Search results for "physics.atm-clus"

showing 10 items of 38 documents

High-resolution spectroscopy and analysis of the V2 + V3 combination band of SF6 in a supersonic jet expansion

2013

International audience; Sulphur hexafluoride is a very strong greenhouse gas whose concentration is increasing in the atmosphere. It is detected through infrared absorption spectroscopy in the strong ν3 fundamental region. Due to the existence of low-lying vibrational states of this molecule, however, many hot bands arise at room temperature and those are still not known. We present here a contribution to the elucidation of this hot band structure, by analysing the ν2 + ν3 combination band. We use a supersonic jet expansion high-resolution spectrum at a rotational temperature of ca. 25 K that was recorded thanks to the Jet-AILES setup at the Source Optimisée de Lumière d'Energie Intermédiai…

010504 meteorology & atmospheric sciencessupersonic jet expansionBiophysicsInfrared spectroscopy7. Clean energy01 natural sciencesHot bandlaw.inventionsymbols.namesake[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]law0103 physical sciencesSupersonic speedPhysical and Theoretical ChemistrySpectroscopy[ PHYS.PHYS.PHYS-ATM-PH ] Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Molecular BiologyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciences[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]010304 chemical physicssulphur hexafluorideChemistry[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Rotational temperatureRotational–vibrational spectroscopyCondensed Matter PhysicsSynchrotron[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]13. Climate actiongreenhouse gassymbolsinfrared absorption[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsHamiltonian (quantum mechanics)tensorial formalism
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Fragmentation of anthracene C14H10, acridine C13H9N and phenazine C12H8N2 ions in collisions with atoms

2014

International audience; We report experimental total, absolute, fragmentation cross sections for anthracene C14H10, acridine C13H9N, and phenazine C12H8N2 ions colliding with He at center-of-mass energies close to 100 eV. In addition, we report results for the same ions colliding with Ne, Ar, and Xe at higher energies. The total fragmentation cross sections for these three ions are the same within error bars for a given target. The measured fragment mass distributions reveal significant contributions from both delayed (≫10−12 s) statistical fragmentation processes as well as non-statistical, prompt (∼10−15 s), single atom knockout processes. The latter dominate and are often followed by sec…

AnthraceneInternal energyPhenazine[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]General Physics and Astronomy01 natural sciencesIonchemistry.chemical_compoundMolecular dynamicschemistryFragmentation (mass spectrometry)0103 physical sciencesAtomAcridine[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryAtomic physics010306 general physics010303 astronomy & astrophysics
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Orientation and Alignment Echoes

2015

We present one of the simplest classical systems featuring the echo phenomenon---a collection of randomly oriented free rotors with dispersed rotational velocities. Following excitation by a pair of time-delayed impulsive kicks, the mean orientation or alignment of the ensemble exhibits multiple echoes and fractional echoes. We elucidate the mechanism of the echo formation by the kick-induced filamentation of phase space, and provide the first experimental demonstration of classical alignment echoes in a thermal gas of ${\mathrm{CO}}_{2}$ molecules excited by a pair of femtosecond laser pulses.

Atomic Physics (physics.atom-ph)FOS: Physical sciencesGeneral Physics and AstronomyPhysics - Classical PhysicsPhysics - Atomic Physicslaw.inventionOpticsFilamentationlawPhysics - Chemical PhysicsChemical Physics (physics.chem-ph)Physics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics][PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]business.industry[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]Echo (computing)Classical Physics (physics.class-ph)LaserOrientation (vector space)Phase spaceExcited stateFemtosecondAtomic physicsbusinessExcitationPhysics - OpticsOptics (physics.optics)Physical Review Letters
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Ab initio angle- and energy-resolved photoelectron spectroscopy with time-dependent density-functional theory

