화학공학소재연구정보센터
Electrochimica Acta, Vol.44, No.12, 1999-2018, 1999
Origins of finite transmission lines for exact representations of transport by the Nernst-Planck equations for each charge carrier
The Barker/Brumleve/Buck (BBB) circuits and-sub-circuit units, are derived and illustrated for the generation of the conventional two-feature mass transport-controlled impedance. This finite 2-port, 4-terminal network for a single salt system, replaces the classical I-port, 2-terminal cable transmission line analog because the latter describes only the lower-frequency Warburg feature. Symmetric or asymmetric cell results depend only on the ion or electron terminals used. Three feature impedance plane plots for slow, potential-dependent ion and/or electron transfers with activation resistance and relaxed double layer capacitance, are generated and illustrated. Residual solution resistance and total cell geometric capacitance are included to generate the expected four-feature impedance plots for cells without special features such as ion pairing and adsorption-reaction processes. This paper presents new results for a circuit description of electron hopping in redox polymers with concomitant counter ion motion. The forms of single species flux equation: Barker, Nernst-Planck, and electron-hopping are compared. The latter two are converted into responses I or j vs phi functions that define "T" circuit elements. Two forms arise that define the implicit R-i or R-e, and C-i or C-e per unit length (i = ion, e = electron), and the corresponding explicit R and C. The analysis uses as examples (I) a single dissolved, inert electrolyte salt M+ X-, and (2) a redox polymer electrolyte radical cation and anion, also M+,X-, undergoing second order electron hopping from M to M+. The corresponding forms for the Rs and Cs are derived. A second case is illustrated to show how the d.c. bias changes the polymer cation/anion compositions (assuming Nernstian behavior), and so determines different R-e and C-e at each composition through the effective second order, concentration-dependent electron hopping.