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Electrosynthesis of Pyrenediones on Carbon Nanotube Electrodes for Efficient Electron Transfer with FAD‐dependent Glucose Dehydrogenase in Biofuel Cell Anodes
Author(s) -
Blanchard PierreYves,
Buzzetti Paulo Henrique M.,
Davies Bridget,
Nedellec Yannig,
Girotto Emerson Marcelo,
Gross Andrew J.,
Le Goff Alan,
Nishina Yuta,
Cosnier Serge,
Holzinger Michael
Publication year - 2019
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.201901666
Subject(s) - electrosynthesis , redox , electron transfer , chemistry , carbon nanotube , cyclic voltammetry , dehydrogenase , glassy carbon , electrode , inorganic chemistry , chemical engineering , electrochemistry , photochemistry , materials science , organic chemistry , nanotechnology , enzyme , engineering
A particularly efficient redox mediator for electron transfer between FAD‐dependent glucose dehydrogenase (FAD‐GDH) and carbon nanotube (CNT) based electrodes can be obtained via electrosynthetic oxidation of pyrene in aqueous buffer solution. 1 H‐NMR spectroscopic studies reveal the formation of a 2 : 1 mixture of 1,6‐pyrenedione and 1,8‐pyrenedione at the electrode. The formed pyrenedione exhibits a well‐defined surface‐bound redox system at −0.1 V vs . SCE and provides excellent electron transfer kinetics with this enzyme. Furthermore, the π‐system of pyrenedione allows improved stacking behavior with the CNT walls, leading to enhanced stabilities compared to commonly used mediators like naphthoquinone. The electrosynthesis of pyrenedione for catalytic glucose oxidation is optimal at pH 2 using cyclic voltammetry or chronoamerometry. It is envisioned that the electrosynthetic methodology can be expanded to form different redox mediators for a series of enzymes.