Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
School of Environmental Science and Engineering, Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Sun Yat-sen University, Guangzhou, 510275, China.
Chemosphere. 2021 Sep;278:130376. doi: 10.1016/j.chemosphere.2021.130376. Epub 2021 Mar 30.
Doping heterogeneous atoms into BiOX is recognized as an effective method to improve its photocatalytic activity. Here, S-doped BiOBr (S-BiOBr) was synthesized via a solvothermal method in the absence of water, which is supposed to substitute O as S in the lattice. This material is firstly used for the visible-light-driven degradation of ibuprofen, a model anti-inflammatory drug. The degradation efficiency of S-BiOBr is much higher than that of pure BiOBr. The degradation kinetic constant for S-BiOBr (2.48 × 10 min) is about 3 times as high as that of pure BiOBr (0.83 × 10 min). It is found that S-doping tunes the band structure of BiOBr, leading to a narrower band gap and thus higher utilization efficiency of visible light. The degradation of ibuprofen on S-BiOBr can be attributed to the generation of HO and OH radicals. OH radical plays a synergistic role along with holes in the photocatalytic degradation process, which is supposed to be better than the reported single hole- or superoxide-dominant reaction. This work reveals a previously unrecognized and more efficient method for the degradation of organic contaminants on BiOBr.
将杂原子掺杂到 BiOX 中被认为是提高其光催化活性的有效方法。本文通过无水电热溶剂法合成了 S 掺杂 BiOBr(S-BiOBr),S 应该替代晶格中的 O。首次将该材料用于模型抗炎药物布洛芬的可见光驱动降解。S-BiOBr 的降解效率远高于纯 BiOBr。S-BiOBr 的降解动力学常数(2.48×10-1 min-1)约为纯 BiOBr(0.83×10-1 min-1)的 3 倍。研究发现,S 掺杂调谐 BiOBr 的能带结构,导致带隙变窄,从而可见光利用率更高。S-BiOBr 上布洛芬的降解归因于 HO 和 OH 自由基的生成。在光催化降解过程中,OH 自由基与空穴协同作用,这似乎比报道的单空穴或超氧自由基主导反应更好。这项工作揭示了一种以前未被认识到的、更有效的 BiOBr 上有机污染物降解方法。