聚吡咯
催化作用
材料科学
聚合
降级(电信)
吸附
纳米线
化学工程
电化学
吡咯
金属有机骨架
氧化还原
单体
光化学
无机化学
电极
化学
纳米技术
聚合物
有机化学
物理化学
计算机科学
工程类
电信
作者
Hui He,Yuexin Wang,Juan Li,Shanliang Jiang,Sidra Subhan,Wenxue Gong,Ying Tang,Yang Hu,Rule Wei,Dongxiao Yang,Xuesheng Li,Zhongxing Zhao
标识
DOI:10.1016/j.cej.2021.131962
摘要
High light adsorption and fast charge separation are crucial for photo-Fenton catalytic activity of MOFs. Herein, bottom-up design was proposed to fabricate polypyrrole (PPyC) nanowires in MIL-88B(Fe) cages as photo-Fenton catalyst for Sulfamethoxazole (SMX) efficient degradation. Pyrrole was prior anchored into MIL-88B(Fe) cluster via Fe-N coordination, and then the additional monomer pyrrole was further triggered bottom-up polymerization in confined cages of MIL-88B(Fe) and formed PPyC@Py-MIL(Fe) composite. These PPyC nanowires were dispersed in Py-MIL(Fe) cages and tightly connected with MOFs clusters via Fe-N bonding. Characterization proved that: (1) Interfacial Fe-N can significantly promote the efficient electron transport from PPyC nanowires to Py-MIL(Fe), enhance optical absorption property, and construct strong Lewis acidic sites and ligand vacancies in PPyC@Py-MIL(Fe). (2) The confined PPyC nanowire via Fe-N connection remarkably promote photo-generated electron-hole separation, Fe2+|Fe3+ redox ability of MOF, and improved photo-electric corrosion ability. As a result, it significantly enhanced the photo-Fenton catalytic performance for SMX degradation. Catalytic oxidation was attributed to the generation of ‧OH species that oxidized 93% SMX in 60 min, showing ultra-rapid degradation and TOC removal rates of 33.7 min−1·mg·g−1 and 8.68 min−1·mg·g−1 respectively, which was about 4–220 times higher than those reported state-of-the-art catalysts. Additionally, the PPyC@Py-MIL(Fe) catalyst showed minimal loss in catalytic activity even after recycling for 10 times, exhibiting good recycling stability compared to many MOFs. Systematic analysis shown that in-situ anchored growth of polypyrrole in confined porous cages of MOF can effectively enhance the catalytic activity and stability of MIL-88B(Fe), and has great development potential applications for photo-Fenton catalytic degradation of organic pollutants.
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