Abstract
Photoelectrochemical (PEC) water splitting is a promising method for the conversion of 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 a highly efficient charge carrier generation and collection due to its large specific surface area and the short minority carrier diffusion length. In the present work, the PEC water splitting performance of nanostructured α‐Fe
2
O
3
is investigated which was prepared by anodization followed by annealing in a low oxygen ambient (0.03 % O
2
in Ar). It was found that low oxygen annealing can activate a significant PEC response of α‐Fe
2
O
3
even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The photocurrent of the α‐Fe
2
O
3
annealed in the low oxygen at 1.5 V vs. RHE results as 0.5 mA cm
−2
, being 20 times higher than that of annealing in air. The obtained results show that the α‐Fe
2
O
3
annealed in low oxygen contains beneficial defects and promotes the transport of holes; it can be attributed to the improvement of conductivity due to the introduction of suitable oxygen vacancies in the α‐Fe
2
O
3
. Additionally, we demonstrate the photocurrent of α‐Fe
2
O
3
annealed in low oxygen ambient can be further enhanced by Zn‐Co LDH, which is a co‐catalyst of oxygen evolution reaction. This indicates low oxygen annealing generates a promising method to obtain an excellent PEC water splitting performance from α‐Fe
2
O
3
photoanodes.
Low oxygen annealing
can activate a significant photoelectrochemical response of α‐Fe
2
O
3
even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The α‐Fe
2
O
3
annealed in low oxygen ambient contains beneficial defects and promotes the transport of photogenerated holes; it can be attributed to the introduction of suitable oxygen vacancies in the α‐Fe
2
O
3
.