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Artículo

Electrocatalytic kinetics and mechanistic insights into indole oxidation reaction on highly oriented pyrolytic graphite electrodes

Rojas, Mariana IsabelIcon ; Gomez, Cesar GerardoIcon ; Avalle, Lucia BernarditaIcon ; Linarez Pérez, Omar EzequielIcon
Fecha de publicación: 05/2025
Editorial: Springer
Revista: Journal of Solid State Electrochemistry (print)
ISSN: 1432-8488
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Físico-Química, Ciencia de los Polímeros, Electroquímica

Resumen

The kinetics and mechanism of the indole oxidation reaction (IOR) on a highly oriented pyrolytic graphite (HOPG) electrode were investigated using various electrochemical techniques. The HOPG electrode exhibited excellent electrocatalytic activity, reaching current densities of up to 35 µA/cm2 over a concentration range of 0.1 and 200.0 µM and a detection limit of 0.02 µM. Chronoamperometric transients were analyzed through a kinetic model that described the relationship between the observed current density and the distribution of free and occupied active sites on the electrode surface. The number of active sites was quantified, revealing a moderate turnover frequency (TOF) under non-saturating conditions, showing the efficiency of the electrode during IOR. Electrochemical impedance spectroscopy (EIS) was employed to characterize the electrode surface and electrode/electrolyte interface. The EIS spectra, fitted using an equivalent circuit model, allowed the evaluation of charge transfer resistance and effective capacitance as a function of indole concentration. This study highligThe kinetics and mechanism of the indole oxidation reaction (IOR) on a highly oriented pyrolytic graphite (HOPG) electrode were investigated using various electrochemical techniques. The HOPG electrode exhibited excellent electrocatalytic activity, reaching current densities of up to 35 µA/cm2 over a concentration range of 0.1 and 200.0 µM and a detection limit of 0.02 µM. Chronoamperometric transients were analyzed through a kinetic model that described the relationship between the observed current density and the distribution of free and occupied active sites on the electrode surface. The number of active sites was quantified, revealing a moderate turnover frequency (TOF) under non-saturating conditions, showing the efficiency of the electrode during IOR. Electrochemical impedance spectroscopy (EIS) was employed to characterize the electrode surface and electrode/electrolyte interface. The EIS spectra, fitted using an equivalent circuit model, allowed the evaluation of charge transfer resistance and effective capacitance as a function of indole concentration. This study highlights the technological importance of understanding IOR, especially in the development of sensors for clinical and environmental applications requiring precise detection and quantification of indole.hts the technological importance of understanding IOR, especially in the development of sensors for clinical and environmental applications requiring precise detection and quantification of indole.
Palabras clave: INDOLE OXIDATION REACTION , HOPG , ELECTROCHEMICAL ANALYSIS , EIS
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/274031
URL: https://link.springer.com/10.1007/s10008-025-06339-5
DOI: http://dx.doi.org/10.1007/s10008-025-06339-5
Colecciones
Articulos(IFEG)
Articulos de INST.DE FISICA ENRIQUE GAVIOLA
Articulos(INFIQC)
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Articulos(IPQA)
Articulos deINSTITUTO DE INVESTIGACION Y DESARROLLO EN INGENIERIA DE PROCESOS Y QUIMICA APLICADA
Citación
Rojas, Mariana Isabel; Gomez, Cesar Gerardo; Avalle, Lucia Bernardita; Linarez Pérez, Omar Ezequiel; Electrocatalytic kinetics and mechanistic insights into indole oxidation reaction on highly oriented pyrolytic graphite electrodes; Springer; Journal of Solid State Electrochemistry (print); 29; 11; 5-2025; 4721-4733
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