Environ Technol. 2014 Mar-Apr;35(5-8):925-30. doi: 10.1080/09593330.2013.856953.
A perovskite-type oxide La(0.4)Ba(0.6)Fe(0.8)Zn(0.2)O(3-delta) (LBFZ) was investigated as the cathode material for simultaneous NO reduction and electricity generation in solid oxide fuel cells (SOFCs). The microstructure of LBFZ was demonstrated by X-ray diffraction and scanning electron microscopy. The results showed that a single cubic perovskite LBFZ was formed after calcined at 1100 degrees C. Meanwhile, the solid-state reaction between LBFZ and Ce(0.8)Sm(0.2)O(1.9) (SDC) at 900 degrees C was negligible. To measure the electrochemical properties, SOFC units were constructed with Sm(0.9)Sr(0.1)Cr(0.5)Fe(0.5)O3 as the anode, SDC as the electrolyte and LBFZ as the cathode. The maximum power density increased with the increasing NO concentration and temperature. The cell resistance is mainly due to the cathodic polarization resistance.
钙钛矿型氧化物 La(0.4)Ba(0.6)Fe(0.8)Zn(0.2)O(3-delta) (LBFZ) 被用作固体氧化物燃料电池 (SOFC) 中同时进行 NO 还原和发电的阴极材料。LBFZ 的微观结构通过 X 射线衍射和扫描电子显微镜进行了证明。结果表明,在 1100°C 煅烧后形成了单一的立方钙钛矿 LBFZ。同时,LBFZ 和 Ce(0.8)Sm(0.2)O(1.9) (SDC) 在 900°C 下的固态反应可以忽略不计。为了测量电化学性能,用 Sm(0.9)Sr(0.1)Cr(0.5)Fe(0.5)O3 作为阳极、SDC 作为电解质和 LBFZ 作为阴极构建了 SOFC 单元。最大功率密度随着 NO 浓度和温度的升高而增加。电池电阻主要归因于阴极极化电阻。