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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 1194-1205 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We examine the role of electronic continua in time-resolved photoelectron spectroscopy studies of polyatomic nonadiabatic dynamics. We have investigated the two limiting cases for such studies. We consider here the limiting case of complementary ionization correlations where the two nonadiabatically coupled excited electronic states (S2 and S1) correlate (in the Koopmans' picture) to different cation electronic states. We show, using an example of ultrafast internal conversion a linear polyene, that this favorable case allows for disentangling of the electronic population dynamics from the coupled vibrational dynamics. In the following paper, we investigate the unfavorable case of corresponding ionization correlations. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 117 (2002), S. 1575-1588 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report the observation and characterization of a new nonresonant strong field ionization mechanism in polyatomic molecules: Nonadiabatic multi-electron (NME) dynamics. The strong field response of a given molecule depends on important properties such as molecular geometry and bonding, the path length of delocalized electrons and/or ionization potential as well as on basic laser pulse parameters such as wavelength and intensity. Popular quasi-static tunnelling models of strong field molecular ionization, based upon the adiabatic response of a single active electron, are demonstrated to be inadequate when electron delocalization is important. The NME ionization mechanism greatly affects molecular ionization, its fragmentation and its energetics. In addition, multi-electron effects are shown to be present even in the adiabatic long wavelength limit. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-6079
    Keywords: PACS. 32.80.Qk Coherent control of atomic interactions with photons - 32.80.Rm Multiphoton ionization and excitation to highly excited states (e.g., Rydberg states) - 42.50.Md Optical transient phenomena: quantum beats, photon echo, free-induction decay, dephasings and revivals, optical nutation, and self-induced transparency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: The interaction of a sequence of two identical ultrashort laser pulses with an atomic system results in quantum interferences as in Ramsey fringes experiments. These interferences allow achievement of temporal coherent control of the excitation probability. We present the results of a temporal coherent control experiment on two different atomic systems: one-photon absorption in K (4s-4p) and two-photon absorption in Cs (6s-7d). In K, the quantum interferences between the two excitation paths associated with the laser pulses are revealed through rapid oscillations of the excitation probability as a function of the time delay between the two pulses. These oscillations take place at the transition frequency (period T = 2.56 fs). The interferences are modulated by beats (at about 580 fs) resulting from the doublet structure of the excited state (4p (2 P 1/2 , 2 P 3/2 )). Three complementary interpretations of this experiment are presented: in terms of beats of quantum interferences, of variation in the spectrum intensity, and of wave packet interferences. Whenever the two laser pulses are temporally overlapped, optical interferences are superimposed on to the quantum interferences. The distinction between these two types of interference is clearly revealed in the two-photon excitation scheme performed on Cs (6s-7d (2 D 3/2 , 2 D 5/2 )) because quantum interferences occur at twice the frequency of the optical interferences.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1434-6079
    Keywords: PACS. 32.80.Qk Coherent control of atomic interactions with photons[:AND:] 32.80.Rm Multiphoton ionization and excitation to highly excited states (e.g., Rydberg states) - 42.50.Md Optical transient phenomena: quantum beats, photon echo, free-induction decay, dephasings and revivals, optical nutation, and self-induced transparency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: Spin precession is investigated through a pump-probe technique which represents an alternative method to previous investigations by wavepacket interferometry. The excited wavepacket corresponds to a precession of spin and orbital angular momentum around the total angular momentum. We discuss and compare two equivalent descriptions of the phenomena, one given in the stationary states and the other in the bright state-dark state formalism. We show that this latter formalism is the most appropriate to describe the dynamics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 28 (2004), S. 361-366 
    ISSN: 1434-6079
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract. This paper describes the spectroscopy of Na3F both in the frequency and time domains. The photoionization efficiency curve shows two thresholds, associated to two isomers. The excited electronic states of the C2v isomer have been probed by photodepletion spectroscopy, and the results are used to analyze a time-resolved study of photoexcited Na3F, probed by photoionization. The pump-probe signal clearly shows damped oscillations, the period of which is fitted to $390\pm10$ fs, close to twice the previously measured bending mode of Na2F [1], while the relaxation time is $1275\pm50$ fs.
    Type of Medium: Electronic Resource
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