Photofragment imaging and electronic spectroscopy of Al2.

Abstract

A combination of photodissociation spectroscopy, ion imaging, and high-level theory is employed to refine the bond strength of the aluminum dimer cation (Al2+) and elucidate the electronic structure and photodissociation dynamics between 38 500 and 42 000 cm-1. Above 40 400 cm-1, structured photodissociation is observed from an extremely anharmonic excited state, which calculations identify as the double minimum G 2Σ+u state. The photodissociation spectrum of the G 2Σ+u ← X 2Σ+g transition in Al2+ gives an average vibrational spacing of 170 cm-1 for the G 2Σ+u state and ν0 = 172 cm-1 for the ground state. Photofragment images of G 2Σ+u ← X 2Σ+g transitions indicate that once the Al (4P) + Al+ (1S) product channel is energetically accessible, it dominates the lower energy, spin-allowed pathways despite being spin-forbidden. This is explained by a proposed competition between radiative and non-radiative decay pathways from the G 2Σ+u state. The photofragment images also yield D0 (Al+-Al) = 136.6 ± 1.8 kJ/mol, the most precise measurement to date, highlighting the improved resolution achieved from imaging at near-threshold energies. Additionally, combining D0 (Al+-Al) with IE (Al) and IE (Al2) gives an improved neutral D0 (Al-Al) = 136.9 ± 1.8 kJ/mol.