共 50 条
Functionality of an oxygen Ca3Co4O9+δ electrode for reversible solid oxide electrochemical cells based on proton-conducting electrolytes
被引:49
|作者:
Pikalova, E.
[1
,2
]
Kolchugin, A.
[1
,2
]
Koroleva, M.
[3
]
Vdovin, G.
[1
]
Farlenkov, A.
[1
,2
]
Medvedev, D.
[1
,2
]
机构:
[1] Inst High Temp Electrochem, Ekaterinburg 620137, Russia
[2] Ural Fed Univ, Ekaterinburg 620002, Russia
[3] Komi Sci Ctr, Inst Chem, Syktyvkar 167982, Russia
基金:
俄罗斯基础研究基金会;
关键词:
Energy conversion;
Reversible solid oxide cells;
Proton conductors;
Misfit layered phases;
Long-term stability;
DRT analysis;
MEMBRANE FUEL-CELLS;
MISFIT CA-COBALTITE;
RELAXATION-TIMES;
CATHODE MATERIAL;
CA3CO4O9-DELTA CATHODE;
LAYERED PEROVSKITES;
REDUCTION REACTION;
PERFORMANCE;
TEMPERATURE;
SOFC;
D O I:
10.1016/j.jpowsour.2019.226996
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:
Reversible solid oxide cells (rSOCs) based on proton-conducting electrolytes represent an advanced electrochemical technology aimed at reversible energy conversion. Their high levels of efficiency, minimal impact on the environment and economic viability point to a positive future for rSOCs. In this study we present the results of electrochemical characterization of the Ca3Co4O9+delta-based oxygen (or steam) electrodes for rSOCs with the BaCe0.5Zr0.3Y0.2O3-delta electrolyte. The electrodes developed display excellent electrochemical activity both in the symmetrical and reversible cells. In detail, the electrode polarization resistance at 700 degrees C amounts to less than 0.25 Omega cm(2) after long-term measurements (1500 h, symmetrical cell mode of operation) and lower than 0.13 Omega cm(2) (open circuit voltage mode of operation), exceeding the electrode performances of other Co-based materials of "112" (LnBaCo(2)O(5+delta), Ln is the lanthanide) and "114" (YBaCo4O7+delta) families. Analysis of these data shows that Ca3Co4O9+delta can be considered to be a promising alternative to the state-of-the-art electrodes utilized in protonic ceramic fuel and electrolysis cells.
引用
收藏
页数:12
相关论文