Method for preparing lithium iron phosphate as a positive electrode active material for a lithium ion secondary battery
A cathode active material, lithium iron phosphate technology, applied in secondary batteries, battery electrodes, chemical instruments and methods, etc., can solve the problem of low initial discharge specific capacity, high current discharge performance and cycle performance, lithium iron phosphate Large crystal grain size and other problems, to achieve high initial discharge specific capacity, high current discharge performance and cycle performance improvement, and high current discharge performance and cycle performance.
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Embodiment 1
[0028] This example illustrates the preparation method of the positive electrode active material lithium iron phosphate provided by the present invention.
[0029] 43.3 g LiOH·H 2 O (Shanghai Zhongli Industrial Co., Ltd., special grade for batteries, LiOH·H 2 O content is 97.01% by weight), 80.4 grams median particle diameter D 50 0.37 microns, D 95 2.50 µm Fe 2 o 3 (ELEMENTIS, Fe 2 o 3 The content is 99.3%), 115.0 grams of H 3 PO 4 (Guangdong Guanghua Chemical Factory Co., Ltd., analytically pure, H 3 PO 4 content is 85.2%), 38.2 grams of sucrose (Guangdong Guanghua Chemical Factory Co., Ltd., analytically pure) and 200 milliliters of deionized water are placed in the reactor, stirred at a rate of 200 rpm for 1.5 hours, then dried at 120 ° C After 8 hours, the precursor was obtained. The precursor is heated up to 690°C at a rate of 5°C / min, sintered at a constant temperature of 690°C in a nitrogen atmosphere for 8 hours, and naturally cooled to room temperature to ...
Embodiment 2-6
[0032] Prepare the positive electrode active material lithium ferrous phosphate according to the method of Example 1, the difference is the type and amount of lithium source, the amount and particle size of ferric oxide, the amount of phosphoric acid, the type and amount of carbon source, solvent The type and dosage, drying temperature and drying time, and sintering temperature and sintering time are shown in Table 1.
[0033] Table 1
[0034] Example
Embodiment 7
[0036] 43.3 g LiOH·H 2 O (Shanghai Zhongli Industrial Co., Ltd., special grade for batteries, LiOH·H 2 O content is 97.01% by weight), 80.4 grams median particle diameter D 50 0.37 microns, D 95 2.50 µm Fe 2 o 3 (ELEMENTIS, Fe 2 o 3 The content is 99.3%), 115.0 grams of H 3 PO 4 (Guangdong Guanghua Chemical Factory Co., Ltd., analytically pure, H 3 PO 4 Content is 85.2%), 38.2 grams of sucrose (Guangdong Guanghua Chemical Factory Co., Ltd., analytically pure), 2.45 grams (0.01 mole) Ni(NO 3 ) 3 , 1.89 g (0.01 mol) Zn(NO 3 ) 2 and 200 ml of deionized water were placed in a reactor, stirred at a rate of 200 rpm for 1.5 hours, and then dried at 120° C. for 8 hours to obtain a precursor. The precursor was heated up to 500°C at a rate of 2°C / min in a nitrogen atmosphere, and sintered at 500°C for 4 hours. Then continue to heat up to 700°C at a rate of 2°C / min, and sinter at 700°C for 10 hours. The sintered product is naturally cooled to room temperature, and the posi...
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