Bismuth-based oxides are promising electrolyte materials for Reversible Solid Oxide Cells (RSOCs) due to their high ion conductivity and rapid surface oxygen exchange kinetics. In this work we propose a multi-element doping strategy to obtain a novel Dy0.06Gd0.02Er0.02Bi1.9O3 (DGESB) quaternary oxide bismuth material whose ionic conductivities and crystal structure are characterized by AC impedance and X-ray diffraction technique in the temperature range from 600 to 700 °C. Along with promising structure stability and durability, our novel DGESB showed a remarkable ionic conductivity that is 65 times higher than the commercial yttria-stabilized zirconia (YSZ) electrolyte at 700 °C. With composite electrode of DGESB + LCN (LaCo0.6Ni0.4O3) and DGESB/YSZ bilayer electrolyte consisting of RSOC symmetric cell, which achieves a high peak power density (PPD) of 1.62 W/cm2 in fuel cell mode which is 2.7 times higher than that of YSZ single-layer electrolyte, while the electrolysis current density is as high as 1.66 A/cm2 at 1.3 V under H2/H2O:50/50 in electrolysis mode at the same operation temperature of 700 °C. The electrochemical performance measurements revealed a certain stable operation for 200 h in fuel cell mode. The performance degradation can be attributed to the microstructure evolution at the interface between electrolyte and electrodes. The high ionic conductive DGESB proves to be an excellent intermediate electrolyte layer for improving cell performance in RSOCs
Read full abstract