首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Evaluation of cation migration in lanthanum strontium cobalt ferrite solid oxide fuel cell cathodes via in-operando X-ray diffraction
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Evaluation of cation migration in lanthanum strontium cobalt ferrite solid oxide fuel cell cathodes via in-operando X-ray diffraction

机译:逆转X射线衍射镧锶铁氧体固体固体氧化物燃料电池阴极阳离子迁移评价

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摘要

Anode-supported SOFC button cells with LSCF-6428 cathodes were operated at various temperatures under constant current conditions for hundreds of hours in dry or humid (similar to 3% water) cathode air while continuously collecting 1 hour XRD scans throughout the test duration. Additionally, one cell in dry air was held at OCV, and 12% CO2 was added to the humid air for another cell. Long cumulative XRD count times allowed minor phases in concentrations of less than 0.1 wt% to be identified. In humid air, cell performance increased during the first couple of hundred hours. XRD measured a gradual shift of Fe-rich Fe,Co spinel peaks to lower angles while post-mortem SEM discovered nano-nodules on the LSCF surfaces. When 12% CO2 was added to humid air, performance degradation was observed after the initial conditioning response, unlike in tests without CO2, which were stable after conditioning. XRD also measured a shift in the peaks of the major LSCF phase in the test with CO2 indicative of some degree of gradual decomposition. Cells tested at constant current in dry air exhibited fast initial degradation that decelerated over time, while the cell held at OCV maintained a stable voltage. XRD of the cathodes held at OCV at 750 degrees C and operated at constant current at 700 degrees C in dry air measured a slower shift of the Fe-rich spinel peaks to lower angles than was seen in tests in humid air, along with a shift in the peaks of a Co-rich Fe, Co spinel to higher angles. Post-mortem SEM of cells exposed to dry air discovered smaller nano-nodules on the LSCF surfaces than had been present in cells tested in humid air. Cells tested at constant current in dry air at 750 degrees C and 800 degrees C did not exhibit any gradual changes in the XRD patterns nor were nano-nodules discovered.
机译:具有LSCF-6428阴极的阳极支持的SOFC按钮单元在恒定电流条件下的各种温度下操作数百小时干燥或潮湿(类似于3%水)阴极空气,同时连续收集在整个测试持续时间内的1小时XRD扫描。另外,在OCV下保持干燥空气中的一个细胞,将12%CO 2加入到另一个细胞的湿气中。长累积XRD计数次数使得浓度小于0.1wt%的浓度小相。在潮湿的空气中,在第一百小时内,细胞性能增加。 XRD测量了Fe Rich Fe的逐渐转移,Co尖晶石峰值降低角度,而验尸SEM在LSCF表面上发现纳米结节。当向潮湿空气中加入12%CO 2时,在初始调理响应后观察到性能降解,与没有CO2的试验不同,在调节后稳定。 XRD还测量了在测试中主要LSCF相的峰值的转变,CO2指示一定程度的逐渐分解。在干燥空气中恒定电流测试的细胞表现出快速的初始劣化,随着时间的推移减速,而在OCV处保持的电池保持稳定的电压。在750℃下保持在OCV的阴极的XRD并以700摄氏度的恒定电流在干燥空气中操作,测量Fe富尖晶石峰值的较慢的偏移,比在潮湿空气中的测试中观察到的较低角度。在共同富含Fe的峰值中,CO尖晶石到更高的角度。暴露于干燥空气的细胞的后验验SEM在LSCF表面上发现了比在潮湿空气中测试的细胞中的较小纳米结节。在750℃和800摄氏度下在干燥空气中测试的细胞在XRD图案中没有表现出XRD图案的任何逐渐变化,也不存在纳米结节。

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