Nitrobenzoic acid-functionalized gold nanoparticles: DET promoter of multicopper oxidases and electrocatalyst for NAD-dependent glucose dehydrogenase. (10th March 2022)

• Record Type: Journal Article
• Authors: Lalaoui, Noémie; Gentil, Kilian; Ghandari, Ilyass; Cosnier, Serge; Giroud, Fabien
• Is Part Of: Electrochimica acta. Volume 408(2022)
• Publication Date: 2022-03-10
• Subjects: Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2022.139894
• Languages: English
• ISSNs: 0013-4686

Abstract

Abstract: We report the synthesis of coated gold nanoparticles with nitrobenzoic moieties (AuNPs-TNB). They displayed small and narrow size distribution (2 nm) as shown by TEM imaging. These functionalized AuNPs-TNB were physically adsorbed on multi-walled carbon nanotubes (MWCNTs) electrodes. Their stable adsorption was monitored by electrochemical methods. The stability of the activated hydroxylamine layer was enhanced compared to the adsorption of the dinitro precursor onto the CNTs layer. Unactivated AuNPs-TNB enhanced the oxygen reduction reaction catalyzed by multicopper oxidases through increased aromatic and electrostatic interactions with limiting current densities higher than 500 µA cm −2 . Next, the electrocatalytic properties of the active form toward the oxidation of the reduced form of nicotinamide adenine dinucleotide (NADH) with low overpotential was shown at near neutral pH. Associated with a NAD-dependent glucose dehydrogenase, the bioelectrodes were assessed for glucose electrooxidation. A complete glucose/O2 enzymatic fuel cell was developed based on unactived and activated AuNPs as cathodic DET promoter and anodic electrocatalyst respectively. The nanostructured assembly exhibited efficient glucose oxidation with current densities of 450 µA cm −2 in high glucose concentration and O2 saturated conditions. In concentration close to those found in physiological fluids (0.04 to 4.00 mmol L −1 ), the enzymatic biofuel cell displayed a linear range for glucose concentration and a low limit of detection (2.5 ± 0.9 µmol L −1 ).