Search results for "Vibronic coupling"

showing 10 items of 42 documents

Low-temperature optical absorption of nickel fluosilicate crystals

1964

Abstract The vibronic absorption spectrum of the Ni++ ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, together with their associated fine structures. In particular, the complex structure of the red band is well explained in detail as a consequence of the mutual perturbation of the 1E and 3T4 levels, which strongly modifies the vibronic coupling and results in two fairly narrow bands, each showing resolved vibrational structure, superposed on a broad band. A Trees correction term, αL(L+1), helps …

Ligand field theoryVibronic couplingNickelAbsorption spectroscopyChemistryElectric fieldPerturbation (astronomy)chemistry.chemical_elementTrigonal crystal systemAtomic physicsIonPhilosophical Magazine
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VIBPACK: A package to treat multidimensional electron-vibrational molecular problems with application to magnetic and optical properties

2018

We present a FORTRAN code based on a new powerful and efficient computational approach to solve multidimensional dynamic Jahn-Teller and pseudo Jahn-Teller problems. This symmetry-assisted approach constituting a theoretical core of the program is based on the full exploration of the point symmetry of the electronic and vibrational states. We also report some selected examples of increasing complexity aimed to display the theoretical background as well as the advantages and capabilities of the program to evaluate of the energy pattern, magnetic and optical properties of large multimode vibronic systems. © 2018 Wiley Periodicals, Inc.

Multi-mode optical fiberComputer scienceFortran02 engineering and technologyGeneral ChemistryElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSymmetry (physics)0104 chemical sciencesComputational scienceComputational MathematicsVibronic couplingCore (graph theory)Code (cryptography)Condensed Matter::Strongly Correlated Electrons0210 nano-technologycomputerEnergy (signal processing)computer.programming_languageJournal of Computational Chemistry
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Time-Resolved Coherent Anti-Stokes Raman Scattering of Graphene: Dephasing Dynamics of Optical Phonon.

2017

We report dynamics of the G-mode in graphene probed with time-resolved coherent anti-Stokes Raman scattering measurements. By applying BOXCARS excitation geometry with three different excitation wavelengths, various nonlinear processes can be selectively detected due to energy and momentum conservation and temporal sequence of the pulses. The Raman signal due to resonant coherent excitation of the G-mode shows exponential decay with lifetime of ∼325 ± 50 fs. This decay time is shorter than expected based on the line width of the G-mode in the Raman spectrum. We propose that the unexpectedly short dephasing time is a result of dynamic variation of nonadiabatic coupling of the photoexcited el…

PhononDephasingphonons02 engineering and technology01 natural sciencessymbols.namesake0103 physical sciencesscattering (physics)grafeeniGeneral Materials SciencesirontaCoherent anti-Stokes Raman spectroscopyPhysical and Theoretical ChemistryExponential decay010306 general physicsta116fononitPhysicsta114graphene021001 nanoscience & nanotechnologyVibronic couplingsymbolsAtomic physics0210 nano-technologyRaman spectroscopyExcitationRaman scatteringThe journal of physical chemistry letters
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Theory of Nuclear Quantum Dynamics Simulations

2016

In Chap. 2, we have seen that the theoretical study of a molecular system is, in a vast majority of cases, separated in two steps. In a first step, the electronic structure of the system is studied by solving the electronic Schrodinger equation with fixed nuclei. This approach, combined with geometry optimization techniques, allows one to locate the important features of the various potential energy surfaces (PESs) of the electronic states of interest. In the context of photochemistry, as seen in Chap. 3, this approach allows one to characterize the various decay pathways of the molecule after photoexcitation. This information can then be used to interpret the various decay time constants o…

PhotoexcitationPhysicsVibronic couplingsymbols.namesakeQuantum dynamicssymbolsContext (language use)Statistical physicsElectronic structureQuantum dissipationPotential energySchrödinger equation
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Modelling the properties of magnetic clusters with complex structures: how symmetry can help us

2020

The purpose of this article is to answer the question of how symmetry helps us to investigate and understand the properties of nanoscopic magnetic clusters with complex structures. The systems of choice will be the three types of polyoxometalates (POMs): (1) POMs containing localised spins; (2) reduced mixed-valence (MV) POMs; (3) partially delocalised POMs in which localised and delocalised subunits coexist and interact. The theoretical tools based on various kinds of symmetry are the following: (1) irreducible tensor operator (ITO) approach based on the so-called 'spin-symmetry' and MAGPACK program; (2) group-theoretical assignment of the exchange multiplets based on spin- and point symme…

PhysicsAntisymmetric exchange010304 chemical physicsCondensed matter physicsJahn–Teller effect010402 general chemistry01 natural sciencesSymmetry (physics)0104 chemical sciencesVibronic couplingMagnetic anisotropy0103 physical sciencesPhysical and Theoretical ChemistrySimetria (Física)Nanoscopic scaleFisicoquímica
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Localization vs. Delocalization in Molecules and Clusters: Electronic and Vibronic Interactions in Mixed Valence Systems

