摘要
As modern industry continues to develop rapidly, water pollution caused by antibiotics and synthetic dyes has become increasingly severe. To address the challenge of efficient treatment of such organic wastewater, a novel modified MIL-101(Fe) photocatalyst was constructed via a synergistic strategy of Cu²⁺ doping and in-situ polymerization of aniline. Under simulated solar irradiation, the composite photocatalyst achieved degradation efficiencies of 93.06% for tetracycline and 94.2% for methylene blue, exhibiting broad-spectrum photocatalytic activity toward various organic dyes. Cu²⁺ and PANI synergistically optimize the band structure, narrowing the bandgap to 2.23 eV while broadening the visible-light response range, promoting charge transport, and forming a stable Z-scheme heterojunction at the interface to suppress the recombination of photogenerated charge carriers. The results of reactive species trapping experiments showed that ·OH, h⁺, and ·O 2 - collectively governed the degradation process. The core mechanism stems from the ligand-to-metal charge transfer (LMCT) characteristics of MIL-101(Fe), the electron-trapping effect of Cu²⁺, and the conjugated conductive network of PANI. In addition, the composite photocatalyst exhibited strong resistance to ionic interference and maintained degradation efficiencies above 80% after five consecutive cycles, demonstrating excellent stability and reusability. This work provides an efficient photocatalytic material and a promising strategy for the comprehensive treatment of organic wastewater.
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