Laser-induced Coulomb Explosion Imaging of Alkali Dimers on Helium Nanodroplets

Abstract

Alkali dimers, Ak2, residing on the surface of He nanodroplets are doubly ionized due to multiphoton absorption from an intense, 50-fs laser pulse leading to fragmentation into a pair of alkali cations. Based on the measured kinetic energy distributions, P(Ekin), of the Ak+ fragment ions, we retrieve the distribution of internuclear distances, P(R), via the Ak22+ potential curve. Results are obtained for Na2, K2, Rb2, and Cs2 in both the 1 1g+ ground state and in the lowest-lying triplet state 1 3u+, and for Li2 in the 1 3u+ state. For Li2, K2, and Rb2, the center of the measured P(R)'s is close to the center of the wave function, (R), of the vibrational ground state in the 1 1g+ and 1 3u+ states, whereas for Na2 and Cs2 small shifts are observed. For all the Ak2, the width of the measured P(R) is broader than |(R)|2 by a factor of 2-4. We discuss that resonance effects in the multiphoton ionization and interaction of the Ak+ ion with the He droplet give rise to the observed deviations of P(R) from |(R)|2. Despite these deviations, we deem that timed Coulomb explosion will allow imaging of vibrational wave packets in alkali dimers on He droplets surfaces.

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