Sintering behavior of BaCe0.7Zr0.1Y0.2O3-δ electrolyte at 1150 °C with the utilization of CuO and Bi2O3 as sintering aids and its electrical performance

被引:62
作者
Babar, Zaheer Ud Din [1 ]
Hanif, Muhammad Bilal [1 ,2 ]
Jiu-Tao Gao [1 ]
Chang-Jiu Li [1 ]
Cheng-Xin Li [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Mech Behav Mat, Xian, Shaanxi, Peoples R China
[2] Comenius Univ, Fac Nat Sci, Dept Inorgan Chem, Bratislava 84215, Slovakia
关键词
BaCe0.7Zr0.1Y0.2O3-delta; Sinterability; Densification; CuO-Bi2O3; Solid oxide fuel cell; PROTON CONDUCTING ELECTROLYTE; DOPED BARIUM ZIRCONATE; FUEL-CELLS; ELECTROCHEMICAL PERFORMANCE; OXIDE; TEMPERATURE; TRANSPORT; ZNO; BA(ZR0.1CE0.7Y0.2)O3-DELTA; BACE0.35ZR0.5Y0.15O3-DELTA;
D O I
10.1016/j.ijhydene.2021.12.075
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
BaCe0.7Zr0.1Y0.2O3-delta (BCZY) is one of the promising electrolytic candidate for solid oxide fuel cell (SOFC) due to its good proton conductivity and better stability. Herein, the effect of dual sintering aids such as CuO-Bi2O3 upon the sinterability at low temperature, improved electrochemical properties, and thermo-chemical changes about proton-conducting BaCe(0.7)Zr(0.1)Y(0.2)O(3-delta )electrolyte were investigated in detail. FESEM micrographs and shrinkage curves revealed significant improvement in sinterability and densifications of BCZY electrolyte. The dense pellets were sintered with CuO-Bi2O3 (2-3 mol %) as sintering aids at a temperature of 1150 degrees C for 5 h. The perfectly uniform distribution of sintering aids increased the linear shrinkage of BCZY from 5% till 19-21%. The crystallite size and grain growth within the structure was enhanced due to the formation of the melting phase of Bi2O3 and Cu2+ incorporation in the perovskite structure. The elevated and improved electrochemical measurement for BCZY with 2 mol% of CuO-Bi2O3 as sintering aid categorized it well suited for solid oxide fuel cells. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7403 / 7414
页数:12
相关论文
共 52 条
[1]   Effect of Nickel Addition on Sintering Behavior and Electrical Conductivity of BaCe0.35Zr0.5Y0.15O3-δ [J].
An, Hyegsoon ;
Shin, Dongwook ;
Ji, Ho-Il .
JOURNAL OF THE KOREAN CERAMIC SOCIETY, 2019, 56 (01) :91-97
[2]  
Babilo P, 2007, J MATER RES, V22, P1322, DOI 10.1557/JMR.2007.0163
[3]   Sintering aid (ZnO) effect on proton transport in BaCe0.35Zr0.5Y0.15O3-δ and electrode phenomena studied by distribution function of relaxation times [J].
Baral, Ashok Kumar ;
Tsur, Yoed .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2019, 102 (01) :239-250
[4]   Reduction in sintering temperature of stable proton conductor BaCe0.35Zr0.5Y0.15O3-δ prepared by sol-gel method and its transport properties [J].
Baral, Ashok Kumar .
SOLID STATE IONICS, 2015, 272 :107-111
[5]   Enhanced sintering of Ce0.8Nd0.2O2_δ-La0.8Sr0.2Ga0.8Mg0.2O3_δ using CoO as a sintering aid [J].
Chen, Lei ;
Zhou, De Feng ;
Wang, Yuan ;
Zhu, Xiao Fei ;
Meng, Jian .
CERAMICS INTERNATIONAL, 2017, 43 (04) :3583-3589
[6]   Effects of CoO and Bi2O3 single/dual sintering aids doping on structure and properties of Ce0.8Nd0.2O1.9 [J].
Chen, Xu ;
Sun, Xi ;
Zhou, Jing ;
Zhou, Defeng ;
Zhu, Xiaofei ;
Meng, Jian .
CERAMICS INTERNATIONAL, 2020, 46 (14) :22727-22732
[7]   Structural and electrochemical properties of yttrium-doped barium zirconate by addition of CuO [J].
Gao, Dongyun ;
Guo, Ruisong .
JOURNAL OF ALLOYS AND COMPOUNDS, 2010, 493 (1-2) :288-293
[8]   Enhanced sinterability and conductivity of BaZr0.3Ce0.5Y0.2O3-δ by addition of bismuth oxide for proton conducting solid oxide fuel cells [J].
Gui, Liangqi ;
Ling, Yihan ;
Li, Geng ;
Wang, Zhihao ;
Wan, Yanhong ;
Wang, Ranran ;
He, Beibei ;
Zhao, Ling .
JOURNAL OF POWER SOURCES, 2016, 301 :369-375
[9]   Zirconium doping effect on the performance of proton-conducting BaZryCe0.8-yY0.2O3-δ (0.0 ≤ y ≤ 0.8) for fuel cell applications [J].
Guo, Youmin ;
Lin, Ye ;
Ran, Ran ;
Shao, Zongping .
JOURNAL OF POWER SOURCES, 2009, 193 (02) :400-407
[10]  
Hanif MB, 2021, CHEM ENG J, V428