A kind of preparation method of supercapacitor electrode material carbon-coated nickel oxide niO/c
A technology for supercapacitors and electrode materials, which is applied in the manufacture of hybrid capacitor electrodes, hybrid/electric double layer capacitors, etc., can solve problems such as the inability to uniformly coat NiO electrode materials, and solve the difficulty of large-scale application, increase specific capacitance, and improve Effect of rate ratio capacitance
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Embodiment 1
[0024] (1) Weigh the raw material nickel acetate (Ni(CH 3 COO) 2 4H 2 (0) 5mmol, urea (2g) and polyvinylpyrrolidone (PVP) 1g were dissolved in absolute ethanol and water, and stirred to prepare a mixed solution; wherein, the volumes of the absolute ethanol and water were 10ml and 40ml respectively;
[0025] (2) Pour the above mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle, keep the filling degree of 80%, put the hydrothermal reaction kettle into a blast drying oven, and react under hydrothermal conditions of 180°C for 8 hours , and then cooled the reactor to room temperature.
[0026] (3) The obtained product was centrifuged, washed with deionized water and ethanol solvent, and dried; the dried sample was put into a muffle furnace and calcined at 1°C / min to 450°C for 40min.
[0027] (4) Weigh 0.2 g of the NiO sample and dissolve it in 36 ml of glucose solution, and stir to prepare a mixed solution; wherein, the concentration of the glucose soluti...
Embodiment 2
[0031] (1) Weigh the raw material nickel acetate (Ni(CH 3 COO) 2 4H 2 (0) 5mmol, urea (3g) and polyvinylpyrrolidone (PVP) 1g were dissolved in absolute ethanol and water, and stirred to prepare a mixed solution; wherein, the volumes of the absolute ethanol and water were 10ml and 40ml respectively;
[0032] (2) Pour the above mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle, keep the filling degree of 80%, put the hydrothermal reaction kettle into a blast drying oven, and react for 3 hours under the hydrothermal condition of 200°C , and then cooled the reactor to room temperature.
[0033] (3) The obtained product was centrifuged, washed with deionized water and ethanol solvent, and dried; the dried sample was put into a muffle furnace and calcined at 1°C / min to 450°C for 40min.
[0034] (4) Weigh 0.3 g of the NiO sample and dissolve it in 36 ml of glucose solution, and stir to prepare a mixed solution; wherein, the concentration of the glucose sol...
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