金属陶瓷
阳极
材料科学
氧化钇稳定氧化锆
甲烷
氧化物
直接乙醇燃料电池
化学工程
固体氧化物燃料电池
丙烷
氧化还原
电化学
电解质
阴极
无机化学
燃料电池
电极
法拉第效率
立方氧化锆
电化学能量转换
冶金
化学
有机化学
陶瓷
物理化学
工程类
作者
Shanwen Tao,John T. S. Irvine
出处
期刊:Nature Materials
[Springer Nature]
日期:2003-05-01
卷期号:2 (5): 320-323
被引量:950
摘要
Solid-oxide fuel cells (SOFCs) promise high efficiencies in a range of fuels. Unlike lower temperature variants, carbon monoxide is a fuel rather than a poison, and so hydrocarbon fuels can be used directly, through internal reforming or even direct oxidation. This provides a key entry strategy for fuel-cell technology into the current energy economy. Present development is mainly based on the yttria-stabilized zirconia (YSZ) electrolyte. The most commonly used anode materials are Ni/YSZ cermets, which display excellent catalytic properties for fuel oxidation and good current collection, but do exhibit disadvantages, such as low tolerance to sulphur and carbon deposition when using hydrocarbon fuels, and poor redox cycling causing volume instability. Here, we report a nickel-free SOFC anode, La0.75Sr0.25Cr0.5Mn0.5O3, with comparable electrochemical performance to Ni/YSZ cermets. The electrode polarization resistance approaches 0.2 Omega cm2 at 900 degrees C in 97% H2/3% H2O. Very good performance is achieved for methane oxidation without using excess steam. The anode is stable in both fuel and air conditions, and shows stable electrode performance in methane. Thus both redox stability and operation in low steam hydrocarbons have been demonstrated, overcoming two of the major limitations of the current generation of nickel zirconia cermet SOFC anodes.
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