Preparation method of lithium iron phosphate cathode material co-coated with conductive polymer/nano metal particles
A technology of nano metal particles and conductive polymers, applied in battery electrodes, circuits, electrical components, etc., can solve problems such as loss of electrical conductivity, achieve good electronic conductivity, improve weak conductivity, and maintain the effect of cycle performance
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Embodiment 1
[0024] Dissolve 0.11 g of aniline in 20.0 mL of 0.4 mol / L formic acid solution, stir and disperse for 30 min, then weigh 4.08 g of lithium iron phosphate powder, stir and disperse in the above solution and ultrasonically disperse for 2 h. After that, 0.1287 g of silver nitrate was weighed, poured into the mixed solution, and the reaction mixture was ultrasonically dispersed for 10 min to dissolve. Then weigh 0.27g of ammonium persulfate as the oxidant ammonium persulfate according to the 1:1 molar ratio of oxidant and polymer monomer, pour it into a flask, and keep the reaction mixture in an ultrasonic water bath at 0°C for 4h, cool to room temperature, and let it stand for 2h , and then filtered and washed three to five times with corresponding concentrations of acid solution and acetone, and vacuum dried at 80°C for 12 hours to obtain a high-rate lithium iron phosphate cathode material.
[0025] Take the active material polymer-coated lithium iron phosphate powder, acetylene...
Embodiment 2
[0028] Dissolve 0.11 g of aniline in 20.0 mL of 0.4 mol / L formic acid solution, stir and disperse for 30 min, then weigh 4.08 g of lithium iron phosphate powder, stir and disperse in the above solution and ultrasonically disperse for 2 h. Take by weighing 0.1287g nickel nitrate Ni (NO 3 ) 2 ·6H 2 O, poured into the mixed solution, and the reaction mixture was ultrasonically dispersed for 10 min to dissolve. Then weigh 0.27g of ammonium persulfate as the oxidant ammonium persulfate according to the 1:1 molar ratio of oxidant and polymer monomer, pour it into a flask, and keep the reaction mixture in an ultrasonic water bath at 0°C for 4h, cool to room temperature, and let it stand for 2h , and then filtered and washed three to five times with corresponding concentrations of acid solution and acetone, and vacuum dried at 80°C for 12 hours to obtain a high-rate lithium iron phosphate cathode material.
[0029] Take the active material polymer-coated lithium iron phosphate powd...
Embodiment 3
[0032] Dissolve 0.11 g of aniline in 20.0 mL of 0.4 mol / L formic acid solution, stir and disperse for 30 min, then weigh 4.08 g of lithium iron phosphate powder, stir and disperse in the above solution and ultrasonically disperse for 2 h. Take by weighing 0.1287g copper nitrate Cu (NO 3 ) 2 ·3H 2O, poured into the mixed solution, and the reaction mixture was ultrasonically dispersed for 10 min to dissolve. Then weigh 0.27g of ammonium persulfate as the oxidant ammonium persulfate according to the 1:1 molar ratio of oxidant and polymer monomer, pour it into a flask, and keep the reaction mixture in an ultrasonic water bath at 0°C for 4h, cool to room temperature, and let it stand for 2h , and then filtered and washed three to five times with corresponding concentrations of acid solution and acetone, and vacuum dried at 80°C for 12 hours to obtain a high-rate lithium iron phosphate cathode material.
[0033] Take the active material polymer-coated lithium iron phosphate powde...
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