碳量子点/Bi2WO6复合材料的制备及其高效光催化降解诺氟沙星性能

Preparation of carbon quantum dots/Bi2WO6 composite materials and their high-efficiency photocatalytic degradation performance of norfloxacin

  • 摘要: 钨酸铋(Bi2WO6,BWO)作为光催化材料,存在光吸收范围窄、光生载流子易复合等缺陷,限制了其对污染物的降解。以玉米秸秆粉末为碳量子点主要原料,通过水热法成功制备了碳量子点/钨酸铋(CQDs/BWO)复合材料,并将其用于光催化降解诺氟沙星(NOR)。通过SEM、XRD、FT-IR、XPS、UV-vis DRS、PL及电化学表征技术证实其成功合成。引入CQDs后,BWO形貌更规则,晶体结构未被破坏,且复合材料光吸收范围拓宽,光生电子-空穴对复合率显著降低,电荷转移效率提升。探究了不同CQDs添加量对CQDs/BWO体系降解NOR的影响,其中CQDs/BWO-2光催化活性最优,在模拟太阳光照射60分钟内对15 mg/L诺氟沙星(NOR)的降解率达97.23%,这得益于CQDs与BWO形成异质结促进电荷有效分离。循环使用3次后,CQDs/BWO体系对NOR的去除率仍可达95.78%。自由基捕获实验及ESR表明,光生空穴(h+)和超氧自由基(·O2)为主要活性物种,羟基自由基(·OH)为次要活性物种,上述光电性能优化与活性物种高效生成共同实现NOR的高效降解。

     

    Abstract: Bismuth tungstate (Bi2WO6, BWO) as a photocatalytic material has some drawbacks such as a narrow light absorption range and easy recombination of photogenerated carriers, which limit its degradation of pollutants. Using corn stalk powder as the main raw material for carbon quantum dots, the carbon quantum dot/bismuth tungstate (CQDs/BWO) composite material was successfully prepared by the hydrothermal method and applied to the photocatalytic degradation of norfloxacin (NOR). The successful synthesis was confirmed by SEM, XRD, FT-IR, XPS, UV-vis DRS, PL and electrochemical characterization techniques. After the introduction of CQDs, the morphology of BWO is more regular, the crystal structure is not damaged, and the light absorption range of the composite material is broadened. The recombination rate of photogenerated electron-hole pairs is significantly reduced, and the charge transfer efficiency is improved. The influence of different addition amounts of CQDs on the degradation of NOR in the CQDs/BWO system was investigated. Among them, the photocatalytic activity of CQDs/BWO-2 was the best. Within 60 minutes of simulated sunlight irradiation, the degradation rate of 15 mg/L norfloxacin (NOR) reached 97.23%, which was attributed to the formation of a heterojunction between CQDs and BWO promoting the effective separation of charges. After being recycled three times, the removal rate of NOR by the CQDs/BWO system can still reach 95.78%. Free radical capture experiments and ESR indicated that photogenerated holes (h+) and superoxide radicals (·O2) were the main active species, while hydroxyl radicals (·OH) were the secondary active species. The optimization of the above photoelectric performance and the efficient generation of active species jointly achieved the efficient degradation of NOR.

     

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