A Non-Rate-Determining Redox Process Dictates the Oxygen Evolution Tafel Slope of MnO2

Electrocatalytic activity is markedly influenced by the Tafel slope, which dictates the sensitivity of the catalytic current, with respect to the potential. Differences in the Tafel slope between electrocatalysts have been rationalized based on redox pre-equilibria preceding the rate-determining step. However, no study has experimentally observed a direct correlation between a non-rate-determining redox event and the Tafel slope. Here, we show that the Tafel slope of the oxygen evolution reaction (OER) on α-MnO2 is markedly influenced by a MnIII/MnII redox process located 500 mV more negative than the OER onset potential. Upon repeated cyclic voltammetry sweeps in an alkaline media, a correlation was observed between the Tafel slope and the peak position of a redox event, which was assigned to a MnIII/MnII redox couple based on the potential dependence of the UV–vis spectra. Notably, the UV–vis absorption of MnIII did not diminish even after the OER was initiated, and another redox process was observed at the OER onset, indicating that MnIII/MnII is not the rate-determining step for OER on α-MnO2 in alkaline pH. Numerical simulations using physicochemical parameters of MnIII/MnII obtained from trumpet plot analyses reproduce the experimental Tafel slopes, indicating that the Tafel slope can be influenced by a non-rate-determining step.