4.6 Article

Electrocatalytic Investigation by Improving the Charge Kinetics between Carbon Electrodes and Dopamine Using Bio-Synthesized CuO Nanoparticles

Journal

CATALYSTS
Volume 12, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/catal12090994

Keywords

CuO nanoparticles; charge kinetics; frontier molecular orbitals; cyclic voltammetry; dopamine sensor

Funding

  1. Bartin University Scientific Research Projects Unit, Turkey [2019-FEN-A-006]

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In this study, the charge transfer kinetics between carbon paste electrodes and dopamine using green synthesized CuO nanoparticles were successfully investigated. The CuO nanoparticles exhibited excellent electrocatalytic activity for the electro-oxidation of dopamine, and the modified electrode showed exceptional selectivity, robustness, and sensitivity for the analysis of dopamine.
We have successfully studied the charge transfer kinetics between carbon paste electrodes and dopamine using green synthesized rectangular monoclinic CuO nanoparticles (NPs) prepared by Alchemilla vulgaris leaves with the one-pot green synthesis method. The scanning electron microscopy (SEM) results confirmed the monoclinic structure with a particle size of around 85 nm. The investigation of thermal properties was carried out by thermogravimetric (TG) and differential thermal analysis (DTA). We also studied the electrochemical response of green synthesized CuO nanoparticles to detect Dopamine (DA) using cyclic voltammetry, which was proven to be an excellent electrocatalyst for the electro-oxidation of DA. The fabricated CuO nanoparticle modified carbon paste electrode (CMCPE) depicts fantastic selectivity, robustness, and sensitivity in analyzing DA in clinical and pharmaceutical preparations. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) orbitals of the DA were studied using positive and negative charges at the CuO modified carbon paste electrode interface. Frontier molecular orbitals of DA are plotted to understand electron transfer reactivity at the electrode interface.

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