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Long Term Testing of Solid Oxide Electrolysis Cells Under Co-Electrolysis Conditions

机译:在共电解条件下的固体氧化物电解细胞长期检测

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SOECs consisting of a nickel-yttria stabilized zirconia (Ni-YSZ) fuel electrode, YSZ electrolyte and lanthanum strontium cobalt ferrite-gadolinium doped ceria (LSCF-GDC) composite oxygen electrode were tested under co-electrolysis (H_2O+CO_2) conditions. The aim in this study was to compare the SOEC durability under co-electrolysis conditions between galvanostatic and potentiostatic modes. Specifically, the cells were operated at 0.75 A/cm~2 (galvanostatic) and at 1.2 V (potentiostatic) at 750 °C for over 1000 hours. In both modes, a larger degradation was observed initially for the first 200 hours of testing, followed by a more stable performance over longer operating times. Trends of the area specific resistance (ASR) and detailed electrochemical analysis of the cell's performance under durability conditions for both modes indicated that the degradation was predominantly due to the fuel electrode along with a slight contribution from the oxygen electrode. Microstructural analysis also confirmed the degradation of the active fuel electrode.
机译:在共电解(H_2O + CO_2)条件下,测试由镍钇稳定的氧化锆(Ni-YSZ)燃料电极,YSZ电解质和镧系钴 - 钆掺杂的二氧化铈(LSCF-GDC)复合氧电极的掺杂二氧化碳(LSCF-GDC)复合氧电极。本研究的目的是在加管静脉和电位模式之间的共同电解条件下比较SOEC耐久性。具体地,在750℃下以0.75A / cm〜2(Galvanostatic)和1.2V(肺部)以1000小时以1.2V(肺部静脉)操作。在两种模式中,最初观察到更大的降解,用于测试前200小时的测试,然后在较长较长的操作时间内进行更稳定的性能。面积特异性电阻(ASR)的趋势和细胞在两种模式下耐久性条件下的细胞性能的详细电化学分析表明,由于燃料电极以及来自氧电极的微小贡献,因此劣化主要是由于氧电极的略有贡献。微结构分析还证实了活性燃料电极的劣化。

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