(452g) Kinetic Mechanism of Oxygen Reduction Reaction on Fe–N–C Catalysts

Oxygen reduction reaction (ORR) is essential to various renewable energy technologies. An important catalyst for ORR is single iron atoms embedded in nitrogen-doped graphene (Fe–N–C). However, the rate-limiting step of the ORR on Fe–N–C is unknown, significantly impeding understanding and improvement. We have studied the activation energies of all steps, calculated by ab initio molecular dynamics simulations under constant electrode potential. In contrast to the common belief that a hydrogenation step limits the reaction rate, we find that the rate-limiting step is oxygen molecule replacing adsorbed water on Fe. This occurs through concerted motion of H₂O desorption and O₂ adsorption, without leaving the site bare. Interestingly, despite being an apparent “thermal” process that is often considered to be potential-independent, the barrier reduces with the electrode potential. This can be explained by stronger Fe–O₂ binding and weaker Fe–H₂O binding at a lower potential due to O₂ gaining electrons and H₂O donating electrons to the catalyst. Our study offers new insights into the ORR on Fe–N–C and highlights the importance of kinetic studies in heterogeneous electrochemistry.