Theoretical screening of single atom doping on β-Ga2O3 (100) for photoelectrochemical water splitting with high activity and low limiting potential

Abstract

Photoelectrochemical (PEC) water splitting combined with renewable energy is an appealing approach for solar energy conversion and storage. Monoclinic gallium oxide (β-Ga₂O₃) has been identified as a promising photoelectrode for PEC because of its good electrical conductivity and chemical and thermal stability. However, the wide bandgap (around 4.8 eV) and the recombination of photogenerated electrons and holes inside β-Ga₂O₃ limit its performance. Doping β-Ga₂O₃ is a practical strategy to enhance photocatalytic activity, but studies on doped β-Ga₂O₃ based photoelectrodes are lacking. In this study, we evaluate the doping effect of ten different dopants for β-Ga₂O₃ photoelectrode at the atomic level using density functional theory calculations. In addition, the oxygen evolution performance is evaluated on doped structures as it is considered the bottleneck reaction in water slitting on the anode of the PEC cell. Our results suggest that rhodium doping is optimal as it demonstrated the lowest overpotential for oxygen evolution reaction. We performed further electronic structure analysis, indicating the narrower bandgap and enhanced photogenerated electron–hole transfer comparing with β-Ga₂O₃ are the main reasons for the improved performance after Rh doping. This study demonstrates that doping is an attractive strategy for the development of efficient Ga₂O₃-based photoanodes and it will be of great importance in helping the design of other semiconductor-based photoelectrodes for practical application.