Kinetic studies of dioxygen and superoxide ion in acetonitrile at gold electrodes using ultrafast cyclic voltammetry

Abstract

On the basis of a circuit with ohmic drop compensation by electronic positive feedback, ultrafast cyclic voltammetry was used to study the electrochemical behavior of dioxygen and superoxide ion at gold electrodes in acetonitrile containing 0.9 M tetraethylammonium tetrafluoroborate as the supporting electrolyte. At low scan rates, the O 2 / O 2 - couple is controlled by diffusion, and its redox process is an irreversible one with the rate constant (7.38 ± 1.25) × 10 −3 cm s −1. The diffusion coefficient of O 2 in such a solution was deduced as (4.87 ± 0.08) × 10 −5 cm 2 s −1, while at high scan rates, it is controlled by the adsorbed O 2 at a rate constant (5.21 ± 0.66) × 10 4 s −1. At moderate scan rates, it is controlled by both of them simultaneously. As to the O 2 - / O 2 2 - couple, its faradaic signal was greatly distorted at low scan rates. However, when the scan rate was increased sufficiently, the perturbing reactions would be ‘out-run’ by a transient experiment. Then, kinetic information could be obtained from the well-shaped voltammograms. In our experiments, the adsorption of O 2 - was found, and the rate constant was deduced as (1.95 ± 0.28) × 10 4 s −1.