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Abstract

Spectroscopic studies of aluminum monofluoride (AlF) have revealed its highly favorable properties for direct laser cooling. All Q lines of the strong A¹Π ← X¹Σ⁺ transition around 227 nm are rotationally closed and thereby suitable for the main cooling cycle. The same holds for the narrow, spin-forbidden a³Π ← X¹Σ⁺ transition around 367 nm, which has a recoil limit in the µK range. We here report on the spectroscopic characterization of the lowest rotational levels in the a³Π state of AlF for v = 0–8 using a jet-cooled, pulsed molecular beam. An accidental AC Stark shift is observed on the a³Π₀, v = 4 ← X¹Σ⁺, v = 4 band. By using time-delayed ionization for state-selective detection of the molecules in the metastable a³Π state at different points along the molecular beam, the radiative lifetime of the a³Π₁, v = 0, J = 1 level is experimentally determined as τ = 1.89 ± 0.15 ms. A laser/radio frequency multiple resonance ionization scheme is employed to determine the hyperfine splittings in the a³Π₁, v = 5 level. The experimentally derived hyperfine parameters are compared to the outcome of quantum chemistry calculations. A spectral line with a width of 1.27 kHz is recorded between hyperfine levels in the a³Π, v = 0 state. These measurements benchmark the electronic potential of the a³Π state and yield accurate values for the photon scattering rate and for the elements of the Franck–Condon matrix of the a³Π–X¹Σ⁺ system.