Preparation method of zirconium, barium activated lithium iron phosphate anode material
A technology of lithium iron phosphate and positive electrode materials, applied in chemical instruments and methods, phosphorus compounds, inorganic chemistry, etc.
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Embodiment 1
[0026] With Li2CO3 (99.73%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, after mixing according to the ratio of 1molLi: 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. That is, the lithium ion positive electrode material is obtained.
Embodiment 2
[0027] Using the testing equipment of the prior art and the testing method of the prior art, the zirconium, 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:
[0028] The zirconium and barium activated lithium iron phosphate positive electrode material in Example 1 of the present invention has an initial discharge capacity of more than 155.52mAh / g; the initial discharge capacity of undoped LiFePO4 is only within 116.25mAh / g.
[0029] The barium-activated lithium iron phosphate positive electrode material in Example 1 of the present invention has a charge-discharge platform with a potential of about 3.5V relative to the lithium electrode, an initial discharge capacity of more than 164mAh / g, and a capacity decay of about 3.0% after 100 charge-discharge cycles.
[0030] The barium-activated lithium iron phosphate positive electrode material preparation met...
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