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High performance photocatalyst TiO(2)@UiO-66 applied to degradation of methyl orange

MOFs have considerable adsorption capacity due to their huge specific surface area. They have the characteristics of photocatalysts for their organic ligands can absorb photons and produce electrons. In this paper, the photodegradation properties of TiO(2) composites loaded with UiO-66 were investig...

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Detalles Bibliográficos
Autores principales: Yang, Jingyi, Chang, Xue, Wei, Fang, Lv, Zixiao, Liu, Huiling, Li, Zhan, Wu, Wangsuo, Qian, Lijuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495301/
https://www.ncbi.nlm.nih.gov/pubmed/37695406
http://dx.doi.org/10.1186/s11671-023-03894-6
Descripción
Sumario:MOFs have considerable adsorption capacity due to their huge specific surface area. They have the characteristics of photocatalysts for their organic ligands can absorb photons and produce electrons. In this paper, the photodegradation properties of TiO(2) composites loaded with UiO-66 were investigated for the first time for MO. A series of TiO(2)@UiO-66 composites with different contents of TiO(2) were prepared by a solvothermal method. The photocatalytic degradation of methyl orange (MO) was performed using a high-pressure mercury lamp as the UV light source. The effects of TiO(2) loading, catalyst dosage, pH value, and MO concentration were investigated. The results showed that the degradation of MO by TiO(2)@UiO-66 could reach 97.59% with the addition of only a small amount of TiO(2) (5 wt%). TiO(2)@UiO-66 exhibited significantly enhanced photoelectron transfer capability and inhibited efficient electron–hole recombination compared to pure TiO(2) in MO degradation. The composite catalyst indicated good stability and reusability when they were recycled three times, and the photocatalytic reaction efficiencies were 92.54%, 88.76%, and 86.90%. The results provide a new option to design stable, high-efficiency MOF-based photocatalysts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11671-023-03894-6.