Search results for "atomic physics"

showing 10 items of 5530 documents

Determination of the first ionization potential of einsteinium by resonance ionization mass spectroscopy (RIMS)

1998

Abstract The first ionization potential of einsteinium (IP Es ) was determined by resonance ionization mass spectroscopy (RIMS) using samples with ≤10 12 atoms of 254 Es ( T 1/2 =276 days). This method is based on the measurement of photoionization thresholds as a function of applied electric field strength, followed by extrapolation to zero field strength to yield IP Es . An atomic beam of Es was created by heating a filament on which einsteinium was electrodeposited from an aqueous solution onto a tantalum backing and covered with titanium metal. Es atoms were ionized via a three-step excitation scheme, and the ions mass-selectively detected in a time-of-flight (TOF) mass spectrometer. Th…

ChemistryMechanical EngineeringMetals and AlloysAnalytical chemistryThermal ionizationPhotoionizationMass spectrometryAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsIonization energyElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Determination of the first ionization potential of nine actinide elements by resonance ionization mass spectroscopy (RIMS)

1998

The high sensitivity of RIMS enables the precise determination of the first ionization potential of actinide elements with a sample size of ≤1012 atoms. By multiple resonant laser excitation, the actinide atoms under investigation are ionized in the presence of an electric field, and the ions are mass-selectively detected in a time-of-flight spectrometer. The first ionization potential is obtained by scanning the wavelength of the laser used for the last excitation step across the ionization threshold Wth—indicated by a sudden increase of the ion count rate—at various electric field strengths. Extrapolation of Wth to electric field strength zero leads directly to the first ionization potent…

ChemistryMechanical EngineeringMetals and AlloysThermal ionizationPhotoionizationMolar ionization energies of the elementsIon sourceAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Localized molecular orbitals for excited states of polyenals, polyendials, and polyenones

2003

The work is focused on the generation of localized molecular orbitals for excited states. A recently developed a priori method based in a CAS-SCF–type algorithm is applied. The method generates directly localized orbitals and can be applied to multireference wavefunctions. A detailed description of the performance of the method as well as the locality of the MOs for the example of the singlet nπ* (CO) excited state is given. It is in general possible to obtain local orbitals for the doubly occupied and virtual valence orbitals. The partial delocalization of the π* (CO) orbital is discussed, as is the effect of the use of different CAS spaces. The systems under study are polyenals, polyendia…

ChemistryMolecular orbital theoryLocalized molecular orbitalsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsSlater-type orbitalLinear combination of atomic orbitalsMolecular orbitalValence bond theoryComplete active spacePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsNatural bond orbitalInternational Journal of Quantum Chemistry
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Negative ions and their importance for the analysis of residual gas

1963

Abstract In the case of heavy molecules, mass spectre obtained with the help of positive ions generally lead to the recording of fragments only, and thus do not indicate the true original mass. In order to overcome this drawback, an attempt was made to attach slow electrons to heavy molecules, since less dissociation products are expected with spectre produced by negative ions. As a preliminary experiment, a simple and cheap form of ion source was constructed which produces mainly atomic negative ions.

ChemistryMoleculeElectronAtomic physicsCondensed Matter PhysicsResidualInstrumentationIon sourceDissociation (chemistry)Surfaces Coatings and FilmsIonVacuum
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Precision experiments on exotic nuclei at IGISOL

2006

Abstract Cooling and trapping techniques of low-energy radioactive ion beams of refractory elements employed at the IGISOL facility are presented with emphasis on high-precision measurements of the ground state properties of exotic nuclei. The impact of the new generation Paul and Penning traps on mass measurements of short-lived nuclei is discussed with examples on precision measurements of masses of super-allowed beta emitters and neutron-rich nuclei. As a new concept the trap-assisted spectroscopy of radioactive ions is presented with applications in collinear laser spectroscopy, decay spectroscopy of isobarically purified sources and in nuclear cross-section measurements by ion counting.

