An insight into the effects of B-site transition metals on the activity, activation effect and stability of perovskite oxygen electrodes for solid oxide electrolysis cells

An insight into the effects of B-site transition metals on the activity, activation effect and stability of perovskite oxygen electrodes for solid oxide electrolysis cells
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深入探讨B位过渡金属对固体氧化物电解电池钙钛矿氧电极活性、活化效果和稳定性的影响

DOI:
10.1016/j.jpowsour.2017.07.118
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发表时间:
2017-09
影响因子:
9.2
通讯作者:
Liu Yihui
Liu Yihui
中科院分区:
工程技术2区
文献类型:
--
作者:
Bi Jiaxin;Yang Shengbing;Zhong Shaohua;Wang Jian-Qiang;Fan Chou;Chen Xinbing;Liu Yihui

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本文讨论了(La0.6Sr0.4)XO 3-δ(X = Mn,Fe,Co)钙钛矿结构中B位过渡金属(TM)对高温电解过程中氧电极活性和稳定性的影响,以加深对阳极极化下不同氧电极所观察到的现象的理解。当TM从Mn变为Fe和Co时,电极的性能和稳定性在800 °C下显著变化,这归因于材料的不同离子电导率和表面化学,其对TM的价态和电子结构具有强烈的依赖性。在800 °C下,在200 mA cm− 2的阳极电流通过下,(La0.6Sr0.4)MnO 3-δ(LSM)电极在1200 min的测试过程中显著降低了1.75 Ω cm 2和101 mV,与(La_(0.6)Sr_(0.4))FeO_(3-δ)(LSF)和(La_(0.6)Sr_(0.4)CoO_(3-δ)(LSC))电极的RE和η的恒定值相比较,表明B位TMs对电极性能和稳定性的影响。在(La0.6Sr0.4)MnO 3-δ电极上观察到最严重的降解,这是由于电极/电解质界面附近的SrO表面偏析和LSM颗粒的相关崩解引起的电极脱离。
Here, effects of B-site transition metals (TMs) in the (La0.6Sr0.4)XO3-δ(X = Mn, Fe, Co) perovskite structure on the activity and stability of the oxygen electrodes during high temperature electrolysis are discussed to provide a deep understanding of the phenomena observed for different oxygen electrodes under anodic polarizations. Performance and stability of the electrodes vary significantly at 800 °C as the TMs changed from Mn to Fe and Co, which is attributed to the different ionic conductivities and surface chemistry of the materials that have a strong dependence on the valence state and electronic structure of TMs. Under an anodic current passage of 200 mA cm−2at 800 °C, electrode polarization resistance (RE) and overpotential (η) of the (La0.6Sr0.4)MnO3-δ(LSM) electrode decrease significantly by 1.75 Ω cm2and 101 mV during the 1200 min test, compared with the constant values ofREandηfor the (La0.6Sr0.4)FeO3-δ(LSF) and (La0.6Sr0.4)CoO3-δ(LSC) electrodes, an indication of the influence of B-site TMs on the electrode performance and stability. Most serious degradation is observed at the (La0.6Sr0.4)MnO3-δelectrode due to the electrode detachment arising from the accelerated SrO surface segregation and related disintegration of LSM particles near the electrode/electrolyte interface.
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