Design of cluster structure units with large surface areas for high-capacity hydrogen storage: In the case of Si12C12H24

Abstract

Using density functional theory, we designed novel cluster structure units with large surface areas for hydrogen storage through the surface functionalization of a stable Si12C12H24 nanocage with CONH2 organic molecules and Li atoms. Two structures, namely, Si12C12H12(CONHLi)12 and Si12C12H12(CONLi2)12, are proposed. The structures are stable at room temperature and show suitable hydrogen adsorption energies. Modification can enlarge the surface area of the two structures compared with the original cluster. In addition, the O and N anions participate in the adsorption of H2 molecules in addition to the Li cations. The average hydrogen binding energy for Si12C12H12(CONHLi)12·82H2 is 0.135 eV/H2 and the average hydrogen binding energy for Si12C12H12(CONLi2)12·84H2 is 0.134 eV/H2 when these cluster structure units reach their maximum H2 uptake capacity. The gravimetric hydrogen percentages are 13.18 and 12.60 wt%, respectively. With such a structural unit, a suitable linker allows the assembly of metal organic framework-like porous materials that display satisfactory hydrogen storage properties at room temperature.