Preparation method of manganese and barium activated lithium iron phosphate as cathode material

A technology of lithium iron phosphate and cathode material, applied in chemical instruments and methods, phosphorus compounds, inorganic chemistry, etc., can solve problems such as poor conductivity and low tap density, and achieve improved electrical conductivity, improved electronic conductivity, and improved unit cell Volume reduction effect

Active Publication Date: 2012-05-02
桐乡乐维新材料有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] At present, there is a consensus that lithium iron phosphate has the advantages of good safety, no pollution, stable cycle performance, high specific capacity and low price, but it also has poor conductivity and the disadvantage of lower tap density

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] 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 for 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 manganese and barium activated lithium iron phosphate cathode material of the present invention is obtained.

Embodiment 2

[0027] Li2CO3 (99.73%), MnO2 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, according to 1mol Li: 0.00004mol Mn: 0.001mol Ba: 1mol Fe: 1mol P After proportional mixing, high-speed ball milling (rotating speed 200r / min) in absolute ethanol (AR) medium 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 3

[0029] Li2CO3 (99.73%), MnO2 (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw material, according to 1mol Li: 0.00005mol Mn: 0.003mol Ba: 1mol Fe: 1mol P After proportional mixing, high-speed ball milling (rotating speed 200r / min) in absolute ethanol (AR) medium 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.

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Abstract

The invention discloses a preparation method of manganese and barium activated lithium iron phosphate as a cathode material. The preparation method comprises the steps of: mixing raw materials including a lithium source, a manganese source, a barium source, an iron source and a phosphate source according to the proportion of 1mol:(0.00002-0.00005)mol:(0.0003)mol:1mol:1mol; then, performing high-speed ball milling at the rotation speed of 200r/min for 20h in an absolute ethyl alcohol medium; drying at 105-120 DEG C to obtain a precursor; placing the precursor obtained through drying in a high-temperature furnace; and calcinating for 24h at the high temperature of 500-750 DEG C in a common pure nitrogen atmosphere to obtain the manganese and barium activated lithium iron phosphate as the cathode material. Because a small amount of substitutive manganese and barium are doped, the shape and the particle size of a product are favorably controlled to obtain a stable lithium iron phosphate compound, of which the crystal lattice is activated, the lithium ion diffusion coefficient is increased, and the initial discharge capacity of the obtained cathode material reaches 160.52mAh/g; a charge-discharge platform of the cathode material is about 3.5V relative to a lithium electrode potential, the initial discharge capacity exceeds 168mAh/g, and the capacity is attenuated by about 1.2% after 100 times of charge-discharge cycles; and compared with a control embodiment, namely undoped LiFePO4, the cathode material is greatly improved in specific capacity and cyclic stability.

Description

technical field [0001] The preparation method of the manganese and barium activated lithium iron phosphate cathode material of the invention belongs to a preparation method of the cathode material of a lithium battery, and in particular relates to a preparation method of the cathode material of the lithium iron phosphate battery. Background technique [0002] At present, the research status of lithium iron phosphate doping modification: lithium iron phosphate LiFePO4 is non-toxic, environmentally friendly, high in safety, rich in raw materials, high in specific capacity, stable in cycle performance, and low in price. The stable discharge platform with a theoretical capacity of 3.5V, the lithium iron phosphate material has high energy density, low price, and excellent safety, and is especially suitable for power batteries. But it has a higher resistivity. Due to lithium iron phosphate, the kinetics of LiFePO4 is not good at room temperature, and the rate performance is extre...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/58C01B25/45
CPCY02E60/12Y02E60/10
Inventor 张健张新球吴润秀王晶张雅静李杰李安平李先兰严积芳黄景诚韦谷林
Owner 桐乡乐维新材料有限公司
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