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Effect of Low Oxygen Annealing on Photoelectrochemical Water Splitting Properties of $α$-Fe$_2$O$_3$

Photoelectrochemical (PEC) water splitting is a promising method for conversing solar energy into chemical energy stored in the form of hydrogen. Nanostructured hematite ($α$-Fe$_2$O$_3$) is one of the most attractive materials for highly efficient charge carrier generation and collection due to its large specific surface area and shortening minority carrier diffusion length required to reach the surface. In the present work, PEC water splitting performance of $α$-Fe$_2$O$_3$ prepared by anodization of thin iron layers on an FTO glass and subsequent annealing in low O$_2$-Ar ambient with only 0.03% O$_2$ was investigated. The key finding is that annealing the anodic nanostructures with low oxygen concentration provides a strongly enhanced PEC performance compared with classic air annealing. The photocurrent of the former at 1.5 V vs. RHE results in 1.1 mA/cm2, being 11 times higher than that of the latter. The enhancement of the PEC performance for $α$-Fe$_2$O$_3$ annealed in low oxygen atmosphere can be attributed to controlled morphology, Sn doping, and introduction of oxygen vacancies, which contribute to the enhancement of the hole flux from the photogenerated site to the reactive surface and additionally lead to an enhanced hole transfer at the interface between the $α$-Fe$_2$O$_3$ and the electrolyte. From the obtained results, it is evident that low oxygen annealing is a surprisingly effective method of defect engineering and optimizing $α$-Fe$_2$O$_3$ electrodes for a maximized PEC water splitting performance.