A lithium-sulfur pole piece with a functional protective layer and its preparation method and application
A protective layer, lithium-sulfur technology, applied in battery electrodes, lithium batteries, non-aqueous electrolyte battery electrodes, etc., can solve the problems of increasing electrolyte viscosity, low conductivity, destroying electrode structure, etc., and achieve the effect of improving capacity retention.
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Embodiment 1
[0037] 0.45g of perfluorosulfonic acid resin grafted with polytetrafluoroethylene and 0.05g of sodium hydroxymethylcellulose (CMC), styrene-butadiene and rubber (SBR) (2:3, w:w) mixed binder Add 20 g of a mixed solution of deionized water and ethanol (1:1, v:v) and stir it magnetically for 5 h. With elemental sulfur as the active material, the mass ratio of elemental sulfur: acetylene black: polyvinylidene fluoride is 7:2:1, and the aluminum foil is used as the current collector. No active material area, used for subsequent experiments. Evenly scrape-coat the coating slurry prepared above on the surface of the pole piece, control the thickness of the coating layer to 1 μm, wait for most of the solvent to volatilize, put it in a vacuum oven at 60°C to dry overnight to remove the solvent, and obtain elemental sulfur with a functional protective layer Pole piece (scanning electron microscope photo of elemental sulfur as figure 1 As shown, the scanning electron micrograph of the...
Embodiment 2
[0039]Put 0.9 g of graphene oxide and 0.1 g of polyethylene oxide (PEO) binder into 50 g of a mixed solution of deionized water and ethanol (1:1, v:v) and stir magnetically for 10 h. Copper sulfide is used as the active material, and the mass ratio of copper sulfide: acetylene black: polyvinylidene fluoride is 6:3:1, and the copper foil is used as the current collector. Active material area, used for subsequent experiments. Evenly scrape and coat the coating slurry prepared above on the surface of the pole piece, control the thickness of the coating layer to 3 μm, wait for most of the solvent to volatilize, put it in a vacuum oven and dry it at 60°C overnight to completely remove the solvent, and obtain a graphene oxide protective film. layer of copper sulfide pole piece.
[0040] The cross-sectional view of the copper sulfide pole piece is shown in image 3 As shown, the cross-sectional scanning electron microscope image of the copper sulfide pole piece with the graphene ox...
Embodiment 3
[0042] Put 1.9g of partially fluorinated sulfonic acid resin and 0.1g mixed binder of sodium hydroxymethylcellulose (CMC) and styrene-butadiene rubber (SBR) (2:3, w:w) into deionized water and ethanol (1:1, v:v) 100 g of the mixed solution was magnetically stirred for 20 h. Using polythiopyrrole as the active material, make polythiopyrrole: acetylene black: polyvinylidene fluoride with a mass ratio of 7:2:1, and use aluminum foil as the current collector with an area of 15cm×15cm, and reserve the edge of the electrode A 1.5 mm area of no active material was used for subsequent experiments. Evenly scrape-coat the coating slurry prepared above on the surface of the pole piece, control the thickness of the coating layer to 5 μm, wait for most of the solvent to volatilize, put it in a vacuum oven and dry it overnight at 60°C to completely remove the solvent, and obtain a partially fluorinated sulfonate Polythiopyrrole battery pole piece with acid resin protective layer.
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