Temperature-dependent oxygen electrochemistry on platinum low-index single crystal surfaces in acid solutions

Using the rotating ring-disk technique (RRD Pt(hkl) E), the oxygen-reduction reaction (ORR) was studied in sulfuric acid solution over the temperature range 298–333 K At the same temperature, the exchange current density increased in the order, Formula: see text which gives the order of absolute kinetic activities of Pt(hkl) in 0.05 mol/L H 2 SO 4 : Pt(111) < Pt(100) < Pt(110). We found that at high current densities every crystal face has an ideally temperature-dependent Tafel slope, i.e., −2 × 2.3(RT/F). The activation energy for the ORR is independent of the surface geometry, Formula: see text. The insensitivity of the activation energy to surface structure implies that the reaction pathway for the ORR is the same on all three single-crystal faces. A "series" pathway for the ORR was proposed, with the first electron transfer being the rate-determining step. The structure sensitivity in the kinetics of the ORR on Pt(hkl) is attributed to the structure-sensitive adsorption of bisulfate and hydroxyl anions and a simple site-blocking effect of these adsorbed anions on the rate of the ORR. Keywords: platinum single crystals, oxygen reduction, peroxide reduction, temperature effects, activation energy.