Platinum nanoparticles-doped sol-gel/carbon nanotubes composite electrochemical sensors and biosensors

被引:321
作者
Yang, MH [1 ]
Yang, YH [1 ]
Liu, YL [1 ]
Shen, GL [1 ]
Yu, RQ [1 ]
机构
[1] Hunan Univ, Chem & Chem Engn Coll, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
biosensors; carbon nanotube; enzymes; platinum nanoparticle; synergistic action;
D O I
10.1016/j.bios.2005.04.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Platinum nanoparticle-doped sol-gel solution is prepared and used as a binder for multi-walled carbon nanotubes (CNT) for the fabrication of electrochemical sensors. Amine group containing sol-gel solution is selected to utilize the affinity of -NH2 groups toward metal nanoparticles for stabilization the nanoparticles in solution. The resulting CNT-silicate material brings new capabilities for electrochemical devices by using the synergistic action of the electrocatalytic activity of Pt nanoparticles and CNT. The combined electrocatalytic activity permits low-potential detection of hydrogen peroxide with remarkably improved sensitivity. With the incorporation of glucose oxidase within the Pt-CNT-silicate matrix, a Pt-CNT paste-based biosensor has been constructed that responds more sensitively to glucose than CNT-based biosensor. The influences of the composite of the sol-gel solution, the quantity of the solution and the Pt nanoparticles loading are examined. In pH 6.98 phosphate buffer, almost interference free determination of glucose is realized at 0.1 V versus SCE with a linear range from 1 to 25 mM, a response time < 15 s, and the sensitivity is 0.98 mu A mM(-1) cm(-2). The sensitivity of the Pt-CNT paste-based biosensor is almost four times larger than that of the CNT-based biosensor (0.27 mu A mM(-1) cm(-2) at 0.1 V). The improved electrocatalytic activity and surface renewability made the Pt-CNT-silicate system a potential platform to immobilize different enzymes for other bioelectrochemical applications. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1125 / 1131
页数:7
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