Oxygen-Electrode Catalysis on Oxoperovskites at 700 °C versus 20 °C

被引:15
作者
Shin, Hyun Ho [1 ,2 ]
Mullins, C. Buddie [1 ,3 ,4 ]
Goodenough, John B. [1 ]
机构
[1] Univ Texas Austin, Texas Mat Inst, Austin, TX 78712 USA
[2] Seoul Natl Univ, Global Frontier Ctr Multiscale Energy Syst, Seoul 08826, South Korea
[3] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
[4] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
关键词
OXIDE FUEL-CELLS; TRANSITION-METAL OXIDES; CATHODE MATERIALS; SOFC CATHODE; TEMPERATURE; PERFORMANCE; PRINCIPLES; STABILITY;
D O I
10.1021/acs.chemmater.7b03281
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The oxygen-reduction and oxygen-evolution reactions (ORR and OER) at 700 degrees C on the perovskites ABO(3-delta) (A = La, Sr and B = Co, Fe, Mn, Cr with undoped versus Nb- or Ta-doped SrCoO3-delta) have been evaluated experimentally with a reversible solid oxide fuel cell (R-SOFC). The predictor for active ORR catalysis at 20 degrees C in alkaline solution is not applicable at 700 degrees C; the adsorbed water on the oxide catalyst surface is lost. In a SOFC, the ORR is split between the fuel and the oxygen electrode; in an alkaline air battery, the entire ORR occurs at the oxygen electrode. On the other hand, the OER reaction occurs by a similar process at the oxygen electrode in a R-SOFC at 700 degrees C and in an air battery or room-temperature fuel cell in an alkaline solution. A proposed condition for both the ORR and the OER occurring at the same oxoperovskite surface at 700 degrees C is a transition-metal cation of the perovskite at its equilibrium oxidation state at the operating temperature and pO(2).
引用
收藏
页码:629 / 635
页数:7
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