info:eu-repo/semantics/article
The bismuth oxyhalide family: thin film synthesis and periodic properties
Fecha
2018-08Registro en:
Gómez Velázquez, Laura Sthefania; Hernández Gordillo, Agileo; Robinson, Matthew J.; Leppert, Valerie J.; Rodil, Sandra E.; et al.; The bismuth oxyhalide family: thin film synthesis and periodic properties; Royal Society of Chemistry; Dalton Transactions; 47; 35; 8-2018; 12459-12467
1477-9226
CONICET Digital
CONICET
Autor
Gómez Velázquez, Laura Sthefania
Hernández Gordillo, Agileo
Robinson, Matthew J.
Leppert, Valerie J.
Rodil, Sandra E.
Bizarro, Monserrat
Resumen
Bismuth oxyhalides (BiOX, where X = F, Cl, Br, I) are interesting materials due to their layered structure, which can be useful for different applications. In this work, we present the synthesis of the complete BiOX family in the thin film form. The tetragonal phase Bi2O3 film deposited onto a glass substrate was transformed into BiOF, BiOCl or BiOBr by a simple immersion at ambient temperature in a halide (X = F, Cl, Br) containing solution. For these films, a residual phase from the oxide was present and for BiOF another phase (tentatively identified as Bi7O5F11) was present too. For the BiOI film synthesis, an iodine and bismuth containing solution was sprayed onto the glass substrate heated at 275 °C and a pure phase was obtained. Microstructural and morphological characterization was performed by X-ray diffraction and scanning electron microscopy, while the chemical environment was studied by X-ray photoelectron spectroscopy. Optical and photocatalytic properties were also obtained. The physical and chemical characteristics of the BiOX films follow a correlation with the atomic radius of the halogen atom incorporated into the corresponding lattice. All the BiOX films showed a photocatalytic response for the photodiscoloration of indigo carmine dye under simulated sunlight irradiation in an alkaline medium. The photocatalytic reactions occurred via 2 proton-electron transfer from the oxide or oxyhalide to the adsorbed IC dye, favoring its reduction to the corresponding leuco IC form.