Method for preparing antimony and barium activated lithium iron phosphate cathode material
A technology of lithium iron phosphate and positive electrode materials, which is applied in the direction of battery electrodes, electrical components, circuits, etc., can solve the problems of poor conductivity and low tap density, and achieve improved electrical conductivity, electronic conductivity, and high-rate charge and discharge performance effect
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Embodiment 1
[0025] Li2CO3 (99.73%), Sb2O3 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials, according to 1mol Li: 0.00002mol Sb: 0.0003mol Ba: 1mol Fe: 1mol P After proportional mixing, high-speed ball milling in absolute ethanol (AR) medium for 20h (rotation speed 200r / min. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. In a pure nitrogen (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the antimony and barium activated lithium iron phosphate cathode material of the present invention.
Embodiment 2
[0027] Li2CO3 (99.73%), Sb2O3 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, according to 1mol Li: 0.00004mol Sb: 0.001mol Ba: 1mol Fe: 1mol P After proportional mixing, high-speed ball milling in absolute ethanol (AR) medium for 20h (rotation speed 200r / min. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. In a pure nitrogen (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the antimony and barium activated lithium iron phosphate cathode material of the present invention.
Embodiment 3
[0029] Li2CO3 (99.73%), Sb2O3 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, according to 1mol Li: 0.00005mol Sb: 0.003mol Ba: 1mol Fe: 1mol P After proportional mixing, high-speed ball milling in absolute ethanol (AR) medium for 20h (rotation speed 200r / min. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. In a pure nitrogen (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the antimony and barium activated lithium iron phosphate cathode material of the present invention.
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