first excited vibrational sta…

010304 chemical physicsChemistryBinding energyIntermolecular forceAnharmonicityVan der Waals surfaceGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeLennard-Jones potentialExcited state0103 physical sciencesPotential energy surface[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysics::Atomic and Molecular ClustersPhysical and Theoretical Chemistryvan der Waals forceAtomic physicsPhysics::Chemical Physics
researchProduct

Fourier-transform spectroscopy and deperturbation analysis of the spin-orbit coupled A(1)Σ(+) and b(3)Π states of KRb.

2016

Fourier-transform A(1)Σ(+) - b(3)Π → X(1)Σ(+) laser-induced fluorescence spectra were recorded for the natural mixture of (39,41)K(85,87)Rb isotopologues produced in a heatpipe oven. Overall 4200 rovibronic term values of the spin-orbit coupled A(1)Σ(+) and b(3)Π states were determined with an uncertainty of about 0.01 cm(-1) in the energy range [10 850, 14 200] cm(-1) covering rotational quantum numbers J' ∈ [3, 280]. Direct deperturbation analysis of the A ∼ b complex performed within the framework of the A(1)Σ(+) ∼ b(3)ΠΩ=0,1,2 coupled-channel approach reproduced experimental data with a standard deviation of 0.004 cm(-1). Initial parameters of the internuclear potentials and spin-orbit …

010304 chemical physicsChemistryGeneral Physics and AstronomyElectronic structureQuantum number01 natural sciencesFourier transform spectroscopyB vitamins0103 physical sciencesKinetic isotope effectIsotopologueEmission spectrumPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyThe Journal of chemical physics
researchProduct

Communication: multireference equation of motion coupled cluster: a transform and diagonalize approach to electronic structure.

2014

The novel multireference equation-of-motion coupled-cluster (MREOM-CC) approaches provide versatile and accurate access to a large number of electronic states. The methods proceed by a sequence of many-body similarity transformations and a subsequent diagonalization of the transformed Hamiltonian over a compact subspace. The transformed Hamiltonian is a connected entity and preserves spin- and spatial symmetry properties of the original Hamiltonian, but is no longer Hermitean. The final diagonalization spaces are defined in terms of a complete active space (CAS) and limited excitations (1h, 1p, 2h, …) out of the CAS. The methods are invariant to rotations of orbitals within their respective…

010304 chemical physicsChemistryGeneral Physics and AstronomyEquations of motionElectronic structure010402 general chemistry7. Clean energy01 natural sciencesLinear subspace0104 chemical sciencessymbols.namesakeCoupled clusterAtomic orbitalQuantum mechanics0103 physical sciencessymbolsComplete active spacePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Subspace topologyThe Journal of chemical physics
researchProduct