CuO nanoparticles/nitrogen-doped carbon nanofibers modified glassy carbon electrodes for non-enzymatic glucose sensors with improved sensitivity

被引:70
|
作者
Lu, Na
Shao, Changlu [1 ]
Li, Xinghua [1 ]
Miao, Fujun
Wang, Kexin
Liu, Yichun
机构
[1] NE Normal Univ, Ctr Adv Optoelect Funct Mat Res, Minist Educ, 5268 Renmin St, Changchun 130024, Peoples R China
基金
中国国家自然科学基金;
关键词
Nitrogen-doped; Carbon nanofibers; Polyaniline; CuO nanoparticles; Non-enzymatic glucose sensor; GRAPHENE; OXIDE; ELECTROCATALYSTS; PERFORMANCE; BIOSENSORS; REDUCTION; NANOCOMPOSITES; NANOMATERIALS; NANOTUBES; OXIDATION;
D O I
10.1016/j.ceramint.2016.04.046
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nitrogen-doped carbon nanofibers (N-CNFs) were facilely prepared by carbonizing electrospun polyacrylonitrile@polyaniline core shell nanofibers. The obtained N-CNFs possessed the favorable properties of high nitrogen content, large surface area, hierarchical porosity and good conductivity, which as ideal supports have been decorated by CuO nanoparticles through a facile solvothermal approach. Benefiting from the synergistic effect of the properties of N-CNFs and CuO nanoparticles, the obtained CuO/N CNFs modified on glassed carbon electrodes (CuO/N CNEs/GCE) have demonstrated desirable activity for direct electrocatalytic oxidation of glucose with much higher sensitivity than that of pure CuO nanoparticles and CuO/CNEs composites. This could be ascribed to the fast electron transport/collect within the 3D conductive networks, which was very beneficial to improve the sensitivity to glucose detection for CuO/CNEs modified electrodes. In addition, the CuO/N-CNEs/GCE also presented a low detection limit to glucose, good selectivity to the general interferences in blood as well as high stability with long-term exposed in air. Therefore, the prepared CuO/N-CNFs modified electrodes by the facile synthesis method presents the potential possibility for practical application in non-enzymatic glucose sensor. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:11285 / 11293
页数:9
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