Novel heterostructured NaTaO<inf>3</inf>/WO<inf>3</inf> systems with improved photocatalytic properties for water decontamination under UV and Visible illumination

In this work, we present the preparation of NaTaO3/WO3 systems, a broad-bandgap and a narrow-bandgap semiconductor, respectively, for photocatalytic applications. The samples were prepared by two different methods, microwave-assisted and conventional hydrothermal method, with different NaTaO3/WO3 mo...

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Detalles Bibliográficos
Autores: Hernández-Laverde, M., Murcia-Mesa, Julie Joseane., Navío, José Antonio, Hidalgo, M. C.
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2024
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/380681
Acceso en línea:http://hdl.handle.net/10261/380681
https://api.elsevier.com/content/abstract/scopus_id/85192536907
Access Level:acceso abierto
Palabra clave:Molar ratio
Heterojunctions
Degradation
Narrow band gap semiconductors
Photocatalytic activity
Sodium compounds
Descripción
Sumario:In this work, we present the preparation of NaTaO3/WO3 systems, a broad-bandgap and a narrow-bandgap semiconductor, respectively, for photocatalytic applications. The samples were prepared by two different methods, microwave-assisted and conventional hydrothermal method, with different NaTaO3/WO3 molar ratios. All samples were extensively characterized, and the photocatalytic behavior was studied in the degradation reaction of rhodamine B under simulated solar illumination. A significant synergistic effect in the coupling of the two components could be observed, with an important improvement in the rhodamine degradation rate, especially for the microwave-prepared sample with 1:1 (NaTaO3/WO3) molar ratio. The enhancement of the activity can be explained by the formation of type II and Z-Scheme heterojunctions. The obtained results are promising for the development of more efficient photocatalyst materials under solar or visible illumination.