A Gd0.2Ce0.8O1.9 impregnated Pr0.4Sr0.6Co0.2Fe0.7Nb0.1O3-δ nanofiber-structured composite anode in solid oxide fuel cells

被引:9
作者
Liu, Xiaotian [1 ]
Wang, Zhuang [1 ]
Fan, Liquan [1 ]
Gao, Keqing [1 ]
Xiong, Yueping [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Peoples R China
关键词
NATURAL-GAS; SOFC ANODE; METHANE; MICROSTRUCTURE; PERFORMANCE; DEPENDENCE; SCAFFOLDS; OXIDATION; HYDROGEN; CERMET;
D O I
10.1039/c6ra19580f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, comparative experiments were conducted based on La0.8Sr0.2Ga0.8Mg0.2O3-delta (LSGM) electrolytes, which supported single solid oxide fuel cells (SOFCs) with pure nanofiber-structured Pr0.4Sr0.6Co0.2Fe0.7Nb0.1O3-delta (PSCFN) anodes or Gd0.2Ce0.8O1.9 (GDC) impregnated PSCFN nanofiber-structured composite anodes. The polarization resistance (R-p) values of the pure nanofiber-structured PSCFN anode and the PSCFN-GDC nanofiber-structured composite anode with an optimal mass ratio of 1 : 0.56 were recorded as 1.573 Omega cm(2) and 0.212 Omega cm(2) at 850 degrees C in wet H-2 (97% H-2-3% H2O), respectively. After impregnating the GDC materials, the maximum power density (P-max) of the single cell with the PSCFN-GDC nanofiber-structured composite anode was found to be about 1.5 times greater than that of the pure nanofiber-structured PSCFN anode at 850 degrees C in wet H-2. The cell with the PSCFNGDC nanofiber-structured composite anode presented a significant electrochemical performance in wet H-2. Meanwhile it also showed excellent thermal cycling and long-term stability during the redox and constant-current discharge testing (300 mA cm(-2)) at 850 degrees C in wet H-2. All of these results indicated that the PSCFN-GDC nanofiber-structured composite anode acted as an efficient and competitive power anode operating in hydrogen fuels.
引用
收藏
页码:87843 / 87847
页数:5
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