Search results for "physics and astronomy"

showing 10 items of 8108 documents

Towards highly accurate ab initio thermochemistry of larger systems: benzene.

2011

The high accuracy extrapolated ab initio thermochemistry (HEAT) protocol is applied to compute the total atomization energy (TAE) and the heat of formation of benzene. Large-scale coupled-cluster calculations with more than 1500 basis functions and 42 correlated electrons as well as zero-point energies based on full cubic and (semi)diagonal quartic force fields obtained with the coupled-cluster singles and doubles with perturbative treatment of the triples method and atomic natural orbital (ANO) triple- and quadruple-zeta basis sets are presented. The performance of modifications to the HEAT scheme and the scaling properties of its contributions with respect to the system size are investiga…

010304 chemical physicsChemistryAb initioGeneral Physics and AstronomyBasis function010402 general chemistry01 natural sciences7. Clean energyStandard enthalpy of formation0104 chemical sciencesChemical thermodynamicsAb initio quantum chemistry methodsQuartic function0103 physical sciencesThermochemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsScalingThe Journal of chemical physics
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Theoretical investigation of the potential energy surface of the van der Waals complex CH4-N-2

2009

International audience; The interaction potential energy surface of the van der Waals CH4-N-2 complex has been calculated for a broad range of intermolecular separations and configurations in the approximation of rigid interacting molecules at the CCSD(T) and MP2 levels of theory using the correlation consistent aug-cc-pVTZ basis set. The BSSE correction was taken into account for all the calculations. The most stable configurations of the complex were found. Binding energies were calculated in the CBS limit with accounting for the molecular deformations. The harmonic and anharmonic fundamental vibrational frequencies and rotational constants for the ground and first excited vibrational sta…

010304 chemical physicsChemistryBinding energyIntermolecular forceAnharmonicityVan der Waals surfaceGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeLennard-Jones potentialExcited state0103 physical sciencesPotential energy surface[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysics::Atomic and Molecular ClustersPhysical and Theoretical Chemistryvan der Waals forceAtomic physicsPhysics::Chemical Physics
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Laser control in open molecular systems: STIRAP and Optimal Control

2007

We examine the effect of dissipation on the laser control of a process that transforms a state into a superposed state. We consider a two-dimensional double well of a single potential energy surface. In the context of reactivity, the objective of the control is the localization in a given well, for instance the creation of an enantiomeric form whereas for quantum gates, this control corresponds to one of the transformation of the Hadamard gate. The environment is either modelled by coupling few harmonic oscillators (up to five) to the system or by an effective interaction with an Ohmic bath. In the discrete case, dynamics is carried out exactly by using the coupled harmonic adiabatic channe…

010304 chemical physicsChemistryGeneral Chemical EngineeringStimulated Raman adiabatic passageGeneral Physics and AstronomyContext (language use)General ChemistryOptimal control01 natural sciencesQuantum gateQuantum mechanicsQubit0103 physical sciencesHarmonic010306 general physicsAdiabatic processHarmonic oscillatorJournal of Photochemistry and Photobiology A: Chemistry
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Fourier-transform spectroscopy and deperturbation analysis of the spin-orbit coupled A(1)Σ(+) and b(3)Π states of KRb.

2016

Fourier-transform A(1)Σ(+) - b(3)Π → X(1)Σ(+) laser-induced fluorescence spectra were recorded for the natural mixture of (39,41)K(85,87)Rb isotopologues produced in a heatpipe oven. Overall 4200 rovibronic term values of the spin-orbit coupled A(1)Σ(+) and b(3)Π states were determined with an uncertainty of about 0.01 cm(-1) in the energy range [10 850, 14 200] cm(-1) covering rotational quantum numbers J' ∈ [3, 280]. Direct deperturbation analysis of the A ∼ b complex performed within the framework of the A(1)Σ(+) ∼ b(3)ΠΩ=0,1,2 coupled-channel approach reproduced experimental data with a standard deviation of 0.004 cm(-1). Initial parameters of the internuclear potentials and spin-orbit …

010304 chemical physicsChemistryGeneral Physics and AstronomyElectronic structureQuantum number01 natural sciencesFourier transform spectroscopyB vitamins0103 physical sciencesKinetic isotope effectIsotopologueEmission spectrumPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyThe Journal of chemical physics
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Communication: multireference equation of motion coupled cluster: a transform and diagonalize approach to electronic structure.

2014

The novel multireference equation-of-motion coupled-cluster (MREOM-CC) approaches provide versatile and accurate access to a large number of electronic states. The methods proceed by a sequence of many-body similarity transformations and a subsequent diagonalization of the transformed Hamiltonian over a compact subspace. The transformed Hamiltonian is a connected entity and preserves spin- and spatial symmetry properties of the original Hamiltonian, but is no longer Hermitean. The final diagonalization spaces are defined in terms of a complete active space (CAS) and limited excitations (1h, 1p, 2h, …) out of the CAS. The methods are invariant to rotations of orbitals within their respective…

