A Non-Rate-Determining Redox Process Dictates the Oxygen Evolution Tafel Slope of MnO <sub>2</sub>
Koichi Yatsuzuka, Kiyohiro Adachi, Ailong Li, Shuang Kong, Satoru Hamamoto, Daisuke Hashizume, Ryuhei Nakamura, Hideshi Ooka
Abstract
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-MnO 2 is markedly influenced by a Mn III /Mn II 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 Mn III /Mn II redox couple based on the potential dependence of the UV–vis spectra. Notably, the UV–vis absorption of Mn III did not diminish even after the OER was initiated, and another redox process was observed at the OER onset, indicating that Mn III /Mn II is not the rate-determining step for OER on α-MnO 2 in alkaline pH. Numerical simulations using physicochemical parameters of Mn III /Mn II obtained from trumpet plot analyses reproduce the experimental Tafel slopes, indicating that the Tafel slope can be influenced by a non-rate-determining step.