Search results for "Molecular physics"

showing 10 items of 5665 documents

Light-induced nonthermal population of optical phonons in nanocrystals

2017

Raman spectroscopy is widely used to study bulk and nanomaterials, where information is frequently obtained from spectral line positions and intensities. In this study, we monitored the Raman spectrum of ensembles of semiconductor nanocrystals (NCs) as a function of optical excitation intensity (optical excitation experiments). We observe that in NCs the red-shift of the Raman peak position with increasing light power density is much steeper than that recorded for the corresponding bulk material. The increase in optical excitation intensity results also in an increasingly higher temperature of the NCs as obtained with Raman thermometry through the commonly used Stokes/anti-Stokes intensity …

010302 applied physicseducation.field_of_studyMaterials sciencePhononPopulation02 engineering and technologyPhysik (inkl. Astronomie)021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsSpectral lineNanomaterialssymbols.namesakeElectrical resistivity and conductivityExcited state0103 physical sciencessymbols0210 nano-technologyeducationRaman spectroscopyExcitation
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Ab initio multi-reference perturbation theory calculations of the ground and low-lying electronic states of the KRb molecule

2016

The potential energy curves of the low-lying electronic states correlating up to the limit K(4p) + Rb(5s) of KRb molecule have been calculated using the multi-reference perturbation theory method at the CASSCF/ XMCQDPT2 level of theory without and with spin–orbit coupling. The calculated parameters of the ground X 1 R + state are in the best agreement among all previously performed ab initio calculations for the KRb molecule. The calculated vibrational intervals of the ground electronic term of the 39 K 85 Rb molecule describe the experiment with the accuracy within ±1 cm ?1 . The calculated intensities of the 2 1 R + (v 0 = 3, J 0 = 26) ? X 1 R + (v 00 = 0...24, J 00 = 25, 27) transitions …

010304 chemical physicsAb initiochemistry.chemical_elementOvertone bandSpin–orbit interactionCondensed Matter Physics01 natural sciencesBiochemistryMolecular physicsPotential energyDissociation (chemistry)Rubidiumsymbols.namesakeDipolechemistryFranck–Condon principle0103 physical sciences:ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Физика [ЭБ БГУ]Physics::Atomic and Molecular ClusterssymbolsPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physics010306 general physics
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Carbonyl-functionalized quaterthiophenes: a study of the vibrational Raman and electronic absorption/emission properties guided by theoretical calcul…

2011

This work investigates the evolution of the molecular, vibrational, and optical properties within a family of carbonyl-functionalized quaterthiophenes: 5,5'''-diheptanoyl-2,2':5',2'':5'',2'''-quaterthiophene (1), 5,5'''-diperfluorohexylcarbonyl-2,2':5',2'':5'',2'''-quaterthiophene (2), and 2,7-[bis(5-perfluorohexylcarbonylthien-2-yl)]-4H-cyclopenta[2,1-b:3,4-b']-dithiophene-4-one (3). The analysis is performed by Raman and UV/Vis absorption/excitation/fluorescence spectroscopy in combination with density functional calculations. Theoretical calculations show that substitution with carbonyl groups and perfluorohexyl chains induces progressive quinoidization of the π-conjugated backbone in co…

010304 chemical physicsAbsorption spectroscopyChemistryTime-dependent density functional theory010402 general chemistryResonance (chemistry)Photochemistry01 natural sciencesAtomic and Molecular Physics and OpticsFluorescence spectroscopyMolecular electronic transition0104 chemical sciencesCrystallographysymbols.namesakeUltraviolet visible spectroscopy0103 physical sciencesBathochromic shiftsymbolsPhysical and Theoretical ChemistryRaman spectroscopyChemphyschem : a European journal of chemical physics and physical chemistry
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Multiple vibrational resonances in the Raman spectra of liquid ethanes

1990

The Raman spectra of liquid ethane, ethane-d3 and ethane-d6 were recorded and analysed. The CH3 and CD3 stretching regions were computer resolved using Cauchy-Gaussian and Voigt functions to account for asymmetric band shapes. Multiple vibrational resonances were investigated using the wavenumbers and observed intensities in these regions. The developed basis functions show strong mixing of the levels in these regions. In general the resonances appear to be less strong in the liquid phase than reported in previous studies of the gaseous state. Some new assignments in the liquid-state spectra of ethanes could be suggested.

