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Redox-Active Green Electrode: Plant-Based Betanin Immobilized on Carbon Black for Drift-Free Voltammetric and
Jayaprakash Meena1,2, Kannappan Santhakumar2, Annamalai Senthil Kumar1,2
1Nano and Bioelectrochemistry Research Laboratory, Carbon Dioxide Research and Green Technology Centre, Vellore Institute of Technology, Vellore 632 014, India.
Abstract:
The development of eco-friendly chemicals and material-based electrode systems with a reduced carbon footprint is a novel initiative for future technological applications. While electrochemical systems based on plant phytochemicals meet the requirements, comprehending the fundamental electron-transfer reactions and preparing stable surface-confined redox systems pose significant research challenges. In this study, we have demonstrated an in situ electrochemical reaction-assisted entrapment of redox-active betanin molecular species from native beetroot plants on a carbon black-modified glassy carbon surface (GCE/CB@Betn-Redox, where Betn-Redox stands for redox-active betanin molecular species) in a pH 2.2 KCl-HCl solution. In general, direct access to native plant phytochemicals is a formidable task due to the matrix effect. Isolating the desired phytochemicals necessitates a series of time-consuming chemical separation steps. Unlike previous literature reports on the unstable nature of Betn, GCE/CB@Betn-Redox exhibited a stable and well-defined proton-coupled electron-transfer peak at an apparent electrode potential, Eo' = 0.4 V vs Ag/AgCl, with a surface-excess value of 17.02 × 10-9 mol cm-2. Using several physicochemical techniques (transmission electron microscopy (TEM), Fourier-transform infrared (FTIR), and Raman), molecular techniques (UPLC), and electrochemical methods (in situ electrochemical quartz crystal microbalance (EQCM) and scanning electrochemical microscopy (SECM)), we have demonstrated the biomimicking electron-transfer functionality of CB@Betn-Redox. The unique feature of CB@Betn-Redox is its nonmediated effect on common biochemicals. This advantage makes it an interesting option for use as a selective pH sensor system without the complications of voltage drift that occur with the mediated oxidation/reduction functionality. We have successfully demonstrated highly selective and stable voltammetric and potentiometric pH sensor applications with practical real samples.
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