Search results for "POLARIZABILITY"

showing 10 items of 240 documents

Shuttling of Rydberg ions for fast entangling operations

2019

We introduce a scheme to entangle Rydberg ions in a linear ion crystal, using the high electric polarizability of the Rydberg electronic states in combination with mutual Coulomb coupling of ions that establishes common modes of motion. After laser-initialization of ions to a superposition of ground- and Rydberg-state, the entanglement operation is driven purely by applying a voltage pulse that shuttles the ion crystal back and forth. This operation can achieve entanglement on a sub-$\mu$s timescale, more than two orders of magnitude faster than typical gate operations driven by continuous-wave lasers. Our analysis shows that the fidelity achieved with this protocol can exceed $99.9\%$ with…

CouplingPhysicsQuantum PhysicsAtomic Physics (physics.atom-ph)General Physics and AstronomyFOS: Physical sciencesQuantum entanglementQuantum Physics7. Clean energy01 natural sciencesIonPhysics - Atomic PhysicsSuperposition principlesymbols.namesakeOrders of magnitude (time)Polarizability0103 physical sciencesRydberg formulasymbolsCoulombPhysics::Atomic PhysicsAtomic physics010306 general physicsQuantum Physics (quant-ph)
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Quantum effects in the capture of charged particles by dipolar polarizable symmetric top molecules. II. Interplay between electrostatic and gyroscopi…

2013

ally nonadiabatic channel treatment of the capture of charged particles by dipolar polarizable symmetric top molecules with the aim to reveal quantum effects in the collision dynamics. In general, these effects are related to the discrete nature of the intrinsic, orbital, and total angular momenta, to the quantum character of passage of collision partners across effective potential barriers and drops, and to the interplay of two types of anisotropic interactions, the gyroscopic (Coriolis) and the electrostatic ones. The latter feature, in principle, leads to a coupling of capture channels. In the calculation of capture cross sections or rate coefficients, however, this coupling can be ignor…

CouplingSurface PropertiesChemistryStatic ElectricityIntermolecular forceGeneral Physics and AstronomyDeuteriumTritiumResonance (particle physics)Charged particleDipolePolarizabilityQuantum mechanicsQuantum TheoryParticle SizePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processMethaneQuantumHydrogenThe Journal of Chemical Physics
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Structure determination to calculate nonlinear optical coefficients in a class of organic material

1999

A class of molecules with intramolecular two-dimensional charge transfer upon excitation has been synthesized. It is expected that these materials should be prospective candidates for nonlinear optical (NLO) applications such as second harmonic (SHG) generation. In order to optimize the macroscopic NLO properties of the compounds, it is necessary to relate their first hyperpolarizability tensors at a molecular level to those at a crystal bulk level. This requires a complete structure determination and refinement. However, the growth of sufficiently large single crystals, which are needed for structural analysis and refinement by x-ray methods, is a time-consuming and sometimes impossible ta…

CrystalMaterials scienceOpticsElectron diffractionbusiness.industryAb initioHyperpolarizabilityNonlinear opticsTensorCrystal structurebusinessMolecular physicsExcitationPhysical Review B
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ChemInform Abstract: Electron Crystallography and Organic Materials with Non-Linear Optical Properties

2010

Results of electron microscopic studies of crystal structures of a number of bis-benzylidene cyclohexanones are presented. It is shown that some of these compounds are efficient crystalline non-linear optically active (NLO) chromophores with second harmonic generation (SHG) properties. Appropriately functionalized chromophores of this type can be used as a polycondensation comonomer to produce partly crystalline main-chain NLO-active polymers. Electron diffraction crystal structural data, obtained for very small crystals, allowed us to get reasonable estimations of macroscopic crystal NLO-coefficients, relating quantum-chemically calculated molecular first hyperpolarizability components to …

Crystalchemistry.chemical_classificationCrystallographyElectron diffractionChemistryElectron crystallographyPhysics::OpticsHyperpolarizabilitySecond-harmonic generationGeneral MedicineCrystal structurePolymerChromophoreChemInform
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Quadratic Nonlinear Behaviour of Various Langmuir-Blodgett Molecules

1989

The Langmuir-Blodgett (L-B) technique is well known as a method of building-up ordered arrays of organic molecules, and especially as a means of imposing a noncentrosymmetric structure from molecules that crystallize in a centrosymmetric space group(1–3). L-B films for use in quadratic nonlinear optics can be ordered in a statistically noncentrosymmetric lattice. The method involves the compression of a mono-layer of the organic molecule, spread on top of a water surface, into a two-dimensional solid, followed by the repeated dipping of the substrate to be coated into and out of the subphase. Monolayers may be deposited onto the substrate both on immersion and withdrawal, resulting in a cen…

CrystallographyChemistryPolarizabilityStereochemistryLattice (order)MonolayerNonlinear opticsMoleculeSecond-harmonic generationAcceptorLangmuir–Blodgett film
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The influence of sigma and pi acceptors on two-photon absorption and solvatochromism of dipolar and quadrupolar unsaturated organic compounds.

