Search results for "polarization [Upsilon(9460)]"

showing 10 items of 915 documents

Shaping of a ground state rotational wavepacket by frequency-chirped pulses

2001

0953-4075; A coherent rotational superposition state is produced in the ground vibronic level of N2 through the interaction of the molecule with the electric field vector of a nonresonant laser pulse. This rotational wavepacket is shaped with a linear frequency chirp of the laser field. The structural shape of the rotational coherences shows a strong dependence with the frequency-chirp amplitude. A comparison with a theoretical model allows the interpretation of the observed effects in terms of dephasing of the wavepacket induced by the laser phase distortion. Application of the presented results to the phase characterization of short XUV pulses is suggested.

CONTROLDephasingPhase (waves)Physics::Opticslaw.inventionCOHERENTSuperposition principleINDUCED POLARIZATION SPECTROSCOPYlawPhysics::Atomic and Molecular ClustersChirpPhysics::Atomic PhysicsFIELDFEMTOSECOND LASER-PULSESINTERFERENCEPhysicsPhase distortionPHOTODISSOCIATIONCondensed Matter PhysicsLaserEVOLUTIONN-2Atomic and Molecular Physics and OpticsAmplitudeAtomic physicsGround stateJournal of Physics B: Atomic, Molecular and Optical Physics
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Controlling molecular alignment rephasing through interference of Raman-induced rotational coherence

2000

0021-9606; Quantum control over molecular alignment rephasing is experimentally investigated in gaseous CO2. The control process is achieved by illuminating the medium with a pair of pump-pulses separated in time by approximately an integer value of T0=1/8B(0), where B(0) is the rotational constant. Through a Raman-type process, each pulse alone produces rotational coherence leading to a periodic orientational anisotropy. It is the combination of the two pulses that yields to quantum interference, resulting in a modification of this anisotropy probed by a third delayed pulse. The effect is accurately analyzed for different time delays between the two pulses. A theoretical analysis supplies …

CONTROLGeneral Physics and AstronomyRotational transitionTRANSITIONS01 natural sciencesMolecular physicssymbols.namesakeOpticsINDUCED POLARIZATION SPECTROSCOPYTIME-RESOLVED DYNAMICSMULTIPHOTON IONIZATIONSYSTEMSElectric field0103 physical sciencesPhysical and Theoretical ChemistryMolecular alignmentFIELD010306 general physicsAnisotropyPhysicsQuantum optics010304 chemical physicsbusiness.industryWAVE-PACKETSPHOTODISSOCIATIONINDUCED CONTINUUM STRUCTUREsymbolsLASERRotational spectroscopyRaman spectroscopybusinessCoherence (physics)
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High-Frequency Polarization Variability from Active Galactic Nuclei

2021

The linear polarization of non-thermal emission encodes information about the structure of the magnetic fields, either from the region where the emission is produced (i.e., the intrinsic polarization angle) and/or from the screens of magnetized plasma that may be located on its way towards Earth (i.e., the effect of Faraday rotation). In addition, the variability timescale of the polarized emission, or its Faraday rotation, can be used to estimate the size of the region where the emission (or the Faraday rotation) originates. The observation of polarized emission from active galactic nuclei (AGN) and, in particular, its time evolution, also provides information about the critical role that …

Camps magnèticsActive galactic nucleusAstrophysics::High Energy Astrophysical PhenomenaAstronomyquasarsblazarsQB1-991AstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics01 natural sciencessymbols.namesake0103 physical sciencesFaraday effectBlazar010303 astronomy & astrophysicsAstrophysics::Galaxy AstrophysicsPhysicspolarization010308 nuclear & particles physicsLinear polarizationAstronomy and AstrophysicsQuasarPlasmaPolarization (waves)Magnetic fieldgamma raysgeneralsymbolsAstronomia
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Photochemically induced dynamic nuclear polarization of heteronuclear singlet order

2021

Photochemically induced dynamic nuclear polarization (photo-CIDNP) is a method to hyperpolarize nuclear spins using light. In most cases, CIDNP experiments are performed in high magnetic fields and the sample is irradiated by light inside a nuclear magnetic resonance (NMR) spectrometer. Here we demonstrate photo-CIDNP hyperpolarization generated in the Earth's magnetic field and under zero- to ultralow-field (ZULF) conditions. Irradiating a sample containing tetraphenylporphyrin and para-benzoquinone for several seconds with light-emitting diodes produces strong hyperpolarization of 1H and 13C nuclear spins, enhancing the NMR signals more than 200 times. The hyperpolarized spin states at th…

Chemical Physics (physics.chem-ph)Materials scienceSpin statesSpinsField (physics)CIDNPPhysics::Medical PhysicsFOS: Physical sciences02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPolarization (waves)7. Clean energy01 natural sciences0104 chemical sciencesMagnetic fieldHeteronuclear moleculePhysics - Chemical Physicsddc:530General Materials ScienceSinglet statePhysical and Theoretical ChemistryAtomic physics0210 nano-technology
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Synergies between Hyperpolarized NMR and Microfluidics: A Review

2021

Hyperpolarized nuclear magnetic resonance and lab-on-a-chip microfluidics are two dynamic, but until recently quite distinct, fields of research. Recent developments in both areas increased their synergistic overlap. By microfluidic integration, many complex experimental steps can be brought together onto a single platform. Microfluidic devices are therefore increasingly finding applications in medical diagnostics, forensic analysis, and biomedical research. In particular, they provide novel and powerful ways to culture cells, cell aggregates, and even functional models of entire organs. Nuclear magnetic resonance is a non-invasive, high-resolution spectroscopic technique which allows real-…

