Vibronic structure in C2H and C2D from anion slow electron velocity-map imaging spectroscopy.

The C2H and C2D radicals are investigated by slow electron velocity-map imaging (SEVI) of the corresponding anions. This technique offers considerably higher resolution (<0.5 meV) than photoelectron spectroscopy. As a result, SEVI spectra of the two isotopomers yield improved electron affinities and reveal many new structures that are particularly sensitive to vibronic coupling between the ground 2Sigma+ and low-lying excited 2Pi states. These structures, which encompass more than 5000 cm(-1) of internal excitation, are assigned with the aid of previous experimental and theoretical work. We also show that SEVI can be applied to photodetachment transitions resulting in ejection of an electron with orbital angular momentum l=1, a p wave, in contrast to anion zero-electron kinetic energy spectroscopy which is restricted to s-wave detachment.