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Sunlight driven photocatalytic degradation of organic pollutants using a MnV(2)O(6)/BiVO(4) heterojunction: mechanistic perception and degradation pathways
In the field of photocatalysis, fabrication of a heterojunction structure with effective charge separation at the interface and charge shift to enhance the photocatalytic activity has acquired extensive consideration. In the present investigation, MnV(2)O(6)/BiVO(4) heterojunction samples with excel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419509/ https://www.ncbi.nlm.nih.gov/pubmed/36133498 http://dx.doi.org/10.1039/d1na00499a |
Sumario: | In the field of photocatalysis, fabrication of a heterojunction structure with effective charge separation at the interface and charge shift to enhance the photocatalytic activity has acquired extensive consideration. In the present investigation, MnV(2)O(6)/BiVO(4) heterojunction samples with excellent photocatalytic performance under sunlight irradiation were conveniently synthesized by a hydrothermal technique, and characterized by UV-Vis, FTIR, XRD, FESEM, HRTEM, PL, BET and XPS techniques. The prepared samples were investigated as photocatalysts for degrading MB and RhB dyes under sunlight. Among various samples of MnV(2)O(6)/BiVO(4), the S-V hetero-junction sample exhibited maximum photocatalytic activity with 98% and 96% degradation of MB and RhB dyes, respectively, in 6 and 35 min. The high photocatalytic activity of MnV(2)O(6)/BiVO(4) may be due to the successful generation and shift of charges in the presence of visible light. The average reduction of chemical oxygen demand (COD) was found to be 75% after irradiation with direct sunlight. In the degradation process of dyes, superoxide anion radicals were the main responsive species, as revealed by trapping experiments. The degradation efficiency of MnV(2)O(6)/BiVO(4) heterojunction did not diminish even after four cycles. In addition, the catalytic performance of the fabricated heterojunction was also explored for reducing 4-nitrophenols (4-NP) by using NaBH(4). Absolute conversion of 4-NP to 4-aminophenol (4-AP) occurred without the production of intermediate byproducts. |
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