2003

Two-photon absorption cross sections delta and solvatochromic properties were determined for a series of quadrupolar and dipolar compounds by using femtosecond excitation in the spectral range between 710 and 960 nm. The compounds investigated were distyrylbenzenes and polyenes bearing appropriate pi or sigma acceptors. The delta values for the centrosymmetric compounds trans, trans- 1,4-bis[2-(2',5'-dihexyloxy)phenylethenyl]-2,3,5,6-tetrafluorobenzene (6), trans, trans-1,4-bis[2-(4'-dibutylamino)phenylethenyl]- 2,3,5,6-tetrafluorobenzene (2), trans, trans-1,4-bis[2-(4'dimethylamino)phenylbutadienyl]- 2,3,5,6-tetrafluorobenzene (7), trans,-trans-1,4-bis[2-(4'-dimethylamino)phenylethenyl]2,5…

CrystallographyDipoleChemistryExcited stateIntramolecular forceSolvatochromismHyperpolarizabilityPhysical and Theoretical ChemistryChromophorePhotochemistryTwo-photon absorptionFluorescenceAtomic and Molecular Physics and OpticsChemphyschem : a European journal of chemical physics and physical chemistry
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Rotational Raman spectroscopy of ethylene using a femtosecond time-resolved pump-probe technique.

2005

154309; Femtosecond Raman-induced polarization spectroscopy (RIPS) was conducted at low pressure (250 mb at 295 K and 400 mb at 373 K) in ethylene. The temporal signal, resulting from the beating between pure rotational coherences, was measured with a heterodyne detection. The temporal traces were converted to the frequency domain using a Fourier transformation and then analyzed thanks to the D2hTDS software (http://www.u-bourgogne.fr/LPUB/shTDS.html) dedicated to X2Y4 molecules with D2h symmetry. The effective Hamiltonian was expanded up to order 2, allowing the determination of five parameters with an rms of 0.017 cm(-1). Special care was taken in the precise modeling of intensities, taki…

DYNAMICSLIQUID WATERTENSORIAL FORMALISMGeneral Physics and Astronomy02 engineering and technology01 natural sciencessymbols.namesakeMOLECULESOpticsINDUCED POLARIZATION SPECTROSCOPYPolarizability0103 physical sciencesCOHERENCEHeterodyne detectionPhysical and Theoretical ChemistrySpectroscopySPECTRUM010304 chemical physicsChemistrybusiness.industry021001 nanoscience & nanotechnologyPolarization (waves)Fourier transformFrequency domainFemtosecondsymbolsZEOLITEMODESCO2Atomic physics0210 nano-technologyRaman spectroscopybusinessThe Journal of chemical physics
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Nonintrusive monitoring and quantitative analysis of strong laser-field-induced impulsive alignment

2004

We report the observation of impulsive alignment of $\mathrm{C}{\mathrm{O}}_{2}$ molecules produced through their interaction with a nonresonant, strong laser pulse. The periodic alignment is monitored using a polarization technique generally employed in optical Kerr effect experiments; the birefringence produced by alignment of the molecular sample is measured with a weak pulse, time-delayed with respect to the alignment pulse. The technique provides a signal proportional to $⟨{\mathrm{cos}}^{2}\phantom{\rule{0.2em}{0ex}}\ensuremath{\theta}⟩\ensuremath{-}\frac{1}{3}$, where $\ensuremath{\theta}$ is the polar angle between the molecular axis and the strong-field polarization axis. Experimen…

DYNAMICSPhysicsI-2BirefringenceKerr effectWave packetWAVE-PACKETSALIGNING MOLECULESPOLARIZABILITYPolarization (waves)Electromagnetic radiationAtomic and Molecular Physics and OpticsPULSESSchrödinger equationMOLECULAR ALIGNMENTMOLECULESsymbols.namesakeREVIVAL STRUCTURESPolarizabilityIonizationQuantum mechanicssymbolsAtomic physicsPhysical Review A
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Dipolar coupling of nanoparticle-molecule assemblies: An efficient approach for studying strong coupling

2021

Strong light-matter interactions facilitate not only emerging applications in quantum and non-linear optics but also modifications of materials properties. In particular the latter possibility has spurred the development of advanced theoretical techniques that can accurately capture both quantum optical and quantum chemical degrees of freedom. These methods are, however, computationally very demanding, which limits their application range. Here, we demonstrate that the optical spectra of nanoparticle-molecule assemblies, including strong coupling effects, can be predicted with good accuracy using a subsystem approach, in which the response functions of the different units are coupled only a…

Degrees of freedom (statistics)General Physics and AstronomyNanoparticleFOS: Physical sciences010402 general chemistryoptiset ominaisuudet01 natural scienceslinear combination of atomic orbitalstime dependent density functional theorynanorakenteet0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)MoleculePhysical and Theoretical Chemistryoptical spectroscopyQuantumPhysicssurface optics010304 chemical physicsCondensed Matter - Mesoscale and Nanoscale Physicstiheysfunktionaaliteoriapolarizability0104 chemical sciencesplasmonitRange (mathematics)DipoleChemical physicsDensity functional theorynanoparticlesnanohiukkasetplasmonsMagnetic dipole–dipole interaction
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Organic Materials for Non-Linear Optics: The 2D Approach

1998

Conventional organic molecules for applications in second-order non-linear optics are donor–acceptor substituted π systems that show only one intense charge-transfer (CT) transition. Thus, only a single element of the second-order polarizability tensor, β, is significant in these one-dimensional systems. The advantages and optimization strategies for two new classes of molecules with multiple CT transitions and two-dimensional second-order polarizability are reviewed. These are donor–acceptor substituted π systems that lack a dipole and have a molecular symmetry of C3 or higher, and dipolar molecules of symmetry C2v. A basic introduction to the field is also given.

DipoleField (physics)ChemistryChemical physicsPolarizabilityMolecular symmetryMoleculeNonlinear opticsNanotechnologySingle elementGeneral MedicinePhysics::Chemical PhysicsSymmetry (physics)Journal f�r Praktische Chemie/Chemiker-Zeitung
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