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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Advanced electrochemical properties of Pr0.9Y0.1BaCo1.8Ni0.2O6-delta - Ce0.8Sm0.2O1.9 composite as cathode material for IT-SOFCs
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Advanced electrochemical properties of Pr0.9Y0.1BaCo1.8Ni0.2O6-delta - Ce0.8Sm0.2O1.9 composite as cathode material for IT-SOFCs

机译:PR0.9Y0.1Baco1.8NI0.2O6-Delta - Ce0.8sm0.2O1.9复合作为IT-SOFC的阴极材料的高级电化学性能

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摘要

The co-doped double perovskite-type cobaltite Pr0.9Y0.1BaCo1.8Ni0.2O6-delta (PYBCN) is synthesized via organo-metallic precursors. The concentrations of electronic and ionic defects in PYBCN at variations of gaseous environment are obtained from the analysis of the experimental isothermal plots for equilibrium oxygen content (6 - delta) vs. oxygen partial pressure P-O2, in the ambient gaseous phase. It is argued that nickel doping is beneficial for enhanced formation of vacancies in O2- positions controlling oxygen ion transport in the cobaltite. The cobaltite based dual-phase composite with 30 wt% addition of samarium doped ceria Ce0.8Sm0.2O1.9 (SDC) is found to have considerably reduced thermal expansion compared to the parent cobaltite. The impedance measurements show that the area specific resistance (ASR) of the composite decreases to 0.11 Omega cm(2) at 973 K with the activation energy 1.2 eV. Further increase of the temperature is accompanied by the decline of the activation energy to 0.9 eV, and ASR attains 0.045 Omega cm(2) at 1073 K. The observed small ASRs are attributed to a large concentration of O2-vacancies in the cobaltite component of the composite. The cathodic overvoltage for oxygen reduction that does not exceed 40 mV at 1073 K and current density 1000 mA cm(-2), moderate thermal expansion, good conductivity and high electro-chemical activity distinguish the developed composite as one of the promising cathode materials for intermediate temperature solid oxide fuel cell applications. (C) 2018 Elsevier B.V. All rights reserved.
机译:共掺杂双钙钛矿型钴矿Pr0.9Y0.1BaCo1.8Ni0.2O6-Δ(PYBCN)经由有机金属前体的合成。在PYBCN电子和离子在缺陷气体环境的变化的浓度从平衡氧含量(6 - 增量)实验等温曲线的分析获得对氧气分压P-O2,在环境气相。有人认为,镍掺杂为增强在O2-位置控制在钴氧离子迁移空位的形成是有益的。用30%(重量)另外钐掺杂的氧化铈Ce0.8Sm0.2O1.9(SDC)的辉钴矿基于双相复合被发现相比于亲本辉钴矿已经显着地减少热膨胀。阻抗测量结果表明,该复合减小到0.11厘米欧米茄(2)在973 K的活化能1.2电子伏特的面积比电阻(ASR)。温度的进一步增加伴随着的活化能的下降至0.9电子伏特,而在ASR K. 1073的达到0.045欧米茄厘米(2)观察到的小的ASRs归因于大的浓度O 2空位中的钴酸成分复合。氧还原阴极过电压不超过40毫伏在1073 K和电流密度千毫安厘米(-2),中度热膨胀,良好的导电性和高电化学活性区分发达复合作为有前途的正极材料中的一个中温固体氧化物燃料电池应用。 (c)2018年elestvier b.v.保留所有权利。

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