Why Does a B₁₂H₁₂ Icosahedron Need Two Electrons to be Stable: A First-Principles Electron-Correlated Investigation...

In this work, we present large-scale electron-correlated computations on various conformers of B₁₂H₁₂ and B₁₂H₆ clusters to understand the reasons behind the high stability of dianion icosahedron (I) and cage-like B₁₂H₆ geometries. Although the B₁₂ icosahedron is the basic building block in some structures of bulk boron, it is unstable in its free form. Furthermore, its H-passivated entity, i.e., a B₁₂H₁₂ icosahedron, is also unstable in the free form. However, dianion B₁₂H₁₂ has been predicted to be stable as a perfect icosahedron in the free-standing form. To capture the correct picture for the stability of B₁₂H₁₂^2- and B₁₂H₆ clusters, we optimized these structures by employing the coupled-cluster singles and doubles (CCSD) approach and the cc-pVDZ basis set. We also performed the vibrational frequency analysis of the isomers of these clusters using the same level of theory to ensure the stability of the structures. For all of the stable geometries obtained from the vibrational frequency analysis, we additionally computed their optical absorption spectra using the time-dependent density functional theory (TDDFT) approach at the B3LYP/6-31G* level of theory. Our calculated absorption spectra could be probed in future experiments on these clusters.