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The oxygen transfer process on solid oxide/noble metal electrodes, studies with impedance spectroscopy, polarization and isotope exchange

机译:固体氧化物/贵金属电极上的氧转移过程,用阻抗光谱,极化和同位素交换进行研究

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摘要

The electrochemical oxygen transfer process at the yttria stabilized zirconia (YSZ) and Fe-implanted YSZ, and at the erbia stabilized bismuth oxide (BE25) surface is studied with dc polarization and impedance spectroscopy using gold electrodes, and with 18O gas phase exchange. The surface modification by Fe-implantation increases the exchange current density up to a factor of 50, but analysis of the impedance spectra at different polarization levels indicates that the type of electrode reaction is not changed by the implantation. Inductive effects at cathodic polarizations are interpreted with a stepwise transfer of electrons. Isotope exchange experiments show an increase in adsorption/reaction sites at the surface after implantation. The high exchange current density, I0, for BE25 is independent of type of electrode but does depend on electrode morphology. I0 can be equated to the surface oxygen exchange rate, indicating that the entire electrolyte surface is active in the electrode exchange process. Qualitative interpretation of the impedance spectra measured at different levels of polarization results in a model where adsorbed oxygen species diffuse over the oxide surface, while charge transfer occurs across the surface.
机译:使用金电极和18O气相交换,通过dc极化和阻抗谱研究了在氧化钇稳定的氧化锆(YSZ)和注入铁的YSZ以及在稳定化的氧化铋(BE25)表面上的电化学氧转移过程。通过Fe注入进行的表面改性将交换电流密度提高到50倍,但是对不同极化水平下的阻抗谱的分析表明,注入不会改变电极反应的类型。阴极极化的感应效应可以通过电子的逐步转移来解释。同位素交换实验表明,植入后表面吸附/反应位点增加。 BE25的高交换电流密度I0与电极的类型无关,但确实取决于电极的形态。 I 0可以等于表面氧交换速率,表明整个电解质表面在电极交换过程中是活跃的。定性解释在不同极化水平下测得的阻抗谱会形成一个模型,在该模型中,吸附的氧种类会扩散到氧化物表面,而电荷转移会在整个表面上发生。

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