Electrochemical quartz crystal microbalance analysis of the oxygen reduction reaction on Pt-based electrodes. part 1: Effect of adsorbed anions on the oxygen reduction activities of pt in HF, HClO_4, and H _2SO_4 Solutions

摘要

The effects of anion adsorption on the activities for the oxygen reduction reaction (ORR) at a Pt film electrode in electrolyte solutions (HClO_4 and HF at various concentrations) were analyzed using an electrochemical quartz crystal microbalance (EQCM) and a rotating disk electrode (RDE). With an increasing HClO4 concentration [HClO_4], the onset potential for the Pt oxide formation in the voltammogram shifted in the positive direction, accompanied by a compression of the hydrogen adsorption/oxidation wave to less positive potentials. This is ascribed to a specific adsorption of the ClO_4- anion, because the [HClO_4] dependence of the mass change δm detected by EQCM in the double-layer region was found to be fitted well by a Frumkin-Temkin adsorption isotherm. The potential dependencies of δm in both 0.1 and 0.5 M HClO_4 solutions accord well with those of the ν(Cl-O) intensities observed by in situ Fourier transform infrared (FTIR) spectroscopy in the potential range from 0.3 to 0.6 V. The kinetically controlled current densities jk for the ORR at the Pt-RDE were found to decrease with increasing [HClO4], because of the blocking of the active sites by specifically adsorbed ClO4-. The values of jk in the non-adsorbing 0.1MHF electrolyte solution, however, were smaller than those in 0.1MHClO4. It was found that the low ORR activity could be ascribed to the lowH+ activity in the weak acid solution of HF. We, for the first time, detected a reversible mass change for one or more adsorbed oxygen species on the Pt-EQCM in O_2-saturated and He-purged HF and HClO_4 solutions. The coverages of oxygen species θO on Pt were found to increase in theO2-saturated solution. High values of θO inO_2-saturated 7mMHF suggest that the ORR rate was limited by the very low H~+ activity in the solution, and the adsorbed oxygen species remained on the surface because of a slow consumption rate.