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Updated: Jul 11, 2026

Adapting Taylor Dispersion to Measure the Dispersion Coefficient of Electrolyte Solutions via an Accessible Microfluidic Setup
Published on: October 7, 2025
Use of microdevices to determine the diffusion coefficient of electrochemically generated species: application to
Tiago L Ferreira1, Thiago R L C Paixão, Eduardo M Richter
1Instituto de Química, Universidade de São Paulo, São Paulo, SP, Brazil 05508-900.
Abstract:
A new approach for the determination of diffusion coefficient, D, of redox species is presented. It is based on the use of a home-constructed twin electrode within a thin-layered cell (TETLC) filled with a solution of electroactive species. Values of D are readily calculated, provided that the time required for the electrochemically generated species (produced at the generator electrode) to reach the collector electrode and the distance between both electrodes are known. Other parameters typically required to calculate D, e.g., concentration of the redox species, area of the electrode, and number of electrons transferred, are not needed. Diffusion coefficients of Fe(CN)(6)(3-), Ru(NH3)(6)(2+), and quinone were determined in water and, for Fe(CN)(6)(4-), in binary mixtures with glycerol. The results obtained were in good agreement with literature values. Aqueous glycerol solutions are microheterogeneous, as shown by the dependence on medium composition of the empirical solvent polarity scale, ET(30), determined by the solvatochromic probe RB. The responses of RB and the electrochemically generated species (Fe(CN)(6)(4-)) to the composition of aqueous glycerol mixtures were found to be remarkably similar. Measurements of D of ferrocene in micellar solutions of the cationic surfactant CTABr were also performed. Values of D for ferrocene and the ferrocenium cation are very different, in agreement with the chemical affinity of both species for the cationic micelle.
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