Preparation method of super capacitor electrode material (nickel oxide)
A technology for supercapacitors and electrode materials, applied in nickel oxide/nickel hydroxide and other directions, can solve the problems of high cost and complicated preparation process, and achieve the effects of low cost, simple preparation method and good electrochemical stability.
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Embodiment 1
[0025] (1) Weigh the raw material nickel nitrate hexahydrate (Ni(NO 3 ) 2 ·6H 2 O) 3.4mmol and 0.5g of polyvinylpyrrolidone (PVP) were dissolved in methanol and water, and stirred to prepare a mixed solution; wherein, the volumes of methanol and water were 43ml and 5ml respectively;
[0026] (2) Pour the above mixed solution into a polytetrafluoroethylene hydrothermal reaction kettle to maintain a filling degree of 80%, put the hydrothermal reaction kettle into a blast drying oven, react at 180°C for 6 hours, and then cool Reactor to room temperature.
[0027] (3) The product obtained by centrifugation was washed with deionized water and ethanol solvent respectively, and dried; the dried sample was placed in a muffle furnace and calcined at 450°C for 40 minutes; the final black sample obtained was supercapacitor oxidation Nickel electrode material.
Embodiment 2
[0029] (1) Weigh the raw material nickel nitrate hexahydrate (Ni(NO 3 ) 2 ·6H 2 (0) 2mmol and 0.05g of polyvinylpyrrolidone (PVP) were dissolved in methanol and water, and stirred to prepare a mixed solution; wherein, the volumes of methanol and water were 41ml and 7ml respectively;
[0030] (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, react at 150°C for 24 hours, and then cool Reactor to room temperature.
[0031] (3) The product obtained by centrifugation was washed with deionized water and ethanol solvent respectively, and dried; the dried sample was placed in a muffle furnace and calcined at 450°C for 40 minutes; the final black sample obtained was supercapacitor oxidation Nickel electrode material.
Embodiment 3
[0033] (1) Weigh the raw material nickel nitrate hexahydrate (Ni(NO 3 ) 2 ·6H 2 (0) 4mmol and 1g of polyvinylpyrrolidone (PVP) were dissolved in methanol and water, and stirred to prepare a mixed solution; wherein, the volumes of methanol and water were 40ml and 8ml respectively;
[0034] (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, react at 180°C for 3 hours, and then cool Reactor to room temperature.
[0035] (3) The product obtained by centrifugation was washed with deionized water and ethanol solvent respectively, and dried; the dried sample was placed in a muffle furnace and calcined at 450°C for 40 minutes; the final black sample obtained was supercapacitor oxidation Nickel electrode material.
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