The competition of intense-field multiple-detachment with efficient photodissociation of F 2 ¯ is studied as a function of laser peak intensity. The main product channels are disentangled and characterized by 3D coincidence fragment imaging. The presented kinetic energy release spectra, angular distributions, as well as two-color pump–probe measurements allow identification of competing sequential and nonsequential mechanisms. Dissociative detachment, producing two neutral atoms (F + F), is found to be dominated by a sequential mechanism of photodissociation (F¯ + F), followed by detachment of the atomic anion fragment. In contrast, dissociative ionization (F + F + ) shows competing contributions of both a sequential two-step mechanism as well as a nonsequential double-detachment of the molecular anion, which are distinguished by the kinetic energy released in the dissociation. Triple-detachment is found to be nonsequential in nature and results in Coulomb explosion (F + + F + ). Furthermore, the measured kinetic energy release for dissociation on the 2 Σ g + state provides a direct measurement of the F 2 ¯ dissociation energy, D 0 = 1.26 ± 0.03 eV.
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Shahi et al. (2017) studied this question.
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