4.7 Article

Simultaneous electrochemical detection of ascorbic acid, dopamine and uric acid based on graphene anchored with Pd-Pt nanoparticles

期刊

COLLOIDS AND SURFACES B-BIOINTERFACES
卷 111, 期 -, 页码 392-397

出版社

ELSEVIER
DOI: 10.1016/j.colsurfb.2013.06.030

关键词

Graphene; Pd-Pt bimetallic nanoparticles; Ascorbic acid; Dopamine; Uric acid; Simultaneous detection

资金

  1. Natural Science Foundation of Jiangsu Education Committee [10KJB150011]
  2. National Natural Science Foundation of China [21175070, 81273480]

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Pd-Pt bimetallic nanoparticles anchored on functionalized reduced graphene oxide (RGO) nanomaterials were synthesized via a one-step in situ reduction process, in which Pt and Pd ions were first attached to poly(diallyldimethylammonium chloride) (PDDA) functionalized graphene oxide (GO) sheets, and then the encased metal ions and GO were subjected to simultaneous reduction by ethylene glycol. The as-prepared Pd3Pt1/PDDA-RGO nanocomposites were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and electrochemical methods. In addition, an electrochemical sensor based on the graphene nanocomposites was fabricated for the simultaneous detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA) in their ternary mixture. Three well-separated voltammetric peaks along with remarkable increasing electro-oxidation currents were obtained in differential pulse voltammetry (DPV) measurements. Under the optimized conditions, there were linear relationships between the peak currents and the concentrations in the range of 40-1200 mu M for AA, 4-200 mu M for DA and 4-400 mu M for UA, with the limit of detection (LOD) (based on S/N =3) of 0.61, 0.04 and 0.10 mu M for AA, DA and UA, respectively. This improved electrochemical performance can be attributed to the synergistic effect of metallic nanoparticles and RGO and the combination of the bimetallic nanoparticles. Furthermore, the practical electroanalytical utility of the sensor was demonstrated by the determination of AA, DA and together with UA in human urine and blood serum samples with satisfactory results. (C) 2013 Elsevier B.V. All rights reserved.

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