A-Site Engineering of the High-Entropy Perovskite Pr_0.4La_0.4Ba_0.4Sr_0.4Ca_0.4Fe₂O_5+δ Cathode for...

Mixed-oxygen ionic and electronic conduction is crucial for the cathode materials of solid oxide fuel cells, ensuring high efficiency and low-temperature operation. However, the electronic and oxygen ionic conductivity of traditional Fe-based layered perovskite cathode materials is low, resulting in insufficient oxygen reduction reactivity. Herein, a type of high-entropy perovskite oxide consisting of five equimolar metals, Pr_0.4La_0.4Ba_0.4Sr_0.4Ca_0.4Fe₂O_5+δ (PLBSCF), a high-performance cobalt-free cathode derived from the PrBaFe₂O_5+δ (PBF), is proposed. Such A-site engineering could not only increase the oxygen vacancy concentration of PLBSCF but also give higher conductivity than PBF, thus significantly reducing the polarization impedance of the symmetric cell to only 0.052 Ω·cm² at 750 °C. The good output performance of a single cell is also realized. The peak power density of the single cell with PLBSCF-Ce_0.9Gd_0.1O_2-δ (GDC) as the cathode at 750 °C was 0.853 W·cm^-2. Additionally, the single cell with the PLBSCF cathode exhibits a good durable performance of 100 h at 750 °C. Combining the distribution of relaxation time analysis, it can be seen that the enhancement of the oxygen reduction reaction is due to the reduction of intermediate-frequency and low-frequency resistance, indicating an improvement in the charge transfer process and adsorption/dissociation process of molecular oxygen.