1996

The interplay between electron delocalization and magnetic interactions play a key role in areas as diverse as solid state chemistry (bulk magnetic materials, superconductors,...) [1] and biology (iron-sulfur proteins, manganese-oxo clusters ...) [2]. In molecular inorganic chemistry these two electronic processes have been traditionally studied independently. Thus, the electron dynamics has been extensively investigated in mixedvalence dimers [3] as exemplified by the Creutz-Taube complex [(NH3)5RuII(pyrazine)RuIII(NH3)5]. In this kind of molecular complexes one extra electron is delocalized over two diamagnetic metal sites. Therefore, they constitute model systems for the study of the ele…

PhysicsDelocalized electronVibronic couplingElectron transferCoordination sphereValence (chemistry)Spin statesChemical physicsVibronic spectroscopyMolecule
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Exceptional points in a non-Hermitian extension of the Jaynes-Cummings Hamiltonian

2016

We consider a generalization of the non-Hermitian \({\mathcal PT}\) symmetric Jaynes-Cummings Hamiltonian, recently introduced for studying optical phenomena with time-dependent physical parameters, that includes environment-induced decay. In particular, we investigate the interaction of a two-level fermionic system (such as a two-level atom) with a single bosonic field mode in a cavity. The states of the two-level system are allowed to decay because of the interaction with the environment, and this is included phenomenologically in our non-Hermitian Hamiltonian by introducing complex energies for the fermion system. We focus our attention on the occurrence of exceptional points in the spec…

PhysicsExceptional pointFermionic systemFermionHermitian matrixNon-Hermitian HamiltonianJaynes-Cummings HamiltonianVibronic couplingsymbols.namesakeQuantum mechanicsBosonic fieldsymbolsHamiltonian (quantum mechanics)Settore MAT/07 - Fisica MatematicaMathematical physicsExceptional point
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Toward multifunctional molecular cells for quantum cellular automata: exploitation of interconnected charge and spin degrees of freedom

2021

We discuss the possibility of using mixed-valence (MV) dimers comprising paramagnetic metal ions as molecular cells for quantum cellular automata (QCA). Thus, we propose to combine the underlying idea behind the functionality of QCA of using the charge distributions to encode binary information with the additional functional options provided by the spin degrees of freedom. The multifunctional ('smart') cell is supposed to consist of multielectron MV d(n)-d(n+1)-type (1 ≤ n ≤ 8) dimers of transition metal ions as building blocks for composing bi-dimeric square planar cells for QCA. The theoretical model of such a cell involves the double exchange (DE), Heisenberg-Dirac-Van Vleck (HDVV) excha…

PhysicsGeneral Physics and Astronomy02 engineering and technologyElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics0104 chemical sciencesVibronic couplingFerromagnetismElectric fieldCoulombAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical Chemistry0210 nano-technologyFisicoquímicaQuantum cellular automatonSpin-½Physical Chemistry Chemical Physics
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Spectroscopy of Hexafluorides with an Odd Number of Electrons: The Vibronic Bands of IrF6

1996

Abstract The low resolution absorption spectroscopy of the first five excited electronic states of IrF 6 has made possible some new assignments for the vibronic transitions of this molecule, and the determination of new vibronic parameter values. They are more accurate than those found in the literature. In this aim, we introduce a simplified tensorial formulation for the linear Jahn–Teller terms in a fourfold degenerate electronic state of an XY 6 -type molecule, which allows easier computation of matrix elements and avoids the use of perturbation theory. Methods for IrF 6 synthesis (using a dynamical flow system) and purification are also presented.

PhysicsMatrix (mathematics)Vibronic couplingAbsorption spectroscopyDegenerate energy levelsVibronic spectroscopyElectronPhysical and Theoretical ChemistryAtomic physicsPerturbation theorySpectroscopySpectroscopyAtomic and Molecular Physics and OpticsJournal of Molecular Spectroscopy
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Measuring the mean value of vibrational observables in trapped ion systems

2002

The theoretical foundations of a new general approach to the measurement problem of vibrational observables in trapped ion systems is reported. The method rests upon the introduction of a simple vibronic coupling structure appropriately conceived to link the internal ionic state measurement outcomes to the mean value of a motional variable of interest. Some applications are provided and discussed in detail, bringing to light the feasibility and the wide potentiality of the proposal.

PhysicsQuantum PhysicsFOS: Physical sciencesObservableMeasurement problemElectromagnetic radiationAtomic and Molecular Physics and OpticsCharged particleIonCoupling (physics)Vibronic couplingExcited stateQuantum mechanicsQuantum Physics (quant-ph)
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