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Fabrication of rGO/α-Fe2O3 electrodes: characterization and use in photoelectrocatalysis

In the current study, the synthesis of hematite ( α -Fe 2 O 3 ) at different temperatures (750 and 900 °C), and reduced graphene oxide (rGO), obtained from an adaptation to the Hummers’s method, was evaluated. These materials were characterized by X-ray diffraction, Raman spectroscopy, Fourier-trans...

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Published in:Journal of materials science. Materials in electronics 2020-10, Vol.31 (19), p.16882-16897
Main Authors: Leão-Neto, Vanildo Souza, da Silva, Aruã Clayton, Camargo, Luan Pereira, Da Silva Pelissari, Marcelo Rodrigues, da Silva, Paulo Rogério Catarini, Parreira, Paulo Sergio, Segatelli, Mariana Gava, Dall′Antonia, Luiz Henrique
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Language:English
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Summary:In the current study, the synthesis of hematite ( α -Fe 2 O 3 ) at different temperatures (750 and 900 °C), and reduced graphene oxide (rGO), obtained from an adaptation to the Hummers’s method, was evaluated. These materials were characterized by X-ray diffraction, Raman spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, among others. The deposition of samples on the conductive surface of tin-doped indium oxide coated glass substrate, was performed by the Layer-by-Layer technique. The films were prepared with 1- and 4-bilayers α -Fe 2 O 3 , using a cationic polyelectrolyte diallyldimethylammonium chloride (PDDA) or rGO. It was observed that the rGO/ α -Fe 2 O 3 films presented higher photocurrent and less resistivity when compared to the PDDA/ α -Fe 2 O 3 films. The largest photocurrent was obtained with the 4-bilayers rGO/ α -Fe 2 O 3 at 900 °C film, with 2.15 µA cm −2 . In addition, a kinetic study for photoelectrocatalytic decolorization of the methylene blue dye under visible light was performed. The electrode that showed the greatest photoelectroactivity was the 4-bilayers rGO/ α -Fe 2 O 3 at 900 °C film, resulting in k obs  = 11.90 × 10 −3  min −1 and about 78% decolorization after 120 min.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-020-04244-3