A kind of doped manganese silicate lithium/carbon composite material and its preparation method
A technology of carbon composite materials and lithium manganese silicate, which is applied in the direction of structural parts, electrical components, battery electrodes, etc., can solve the problems of poor cycle stability, low energy density and poor conductivity of olivine-type lithium iron phosphate, and achieve electrochemical Excellent performance, improved electrochemical cycle stability, and favorable conductivity
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Embodiment 1
[0016] Step 1: Dissolve 1.6 g of poloxamer F127 in 10 mL of absolute ethanol at 30° C. for use. Dissolve 0.01mol of tetraethyl silicate and 0.5mL of 0.2mol / L dilute hydrochloric acid solution in 1mL of water, stir for hydrolysis reaction until the solution is no longer separated, tetraethyl silicate is completely dissolved, the reaction time is about 30min, and then Add 0.01mol of manganese nitrate, 0.02mol of lithium nitrate and 0.03g of boric acid in molar ratio, stir for a period of time until the system is clarified, then add 2.5g of 20wt% phenolic resin aqueous solution to it, and form the sol with the poloxa prepared before Mix F127 ethanol sol, stir at 30°C for 1h to obtain a stable sol system, put the above sol system at 30°C for 12h to obtain a precursor gel, then treat the gel at 150°C for 24h in an air atmosphere, and grind to obtain Precursor powder;
[0017] Step 2: Heat the precursor powder prepared in Step 1 under the protection of argon atmosphere. The heat tr...
Embodiment 2
[0021] Step 1: Dissolve 1 g of poloxamer F127 in 10 mL of water at 30°C for use. Dissolve 0.01mol tetraethyl silicate and 1mL 0.2mol / L dilute nitric acid solution in 1mL water, adjust the pH of the system to stir and carry out the hydrolysis reaction until the solution no longer separates, tetraethyl silicate is completely dissolved, and the reaction time is about For 50min, then add 0.01mol manganese nitrate, 0.02mol lithium nitrate and 0.06g boric acid in molar ratio, stir for a period of time until the system is clear, then add 2.5g 20wt% phenolic resin aqueous solution to it, and the sol that forms is mixed with the previously prepared Poloxamer F127 water sol was mixed, stirred at 30°C for 1 hour to obtain a stable sol system, and the above sol system was left to stand at 30°C for 12 hours to obtain a precursor gel, and then the gel was treated at 150°C for 24 hours in an air atmosphere. Grinding to obtain precursor powder;
[0022] Step 2: Heat the precursor powder prep...
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