Lithium iron phosphate/carbon composite electrode material and preparation method thereof
A lithium iron phosphate, composite electrode technology, applied in electrode manufacturing, battery electrodes, circuits, etc., can solve the problems of difficult particle size control, large particle size, long time consumption, etc. good coverage effect
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Embodiment 1
[0021] Example 1 Preparation of lithium iron phosphate / C composite electrode material of the present invention
[0022] Add 10.7692g (0.2mol) lithium hydroxide to the three-necked flask, and neutralize it by titration with 18.4615g (0.2mol) of acrylic acid dissolved in 70.7692g of water. The titration process should be slow and constantly stirred. Polymerize under the action of initiator ammonium persulfate and chain transfer agent isopropanol. After the polymerization is completed, move the polymerization product into a ball mill tank, add iron phosphate according to the stoichiometric ratio and mix it. The mixture is ball milled for 6 hours and then dried. The resulting mixture was ball milled for another 6 hours. Weigh the ball-milled product and place it in a temperature-controlled reaction furnace replaced by non-oxidizing gas for calcination. The calcination condition is to raise the temperature from 20°C to 500°C, the heating rate is 10°C / min, keep the temperature at 50...
Embodiment 2
[0025] Embodiment 2 Preparation of lithium iron phosphate / C composite electrode material of the present invention
[0026] Other conditions were the same as in Example 1, except that the polyacrylic acid needed for the lithium carboxylate polymer was replaced by a poly(acrylic acid acrylonitrile) copolymer, wherein the ratio of acrylic acid:acrylonitrile was 8:2.
[0027] The electrical performance test method is the same as that of Example 1.
[0028] The Lithium Ferrous Phosphate / C material prepared by the method and proportioning in Example 2 is a black powder with uniform particle size. The discharge capacity is 116mAh / g at 0.2C, and 99mAh / g at 1C. The carbon content is 5.22%. .
Embodiment 3
[0029] Example 3 Preparation of lithium iron phosphate / C composite electrode material of the present invention
[0030] Add 10.7692g (0.2mol) lithium hydroxide to the three-necked flask, and neutralize it by titration with 18.4615g (0.2mol) of acrylic acid dissolved in 70.7692g of water. The titration process should be slow and constantly stirred. Polymerize under the action of initiator ammonium persulfate and chain transfer agent isopropanol. After the polymerization is completed, move the polymerized product into a ball mill tank, add iron phosphate according to the stoichiometric ratio and mix it. The mixture is ball milled for 6 hours and then dried. Weigh the ball-milled product and place it in a temperature-controlled reaction furnace replaced by non-oxidizing gas for calcination. The calcination condition is to raise the temperature from 20°C to 450°C at a heating rate of 10°C / min, keep it at 450°C for 2 hours, and then continue to heat up To 700°C, the heating rate is...
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