Preparation method of nano-network conductive polymer coated lithium iron phosphate anode material
A conductive polymer, lithium iron phosphate technology, applied in battery electrodes, circuits, electrical components, etc., to achieve the effect of improving conductivity, improving rate performance, and restricting generation
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Embodiment 1
[0018] 1. Add 3.64g of cetyltrimethylammonium bromide into 100ml of 0.1mol / L sulfuric acid solution and stir until completely dissolved. Then 7.29g of lithium iron phosphate powder was dispersed in the solution, and ultrasonically stirred for 30 minutes to fully mix the lithium iron phosphate and cetyltrimethylammonium bromide. Add 1.8ml of aniline monomer under the condition of ultrasonic stirring, and continue ultrasonic stirring for 60min to obtain the mixed solution A;
[0019] 2. Cool the mixed solution A to -5°C, dissolve 6.49g of ferric chloride in 100ml of 0.1mol / L sulfuric acid to form a solution B, add B dropwise to the mixed solution A under the condition of nitrogen protection, at -5 The reaction was stirred at ℃ for 5 hours, the product was alternately washed with deionized water and ethanol until the filtrate was colorless, and dried in vacuum at 40℃ for 20 hours to obtain the nano-network polyaniline-coated lithium iron phosphate cathode material.
Embodiment 2
[0021] 1. Add 7.29g of cetyltrimethylammonium bromide to 100ml of 0.2mol / L hydrochloric acid solution and stir until completely dissolved. Then 7.29g of lithium iron phosphate powder was dispersed in the solution, and ultrasonically stirred for 60 minutes to fully mix the lithium iron phosphate and cetyltrimethylammonium bromide. Add 0.69ml of pyrrole monomer under the condition of ultrasonic stirring, and continue ultrasonic stirring for 30min to obtain the mixed solution A;
[0022] 2. Cool the mixed solution A to -2°C, dissolve 4.74g of potassium permanganate in 100ml of 0.2mol / L hydrochloric acid to form a solution B, add B dropwise to the mixed solution A under the protection of argon, and The reaction was stirred at -2°C for 15 hours, the product was alternately washed with deionized water and ethanol until the filtrate was colorless, and dried in vacuum at 60°C for 24 hours to obtain the nano-network polypyrrole-coated lithium iron phosphate cathode material.
Embodiment 3
[0024] 1. Add 6.4g of cetyltrimethylammonium chloride into 100ml of 0.2mol / L hydrochloric acid solution and stir until completely dissolved. Then 3.2 g of lithium iron phosphate powder was dispersed in the solution, and ultrasonically stirred for 60 minutes to fully mix the lithium iron phosphate and cetyltrimethylammonium chloride. Add 1.38ml of pyrrole monomer under the condition of ultrasonic stirring, and continue ultrasonic stirring for 60min to obtain the mixed solution A;
[0025] 2. Cool the mixed solution A to 0°C, dissolve 4.56g of ammonium persulfate in 100ml of 0.2mol / L hydrochloric acid to form a solution B, add B dropwise to the mixed solution A under nitrogen protection, and stir at 0°C After reacting for 24 hours, the product was alternately washed with deionized water and ethanol until the filtrate was colorless, and dried in vacuum at 60°C for 48 hours to obtain the nano-network polypyrrole-coated lithium iron phosphate cathode material.
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