Zekri Atef, Knipper Martin, Parisi Jürgen, Plaggenborg Thorsten
Energy and Semiconductor Research Laboratory, Department of Physics, University of Oldenburg, Carl-von-Ossietzky Strasse 9-11, 26129 Oldenburg, Germany.
Phys Chem Chem Phys. 2017 May 31;19(21):13767-13777. doi: 10.1039/c7cp02186k.
Solid oxide fuel cells (SOFCs) are electrochemical conversion devices, which essentially consist of two porous electrodes separated by a dense, oxide ion conducting electrolyte. The performance and the durability of SOFCs strongly depend on the electrode microstructure. In this paper, the impact of a relatively long exposure time (up to 20 000 h) under realistic operation terms (temperature (T) = 850 °C, current density (J) = 190-250 mA cm) in the kinetics of microstructural degradation are investigated for porous nickel (Ni)/ceria gadolinium oxide (CGO) anodes, to understand the microstructural evolution in SOFC cermet anodes. A combined system of Focused Ion Beam (FIB) and Scanning Electron Microscope (SEM) tomography was used to analyze various anode microstructures aged during different operating times (2500 h, 15 000 h and 20 000 h). The methodologies of image acquisition as well as the segmentation and the object recognition were improved, offering a reliable quantification of Ni-grain growth, connectivity, tortuosity factor and triple phase boundary length (TPBL). The representative volume element (RVE) was also studied, and its dependence on aging time was confirmed. To construct a volume that can be accurate and representative for the whole sample, the necessary corresponding 3D reconstruction size was adjusted by increasing operating time, in order to suppress the influence of microstructure variation caused by Ni and CGO agglomeration. Statistically significant 3D microstructural changes were observed in the anode by increasing the operating time, including nickel particle size distribution, changes in connectivity of the ceramic part (CGO) and a significant decrease of contiguous triple phase boundary densities. Additional qualitative observations were done in order to gain a complete insight of the degradation phenomena in nickel based cermet anodes.
固体氧化物燃料电池(SOFC)是一种电化学转换装置,它主要由两个多孔电极组成,中间隔着一层致密的、传导氧离子的电解质。SOFC的性能和耐久性在很大程度上取决于电极的微观结构。本文研究了在实际运行条件下(温度(T)=850°C,电流密度(J)=190 - 250 mA/cm),较长暴露时间(长达20000小时)对多孔镍(Ni)/氧化铈钆(CGO)阳极微观结构降解动力学的影响,以了解SOFC金属陶瓷阳极的微观结构演变。采用聚焦离子束(FIB)和扫描电子显微镜(SEM)断层扫描的组合系统,分析了在不同运行时间(2500小时、15000小时和20000小时)老化后的各种阳极微观结构。改进了图像采集以及分割和目标识别方法,能够可靠地量化镍晶粒生长、连通性、曲折因子和三相边界长度(TPBL)。还研究了代表性体积单元(RVE),并证实了其对老化时间的依赖性。为了构建一个能够准确代表整个样品的体积,通过增加运行时间来调整必要的相应三维重建尺寸,以抑制由镍和CGO团聚引起的微观结构变化的影响。通过增加运行时间,在阳极中观察到了具有统计学意义的三维微观结构变化,包括镍颗粒尺寸分布、陶瓷部分(CGO)连通性的变化以及连续三相边界密度的显著降低。还进行了额外的定性观察,以便全面了解镍基金属陶瓷阳极的降解现象。