摘要
Photocatalytic technology is widely used to solve environmental pollution problems, while most photocatalysts have a weak response to visible light, photogenerated charges are easy to recombine, and catalytic activity is limited. Herein, we used electrostatic self-assembly to tightly load Ti 3 C 2 MXene quantum dots (MQDs) onto Bi 2 WO 6 with oxygen vacancies (BWO) to obtain BWO@MQDs composite photocatalytic materials for the degradation of tetracycline (TC). The presence of oxygen vacancies in BWO provided more active sites, facilitating the reduction of O 2 to ·O 2 - by electrons. Moreover, MQDs and BWO could form a Schottky junction at the contact interface, and then the electrons on the BWO conduction band were transferred to MQDs, reducing the photogenerated electron-hole recombination. Under the optimal experimental conditions, the TC degradation efficiency of the BWO@MQDs photocatalyst was 88.12 %, which was 1.61 times that of original Bi 2 WO 6 , and the catalytic activity was well preserved after cycle stability testing. The possible photocatalytic mechanism and photodegradation pathway were revealed by UV–vis, XPS, ESR and LC-MS, the results indicated that ·O 2 - played the most dominant role in TC degradation and the final degradation products were mainly CO 2 and H 2 O. This study has important implications in oxygen vacancies and quantum dots co-modified bismuth-based materials for photocatalysis to solve water pollution problems.
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