首页> 外文期刊>Journal of industrial and engineering chemistry >Ce_(0.8)Gd_(0.2)O2 modification on La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O3 cathode for improving a cell performance in intermediate temperature solid oxide fuel cells
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Ce_(0.8)Gd_(0.2)O2 modification on La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O3 cathode for improving a cell performance in intermediate temperature solid oxide fuel cells

机译:在La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O3阴极上修饰Ce_(0.8)Gd_(0.2)O2以改善中温固体氧化物燃料电池的电池性能

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摘要

To increase the cell performance of solid oxide fuel cells operated at intermediate temperature (600-800 °C), Ce_(0.8)Gd_(0.2)O2 (GDC) was applied to the La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O3(LSCF) cathode in electrode microstructure using sol-gel coating. We employed a GDC as a diffusion barrier layer on the yttria-stabilized zironia (YSZ) electrolyte to prevent the interlayer formation of SrZrO3, which has poor ionic conductivity. This interfacial reaction product was hardly formed at the electrolyte-cathode interlayer after sintering the GDC layer resulting to reduce the cathode polarization resistance. Moreover, we use sol-gel method to coat GDC thin layer through the cathode pore wall surface to extend the triple phase boundary (TPB) area. The cathode polarization resistance also reduced due to the additional TPB area. For the single cell featuring LSCF cathode modified with GDC sol-gel coating, the maximum densities were 0.41 W/cm~2 and 0.89 W/cm~2 at 700 °C and 800 °C.
机译:为了提高在中等温度(600-800°C)下操作的固体氧化物燃料电池的电池性能,将Ce_(0.8)Gd_(0.2)O2(GDC)应用于La_(0.6)Sr_(0.4)Co_(0.2)使用溶胶-凝胶涂层的电极微结构中的Fe_(0.8)O3(LSCF)阴极。我们在氧化钇稳定的氧化锆(YSZ)电解质上采用了GDC作为扩散阻挡层,以防止SrZrO3的层间形成,而SrZrO3的离子导电性较差。在烧结GDC层之后,几乎不在电解质-阴极中间层上形成该界面反应产物,从而降低了阴极极化电阻。此外,我们使用溶胶-凝胶法通过阴极孔壁表面涂覆GDC薄层,以扩展三相边界(TPB)区域。由于额外的TPB面积,阴极极化电阻也降低了。对于具有GDC溶胶-凝胶涂层改性的LSCF阴极的单电池,在700°C和800°C时,最大密度分别为0.41 W / cm〜2和0.89 W / cm〜2。

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