Ba1-xSrxCe0.8-yZryY0.2O3-δ protonic electrolytes synthesized by hetero-composition-exchange method for solid oxide fuel cells

被引:9
作者
Lee, Kan-Rong [1 ,2 ]
Tseng, Chung-Jen [2 ]
Chang, Jeng-Kuei [1 ,2 ,3 ]
Wang, Kuan-Wen [1 ,2 ]
Huang, Yu-Shuo [1 ]
Chou, Tzu-Chi [4 ]
Chiu, Kuo-Chuang [4 ]
Tsai, Li-Duan [4 ]
Lee, Sheng-Wei [1 ,2 ,3 ]
机构
[1] Natl Cent Univ, Inst Mat Sci & Engn, 300 Zhongda Rd, Taoyuan 32001, Taiwan
[2] Natl Cent Univ, Dept Mech Engn, Taoyuan 32001, Taiwan
[3] Natl Cent Univ, Dept Chem & Mat Engn, Taoyuan 32001, Taiwan
[4] Ind Technol Res Inst, Mat & Chem Res Labs, Hsinchu 31040, Taiwan
关键词
Proton -conducting electrolyte; Solid oxide fuel cells; Ba1-xSrxCe0.8-yZryY0.2O3-delta; Chemical stability; Ionic conductivity; CHEMICAL-STABILITY; CONDUCTIVITY; ANODE; CATHODE; BACE0.8-XZRXY0.2O3-DELTA; PERFORMANCE; TRANSPORT; METHANE; SOFC;
D O I
10.1016/j.ijhydene.2017.01.200
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
This study reports the synthesis of proton-conducting Ba0.8Sr0.2Ce0.6Zr0.2Y0.2O3-delta oxides by using a combination of the sol gel process and hetero-composition-exchange technique. The experimental results show that the sintered Ba0.8Sr0.2Ce0.6Zr0.2Y0.2O3-delta pellet synthesized by the hetero-composition-exchange method exhibits excellent sinterability, good relatively density, and high protonic conduction. Furthermore, the Pt/electrolyte/Pt single cell with such an electrolyte shows a significantly higher maximum power density as compared to those oxides prepared from conventional sol gel powders. Based on the experimental results, we attempt to explain the improvement mechanism in terms of as calcined particle characteristics and proton hopping distance. This work shows that the Bai(1-x)Sr(x)Ce(0.8-y)Zr(y)Y(0.2)O(3-delta) oxides synthesized by the sol gel combined with heterocomposition-exchange method would be a promising electrolyte for H+-SOFC applications. More importantly, this new fabrication approach could be applied to other similar perovskite-type electrolyte systems. (C) 2017 Hydrogen Energy Publications LLC.
引用
收藏
页码:22222 / 22227
页数:6
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