材料科学
介电谱
电极
电解
氧化物
氧化钇稳定氧化锆
极化(电化学)
分析化学(期刊)
克拉克电极
氧气
电化学
固体氧化物燃料电池
化学工程
复合材料
陶瓷
化学
电解质
冶金
色谱法
物理化学
有机化学
工程类
立方氧化锆
作者
Scott A. Barnett,Beom‐Kyeong Park,Roberto Scipioni,Matthew Y. Lu,Jerren Grimes,Yvonne Chart,Tianrang Yang
出处
期刊:Meeting abstracts
日期:2020-11-23
卷期号:MA2020-02 (40): 2644-2644
标识
DOI:10.1149/ma2020-02402644mtgabs
摘要
PrO x -infiltrated oxygen electrodes can yield relatively low polarization resistances even at reduced operating temperature. Similarly, Gd-doped Ceria (GDC) infiltration into Ni-YSZ fuel electrodes has been shown to reduce polarization resistance while also helping to maintain stable electrolysis operation. Here we review the literature on these electrodes and discuss recent results on electrochemical impedance spectroscopy (EIS) studies of PrO x -infiltrated La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) and SrTi0.3Fe0.55Co0.15O3 (STFC) oxygen electrodes and GDC-infiltrated Ni-YSZ. Physically-based equivalent circuit models are developed using the distribution of relaxation times method and used to fit the symmetric cell EIS data, comparing PrO x - and GDC-infiltrated electrodes with un-infiltrated electrodes. The results suggest that PrO x improves oxygen dissociative adsorption/desorption, oxygen surface exchange, and transport of oxygen in the perovskites; while GDC reduces the reaction resistance associated with three-phase boundaries and improves oxygen transport in Ni-YSZ. Full cells employing the PrO x -infiltrated STFC and Ni-YSZ:GDC electrodes achieve high performance (e.g. fuel cell power density nearly 3 W/cm 2 at 750 o C and > 1 W/cm 2 at 600 o C; and electrolysis current density at 1.3 V of nearly 4 A/cm 2 at 750 o C), while exhibiting promising stability. Combining the equivalent circuit models from the symmetric cell data for each electrode provides a detailed explanation and fit of the full cell EIS results.
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