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Microstructure and Performance of Ni-Free Nano La0.75Sr0.25Cr0.5Mn0.5O3 - Gd0.2Ce0.8Ox Composite Anode

材料科学 微观结构 阳极 成核 固体氧化物燃料电池 氧化钇稳定氧化锆 化学工程 复合数 金属陶瓷 电解质 纳米- 晶粒生长 粒度 氧化物 冶金 纳米颗粒 陶瓷 立方氧化锆 纳米技术 复合材料 电极 化学 有机化学 工程类 物理化学
作者
Anna Ściążko,Jo Kubota,Kazuyoshi Sato,Yosuke Komatsu,Naoki Shikazono
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2021-03 (1): 273-273
标识
DOI:10.1149/ma2021-031273mtgabs
摘要

Degradation of conventional solid oxide fuel cell (SOFC) anode is often associated with nickel coarsening and redox instability. Great efforts have been made to find alternative materials to replace the state-of-the-art nickel - yttria-stabilized zirconia (Ni-YSZ) anode cermet. In the previous study, La 0.9 Sr 0.1 Cr 0.5 Mn 0.5 O 3 -Gd 0.1 Ce 0.9 O x (LSCM-GDC) composite anode was investigated as one of the possible alternatives for Ni-free SOFC (1). The LSCM-GDC composite was fabricate by mixing commercial powders in the designated proportion. It was shown that the surface area of GDC has to be increased and the grain size has to be decreased in order to compensate for the poor electrocatalytic properties. In this study, the microstructure and electrochemical performance of Ni-free anode fabricated with La 0.75 Sr 0.25 Cr 0.5 Mn 0.5 O 3 : Gd 0.2 Ce 0.8 O x = 50 : 50 w.% (LSCM-GDC) nano-powder are investigated. The LSCM-GDC nano-composite particles were prepared through colloidal-processing-based approach (2). The growth of homogenous nano-particles is induced by the heterogeneous nucleation of a LSCM precursor on the surface of GDC nanocrystals. The nucleation is further followed by heat treatment at 1000 o C to convert precursors into oxides. The resulting nano-powder consists of well dispersed LSCM and GDC nano-particles with the size of approximately 50 nm. The electrolyte-supported SOFC cells are fabricated by screen-printing LSCM-GDC anode and pure LSCM current collector on the surface of YSZ pellet. The cathode is fabricated on the opposite of the YSZ pellet by screen-printing GDC blocking layer and LSCF electrode. The effects of sintering temperature (1100 o C and 1200 o C) and LSCM-GDC anode thickness are investigated. The characterization of the cells is conducted by a series of electrochemical impedance spectroscopy (EIS) measurements at 800 – 500 o C. The high resolution focused ion beam - scanning electron microscopy (FIB-SEM) is used to evaluate 3-D microstructures of the anodes sintered at 1100 o C and at 1200 o C. The microstructures of samples are shown in Fig. 1. The well dispersed 50 nm LSCM and GDC particles moderate grain growth of the composite and result in fine microstructure. The GDC average intercept lengths are 80 and 134 nm for samples sintered at 1100 and 1200 o C, respectively. The polarization resistance strongly depends on the electrode thickness and sintering temperature. The higher sintering temperature induces grains coarsening and decreases the GDC surface area. Therefore, better performance is achieved for samples sintered at 1100 o C than at 1200 o C. The best performance of 0.14 Ω cm -2 (measured at 800 o C with H 2 : H 2 O : N 2 = 40 : 20 : 40 %) is achieved for the thinnest LSCM-GDC-1100 o C electrode of 6 µm. Polarization resistance increased with the electrode thickness. This is attributed to the poor connectivity of the LSCM network. The connectivity of LSCM is lost in the range of 1.5 µm from the current collector layer for LSCM-GDC-1100 o C, and the electron transport has to be maintained by GDC. Due to the relatively low electronic conductivity of GDC, the electrode thickness has to be limited. 1. A. Sciazko, R. Yokoi, Y. Komatsu, T. Shimura, and N. Shikazono, ECS Trans. , 91 , 1711–1720 (2019). 2. K. Sato, C. Iwata, N. Kannari, and H. Abe, J. Power Sources , 414 , 502–508 (2019). Figure 1

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