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Incorporation of reduced graphene oxide into faceted flower-like {001} TiO(2) for enhanced photocatalytic activity

Anatase TiO(2) with {001} facets is much more active than that with {101} facets, which has been verified via experiments and theoretical calculations. Graphene has garnered much attention since it was initially synthesized, due to its unique properties. In this study, reduced graphene oxide (RGO)/{...

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Detalles Bibliográficos
Autores principales: Liu, Haijin, Li, Peiyao, Bai, Haokun, Du, Cuiwei, Wei, Dandan, Su, Yuzhao, Wang, Yuqian, Yang, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124043/
https://www.ncbi.nlm.nih.gov/pubmed/30225058
http://dx.doi.org/10.1098/rsos.180613
Descripción
Sumario:Anatase TiO(2) with {001} facets is much more active than that with {101} facets, which has been verified via experiments and theoretical calculations. Graphene has garnered much attention since it was initially synthesized, due to its unique properties. In this study, reduced graphene oxide (RGO)/{001} faceted TiO(2) composites were fabricated via a solvothermal method. The composites were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectrophotometry, photoluminescence and Raman analysis. The results revealed that the graphene oxide was reduced during the preparation process of the {001} faceted TiO(2), and combined with the surface of {001} TiO(2). The photocatalytic activities of the composites were evaluated through the degradation of basic violet, under both white light (λ > 390 nm) and visible light (λ = 420 nm) irradiation. The results indicated that the photocatalytic activities of the {001} faceted TiO(2) were significantly improved following the incorporation of RGO, particularly under visible light irradiation. Theoretical calculations showed that the band structure of the {001} faceted TiO(2) was modified via graphene hybridization, where the separation of photoinduced electron–hole pairs was promoted; thus, the photocatalytic activity was enhanced.