Carbon nanotubes-nanoflake-like SnS2 nanocomposite for direct electrochemistry of glucose oxidase and glucose sensing

被引:99
作者
Li, Juan [1 ]
Yang, Zhanjun [1 ]
Tang, Yan [1 ]
Zhang, Yongcai [1 ]
Hu, Xiaoya [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Jiangsu Key Lab Environm Engn & Monitoring, Yangzhou 225002, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanoflake-like SnS2; Carbon nanotubes; Glucose oxidase; Direct electrochemistry; Glucose; Biosensor; DIRECT ELECTRON-TRANSFER; LITHIUM-ION BATTERIES; PHOTOCATALYTIC ACTIVITY; REDOX PROTEINS; THIN-FILMS; BIOSENSOR; IMMOBILIZATION; MATRIX; NANOSTRUCTURES; COMPOSITES;
D O I
10.1016/j.bios.2012.09.059
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Multi-walled carbon nanotubes (MWCNTs)-nanoflake-like SnS2 nanocomposite were designed for immobilization of glucose oxidase (GOx). The direct electrochemistry of GOx and glucose sensing at MWCNTs-SnS2 modified glassy carbon electrode were studied. Compared with single MWCNTs or SnS2, the MWCNTs-SnS2 film has larger surface area and provides a more favorable microenvironment for facilitating the electron transfer between enzyme and electrode surface. The properties of GOx/MWCNTs-SnS2 were examined by scanning electron microscopy, UV-vis spectroscopy, Fourier transform infrared spectroscopy and cyclic voltammetry. The immobilized enzyme on MWCNTs-SnS2 composite film retained its native structure and bioactivity and showed a surface controlled, reversible two-proton and two-electron transfer reaction with a apparent electron transfer rate constant of 3.96 s(-1). The constructed glucose biosensor exhibits wider linear range from 2.0 x 10(-5) M to 1.95 x 10(-3) M, much lower detection limit of 4.0 x 10(-6) M at signal-to-noise of 3 and higher sensitivity of 21.65 mA M-1 cm(-2) than our previous nanoflake-like SnS2-based glucose sensor. The proposed biosensor has excellent selectivity, good reproducibility, and acceptable operational stability and can be successfully applied in the reagentless glucose sensing at -0.43 V. This MWCNTs-SnS2 composite provides a new avenue for immobilizing proteins and fabricating excellent biosensors. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:698 / 703
页数:6
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