期刊
NEW JOURNAL OF CHEMISTRY
卷 41, 期 3, 页码 1028-1036出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6nj03575b
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资金
- National Natural Science Foundation of China [21663027, 51262028]
- Science and Technology Support Project of Gansu Province [1504GKCA027]
- Program for the Young Innovative Talents of Longyuan
- Program for Innovative Research Team [NWNU-LKQN-15-2]
- Opening Project of Key Laboratory of Green Catalysis of Sichuan Institutes of High Education [LZJ1502]
- Research Fund for Higher Education of Gansu Province [2016A-002]
- Undergraduate Academic Innovative Research Team of Northwest Normal University
C3N4/CdS-CdWO4 core-shell heterostructure photocatalysts were prepared via a facile solvent volatilization method. High-resolution transmission electron microscopy (HRTEM) analysis demonstrated that an interfacial structure was present between the C3N4 shell and the CdS-CdWO4 core, and the specific function of the modification of C3N4 was investigated by room-temperature photoluminescence spectroscopy and transient photocurrent measurement. The heterostructure photocatalysts displayed enhanced photocatalytic activity in the degradation of RhB dye than that of the single components and binary composites. Among the as-prepared samples, the best photocatalytic performance was achieved by 10 wt% C3N4/CdS-CdWO4, which was about 5.7 and 14.6 times that of CdS-CdWO4 and C3N4, respectively, under UV-visible light irradiation. Owing to the formation of a C3N4/CdS-CdWO4 ternary heterostructure, its efficient pollutant-removing ability and stability can be attributed to the improved separation of photogenerated carriers and transfer efficiency for the intensive built-in electric field intensity. Radical trapping experiments proved that h(+) and O-center dot(2)- play crucial roles in the photocatalytic process.
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