共流延法制備固體氧化物燃料電池陽極的優(yōu)化
發(fā)布時間:2018-02-24 01:12
本文關鍵詞: 固體氧化物燃料電池 活性層 優(yōu)化 流延法 出處:《無機材料學報》2014年02期 論文類型:期刊論文
【摘要】:采用共流延成型、共燒結法制備了以Ni-YSZ陽極支撐的氧化鈧穩(wěn)定的氧化鋯(SSZ)電解質膜。為提高電化學活性在支撐陽極與電解質膜之間引入了Ni-SSZ活性陽極。通過調整活性陽極的厚度和SSZ:NiO的質量比優(yōu)化了陽極活性;通過比較支撐陽極中添加不同造孔劑含量時的性能,優(yōu)化了支撐陽極的孔隙率。研究結果表明,當活性層厚度為35μm,質量比為w(SSZ):w(NiO)=1:1,支撐層造孔劑含量為10wt%時,陽極活性最佳;采用絲網印刷并燒結LSM-SSZ復合陰極后,所得單電池在750℃的最高功率密度達到0.96 W/cm2,比優(yōu)化前本課題組前期報道的性能提高了2.3倍。
[Abstract]:Common flow forming, In order to improve the electrochemical activity, Ni-SSZ active anode was introduced between the supporting anode and the electrolyte film in order to improve the electrochemical activity. The thickness of the active anode was adjusted by adjusting the thickness of the active anode. The anodic activity was optimized by the mass ratio of SSZ:NiO. The porosity of the supporting anode was optimized by comparing the properties of the supporting anode with different content of pore-forming agent. The results showed that the anode activity was the best when the active layer thickness was 35 渭 m, the mass ratio was 1: 1 and the propping layer pore-making agent content was 10 wt%. The maximum power density of the single cell is 0.96W / cm ~ 2 at 750 鈩,
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