Oxidation rate of Fe and electrochemical performance of Fe-air solid oxide rechargeable battery using LaGaO3 based oxide ion conductor

被引:22
|
作者
Inoishi, Atsushi [1 ]
Okamoto, Yohei [2 ]
Ju, Young-Wan [2 ]
Ida, Shintaro [2 ]
Ishihara, Tatsumi [2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Integrated Frontier Sci, Dept Automot Sci, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Dept Appl Chem, Fac Engn, Nishi Ku, Fukuoka 8190395, Japan
[3] Kyushu Univ, Fac Engn, Int Inst Carbon Neutral Energy WPI I2CNER, Higashi Ku, Fukuoka 812, Japan
关键词
CARBON;
D O I
10.1039/c3ra23337e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Effects of oxidation rate of Fe powder in Fe-air solid oxide rechargeable battery on discharge potential and capacity were studied. From the measurement of P-O2 in Fe set chamber and AC impedance for electrode reaction, oxidation rate of Fe, i.e., formation rate of H-2, was an important parameter for discharge performance of Fe-air solid oxide battery. Slow oxidation rate of Fe, namely, low current density, shows high discharge potential, however, caused sintering of Fe powder resulting in the decreased discharge capacity and so decreased usage efficiency of Fe powder. On the other hand, larger capacity (1145 mAh g(Fe)(-1)), which is close to the theoretical capacity, can be achieved at higher discharge rate of 30 mA cm(-2) at 873 K. Therefore, higher current density seems to be suitable for larger discharge capacity. Concentration overpotential is negligibly small at initial stage of discharge, however, with discharge period, diffusion overpotential became significantly enlarged caused by the slow oxidation rate of Fe. Sintering of Fe powder was observed after discharge at 5 mA cm(-2) by SEM and TEM observations and so fast oxidation rate at larger current density can be assigned to bulk oxidation of Fe powder with small particle size sustained during discharge.
引用
收藏
页码:8820 / 8825
页数:6
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