Modification of electrocatalytic activity of BaCe0.40Sm0.20Fe0.40O3-δ with Co3O4 as cathode for proton-conducting solid oxide fuel cell

被引:17
作者
Zhang, Cuijuan [1 ]
Du, Zhihong [1 ]
Zhao, Hailei [1 ,2 ]
Zhang, Xinxin [1 ]
机构
[1] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
[2] Beijing Key Lab New Energy Mat & Technol, Beijing 100083, Peoples R China
关键词
Proton-conducting solid oxide fuel cell; Cathode; Electrocatalytic activity; Electrical conductivity; RESISTANT CE0.8SM0.2O1.9 ELECTROLYTE; ELECTRICAL-CONDUCTIVITY; THIN BACE1-XSMXO3-ALPHA; COMPOSITE CATHODE; REDUCTION; ION; POLARIZATION; PERFORMANCE; PEROVSKITE; LAYER;
D O I
10.1016/j.electacta.2013.06.124
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Tailoring the properties of cathode is of great importance to improve the performance of proton-conducting solid oxide fuel cells (SOFC-H). This work demonstrates that the performance of BaCe0.40Sm0.20Fe0.40O3-delta cathode can be optimized by introducing appropriate amount of Co3O4. The 5-10 wt% Co3O4 reacts with BaCe0.40Sm0.20Fe0.40O3-delta, forming conductive mixed oxygen ionic-electronic phases. The materials with 5-10 wt% Co3O4 exhibits protonic and improved oxygen ionic-electronic conductivity in wet air, which contributes greatly to the electrocatalytic activity toward the reaction on the cathode. The (95-90%) BaCe0.40Sm0.20Fe0.40O3-delta (5-10%) Co3O4 demonstrates lower ASR, lower cathode overpotential, higher exchange current density, and higher peak power density. Higher content of Co3O4 (20%) will result in the disappearance of protonic conducting phase and denser electrode microstructure, which are detrimental to the performance. This work demonstrates that designing cathode materials with modified microstructure, which is simultaneously protonic, oxygen ionic and electronic conductive, is crucial to improve the performance of SOFC-H. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:369 / 375
页数:7
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