Signature of a conical intersection in the dissociative photoionization of formaldehyde

The valence-shell photoionization of formaldehyde is investigated by means of combining Photo-Electron Photo-Ion COincidence (PEPICO) experiments and ab initio calculations. The formation of three ion fragments: HCO + , CO + and H + 2 , via dissociative photoionization following excitation at 17 eV is discussed. The experimental results consisting of electron-ion kinetic energy correlation diagrams for the corresponding coincident events, i.e. (HCO + , e − ), (CO + , e − ) and (H + 2 , e − ), as well as the fragment abundance as a function of the binding energy, are complemented by high level electronic structure calculations including potential energy curves and on-the-fly trajectories. The results are consistent with a main relaxation process via internal conversion into rovibrationally excited levels of the H 2 CO + ground state, followed by statistical dissociation, preferentially into HCO + . The analysis of the experimental results reveals nevertheless the signature of a conical intersection controlling the dynamics and favoring dissociation into the molecular channel, CO + + H 2 . In addition, the minor formation of the H + 2 ion is suggested to occur through a roaming pathway on the cation excited state. Electron/ion coincidence experiments and ab initio calculations of the dissociative photoionization of formaldehyde reveal the presence of a conical intersection controlling the dynamics and favoring dissociation into the molecular channel, CO + + H 2 .