2018
DOI: 10.1021/acssuschemeng.8b02835
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Hybridization of Co3O4 and α-MnO2 Nanostructures for High-Performance Nonenzymatic Glucose Sensing

Abstract: This work reports a highly sensitive and selective nonenzymatic detection of glucose that has been achieved by hybridization of 1D α-MnO2 nanorods modified with surface decoration of Co3O4 nanoparticles. The rational design and controlled synthesis of the hybrid nanostructures are of great importance in enabling the fine tuning of their properties and functions. First-principles-based periodic hybrid unrestricted HSE06 DFT with Grimme’s long-range dispersion corrections are employed to compute the equilibrium … Show more

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Cited by 58 publications
(54 citation statements)
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“…Sensors for glucose detection, including enzymatic and non-enzymatic detection methods, are the most convenient and promising method due to its sensitivity and reproducibility 15,16 . Enzyme-immobilized glucose sensors suffer from some intrinsic drawbacks such as lack of temperature and pH stability, high cost and low shelf-life 1719 .…”
Section: Introductionmentioning
confidence: 99%
“…Sensors for glucose detection, including enzymatic and non-enzymatic detection methods, are the most convenient and promising method due to its sensitivity and reproducibility 15,16 . Enzyme-immobilized glucose sensors suffer from some intrinsic drawbacks such as lack of temperature and pH stability, high cost and low shelf-life 1719 .…”
Section: Introductionmentioning
confidence: 99%
“…Transition metals are low cost and can be used as electrocatalytic materials for glucose. There are many electrocatalysts reported for transition metals, including pure metals [6,25], bimetals [7,26,27,28], compounds [29,30,31,32], and composites [33,34,35,36,37,38,39,40,41,42,43,44] for non-enzymatic glucose sensors. The catalytic principle of non-enzymatic glucose sensors based on transition metals is by using the d-electron of d-orbital to form medium-strength bonds with substrates, so that the analyte can be easily adsorbed at any time, and its products can be easily desorbed [3].…”
Section: Introductionmentioning
confidence: 99%
“… 34 Moreover, the continuous increase in peak current until the potential of 0.6 V proved the involvement of redox species in glucose oxidation. 35 Further, CV of the HMCA electrode in the presence of glucose solution (0.5 mM) on different scan rates was performed as shown in Figure 1 c. The peak current of glucose oxidation in the HMCA electrode is proportional to the scan rate and shows good linearity in the range of 5-100 mV s –1 , as shown in Figure 1 d. It matches with the linear regression equation j (mA cm –2 ) = 0.122ν 1/2 (mV s –1 ) 1/2 + 0.368 with a correlation coefficient of 0.941. The outcome shows that the electrochemical activity is controlled by glucose adsorption on the electroactive surface.…”
Section: Results and Discussionmentioning
confidence: 99%