Preparation method of bismuth 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
[0026] Li2CO3 (99.73%), Bi2O3 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials, according to the ratio of 1mol Li:0.00002mol Bi:0.0003molBa:1mol Fe:1mol P After mixing, in anhydrous ethanol (AR) medium, high-speed ball milling for 20h (rotational speed 200r / min). After drying at 105-120°C, the precursor is obtained. The precursor obtained by drying is placed in a high-temperature furnace and calcined at 500-750°C at high temperature for 24h in an ordinary pure nitrogen (>99.5%) atmosphere. That is, the bismuth and barium activated lithium iron phosphate cathode material of the present invention is obtained.
Embodiment 2
[0027] Example 2 (no mixed control)
[0028] The Li2CO3 (99.73%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials were mixed according to the ratio of 1molLi:1mol Fe:1mol P, and then in anhydrous ethanol (AR) medium, high-speed ball milling for 20h (rotating speed 200r) / min. After drying at 105-120°C, the precursor is obtained, and the precursor obtained by drying is placed in a high-temperature furnace, and calcined at 500-750°C at high temperature for 24h in an ordinary pure nitrogen (>99.5%) atmosphere. The lithium ion cathode material is obtained.
[0029] Using prior art testing equipment and prior art testing methods, the test results of the bismuth and barium activated lithium iron phosphate cathode material of Example 1 and the non-incorporated Comparative Example 2 are:
[0030] The bismuth and barium activated lithium iron phosphate cathode material of Example 1 of the present invention has an initial discharge capacity of more than 155.52 mAh / g; the first discharge ca...
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