### Abstract

We present very accurate calculations of the ground-state potential energy curve (PEC) of the LiH molecule performed with all-electron explicitly correlated Gaussian functions with shifted centers. The PEC is generated with the variational method involving simultaneous optimization of all Gaussians with an approach employing the analytical first derivatives of the energy with respect to the Gaussian nonlinear parameters (i.e., the exponents and the coordinates of the shifts). The LiH internuclear distance is varied between 1.8 and 40 bohrs. The absolute accuracy of the generated PEC is estimated as not exceeding 0.3 cm^{-1}. The adiabatic corrections for the four LiH isotopologues, i.e., ^{7}LiH, ^{6}LiH, ^{7}LiD, and ^{6}LiD, are also calculated and added to the LiH PEC. The aforementioned PECs are then used to calculate the vibrational energies for these systems. The maximum difference between the computed and the experimental vibrational transitions is smaller than 0.9 cm^{-1}. The contribution of the adiabatic correction to the dissociation energy of ^{7}LiH molecule is 10.7 cm^{-1}. The magnitude of this correction shows its importance in calculating the LiH spectroscopic constants. As the estimated contribution of the nonadiabatic and relativistic effects to the ground state dissociation energy is around 0.3 cm^{-1}, their inclusion in the LiH PEC calculation seems to be the next most important contribution to evaluate in order to improve the accuracy achieved in this work.

Original language | English (US) |
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Article number | 064117 |

Journal | Journal of Chemical Physics |

Volume | 134 |

Issue number | 6 |

DOIs | |

State | Published - Feb 14 2011 |

### ASJC Scopus subject areas

- Physics and Astronomy(all)
- Physical and Theoretical Chemistry

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## Cite this

*Journal of Chemical Physics*,

*134*(6), [064117]. https://doi.org/10.1063/1.3554211