First-principle investigation of structural, electronic, and phase stabilities in chalcopyrite semiconductors: insights from Meta-GGA functionals

Abstract

Abstract We undertake a comprehensive first-principles investigation into the factors influencing the optoelectronic efficiencies of P I Q I I I R 2 V I chalcopyrite semiconductors. The structural attributes, electronic properties, and phase stabilities are explored using various meta-GGA exchange-correlation (XC) functionals within the density functional framework. In particular, we assess the relative performance of these XC functionals in obtaining estimates of various relevant parameters. The structural parameter u in chalcopyrite semiconductors is a noteworthy aspect, as it is intrinsically tied to the extent of orbital hybridization between distinct atoms and thereby strongly influences the electronic properties. In general, the application of widely used GGA-PBE XC functional to these chalcopyrites results in unreliable predictions of band gaps and ‘u’ parameter due to delocalization errors that in turn arise due to the inclusion of d and f core electrons. While hybrid functionals offer remarkable accuracy through state-of-the-art methods, their main drawback lies in their computational expense and resource demands. Our findings strongly suggest that in comparison to GGA-PBE, the meta-GGA XC functionals perform quite well and provide results that closely align with experimental values. In particular, the r 2SCAN and rMGGAC XC functionals are preferable and superior for investigating chalcopyrites and other solid-state systems. This preference is rooted in their excellent performance and substantially reduced computational costs compared to hybrid functionals.