Search results for "Citation"

showing 10 items of 1710 documents

Low-lying levels of201Hg from the decay of201Au

1972

The decay of 26.4-min201Au has been investigated using chemically separated sources and Ge(Li), Si(Li), plastic and Nal(Tl) detectors in different singles and coincidence arrangements. The β-disintegration energy was measured to be 1.27 ± 0.10 MeV. Thirteen γ-rays were observed to belong to this decay and the new levels at 543, 549.2, 552.8, 559.1, 605.7, 645.4, 732 and 1188 keV were established in201Hg, in addition to the three previously known excited states below 200 keV.

PhysicsNuclear and High Energy PhysicsDecay schemeIsotopes of germaniumExcited stateIsotopes of protactiniumIsotopes of zirconiumCoulomb excitationNuclear isomerAtomic physicsIsotopes of europiumZeitschrift für Physik A Hadrons and nuclei
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Hyperfine interaction in the Autler-Townes effect: The formation of bright, dark, and chameleon states

2017

This paper is devoted to clarifying the implications of hyperfine (HF) interaction in the formation of adiabatic (i.e., ``laser-dressed'') states and their expression in the Autler-Townes (AT) spectra. We first use the Morris-Shore model [J. R. Morris and B. W. Shore, Phys. Rev. A 27, 906 (1983)] to illustrate how bright and dark states are formed in a simple reference system where closely spaced energy levels are coupled to a single state with a strong laser field with the respective Rabi frequency ${\mathrm{\ensuremath{\Omega}}}_{S}$. We then expand the simulations to realistic hyperfine level systems in Na atoms for a more general case when non-negligible HF interaction can be treated as…

PhysicsAutler–Townes effectCoupling (probability)01 natural sciencesOmegaSpectral line010305 fluids & plasmas0103 physical sciencesAtomic physics010306 general physicsGround stateHyperfine structureEnergy (signal processing)ExcitationPhysical Review A
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Defect Luminescence of LiBaF3 Perovskites

2000

Blue and red luminescence of undoped LiBaF3 crystals was studied. A broad, isotropic photoluminescence band centered at 410 nm can be excited by 210 nm — 275 nm light in as grown crystals. After X-irradiation at RT a new narrower, anisotropic luminescence band appears at 425 mn which has an additional excitation band at 290 nm. The X-irradiation also creates the F- type centres and anisotropic centres with an absorption band at 630 nm and a luminescence band at 700 nm. No F- centre luminescence is observed. All the other centres mentioned act as radiative recombination centers as well. It is speculated that the origin of the blue luminescence is due to oxygen defects and that the red lumine…

PhotoluminescenceMaterials scienceImpurityAbsorption bandExcited stateSpontaneous emissionLuminescenceAnisotropyMolecular physicsExcitation
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Photoluminescence of Ga-face AlGaN/GaN single heterostructures

2001

Abstract The radiative recombination in Ga-face Al 0.30 Ga 0.70 N/GaN single heterostructures (SHs) was studied by photoluminescence (PL) measurements. An energy shift of the excitonic transitions toward higher energies was observed, indicating the presence of residual compressive strain in the GaN layer. In addition to these exciton lines, a broad band energetically localized between the exciton lines and the LO-phonon replica was noticed in the undoped SH. From its energy position, excitation power dependence, as well as temperature behaviour, we have attributed this luminescence to the H -band (HB), which is representative of the two-dimensional electron gas (2DEG) recombination.

PhotoluminescenceMaterials scienceCondensed matter physicsCondensed Matter::OtherMechanical EngineeringExcitonHeterojunctionCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsCondensed Matter::Materials ScienceMechanics of MaterialsGeneral Materials ScienceSpontaneous emissionFermi gasLuminescenceExcitationRecombinationMaterials Science and Engineering: B
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<title>Low-frequency excitation of double quantum dots</title>

2008

We address theoretically adiabatic regime of charge transport for a model of two tunnel-coupled quantum dots connected in series. The energy levels of the two dots are harmonically modulated by an external potential with a constant phase shift between the two. Motivated by recent experiments with surface-acoustic-wave excitation, we consider two situations: (a) pure pumping in the absence of external voltage (also at finite temperature), and (b) adiabatic modulation of the current driven by large external bias. In both cases we derive results consistent with published experimental data. For the case (b) we explicitly derive the adiabatic limit of Tien-Gordon formula for photon-assisted tunn…

PhysicsQuantum dotQuantum mechanicsConductanceLow frequencyDouble quantumAdiabatic processExcitationQuantum tunnellingVoltageSPIE Proceedings
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Piezoelectric Actuated Nonlinear Energy Sink With Tunable Attenuation Efficiency

2019

Abstract Comparing to linear vibration absorbers, nonlinear energy sinks (NESs) have attracted worldwide attention for their intrinsic characteristics of targeted energy transfer or energy pumping in a relatively wide frequency range. Unfortunately, they are highly dependent on the vibration amplitude to be attenuated and will play its role only if the external load exceeds a specific threshold value. Different from the passive bistable NES, a novel piezoelectric nonlinear energy sink (PNES) is designed by introducing in-phase actuation to compensate or enhance the external vibration loads, thus triggering the NES operating in high attenuation efficiency. The nonlinear mathematic model of t…

Physicsgeographygeography.geographical_feature_categoryCantileverbusiness.industryMechanical EngineeringAttenuationCondensed Matter Physics01 natural sciencesPiezoelectricitySink (geography)010305 fluids & plasmasNonlinear systemMechanics of Materials0103 physical sciencesOptoelectronicsbusiness010301 acousticsExcitationJournal of Applied Mechanics
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Rydberg excitation of trapped cold ions: a detailed case study

2011

We provide a detailed theoretical and conceptual study of a planned experiment to excite Rydberg states of ions trapped in a Paul trap. The ultimate goal is to exploit the strong state dependent interactions between Rydberg ions to implement quantum information processing protocols and to simulate the dynamics of strongly interacting spin systems. We highlight the promises of this approach when combining the high degree of control and readout of quantum states in trapped ion crystals with the novel and fast gate schemes based on interacting giant Rydberg atomic dipole moments. We discuss anticipated theoretical and experimental challenges on the way towards its realization.

