Plasmonic-driven charge separation through combining Ag nanoparticles (Ag NPs) to form a double Z-scheme heterostructure in WO3/BiOCl/g-C3N4 for the photocatalytic degradation of antibiotics.

Abstract

Integrating a heterojunction system with the impact of surface plasmon resonance (SPR) is an executable and innovative tactic for photocatalyst amelioration. Ag nanoparticle (Ag NP)-modified WO3/BiOCl/g-C3N4 (WB-CN) was favorably fabricated through in situ photo deposition assembly to form double heterojunctions (A-WBCN). The degradation performance of A-WBCN is better than that of pure g-C3N4 (CN) and WO3/BiOCl (WB), it can degrade more than 90% of OFLX within 20 minutes, due to Ag NPs performing as a bridge for electron mediators, apart from the implications of SPR in A-WBCN. The results of UV diffuse reflectance spectroscopy indicate that loading with Ag NPs can expand the light absorption range of WB-CN to near-infrared. The photoluminescence spectra and transient photocurrent spectra indicate that Ag NP loading significantly improves the separation efficiency of photogenerated carriers. Density functional theory (DFT) simulation results show that the introduction of Ag NPs can change the direction of carrier movement, resulting in bending of the energy bands of WB and CN, improving the redox ability of A-WBCN, and improving its photocatalytic efficiency. In addition, the intermediate products of OFLX was determined by HPLC-MS analysis. The spin electron resonance (ESR) results indicate that ˙O2- and ˙OH are the main active species in photocatalytic degradation. This work furnishes a fresh idea for upgrading photocatalytic performance and advancing electron transfer.