1. Electrochemical performance of La0.65Sr0.35MnO3 oxygen electrode with alternately infiltrated Sm0.5Sr0.5CoO3-δ and Sm0.2Ce0.8O1.9 nanoparticles for reversible solid oxide cells
- Author
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Xu Zhang, Pingping Wu, Yanting Tian, Zhe Lü, and Lili Ding
- Subjects
Materials science ,Renewable Energy, Sustainability and the Environment ,Oxide ,Energy Engineering and Power Technology ,Condensed Matter Physics ,Electrochemistry ,Redox ,law.invention ,chemistry.chemical_compound ,Fuel Technology ,chemistry ,Chemical engineering ,law ,Electrode ,Ionic conductivity ,Polarization (electrochemistry) ,Clark electrode ,Yttria-stabilized zirconia - Abstract
La1-xSrxMnO3 is a well-known oxygen electrode for reversible solid oxide cells (RSOCs). However, its poor ionic conductivity limits its performance in redox reaction. In this study, we selected Sm0.5Sr0.5CoO3-δ (SSC) as catalyst and Sm0.2Ce0.8O1.9 (SDC) as ionic conductor and sintering inhibitor to co-modify the La0.65Sr0.35MnO3 (LSM) oxygen electrode through an alternate infiltration method. The infiltration sequence of SSC and SDC showed an influence on the morphology and performance of LSM oxygen electrode, and the influence was gradually weakened with the increasing infiltration time. The polarization resistance of the alternately infiltrated LSM-SSC/SDC electrode was 0.08 Ω cm2 at 800 °C in air, which was 3.36% of the LSM electrode (2.38 Ω cm2). The Ni-YSZ/YSZ/LSM-SSC/SDC single cell attained a maximum power density of 1205 mW cm−2 in SOFC mode at 800 °C, which was 8.73 times more than the cell with LSM electrode. The current density achieved 1620 mA .cm−2 under 1.5 V at 800 °C in SOEC mode and the H2 generation rate was 3.47 times of the LSM oxygen electrode.
- Published
- 2022