Praseodymium-cerium oxide thin film cathodes: Study of oxygen reduction reaction kinetics

被引:82
作者
Chen, Di [1 ]
Bishop, Sean R. [1 ,2 ]
Tuller, Harry L. [1 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Kyushu Univ, Int Inst Carbon Neutral Energy Res I2CNER, Nishi Ku, Fukuoka 8190395, Japan
基金
美国国家科学基金会;
关键词
Ceria; Three-way catalyst; Oxygen storage; Oxygen separation; Permeation membrane mixed ionic electronic conduction; Solid oxide fuel cell; POINT-DEFECTS; IMPEDANCE; TRANSPORT; CATALYSTS;
D O I
10.1007/s10832-011-9678-z
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Praseodymium-Cerium Oxide (PrxCe1-xO2-delta; PCO), a potential three way catalyst oxygen storage material and solid oxide fuel cell (SOFC) cathode, exhibits surprisingly high levels of oxygen nonstoichiometry, even under oxidizing (e.g. air) conditions, resulting in mixed ionic electronic conductivity (MIEC). In this study we examine the redox kinetics of dense PCO thin films using impedance spectroscopy, for x = 0.01, 0.10 and 0.20, over the temperature range of 550 to 670A degrees C, and the oxygen partial pressure range of 10(-4) to 1 atm O-2. The electrode impedance was observed to be independent of electrode thickness and inversely proportional to electrode area, pointing to surface exchange rather than bulk diffusion limited kinetics. The large electrode capacitance (10(-2)F) was found to be consistent with an expected large electrochemically induced change in stoichiometry for x = 0.1 and x = 0.2 PCO. The PCO films showed surprisingly rapid oxygen exchange kinetics, comparable to other high performance SOFC cathode materials, from which values for the surface exchange coefficient, k (q) , were calculated. This study confirms the suitability of PCO as a model MIEC cathode material compatible with both zirconia and ceria based solid oxide electrolytes.
引用
收藏
页码:62 / 69
页数:8
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