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Rationally designed NiMn LDH@NiCo <sub>2</sub> O <sub>4</sub> core–shell structures for high energy density supercapacitor and enzyme-free glucose sensor
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Citations
65
References
2021
Year
Exploring high-efficiency and low-cost bifunctional electrodes for supercapacitors and sensors is significant but challenging. Most of the existing electrodes are mostly single-functional materials with simple structure. Herein, NiCo<sub>2</sub>O<sub>4</sub>nanowires as the core and NiMn layered double hydroxide (LDH) as the shell is directly grown<i>in situ</i>on carbon cloth (CC) to form a heterostructure (NiMn LDH@NiCo<sub>2</sub>O<sub>4</sub>/CC). The performance in supercapacitors and enzyme-free glucose sensing has been systematically studied. Compared with a single NiCo<sub>2</sub>O<sub>4</sub>nanowire or NiMn LDH nanosheet, the heterogeneous interface produced by the unique core-shell structure has stronger electronic interaction and abundant active surface area, which shows excellent electrochemical performance. Electrochemical tests demonstrate that the NiMn LDH@NiCo<sub>2</sub>O<sub>4</sub>/CC core-shell electrode possesses an area specific capacitance of 2.40 F cm<sup>-2</sup>and a rate capability of 76.22% at 20 mA cm<sup>-2</sup>. Simultaneously, asymmetric supercapacitor is assembled with it as the positive electrode and NiFe LDH@NiCo<sub>2</sub>O<sub>4</sub>/CC as the negative electrode. The supercapacitor possesses an energy density of 47.74 Wh kg<sup>-1</sup>when the power density is 175 W kg<sup>-1</sup>, revealing excellent performance and maintains cycle stability of 93.48% after 6000 cycles at 10 mA cm<sup>-2</sup>. Additionally, the electrode applied as enzyme-free glucose sensor electrode also displays outstanding sensitivity of 2139<i>μ</i>A mM<sup>-1</sup>cm<sup>-2</sup>, wide detection range (2<i>μ</i>M<sup>-3</sup>mM and 4-8 mM) and low detection limit of 210 nM, representing good anti-interference performance. This work reveals the multi-metal synergy and rationally designed core-shell structure is critical to the electrochemical performance of bifunctional electrodes.
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