摘要
Organic photocatalysts have recently drawn intense attention to wastewater treatment through the efficient utilization of solar energy. Rational design and synthesis of organic photocatalysts with facilitated charge-carrier transfer are crucial for achieving high-performance photodegradation of pollutants. In this work, functional polymers of intrinsic microporosity (PIMs) were synthesized by a quaternization reaction, and the zwitterionic and D–π–A structured polymers show visible-light-driven catalytic activity for the degradation of organic pollutants. The formation of D–π–A structures in PIMs is demonstrated to extend visible-light absorption and promote charge-transfer transition. Besides, the zwitterionic structures improve hydrophilicity and induce the aggregation of polymer chains, facilitating charge-carrier diffusion at the polymer–water and polymer–polymer interfaces. The combination of these favorable features endows the resulting PIMs with high catalytic degradation ability toward organic dyes under visible-light irradiation, which prevails over state-of-the-art organic photocatalysts.
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