Quantitative in Situ Measurement of Ion Transport in Polypyrrole/Poly(styrenesulfonate) Films Using Rotating Ring−Disk Voltammetry

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Abstract
An approach based on rotating ring−disk electrode (RRDE) voltammetry is described for the quantitative, in situ measurement of ion transport between solution and conducting polymer films. The specific composite film studied in this report is polypyrrole/poly(styrenesulfonate) (pPy+/pSS-). Cation flux in and out of the polymer was obtained from the mass-transport-limited reduction current for the dopant cation(s) measured at the ring during redox cycling of the polymer. Crucial to this method is the use of a supporting electrolyte that is sterically inhibited from passing into the film and the use of dopant ions that adhere to specific electrochemical constraints. With this method it was possible to quantitatively account for all changes in charge compensation in the film by the specific cation(s) involved. Three different cations were explored alone and in paired combinations. Solutions containing mixtures of dopant cations were studied to determine whether the pPy+/pSS- films exhibit preferential doping. Kinetic factors, likely due to steric differences in the dopant cations, were found to lead to significant preferential doping of the polymer.

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