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Physical Review Letters

Inner-electron multiphoton ionization of barium Rydberg states with picosecond pulses

Henrik Stapelfeldt, Dimitrios G. Papaioannou, Lambertus D. Noordam, Thomas F. Gallagher

Published Dec 2, 1991• 56 citations
Publisher

Abstract

We have studied multiphoton ionization of Ba 6snl Rydberg states by intense ps pulses and have shown that the duration of the laser pulse compared to the orbit time of the Rydberg electron determines the laser-atom interaction. For high-n states with a long orbit time, the loosely bound Rydberg electron is not affected by the intense laser pulse. Instead the inner electron is ejected by absorption of five photons, leaving the ${\mathrm{Ba}}^{+}$ ion in a Rydberg state. For low-n states the outer electron is ejected and the residual ${\mathrm{Ba}}^{+}$ ion can subsequently be multiphoton ionized to ${\mathrm{Ba}}^{++}$.

DOI
10.1103/physrevlett.67.3223

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Journal of the Optical Society of America B•Jan 1, 1988•6 citations
We have studied multiphoton ionization of Ba 6snl Rydberg states by intense ps pulses and have shown that the duration of the laser pulse compared to the orbit time of the Rydberg electron determines the laser-atom interaction. For high-n states with a long orbit time, the loosely bound Rydberg electron is not affected by the intense laser pulse. Instead the inner electron is ejected by absorption of five photons, leaving the Ba+{\mathrm{Ba}}^{+}Ba+ ion in a Rydberg state. For low-n states the outer electron is ejected and the residual Ba+{\mathrm{Ba}}^{+}Ba+ ion can subsequently be multiphoton ionized to Ba++{\mathrm{Ba}}^{++}Ba++.
We have investigated multiphoton ionization of Ba 6snl6snl6snl Rydberg states by intense 200-fs laser pulses. Specifically, we have excited Ba atoms to the 6sns6sns6sns and 6snd6snd6snd 15\ensuremath{\infty} states using two nanosecond lasers. The atoms were then irradiated with the fs pulses produced by a mode-locked, regeneratively amplified Ti:sapphire laser that is stepwise-tunable between 790 and 850 nm. We have used both the fundamental light and the second harmonic (395--425 nm) to investigate the ionization dynamics in these two wavelength regions. In contrast to previous experiments, in which laser pulses 5 ps or longer were used, our results indicate that excitation of Ba+{\mathrm{Ba}}^{+}Ba+ Rydberg states and Ba2+{\mathrm{Ba}}^{2+}Ba2+ photoions is relatively insensitive to the femtosecond laser wavelength. In addition, we find that, as the Kepler orbital period of the Ba Rydberg electron becomes comparable to this very small laser pulse width, the inner electron ionization process no longer appears to be instantaneous to the outer electron, and the outer electron is not projected onto Ba+{\mathrm{Ba}}^{+}Ba+ Rydberg states.
We have observed that the amount of photoionization from an atomic Rydberg state with a pulsed laser depends critically on the length of the pulse, whereas lowest-order perturbation theory implies that the yield depends only on the fluence (the integrated intensity) of the pulse. We have measured the yield for one-photon ionization with short (0.5–2.7-ps) high-intensity laser pulses from the 27d Rydberg state in barium. With equal fluence, the yield decreases for pulses shorter than the Kepler orbit time of the outer electron (2.2 ps) because not all of its wave function comes near the core during the length of the pulse. The observations and this classical picture are confirmed by quantum-mechanical calculations.
The authors have studied double ionization of Ba 6snl Rydberg states through resonant two-photon excitation of 8snl double-Rydberg states with n=13 and 14 and different l. The laser intensity dependence of Ba 2+ yield measured for l>or=8, when the electrons suffer long-range dipole interaction, shows a decrease from four-photon for l=8 to less than three for l=11. The four-photon dependence is due to autoionization decay populating the Ba + (7p) levels which gives an indirect signature to the Ba 2+ production. By increasing l this decay vanishes and the data show evidence of a direct double-ionization process via planetary-electron states for l>or=10. Additional intensity measurements performed for low l=6 states strongly mixed with 5fn'l' ones by short-range multipole interaction, reveal indirect Ba 2+ production and an individual case of partial stabilization due to destructive interference leading to direct double ionization.
We have observed suppression of ionization in Rydberg atoms irradiated by an intense short-pulse laser field. We find that single-photon ionization of the outer electron in a Ba 6snk Stark state can be severely suppressed relative to high-order (\ensuremath{\ge}3 photon) nonresonant multiphoton ionization of the tightly bound 6s core electron. This population trapping occurs in intense short laser pulses, where the bandwidth of the ionizing laser is greater than the spacings between adjacent Stark states, and may be due to a substantial modification of the initial Stark state via stimulated Raman processes through the continuum. The Ba+∗{\mathrm{Ba}}^{+\mathrm{*}}Ba+∗ ion should be left in a higly excited superposition state, or wave packet.
The authors have observed the production of Ba2+ from neutral Ba by intense picosecond laser pulses in the range 560-650 nm. Several new features have been observed, which were not observed with nanosecond pulses. Most of the strong resonances in Ba2+ production can be attributed to Ba+ transitions originating in the 6s1/2 or 5dj states, suggesting that the dominant process in double ionization in this intensity and wavelength regime is sequential removal of electrons. However, there are several resonances which cannot be attributed in this manner, evidence for possible alternative ionization mechanisms. Ba2+ production is strong throughout the region studied, at times comparable to that of Ba+. The authors have also looked for Ba2+ production in the range 280-325 nm, but no Ba2+ signal was observed in this part of the ultraviolet.