2012

We present a time-dependent density-functional method able to describe the photoelectron spectrum of atoms and molecules when excited by laser pulses. This computationally feasible scheme is based on a geometrical partitioning that efficiently gives access to photoelectron spectroscopy in time-dependent density-functional calculations. By using a geometrical approach, we provide a simple description of momentum-resolved photoemission including multiphoton effects. The approach is validated by comparison with results in the literature and exact calculations. Furthermore, we present numerical photoelectron angular distributions for randomly oriented nitrogen molecules in a short near-infrared…

Atomic Physics (physics.atom-ph)Photoemission spectroscopyAb initioFOS: Physical sciences02 engineering and technology01 natural sciences7. Clean energySpectral lineSettore FIS/03 - Fisica Della MateriaPhysics - Atomic PhysicsX-ray photoelectron spectroscopyTDDFTABOVE-THRESHOLD IONIZATION; LASER FIELDS; WAVE-FUNCTIONS; PHOTOEMISSION; CLUSTERS; SYSTEMS; PULSESMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersPhysics::Atomic Physics010306 general physicsPhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsAtoms in moleculesTime-dependent density functional theory021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics3. Good healthStrong field ionizationExcited stateDensity functional theoryAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)0210 nano-technology
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Setting the photoelectron clock through molecular alignment

2020

The interaction of strong laser fields with matter intrinsically provides a powerful tool for imaging transient dynamics with an extremely high spatiotemporal resolution. Here, we study strong-field ionisation of laser-aligned molecules, and show a full real-time picture of the photoelectron dynamics in the combined action of the laser field and the molecular interaction. We demonstrate that the molecule has a dramatic impact on the overall strong-field dynamics: it sets the clock for the emission of electrons with a given rescattering kinetic energy. This result represents a benchmark for the seminal statements of molecular-frame strong-field physics and has strong impact on the interpreta…

Chemical Physics (physics.chem-ph)Atomic Physics (physics.atom-ph)ScienceChemical physicsQQuantum physicsFOS: Physical sciencesSettore FIS/03 - Fisica Della MateriaArticlePhysics - Atomic PhysicsStrong field ionizationTDDFTPhysics - Chemical Physicslcsh:QAtomic and molecular physicsddc:500Physics - Atomic and Molecular Clusterslcsh:ScienceAtomic and Molecular Clusters (physics.atm-clus)Applied optics
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Electronic Structure and Bonding of Icosahedral Core–Shell Gold–Silver Nanoalloy Clusters Au144–xAgx(SR)60

2011

Atomically precise thiolate-stabilized gold nanoclusters are currently of interest for many cross-disciplinary applications in chemistry, physics and molecular biology. Very recently, synthesis and electronic properties of "nanoalloy" clusters Au_(144-x)Ag_x(SR)_60 were reported. Here, density functional theory is used for electronic structure and bonding in Au_(144-x)Ag_x(SR)_60 based on a structural model of the icosahedral Au_144(SR)_60 that features a 114-atom metal core with 60 symmetry-equivalent surface sites, and a protecting layer of 30 RSAuSR units. In the optimal configuration the 60 surface sites of the core are occupied by silver in Au_84Ag_60(SR)_60. Silver enhances the electr…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceAbsorption spectroscopyIcosahedral symmetryFermi levelSuperatomElectron shellMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronic structureNanoclustersCrystallographysymbols.namesakePhysics - Chemical PhysicssymbolsGeneral Materials ScienceDensity functional theoryPhysics - Atomic and Molecular ClustersPhysical and Theoretical ChemistryAtomic and Molecular Clusters (physics.atm-clus)The Journal of Physical Chemistry Letters
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The spectra of mixed $^3$He-$^4$He droplets

2005

The diffusion Monte Carlo technique is used to calculate and analyze the excitation spectrum of $^3$He atoms bound to a cluster of $^4$He atoms, by using a previously determined optimum filling of single-fermion orbits with well defined orbital angular momentum $L$, spin $S$ and parity quantum numbers. The study concentrates on the energies and shapes of the three kinds of states for which the fermionic part of the wave function is a single Slater determinant: maximum $L$ or maximum $S$ states within a given orbit, and fully polarized clusters. The picture that emerges is that of systems with strong shell effects whose binding and excitation energies are essentially determined over configur…

