Iridium Surface Oxide Affects the Nafion Interface in Proton-Exchange-Membrane Water Electrolysis
Sarah A. Berlinger, Xiong Peng, Xiaoyan Luo, Peter J. Dudenas, Guosong Zeng, Haoran Yu, David A. Cullen, Adam Z. Weber, Nemanja Danilovic, Ahmet Kusoglu
Abstract
Proton-exchange-membrane water electrolyzer (PEMWE) catalyst layers consist of aggregates of catalyst particles (typically iridium) and ionomer (typically Nafion). Prior work suggests that the oxide form of Ir affects the kinetics of the oxygen-evolution reaction. However, because most catalyst-benchmarking studies are conducted ex situ in liquid electrolytes, it remains unclear how the ionomer is influenced by the catalyst oxide and affects overall cell performance. Using a suite of experimental techniques, we conduct fundamental investigations into model ink (catalyst and ionomer dispersed in solution) and thin-film systems to inform cell-level overpotential analysis as a function of three forms of Ir (metallic Ir m, oxyhydroxide IrOOH, and oxide IrO 2 ). Nafion on Ir m has a high degree of phase separation and higher swelling, likely improving the ionic conductivity. Additionally, Nafion binds most strongly to IrOOH, likely yielding reduced kinetic overpotentials. These findings highlight the intricacies of the ionomer/Ir interface and provide insight into all catalyst-layer systems.