Photodetachment and Tunneling Dissociation of Cryogenic Double-Rydberg Anions NH4.

The Rydberg radical NH4 and the double Rydberg anion (DRA) NH4- have long aroused researchers' interests due to their potential for exploring the reaction dynamics of the H + NH3 → H2 + NH2 reaction, a prototypical penta-atomic system. In this study, we present high-resolution photodetachment spectroscopy of DRA NH4- and ion-molecule complex H-(NH3). We observed multiple new photodetachment channels of DRA NH4-. The energy level of the excited state (3p 2T2) of the Rydberg radical NH4 was determined to be 15052(94) cm-1, in excellent agreement with the principal Schüler band (15061.61 cm-1). Additionally, we observed the tunneling dissociation of NH4- in a cryogenic ion trap with its dissociation lifetime determined to be 19(2) ms.