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Degradation of Metal-supported Cells with Ni-YSZ or Ni-Ni_3Sn-YSZ Anodes Operated with Methane-based Fuels

机译:用基于甲烷的燃料操作的Ni-YSZ或Ni-Ni_3SN-YSZ阳极的金属负载细胞的降解

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Ni-Ni_3Sn-YSZ and Ni-YSZ anodes were incorporated into metal-supported SOFCs that consisted of a porous metal support (Sandvik Sanergy), samaria-doped ceria (SDC) barrier layer, anode as previously described, YSZ electrolyte, and La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)-SDC cathode. Cells were tested at 750°C with air as the oxidant and fuel consisting of 65% CH_4, 32% H_2, and 3% H_2O. The cells were held at a current density of 0.15 A·cm~(-2) for 500 hours. The cell without tin in the anode began to degrade after approximately 200 hours and catastrophically failed at approximately 425 hours. After testing, we observed that the anode had disintegrated, and as a result, the electrolyte and cathode were completely detached from the metal support. On the other hand, the cell with an anode containing tin did not catastrophically fail, and the cell remained intact after 500 hours of operation. Over 500 hours, the cell potential degraded from 0.841 V to 0.743 V, and scanning electron micrographs showed that the anode had delaminated from the electrolyte in some areas. Nonetheless, the cell with the Ni-Ni_3Sn-YSZ anode degraded significantly less than the cell containing a Ni-YSZ anode, suggesting that the addition of Ni_3Sn to an anode could be a useful strategy for improving durability of SOFC anodes using hydrocarbon fuels.
机译:Ni-Ni_3SN-YSZ和Ni-YSZ阳极掺入金属负载的SOFC中,该金属支撑的SOFC组成,由多孔金属载体(Sandvik Sanergy),撒玛利亚掺杂的二氧化铈(SDC)阻挡层,阳极如前所述,YSZ电解质和LA_( 0.6)SR_(0.4)CO_(0.2)FE_(0.8)O_(3-Δ)-SDC阴极。用空气在750℃下测试细胞,作为氧化剂和由65%CH_4,32%H_2和3%H_2O组成的燃料。将细胞保持在0.15a·cm〜(-2)的电流密度500小时。在大约200小时后,没有锡中没有锡的细胞开始在大约200小时后降解,并且在大约425小时的灾难性失效。在测试之后,我们观察到阳极已经崩解,结果,电解质和阴极完全从金属载体中脱离。另一方面,含有锡的阳极的细胞没有灾难性地失败,并且在操作的500小时后细胞保持完整。超过500小时,电池电位从0.841 V降解到0.743V,扫描电子显微照片显示阳极在某些区域中的电解质中划分。尽管如此,具有Ni-Ni_3Sn-ysz阳极的细胞显着低于含有Ni-YSZ阳极的细胞,表明Ni_3Sn与阳极的添加可以是用于使用烃燃料改善SOFC阳极耐久性的有用策略。

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