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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

Inactive Publication Date: 2013-02-13
浙江远志新材料有限公司
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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%), 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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Abstract

The invention discloses a method for preparing an antimony and barium activated lithium iron phosphate cathode material. The method comprises the following steps of: mixing a lithium source, an iron source, a phosphate group source, an antimony source and a barium source which serve as raw materials according to the ratio of Li to Sb to Ba to Fe to P of 1:(0.00002-0.00005):(0.0003-0.003):1:1, performing high-speed ball milling in an absolute ethanol medium at the rotating speed of 200r / min for 20 hours, drying at the temperature of between 105 and 120 DEG C, and thus obtaining a precursor; and putting the dried precursor into a high temperature furnace, calcining in a nitrogen atmosphere at the temperature of between 500 and 750 DEG C for 24 hours, and thus obtaining the antimony and barium activated lithium iron phosphate cathode material. A small amount of antimony and barium is doped, so that control over the appearance and the particle size of a product is facilitated, a stable lithium iron phosphate compound is obtained, the crystal lattice of the material is activated, a lithium ion diffusion coefficient is improved, and the material has the initial discharging capacity of 160.52mAh / g; a charging / discharging platform of the material has a relative lithium electrode potential of about 3.5V, and material has the initial discharging capacity of more than 168mAh / g and has the capacity which is reduced by about 1.2 percent after 100-time charging / discharging operation; and compared with an undoped LiFePO4 comparison embodiment, the method has the advantage that the specific capacity and the circulating stability of the material are greatly improved.

Description

technical field [0001] The antimony and barium activated lithium iron phosphate positive electrode material preparation method of the present invention belongs to a lithium battery positive electrode material preparation method, in particular to a lithium iron phosphate battery positive electrode material preparation method. 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 extremely ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/58
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
Owner 浙江远志新材料有限公司
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