Department of Environmental Science, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor, P.O. Box: 46414-356, Mazandaran, Iran.
Department of Environmental Science, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor, P.O. Box: 46414-356, Mazandaran, Iran.
Chemosphere. 2024 Sep;364:142980. doi: 10.1016/j.chemosphere.2024.142980. Epub 2024 Aug 6.
In the present study, we introduce a covalent organic triazine framework polymer (COTF-P) using 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) with triazine-based amine. The resulting dark red COTF-P illustrated potential behavior as a photocatalyst under visible light. Due to the inadequate solar energy capture and ultrafast charge recombination of the resulting COTF-P, the prepared COTF-P has been decorated with CQDs (N-CQD and N-S-CQD) to build a Z-scheme CQDs/COTF-P heterojunction photocatalyst and utilizes as photocatalyst for the breakdown of phenanthrene (PHE) exposed to visible light. The prepared COTF-P and CQDs/COTF-P were fully characterized, analyzing the textural (N isotherms), structural (XRD and FTIR), chemical (EDX and XPS), morphological (FESEM and TEM), optical (DRS-UV-Vis and photoluminescence), and electrochemical properties (EIS impedance, transient photocurrent, and flat band potential). The prepared N-S-CQD/COTF-P heterojunction displayed optimum activity for the photocatalytic oxidation of PHE from water, owing to an enhanced separation of the photogenerated charges and lower bandgap value, 2.1 vs. 1.9 eV. The N-S-CQD/COTF-P heterojunction showed acceptable stability in terms of activity and structural properties after 5 cycles of reuse. The mechanism of activation highlights the importance played by superoxide radicals and hydroxyl radicals. This project sheds light on the potential use of CQDs for the decoration of polymers, extending the absorbance in the visible region and boosting the migration of charge, which boosts the activity of the resulting material.
在本研究中,我们使用 3,4,9,10-苝四羧酸二酐(PTCDA)和三嗪基胺合成了一种共价有机三嗪框架聚合物(COTF-P)。所得的暗红色 COTF-P 表现出在可见光下作为光催化剂的潜在性能。由于所得 COTF-P 对太阳能的捕获不足和超快电荷复合,因此用 CQDs(N-CQD 和 N-S-CQD)对其进行了修饰,以构建 Z 型 CQDs/COTF-P 异质结光催化剂,并将其用作可见光下暴露的菲(PHE)的光催化剂。对制备的 COTF-P 和 CQDs/COTF-P 进行了全面表征,分析了其结构(XRD 和 FTIR)、化学(EDX 和 XPS)、形貌(FESEM 和 TEM)、光学(DRS-UV-Vis 和光致发光)和电化学性质(EIS 阻抗、瞬态光电流和平带电位)。制备的 N-S-CQD/COTF-P 异质结由于光生载流子的分离增强和更低的能带隙值(2.1 对 1.9 eV),对水中 PHE 的光催化氧化表现出最佳活性。N-S-CQD/COTF-P 异质结在 5 次重复使用后在活性和结构性能方面表现出良好的稳定性。激活机理突出了超氧自由基和羟基自由基的重要性。该项目阐明了 CQDs 用于聚合物修饰的潜力,扩展了在可见光区域的吸收并促进了电荷的迁移,从而提高了所得材料的活性。