Effect of palladium oxidation state on the kinetics and mechanism of the charge transfer reaction taking place at the Pd/YSZ interface

被引:8
作者
Kalimeri, K.
Pekridis, G.
Vartzoka, S.
Athanassiou, C.
Marnellos, G. [1 ]
机构
[1] Univ Western Macedonia, Dept Engn & Management Energy Resources, GR-50100 Kozani, Greece
[2] Aristotle Univ Thessaloniki, Dept Chem Engn, GR-54006 Thessaloniki, Greece
[3] Ctr Res & Technol, Chem Proc Engn Res Inst, GR-57001 Thessaloniki, Greece
关键词
palladium; Pd; palladium oxide; PdO; YSZ; Pd/YSZ interface; electrode polarization; charge transfer reaction mechanism; Butler-Volmer equation;
D O I
10.1016/j.ssi.2006.03.035
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrode polarization and conductivity measurements were carried out at the Pd/YSZ interface and at conditions close to the Pd-PdO thermodynamic equilibrium. The steady-state current-overpotential characteristics were analyzed with a Butler-Volmer type of equation. Both, apparent exchange current density, I-o, and anodic/cathodic charge transfer coefficients (alpha(a)/alpha(c)), were calculated. Based on the experimental results, it was concluded that the charge transfer at the electrode is rate-determining in the case of PdO during anodic operation and Pd during cathodic operation, while in the other case mass transport of adsorbed oxygen species along the electrode/solid electrolyte interface is in competition with the charge transfer process. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:979 / 988
页数:10
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