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Il Nuovo Cimento D

Laser-assisted particle-atom ionization. Analysis of triple and double differential cross-sections

R. Burlon, P. Cavaliere, G. Ferrante

Published Jul 1, 1984• 5 citations
Publisher
DOI
10.1007/bf02451868

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Laser highly selective ionization detector of single atoms and its applications

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IEEE Journal of Quantum Electronics•Sep 1, 1979•0 citations
Above 54.4eV54.4\phantom{\rule{0.3em}{0ex}}\mathrm{eV}54.4eV, two-photon double ionization of helium is dominated by a sequential absorption process, producing characteristic behavior in the single and triple differential cross sections. We show that the signature of this process is visible in the nuclear recoil cross section, integrated over all energy sharings of the ejected electrons, even below the threshold for the sequential process. Since nuclear recoil momentum imaging does not require coincident photoelectron measurement, the predicted images present a viable target for future experiments with new short-pulse vacuum ultraviolet (vuv) and soft x-ray sources.
We investigate the two-photon double ionization of beryllium atom induced by ultrashort pulses. We use a time-dependent formalism to evaluate the ionization amplitudes and generalized cross sections for the ejection of the 2s22{s}^{2}2s2 valence shell electrons in the presence of a fully occupied 1s21{s}^{2}1s2 frozen core shell. The relative contributions of the two-photon direct and sequential process are systematically explored by varying both pulse duration and central frequency. The energy and angular differential ionization yields reveal the signatures of both mechanisms, as well as the role of electron correlation in both the single and double ionization continua. In contrast with previous results on the helium atom, the presence of an electronic core strongly affects the final state leading to back-to-back electron emission even in the a priori less correlated two-photon sequential mechanism. In particular, a dominant pathway via excitation ionization through the Be+(2p){\mathrm{Be}}^{+}(2p)Be+(2p) determines the profiles and pulse-duration dependencies of the energy and angle differential yields.
Formulas are derived for the differential and integral cross sections associated with laser-induced excitation transfer. The theory is patterned closely after our recent treatment of laser-induced chemi-ionization. It is found that cross sections specific to single-photon absorption are proportional to the square of the cosine of the angle between the laser polarization and the initial relative velocity of the two colliding atoms. The distortion by a laser of the cross section for an elastic scattering event also is treated. Finally, a cross-section formula is derived for a collision-induced two-photon absorption, mediated by a single intermediate electronic state.