The influence of dioxygen reduction on oxide growth and dissolution at the surface of AA2024-T3 has been investigated in near-neutral, unbuffered conditions. Dioxygen reduction at Fe and Cu also was examined to compare with the behavior of intermetallic particles in AA2024-T3. Electrodes were exposed alternately to N-2-saturated or O-2-saturated 0.1 M Na2SO4 solution in a characterized wall-jet flow cell. Limiting current densities associated with O-2 reduction on Fe and Cu range between 1.5 and 2.0 mA cm(-2), whereas AA2024-T3 displays significantly lower values. AA2024-T3 samples also display potential-dependent current density transients when the solution is alternated between N-2-saturated and O-2-saturated supporting electrolyte. The data show that the current density transient behavior is due to competition between interfacial etching of oxide due to high local pH, which is a result of the cathodic oxygen reduction reaction (ORR) at intermetallic particles, and anodic oxide growth on the alloy, which is driven by the electric field produced at a given potential. Scanning electron microscopy shows significant differences in oxide thickness with radial distance from the center of the jet impingement region. Energy-dispersive spectroscopic imaging reveals an increase in near-surface Cu and Fe in areas that experience high current densities. (C) 2007 The Electrochemical Society.