光催化
可见光谱
电子顺磁共振
光化学
降级(电信)
材料科学
核化学
复合数
激进的
化学
催化作用
有机化学
复合材料
电信
物理
光电子学
核磁共振
计算机科学
作者
Ye-Xia Li,Wen-Long Duan,Baoyi Ren,Jian Luan,Fang Guo
标识
DOI:10.1016/j.seppur.2023.123337
摘要
We developed the novel Fe-doped Zn-based coordination polymer (CP) composites ([email protected], n = 1–3) with superior visible-light-driven photocatalytic activity. Herein, the [email protected] composites were prepared using a newly designed Zn-CP {[Zn(3-padpe)(1,3-BDC)]·H2O}n using mixed ligands 4,4′-bis(3-pyridylformamide)diphenylether (3-padpe) and 1,3-benzenedicarboxylic acid (1,3-H2BDC) and FeSO4 by a facile approach at room temperature. The degradation of several tetracyclines (TCs), such as chlortetracycline (CTC), tetracycline hydrochloride (TC), and oxytetracycline (OTC) under visible-light irradiation were used to assess the photocatalytic performance. The generated ideal [email protected] composite showed high photocatalytic activity under visible light irradiation, for which the removal rate of antibiotics were 90.60% for CTC in 100 min, 90.00% for TC in 100 min, and 87.70% for OTC in 30 min, respectively. The superior photocatalytic performance was attributed to the Fe–O bond formation which expanded the optical absorption range and significantly increased the separation effectiveness of photogenerated charges. These properties enhanced the photoactivity of [email protected] for photocatalytic reaction under visible light irradiation. Additionally, the [email protected] showed excellent photostability and recycleability. The detailed intermediates and pathway of CTC degradation were also illustrated. According to the quenching studies and electron spin resonance (ESR) spectra characterization, the main species involved in the photocatalytic reaction were the radicals h+ and O2–. In addition, the possible photocatalytic reaction mechanisms were deeply discussed. This work offers fresh insight into the design of CP-based photocatalytic materials and demonstrates the broad application potential of [email protected] composites in environmental remediation.
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