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Sintering Mechanisms of Cobalt-Doped Ceria and Zirconia Electrolytes in Intermediate-Temperature Solid Oxide Fuel Cells

机译:中温固体氧化物燃料电池中钴掺杂二氧化铈和氧化锆电解质的烧结机理

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摘要

Ce_(0.9)Gd_(0.1)O_(1.95)(CGO) and (ZrO_2)_(0.89)(Sc_2O_3)_(0.1)(Ceo_2)_(0.01)(ScSZ) have been proposed as possible alternative electrolytes in intermediate-temperature solid oxide fuel cells (SOFCs). In this study, the mechanisms of densely sintering Co-doped CGO and ScSZ electrolytes during the SOFC fabrication process were investigated using synchrotron X-ray diffraction (SR-XRD) analysis. The addition of CoO enhanced the sintering characteristics of both CGO and ScSZ. Based on the results of the SR-XRD analysis, it was found that CGO and CoO did not form a solid solution after heat treatment at 1200℃ for 10 h. On the other hand, the solubility limit of Co in ScSZ was estimated to be ≤3 mol% after firing at 1400℃, and Co doping accelerated the conversion of the two phases of the fluorite structures with cubic and rhombohedral phases into a single cubic phase. Because no significant densification of the Co-doped ScSZ samples was observed before and after the phase change and Co diffusion, it suggests that these reaction sintering processes should not be strongly related to densification. From the results of scanning electron microscopy, Co doping suggests to assist the densification of the ScSZ samples through liquid phase sintering, similar to Co-doped CGO.
机译:已提出Ce_(0.9)Gd_(0.1)O_(1.95)(CGO)和(ZrO_2)_(0.89)(Sc_2O_3)_(0.1)(Ceo_2)_(0.01)(ScSZ)的建议高温固体氧化物燃料电池(SOFC)。在这项研究中,使用同步加速器X射线衍射(SR-XRD)分析了在SOFC制备过程中致密烧结Co掺杂CGO和ScSZ电解质的机理。 CoO的添加增强了CGO和ScSZ的烧结特性。根据SR-XRD分析的结果,发现CGO和CoO在1200℃热处理10 h后没有形成固溶体。另一方面,在1400℃烧成后,Co在ScSZ中的溶解度极限估计为≤3mol%,并且Co掺杂促进了具有立方和菱形面相的萤石结构两相向单立方相的转化。 。由于在相变和Co扩散之前和之后均未观察到Co掺杂的ScSZ样品的显着致密化,因此表明这些反应烧结过程不应与致密化密切相关。根据扫描电子显微镜的结果,Co掺杂建议通过液相烧结来协助ScSZ样品的致密化,类似于Co掺杂的CGO。

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