Highly efficient photocatalytic performance of Z-scheme BTe/HfS2 heterostructure for H2O splitting

Abstract

Constructing van der Waals (vdW) heterostructures is one of the effective strategies for developing highly efficient photocatalysts. In this study, we have designed a novel BTe/HfS₂ heterostructure and systematically investigated its electronic properties and photocatalytic performance using first-principles calculations. The dynamic stability and thermodynamic stability of the heterostructure are verified through phonon spectrum simulations and ab initio molecular dynamics (AIMD) simulations, respectively, enhancing the likelihood of experimental synthesis. The bandgap of the BTe/HfS₂ heterostructure is 0.12 eV, and the band edge positions satisfy the overall water splitting requirements for photocatalysts. The charge density difference, work function, Bader charge, and band alignment all confirm that the BTe/HfS₂ heterostructure is a typical direct Z-scheme heterostructure, effectively facilitating the separation of photogenerated charge carriers and exhibiting strong redox capability. The solar-to-hydrogen (STH) efficiency of the BTe/HfS₂ heterostructure reaches as high as 17.32 %. Moreover, the heterostructure exhibits strong light absorption capability, reaching a magnitude of 10⁵. The carrier mobility of the BTe/HfS₂ heterostructure surpasses that of two individual monolayer materials, with the hole mobility in the x-direction reaching an impressive 28357.15 cm²s^-1V^-1. Simultaneously, the Gibbs free energy indicates that the BTe/HfS₂ heterostructure can undergo the hydrogen evolution reaction (HER) with only 0.19 eV of external potential at pH = 0. Moreover, at pH = 7, it can spontaneously convert H₂O into O₂. Therefore, the newly designed BTe/HfS₂ heterostructure offers a new direction for practical applications of photocatalysts.