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Electrochemical behavior of ceria with selected metal electrodes

机译:二氧化铈与选定金属电极的电化学行为

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The electrochemical properties of the metal | doped ceria | metal system have been examined by A.C. impedance spectroscopy at a range of temperatures (575-650℃) and oxygen partial pressures (8×10-26-0.21 atm). Under reducing conditions, the inverse of the interfacial resistances for both Pt and Au electrodes on samarium-doped ceria (SDC) displayed a po2-1/4 dependence on oxygen partial pressure and an Arrhenius dependence on temperature with an activation energy of ~2.7 eV. The similarity in the characteristics of the two types of electrode materials indicates that the electrochemical oxidation of hydrogen occurs predominantly at the ceria | gas interface. Moreover, the behavior, which is similar to that of the electronic conductivity of SDC, is consistent with the hypothesis that electron migration from the reaction site to the metal current collector is the rate-limiting step.
机译:金属的电化学性质掺杂的二氧化铈|金属体系已通过交流阻抗谱在温度范围(575-650℃)和氧分压(8×10-26-0.21 atm)下进行了检查。在还原条件下,掺杂t的二氧化铈(SDC)上的Pt和Au电极的界面电阻的倒数表现出对氧分压的po2-1 / 4依赖性和对温度的Arrhenius依赖性,活化能为〜2.7 eV 。两种电极材料的特性相似,表明氢的电化学氧化主要发生在二氧化铈处。气体接口。此外,该行为类似于SDC的电子电导率,与以下假设相符:电子从反应位点迁移到金属集电器是限速步骤。

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