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Direct electrochemistry of glucose oxidase and sensing glucose using a screen-printed carbon electrode modified with graphite nanosheets and zinc oxide nanoparticles
| Content Provider | Semantic Scholar |
|---|---|
| Author | Karuppiah, Chelladurai Palanisamy, Selvakumar Chen, Shen-Ming Veeramani, Vediyappan Periakaruppan, Prakash |
| Copyright Year | 2014 |
| Abstract | AbstractWe have studied the direct electrochemistry of glucose oxidase (GOx) immobilized on electrochemically fabricated graphite nanosheets (GNs) and zinc oxide nanoparticles (ZnO) that were deposited on a screen printed carbon electrode (SPCE). The GNs/ZnO composite was characterized by using scanning electron microscopy and elemental analysis. The GOx immobilized on the modified electrode shows a well-defined redox couple at a formal potential of −0.4 V. The enhanced direct electrochemistry of GOx (compared to electrodes without ZnO or without GNs) indicates a fast electron transfer at this kind of electrode, with a heterogeneous electron transfer rate constant (Ks) of 3.75 s−1. The fast electron transfer is attributed to the high conductivity and large edge plane defects of GNs and good conductivity of ZnO-NPs. The modified electrode displays a linear response to glucose in concentrations from 0.3 to 4.5 mM, and the sensitivity is 30.07 μA mM−1 cm−2. The sensor exhibits a high selectivity, good repeatability and reproducibility, and long term stability. FigureGraphical representation for the fabrication of GNs/ZnO composite modified SPCE and the immobilization of GOx |
| Starting Page | 1843 |
| Ending Page | 1850 |
| Page Count | 8 |
| File Format | PDF HTM / HTML |
| DOI | 10.1007/s00604-014-1256-z |
| Alternate Webpage(s) | https://static-content.springer.com/esm/art:10.1007%2Fs00604-014-1256-z/MediaObjects/604_2014_1256_MOESM1_ESM.pdf |
| Alternate Webpage(s) | https://doi.org/10.1007/s00604-014-1256-z |
| Volume Number | 181 |
| Journal | Microchimica Acta |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |