Search results for "Quantum"

showing 10 items of 9714 documents

Large numbers of cold positronium atoms created in laser-selected Rydberg states using resonant charge exchange

2016

Lasers are used to control the production of highly excited positronium atoms (Ps*). The laser light excites Cs atoms to Rydberg states that have a large cross section for resonant charge-exchange collisions with cold trapped positrons. For each trial with 30 million trapped positrons, more than 700 000 of the created Ps* have trajectories near the axis of the apparatus, and are detected using Stark ionization. This number of Ps* is 500 times higher than realized in an earlier proof-of-principle demonstration (2004 Phys. Lett. B 597 257). A second charge exchange of these near-axis Ps* with trapped antiprotons could be used to produce cold antihydrogen, and this antihydrogen production is e…

ANTIHYDROGENGeneral PhysicsAntiparticlepositronium0205 Optical Physics0307 Theoretical And Computational ChemistryPLASMASCONFINEMENTPhysics Atomic Molecular & Chemical01 natural sciences010305 fluids & plasmasPositroniumsymbols.namesake0202 Atomic Molecular Nuclear Particle And Plasma PhysicsIonization0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Atomic Physics010306 general physicsAntihydrogenpositronsPhysicsCondensed Matter::Quantum GasesScience & TechnologyPhysicsOpticsRydberg statesCondensed Matter PhysicsAtomic and Molecular Physics and Opticscharge-exchangeExcited stateAntimatterPhysical SciencesRydberg formulasymbolsAtomic physicsLepton
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Nuclear anapole moment interaction in BaF from relativistic coupled-cluster theory

2018

We present high accuracy relativistic coupled cluster calculations of the P-odd interaction coefficient $W_A$ describing the nuclear anapole moment effect on the molecular electronic structure. The molecule under study, BaF, is considered a promising candidate for the measurement of the nuclear anapole moment, and the preparation for the experiment is now underway [Altunas et al., Phys. Rev. Lett. 120, 142501 (2018)]. Influence of various computational parameters (size of the basis set, treatment of relativistic effects, and treatment of electron correlation) on the calculated $W_A$ coefficient is investigated and a recommended value of 147.7 Hz with an estimated uncertainty of 1.5% is prop…

ATOMIC PARITY NONCONSERVATIONDIATOMIC-MOLECULESP-ODDVIOLATIONAtomic Physics (physics.atom-ph)Nuclear TheoryDENSITY FUNCTIONALSFOS: Physical sciences01 natural sciences010305 fluids & plasmasPhysics - Atomic PhysicsENHANCEMENTMolecular electronic structure0103 physical sciencesIMPLEMENTATIONNuclear Experiment010306 general physicsBasis setPhysicsElectronic correlationELECTRIC-FIELD GRADIENTSDiatomic moleculeWEAK-INTERACTIONSCoupled clusterMoment (physics)Atomic physicsRelativistic quantum chemistryAPPROXIMATIONPhysical Review A
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Theoretical study of photoinduced ring-isomerization in the 1,2,4-oxadiazole series

2004

Abstract A theoretical study of photoinduced ring-isomerization of 3-amino-5-methyl- and 3-amino-5-phenyl-1,2,4-oxadiazoles is reported. The results well agree with the reported experimental data: in particular, they explain the ring-photoisomerization into the corresponding 2-amino-1,3,4-oxadiazoles through a ring contraction-ring expansion route; moreover, the occurrence of competing pathways involving both the ring contraction and the internal cyclization–isomerization mechanism during irradiation of the 5-alkyl substituted substrates in the presence of a base has been also substantiated.

Ab initio calculationPhotoisomerizationPhotochemistryChemistryHeterocycleOrganic ChemistryOxadiazoleSettore CHIM/06 - Chimica OrganicaPhotochemistryBiochemistrychemistry.chemical_compoundComputational chemistryAb initio quantum chemistry methodsPhotoisomerizationDrug Discovery124-OxadiazoleIsomerizationTetrahedron
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Revisiting the Nonadiabatic Process in 1,2-Dioxetane.

2015

Determining the ground and excited-state decomposition mechanisms of 1,2-dioxetane is essential to understand the chemiluminescence and bioluminescence phenomena. Several experimental and theoretical studies has been performed in the past without reaching a converged description. The reason is in part associated with the complex nonadiabatic process taking place along the reaction. The present study is an extension of a previous work (De Vico, L.; Liu, Y.-J.; Krogh, J. W.; Lindh, R. J. Phys. Chem. A 2007, 111, 8013-8019) in which a two-step mechanism was established for the chemiluminescence involving asynchronous O-O' and C-C' bond dissociations. New high-level multistate multi configurati…

Ab initio molecular dynamicschemistry.chemical_compound12-DioxetanechemistryComputational chemistryQuantum mechanicsTheoretical chemistrySinglet statePhysical and Theoretical ChemistryHigh ratioComputer Science ApplicationsJournal of chemical theory and computation
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Low temperature rate coefficients of the H + CH+ → C+ + H2 reaction: New potential energy surface and time-independent quantum scattering

2015

The observed abundances of the methylidyne cation, CH(+), in diffuse molecular clouds can be two orders of magnitude higher than the prediction of the standard gas-phase models which, in turn, predict rather well the abundances of neutral CH. It is therefore necessary to investigate all the possible formation and destruction processes of CH(+) in the interstellar medium with the most abundant species H, H2, and e(-). In this work, we address the destruction process of CH(+) by hydrogen abstraction. We report a new calculation of the low temperature rate coefficients for the abstraction reaction, using accurate time-independent quantum scattering and a new high-level ab initio global potenti…

