Enhanced electrochemical oxidation of ethanol using a hybrid catalyst cascade architecture containing pyrene-TEMPO, oxalate decarboxylase and carboxylated multi-walled carbon nanotube

Abstract The work presented herein demonstrates a hybrid bi-catalytic architecture for the complete electrochemical oxidation of ethanol. The new catalytic system contains pyrene-TEMPO (TEMPO = 2,2,6,6-tetramethylpiperidinyl-N-oxyl) immobilized on the surface of carboxylated multi-walled carbon nanotubes (MWCNT-COOH), and oxalate decarboxylase enzyme (OxDc) immobilized onto a carbon cloth electrode. Electrolysis revealed a stable amperometric curve and an excellent current density value over a duration of 10 h. In addition, the hybrid system immobilized on the carbon electrode exhibits outstanding stability after electrolysis. Nuclear magnetic resonance (NMR) and gas chromatography (GC) demonstrate that the hybrid electrode system is able to oxidize ethanol to CO2 after 10 h of electrolysis. Overall, this study illustrates the enhancement of an enzymatic biofuel cell through the hybrid multi-catalytic systems, which exhibit high oxidation rates for all substrates involved in complete ethanol oxidation, enabling the collection of up to 12 electrons per molecule of ethanol.