To explore a natural nonenzymatic electrode catalyst for highly sensitive and selective molecular detection for targeting biomolecules is a very challenging task. Metal nitrides have attracted huge interest as promising electrodes for glucose and hydrogen peroxide (H 2 O 2 ) sensing applications due to their exceptional redox properties, superior electrical conductivity, and superb mechanical strength. However, the deprived electrochemical stability extremely limits the commercialization opportunities. Herein, novel nitrogen-doped graphene-encapsulated nickel cobalt nitride (Ni x Co 3– x N/NG) core–shell nanostructures with a controllable molar ratio of Ni/Co are successfully fabricated and employed as highly sensitive and selective electrodes for glucose and H 2 O 2 sensing applications. The highly sensitive and selective properties of the optimized core–shell NiCo 2 N/NG electrode are because of the high synergistic effect of the NiCo 2 N core and the NG shell, as evidenced by a superior glucose sensing performance with a short response time of <3 s, a wide linear range from 2.008 μM to 7.15 mM, an excellent sensitivity of 1803 μA mM –1 cm –2, and a low detection limit of 50 nM (S/N = 3). Furthermore, the core–shell NiCo 2 N/NG electrode shows excellent H 2 O 2 sensing performances with a short response time of ∼3 s, a wide detection range of 200 nM to 3.4985 mM, a high sensitivity of 2848.73 μA mM –1 cm –2, and ultra-low limit detection of 200 nM (S/N = 3). The NiCo 2 N/NG sensor can also be employed for glucose and H 2 O 2 detection in human blood serum, promising its application toward the determination of glucose and H 2 O 2 in real samples.
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Deepalakshmi et al. (2018) studied this question.
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