Issue 95, 2015

Direct electrochemistry of glucose oxidase and sensing of glucose at a glassy carbon electrode modified with a reduced graphene oxide/fullerene-C60 composite

Abstract

In the present work, a glucose biosensor was fabricated based on the direct electrochemistry of glucose oxidase at glassy carbon modified with a reduced graphene oxide (RGO) and fullerene-C60 (C60) composite. The reduced graphene oxide/fullerene (RGO–C60) composite was prepared by electrochemical reduction of a graphene oxide (GO) and C60 composite at −1.4 V for 200 s in pH 5 solution; while the GO–C60 composite was prepared by a simple sonication of C60 in GO solution for 6 hours at 45 °C. A well-defined and enhanced reversible redox peak of GOx was observed at RGO–C60 composite compared with other modified electrodes. The heterogeneous electron transfer rate constant (Ks) and the surface coverage concentration of GOx at RGO–C60/GOx modified electrode were calculated to be 2.92 s−1 and 1.19 × 10−10 mol cm−2, respectively. Under optimum conditions, the amperometry response of the biosensor was linear against the concentration of glucose from 0.1 to 12.5 mM with a response time of 3 s. The limit of detection was estimated to be 35 μM based on S/N = 3 with a high sensitivity of 55.97 μA mM−1 cm−2. In addition, the fabricated biosensor showed a good practical ability for the detection of glucose in human blood serum samples.

Graphical abstract: Direct electrochemistry of glucose oxidase and sensing of glucose at a glassy carbon electrode modified with a reduced graphene oxide/fullerene-C60 composite

Supplementary files

Article information

Article type
Paper
Submitted
22 Jun 2015
Accepted
04 Sep 2015
First published
07 Sep 2015

RSC Adv., 2015,5, 77651-77657

Author version available

Direct electrochemistry of glucose oxidase and sensing of glucose at a glassy carbon electrode modified with a reduced graphene oxide/fullerene-C60 composite

B. Thirumalraj, S. Palanisamy, S. Chen, C. Yang, P. Periakaruppan and B. Lou, RSC Adv., 2015, 5, 77651 DOI: 10.1039/C5RA12018G

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