ChemistryNuclear TheoryRefractory metalsTrappingCondensed Matter PhysicsPenning trapAtomic massIonBeta (plasma physics)Physics::Atomic PhysicsPhysical and Theoretical ChemistryAtomic physicsNuclear ExperimentGround stateSpectroscopyInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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First Fourier-transform ion cyclotron resonance signals of very highly charged atomic ions

1994

We report on the first application of Fourier-transform ion cyclotron resonance mass spectrometry to the very highly charged ions produced in the high-energy electron beam ion trap (SuperEBIT) at the Lawrence Livermore National Laboratory. Initial results are described, and spectra are presented from ions as highly charged as Cs53+.

ChemistryOrganic ChemistryAnalytical chemistryMass spectrometryFourier transform ion cyclotron resonanceSpectral lineAnalytical ChemistryIonPhysics::Plasma PhysicsSelected ion monitoringIon trapAtomic physicsSpectroscopyIon cyclotron resonanceElectron beam ion trapRapid Communications in Mass Spectrometry
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Up-conversion processes in NaLaF4:Er3+

2009

abstract Structural and spectroscopic investigation of NaLaF 4 :Er 3+ material at different doping concentrations ispresented. X-ray diffraction patterns, up-conversion luminescence spectra and decay curves for 2 H 9/2 ? 4 I 15/2 , 4 S 3/2 ? 4 I 15/2 and 4 F 9/2 ? 4 I 15/2 optical transitions in the material are shown and possibleexcitation routes are discussed. Raman spectrum for the undoped material is presented and the effectivephonon energy of the material is estimated. Based on the obtained results application of rare-earth dopedNaLaF 4 in the field of up-conversion phosphors is evaluated. 2009 Elsevier B.V. All rights reserved. 1. IntroductionFor many years rare-earth (RE) doped materi…

ChemistryOrganic ChemistryDopingAnalytical chemistryNonlinear opticsPhosphorAtomic and Molecular Physics and OpticsPhoton upconversionElectronic Optical and Magnetic MaterialsIonInorganic Chemistrysymbols.namesakesymbolsElectrical and Electronic EngineeringPhysical and Theoretical ChemistryAtomic physicsTime-resolved spectroscopyLuminescenceRaman spectroscopySpectroscopyOptical Materials
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Electric field induced alignment-orientation conversion in diatomic molecules: analysis and observation for NaK

1999

This article reports the observation of the molecular fluorescence circularity under irradiation with linearly polarised light. This alignment-orientation conversion phenomenon arises as a result of partial transformation from alignment of the ensemble of 1 P state molecular angular momenta into their orientation under the effect of non-linear dc Stark effect. Circularity rate up to 0.12 was observed in D 1 P! X 1 S fluorescence of 23 Na 39 K molecules in agreement with the theoretically predicted value.

ChemistryOrganic ChemistryFluorescenceDiatomic moleculeAnalytical ChemistryInorganic Chemistrysymbols.namesakeStark effectOrientation (geometry)Electric fieldsymbolsMoleculeIrradiationAtomic physicsSpectroscopyNAKJournal of Molecular Structure
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Pulsed photodissociation in an ion cyclotron resonance trap: extending the time range for unimolecular dissociation studies of metal clusters

1997

ChemistryOrganic ChemistryPhotodissociationAnalytical chemistryAtomic physicsTandem mass spectrometryTime rangeSpectroscopyFourier transform ion cyclotron resonanceDissociation (chemistry)Ion cyclotron resonanceAnalytical ChemistryMetal clustersRapid Communications in Mass Spectrometry
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Extending Limits of Chlorine Kinetic Isotope Effects

2012

Chlorine kinetic isotope effects exceeding semiclassical limits were observed in enzyme-catalyzed reactions, but their source has not been yet identified. Herein we show that unusually large chlorine kinetic isotope effects are associated with reactions in which chlorine is the central atom that is being passed between two heavy atoms. The origin of these large values is the ratio of imaginary frequencies for light-to-heavy species (the so-called temperature-independent factor).

ChemistryOrganic ChemistryRadiochemistryAnalytical chemistrySemiclassical physicschemistry.chemical_element010501 environmental sciences010402 general chemistryKinetic energy01 natural sciences0104 chemical sciencesAtomKinetic isotope effectpolycyclic compoundsChlorinePhysics::Atomic PhysicsPhysics::Chemical PhysicsNuclear ExperimentAstrophysics::Galaxy Astrophysics0105 earth and related environmental sciencesThe Journal of Organic Chemistry
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