The primary challenge hindering the widespread adoption of hydrogen energy is its storage, highlighting the need for effective storage media. In this study, we utilize first-principles calculations to systematically evaluate the superalkali cluster OLi3 decorated on a CN monolayer for its potential as an efficient hydrogen storage material. Our findings reveal that the OLi3 cluster binds to each side of the CN monolayer through a charge transfer mechanism, exhibiting a binding energy of 12.32 eV per OLi3. The OLi3 cluster, when integrated into the OLi3-decorated CN monolayer, displays a loss of charge, thereby creating a localized electric field around the cluster. This phenomenon facilitates the polarized hydrogen adsorption process through a combination of orbital interactions, electrostatic interactions, and van der Waals forces. The maximum number of hydrogen molecules that can be adsorbed by the 2(OLi3)-decorated CN monolayer is 12. The average adsorption energy per hydrogen molecule is 0.185 eV, with a gravimetric density of 9.45 wt %, significantly exceeding the target set by the U.S. Department of Energy (6.5 wt %). Additionally, the effects of the temperature and pressure on hydrogen storage performance indicate that the hydrogen-adsorbed structures of the OLi3-decorated CN monolayer remain stable at room temperature under mild pressure. These results suggest that the OLi3-decorated CN monolayer may serve as a promising material for reversible hydrogen storage.
Keywords: OLi3 superalkali cluster; first-principles calculations; graphitic carbon nitride; hydrogen storage.