Interactions and dynamics of metastable triplet-state helium dimer with Ne and Ar
arXiv:2609.34713
Abstract
Helium dimer in its metastable triplet electronic state, He, is a promising candidate for direct laser cooling and precision measurements. Interactions and collisions involving He remain unexplored in ultracold and cold energy domains. Here, we present the first theoretical investigation of intermolecular interactions and collision dynamics of He+Ne van der Waals complex. For the ground electronic state, , we employ a spin-restricted coupled cluster method with single, double, and noniterative triple excitations. The resulting interaction potential exhibits an extremely shallow well with a depth of 4.612 cm. We construct a three-dimensional vibrationally averaged potential energy surface. Using this surface, we perform full close-coupling calculations including fine-structure levels of He to investigate collisional excitation and quenching induced by Ne. We analyze the low-energy scattering dynamics and model resonant features associated with quasi-bound states supported by interaction potential. Propensity rule for fine-structure conserving transitions is established. We additionally consider He+Ar collisions and compare their energy dependence and resonance structure with those of He+Ne. The He+Ar system exhibits a richer resonance structure, highlighting the sensitivity of low-energy scattering to interaction potential and reduced mass. Calculated PES and scattering properties provide a reliable benchmark for description of He+Ne van der Waals complex and may be useful for interpretation of future experimental spectra and collision measurements.