Abstract
Here we report on the development of a high-efficiency, dual channel-electrode (DCE) generation-collection system and its application for interrogating redox-active surface-adsorbed thin films. DCE systems consist of two electrodes configured on the base of a microfluidic channel. Under laminar flow conditions, a redox reaction can be driven on the upstream generator electrode, and the products carried by convection to the downstream collector electrode where the reverse redox reaction occurs. One significant outcome of this report is that simple fabrication techniques can be used to prepare DCE systems that have collection efficiencies of up to 97%. This level of efficiency makes it possible to quantitatively measure the charge associated with redox-active thin films interposed between the generator and collector electrodes. This is important, because it provides a means for interrogating species that are not in sufficiently close proximity to an electrode to enable direct electron transfer or electroactive films adsorbed to insulating surfaces. Here, the method is demonstrated by comparing results from this indirect surface interrogation method, using Fe(CN)6(3-) as the redox probe, and direct electroreduction of Au oxide thin films. These experimental results are further compared to finite-element simulations.
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