Ab initio quantum chemistry methodsChemistryScatteringPotential energy surfaceThermochemistryAb initioGeneral Physics and AstronomyThermodynamicsReactivity (chemistry)Scattering theoryPhysical and Theoretical ChemistryAtomic physicsPotential energyThe Journal of Chemical Physics
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Size-consistent ab initio calculation of the electric quadrupole moment of Cl2

2003

Abstract The molecular electric quadrupole moment ( Θ ) of Cl 2 has been calculated using SDCI, and (SC) 2 -SDCI wave functions as well as CCSD, CCSD(T), and CC3 methods. All these correlation methods are single reference. All of them, but SDCI, are free of the size-extensivity error. The variation of Θ from the separated atoms to the equilibrium region is reported. The present results leads to an estimated value of 2.3520 a.u. (10.55 × 10 −40 Cm 2 ) corresponding to a CC(3) calculation at the CBS approach and including the ro-vibrational and thermal averaging corrections. This value is compatible with two experimental values and points to one of them as slightly more reliable.

Ab initio quantum chemistry methodsChemistryThermalQuadrupoleAb initioGeneral Physics and AstronomyCorrelation methodPhysical and Theoretical ChemistryAtomic physicsWave functionBond-dissociation energyDiatomic moleculeChemical Physics Letters
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Semi-Empirical Calculations of Hole Polarons in MgO and KNbO3 Crystals

1998

The semi-empirical quantum chemical INDO method has been used for cluster and large unit cell calculations of hole polarons bound to a cation vacancy in highly ionic MgO and partly covalent perovskite KNbO 3 . In both cases a hole is well localized on an oxygen atom displaced towards the vacancy. The calculated optical and thermal ionization energies for V - and V 0 centers are in excellent agreement with experimental data for MgO. In KNbO 3 we predict the existence of one-site and two-site (molecular) polarons with close absorption energies (1 e V). The relevant experimental data are discussed.

Ab initio quantum chemistry methodsChemistryVacancy defectBound stateIonic bondingThermal ionizationIonization energyAtomic physicsCondensed Matter PhysicsPolaronElectronic Optical and Magnetic MaterialsPerovskite (structure)physica status solidi (b)
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Asymptotic potentials and rate constants in the adiabatic capture centrifugal sudden approximation for X + OH(X-2 Pi) -> OX + H(S-2) reactions where …

2012

International audience; New long-range multipolar coefficients for the X + OH(X-2 Pi) interactions, where X = O(P-3), S(P-3) and N(S-4), are given here. They have been evaluated on the basis or monomer properties of the atoms and OH such as the dipole and quadrupole moments, and the static and dynamic polarizabilities. Each matrix element of the 18 x 18 (8 x 8 for N + OH) quasi-degenerate asymptotic potentials has been built up by means of the perturbation theory up to second order including or not the fine-structure of O, S and OH. The adiabatic potentials, obtained after diagonalization of the full matrix, show many crossings and complex behaviors near the asymptotes. Using the entrance c…

Ab initio010402 general chemistryKinetic energy7. Clean energy01 natural sciencesBiochemistryDIPOLE POLARIZABILITIESATOMSAb initio quantum chemistry methodsLOW-TEMPERATUREOH RADICALS0103 physical sciencesCOUPLED-CLUSTER CALCULATIONSPhysical and Theoretical ChemistryPerturbation theoryAdiabatic processKINETICS010304 chemical physicsChemistryRANGECondensed Matter PhysicsPotential energy0104 chemical sciencesQUADRUPOLE-MOMENTSO-2[SDU]Sciences of the Universe [physics]QuadrupoleCLAtomic physicsGround state
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Study of the electronic and atomic structure of thermally treated SrTiO3(110) surfaces

2003

The electronic structure of heated SrTiO3(110) surfaces was investigated with metastable impact electron spectroscopy and ultraviolet photoelectron spectroscopy (He(I). Scanning tunnelling microscopy and atomic force microscopy (AFM) were used to study the topology of the surface. The crystals were heated up to 1000 °C under reducing conditions in ultrahigh vacuum or under oxidizing conditions in synthetic air for 1 h, respectively. Under both conditions microfacetting of the surface is observed. The experimental results are compared with ab initio Hartree-Fock calculations, also presented here, carried out for both ideal and reconstructed SrTiO 3(110) surfaces. The results give direct evid…

Ab initioAnalytical chemistrySurfaces and InterfacesGeneral ChemistryElectronic structureCondensed Matter PhysicsElectron spectroscopySurfaces Coatings and Filmslaw.inventionCondensed Matter::Materials Sciencechemistry.chemical_compoundchemistryAb initio quantum chemistry methodslawMicroscopyMaterials ChemistryStrontium titanateAtomic physicsScanning tunneling microscopeUltraviolet photoelectron spectroscopySurface and Interface Analysis
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Theoretical study of the NH tautomerism in free base porphyrin

1997

Abstract The NH tautomerism of free base porphyrin is investigated at the semiempirical spin-unrestricted AM1 (UAM1) and ab initio RHF/3-21G levels. The UAM1 method provides delocalized geometries for all stationary structures without imposing any symmetry constraint. RHF/3-21G geometry optimizations have to be performed under symmetry restrictions to ensure that realistic delocalized structures are obtained. Both the semiempirical and the ab initio calculations predict that the interconversion between trans tautomers proceeds in an asynchronous two-step process via intermediate cis tautomers. The cis tautomers are characterized as minima in the potential energy surface and are 8–10 kcal m…

Ab initioFree baseActivation energyCondensed Matter PhysicsBiochemistryPorphyrinTautomerchemistry.chemical_compoundDelocalized electronchemistryComputational chemistryAb initio quantum chemistry methodsPotential energy surfacePhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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