010304 chemical physicsChemistryComputer aidLiquid phaseBasis function02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsSpectral linesymbols.namesakeLiquid stateNuclear magnetic resonance0103 physical sciencessymbolsWavenumberGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysics::Chemical Physics0210 nano-technologyRaman spectroscopySpectroscopyMixing (physics)Journal of Raman Spectroscopy
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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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Germanium Dicarbide: Evidence for a T-Shaped Ground State Structure

2017

The equilibrium structure of germanium dicarbide GeC2 has been an open question since the late 1950s. Although most high-level quantum calculations predict an L-shaped geometry, a T-shaped or even a linear geometry cannot be ruled out because of the very flat potential energy surface. By recording the rotational spectrum of this dicarbide using sensitive microwave and millimeter techniques, we unambiguously establish that GeC2 adopts a vibrationally averaged T-shaped structure in its ground state. From analysis of 14 isotopologues, a precise r0 structure has been derived, yielding a Ge–C bond length of 1.952(1) A and an apex angle of 38.7(2)°.

010304 chemical physicsChemistrychemistry.chemical_elementLinear molecular geometryGermanium02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsBond lengthCrystallography0103 physical sciencesPotential energy surfaceGeneral Materials ScienceMillimeterIsotopologuePhysical and Theoretical Chemistry0210 nano-technologyGround stateMicrowaveThe Journal of Physical Chemistry Letters
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Introduction to the special issue on molecular spectroscopy, atmospheric composition and climate change

2018

International audience

010304 chemical physicsClimate changeMolecular spectroscopy010402 general chemistryAtmospheric sciences01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAtmospheric composition13. Climate action0103 physical sciencesEnvironmental sciencePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSSpectroscopyJournal of Molecular Spectroscopy
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Dynamic Polarizability and Higher-Order Electric Properties of Fluorene, Carbazole, and Dibenzofuran

2019

Static electric properties, from the dipole moment to the second-hyperpolarizability tensor γ, of the 3-membered, isoelectronic ring molecules, fluorene (FL), carbazole (CR), and dibenzofuran (DBF), have been calculated at various levels of approximation. The electron correlation effects have been included at the coupled-cluster (CC) level, using CCSD and CC2 versions of the method. DFT calculations with the CAM-B3LYP functional have also been performed, and the results are compared to the CC values. The electric property-tailored Pol basis set and its more compact Z3Pol version have been employed in all static calculations. Differences between dipole polarizability values computed at the P…

010304 chemical physicsElectronic correlationChemistryCarbazoleFluorene010402 general chemistry01 natural sciencesMolecular physics0104 chemical scienceschemistry.chemical_compoundDipolePolarizabilityExcited state0103 physical sciencesPhysical and Theoretical ChemistryBasis setExcitationJournal of Physical Chemistry A
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Steering the excited state dynamics of a photoactive yellow protein chromophore analogue with external electric fields

2014

Abstract The first excited state of the Photoactive Yellow Protein chromophore exhibits a strong charge transfer character and the dipole moments of the excited and ground states differ significantly. Furthermore, the excited state charge distribution changes during the isomerization of this chromophore. These observations suggest that external electric fields can be used to control photo-isomerization, providing a new concept for developing photochromic devices, such as e-paper or optical memory. To test this idea, we performed excited state dynamics simulations and static calculations of a PYP chromophore analogue (pCK − ) in an external electric field. By adjusting direction and strength…

010304 chemical physicsField (physics)ChemistryCharge densitySurface hoppingChromophore010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesBiochemistryMolecular physics0104 chemical sciencesPhotochromismDipoleElectric fieldExcited state0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical Chemistryta116ComputingMilieux_MISCELLANEOUS
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Inelastic neutron scattering study of proton dynamics in Ca(OH)2 at 20 K

1995

Abstract Inelastic neutron scattering (INS) spectra of Ca(OH) 2 at 20 K are presented from 30 to 4000 cm −1 for a powder sample, from 30 to 12000 cm −1 for an oriented single-crystal. INS band splitting due to the lattice density-of-states is observed. Polarization effects reveal the orientation of atomic displacements for each mode and a new band assignment scheme is proposed. For the single-crystal, the v OH mode and overtones are observed. This oscillator shows only moderate anharmonicity. Spectrum simulation reveals that INS spectral intensities are not consistent with simple normal coordinates and harmonic force-fields for Ca(OH) 2 entities. A new dynamical model is proposed, including…

010304 chemical physicsInfraredChemistryAnharmonicityGeneral Physics and Astronomy02 engineering and technology021001 nanoscience & nanotechnologyPolarization (waves)01 natural sciencesMolecular physicsSpectral lineInelastic neutron scatteringsymbols.namesakeCrystallographyLattice (order)0103 physical sciencessymbolsNormal coordinates[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technologyRaman spectroscopyComputingMilieux_MISCELLANEOUS
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