PhysicsQuantum PhysicsAtomic Physics (physics.atom-ph)FOS: Physical sciencesGeneral Physics and Astronomy01 natural sciencesPhysics - Atomic Physics010305 fluids & plasmasIonsymbols.namesakeDipoleQuantum state0103 physical sciencesRydberg formulasymbolsPhysics::Atomic PhysicsIon trapAtomic physicsQuantum Physics (quant-ph)010306 general physicsSpin (physics)Realization (systems)ExcitationNew Journal of Physics
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Towards an accurate molecular orbital theory for excited states : Ethene, butadiene, and hexatriene

1993

A newly proposed quantum chemical approach for ab initio calculations of electronic spectra of molecular systems is applied to the molecules ethene, trans‐1,3‐butadiene, and trans‐trans‐1,3,5‐hexatriene. The method has the aim of being accurate to better than 0.5 eV for excitation energies and is expected to provide structural and physical data for the excited states with good reliability. The approach is based on the complete active space (CAS) SCF method, which gives a proper description of the major features in the electronic structure of the excited state, independent of its complexity, accounts for all near degeneracy effects, and includes full orbital relaxation. Remaining dynamic ele…

ErrorsGeneral Physics and AstronomyPolyenesElectronic structuresymbols.namesakeRydberg StatesAb initio quantum chemistry methodsComputational chemistrySinglet statePhysical and Theoretical ChemistryTriplet state:FÍSICA::Química física [UNESCO]AccuracyExcitationCalculation MethodsButadieneTripletsChemistryMolecular orbital theoryScf CalculationsExcited StatesCalculation Methods ; Quantum Chemistry ; Ab Initio Calculations ; Electron Spectra ; Butadiene ; Accuracy ; Scf Calculations ; Triplets ; Rydberg States ; Excitation ; Errors ; Polyenes ; Excited StatesQuantum ChemistryUNESCO::FÍSICA::Química físicaElectron SpectraExcited stateRydberg formulasymbolsRydberg stateAtomic physicsAb Initio Calculations
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Empirical determination of Einstein A-coefficient ratios of bright [Fe II] lines

2014

The Einstein spontaneous rates (A-coefficients) of Fe+ lines have been computed by several authors with results that differ from each other by up to 40%. Consequently, models for line emissivities suffer from uncertainties that in turn affect the determination of the physical conditions at the base of line excitation. We provide an empirical determination of the A-coefficient ratios of bright [Fe II] lines that would represent both a valid benchmark for theoretical computations and a reference for the physical interpretation of the observed lines. With the ESO-Very Large Telescope X-shooter instrument between 3000 Å and 24700 Å, we obtained a spectrum of the bright Herbig-Haro object HH 1. …

PhysicsISM: individual objects (HH1)Extinction (astronomy)Hartree–Fock methodFOS: Physical sciencesAstronomy and AstrophysicsAstrophysicsAstronomy and AstrophysicISM: lines and bandCharged particleISM: atomAstrophysics - Solar and Stellar AstrophysicsSpace and Planetary ScienceEmissivityAstrophysics::Solar and Stellar AstrophysicsHerbig–Haro objectAtomic dataHerbig-Haro objectExcitationSolar and Stellar Astrophysics (astro-ph.SR)Astrophysics::Galaxy AstrophysicsDimensionless quantityLine (formation)
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Computational determination of the dominant triplet population mechanism in photoexcited benzophenone

2014

In benzophenone, intersystem crossing occurs efficiently between the S-1(n pi(star)) state and the T-1 state of dominant n pi(star) character, leading to excited triplet states after photoexcitation. The transition mechanism between S-1(n pi(star)) and T-1 is still a matter of debate, despite several experimental studies. Quantum mechanical calculations have been performed in order to assess the relative efficiencies of previously proposed mechanisms, in particular, the direct S-1 -> T-1 and indirect S-1 -> T-2(pi pi(star)) -> T-1 ones. Multiconfigurational wave function based methods are used to discuss the nature of the relevant states and also to determine minimum energy paths a…

STATE DIPOLE-MOMENTSPopulationMechanistic organic photochemistryEXCITED BENZOPHENONEGeneral Physics and AstronomyGAS-PHASEABSORPTION-SPECTROSCOPYchemistry.chemical_compoundORGANIC-PHOTOCHEMISTRYMOLECULAR WAVE-FUNCTIONSBenzophenonePhysical and Theoretical ChemistryeducationWave functioneducation.field_of_studyROW ATOMSChemistryCONICAL INTERSECTIONSPhotoexcitation[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryIntersystem crossingExcited state2ND-ORDER PERTURBATION-THEORYANO BASIS-SETSAtomic physicsPhosphorescence
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