Decoration of TiO2/g-C3N4 Z-scheme by carbon dots as a novel photocatalyst with improved visible-light photocatalytic performance for the degradation of enrofloxacin

Abstract

A novel visible-light-driven carbon dot (CDs)/TiO₂/g-C₃N₄ photocatalyst was successfully synthesized by doping CDs in TiO₂ nanoparticles and the surface of g-C₃N₄ nanosheets via a facile hydrothermal process and was confirmed by characterization methods. UV-vis diffuse reflectance spectra (DRS) revealed that CDs/TiO₂/g-C₃N₄ showed obvious additional absorption in the 370–450 nm region. DMPO spin-trapping ESR spectra demonstrated the existence of O₂˙⁻ and ·OH. The photocatalytic activity of the CDs (1.0 wt%)/TiO₂/g-C₃N₄ was remarkably enhanced as compared to that of the single components (TiO₂ and g-C₃N₄) and double component (TiO₂/g-C₃N₄) towards the degradation of enrofloxacin (ENX) under visible-light irradiation. About 91.6% of ENX was decomposed by CDs (1.0 wt%)/TiO₂/g-C₃N₄ in 1 h, which is nearly 3.95 times, 4.82 times, and 1.69 times that for TiO₂, g-C₃N₄, and TiO₂ (90.0 wt%)/g-C₃N₄, respectively. Scavenging experiments revealed that O₂˙⁻ and ·OH played key roles during the photocatalytic degradation of ENX. This study provides a simple and convenient method to modify materials with enhanced photocatalytic performance, and the CDs/TiO₂/g-C₃N₄ catalyst is efficient, stable, and reusable for environmental practical applications.