In Situ Reduction Fabricated Pt-Mediated Bi₂WO₆/g-C₃N₄ Heterojunction with Unconventional Z-Scheme Charge Transfer for Enhanced Photocatalysis and Hydrogen Evolution

High Resolution Image Download MS PowerPoint Slide A novel Pt-mediated Z-scheme heterojunction photocatalyst, Pt-Bi 2 WO 6 /g-C 3 N 4 (Pt-BWO/g-CN), was synthesized via an in situ reduction strategy, enabling precise Pt positioning as an electron mediator between BWO and g-CN. Structural and morphological analyses (FESEM, HRTEM, and BET) confirmed nanoscale integration, uniform Pt dispersion, and high surface area. X-ray photoelectron spectroscopy (XPS) revealed binding energy shifts indicative of efficient interfacial charge transfer, while UV–vis diffuse reflectance spectroscopy (DRS) and Mott–Schottky analyses confirmed favorable band alignment consistent with a direct Z-scheme pathway. Photoluminescence (PL) and photoelectrochemical measurements demonstrated suppressed electron–hole recombination and enhanced charge separation. Electron paramagnetic resonance (EPR) provided compelling mechanistic evidence: DMPO-trapped spectra detected abundant • OH and • O 2– radicals under light irradiation, TEMP-trapped spectra confirmed 1 O 2 formation, and intrinsic oxygen vacancies ( g ≈ 2.003) were observed even in the dark, decreasing upon illumination, supporting defect-assisted charge transfer. The optimized Pt-BWO/g-CN achieved complete RhB degradation and 85% RR4 removal within 60 min under visible light, alongside a hydrogen generation rate of 5364.96 μmol g –1 h –1 (STH efficiency of 3.4% and AQY of 3.5%). Radical scavenging identified h + and • O 2 – as the dominant active species. This work demonstrates a scalable route to high-performance Z-scheme photocatalysts with dual capability in pollutant degradation and solar hydrogen generation, underpinned by direct spectroscopic validation of the charge transfer pathway.