Voltammetric determination of the heterogeneous charge transfer rate constant for superoxide formation at a glassy carbon electrode in aprotic medium
Abstract
A detailed investigation on the electrochemical reduction of oxygen was carried out using cyclic voltammetry at a glassy carbon electrode in dimethylsulphoxide (DMSO) containing 0.1 M tetrabutylammonium perchlorate (TBAP) as the supporting electrolyte. A diffusion-limited, quasi-reversible one-electron peak corresponding to the oxygen-superoxide anion couple is seen. The quasi-reversibility was supported by the ?Ep and Ip behavior with the square root of the scan rate, which is typical for a quasi-reversible process. We have used the theory developed by Nicholson for a study of the electrode reaction kinetics in order to measure a precise and reproducible value for the standard rate constant, k0, of the quasi-reversible reduction of oxygen to superoxide anion. The k0 mean value obtained was 9.3 × 10-2 with a standard deviation of ±0.4 × 10-2 cm s-1, and a coefficient of variation of 4.6%. The k0 value obtained was compared with both a previous value found in the literature and with simulated curves. © 2003 Elsevier Science B.V. All rights reserved.
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Título según WOS: | Voltammetric determination of the heterogeneous charge transfer rate constant for superoxide formation at a glassy carbon electrode in aprotic medium |
Título según SCOPUS: | Voltammetric determination of the heterogeneous charge transfer rate constant for superoxide formation at a glassy carbon electrode in aprotic medium |
Título de la Revista: | JOURNAL OF ELECTROANALYTICAL CHEMISTRY |
Volumen: | 549 |
Número: | SUPPL. |
Editorial: | Elsevier |
Fecha de publicación: | 2003 |
Página de inicio: | 157 |
Página final: | 160 |
Idioma: | English |
URL: | http://linkinghub.elsevier.com/retrieve/pii/S0022072803002481 |
DOI: |
10.1016/S0022-0728(03)00248-1 |
Notas: | ISI, SCOPUS |