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Hydrogen storage is indeed fundamental to utilizing H 2 effectively, and porous carbon materials have emerged as highly promising supports for this purpose. γ-Graphyne (γGy) possesses abundant chemical bonds, considerable porosity, and exceptional chemical stability, positioning it as a promising candidate for hydrogen storage and transport applications. In this study, we conducted density functional theory calculations to investigate the potential of Li- and Na-loaded γGy as hydrogen storage materials. Our findings reveal that the hydrogen storage capacity (HSC) of Na-loaded γGy falls significantly short of expectations, whereas Li-loaded γGy demonstrates a notably higher HSC. Subsequently, our calculations indicate that B-doping of γGy does not promote favorable HSC, whereas N-doping exhibits a beneficial effect. Furthermore, we observed that tensile strain favors the hydrogen storage properties of 4Li@γGy and 4Li@N-γGy, while compressive strain enhances the hydrogen storage characteristics of 4Li@B-γGy. Notably, we discovered the capacity to adjust the valence band center of Li (ɛ VB), consequently influencing the hydrogen storage performance of γGy. Our investigation suggests that increased overlap between ɛ VB in Li-loaded graphyne and the effective alignment of H 2 and the supporting structure augments the binding force between Li and H 2 , thereby amplifying the HSC. [Display omitted] • Li-loaded γ-Graphyne stores H 2 via Valence-like interaction. • B- and N-doping can enhance storage capacity of Li-loaded γ-Graphyne. • Valence band center of Li tuned by strain achieve efficient adsorption-desorption. [ABSTRACT FROM AUTHOR]