SrCo0.7Fe0.2Ta0.1O3-δ perovskite as a cathode material for intermediate-temperature solid oxide fuel cells

被引:35
作者
Qu, Baoping [1 ]
Long, Wen [1 ]
Jin, Fangjun [1 ]
Wang, Shizhuo [1 ]
He, Tianmin [1 ]
机构
[1] Jilin Univ, Coll Phys, Minist Educ, Key Lab Phys & Technol Adv Batteries, Changchun 130012, Peoples R China
关键词
Solid oxide fuel cell; Doped strontium cobaltite cathode; Thermal expansion; Stability; Electrical conductivity; Electrochemical performance; OXYGEN PERMEATION; THERMAL-EXPANSION; ELECTROCHEMICAL PROPERTIES; TRANSPORT-PROPERTIES; CUBIC PEROVSKITE; PERFORMANCE; SRCO0.8FE0.2O3-DELTA; TRANSITIONS; STABILITY; MEMBRANES;
D O I
10.1016/j.ijhydene.2014.05.150
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
Perovskite oxide SrCo0.7Fe0.2Ta0.1O3-delta (SCFT) was synthesized by a solid-state reaction and investigated as a potential cathode material for intermediate-temperature solid oxide fuel cell (IT-SOFC). The single phase SCFT having a cubic perovskite structure was obtained by sintering the sample at 1200 degrees C for 10 h in air. Introduction of Ta improved the phase stability of SCFT. The SCFT exhibited a good chemical compatibility with the La0.9Sr0.1Ga0.8Mg0.2O3-delta (LSGM) electrolyte at 950 degrees C for 10 h. The average thermal expansion coefficient was 23.8 x 10(-6) K-1 between 30 and 1000 degrees C in air. The electrical conductivities of the SCFT sample were 71-119 S cm(-1) in the 600-800 degrees C temperature range in air, and the maximum conductivity reached 247 S cm(-1) at 325 degrees C. The polarization resistance of the SCFT cathode on the LSGM electrolyte was 0.159 Omega cm(2) at 700 degrees C. The maximum power density of a single-cell with the SCFT cathode on a 300 mu m-thick LSGM electrolyte reached 652.9 mW cm(-2) at 800 degrees C. The SCFT cathode had shown a good electrochemical stability over a period of 20 h short-term testing. These findings indicated that the SCFT could be a suitable alternative cathode material for IT-SOFCs. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12074 / 12082
页数:9
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