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Electrochemical behavior of Azure A/gold nanoclusters modified electrode and its application as non-enzymatic hydrogen peroxide sensor

[Display omitted] ► AzA/gold nanoclusters was prepared and characterized by Absorption spectroscopy, FESEM and confocal Raman microscopy. ► AzA/gold nanoclusters modified electrode was fabricated and characterized by cyclic voltammetry and was applied for the determination of H2O2 under static and d...

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Bibliographic Details
Published in:Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2012-09, Vol.97, p.90-96
Main Authors: Priya, C., Sivasankari, G., Sriman Narayanan, S.
Format: Article
Language:English
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Summary:[Display omitted] ► AzA/gold nanoclusters was prepared and characterized by Absorption spectroscopy, FESEM and confocal Raman microscopy. ► AzA/gold nanoclusters modified electrode was fabricated and characterized by cyclic voltammetry and was applied for the determination of H2O2 under static and dynamic condition. ► A linear range of 3.26×10−6M to 3.2×10−3M with the detection limit of 1.08×10−6M (S/N=3) was obtained for the determination of H2O2. ► The sensor was applied for the determination of H2O2 in commercial milk samples. A novel non-enzymatic hydrogen peroxide sensor was developed using Azure A/gold nanoclusters modified graphite electrode. The method of preparation of Azure A/gold nanoclusters was simple and it was characterized by UV–visible spectroscopy, field emission scanning electron microscopy (FESEM) and confocal Raman microscopy. The electrochemical properties of Azure A/gold nanoclusters modified graphite electrode was characterized by cyclic voltammetry. In 0.1M H2SO4 the modified electrode showed redox peaks which correspond to the redox behavior of gold nanoparticle. In 0.1M PBS the modified electrode exhibited well defined redox peaks with the formal potential of −0.253V which is analogous to the redox reaction of Azure A. The results have shown that the gold nanoclusters has reduced the formal potential of Azure A and enhanced the current due to the fast charge transfer kinetics. Also the modified electrode showed an enhanced electrocatalytic activity towards the reduction of H2O2 in the concentration range of 3.26×10−6M to 3.2×10−3M with a detection limit of 1.08×10−6M (S/N=3). The proposed electrode exhibited good stability and reproducibility, and it has the potential application as a sensor for other biologically significant compounds.
ISSN:0927-7765
1873-4367
DOI:10.1016/j.colsurfb.2012.04.004