光降解
锡
溴化物
铅(地质)
兴奋剂
铯
抗生素
毒性
化学
环境化学
材料科学
无机化学
生物
有机化学
光催化
光电子学
催化作用
生物化学
古生物学
作者
Jingyang Gao,Jianhao Wu,Chunxi Liu,Zhi Chen,Lan Li,Jinglei Hu,Chunyan Li,Yu‐Rong Liu,Xusheng Wang,Wen Wang
标识
DOI:10.1016/j.jclepro.2024.141000
摘要
Inorganic perovskite lead cesium bromide (CsPbBr3) has attracted great attention due to its excellent photocatalytic capability. However, the intrinsic toxicity of Pb hindered its wide application in photo-electric fields. Herein, an effective modification on the CsPbBr3 was proposed by substituting toxic Pb with low-toxic element Sn, and Sn-doped CsPb1-xSnxBr3 perovskites were synthesized by the simple anti-solvent precipitation which showed improved visible-light photodegradation of antibiotic residue in ethanol. The partially substituted CsPb1-xSnxBr3 (x = 0, 0.3, 0.4, 0.5, 0.6, 0.7, 1.0) perovskite can reduce the toxicity of Pb-based perovskite without destroying the initial structure. The CsPb0.5Sn0.5Br3 displayed a maximum photocatalytic efficiency for the degradation of tetracycline hydrochloride (TC-HCl) (79 %, 60 min). The reaction rate constant was calculated to be 0.1201 min−1, which was 2.0 and 28.8 times higher than the pure CsPbBr3 and CsSnBr3, respectively. Cycling tests showed a minor decrease (<5 %) in the degradation of TC-HCl after four cycles. As confirmed by the photo-electrochemical test, the introduction of Sn results in improved charge separation and transfer. Additionally, holes (h+) and superoxide radicals (∙O2−) played major roles in the photodegradation of TC-HCl based on capture experiments. This work represents a promising approach to reducing the toxicity of metal halide perovskite with optimized activity for efficiently treating antibiotics simultaneously, which may contribute to a breakthrough in new applications such as environmental control.
科研通智能强力驱动
Strongly Powered by AbleSci AI