Shin Ji-Seop, Saqib Muhammad, Jo Minkyeong, Park Kwangho, Park Kwang Min, Ahn Jin Soo, Lim Hyung-Tae, Park Jun-Young
HMC, Department of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul 05006, Korea.
Research Institute of Industrial Science and Technology (RIST), Pohang 37673, Korea.
ACS Appl Mater Interfaces. 2021 Oct 27;13(42):49868-49878. doi: 10.1021/acsami.1c13779. Epub 2021 Oct 13.
A critical issue to tackle before successful commercialization of solid oxide fuel cells (SOFCs) can be achieved is the long-term thermal stability required for SOFCs to operate reliably without significant performance degradation despite enduring thermal cycling. In this work, the impact of thermal cycling on the durability of NiO-yttria-stabilized zirconia-based anode-supported cells is studied using three different heating/cooling rates (1, 2, and 5 °C min) as the temperature fluctuated between 400 and 700 °C. Our experiments simulate time periods when power from SOFCs is not required (e.g., as might occur at night or during an emergency shutdown). The decay ratios of the cell voltages are 8.8% (82 μV h) and 19.1% (187 μV h) after thermal cycling testing at heating/cooling rates of 1 and 5 °C min, respectively, over a period of 1000 h. The results indicate SOFCs that undergo rapid thermal cycling experience much greater performance degradation than cells that experience slow heating/cooling rates. The changes in total resistance for thermally cycled cells are determined by measuring the of the electrodes (whereas the ohmic resistances of the cells remain unchanged from their initial value), signifying that electrode deterioration is the main degradation mechanism for SOFCs under thermal cycling. In particular, fast thermal cycling leads to severe degradation in the anode part of SOFCs with substantial agglomeration and depletion of Ni particles seen in our characterizations with field emission-scanning electron microscopy and electron probe microanalysis. In addition, the mean particle size in the cathode after thermal cycling testing increases from 0.104 to 0.201 μm for the 5 °C min cell. Further, the presence of Sr-enriched regions is more significant in the LaSrCoFeO cathode after fast thermally cycled SOFCs.
在实现固体氧化物燃料电池(SOFC)成功商业化之前需要解决的一个关键问题是,SOFC要在经历热循环的情况下仍能可靠运行且性能无显著下降所需的长期热稳定性。在这项工作中,研究了热循环对基于氧化镍-氧化钇稳定氧化锆的阳极支撑电池耐久性的影响,使用了三种不同的加热/冷却速率(1、2和5℃/分钟),温度在400至700℃之间波动。我们的实验模拟了不需要SOFC供电的时间段(例如,可能在夜间或紧急停机时出现)。在1℃/分钟和5℃/分钟的加热/冷却速率下进行1000小时的热循环测试后,电池电压的衰减率分别为8.8%(82μV/小时)和19.1%(187μV/小时)。结果表明,经历快速热循环的SOFC比经历缓慢加热/冷却速率的电池性能下降要大得多。通过测量电极的(此处原文缺失相关内容)来确定热循环电池的总电阻变化(而电池的欧姆电阻保持其初始值不变),这表明电极劣化是热循环下SOFC的主要降解机制。特别是,快速热循环导致SOFC阳极部分严重降解,在我们用场发射扫描电子显微镜和电子探针微分析进行的表征中可以看到镍颗粒大量团聚和耗尽。此外,对于5℃/分钟的电池,热循环测试后阴极中的平均粒径从0.104μm增加到0.201μm。此外,在快速热循环的SOFC之后,LaSrCoFeO阴极中富锶区域的存在更为明显。