Porous cubic ZnSO3@graphene negative electrode material used for sodium ion battery and preparation method for porous cubic ZnSO3@graphene negative electrode material
A sodium-ion battery and graphene-coated technology, which is applied to battery electrodes, secondary batteries, circuits, etc., can solve the problems of unstable material structure, volume change, and poor cycle performance, and achieve improved electrochemical performance and long-term cycle performance. The effect of long life and low cost
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Embodiment 1
[0032] Dissolve 20mmol of zinc sulfate heptahydrate in 100ml of deionized water to form solution A, dissolve 20mmol of tin tetrachloride pentahydrate in 200ml of deionized water to form solution B, mix the two solutions, and stir magnetically at 30°C for 8h , carry out centrifugal drying, and calcinate the dried product in the air atmosphere for 2h, the calcination temperature is 600°C, and the heating rate is 5°C / min, and the porous cubic ZnSnO 3 .
[0033] 0.4gZnSnO 3 Ultrasonic dispersion in 200ml of ethanol, adding 4ml of 3-aminopropyl triethoxy silicon, magnetically stirred at 30°C for 12h, then added 50ml of pre-dispersed graphene oxide aqueous solution (2mg / ml) and continued to stir for 6h, centrifuged after stirring Drying, heat treatment in Ar atmosphere for 2h, the heat treatment temperature is 600°C, and the heating rate is 5°C / min, to obtain ZnSnO 3 rGO composite with a carbon content of 17 wt%.
[0034] Mix the material obtained in Example 1, conductive carbon ...
Embodiment 2
[0040] Dissolve 10mmol of zinc sulfate heptahydrate in 100ml of deionized water to form solution A, dissolve 10mmol of sodium stannate trihydrate in 100ml of deionized water to form solution B, mix the two solutions, and stir magnetically at 30°C for 12h, Centrifugal drying was carried out, and the dried product was calcined for 2 hours in an air atmosphere at a calcination temperature of 550°C and a heating rate of 5°C / min to obtain porous cubic ZnSnO 3 .
[0041] 0.4gZnSnO 3 Ultrasonic dispersion in 200ml of deionized water, adding 1.2g of cetyltrimethylammonium bromide, stirring magnetically at 30°C for 12h, then adding 60ml of pre-dispersed graphene oxide aqueous solution (2mg / ml) and continuing to stir for 6h, stirring After the end, centrifugal drying was carried out, and heat treatment was carried out under Ar atmosphere for 2h, the heat treatment temperature was 600°C, and the heating rate was 5°C / min to obtain ZnSnO 3 rGO composite with a carbon content of 25 wt%. ...
Embodiment 3
[0043] Dissolve 20mmol of zinc sulfate heptahydrate in 100ml of deionized water to form solution A, dissolve 20mmol of sodium stannate trihydrate in 100ml of deionized water + 100ml of absolute alcohol to form solution B, mix the two solutions, and heat at 50°C Stir magnetically at high temperature for 6 hours, and perform centrifugal drying. The dried product is calcined in air atmosphere for 2 hours. The calcining temperature is 550°C, and the heating rate is 5°C / min, to obtain porous cubic ZnSnO 3 .
[0044] 0.5gZnSnO 3 Ultrasonic disperse in 200ml of dimethylformamide, add 5ml of 3-aminopropyltrimethoxysilane, stir magnetically at 30°C for 12h, add 60ml of pre-dispersed graphene oxide aqueous solution (3mg / ml) and continue stirring for 6h, stir After the end, centrifugal drying was carried out, and heat treatment was carried out under Ar atmosphere for 4h, the heat treatment temperature was 600°C, and the heating rate was 2°C / min to obtain ZnSnO 3 rGO composite with a ca...
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