Abstract
The electro-oxidation of ascorbate (AAO) in the presence of urea at NiOx/CoOx/GNs/GC electrode is investigated. Cyclic voltammetry measurements show that the peak current (I
p) of AAO at NiOx/CoOx/GNs/GC electrode is ten times that of GNs/GC electrode. This highlights the role of catalyst composition and order of deposition on the activity of AAO. Interestingly, blending ascorbate (AH− ) with urea caused a significant promotion of AAO. Both the I
p of AAO and the fuel utilization in the AH− /urea fuel blend solution are doubled when compared to those obtained at the same electrode in pure AH− solution (in addition to a favorable negative shift in the onset potential, E
onset = 150 mV). Urea molecules are believed to act as anchoring molecules for AH− molecules at the NiOx/CoOx/GNs/GC surface with a favorable geometry facilitating its oxidation (by two-electron transfer process) to dehydroascorbate (DHA). Four interaction geometries are proposed, and comparative DFT calculations are conducted, displaying the relative stability and dipole moments of AH− in such a way that facilitates its adsorption and oxidation. These findings demonstrate the crucial role of the catalysts tailoring together with the selection of a smart blending fuel with AH−.
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials
Cited by
5 articles.
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