材料科学
电解质
电极
电解
克拉克电极
氧化物
氢
电化学
可逆氢电极
高温电解
氧化钇稳定氧化锆
标准氢电极
氧气
化学工程
参比电极
化学
陶瓷
复合材料
冶金
立方氧化锆
物理化学
工程类
有机化学
作者
Giuseppe Sassone,Ӧzden Çelikbilek,Maxime Hubert,Katherine Develos-Bagarinao,Thomas David,Laure Guétaz,Isabelle Martin,Julie Villanova,Anass Benayad,Léa Rorato,Julien Vulliet,Bertrand Morel,Aline Léon,Jérôme Laurencin
标识
DOI:10.1016/j.jpowsour.2024.234541
摘要
The present work aims to better understand the effect of operating temperature on the degradation of Solid Oxide Electrolysis Cells (SOECs). The studied SOECs consist of La0.6Sr0.4Co0.2Fe0.8O3-δ-Ce0.8Gd0.2O2-δ (LSCF-GDC) oxygen electrode, GDC diffusion barrier layer, Y0.16Zr0.84O1.92 (YSZ) electrolyte and Ni-YSZ hydrogen electrode. Durability tests are carried out at 750, 800 and 850 °C for 2000 h at −1 A cm−2, using 10/90 vol% H2/H2O and dry air at the hydrogen and oxygen electrodes, respectively. The electrochemical impedance spectra measured before and after ageing reveal a strong evolution related to the hydrogen electrode, while the change in the oxygen electrode contribution remains negligible. A set of advanced characterization techniques are employed to study the cell degradation. For the hydrogen electrode, a large Ni depletion is observed after ageing, which increases with the operating temperature. The analysis of the oxygen electrode shows an elemental inter-diffusion between the LSCF-GDC/GDC/YSZ layers on the manufactured cells that seems to not evolve significantly upon operation. Moreover, the presence of SrZrO3 is not detected in the pristine cell and in the operated ones. Besides, only a limited LSCF decomposition is found in good agreement with the electrochemical characterizations. Hypotheses that could explain the good oxygen electrode stability are discussed.
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