Preparation method of strontium and barium activated lithium iron phosphate positive pole material

A technology of lithium iron phosphate and positive electrode materials, which is applied in battery electrodes, electrical components, circuits, etc., can solve problems such as low tap density and poor conductivity, and achieve the goal of increasing electrical conductivity, increasing electronic conductivity, and reducing unit cell volume Effect

Active Publication Date: 2012-02-15
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

[0024] Li2CO3 (99.73%, SrCO (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials, mixed according to the ratio of 1mol Li: 0.00002mol Sr: 0.0003mol Ba: 1mol Fe: 1molP Finally, in absolute ethanol (AR) medium, high-speed ball milling for 20h (rotation speed 200r / mimn. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the strontium and barium activated lithium iron phosphate cathode material of the present invention.

Embodiment 2

[0026] Li2CO3 (99.73%, SrCO (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials, according to the ratio of 1mol Li: 0.00004mol Sr: 0.001mol Ba: 1mol Fe: 1mol P After mixing, high-speed ball milling in absolute ethanol (AR) medium for 20h (rotation speed 200r / mimn. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. In a nitrogen (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the strontium and barium activated lithium iron phosphate cathode material of the present invention.

Embodiment 3

[0028] Li2CO3 (99.73%, SrCO (99.8%), BaCO3 (99.8%), FeC2O4.2H2O (99.06%), NH4H2PO4 (98%) raw materials, according to the ratio of 1mol Li: 0.00005mol Sr: 0.003mol Ba: 1mol Fe: 1mol P After mixing, high-speed ball milling in absolute ethanol (AR) medium for 20h (rotation speed 200r / mimn. After drying at 105-120°C, the precursor was obtained, and the dried precursor was placed in a high-temperature furnace. In a nitrogen (>99.5%) atmosphere, calcining at a high temperature of 500-750° C. for 24 hours to obtain the strontium and barium activated lithium iron phosphate cathode material of the present invention.

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Abstract

The invention discloses a preparation method of a strontium and barium activated lithium iron phosphate positive pole material. The preparation method is characterized by comprising the following steps: mixing a lithium source, an iron source, a phosphate radical source, and a strontium source utilized as a raw material according to the ratio of 1:(0.00002-0.00005):(0.0003-0.003):1:1; in an absolute ethyl alcohol medium, carrying out high-speed ball-milling for 20 hours at the rotation rate of 200r / mimn and drying at the temperature of 105-120 DEG C, thereby obtaining a front body, and placing the drying obtained front body in a high temperature furnace; and carrying out high-temperature calcination for 24 hours at 500-750 DEG C in a common pure nitrogen atmosphere on to obtain the strontium, barium activating lithium iron phosphate positive pole material. According to the invention, strontium and the barium are replaced because of the doping, the feature and the particle diameter of a product are effectively controlled, thereby obtaining a stable lithium iron phosphate compound, the crystal lattice of the lithium iron phosphate compound is activated, the lithium ion diffusion coefficient is improved, and the loading capacity achieves 160.52 m A h / g in the first time; a charge-discharge platform relative to lithium electrode potential is around 3.5V, the initial discharge capacity exceeds 168 m A h / g, and the capacity decays around 1.2% after the charging and discharging are circled for100 times; compared with the unmixed LiFePO4 contrast embodiment, the specific capacity and the cyclical stability are greatly improved.

Description

technical field [0001] The method for preparing a strontium and barium activated lithium iron phosphate positive electrode material of the invention belongs to a method for preparing a lithium battery positive electrode material, and in particular relates to a preparation method for a lithium iron phosphate battery positive electrode material. 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 perfor...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/58
CPCY02E60/10
Inventor 张健张新球吴润秀王晶张雅静李杰李安平李先兰张爱萍何丽萍
Owner 桐乡乐维新材料有限公司
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