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.
