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We calculate the dissociation of H₂⁺ in intense short pulsed laser fields for a variety of wavelengths and a wide range of initial vibrational states (v=0--14). While the low-v levels achieve 100% dissociation in the leading edge of the pulse, for high v there is an onset of stabilization, and significant [(5--50)%] population remains in bound vibrational states throughout the entire pulse. The dissociation is incomplete, and a coherent distribution of excited vibrational states is formed. This survival effect can be attributed to the trapping of portions of the initial vibrational wave packet in transient laser-induced potential wells.
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Giusti‐Suzor et al. (1992) studied this question.
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