Generator-collector experiments at a single electrode : exploring the general applicability of this approach by comparing the performance of surface immobilized versus solution phase sensing molecules

We demonstrate proof-of-concept that generator-collector experiments can be performed at a single macroelectrode and used to determine mechanistic information. The practical advantages of such a system over conventional generator-collector techniques are also outlined. The single-electrode generator...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 26(2010), 2 vom: 19. Jan., Seite 1340-6
1. Verfasser: Henstridge, Martin C (VerfasserIn)
Weitere Verfasser: Wildgoose, Gregory G, Compton, Richard G
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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245 1 0 |a Generator-collector experiments at a single electrode  |b exploring the general applicability of this approach by comparing the performance of surface immobilized versus solution phase sensing molecules 
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520 |a We demonstrate proof-of-concept that generator-collector experiments can be performed at a single macroelectrode and used to determine mechanistic information. The practical advantages of such a system over conventional generator-collector techniques are also outlined. The single-electrode generator-collector technique is applied to study the known mechanism of oxygen reduction in aqueous conditions as a model system. We seek to demonstrate that the single-electrode generator-collector approach is capable of detecting local pH changes, immediately adjacent to the electrode surface during a redox reaction. Experiments are performed using a molecular pH probe attached to the electrode surface. Comparison of experimental data with numerical simulations verifies that the reduction of oxygen at pH 6.8 proceeds via a two-electron, two-proton mechanism. Experiments were also performed with a molecular pH probe dissolved in the electrolyte solution in order to explore the feasibility of this approach, which is potentially applicable to a much wider range of electrochemical systems 
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700 1 |a Wildgoose, Gregory G  |e verfasserin  |4 aut 
700 1 |a Compton, Richard G  |e verfasserin  |4 aut 
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