Manufacturing method of high-energy long-life lithium-sulfur battery
A technology for a lithium-sulfur battery and a manufacturing method, which is applied in the field of high-capacity sulfur positive electrode and lithium-sulfur battery manufacturing, can solve the problems of not reflecting the superiority of lithium-sulfur batteries, difficult to surpass battery energy density, and disadvantageous battery high rate performance, etc. The electrode structure has good stability, which is beneficial to the balance of electrode reaction and the effect of light weight.
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Embodiment 1
[0032] Example 1: Preparation of highly conductive porous carbon precursor
[0033] Dissolve 1 g of gelatin in 5 mL of deionized water at 90°C to form a gelatin solution, and take another 5 g of sodium chloride, dissolve it in 100 mL of deionized water with stirring at 90°C, and slowly introduce it into the gelatin solution. After stirring evenly, drop it into a Dewar bottle filled with liquid nitrogen through a peristaltic pump for flash freezing to obtain cryogel particles; transfer to a lyophilized vacuum dryer for 24 hours to obtain a precursor; raise the temperature of the precursor under the protection of a nitrogen atmosphere Carbonize at 900°C for 2 hours at a constant temperature to form carbonized products; cool to room temperature, pulverize, wash with deionized water to remove sodium chloride, centrifuge, and dry to obtain highly conductive porous carbon.
Embodiment 2
[0034] Example 2: Precursor carbonization
[0035] Dissolve 1 g of gelatin in 10 mL of deionized water at 90°C to form a gelatin solution, and take another 20 g of sodium chloride, dissolve it in 100 mL of deionized water with stirring at 90°C, and slowly introduce it into the gelatin solution. After stirring evenly, drop it into a Dewar bottle filled with liquid nitrogen through a peristaltic pump for flash freezing to obtain cryogel particles; transfer to a lyophilized vacuum dryer for 24 hours to obtain a precursor; raise the temperature of the precursor under the protection of a nitrogen atmosphere Carbonize at 900°C for 2 hours at a constant temperature to form carbonized products; cool to room temperature, pulverize, wash with deionized water to remove sodium chloride, centrifuge, and dry to obtain highly conductive porous carbon.
Embodiment 3
[0036] Example 3: Preparation of conductive porous carbon
[0037] Dissolve 1 g of gelatin in 20 mL of deionized water at 90°C to form a gelatin solution, and take another 30 g of sodium chloride, dissolve it in 100 mL of deionized water with stirring at 90°C, and slowly introduce it into the gelatin solution. After stirring evenly, drop it into a Dewar bottle filled with liquid nitrogen through a peristaltic pump for flash freezing to obtain cryogel particles; transfer to a lyophilized vacuum dryer for 24 hours to obtain a precursor; raise the temperature of the precursor under the protection of a nitrogen atmosphere Carbonize at 900°C for 2 hours at a constant temperature to form carbonized products; cool to room temperature, pulverize, wash with deionized water to remove sodium chloride, centrifuge, and dry to obtain highly conductive porous carbon.
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