An Unbalanced Battle in Excellence: Revealing Effect of Ni/Co Occupancy on Water Splitting and Oxygen Reduction Reactions in Triple-Conducting Oxides for Protonic Ceramic Electrochemical Cells

Porous electrodes that conduct electrons, protons, and oxygen ions with dramatically expanded catalytic active sites can replace conventional electrodes with sluggish kinetics in protonic ceramic electrochemical cells. In this work, a strategy is utilized to promote triple conduction by facilitating proton conduction in praseodymium cobaltite perovskite through engineering non-equivalent B-site Ni/Co occupancy. Surface infrared spectroscopy is used to study the dehydration behavior, which proves the existence of protons in the perovskite lattice. The proton mobility and proton stability are investigated by hydrogen/deuterium (H/D) isotope exchange and temperature-programmed desorption. It is observed that the increased nickel replacement on the B-site has a positive impact on proton defect stability, catalytic activity, and electrochemical performance. This doping strategy is demonstrated to be a promising pathway to increase catalytic activity toward the oxygen reduction and water splitting reactions. The chosen PrNi0.7Co0.3O3-delta oxygen electrode demonstrates excellent full-cell performance with high electrolysis current density of -1.48 A cm(-2) at 1.3 V and a peak fuel-cell power density of 0.95 W cm(-2) at 600 degrees C and also enables lower-temperature operations down to 350 degrees C, and superior long-term durability.

Automated summary

By engineering non-equivalent B-site Ni/Co occupancy in praseodymium cobaltite perovskite, this work promotes triple conduction by facilitating proton conduction, replacing conventional electrodes with sluggish kinetics in protonic ceramic electrochemical cells. Surface infrared spectroscopy is used to study the dehydration behavior and proves the existence of protons in the perovskite lattice. The increased nickel replacement on the B-site positively impacts proton defect stability, catalytic activity, and electrochemical performance, making it a promising pathway for increasing catalytic activity in oxygen reduction and water splitting reactions.