Abstract
Rubidium dimers residing on the surface of He nanodroplets are doubly ionized by an intense fs laser pulse leading to fragmentation into a pair of ions. We show that the kinetic energy of the fragment ions can be used to identify dimers formed in either the X ground state or in the lowest-lying triplet state, a . From the experiment, we estimate the abundance ratio of dimers in the a and X states as a function of the mean droplet size and find values between 4:1 and 5:1. Our technique applies generally to dimers and trimers of alkali atoms, here also demonstrated for , , and , and will enable fs time-resolved measurements of their rotational and vibrational dynamics, possibly with atomic structural resolution.
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