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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Synthesis of Ni–TiO Nanocomposites as Enzyme–Less, Amperometric Sensors for the Electrooxidation of Glucose
The simple synthesis of a Ni–TiO2nanocomposite supported on Vulcan carbon (XC–72 R) for the electrooxidation reaction of glucose is reported. Four transition metal weight ratios were synthesized and characterized. Cyclic voltammetry studies in 0.1 M NaOH demonstrate that the four metal catalysts can effectively oxidize 1 mM glucose, with the 3:1 (60%) Ni to Ti nanocomposite yielding the highest current. The 60% Ni–TiO2/XC72R catalyst was used to construct an enzyme–less, chronoamperometric sensor for glucose detection in an alkaline medium. Using 50μM aliquots of glucose at a potential of +0.7 V (vs Hg/HgO), the sensor responded rapidly (<3 s), provided a sensitivity of 3300μA mM−1cm−2, detection limits of 144 nM (Signal/Noise = 3), and excellent selectivity and reproducibility. The glucose aliquot concentrations were then increased to 1 mM to mimic physiological blood conditions of 1–20 mM. At a potential of +0.7 V (vs Hg/HgO), the sensor continued to respond rapidly (<1 s), showed a sensitivity of 273.7μA mM−1cm−2, detection limits of 3.13μM (S/N = 3), and excellent selectivity and reproducibility. The catalyst also exhibited an ideal anti–poisoning capability to free chloride ions and negligible signals towards other interfering species.
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- Award ID(s):
- 2018740
- PAR ID:
- 10474220
- Publisher / Repository:
- IOP Science
- Date Published:
- Journal Name:
- ECS Advances
- Volume:
- 2
- Issue:
- 2
- ISSN:
- 2754-2734
- Page Range / eLocation ID:
- 026502
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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