Chemical Physics (physics.chem-ph)Excitation spectrumdiffusion[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]wave functionsFOS: Physical sciencesMonte Carlo methodsbinding energyMonte Carlo technique ; Excitation spectrum ;Monte Carlo techniqueliquid theoryliquid helium 3-4 mixturesPhysics - Chemical Physics[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physics - Atomic and Molecular ClustersAtomic and Molecular Clusters (physics.atm-clus)67.60.-g 66.10.Cb 61.20.Jadrops
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Thermal Expansion in Small Metal Clusters and its Impact on the Electric Polarizability

2000

The thermal expansion coefficients of $\mathrm{Na}_{N}$ clusters with $8 \le N \le 40$ and $\mathrm{Al}_{7}$, $\mathrm{Al}_{13}^-$ and $\mathrm{Al}_{14}^-$ are obtained from {\it ab initio} Born-Oppenheimer LDA molecular dynamics. Thermal expansion of small metal clusters is considerably larger than that in the bulk and size-dependent. We demonstrate that the average static electric dipole polarizability of Na clusters depends linearly on the mean interatomic distance and only to a minor extent on the detailed ionic configuration when the overall shape of the electron density is enforced by electronic shell effects. The polarizability is thus a sensitive indicator for thermal expansion. We …

Condensed Matter - Materials ScienceElectron densityMaterials scienceAb initioShell (structure)Materials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyIonic bondingThermal expansionDipoleMolecular dynamicsPolarizabilityPhysics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)
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Multiply charged metal cluster anions

2000

Formation, stability patterns, and decay channels of silver dianionic and gold trianionic clusters are investigated with Penning-trap experiments and a shell-correction method including shape deformations. The theoretical predictions pertaining to the appearance sizes and electronic shell effects are in remarkable agreement with the experiments. Decay of the multiply anionic clusters occurs predominantly by electron tunneling through a Coulomb barrier, rather than via fission, leading to appearance sizes unrelated to those of multiply cationic clusters.

Condensed Matter - Materials ScienceMaterials scienceNuclear TheoryFissionShell (structure)Cationic polymerizationGeneral Physics and AstronomyCoulomb barrierMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectron530MetalNuclear Theory (nucl-th)Chemical physicsvisual_artvisual_art.visual_art_mediumCluster (physics)Physics::Atomic and Molecular ClustersPhysics - Atomic and Molecular ClustersAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)Quantum tunnelling
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Nonmagnetic and magnetic thiolate-protected Au25superatoms on Cu(111), Ag(111), and Au(111) surfaces

2012

Geometry, electronic structure, and magnetic properties of methylthiolate-stabilized Au$_{25}$L$_{18}$ and MnAu$_{24}$L$_{18}$ (L = SCH$_3$) clusters adsorbed on noble-metal (111) surfaces have been investigated by using spin-polarized density functional theory computations. The interaction between the cluster and the surface is found to be mediated by charge transfer mainly from or into the ligand monolayer. The electronic properties of the 13-atom metal core remain in all cases rather undisturbed as compared to the isolated clusters in gas phase. The Au$_{25}$L$_{18}$ cluster retains a clear HOMO - LUMO energy gap in the range of 0.7 eV to 1.0 eV depending on the surface. The ligand layer…

Condensed Matter - Materials ScienceMaterials scienceta114Condensed Matter - Mesoscale and Nanoscale PhysicsMagnetic momentBand gapMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronic structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCrystallographyMesoscale and Nanoscale Physics (cond-mat.mes-hall)Cluster (physics)Density functional theoryPhysics - Atomic and Molecular ClustersAtomic physicsAtomic and Molecular Clusters (physics.atm-clus)Spin (physics)HOMO/LUMOEnergy (signal processing)Physical Review B
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