Synthesis and characterization of α-nickel (II) hydroxide particles on organic-inorganic matrix and its application in a sensitive electrochemical sensor for vitamin D determination

被引:34
作者
Canevari, Thiago C. [1 ]
Cincotto, Fernando H. [1 ]
Landers, Richard [2 ]
Machado, Sergio A. S. [1 ]
机构
[1] State Univ Sao Paulo, Inst Chem, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Estadual Campinas, Gleb Wataghin Inst Phys, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Electrochemical sensor; graphene oxide; hybrid materials; nickel hydroxide; Vitamin D; AMPEROMETRIC DETECTION; LIQUID-CHROMATOGRAPHY; GRAPHENE OXIDE; ELECTRODE; ELECTROANALYSIS; QUANTIFICATION; NANOPARTICLES; THICKNESS; PRODUCTS; SURFACES;
D O I
10.1016/j.electacta.2014.10.012
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This paper describes the synthesis, characterization and application of amorphous nickel (II) hydroxide particles, alpha-Ni(OH)(2), onto a hybrid material composed of silica and graphene oxide, SiO2/GO. The sol-gel process using HF as the catalyst was used to obtain this organic-inorganic matrix. The Ni(OH)(2) were prepared directly on the surface of the matrix using nickel (II) acetate and N, N-dimethylformamide (DMF) as a solvent. The SiO2/GO/Ni(OH)(2) material was characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS) and electrochemical techniques. A glassy carbon electrode modified with the SiO2/GO/Ni(OH)(2) material was used in the development of a sensitive electrochemical sensor for the determination of vitamin D-3 by pulse differential voltammetry. A well-defined electro-oxidation peak of vitamin D-3 was observed in sodium hydroxide at pH 13. The results indicated that the resultant SiO2/GO/Ni(OH)(2) modified electrode is highly selective and very sensitive with a limit of detection, in pure laboratory solutions of 3.26 x 10(-9) mol dm(-3); therefore, it can be used to detect vitamin D3 in real samples. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:688 / 695
页数:8
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