Nano flower spherical carbon-sulfur composite lithium-sulfur battery positive electrode material supported by nickel foam and preparation method thereof
A technology of carbon-sulfur composite and positive electrode materials, applied in battery electrodes, lithium batteries, non-aqueous electrolyte batteries, etc., can solve the problems of surface morphology and microscopic characteristics of sulfur positive electrodes, weakened contact between materials and substrates, and shortened cycle life. Achieve good electron transmission channel, slow down capacity attenuation, increase the effect of contact area
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Embodiment 1
[0036] Weigh 0.6g of zinc nitrate hexahydrate, 0.6g of urea and 0.15g of ammonium fluoride, dissolve them in 80ml of deionized water, stir until completely dissolved to a transparent state, and prepare a homogeneous solution. Put the homogeneous solution formed above into a polytetrafluoroethylene high-pressure hydrothermal tank, and put a foamed nickel substrate in advance. The hydrothermal tank was sealed in a high-pressure reactor, and the hydrothermal reaction was carried out in an oven at 90° C. for 6 hours. After the reaction is complete, cool to room temperature 25° C., wash with deionized water three times, and place in an oven to dry. Afterwards, it was calcined at 500° C. for 1 hour in argon, and cooled naturally to room temperature 25° C. to prepare zinc oxide nanosheets supported by nickel foam.
[0037] Put 80ml of glucose aqueous solution with a molar concentration of 0.1mol / L into a polytetrafluoroethylene high-pressure hydrothermal tank, and put zinc oxide nan...
Embodiment 2
[0040] Weigh 1.2g of zinc nitrate hexahydrate, 1.2g of urea and 0.3g of ammonium fluoride, dissolve them in 80ml of deionized water, stir until completely dissolved to a transparent state, and prepare a homogeneous solution. Put the homogeneous solution formed above into a polytetrafluoroethylene high-pressure hydrothermal tank, and put a foamed nickel substrate in advance. The hydrothermal tank was sealed in a high-pressure reactor, and the hydrothermal reaction was carried out in an oven at 130° C. for 7.5 hours. After the reaction is complete, cool to room temperature, wash with deionized water three times, and place in an oven to dry. Afterwards, it was calcined at 650° C. for 2 hours in argon, and cooled naturally to room temperature 25° C. to prepare zinc oxide nanosheets supported by nickel foam.
[0041] Put 80ml of glucose aqueous solution with a molar concentration of 1mol / L into a polytetrafluoroethylene high-pressure hydrothermal tank, and put zinc oxide nanosheet...
Embodiment 3
[0044] Weigh 1.8 g of zinc nitrate hexahydrate, 1.8 g of urea and 0.45 g of ammonium fluoride and dissolve them in 80 ml of deionized water, stir until completely dissolved to a transparent state, and prepare a homogeneous solution. Put the homogeneous solution formed above into a polytetrafluoroethylene high-pressure hydrothermal tank, and put a foamed nickel substrate in advance. The hydrothermal tank was sealed in a high-pressure reactor, and the hydrothermal reaction was carried out in an oven at 150° C. for 9 hours. After the reaction is complete, cool to room temperature, wash with deionized water three times, and place in an oven to dry. Afterwards, it was calcined in argon at 800° C. for 3 hours, and cooled naturally to room temperature of 25° C. to prepare zinc oxide nanosheets supported by nickel foam.
[0045] Put 80ml of glucose aqueous solution with a molar concentration of 2mol / L into a polytetrafluoroethylene high-pressure hydrothermal tank, and put zinc oxide ...
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