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Electrochemically derived CuO nanorod from copper-based metal-organic framework for non-enzymatic detection of glucose
In this work, we fabricated a novel enzyme-free glucose sensor based on CuO nanorod, which was electrochemically derived from the copper-based metal-organic framework, Cu3(BTC)2 (BTC: benzene tricarboxylate). Repeated potential cycling successfully oxidized Cu3(BTC)2 to CuO, leaving residual carboxy...
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Published in: | Applied surface science 2019-06, Vol.479, p.720-726 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In this work, we fabricated a novel enzyme-free glucose sensor based on CuO nanorod, which was electrochemically derived from the copper-based metal-organic framework, Cu3(BTC)2 (BTC: benzene tricarboxylate). Repeated potential cycling successfully oxidized Cu3(BTC)2 to CuO, leaving residual carboxylate on the catalyst surface. The oxidation process was carefully investigated by X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform IR, and scanning electron microscopy. Cyclic voltammetry and chronoamperometry studies of the electrochemical oxidation of glucose on the CuO nanorod revealed excellent electrocatalytic performance with high sensitivity of 1523.5 μA mM−1 cm−2, linear response up to 1.25 mM, and detection limit of 1 μM. Compared with commercial CuO powder, the CuO nanorod showed much higher sensitivity because of its large surface area (60.2 m2 g−1). Moreover, it exhibited good selectivity to glucose over potential interfering compounds. These results suggest the potential application of the Cu3(BTC)2-derived CuO nanorod as a non-enzymatic glucose sensor.
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•CuO nanorod is electrochemically derived from Cu-based metal-organic framework, Cu3(BTC)2.•The obtained nanorod still has residual carboxylate ligand on the surface.•The sensitivity for glucose oxidation is 1523.5 μA mM−1 cm−2 with detection limit of 1 μM. |
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ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2019.02.130 |