Chemical processNuclear and High Energy PhysicsMedical diagnosticMagnetic Resonance SpectroscopyPHYSICAL MANIPULATIONSComputer scienceProcess (engineering)MicrofluidicsMicrofluidicsFOS: Physical sciencesContext (language use)Nanotechnology02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistryLab-On-A-Chip DevicesPhysics - Chemical PhysicsHyperpolarization (physics)SpectroscopyChemical Physics (physics.chem-ph)021001 nanoscience & nanotechnologyMagnetic Resonance Imaging0104 chemical sciences0210 nano-technologyProgress in Nuclear Magnetic Resonance Spectroscopy
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Chemical Reaction Monitoring Using Zero-Field Nuclear Magnetic Resonance Enables Study of Heterogeneous Samples in Metal Containers

2020

Abstract We demonstrate that heterogeneous/biphasic chemical reactions can be monitored with high spectroscopic resolution using zero‐field nuclear magnetic resonance spectroscopy. This is possible because magnetic susceptibility broadening is negligible at ultralow magnetic fields. We show the two‐step hydrogenation of dimethyl acetylenedicarboxylate with para‐enriched hydrogen gas in conventional glass NMR tubes, as well as in a titanium tube. The low frequency zero‐field NMR signals ensure that there is no significant signal attenuation arising from shielding by the electrically conductive sample container. This method paves the way for in situ monitoring of reactions in complex heteroge…

Chemical substanceMaterials scienceHydrogenAnalytical chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesChemical reaction7. Clean energyCatalysisNMR spectroscopyHyperpolarization (physics)Research Articleshyperpolarization010405 organic chemistryReaction MonitoringGeneral MedicineGeneral ChemistryNuclear magnetic resonance spectroscopyequipment and suppliesMagnetic susceptibility0104 chemical sciencesMagnetic fieldzero-fieldchemistryddc:540Electromagnetic shieldingResearch Article
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Femtosecond polarization spectroscopy in molecular gas mixtures: Macroscopic interference and concentration measurements

2000

0021-9606; Raman-induced polarization spectroscopy (RIPS) experiments combined with homodyne detection have been conducted with a femtosecond laser at room temperature and low pressure (p < 2 atm) in CO2-N2 mixtures as well as in air (O2-N2 mixtures). Each molecule of the mixture produces its own time-dependent signal, measured as a series of recurring transients. Macroscopic interference is observed when transients of both molecules overlap in the time domain. This interference leads to a large modification of the signal, which is well reproduced by calculations. The total signal recorded in CO2-N2 or O2-N2 mixtures of known concentration is analyzed in order to measure the polarizability …

ChemistryAIRAnalytical chemistryGeneral Physics and AstronomyPolarization (waves)01 natural sciencesINVERSE RAMAN-SPECTROSCOPYROTATIONAL COHERENCE010309 opticssymbols.namesakeHomodyne detectionPolarizability0103 physical sciencesFemtosecondsymbolsCO2Time domainPhysical and Theoretical Chemistry010306 general physicsAnisotropySpectroscopyRaman spectroscopy
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Electrical impedance spectroscopy of ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate (ECOENG™ 110)

2011

Abstract Ionic liquid “ECOENG™ 110”, a promising electrolyte for electrochemical devices, was investigated by impedance spectroscopy. Metallic electrodes (Pt, Cu, Ag, and Mo) as well as carbon were used for the electrochemical characterization. The dependences of the real and imaginary impedance, polarization resistance and electrochemical capacity of the double layer on the electrode potential were investigated using electrical equivalent circuits of R1(QR2) and R1[Q(R2W)] types.

ChemistryAnalytical chemistryGeneral ChemistryElectrolyteCondensed Matter PhysicsElectrochemistryDielectric spectroscopychemistry.chemical_compoundIonic liquidEquivalent circuitGeneral Materials SciencePolarization (electrochemistry)Electrical impedanceElectrode potentialSolid State Ionics
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Determination of concentrations in ternary and quaternary molecular gas mixtures using femtosecond Raman spectroscopy

2002

Measurements of concentrations in gas mixtures of three and four molecular components are presented. They rely on a femtosecond time-resolved pump–probe technique based on Raman-induced polarization spectroscopy. The rotational time response of the molecular gas mixture is measured as a function of the pump–probe time delay. No selective frequency tunability is needed as the molecular rotational spectra are excited within the laser bandwidth. The results obtained from experiments performed at room temperature in N2O–CO2–N2 and N2O–CO2–O2–N2 mixtures are presented and the accuracy of the method is discussed. Copyright © 2002 John Wiley & Sons, Ltd.

ChemistryAnalytical chemistryPolarization (waves)LaserSpectral linelaw.inventionsymbols.namesakelawExcited stateFemtosecondsymbolsGeneral Materials ScienceRaman spectroscopySpectroscopyTernary operationSpectroscopyJournal of Raman Spectroscopy
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Interacting induced dipoles polarization model for molecular polarizabilities. Reference molecules, amino acids and model peptides

1999

Abstract We outline a method for the calculation of molecular dipole ( μ ) and quadrupole ( Θ = ) moments and dipole–dipole polarizabilities ( α = ) which we have successfully applied to a series of reference molecules, amino acids and model peptides. The results for μ are in line with CPHF reference calculations. In particular, the calculated positive value of CO is in agreement with both experimental and CI calculations. The computation of ( α = ) has been performed by the interacting induced dipoles polarization model that calculates tensor effective anisotropic point polarizabilities (method of Applequist et al.). The POLAR program cannot be used as a black box. Some tests should be per…

ChemistryComputationCondensed Matter PhysicsPolarization (waves)BiochemistrySmall moleculeMolecular physicsDipoleComputational chemistryQuadrupoleMoleculePolarPhysical and Theoretical ChemistryAnisotropyJournal of Molecular Structure: THEOCHEM
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