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Ultrasensitive and Highly Selective Ni(3)Te(2) as a Nonenzymatic Glucose Sensor at Extremely Low Working Potential

[Image: see text] Developing Nonenzymatic glucose biosensors has recently been at the center of attention owing to their potential application in implantable and continuous glucose monitoring systems. In this article, nickel telluride nanostructure with the generic formula of Ni(3)Te(2) has been rep...

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Detalles Bibliográficos
Autores principales: Golrokh Amin, Bahareh, De Silva, Umanga, Masud, Jahangir, Nath, Manashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649054/
https://www.ncbi.nlm.nih.gov/pubmed/31460215
http://dx.doi.org/10.1021/acsomega.9b01063
Descripción
Sumario:[Image: see text] Developing Nonenzymatic glucose biosensors has recently been at the center of attention owing to their potential application in implantable and continuous glucose monitoring systems. In this article, nickel telluride nanostructure with the generic formula of Ni(3)Te(2) has been reported as a highly efficient electrocatalyst for glucose oxidation, functional at a low operating potential. Ni(3)Te(2) nanostructures were prepared by two synthesis methods, direct electrodeposition on the electrode and hydrothermal method. The electrodeposited Ni(3)Te(2) exhibited a wide linear range of response corresponding to glucose oxidation exhibiting a high sensitivity of 41.615 mA cm(–2) mM(–1) and a low limit of detection (LOD) of 0.43 μM. The hydrothermally synthesized Ni(3)Te(2), on the other hand, also exhibits an ultrahigh sensitivity of 35.213 mA cm(–2) mM(–1) and an LOD of 0.38 μM. The observation of high efficiency for glucose oxidation for both Ni(3)Te(2) electrodes irrespective of the synthesis method further confirms the enhanced intrinsic property of the material toward glucose oxidation. In addition to high sensitivity and low LOD, Ni(3)Te(2) electrocatalyst also has good selectivity and long-term stability in a 0.1 M KOH solution. Since it is operative at a low applied potential of 0.35 V vs Ag|AgCl, interference from other electrochemically active species is reduced, thus increasing the accuracy of this sensor.