Abstract

The double photoionization of N2O and C2H2 molecules by linearly polarized light in the 30-50 eV energy range has been studied by coupling ion imaging and electron-ion-ion coincidence techniques. In the case of N2O, for the two possible dissociative processes leading to N++NO+ and O++N2 +, anisotropic angular distributions of ionic fragments have been measured, indicating that N2O ionizes when its axis is parallel to the light polarization vector and the fragments are separating in a time shorter than the dication rotational period. In the case of C2H2, the two-body dissociation reactions producing C2H++H+ and CH2 ++C+ have shown almost isotropic angular distributions, indicating the double photoionization occurs when acetylene is mainly oriented perpendicularly to the light polarization vector. The analysis of results based on a Monte Carlo trajectory simulation provides: i) the metastable N2O2+ and C2H2 2+ dication lifetimes, ii) the kinetic energy release (KER) distribution for the final ions resulting from the Coulomb explosion, and iii) the anisotropy β parameter values as a function of the investigated photon energy extracted from the measured ionic angular distributions.

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