Semiconductor photocatalysis is widely proposed for decomposing multiple pollutants via photo-generated oxidative species. However, the photocatalytic degradation performance in practical settings still remains unsatisfactory due to the limited production of active oxidative species (AOS). In this work, a defect engineering strategy was developed to explore the superiority of oxygen vacancies (Vo) and their structural regulation to enhance AOS production for boosting photodegradation. Taking anatase TiO2 as a model photocatalyst, ultrathin TiO2 nanosheets containing abundant Vo and appropriate Fe doping exhibited an unprecedented 134 times higher activity in the degradation of Rhodamine B (RhB) (rate as high as 0.3073 min-1) than bulk anatase and were superior to most reported photocatalysts. The defect-rich ultrathin TiO2 nanosheets could be further applied in high-efficiency degradation of tetracycline hydrochloride (TC-HCl) with the degradation rate of 0.0423 min-1. The in situ electron paramagnetic resonance, advanced spectroscopic characterization and electrochemical measurement revealed the key role of Vo and Fe doping in facilitating the production of photo-generated holes and superoxide radicals (˙O2 -) that were identified to be effective to decompose both RhB and TC-HCl. This research provides insight into defect engineering promoting AOS generation and gives inspiration for the design of efficient photocatalysts for photooxidation applications.
This journal is © The Royal Society of Chemistry.