阴极
材料科学
固体氧化物燃料电池
氧化物
介电谱
电解质
电极
化学工程
电化学
化学
冶金
工程类
物理化学
作者
Yidan Zhang,Ankang Zhu,Youmin Guo,Chunchang Wang,Meng Ni,Hao Yu,Chuanhui Zhang,Zongping Shao
出处
期刊:Applied Energy
[Elsevier BV]
日期:2019-01-22
卷期号:238: 344-350
被引量:50
标识
DOI:10.1016/j.apenergy.2019.01.094
摘要
Abstract Proton conducting solid oxide fuel cells are solid state electrochemical devices for power generation at a conversion efficiency (>60%) higher than conventional thermal power plants (∼40%). The cathode is the key component of proton conducting solid oxide fuel cells as it contributes to more than 50% of the total overpotential loss of an H+-SOFC with thin film electrolyte. This work aims to develop high performance and durable cathode for proton conducting solid oxide fuel cells by doping Ba2+ into the Sr-site of the SrSc0.175Nb0.025Co0.8O3-δ perovskite oxide. The influence of moisture on the catalytic activity of Ba0.5Sr0.5Sc0.175Nb0.025Co0.8O3-δ cathode was investigated using electrochemical impedance spectroscopy of symmetric cell at 600 °C. The resistance in the low-frequency range was found to be the rate-limiting step of the oxygen reduction reaction in the dry air, while the resistance in the medium-frequency range became the rate-limiting step in the moist air. With a Ba0.5Sr0.5Sc0.175Nb0.025Co0.8O3-δ cathode, a proton conducting single cell achieved good performance at a temperature of 700 °C with a power density of 633 mW cm−2. However, the performance of single cell decreased with time, probably due to the agglomeration of cathode particles and the coverage of produced water on the active surface. To improve the durability of the proton conducting solid oxide fuel cell, it is critical to minimize the cathode particle agglomeration and remove the produced water effectively. The research results contribute to the development of high-performance fuel cell for efficient energy conversion.
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