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Investigation of Redox Kinetics by Simultaneous In Situ Optical Absorption Relaxation and Electrode Impedance Measurements: Pr Doped Ceria Thin Films

机译:通过同时原位光吸收弛豫和电极阻抗测量研究氧化还原动力学:Pr掺杂的二氧化铈薄膜

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Fast oxygen incorporation, essential for low temperature SOFCs, is enhanced in mixed ionic electronic conducting electrodes. In this study, simultaneous in situ measurement of transient optical absorption changes and electrode impedance is demonstrated as a powerful and convenient means for examining oxygen exchange kinetics in oxide thin films, utilizing Pr_(0.1)Ce_(0.9)O_(2-δ) as a model system. Absorption in the visible spectrum is tied to the fraction of Pr in its oxidized state (4+), which in turn is related to the material's oxygen deficiency. The origin of discrepancies between k_(chem) derived from optical relaxation measurements and k_(elec) from electrochemical measurements is discussed in terms of surface contamination and the potential catalytic effect of metal contacts.
机译:快速的氧掺入对于低温SOFC来说是必不可少的,在混合离子电子导电电极中得到了增强。在这项研究中,以Pr_(0.1)Ce_(0.9)O_(2-δ)作为原位,同时现场测量瞬态光吸收变化和电极阻抗被证明是检查氧化物薄膜中氧交换动力学的一种强大而便捷的方法。模型系统。可见光谱中的吸收与处于氧化态(4+)的Pr的比例有关,而这又与材料的氧缺乏有关。根据表面污染和金属触点的潜在催化作用,讨论了从光学弛豫测量得出的k_(chem)与从电化学测量得出的k_(ele)之间差异的起源。

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