Isotope-dependent Tafel analysis probes proton transfer kinetics during electrocatalytic water splitting
Jinzhen Huang, Ran Wang, Hongyuan Sheng, Xiaorong Zhu, R. Dominic Ross, Daxing Hua, Lin Lei, Yafei Li, Qinghua Zhang, Lin Gu, Xianjie Wang, Ping Xu, Jun Lü, Sida Jiang, Jiecai Han, Bo Song, Song Jin
Abstract
Proton transfer plays an important role in both hydrogen and oxygen evolution reactions during electrocatalytic water splitting to produce green hydrogen. However, directly adapting the conventional proton/deuterium kinetic isotope effect to study proton transfer in heterogeneous electrocatalytic processes is challenging. Here we propose using the shift in the Tafel slope between protic and deuteric electrolytes, or the Tafel slope isotope effect, as an effective probe of proton transfer characteristics. Comparison of the Tafel slope isotope effect for diverse hydrogen and oxygen evolution reaction electrocatalysts in different pH environments reveals that proton transfer is both pH and structure dependent. Using ruthenium oxide as an example, we show that local structure modification can change the rate-determining step from an electrochemical, concerted proton–electron transfer step to a chemical step and improve the oxygen evolution activity in acid. The isotope-dependent Tafel analysis will facilitate a better understanding of the proton transfer behaviours during electrocatalytic processes and provide guidance for designing efficient electrocatalysts. Proton transfer plays a key role in fuel-producing reactions, but directly monitoring these processes in heterogeneous electrocatalysts is challenging. Now it has been shown that shifts in the Tafel slope in protic versus deuteric electrolytes can elucidate the rate-determining step during water splitting and reveal pH- and structure-dependent proton transfer behaviours.