کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6603940 | 1424090 | 2018 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Electrochemical performance and stability of cobalt-free Ln1.2Sr0.8NiO4 (Ln=La and Pr) air electrodes for proton-conducting reversible solid oxide cells
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
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چکیده انگلیسی
Cobalt-free Ruddlesden-Popper structured Ln1.2Sr0.8NiO4 (Lnâ¯=â¯La and Pr) have been synthesized by a modified Pechini method, moreover, their thermal and electrochemical properties as well as performance of cells with proton-conducting electrolytes have been investigated. Experimental results reveal that the thermal expansion coefficients of Ln1.2Sr0.8NiO4 are close to those of Ba(Ce,Zr)O3-based proton conductors. The polarization resistances of symmetrical cells with La1.2Sr0.8NiO4 (LSN) and Pr1.2Sr0.8NiO4 (PSN) electrodes are as low as 0.15 and 0.23â¯Î©â¯cm2 at 700â¯Â°C, respectively. Besides, Ln1.2Sr0.8NiO4 can remain stable structure over 100â¯h in humidified air (20â¯vol% H2O) at 800 °C. Furthermore, proton-conducting reversible solid oxide cells (PC-RSOCs) with LSN and PSN air electrodes exhibit maximum power densities of 0.46 and 0.35â¯Wâ¯cmâ2 in solid oxide fuel cell mode at 700â¯Â°C, respectively. Meanwhile, the same cells achieve current densities as high as 1.37 and 1.12 Aâ¯cmâ2 in solid oxide electrolysis cell mode at 700â¯Â°C with a given voltage of 1.3â¯V, respectively. In addition, both of two cells with LSN and PSN air electrodes present acceptable short-term stability under reversible operation condition. These encouraging results suggest that Ln1.2Sr0.8NiO4 could be suitable candidates of air electrodes in intermediate-temperature PC-RSOCs.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 267, 20 March 2018, Pages 269-277
Journal: Electrochimica Acta - Volume 267, 20 March 2018, Pages 269-277
نویسندگان
Shaojing Yang, Yabing Wen, Jingchao Zhang, Yang Lu, Xiaofeng Ye, Zhaoyin Wen,