Construction of Pt-decorated g-C3N4/Bi2WO6Z-scheme composite with superior solar photocatalytic activity toward rhodamine B degradation

Abstract

Highly efficient visible-light-driven Pt-decorated g-C3N4/Bi2WO6 hybrid photocatalysts were successfully prepared via a photodeposition method. The microstructures and optical properties of the prepared samples were characterized by transient photocurrent experiments, X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), UV–vis diffused reflectance spectra (DRS), photoluminescence (PL), electron spin resonance (ESR) spectroscopy and X-ray photoelectron spectroscopy (XPS) techniques. FESEM and TEM images show that metallic Pt particles disperse on the surface of g-C3N4/Bi2WO6 hybrid. Pt-decorated g-C3N4/Bi2WO6 compsites exhibited excellent DRS attribute to the surface plasmonic resonance (SPR) of Pt particles and g-C3N4/Bi2WO6. The PL results verified that the suitable band potential of g-C3N4 and Bi2WO6 for construction of Z-type photocatalytic system. In the photocatalytic experiment, results showed that Pt(1%)-g-C3N4/Bi2WO6 photocatalysts displayed higher photocatalytic activity than either pure g-C3N4 or Bi2WO6 for the degradation of Rhodamine B (RhB). Additionally, the free-radical trapping experiments and ESR disclose that the hole (h+), superoxide radical (O2−) and hydroxyl radical (·OH) acted as reactive species. Based on above, a possible plasmonic Z-scheme mechanism for organics degradation over Pt-decorated g-C3N4/Bi2WO6 was proposed.