010304 chemical physicsChemistryGeneral Physics and AstronomyEquations of motionElectronic structure010402 general chemistry7. Clean energy01 natural sciencesLinear subspace0104 chemical sciencessymbols.namesakeCoupled clusterAtomic orbitalQuantum mechanics0103 physical sciencessymbolsComplete active spacePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Subspace topologyThe Journal of chemical physics
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Multi-scale multireference configuration interaction calculations for large systems using localized orbitals: Partition in zones

2012

A new multireference configuration interaction method using localised orbitals is proposed, in which a molecular system is divided into regions of unequal importance. The advantage of dealing with local orbitals, i.e., the possibility to neglect long range interaction is enhanced. Indeed, while in the zone of the molecule where the important phenomena occur, the interaction cut off may be as small as necessary to get relevant results, in the most part of the system it can be taken rather large, so that results of good quality may be obtained at a lower cost. The method is tested on several systems. In one of them, the definition of the various regions is not based on topological considerati…

010304 chemical physicsChemistryGeneral Physics and AstronomyMultireference configuration interactionMolecular orbital theory010402 general chemistry01 natural sciences0104 chemical sciencesLinear combination of atomic orbitalsMulti-configurational self-consistent field0103 physical sciencesMolecular orbitalComplete active spaceStatistical physicsPhysical and Theoretical ChemistryAtomic physicsBasis setNatural bond orbital
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Laser-induced enhancement of tunneling in NHD2

2012

We apply and explore techniques aiming at enhancing the tunneling by laser fields, originally developed for a one-dimensional model, to a complete six-dimensional vibrational model of the inversion motion in NHD(2). The computational study is performed with the multi-configuration time-dependent Hartree method. Assuming an ideal three-dimensional alignment we obtain a driven tunneling time twenty times smaller than the natural one, in rather good agreement with an oversimplified three-state model. In the case of one-dimensional alignment, a linearly polarized field leads to a poor enhancement of the tunneling probability, after averaging over the rotation about the alignment axis, whereas a…

010304 chemical physicsChemistryLinear polarizationScanning tunneling spectroscopyGeneral Physics and AstronomyHartreeLaser01 natural scienceslaw.invention[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrylaw0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryPhysical and Theoretical ChemistryAtomic physics010306 general physicsTunneling timeQuantum tunnellingComputingMilieux_MISCELLANEOUS
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A quantum dynamics study of the benzopyran ring opening guided by laser pulses

2014

Abstract The ring-opening photoisomerization of benzopyran, which occurs via a photochemical route involving a conical intersection, has been studied with quantum dynamics calculations using the multi-configuration time-dependent Hartree method (MCTDH). We introduce a mechanistic strategy to control the conversion of benzopyran to merocyanine with laser pulses. We use a six-dimensional model developed in a previous work for the potential energy surfaces (PES) based on an extension of the vibronic-coupling Hamiltonian model (diabatization method by ansatz), which depends on the most active degrees of freedom. The main objective of these quantum dynamics simulations is to provide a set of str…

010304 chemical physicsChemistryQuantum dynamicsDegrees of freedom (physics and chemistry)General Physics and AstronomyHartreeConical intersection010402 general chemistry01 natural sciencesPotential energyMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrysymbols.namesakeStark effectComputational chemistry0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsPhysical and Theoretical ChemistryGround stateAdiabatic processComputingMilieux_MISCELLANEOUS
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Quantum dynamics of 16O in collision with ortho- and para-17O17O

2017

Abstract We report full quantum dynamical observables, such as integral and differential cross sections and rate constants, for the 16 O +  17 O 17 O reactive collision process. We particularly emphasize the effect coming from the nonzero nuclear spin of 17 O, leading to two nuclear spin isomers of 34 O 2 , ortho- and para- 34 O 2 which can be studied independently and behave differently. A comparison with the 16 O +  18 O 18 O collision is given. We find that processes involving 17 O 17 O are always faster than with 18 O 18 O.

010304 chemical physicsChemistryQuantum dynamicsGeneral Physics and AstronomyObservable010402 general chemistryCollision01 natural sciences0104 chemical sciencesReaction rate constant0103 physical sciencesKinetic isotope effectPhysical chemistryPhysical and Theoretical ChemistryAtomic physicsQuantumChemical Physics Letters
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Full-dimensional control of the radiationless decay in pyrazine using the dynamic Stark effect

2014

We present a full quantum-mechanical study of the laser control of the radiationless decay between the B3u(nπ(*)) and B2u(ππ(*)) states of pyrazine using the dynamic Stark effect. In contrast to our previous study [Sala et al., J. Chem. Phys. 140, 194309 (2014)], where a four-dimensional model was used, all the 24 degrees of freedom are now included in order to test the robustness of the strategy of control. Using a vibronic coupling Hamiltonian model in a diabatic representation, the multi-layer version of the multi-configuration time-dependent Hartree method is exploited to propagate the corresponding wave packets. We still observe a trapping of the wavepacket on the B2u(ππ(*)) potential …

010304 chemical physicsChemistryWave packetDiabaticGeneral Physics and AstronomyHartree010402 general chemistry01 natural sciencesPotential energy0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryVibronic couplingsymbols.namesakeStark effectQuantum mechanicsExcited state[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry0103 physical sciencesPotential energy surfacesymbolsPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsComputingMilieux_MISCELLANEOUSThe Journal of Chemical Physics
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