Structure, stability, absorption spectra and aromaticity of the singly and doubly silicon doped aluminum clusters Al(n)Si(m)(0/+) with n = 3–16 and m = 1, 2

Structures of the binary Al(n)Si(m) clusters in both neutral and cationic states were investigated using DFT and TD-DFT (B3LYP/6-311+G(d)) and (U)CCSD(T)/cc-pvTZ calculations. Silicon-doped aluminum clusters are characterized by low spin ground states. For small sizes, the Si dopant prefers to be located at vertices having many edges. For larger sizes, the Si atom prefers to be endohedrally doped inside an Al(n) cage. Relative stability, adiabatic ionization energy and dissociation energies of each cluster size were evaluated. A characteristic of most Si doped Al clusters is the energetic degeneracy of two lowest-lying isomers. Calculated results confirm the high stability of the sizes Al(4)Si(2), Al(12)Si and Al(11)Si(2)(+) as “magic” clusters, that exhibit 20 or 40 shell electrons and are thermodynamically more stable as compared to their neighbors. Electronic absorption spectra of isoelectronic magic clusters Al(13)(−), Al(12)Si, and Al(11)Si(2)(+) that have two pronounced bands corresponding to blue and violet lights, have been rationalized by using the electron shell model. The magnetically included ring current density (MICD) analyses suggest that they are also aromatic structures as a result of the “magic” 40 shell electrons.