Molybdenum-based double perovskites A2CrMoO6-δ (A = Ca, Sr, Ba) as anode materials for solid oxide fuel cells

被引:31
|
作者
Yang, Xin [1 ,2 ,3 ]
Liu, Jincheng [1 ]
Chen, Fanglin [2 ]
Du, Yanhai [3 ]
Deibel, Angela [3 ]
He, Tianmin [1 ]
机构
[1] Jilin Univ, Coll Phys, Key Lab Phys & Technol Adv Batteries, Minist Educ, Changchun 130012, Jilin, Peoples R China
[2] Univ South Carolina, Dept Mech Engn, 300 Main St, Columbia, SC 29208 USA
[3] Kent State Univ, Coll Aeronaut & Engn, 1400 Lefton Esplanade, Kent, OH 44242 USA
基金
美国国家科学基金会;
关键词
Solid oxide fuel cell; Double perovskite anode; Electrochemical stability; Oxygen vacancy formation energy; Sulfur tolerance; STABLE ANODE; NI; SR2MGMOO6-DELTA; IDENTIFICATION; REDUCTION; STABILITY; YSZ; CO;
D O I
10.1016/j.electacta.2018.09.102
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The development of sulfur-tolerant anode materials is vital for solid-oxide fuel cells (SOFCs) that use conventional fossil fuels as fuel source to decrease emissions and increase energy-conversion efficiency. In this work, A(2)CrMoO(6-delta) (A = Ca, Sr, Ba) double perovskite materials are synthesized and evaluated as potential SOFC anode materials to assess their electrocatalytic activity and sulfur tolerance. All samples exhibit well-matched thermal expansion coefficient and satisfactory chemical compatibility with La0.9Sr0.1Ga0.8Mg0.2O3-delta (LSGM) electrolyte over the measured temperature range. Among the compositions investigated, the B-site partially disordered Sr2CrMoO6-delta (SCM) double perovskite exhibits superior electrical conductivity, cycle stability, and polarization resistance on LSGM electrolyte because of its high-symmetry structure and appropriate oxygen-vacancy concentration. The relatively stable single-cell performance in 100 ppm H2S/H-2 demonstrates that the behavior of SCM anode is more stable than that of nickel-yttria-stabilized zirconia. Postexposure characterization by X-ray diffraction is further conducted to evaluate SCM as potential sulfur-tolerant SOFC anode. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:440 / 450
页数:11
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