Title of article :
Synthesis of hollow Pt–Ni–graphene nanostructures for nonenzymatic glucose detection
Author/Authors :
Hu، نويسنده , , Yaojuan and He، نويسنده , , Fengyun and Ben، نويسنده , , Ailing and Chen، نويسنده , , Changyun، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
7
From page :
55
To page :
61
Abstract :
A novel, graphene-supported, and hollow Pt–Ni nanostructure (denoted as hollow Pt–Ni–graphene nanocatalyst) was synthesized using a galvanic replacement approach at ambient temperature. The prepared nanostructures were characterized by transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), X-ray powder diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The electrocatalytic characteristics of the nanostructures pertaining to the oxidation of glucose were evaluated by voltammetry. The results demonstrated that the hollow Pt–Ni–graphene nanocatalysts demonstrate superior electrocatalytic performance in comparison with the solid Pt–Ni–graphene electrocatalysts. A nonenzymatic amperometric glucose sensor was developed using the hollow Pt–Ni–graphene nanostructure as the electrode material. The sensor exhibited good electrocatalytic activity toward the oxidation of glucose and had a rapid response (ca. 2 s), low detection limit (ca. 2 μM), wide linear range (0.5–20 mM), and high sensitivity (ca. 30.3 μA mM−1 cm−2), as well as good stability and repeatability. Additionally, the common interfering species, such as ascorbic acid (AA), uric acid (UA), and 3,4-dihydroxyphenylacetic acid (DOPAC) did not cause any interference due to the use of a low detection potential (−0.35 V vs. SCE). Furthermore, the sensor was successfully applied to the determination of glucose concentration in human serum samples.
Keywords :
Hollow-Pt–Ni–graphene , Glucose oxidation reaction , Nonenzymatic glucose detection
Journal title :
Journal of Electroanalytical Chemistry
Serial Year :
2014
Journal title :
Journal of Electroanalytical Chemistry
Record number :
1678277
Link To Document :
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