Electrochemistry with Stationary Disk and Ring-disk Millielectrodes in Magnetic Fields
Abstract
The most well-known effect of the magnetic field on electrochemical systems is hydrodynamic convection (stirring) of the electrolytic solution. The basic hydrodynamic equations governing mass transport under the magnetic force are well-understood. However, owing to the nonlinear character of those equations and the fact that neither the velocity nor the concentration profile near the electrode is known a priori, rigorous analytical solutions are not available. Retreating to a semiempirical treatment of mass transport, we took the approach of letting the rigorous hydrodynamic equations guide us to the system parameters that should control the steady-state mass-transport-limited current, and subsequently to vary all those parameters systematically using conventional millimeter-sized disk electrodes, and a range of compounds and solvents. To our knowledge, this study comprises the first of its kind, and we concluded that the limiting current i 1 = 4.31 × 10 3 n f+1F A 3/4B 1/3Dv 1/4C bulk 4/3, where n is the number of electrons involved in the redox process, F is the Faraday constant, A is the electrode area, B is the magnetic field strength, D is the diffusion coefficient, C bulk is the bulk concentration of the redox-active species, v is the kinematic viscosity of the electrolyte, and f > 0. The angular flow profile near the electrode surface was mapped using an electrochemical generation/collection method.
Recommended Citation
N. Leventis et al., "Electrochemistry with Stationary Disk and Ring-disk Millielectrodes in Magnetic Fields," Journal of Physical Chemistry B, American Chemical Society (ACS), Jan 1998.
The definitive version is available at https://doi.org/10.1021/jp980498f
Department(s)
Chemistry
International Standard Serial Number (ISSN)
1520-6106
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 1998 American Chemical Society (ACS), All rights reserved.
Publication Date
01 Jan 1998