Abstract

We present the first high-resolution spectroscopic study of LiCs. LiCs is formed in a heat-pipe oven and studied via laser-induced fluorescence Fourier-transform spectroscopy. By exciting molecules through the $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}^{+}\text{\ensuremath{-}}B\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Pi}$ and $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}^{+}\text{\ensuremath{-}}D\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Pi}$ transitions vibrational levels of the $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}^{+}$ ground state have been observed up to $3\phantom{\rule{0.3em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}1}$ below the dissociation limit enabling an accurate construction of the potential. Furthermore, rovibrational levels in the $a\phantom{\rule{0.2em}{0ex}}^{3}\ensuremath{\Sigma}^{+}$ triplet ground state have been observed via singlet-triplet mixing in the higher excited states. With the help of coupled channels calculations, accurate singlet and triplet ground-state potentials were derived reaching the atomic ground-state asymptote. These potentials yield an accurate determination of the singlet and triplet ground-state dissociation energies and allow first predictions of cold collision properties of $\mathrm{Li}+\mathrm{Cs}$ pairs.

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