Photoelectrochemical
(PEC) water splitting activity of
Fe2O3 is restricted by the rapid recombination
of photocarriers
both in bulk and on the surface and slack water oxidation kinetics.
Herein, this work describes a method for designing and constructing
a Fe2O3 photoanode by sequential in-situ and ex-situ incorporation of dopants for an effective
PEC water splitting strategy. In-situ Zr doping can
be used to improve the bulk conductivity of the photoanode by augmenting
the majority carriers while generating surface defects that limit
effective water oxidation at the photoelectrode/electrolyte interface.
Therefore, the main emphasis of this study is on ex-situ codoping with Be, which boosts the surface charge transfer properties via the passivation of surface-trapping states, thus leading
to effective hole migration to the electrolyte. As a consequence,
the Zr/Be codoped Fe2O3 photoanode (Zr/Be-HT)
attained an 83% improved photocurrent density (1.92 mA/cm2) than that of bare-Fe2O3 at a water oxidation
potential of 1.23 V vs. RHE. Mott–Schottky
plots, electrochemical impedance spectroscopy, a transient time constant,
and bulk and surface charge separation efficiency evaluations were
conducted to comprehend the functions of Zr and Be dopants. Finally,
the Co–Pi cocatalyst-coated Zr/Be-HT photoanode produced 33.75
and 17.76 μmol/h H2 and O2 gases, respectively,
at 1.23 V vs. RHE. This codoping strategy could lead
to a more sustainable and efficient method for producing hydrogen
fuel.