Digital Simulation of the Measured Electrochemical Response of Reversible Redox Couples at Microelectrode Arrays: Consequences Arising from Closely Spaced Ultramicroelectrodes.
Interim technical rept.,
MASSACHUSETTS INST OF TECH CAMBRIDGE DEPT OF CHEMISTRY
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Diffusion to arrays of closely spaced 1.2 micron to 0.2 micron ultramicroelectrodes 50 micron x 2.3 micron was studied by digital simulation and experimentally by examing the redox behavior of RuNH363 in H2O. Cylindrical diffusion of solution species resulted in quasi-steady-state currents at the microband electrodes. Generation-collection experiments, analogous to rotating ring-disk collection experiments, resulted in larger generator currents than those observed at a single microelectrode due to the back diffusion of products to the neighboring microelectrode. A collection efficiency of 93 was observed for the re-oxidation of RuNH362 generated at a central microelectrode 0.2 micron from two flanking collector microelectrodes. This experiment as well as generator-single collector electrode pairs was simulated at a two-dimensional rectangular expanding grid and yielded results in good agreement with the experiment. Predictions of the model that the collection efficiency principally depends on the gap size, rather than electrode width, were tested experimentally. The novel application of microelectrode arrays to the study of the follow-up reactions of electrogenerated intermediates is demonstrated. Author
- Physical Chemistry
- Electrical and Electronic Equipment