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Double-Perovskite Anode Materials Sr2MMoO6 (M = Co, Ni) for Solid Oxide Fuel Cells

机译:固体氧化物燃料电池用双钙钛矿阳极材料Sr2MMoO6(M = Co,Ni)

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Double-perovskites Sr2MMoO6 (M = Co, Ni) have been investigated as anode materials for a solid oxide fuel cell. At room temperature, both Sr2CoMoO6 and Sr2NiMoO6 are tetragonal (I4/m). X-ray absorption spectroscopy confirmed the presence of Co~(2+)/Mo~(6+) and Ni~(2+)/Mo~(6+) pairs in the oxygen-stoichiometric compounds. The samples contain a limited concentration of oxygen vacancies in the reducing atmospheres at an anode. Reoxidation is facile below 600 °C; they become antiferromagnetic at low temperatures T_N = 37 and 80 K for M = Co and Ni, respectively. As an anode with a 300 μ m thick La_(0.8)Sr_(0.2)Ga_(0.83)Mg_(0.17)O_(2.815) electrolyte and SrFe_(0.2)Co_(0.8)O_(3-δ) as a cathode, Sr2CoMoO6 exhibited maximum power densities of 735 mW/cm2 in H2 and 527 mW/cm2 in wet CH4 at 800 °C; Sr2NiMoO6 shows a notable power output only in dry CH4. The high performance of Sr2CoMoO6 in wet CH4 may be due to its catalytic effect on steam reforming of methane, but some degradation of the structure that occurred in CH4 obscures identification of the catalytic reaction processes at the surface. However, the stronger octahedral-site preference of Ni~(2+) versus Co~(2+) can account for the lower performance of the M = Ni anode.
机译:已经研究了双钙钛矿Sr2MMoO6(M = Co,Ni)作为固体氧化物燃料电池的阳极材料。在室温下,Sr2CoMoO6和Sr2NiMoO6均为四边形(I4 / m)。 X射线吸收光谱法证实了氧化学计量化合物中存在Co〜(2 +)/ Mo〜(6+)和Ni〜(2 +)/ Mo〜(6+)对。样品在阳极的还原气氛中包含有限浓度的氧空位。低于600°C时容易再氧化;当M = Co和Ni时,它们在低温T_N = 37和80 K时变为反铁磁性。作为具有300μm厚的La_(0.8)Sr_(0.2)Ga_(0.83)Mg_(0.17)O_(2.815)电解质和SrFe_(0.2)Co_(0.8)O_(3-δ)电解质的阳极,Sr2CoMoO6在800°C下,H2的最大功率密度为735 mW / cm2,湿式CH4的最大功率密度为527 mW / cm2; Sr2NiMoO6仅在干燥的CH4中显示出显着的功率输出。 Sr2CoMoO6在湿式CH4中的高性能可能是由于其对甲烷蒸汽重整的催化作用,但是在CH4中发生的某些结构降解使表面的催化反应过程难以识别。但是,Ni〜(2+)相对于Co〜(2+)的八面体位置偏爱性强,可以解释M = Ni阳极的性能较低。

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