“…Hydrogen and oxygen production from photoelectrochemical (PEC) water splitting has attracted heightened interest in solar fuel application. − Hematite (α-Fe 2 O 3 ; E g = 2.2 eV) for water oxidation is stable, inexpensive, and earth-abundant. − With a 16.8% theoretical solar-to-hydrogen conversion efficiency, the PEC performance of α-Fe 2 O 3 is mainly limited by the disagreement between the long light absorption depth (118 nm light penetration depth in λ = 550 nm) and small hole diffusion length (transportation distance of carriers of <4 nm and lifetime of carriers of <10 ps). ,, Most photons absorbed by a relatively thick hematite layer are combined and do not take part in the water oxidation reaction at the PEC system. To shorten the hole-transport distance to the electrode/electrolyte interface and to enhance electrical conductivity for combating the lifetime of short carriers, many works have been studied on the formation of nanostructures − and element doping. − The developed various nanostructures − for hematite contain zero dimension (0D), ,− one dimension (1D), ,− two dimension (2D), − and three dimension (3D). ,− The one-dimensional nanostructure of α-Fe 2 O 3 is proven to be favorable for shortening the charge carrier migration distance. ,,,− There are works that focus on constructing a more favorable morphology and structure to increase the ultraviolet–visible (UV–vis) light absorption, decrease the electrochemical resistance, and reduce the recombination of the surface charge carrier. , Another issue limiting the PEC performance of hematite is the slow kinetics of the oxygen evolution reaction (OER). Transition-metal-based elements as functional catalysts for the OER in alkaline solution have been explored to improve the OER rate and reduce the overpotential, making this four-electron process with higher efficiency.…”