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Fabrication and optimization of La_(0.4)Sr_(0.6)Co_(0.2)Fe_(0.7)Nb_(0.1)O_(3-δ) electrode for symmetric solid oxide fuel cell with zirconia based electrolyte 被引量:4

Fabrication and optimization of La_(0.4)Sr_(0.6)Co_(0.2)Fe_(0.7)Nb_(0.1)O_(3-δ) electrode for symmetric solid oxide fuel cell with zirconia based electrolyte
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摘要 La(0.4)Sr(0.6)Co(0.2)Fe(0.7)Nb(0.1)O(3-δ)(LSCFN)was applied as both anode and cathode for symmetrical solid oxide fuel cells(SSOFCs)with zirconia based electrolyte.The cell with LSCFN electrode was fabricated by tape-casting and screen printing.Fabrication process was optimized firstly by comparing co-sintering and separate-sintering of electrode and electrolyte.To further improve the LSCFN electrode properties,oxygen ionic conductor of Gd(0.1)Ce(0.9)O(2-δ)(GDC)was added into the LSCFN electrode.The preferred composition of LSCFN-GDC composite electrode was found to be 1:1 in weight ratio with polarization resistance of 0.16Ωcm^2at 800~℃.The maximum power densities of LSCFN-GDC||GDC/YSZ/GDC||LSCFN-GDC tested in H2and CH4with 3%H2O were 395 m W cm^(-2)and 124 m W cm^(-2)at 850~?C,respectively,which were much higher than that of LSCFN||GDC/YSZ/GDC||LSCFN cells at same condition,possibly due to the extension of the triple phase boundary induced by the addition of GDC.The cell showed reasonable stability using H2and CH4with 3%H2O as fuels and no significant power output degradation was observed after total 200 h operation. La(0.4)Sr(0.6)Co(0.2)Fe(0.7)Nb(0.1)O(3-δ)(LSCFN)was applied as both anode and cathode for symmetrical solid oxide fuel cells(SSOFCs)with zirconia based electrolyte.The cell with LSCFN electrode was fabricated by tape-casting and screen printing.Fabrication process was optimized firstly by comparing co-sintering and separate-sintering of electrode and electrolyte.To further improve the LSCFN electrode properties,oxygen ionic conductor of Gd(0.1)Ce(0.9)O(2-δ)(GDC)was added into the LSCFN electrode.The preferred composition of LSCFN-GDC composite electrode was found to be 1:1 in weight ratio with polarization resistance of 0.16Ωcm^2at 800~℃.The maximum power densities of LSCFN-GDC||GDC/YSZ/GDC||LSCFN-GDC tested in H2and CH4with 3%H2O were 395 m W cm^(-2)and 124 m W cm^(-2)at 850~?C,respectively,which were much higher than that of LSCFN||GDC/YSZ/GDC||LSCFN cells at same condition,possibly due to the extension of the triple phase boundary induced by the addition of GDC.The cell showed reasonable stability using H2and CH4with 3%H2O as fuels and no significant power output degradation was observed after total 200 h operation.
出处 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2017年第11期1329-1333,共5页 材料科学技术(英文版)
基金 supported by the National Natural Science Foundation of China (No. 51402355) Natural Science Foundation of Beijing Project (Nos. LJ201531 and 2154056) Shanxi Province Project (No. MD2014-08) Guangdong Project (No. 201460720100025)
关键词 LSCFN electrode Triple phase boundary Solid oxide fuel cells LSCFN electrode Triple phase boundary Solid oxide fuel cells
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