A-Site High-Entropy Engineering Enables a Cobalt-Free Perovskite Air Electrode with Exceptional Activity and Durability for Reversible Solid Oxide Cells

Abstract

The limited catalytic activity and durability of cobalt-free perovskite air electrodes exist a significant obstacle to their widespread application in reversible solid oxide cells (RSOCs). Cobalt-free Bi 0.5 Sr 0.5 FeO 3-δ (BSF) air electrode exhibits a comparatively desirable performance and is expected to be further optimized. Herein, an A-site high-entropy perovskite oxide La 0.2 Pr 0.2 Bi 0.2 Sr 0.2 Ca 0.2 FeO 3-δ (LPBSC) through introducing small-sized atoms at the A-site of BSF to induce lattice distortion is designed. The optimized LPBSC demonstrates exceptional oxygen-ion diffusivity (D chem = 4.129 × 10 -2 cm 2 s -1 ) and surface exchange kinetics (K chem = 4.30 × 10 -2 cm 2 s -1 ), leading to a 54.24% reduction in polarization resistance (from 0.148 to 0.059 Ω cm 2 ) at 750 ℃. Moreover, LPBSC exhibits excellent tolerance to CO 2 and Cr poisoning with its polarization resistance remaining unchanged even under 10% CO 2 or accelerated Cr poisoning conditions. In fuel cell mode, the single cell achieves a remarkable peak power density of 921 mW cm -2 at 750 °C. In electrolysis cell mode, a current density of 1915 mA cm -2 is achieved at 750 °C under an applied voltage of 1.5 V in a 70% CO 2 /30% CO atmosphere. The A-site high-entropy strategy induces lattice distortion of BSF, enhancing the structural stability and suppressing the phase transformation and elemental segregation, thereby preserving outstanding catalytic activity. This design significantly improves the resistance to both CO 2 and Cr poisoning, offering a novel approach to enhance the oxygen reduction/evolution reaction (ORR/OER) activity and environmental tolerance of cobalt-free air electrodes for RSOCs.