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Effect of H_2O and CO_2 on LSCF-GDC Composite Cathodes

机译:H_2O和CO_2对LSCF-GDC复合阴极的影响

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Polarization losses associated with the cathode oxygen reduction reaction (ORR) and degradation of cathode materials remain as hurdles for widespread implementation of solid oxide fuel cells (SOFC). Rates of degradation depend significantly on the operating temperature and gas conditions, such as the presence of unwanted oxygen-containing compounds, namely H_2O and CO_2. In this study, we explore H_2O and CO_2 degradation mechanisms for a common composite cathode material, La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ) (LSCF) - Ce_(0.90)Gd_(0.10)O_(1.95) (GDC) using electrochemical impedance spectroscopy (EIS) under various temperatures, oxygen partial pressure, and contaminant conditions to determine the effect of H_2O and CO_2 on LSCF-GDC. Our results suggest that CO_2 and H_2O compete with the ORR, and a strong correlation between blocking, degradation, and sintering effects caused by CO_2 and H_2O is directly observed. The interactions of CO_2 and H_2O with the cathode surface changes as a function of operating temperature, resulting in different short-term or long-term degradation mechanisms.
机译:与阴极氧还原反应(ORR)相关的偏振损失和阴极材料的降解仍然是用于固体氧化物燃料电池(SOFC)的广泛实施的障碍。降解率显着取决于工作温度和气体条件,例如存在不需要的含氧化合物,即H_2O和CO_2。在这项研究中,我们探讨了通用复合阴极材料的H_2O和CO_2劣化机制,LA_(0.6)SR_(0.4)CO_(0.2)FE_(0.8)O_(3-Δ) - CE_(0.90)GD_( 0.10)O_(1.95)(GDC)在各种温度下使用电化学阻抗谱(EIS),氧分压和污染物条件,以确定H_2O和CO_2对LSCF-GDC的影响。我们的结果表明,CO_2和H_2O与ORR竞争,并直接观察到由CO_2和H_2O引起的阻塞,劣化和烧结效应之间的强相关性。 Co_2和H_2O与阴极表面的相互作用随工作温度的函数而变化,导致不同的短期或长期降解机制。

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