Novel NiWO4/ZnFe2O4 based S-Scheme heterojunction for solar light assisted degradation of brilliant green dye and sustainable hydrogen production
摘要
Herein, a novel NiWO4/ZnFe2O4 (NW/ZF) S-scheme heterojunction was fabricated via a precipitation–thermal treatment route and investigated for solar-light-driven photocatalysis, antibacterial performance and hydrogen evaluation. Structural analysis (XRD, FTIR, SEM, and EDX) of NW/ZF confirmed the formation of a well-defined heterointerface, while UV–Vis DRS and PL studies revealed a narrowed band gap (3.07 eV) and reduced charge-carrier recombination compared to pristine ZnFe2O4 (3.19 eV) and NiWO4 (3.30 eV). The band edge positions (ECB = − 0.23 eV for ZF; EVB = 3.43 eV for NW validated the S-scheme configuration, enabling strong redox potentials for radical generation. Under solar irradiation, the NW20/ZF exhibited 99% BG degradation within 50 min, with kapp value of 0.0928 min⁻¹, nearly fourfold higher than pristine ZF. The supporting role of SO4•−, h⁺, and O2•− as the primery species for dye mineralization was further confirmed by the radical quenching experiments. The photocatalyst maintained ca. >93% efficiency after five cycles, indicating high photostability. Antibacterial tests against Aeromonas hydrophila revealed concentration-dependent inhibition zones, reaching 8.33 ± 0.58 mm at 100 mg of catalyst. Synergistic enhancement was achieved upon coupling with PMS, attributed to the additional generation of SO₄•− species. The NW20/ZF shows 70 µmol.h− 1 photocatalytic hydrogen production activity higher than NW10/ZF (33 µmol.h− 1), NW30/ZF (68 µmol.h− 1) and NW40/ZF (59 µmol.h− 1). This study establishes NiWO4/ZnFe2O4 S-scheme heterojunctions as multifunctional photocatalysts with efficient solar-driven charge separation, high redox activity, and multiple applicability in dye remediation, microbial disinfection and hydrogen production.
Graphical Abstract