Accurate control of the covalent functionalization of single-walled carbon nanotubes for the electro-enzymatically controlled oxidation of biomolecules.
Fiche publication
Date publication
janvier 2018
Journal
Beilstein journal of nanotechnology
Auteurs
Membres identifiés du Cancéropôle Est :
Pr FORT Yves
Tous les auteurs :
Allali N, Urbanova V, Etienne M, Devaux X, Mallet M, Vigolo B, Adjizian JJ, Ewels CP, Oberg S, Soldatov AV, McRae E, Fort Y, Dossot M, Mamane V
Lien Pubmed
Résumé
Single-walled carbon nanotubes (SWCNTs) were functionalized by ferrocene through ethyleneglycol chains of different lengths (FcETGn) and the functionalized SWCNTs (f-SWCNTs) were characterized by different complementary analytical techniques. In particular, high-resolution scanning electron transmission microscopy (HRSTEM) and electron energy loss spectroscopy (EELS) analyses support that the outer tubes of the carbon-nanotube bundles were covalently grafted with FcETGn groups. This result confirms that the electrocatalytic effect observed during the oxidation of the reduced form of nicotinamide adenine dinucleotide (NADH) co-factor by the f-SWCNTs is due to the presence of grafted ferrocene derivatives playing the role of a mediator. This work clearly proves that residual impurities present in our SWCNT sample (below 5 wt. %) play no role in the electrocatalytic oxidation of NADH. Moreover, molecular dynamic simulations confirm the essential role of the PEG linker in the efficiency of the bioelectrochemical device in water, due to the favorable interaction between the ETG units and water molecules that prevents π-stacking of the ferrocene unit on the surface of the CNTs. This system can be applied to biosensing, as exemplified for glucose detection. The well-controlled and well-characterized functionalization of essentially clean SWCNTs enabled us to establish the maximum level of impurity content, below which the f-SWCNT intrinsic electrochemical activity is not jeopardized.
Mots clés
biosensing, carbon nanotubes, covalent functionalization, electrocatalysis, ferrocene
Référence
Beilstein J Nanotechnol. 2018 ;9:2750-2762