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Synthesis of highly effective CuO–FeSe2 composites for the photodegradation of RhB under visible light
The release of industrial effluents into fresh water is a major contributor of water contamination. Therefore, it is highly desirable to develop a viable solution to this alarming issue to improve the quality of clean water. To enhance the photocatalytic efficiency and hence utilization ratio of CuO...
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Published in: | Research on chemical intermediates 2024, Vol.50 (6), p.2501-2518 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The release of industrial effluents into fresh water is a major contributor of water contamination. Therefore, it is highly desirable to develop a viable solution to this alarming issue to improve the quality of clean water. To enhance the photocatalytic efficiency and hence utilization ratio of CuO, a series of CuO–FeSe
2
composites with different varying contents of FeSe
2
were prepared through facile synthetic methods. X-ray diffraction (XRD) and energy-dispersive X-rays (EDX) analysis verified that the samples were successfully prepared without any contaminating phases. The average crystallite sizes of CuO and FeSe
2
were computed to be 29 and 21 nm respectively. For the CuO–FeSe
2
composites, the crystallite sizes varied between 25 and 27 nm. The morphology of CuO was comprised of needle-shaped structures, whereas that of FeSe
2
was observed to be flower-shaped structures comprising of irregular crystals. A red shift in the bandgap of CuO–FeSe
2
composites was observed with the increase in FeSe
2
concentration. The prepared photocatalysts were utilized to evaluate their efficiency under visible light against Rhodamine B (RhB). Among all the prepared composites, CuO–75% FeSe
2
revealed a remarkable performance and degraded 96% RhB in 180 min. Rate constants for the degradation of the dye were determined by applying the Langmuir–Hinshelwood model. |
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ISSN: | 0922-6168 1568-5675 |
DOI: | 10.1007/s11164-024-05286-6 |