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Theory and computation of the attosecond dynamics of pairs of electrons excited by high-frequency short light pulses

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dc.contributor.author Mercouris, Th en
dc.contributor.author Komninos, Y en
dc.contributor.author Nicolaides, CA en
dc.date.accessioned 2014-03-01T01:21:38Z
dc.date.available 2014-03-01T01:21:38Z
dc.date.issued 2004 en
dc.identifier.issn 1050-2947 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/16283
dc.subject.classification Optics en
dc.subject.classification Physics, Atomic, Molecular & Chemical en
dc.subject.other Computational methods en
dc.subject.other Continuum mechanics en
dc.subject.other Correlation methods en
dc.subject.other Electronic structure en
dc.subject.other Energy transfer en
dc.subject.other Ground state en
dc.subject.other Hamiltonians en
dc.subject.other Helium en
dc.subject.other Ionization en
dc.subject.other Laser pulses en
dc.subject.other Mathematical models en
dc.subject.other Molecular dynamics en
dc.subject.other Probability distributions en
dc.subject.other Resonance en
dc.subject.other Scattering en
dc.subject.other Attosecond dynamics en
dc.subject.other Doubly excited states (DES) en
dc.subject.other Gaussian pulses en
dc.subject.other Hartree-Fock equations en
dc.subject.other Position vectors en
dc.subject.other Atomic physics en
dc.title Theory and computation of the attosecond dynamics of pairs of electrons excited by high-frequency short light pulses en
heal.type journalArticle en
heal.identifier.primary 10.1103/PhysRevA.69.032502 en
heal.identifier.secondary 032502 en
heal.identifier.secondary http://dx.doi.org/10.1103/PhysRevA.69.032502 en
heal.language English en
heal.publicationDate 2004 en
heal.abstract By defining and solving from first principles, using the state-specific expansion approach, a time-dependent pump-probe problem with real atomic states, we show computationally that, if time resolution reaches the attosecond regime, strongly correlated electronic "motion" can be probed and can manifest itself in terms of time-dependent mixing of symmetry-adapted configurations. For the system that was chosen in this study, these configurations, the He 2s2p,2p3d, and 3s3p P-1(o), whose radials are computed by solving multiconfigurational Hartree-Fock equations, label doubly excited states (DES) of He inside the 1sepsilonp P-1(o) scattering continuum and act as nonstationary states that mix, and simultaneously decay exponentially to 1sepsilonp P-1(o) via the atomic Hamiltonian, H-A. The herein presented theory and analysis permitted the computation of attosecond snapshots of pairs of electrons in terms of time-dependent probability distributions of the angle between the position vectors of the two electrons. The physical processes were determined by solving ab initio the time-dependent Schrodinger equation, using as initial states either the He 1s(2) or the 1s2s S-1 discrete states and two femtosecond Gaussian pulses of 86 fs full width at half-maximum, having frequencies in resonance with the energies of the correlated states represented by the 2s2p and 2p3d configurations. We calculated the probability of photoabsorption and of two-photon resonance ionization and of the simultaneous oscillatory mixing of the configurations 2s2p,2p3d,3s3p, and 1sepsilonp P-1(o), within the attosecond scale, via the interactions present in H-A. Among the possible channels for observing the attosecond oscillations of the occupation probabilities of the DES, is the de-excitation path of the transition to the He 1s3d D-1 discrete state, which emits at 6680 Angstrom. en
heal.publisher AMERICAN PHYSICAL SOC en
heal.journalName Physical Review A - Atomic, Molecular, and Optical Physics en
dc.identifier.doi 10.1103/PhysRevA.69.032502 en
dc.identifier.isi ISI:000220605200050 en
dc.identifier.volume 69 en
dc.identifier.issue 3 en
dc.identifier.spage 032502 en
dc.identifier.epage 1 en


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