Herein,
we have designed nonstoichiometric WO3, coupled
with ZnCr layered double hydroxide (LDH) nanosheeet through Ag nanoparticle
as the solid-state electron mediator to form WO3–X/Ag/ZnCr LDH Z-scheme photocatalyst. The presence
of oxygen defect levels in as-synthesized materials was confirmed
by Raman, X-ray photoelectron spectroscopy (XPS), and photoluminescence
(PL) analyses. The photocatalytic performance of the catalysts was
investigated by the tetracycline degradation and H2 energy
production under visible light irradiation. The WO3–X/Ag/ZnCr LDH ternary heterostructure exhibits superior
activity toward tetracycline degradation and hydrogen evolution. The
excellent photocatalytic performance of the catalyst was attributed
to the synergistic effects among three species (WO3–X, Ag, and ZnCr LDH) and the enhanced separation efficiency
of photoinduced charge carriers through the Z-scheme WO3–X/Ag/ZnCr LDH system. In addition, the created oxygen
deficiency on WO3–X could improve
the photocatalytic behavior of ZnCr LDH in heterostructure by delaying
the recombination efficiency of photoexcited electron–hole
pairs. Furthermore, the higher affinity of tetracycline at the oxygen
defect levels of the photocatalyst supports the high rate of tetracycline
degradation. The enhanced photocatlytic activity of the catalysts
was further supported by PL spectra and photoelectrochemical studies
(electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry
(LSV) plot). The present research opens up a new strategy for designing
highly efficient visible light-induced Z-scheme-based photocatalysts
with high population of active sites for energy and environmental
applications in a sustainable manner.