Comprehensive Study on the Electrochemical Evolution, Reaction Kinetics, and Mass Transport at the Anion Exchange Ionomer–Pt Interface for Oxygen Reduction Reaction

Understanding the structure evolution, kinetics, and mass transfer for the oxygen reduction reaction (ORR) at the ionomer–catalyst interface is fundamental for the development of anion exchange membrane fuel cells (AEMFCs). Herein, we investigate the structural evolution of ionomer–Pt interfaces during the activation process of polycrystalline Pt (poly-Pt) electrodes and their ORR kinetics and mass transfer characteristics at steady state. The results suggest the ionomer thickness as a critical factor in determining the Pt surface structure and the flux of the O 2 diffusion, which in turn affect the subsequent kinetic and mass transfer of the ORR on ionomer–Pt electrode interfaces. Thicker ionomer film leads to a more severe evolution of electrochemical features during the activation process, likely caused by forming more less-active Pt clusters at the ionomer–Pt interface. Thus, the ORR kinetic activity at the steady state decreases with the increase in ionomer thickness. Concurrently, the thicker ionomer leads to a reduced diffusion flux of O 2, culminating in a lower limiting current density for the ORR. Additionally, we calculated the diffusion coefficient and solubility of O 2 within the FAA-3 alkaline ionomer film, with a comparative assessment against those in the proton exchange membrane (PEM). These findings offer valuable insights into the ionomer–Pt interface in AEMFCs and their effects on performance.