Theoretical study of efficiency of metal cations (Mg+, Ca+, and Ag+) for effective hydrogen storage

Abstract

The interaction between the metal cations and H2 molecule has been investigated using dispersion-corrected and -uncorrected hybrid density functional and CCSD(T) methods in conjunction with the correlation consistent triple-ζ quality basis sets for the storage of the H2 molecule. The molecular properties, potential energy surfaces, stability, binding energy and well-depth have been computed for the metal cation–dihydrogen (M+–H2, M = Mg, Ca, and Ag) complexes in the gas phase. The results obtained by the dispersion-corrected hybrid density functional B2PLYP-D method agree very well with the earlier experimental and theoretical results wherever available. Different components of the interaction energy have been estimated by the symmetry adapted perturbation theory (SAPT) to get physical insight into the interaction energy. Among the three complexes, only Ag+–H2 is the most stable complex and it accumulates more H2 molecules as the interaction between the metal cation Ag+ and the H2 molecule is the greatest.