Universal all-particle explicitly-correlated Gaussians for non-Born–Oppenheimer calculations of molecular rotationless states

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Complex explicitly correlated one-center all-particle Gaussian functions (CECGs) are tested as basis functions for molecular non-Born–Oppenheimer (non-BO) calculations. The tests concern the complete spectrum of the 23 bound pure vibrational states of the HD+ ion. The tests show that CECGs are very effective in representing both the nuclear-nuclear correlation and the vibrational oscillation of the wave functions in terms of the internuclear distance. This finding is important because it paves the way for high-accuracy non-BO calculations of bound vibrational states of molecules with more than two nuclei that have never been performed before.