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Synthesis of LaFeO(3)/Ag(2)CO(3) Nanocomposites for Photocatalytic Degradation of Rhodamine B and p-Chlorophenol under Natural Sunlight

[Image: see text] Novel LaFeO(3)/Ag(2)CO(3) nanocomposites are synthesized by co-precipitation method for photocatalytic degradation of Rhodamine B (RhB) and p-chlorophenol under visible light irradiation. Heterostructures between LaFeO(3) and Ag(2)CO(3) semiconductors are formed during the synthesi...

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Detalles Bibliográficos
Autores principales: Pirzada, Bilal M., Pushpendra, Kunchala, Ravi K., Naidu, Boddu S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649104/
https://www.ncbi.nlm.nih.gov/pubmed/31459497
http://dx.doi.org/10.1021/acsomega.8b02829
Descripción
Sumario:[Image: see text] Novel LaFeO(3)/Ag(2)CO(3) nanocomposites are synthesized by co-precipitation method for photocatalytic degradation of Rhodamine B (RhB) and p-chlorophenol under visible light irradiation. Heterostructures between LaFeO(3) and Ag(2)CO(3) semiconductors are formed during the synthesis of these nanocomposites. Among the nanocomposites prepared with different ratios of LaFeO(3) and Ag(2)CO(3), 1% LaFeO(3)/Ag(2)CO(3) shows the highest photocatalytic activity for the degradation of RhB. Maximum electron–hole pair decoupling efficiency is observed in 1% LaFeO(3)/Ag(2)CO(3), which causes the greater activity of the heterostructure. Degradation efficiency of 99.5% for RhB and 59% for p-chlorophenol has been obtained under natural sunlight within 45 min. Interestingly, the stability of Ag(2)CO(3) is improved dramatically after making nanocomposite, and no decomposition of the catalyst was observed even after several photocatalytic cycles. Reactive oxygen species scavenging experiments with p-benzoquinone, isopropyl alcohol, and ammonium oxalate suggest that a major degradation process is caused by holes. Degradation of RhB into small organic moieties is detected using LC–MS technique. Further, the efficient mineralization of the degradation products occurs during the catalytic process.