期刊
CERAMICS INTERNATIONAL
卷 47, 期 14, 页码 19402-19413出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2021.03.277
关键词
CuO; ZnO; p-n Heterojunction; Electrospinning; Photocatalysis; Denitrification
资金
- Doctoral Scientific Research Foundation of Bohai University [0517bs029]
CuO/ZnO p-n heterojunction nanofibers were synthesized for efficient elimination of pyridine in fuel oil. The system was capable of degrading over 90% of pyridine within 60 minutes under visible light, with the p-CuO/n-ZnO nanofibers showing enhanced denitrification efficiency compared to ZnO alone. Mechanistic investigations suggested that photoexcited holes played a key role in generating reactant intermediates during the degradation process.
CuO/ZnO p-n heterojunction nanofibers were fabricated by coupling p-type CuO with n-type ZnO nanofibers for efficacious elimination of pyridine in fuel oil. The structural and photoelectric characteristics of the assynthesized nanofibers were systematically studied. The photodegradation system was appropriate for the oxidation of pyridine from fuel oil utilizing the ambient air without mixing with other oxidants. Under visible light illumination, more than 90% of the pyridine (100 mL, 100 mu g/g) could be degraded within 60 min by 17.5 mg of MCuZn-0.5 (the photocatalyst with a Cu/Zn molar ratio of 0.5 at%). The visible-light-induced photocatalytic denitrification efficiency of the MCuZn-0.5 nanofibers was nearly 1.5 times as high as that of ZnO alone. The superior denitrification activity of p-CuO/n-ZnO heterojunction nanofibers could be attributed to the enhanced optical absorption capacity and efficacious separation of photoexcited charge pairs. In addition, fivecycle experiments confirmed that MCuZn-0.5 nanofibers also displayed satisfactory photocatalytic denitrification properties. Mechanistic investigations proposed that the photoexcited holes played a dominant role in the formation of reactant intermediates, while superoxide radicals promoted the ultimate mineralization process of pyridine.
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