Preparation method of manganese and barium activated lithium iron phosphate as cathode material
A technology of lithium iron phosphate, cathode material, applied in chemical instruments and methods, phosphorus compounds, inorganic chemistry, etc.
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Embodiment 1
[0027] Li2CO3 (99.73%), MnO2 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, according to 1mol Li: 0.00002molMn: 0.0003mol Ba: 1mol Fe: 1mol P ratio After mixing, in absolute ethanol (AR) medium, high-speed ball milling (200r / min) for 20h. After drying at 105-120°C, the precursor is obtained, and the dried precursor is placed in a high-temperature furnace, and calcined at 500-750°C for 24 hours in an ordinary pure nitrogen (>99.5%) atmosphere. That is, the manganese and barium activated lithium iron phosphate cathode material of the present invention is obtained.
Embodiment 2
[0028] Embodiment 2 (no mixed contrast)
[0029] With Li2CO3 (99.73%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, after mixing according to the ratio of 1mol Li: 1mol Fe: 1mol P, in absolute ethanol (AR) medium, high-speed ball milling 20h (rotating speed 200r / mimn. After drying at 105-120°C, the precursor is obtained, and the dried precursor is placed in a high-temperature furnace, and calcined at 500-750°C for 24 hours in an ordinary pure nitrogen (>99.5%) atmosphere The obtained lithium ion cathode material.
[0030] Using the testing equipment of the prior art and the testing method of the prior art, the manganese, barium activated lithium iron phosphate positive electrode material of the above embodiment 1, and the non-doped comparison example 2 are tested and the results are as follows:
[0031] The manganese and barium activated lithium iron phosphate positive electrode material in Example 1 of the present invention has an initial discharge capacity of more tha...
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