Magnesium aluminum pentafluoride/nitrogen-doped carbon lithium-sulfur battery positive electrode material and preparation method thereof
A pentafluoro-magnesium-aluminum, positive electrode material technology, applied in battery electrodes, lithium storage batteries, positive electrodes and other directions, can solve the problems of poor conductivity of sulfur and lithium-sulfur products, cumbersome process, low utilization rate, etc., to improve cycle stability, The preparation process is simple and the effect of providing sulfur-carrying space
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Embodiment 1
[0048] (1) Treatment of attapulgite
[0049] The natural attapulgite was screened with a 200-mesh sieve, and then 6 g of attapulgite was put into 200 mL of hydrochloric acid with a concentration of 4 mol / L, and heated and stirred at 90 ° C for 2 h. Then carry out suction filtration, the product obtained after suction filtration is washed to neutrality, and then the obtained sample is placed in a vacuum drying oven to dry for 12 hours.
[0050] (2) Attapulgite-coated nitrogen-doped carbon
[0051] Weigh the above-mentioned 2g of modified attapulgite, 1.5g of glucose and 0.9g of ammonium chloride into a 100mL beaker, add 40mL of deionized water and continue stirring for 24h, and then put it in a water bath at 80°C until the water is evaporated to obtain the precursor. The above precursor was calcined in a tube furnace under an argon atmosphere at a heating rate of 4°C / min, and calcined at 600°C for 3h to obtain a nitrogen-doped carbon-coated attapulgite composite.
[0052] (3)...
Embodiment 2
[0059] (1) Treatment of attapulgite
[0060] The natural attapulgite was screened with a 200-mesh sieve, and then 6 g of attapulgite was put into 200 mL of hydrochloric acid with a concentration of 6 mol / L, and heated and stirred at 70 ° C for 4 h. Then carry out suction filtration, the product obtained after suction filtration is washed to neutrality, and then the obtained sample is placed in a vacuum drying oven to dry for 12 hours.
[0061] (2) Attapulgite-coated nitrogen-doped carbon
[0062] Weigh the above 2g of modified attapulgite, 1.5g of glucose and 1.35g of ammonium chloride into a 100mL beaker, add 40mL of deionized water and continue to stir for 24h, and then put it in a water bath at 80°C until the water is evaporated to obtain the precursor. The above precursor was calcined in a tube furnace under an argon atmosphere at a heating rate of 6°C / min, and calcined at 900°C for 7h to obtain a nitrogen-doped carbon-coated attapulgite composite.
[0063] (3) HF treatm...
Embodiment 3
[0072] (1) Treatment of attapulgite
[0073] The natural attapulgite was screened with a 200-mesh sieve, and then 6 g of attapulgite was put into 200 mL of hydrochloric acid with a concentration of 6 mol / L, and heated and stirred at 80 ° C for 3 h. Then carry out suction filtration, the product obtained after suction filtration is washed to neutrality, and then the obtained sample is placed in a vacuum drying oven to dry for 12 hours.
[0074] (2) Attapulgite-coated nitrogen-doped carbon
[0075] Weigh the above-mentioned 2g of modified attapulgite, 2g of glucose and 1.2g of ammonium chloride into a 100mL beaker, add 40mL of deionized water and keep stirring for 24h, and then put it in a water bath at 80°C until the water is evaporated to obtain the precursor. The above precursor was calcined in a tube furnace under an argon atmosphere at a heating rate of 5°C / min, and calcined at 800°C for 5h to obtain a nitrogen-doped carbon-coated attapulgite composite.
[0076] (3) HF tr...
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