Photodissociation dynamics of H2S+ via the <i>A</i>2<i>A</i>1 (0, 8, 0) state

The photodissociation dynamics of the hydrogen sulfide cation (H2S+) (X2B1) were investigated using the time-sliced velocity map ion imaging technique. S+ (4Su) product images were measured at four photolysis wavelengths around 393.70 nm, corresponding to the excitation of the H2S+ (X2B1) cation to the A2A1 (0, 8, 0) state. The raw images and the derived total kinetic energy releases (TKERs) spectra exhibited partial rotational resolution for the H2 products. A sensitive dependence on the photolysis wavelength was observed in the TKER spectra and anisotropy parameters. Within a narrow excitation energy range of ∼12 cm-1, the H2 products showed two distinct rotational excitations. Furthermore, clear differences in anisotropy parameters were observed. These phenomena indicate that the rotational excitation of the H2S+ ions plays a role in the non-adiabatic photodissociation dynamics.