Electrocatalysis by nanoparticles: oxygen reduction on gold nanoparticles-electrodeposited platinum electrodes

Abstract

O 2 reduction has been performed at Au nanoparticle-electrodeposited Pt electrodes (Au/Pt electrodes) in O 2–saturated 0.1 M KOH solution. Cyclic voltammetry (CV) and rotating ring-disk electrode (RRDE) techniques have been used in this investigation. Two reduction peaks were observed on the CV for the O 2 reduction at the Au/Pt electrodes. The reduction pathway of O 2 to either HO 2 − or OH − is highly dependent on the electrode potential and the Au surface coverage of the Pt electrode as well. The Au/Pt electrodes exhibit different electrocatalytic behaviour in three potential regions: At E>−300 mV, the 2-electron reduction of O 2 to HO 2 − predominates, at −300> E>−500 mV, the 4-electron reduction predominates, and at E<−500 mV, the 2-electron and 4-electron reduction pathways proceed concurrently. The maximum production of HO 2 − (as a major reduction product) was obtained at a potential of ca. −240 mV versus Ag ∣ AgC ∣ KCl(sat), which is more positive by ca. 250 mV than the corresponding value at the bulk Au electrode (i.e. −500 mV vs. Ag ∣ AgCl ∣ KCl(sat)). The increase of the surface coverage of Au (i.e. increase of deposition time) on the Pt electrodes leads to a loss of this activity towards the O 2 reduction to HO 2 −. At a relatively higher negative potential, i.e. at −400 mV, the 4-electron reduction of O 2 to OH − occurs predominantly at all the examined Au/Pt electrodes with different Au loadings. Further negative increase of the potential (more negative than −400 mV) results in a partial contribution of the 2-electron reduction of O 2 with the 4-electron reduction. This behaviour could be understood in view of the potential dependence of the amount and the nature of the adsorbed species on the Au/Pt disk electrode surface.