Steady-state voltammetry of hydroxide ion oxidation in aqueous solutions containing ammonia

An oxidation process observed in dilute aqueous solutions of ammonia was investigated under steady-state conditions with gold microelectrodes with radii in the range 2.5-30 [micro]m. Over the ammonia concentration range 0.1-10 mM, a well-defined voltammetric wave was observed at ~1.4 V versus Ag/AgCl. It was attributed to the oxidation of hydroxide ions that arise from the dissociation of the weak base. The steady-state limiting current was found to depend on the concentration of supporting electrolyte, and in solution with low electrolyte, it was enhanced by migration contribution, as expected for a negatively charged species that oxidizes on a positively charged electrode. In addition, the steady-state limiting current was proportional to both the ammonia concentration and the electrode radius. The overall electrode process was analyzed in terms of a CE mechanism (homogeneous chemical reaction preceding the heterogeneous electron transfer) with a fast chemical reaction when measurements were carried out in solutions containing N[H.sub.3] at [less than or equal to] 5 mM and with electrodes having a radius of [greater than or equal to] 5 [micro]m. This was ascertained by comparing experimental and theoretical data obtained by simulation. The formation of the soluble complex species Au[(N[H.sub.3]).sub.2.sup.+] was also considered as a possible alternative to explain the presence of the oxidation wave. This process however was ruled out, as the experimental data did not fit theoretical predictions in any of the conditions employed in the investigation. Instead, the direct oxidation of N[H.sub.3], probably to [N.sub.2]O, was invoked to explain the anomalous currents found when the CE process was strongly kinetically hindered. Throughout this study, a parallel was made between the CE mechanism investigated here and that known to occur during the hydrogen evolution reaction from weak acids.