Electrochemistry
Online ISSN : 2186-2451
Print ISSN : 1344-3542
ISSN-L : 1344-3542

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UNCORRECTED PROOF
Enhancement of Electrochemiluminescence by Au Paste Electrode for Bipolar Electroanalysis
Ayane ENDOKoki KUBOTA Takahiro ITO-SASAKIMayo KOMATSUTomoki IWAMAHitoshi SHIKUKumi Y. INOUE
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JOURNAL OPEN ACCESS Advance online publication
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Article ID: 23-68114

UNCORRECTED PROOF: January 16, 2024
ACCEPTED MANUSCRIPT: December 12, 2023
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Abstract

Carbon paste electrodes (CPEs) are widely used because of their malleability and ease of modification of functional molecules. This study introduces the application of Au paste electrodes (AuPEs) as a method for amplifying electrochemiluminescence (ECL), with a focus on bipolar electrochemical analyses. First, the ECL intensities generated by the cathodic and anodic reactions of [Ru(bpy)3]2+ at the glassy carbon disc electrode, Au disc electrode, carbon paste electrode, and AuPE was compared using a three-electrode system. We confirmed that the utilization of the AuPEs resulted in ECL intensities that were 1.4–1.7 times higher than those achieved through the use of other electrodes. A similar ECL enhancement effect was observed with the AuPE mixed with N,N′-dimethyl-3,4,9,10-perylenetetracarboxylicdiimide (PDI-CH3) as a cathodic luminophore. This PDI-CH3 mixed AuPE was used as the cathode in a closed bipolar electrode system. The system successfully detected dopamine concentrations of 1.0 mmol dm−3 in a sample cell. We hypothesize that the observed enhancements in the ECL were attributable to the surface plasmon field-enhancement effect of the Au particles. These results can be applied to highly sensitive bipolar electrochemical microscopy for imaging the dynamics of intracellular transmitter molecules.

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© The Author(s) 2023. Published by ECSJ.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (CC BY-NC-SA, http://creativecommons.org/licenses/by-nc-sa/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium by share-alike, provided the original work is properly cited. For permission for commercial reuse, please email to the corresponding author. [DOI: 10.5796/electrochemistry.23-68114].
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