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A hierarchical Nb(2)O(5)@NiFe-MMO rod array, fabricated and used as a structured photocatalyst
Recently, using sunlight as a driving force with transitional metal oxides as photocatalysts, due to their unique optical and catalytic properties for organic reactions, has been considered to be a promising strategy in synthetic chemistry. Here, a hierarchically structured photocatalyst, a NiFe mix...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060917/ https://www.ncbi.nlm.nih.gov/pubmed/35517279 http://dx.doi.org/10.1039/c8ra10432h |
Sumario: | Recently, using sunlight as a driving force with transitional metal oxides as photocatalysts, due to their unique optical and catalytic properties for organic reactions, has been considered to be a promising strategy in synthetic chemistry. Here, a hierarchically structured photocatalyst, a NiFe mixed metal oxide coated Nb(2)O(5) (denoted as Nb(2)O(5)@NiFe-MMO) rod array has been successfully fabricated using Nb foil as a substrate. The Nb(2)O(5) rod array was synthesized by the oxidative etching of Nb metal on the surface of the a substrate. The coating NiFe-MMO was obtained by the calcination of a NiFe layered double hydroxide (NiFe-LDH) precursor via the in situ epitaxial growing technique. The Nb(2)O(5)@NiFe-MMO rod array extended the photoresponse light region from ultraviolet light around 400 nm to visible light around 600 nm. With the well-designed architecture and highly dispersed NiO and Fe(2)O(3), the as-prepared photocatalyst exhibited excellent activity and recyclability toward the reaction of aerobic coupling under relatively green conditions, with catalytic efficiency of 228 μmol cm(−2) (the area is that of the Ni foil substrate) at 30 °C for 5 h. The present work provides a new strategy for the exploration of excellent structured photocatalysts based on transition metal oxide materials for selective aerobic oxidation of benzylamine to imine. |
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