Engineered SnO 2/BiOI fibers via electrospinning for robust visible-light/peroxymonosulfate -driven multipollutant mineralization

Engineered photocatalysts capable of operating under visible light and realistic water matrices are needed to address emerging pharmaceutical contaminants. Here, we fabricate SnO<sub>2</sub>/BiOI fibrous heterostructures by electrospinning SnO<sub>2</...

Descripción completa

Detalles Bibliográficos
Autores: Huidobro, Laura, Allés, Miquel, Abid, Mahmoud, Bechelany, Mikhael, Sousa Romero, Carmen, Gómez, Elvira, Serrà i Ramos, Albert
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2026
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:dnet:recercat____::417b5b556acb449fe02fe14651d4f5ab
Acceso en línea:https://hdl.handle.net/2445/229484
Access Level:acceso abierto
Palabra clave:Fotoelectroquímica
Fotocatàlisi
Absorció de la llum
Photoelectrochemistry
Photocatalysis
Light absorption
Descripción
Sumario:Engineered photocatalysts capable of operating under visible light and realistic water matrices are needed to address emerging pharmaceutical contaminants. Here, we fabricate SnO<sub>2</sub>/BiOI fibrous heterostructures by electrospinning SnO<sub>2</sub> nanofibers decorated with solvothermally synthesized BiOI followed by calcination. The electrospun fibers provide a mechanically robust, high-surface-area scaffold, while BiOI incorporation enhances visible-light absorption and creates SnO<sub>2</sub>/BiOI heterointerfaces. Textural, optical, and spectroscopic analyses reveal progressive surface decoration, increased surface area, and defect-rich Bi environments as BiOI loading increases. Using tetracycline (TC) as a model contaminant at neutral pH, SnO<sub>2</sub>/BiOI composites markedly outperform pristine SnO<sub>2</sub> under visible light and/or peroxymonosulfate (PMS), with an optimal BiOI content (SBO2) under single-stimulus conditions and near-complete TC mineralization for the highest loading (SBO3) in the PMS + visible-light system. Radical scavenging indicates that SO<sub>4</sub><sup>•−</sup> and <sup>•</sup>OH are the dominant reactive species, with O<sub>2</sub><sup>•−</sup>, h<sup>+</sup> and e<sup>−</sup> playing secondary roles. A multipollutant mixture (TC, sulfamethoxazole, levofloxacin, lansoprazole) is mineralized by >80% in both Milli-Q and tap water, and SBO3 retains high activity over nine cycles with Bi and I leaching below 0.05% after 48 h. Density functional theory calculations, combined with XPS, support an S-scheme SnO<sub>2</sub>/BiOI heterojunction, enabling spatial separation of strongly reducing electrons in BiOI and oxidizing holes in SnO<sub>2</sub>. Although high PMS loadings can partially mask intrinsic catalyst differences, these results outline a practical design platform for heterogeneous (slurry), visible-responsive, PMS-assisted photocatalysts for pharmaceutical-laden effluents.