부산대학교 도서관

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-MnO2is markedly influenced by a MnIII/MnIIredox 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/MnIIredox couple based on the potential dependence of the UV–vis spectra. Notably, the UV–vis absorption of MnIIIdid not diminish even after the OER was initiated, and another redox process was observed at the OER onset, indicating that MnIII/MnIIis not the rate-determining step for OER on α-MnO2in alkaline pH. Numerical simulations using physicochemical parameters of MnIII/MnIIobtained from trumpet plot analyses reproduce the experimental Tafel slopes, indicating that the Tafel slope can be influenced by a non-rate-determining step.