In this study, density functional theory (DFT)-based investigations are carried out using the CASTEP code. The plane-wave pseudopotential method is used to explore the multifunctional properties, including the structural, electronic spectra, thermo-mechanical and hydrogen storage properties, of hydrogen-rich mixed-anionic (Li3H4N2X, where X = F, Cl, Br, and I) halides. The exchange–correlation interactions are treated within the generalized gradient approximation (GGA) using the Perdew–Burke–Ernzerhof (PBE) functional, while the hybrid HSE06 function is used for accurate band gap predictions. Moreover, the optical properties of the halides are analyzed under the influence of UV–Vis radiation instances. The band gap values of these orthorhombic-structured halides lie in the visible-to-UV regions of radiation, with values of 2.97 eV, 3.12 eV, 3.06 eV and 3.28 eV, respectively. Such band gap values allow these materials to absorb nearly 75% to 90% of incoming radiation, with absorption values around (105 cm−1). These favorable opto-electronic responses make these halides suitable for solar radiation energy conversion applications. Stable thermodynamic responses and the mechanical nature of the mixes (brittle for Li3H4N2Br and ductile for the rest) reveal their practical applicability for flexible photonics. Moreover, due to the presence of rich hydrogen atoms, the Li3H4N2F halide exhibits a gravimetric ratio of around 6.0 wt%, which is higher than the standard (5.5 wt%) value defined by the US DOE. Similarly, GHSC values of 2.5 wt% for Li3H4N2I, 3.5 wt% for Li3H4N2Br, and 5.0 wt% for Li3H4N2Cl are reported; these values indicate that these compounds possess strong potential for use in the hydrogen fuel cells required in light-duty vehicles.
Yaqoob et al. (Mon,) studied this question.