Search results for " laser"

showing 10 items of 1455 documents

Internal ion impact ionization for Fourier-transform ion cyclotron resonance

1994

A general scheme for ionization and fragmentation of ions in Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICRMS) is introduced. The technique is based upon excitation of high-frequency (i.e. lowmass) primary ions (e.g. N, Al+, H2O+·) which may be generated by standard ionization methods (e.g. electron ionization or laser desorption) inside the trap. Generation of the primary ions is followed by excitation of their cyclotron motion to high translational energy to serve as projectile ions. The projectiles serve two functions: to ionize neutral gas atoms and/or molecules (secondary ions) within the trap internal ion impact ionization (IIII), and to collisionally activate the…

Chemical ionizationChemistryOrganic ChemistryAnalytical chemistryThermal ionizationFourier transform ion cyclotron resonanceIon sourceAnalytical ChemistryAtmospheric-pressure laser ionizationPhysics::Plasma PhysicsIonizationAtomic physicsSpectroscopyElectron ionizationIon cyclotron resonanceRapid Communications in Mass Spectrometry
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Determination of a three-step excitation and ionization scheme for resonance ionization and ultratrace analysis of Np-237

2011

Abstract The long-lived radio isotope 237 Np is generated within the nuclear fuel cycle and represents a major hazard in the final disposal of nuclear waste. Related geochemical research requires sensitive methods for the detection of ultratrace amounts of neptunium in environmental samples. Resonance ionization mass spectrometry (RIMS) has proven to be one of the most sensitive methods for the detection of plutonium. A precondition for the application of RIMS to ultratrace analysis of neptunium is the knowledge of an efficient and selective scheme for optical excitation and ionization. Therefore, a multitude of medium to high-lying atomic levels in neptunium was located by applying in-sour…

Chemical ionizationNeptuniumAnalytical chemistrychemistry.chemical_elementThermal ionizationThermal ionization mass spectrometryMass spectrometryAtomic and Molecular Physics and OpticsAnalytical ChemistryAtmospheric-pressure laser ionizationchemistryIonizationAtomic physicsInstrumentationSpectroscopyElectron ionizationSpectrochimica Acta Part B: Atomic Spectroscopy
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Fine-structure mixing collisions of Rb(52D) excited in a two-photon transition using external-cavity cw diode laser

1999

We present an experimental study of fine structure (fs)- mixing in the 5 2 D state of Rb, and details of construction and performance of an external cavity cw diode laser, developed to provide a light source at 778 nm for two-photon excitation of Rb(5 2 D). Cross section for the fs-mixing Rb(5 2 D 5/2 ) yields Rb(5 2 D 3/2 ) in collisions with the ground state Rb(5 2 S 1/2 ) atoms was found to be 5.8 +/- 1.9 (DOT) 10 -14 cm 2 .

Chemical speciesPhotonChemistrylawExcited stateAtomic physicsGround stateLaserExcitationSemiconductor laser theoryDiodelaw.inventionSPIE Proceedings
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Study of Mechanisms of Light-Induced Dissociation of Ru(dcbpy)(CO)2I2 in Solution down to 20 fs Time Resolution

2006

Mechanisms of the light-induced ligand exchange reaction of (trans-I) Ru(dcbpy)(CO)2I2 (dcbpy = 4,4'-dicarboxylic acid-2,2'-bipyridine) in ethanol have been studied by transient absorption spectroscopy. Ultraviolet 20 fs excitation pulses centered at 325 nm were used to populate a vibrationally hot excited pi bipyridyl state of the reactant that quickly relaxes to a dissociative Ru-I state resulting in the release of one of the carbonyl groups. Quantum yield measurements have indicated that about 40% of the initially exited reactant molecules form the final photoproduct. A 62 fs rise component in the transient absorption (TA) signal was observed at all probe wavelengths in the visible regio…

ChemistryAnalytical chemistryQuantum yieldPhotochemistrymedicine.disease_causeDissociation (chemistry)Surfaces Coatings and FilmsExcited stateUltrafast laser spectroscopyMaterials ChemistrymedicineMoleculePhysical and Theoretical ChemistrySpectroscopyExcitationUltravioletThe Journal of Physical Chemistry B
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High resolution spectroscopy and potential determination of the (3)1Pi state of NaCs.

