Full-Dimensional Ab Initio Potential Energy Surface and Vibrational Energy Levels of Li?H.

ABSTRACT: We built a full-dimensional analytical potential energy surface of the ground electronic state of Li?H from ca. 20,000 ab initio multi-reference configuration interaction calculations, including core?valence correlation effects. The surface is flexible enough to accurately describe the three dissociation channels: Li (2s ²S) + LiH (¹??), Li? (¹?_g?) + H (1s ²S) and 2Li (2s ²S) + H (1s ²S). Using a local fit of this surface, we calculated pure (J = 0) vibrational states of Li?H up to the barrier to linearity (ca. 3400 cm^-1 above the global minimum) using a vibrational self-consistent field/virtual state configuration interaction method. We found 18 vibrational states below this barrier, with a maximum of 6 quanta in the bending mode, which indicates that Li?H could be spectroscopically observable. Moreover, we show that some of these vibrational states are highly correlated already ca. 1000 cm^-1 below the height of the barrier. We hope these calculations can help the assignment of experimental spectra. In addition, the first low-lying excited states of each B?, B? and A? symmetry of Li?H were characterized.

SUBMITTER: Ahn Furudate M 

PROVIDER: S-EPMC6337435 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature