Engineering Z-scheme TiO2-OV-BiOCl via oxygen vacancy for enhanced photocatalytic degradation of imidacloprid.

The development and application of photocatalysts with strong redox ability to degrade refractory pesticides is the key to eliminating pesticide contamination. In this work, we develop a facile, time-saving, and surfactant-assisted method to fabricate a new Z-scheme heterojunction based on TiO2/BiOCl. This photocatalyst is rich in oxygen vacancy defects (TiO2-OV-BiOCl), and displays an excellent photocatalytic degradation performance for imidacloprid (IMD), and a possible degradation pathway of IMD is provided. The surfactant F127 plays an essential role in regulating the oxygen vacancy defects (OVDs) of TiO2-OV-BiOCl, where the OVD mainly exists in 5 layer BiOCl ultrathin nanosheets. Free radical trapping experiments demonstrate that the introduction of an OVD in BiOCl as a 'charge mediator' changes the charge-transfer mode from a type-II mechanism to a Z-scheme mechanism. The formation of a Z-scheme heterojunction leads to an excellent light utilization and higher separation efficiency of photogenerated charge carriers with a prolonged lifetime compared to those of BiOCl and TiO2/BiOCl. This work highlights the critical role of an OVD in the construction of a Z-scheme heterojunction of TiO2/BiOCl, and it can be applied to construct efficient photocatalytic systems for pesticide degradation.