Photoelectrochemical
(PEC) water splitting serves as one of the
promising approaches for producing clean and renewable energy, and
their solar–hydrogen energy conversion efficiency depends on
the interfacial charge separation and carrier mobility. Herein, we
report an effective strategy to promote the PEC performance by fabricating
a WO3 photoanode rich in oxygen vacancies (Ov) modified
by NiFe-based layered double hydroxide (LDH). When WO3–Ov/NiFe-LDH
is used as a photoanode, the maximum photocurrent density at 1.8 V
versus RHE has been significantly enhanced to 2.58 mA·cm–2, which is 4.3 times higher than that of WO3. In addition, analogues were studied in controlled experiments without
Ov, which further demonstrated that the synergistic effect of NiFe-LDH
and Ov resulted in increased carrier concentration and driving force.
According to electrical impedance spectroscopy, X-ray photoelectron
spectroscopy, and Mott–Schottky analysis, the built-in electronic
field in WO3 homojunction, along with the accelerated hole
capture by the NiFe-LDH cocatalyst contributes to the improved charge
separation and transport in the WO3–Ov/NiFe-LDH
electrode. This work proposes an efficient and valuable strategy for
designing the structure of WO3-based photoelectrodes.