Cathode material LiMn1-xFexPO4 for lithium ion cell and preparation method of cathode material LiMn1-xFexPO4
A lithium iron manganese phosphate and lithium ion battery technology, applied in battery electrodes, chemical instruments and methods, circuits, etc., can solve problems such as poor cyclability, capacity fading, core-shell structure interface separation, etc., and achieve excellent rate performance and cycle performance. Good, high energy density effect
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Embodiment 1
[0025] (1) Preparation of reaction solution
[0026] Preparation of 0.5 mol / L manganese-rich solution A: Dissolve manganese oxalate and ferrous oxalate in deionized water at a molar ratio of 5:1;
[0027] Prepare 0.5 mol / L manganese-poor solution B: dissolve manganese oxalate and ferrous oxalate in deionized water at a molar ratio of 0.05:1;
[0028] Prepare 0.5 mol / L phosphorus source solution C: dissolve ammonium dihydrogen phosphate in deionized water;
[0029] (2) Add the manganese-poor solution B in step (1) to the manganese-rich solution A at a rate of 1 L / h. After mixing evenly, add the mixed solution to the phosphorus source solution C, and control the concentration of metal ions in the mixed solution. The molar ratio of phosphorus source is 1:1, under the protection of nitrogen, stir, heat at 50 ℃ for 20 h, wash and dry, and obtain the precursor of ferromanganese phosphate with gradient structure, and the precursor is from the inside to the outside along the particle...
Embodiment 2
[0033] (1) Preparation of reaction solution
[0034] Prepare 5 mol / L manganese-rich solution A: dissolve manganese chloride and ferrous chloride in deionized water at a molar ratio of 9:1;
[0035] Prepare 5 mol / L manganese-poor solution B: dissolve manganese chloride and ferrous chloride in deionized water at a molar ratio of 1:1;
[0036] Prepare 5 mol / L phosphorus source solution C: dissolve ammonium dihydrogen phosphate in deionized water;
[0037] (2) Add the manganese-poor solution B in step (1) to the manganese-rich solution A at a rate of 3 L / h. After mixing evenly, add the mixed solution to the phosphorus source solution C to control the concentration of metal ions in the mixed solution. The molar ratio to the phosphorus source is 1:1, stirred under the protection of nitrogen, heated at 100 °C for 5 h, washed and dried, and the precursor of ferromanganese phosphate with gradient structure is obtained. The precursor is from the inside to the inside along the particle ...
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