钙钛矿(结构)
阴极
兴奋剂
氧化物
电解质
氧气
氟
固体氧化物燃料电池
无机化学
材料科学
化学工程
化学
电极
电化学
光电子学
物理化学
冶金
有机化学
工程类
作者
Yongna Liu,Xiuxia Meng,Fangyong Yu,Mengjie Yin,Naitao Yang,Bo Meng,M. Veronica Sofianos,Shaomin Liu
标识
DOI:10.1016/j.ijhydene.2018.04.167
摘要
Possessing a high oxygen reduction reaction (ORR) activity is one of the most important prerequisites for the cathode to ensure an efficient solid oxide fuel cell. Herein, a highly active cathode is developed by doping the fluorine anion in anion sites of perovskite oxides (ABO3). The electrocatalytic activities of three different cathode samples including the original perovskite La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF), the doped La0.6Sr0.4Co0.2Fe0.8O2.95-δF0.05 (LSCFF0.05) and La0.6Sr0.4Co0.2Fe0.8O2.9-δF0.1 (LSCFF0.1) are comparatively investigated. The fluorine doped perovskites reveal higher electrochemical performance than the original perovskite. Based on three cathodes of LSCF, LSCFF0.05 and LSCFF0.1 operated at 850 °C, the measured area specific resistance was 0.018, 0.017 and 0.91 Ω cm2, respectively; and the respective maximum power density of the single fuel cell using the 9-μm-thick YSZ electrolyte was 754, 1005, and 737 mW cm−2. Such performance results vividly indicate that, the obtained perovskite oxyfluoride by doping an optimum amount of F ions can efficiently improve ORR activity and thus is a feasible strategy to develop cathode for high-performance solid oxide fuel cells.
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