Uniform and porous CoNi 2 Se 4 was successfully synthesized by electrodeposition onto a composite electrode comprising reduced graphene oxide (rGO) anchored on a Ni foam substrate (prepared hydrothermally). This CoNi 2 Se 4 –rGO@NF composite electrode has been employed as an electrocatalyst for the direct oxidation of glucose, thereby acting as a high-performance non-enzymatic glucose sensor. Direct electrochemical measurement with the as-prepared electrode in 0.1 M NaOH revealed that the CoNi 2 Se 4 –rGO nanocomposite has excellent electrocatalytic activity towards glucose oxidation in an alkaline medium with a sensitivity of 18.89 mA mM −1 cm −2 and a wide linear response from 1 μM to 4.0 mM at a low applied potential of +0.35 V vs. Ag|AgCl. This study also highlights the effect of decreasing the anion electronegativity on enhancing the electrocatalytic efficiency by lowering the potential needed for glucose oxidation. The catalyst composite also exhibits high selectivity towards glucose oxidation in the presence of several interferents normally found in physiological blood samples. A low glucose detection limit of 0.65 μM and long-term stability along with a short response time of approximately 4 seconds highlights the promising performance of the CoNi 2 Se 4 –rGO@NF electrode for non-enzymatic glucose sensing with high precision and reliability.
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Nanostructured copper selenide as an ultrasensitive and selective non-enzymatic glucose sensor
CuSe nanostructures exhibit high-efficiency for glucose detection with high sensitivity (19.419 mA mM −1 cm −2 ) and selectivity at a low applied potential of +0.15 V vs. Ag|AgCl, a low detection limit of 0.196 μM and a linear range of glucose detection from 100 nM to 40 μM.
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- Award ID(s):
- 1710313
- NSF-PAR ID:
- 10244772
- Date Published:
- Journal Name:
- Materials Advances
- Volume:
- 2
- Issue:
- 3
- ISSN:
- 2633-5409
- Page Range / eLocation ID:
- 927 to 932
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/d0ma00890g
