Abstract
Recent advances in energy conversion technologies, especially solar-driven photocatalytic water splitting, are vital for satisfying the increasing global need for sustainable and clean energy. Perovskite oxides have attracted considerable attention among photocatalytic materials due to their tunable electronic structures, exceptional stability, and promise for effective hydrogen generation and environmental remediation. In this study, the optoelectronic and photocatalytic (PC) characteristics of ATiO(3) (A = Ca, Mg) perovskites, undoped and codoped with Se and Zr, have been analyzed using ab initio simulations based on the density functional theory (DFT). The calculated formation energies for codoped systems range from -1.01 to -3.32 Ry/atom, confirming their thermodynamic stability. Furthermore, band structure calculations indicate that the undoped compounds CaTiO(3) and MgTiO(3) possess indirect band gaps of 2.766 eV and 2.926 eV, respectively. In contrast, codoping alters the electronic properties by changing the band gap from indirect to direct and reducing its energy, resulting in the direct band gap values 2.153 eV, 1.374 eV, 2.159 eV, and 1.726 eV for the compounds Ca8Ti7Zr1O23Se1, Ca8Ti6Zr2O22Se2, Mg8Ti7Zr1O23Se1, and Mg8Ti6Zr2O22Se2, respectively. Additionally, this codoping improves light absorption and optical conductivity in the visible and ultraviolet ranges. These enhancements become increasingly evident with elevated dopant concentrations, leading to intensified light-matter interactions. Analysis of the band edge potentials reveals that the Se-/Zr-codoped CaTiO(3) compounds satisfy the necessary criteria for the photodissociation of water, conferring on them an ability to generate H(2) and O(2) under light irradiation. However, under different pH conditions, Se-/Zr-codoped MgTiO(3) is expected to perform better at higher pH levels, while Se-/Zr-codoped CaTiO(3) is more effective at lower pH levels. These findings highlight the promise of codoped materials for renewable energy applications, such as solar-driven hydrogen production and optoelectronic devices, with pH being a critical factor in enhancing their photocatalytic performance.