共 50 条
Influence of nanoporous carbon electrode thickness on the electrochemical characteristics of a nanoporous carbon|tetraethylammonium tetrafluoroborate in acetonitrile solution interface
被引:42
|作者:
Lust, E
Jänes, A
Pärn, T
Nigu, P
机构:
[1] Univ Tartu, Inst Phys Chem, EE-51014 Tartu, Estonia
[2] Tartu Technol Ltd, EE-51014 Tartu, Estonia
关键词:
electrical double layer;
nanoporous carbon;
nonaqueous electrolyte solution;
zero charge potential;
D O I:
10.1007/s10008-003-0396-6
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
Electrochemical characteristics for the nanoporous carbon|Et4NBF4+acetonitrile interface have been studied by cyclic voltammetry and impedance spectroscopy methods. The influence of the electrolyte concentration and thickness of the nanoporous electrode material on the shape of the cyclic voltammetry and impedance curves has been established and the reasons for these phenomena are discussed. A value of zero charge potential, depending slightly on the structure and concentration of the electrolyte, the region of ideal polarizability and other characteristics have been established. The nanoporous nature of the carbon electrodes introduces a distribution of resistive and capacitive elements, giving rise to complicated electrochemical behaviour. Analysis of the complex plane plots shows that the nanoporous carbon|Et4NBF4+acetonitrile electrolyte interface can be simulated by an equivalent circuit, in which two parallel conduction paths in the solid and liquid phases are interconnected by the double-layer capacitance in parallel with the complex admittance of the hindered reaction of the charge transfer or of the partial charge transfer (i.e. adsorption stage limited) process. The values of the characteristic frequency depend on the electrolyte concentration and electrode potential, i.e. on the nature of the ions adsorbed at the surface of the nanoporous carbon electrode. The value of the solid state phase resistance established is independent of the thickness of the electrode material.
引用
收藏
页码:224 / 237
页数:14
相关论文