Ab initio studies of the ground and first excited states of the Sr-H${}_2$ and Yb-H${}_2$ complexes

Abstract

Accurate intermolecular potential-energy surfaces (IPESs) for the ground and first excited states of the Sr-H${}_2$ and Yb-H${}_2$ complexes were calculated. After an extensive methodological study, the CCSD(T) method with the Douglas-Kroll-Hess Hamiltonian and correlation-consistent basis sets of triple-$\zeta$ quality extended with 2 sets of diffuse functions and a set of midbond functions were chosen. The obtained ground-state IPESs are similar in both complexes, being relatively isotropic with two minima and two transition states (equivalent by symmetry). The global minima correspond to the collinear geometries with $R=$ 5.45 and 5.10~Å and energies of $-$27.7 and $-$31.7~cm${}^{-1}$ for the Sr-H${}_2$ and Yb-H${}_2$ systems, respectively. The calculated surfaces for the Sr(${}^{3}P$)-H${}_2$ and Yb(${}^{3}P$)-H${}_2$ states are deeper and more anisotropic and they exhibit similar patterns within both complexes. The deepest surfaces, where the singly occupied \textit{p}-orbital of the metal atom is perpendicular to the intermolecular axis, are characterised by the global minima of ca. $-$2053 and $-$2260~cm${}^{-1}$ in the T-shape geometries at $R=$ 2.41 and 2.29~Å for Sr-H${}_2$ and Yb-H${}_2$, respectively. Additional calculations for the complexes of Sr and Yb with the He atom revealed a similar, strong dependence of the interaction energy on the orientation of the \textit{p}-orbital in the the Sr(${}^{3}P$)-He and Yb(${}^{3}P$)-He states.

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