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Nafion/tetraruthenated porphyrin glassy carbon-modified electrode: characterization and voltammetric studies of sulfite oxidation in water–ethanol solutions
Authors:Karla Calfumán  María Jesus Aguirre  Diego Villagra  Claudia Yañez  Carmen Arévalo  Betty Matsuhiro  Leonora Mendoza  Mauricio Isaacs
Institution:1. Departamento de Química, Facultad de Ciencias, Universidad de Chile, Las Palmeras #3425, Casilla 653, ?u?oa, Santiago, Chile
2. Departamento de Química de los Materiales, Facultad de Química y Biología, Universidad de Santiago de Chile, Casilla 40-Correo 33, Santiago, Chile
3. Departamento de Química, Facultad de Ciencias, Universidad de Tarapacá, Arica, Av. General Velásquez 1775, Casilla 7-D, Arica, Chile
4. Departamento de Química Orgánica y Físico-Química, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, P.O. Box?233, Santiago, Chile
5. Departamento de Química Física, Facultad de Química, Universidad de La Laguna, 38071-La Laguna, Santa Cruz de Tenerife, Spain
Abstract:In this work, the modification of a glassy carbon electrode with tetraruthenated porphyrins electrostatically assembled onto a Nafion film, previously adsorbed on the electrode surface, is reported. This modified electrode was characterized by scanning electron microscopy–energy-dispersive X-ray, Raman spectroscopy, UV-Vis spectroelectrochemistry, and cyclic voltammetry. The Nafion film onto the glassy carbon electrode shows a smooth disposition; when the tetraruthenated porphyrin is incorporated on the Nafion film, the complex is adsorbed in a homogeneous way. The modified electrode catalyzes HSO3 oxidation in water–ethanol solutions and shows an enhanced stability compared with the electrode modified with the dip coating method. Rotating disk electrode experiments showed a kinetic limitation to the electron transfer controlled by charge propagation in the film. I/E curves show a Tafel slope of 120 mV/decade corresponding to a first electron-transfer reaction, depending on the potential, as the determining step. Spectroelectrochemical experiments demonstrated that Ru(II) is the active site for the electrocatalysis.
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