2006

The (3)(1)Pi state of the NaCs molecule was studied by high resolution Fourier-transform spectroscopy. The (3)(1)Pi--X (1)Sigma(+) laser induced fluorescence was excited by an Ar(+) ion laser or by a single-mode frequency-doubled cw Nd:YAG laser. The presence of argon buffer gas yielded rich rotational relaxation spectra allowing to enlarge the data set for the (3)(1)Pi state term values, as well as to observe Lambda splittings in a wide range of vibrational (v(')) and rotational (J(')) quantum numbers. The data field includes about 820 energy levels of (3)(1)Pi NaCs in the range from v(')=0 to 37 and from J(')=3 to 190, which corresponds to ca. 95% of the potential well depth. Direct fit o…

ChemistryBuffer gasGeneral Physics and AstronomyIon laserQuantum numberLaserPotential energylaw.inventionlawExcited statePhysical and Theoretical ChemistryAtomic physicsLaser-induced fluorescenceSpectroscopyThe Journal of chemical physics
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Intense laser effects on donor impurity in a cylindrical single and vertically coupled quantum dots under combined effects of hydrostatic pressure an…

2010

WOS: 000280235800010

ChemistryHydrostatic pressureBinding energyGeneral Physics and AstronomySurfaces and InterfacesGeneral ChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsSurfaces Coatings and FilmsEffective mass (solid-state physics)Quantum wellsImpurityQuantum dotIntense laser effectsElectric fieldElectric fieldRectangular potential barrierAtomic physicsHydrostatic pressureImpurityQuantum well
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Femtosecond Transient Absorption Study of the Dynamics of Acrylodan in Solution and Attached to Human Serum Albumin

2003

The excited-state relaxation dynamics of the protein-labeling dye acrylodan in solution and attached to human serum albumin has been studied by femtosecond transient absorption spectroscopy. Time-resolved spectra and kinetics of stimulated emission and excited-state absorption in the wavelength region from 400 to 800 nm were studied in ethanol and dimethylformamide. The excited-state solvation dynamics is characterized by multiexponential behavior in both solvents. In ethanol solution, the time dependence of the transient spectra is interpreted in terms of fast solvent relaxation followed by excited-state isomerization of the dye. Acrylodan attached to the protein shows a relaxation compone…

ChemistryKineticsSolvationAnalytical chemistryHuman serum albuminPhotochemistryFluorescenceSurfaces Coatings and FilmsFemtosecondUltrafast laser spectroscopyMaterials ChemistrymedicineRelaxation (physics)Physical and Theoretical ChemistryAbsorption (chemistry)medicine.drugThe Journal of Physical Chemistry B
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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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Impact of the synergistic collaboration of oligothiophene bridges and ruthenium complexes on the optical properties of dumbbell-shaped compounds.

2012

The linear and non-linear optical properties of a family of dumbbell-shaped dinuclear complexes, in which an oligothiophene chain with various numbers of rings (1, 3, and 6) acts as a bridge between two homoleptic tris(2,2'-bipyridine)ruthenium(II) complexes, have been fully investigated by using a range of spectroscopic techniques (absorption and luminescence, transient absorption, Raman, and non-linear absorption), together with density functional theory calculations. Our results shed light on the impact of the synergistic collaboration between the electronic structures of the two chemical moieties on the optical properties of these materials. Experiments on the linear optical properties …

ChemistryOrganic Chemistrychemistry.chemical_elementGeneral ChemistryThiophenesConjugated systemPhotochemistryLigandsSpectrum Analysis RamanCatalysisRutheniumRutheniumchemistry.chemical_compoundBipyridineCoordination ComplexesUltrafast laser spectroscopyThiopheneQuantum TheoryThermodynamicsHomolepticAbsorption (electromagnetic radiation)LuminescenceChemistry (Weinheim an der Bergstrasse, Germany)
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