阴极
氧化还原
极化(电化学)
介电谱
分析化学(期刊)
氧化物
固体氧化物燃料电池
电极
吸收光谱法
非阻塞I/O
材料科学
氧化镍
化学
电解质
无机化学
电化学
物理化学
光学
催化作用
物理
冶金
生物化学
色谱法
作者
Russell J. Woolley,Mary P. Ryan,Stephen J. Skinner
出处
期刊:Fuel Cells
[Wiley]
日期:2013-11-08
卷期号:13 (6): 1080-1087
被引量:14
标识
DOI:10.1002/fuce.201300174
摘要
Abstract A solid oxide fuel cell in operando is a complex multiphasic entity under electrical polarization and operating at high temperatures. In this work, we reproduce these conditions while studying transition metal redox chemistry in situ at the cathode. This was achieved by building a furnace that allowed for X‐ray absorption near‐edge structure and AC impedance spectroscopy data to be obtained simultaneously on symmetrical cells while at operating temperatures. The cell electrodes consisted of phases from the Ruddlesden–Popper family; La 2 NiO 4+δ , La 4 Ni 3 O 10–δ , and composites thereof. The redox chemistry of nickel in these cathodes was probed in situ through investigation of changes in the position of the X‐ray absorption K‐edge. An oxidation state reduction (Ni 3+ to Ni 2+ ) was observed on heating the cells; this was correlated to changing concentrations of ionic charge carriers in the electrode. Polarizing the cells resulted in dramatic changes to their electrical performance but not to the bulk redox chemistry of the electrode. The implications of this with respect to explaining the polarization behavior are discussed.
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