Mn2+-Doped CeP2O7 Composite Electrolytes for Application in Low Temperature Proton-Conducting Ceramic Electrolyte Fuel Cells

被引:18
|
作者
Singh, Bhupendra [1 ,2 ]
Kim, Ji-Hye [1 ]
Jeon, Sang-Yun [1 ]
Park, Jun-Young [3 ]
Song, Sun-Ju [1 ,2 ]
机构
[1] Chonnam Natl Univ, Sch Mat Sci & Engn, Ion Lab, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Res Inst Catalysis, Kwangju 500757, South Korea
[3] Sejong Univ, Dept Adv Mat Engn, Seoul 143747, South Korea
基金
新加坡国家研究基金会;
关键词
CERIUM PYROPHOSPHATE; INTERMEDIATE TEMPERATURES; ELECTRICAL-CONDUCTIVITY; SUNSCREEN MATERIALS; AMORPHOUS CERIUM; BEHAVIOR; PHOSPHATE; SNP2O7;
D O I
10.1149/2.090401jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The proton conducting Ce1-xMnxP2O7 (x = 0.05, 0.075, 0.1, 0.125 and 0.15) composite electrolytes were synthesized by two-step slow digestion method with different P/(Ce+Mn) molar ratio. X-ray diffraction (XRD) patterns show that powders as-calcined at 300 degrees C contain pyrophosphate as the only crystalline phase, but sintering at 400 degrees C leads to the formation of a composite with additional crystalline phases of proton conducting metaphosphate, polyphosphate and orthophosphate. The microstructure of sintered pellets of Ce1-xMnxP2O7 (CMP) was analyzed by scanning electron microscopy (SEM). The CMP samples with high phosphate content become denser on sintering. The variation of ionic conductivity with temperature is studied in unhumidified and humidified air for the potential application of CMPs as electrolytes in proton-conducting ceramic electrolyte fuel cells (PCFCs). Among various CMP samples, Ce0.9Mn0.1P2O7 with P/(Ce+Mn) = 2.7 shows maximum conductivity of 6.54 x 10(-6) S cm(-1) at 450 degrees C in unhumidified air and 1.78 x 10(-2) S cm(-1) at 170 degrees C in humidified air with water vapor pressure (pH(2)O) of 0.12 atm. The ionic conductivity of CMPs increases with the increasing pH(2)O and Ce0.9Mn0.1 P2O7 shows maximum conductivity of 2.24 x 10(-2) S cm(-1) at 170 degrees C in pH(2)O = 0.16 atm. (c) 2013 The Electrochemical Society. All rights reserved.
引用
收藏
页码:F133 / F138
页数:6
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