Insight into the Effect of Anionic–Anionic Co-Doping on BaTiO3 for Visible Light Photocatalytic Water Splitting: A First-Principles Hybrid Computational Study

Abstract

In this research, we thoroughly studied the electronic properties and optical absorption characteristics with double-hole coupling of anions–anion combinations for designing effective photocatalysts for water redox using first-principles methods within the hybrid Heyd–Scuseria–Ernzerhof (HSE06) exchange–correlation formalisms. The findings reveal that the values of formation energy of both the anion mono- and co-doped configurations increase monotonically as the chemical potential of oxygen decreases. The N–N co-doped BaTiO3 exhibits a more favorable formation energy under an O-poor condition compared with other configurations, indicating that N and N pairs are more likely to be synthesized successfully. Interestingly, all the co-doping configurations give a band gap reduction with suitable position for oxygen production and hydrogen evolution. The obtained results demonstrate that all the co-doped systems constitute a promising candidate for photocatalytic water-splitting reactions. Furthermore, the enhanced ability of the anionic-anionic co-doped BaTiO3 to absorb visible light and the positions of band edges that closely match the oxidation-reduction potentials of water suggest that these configurations are viable photocatalysts for visible-light water splitting. Therefore, the wide-band gap semiconductor band structures can be tuned by double-hole doping through anionic combinations, and high-efficiency catalysts for water splitting using solar energy can be created as a result.