Preparation method of lithium ion battery electrode material

A lithium-ion battery and electrode material technology, applied in battery electrodes, non-aqueous electrolyte battery electrodes, circuits, etc., can solve the problems of electrode material structure deformation, low electronic conductivity, high energy consumption, etc., to achieve changing distribution, high electronic Effects of conductivity and high degree of graphitization

Active Publication Date: 2018-08-28
PULEAD TECH IND
View PDF11 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the limitation of the material synthesis temperature (650-1000°C), the carbon coating layer in method 1) is mainly composed of amorphous carbon. Compared with highly graphitized graphene and carbon nanotubes, the amorphous carbon The electronic conductivity is relatively low. Therefore, it is far from meeting the needs of future battery development to improve the electronic conductivity of the electrode material only by the amorphous carbon coating layer.
At present, the most direct and effective way is to increase the sintering temperature (≥1800°C) to increase the degree of graphitization of the carbon layer, but this method consumes a lot of energy, and the high sintering temperature will deform the structure of the electrode material and even deactivate it.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of lithium ion battery electrode material
  • Preparation method of lithium ion battery electrode material
  • Preparation method of lithium ion battery electrode material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] The present embodiment provides a kind of preparation method of lithium-ion battery electrode material, specifically as follows:

[0041] Add 3g of citric acid, tetraphenylboronic acid, and dibenzyl disulfide to 100g of V (去离子水) :V (乙醇) = 4:1 mixed dispersant, stirred evenly in the reactor to form the first mixture. Add 0.5 g of lithium carbonate, ferrous oxalate, and ammonium dihydrogen phosphate to the first mixture in sequence according to the molar ratio of Li:Fe:P of 1:1:1, and stir evenly to form the second mixture. The second mixture was heated at 80° C. and stirred at 300 rpm until the solution evaporated to dryness to form a solid. Then vacuum-dry at 80°C for 10h, then heat to 350°C for 4h under nitrogen atmosphere at a rate of 5°C per minute for calcination, then cool and grind. Then, it is heated to 800° C. for 15 hours at a heating rate of 5° C. per minute and calcined for 15 hours. The obtained solid product is ground and sieved to obtain a boron-sulfur ...

Embodiment 2

[0049] The present embodiment provides a kind of preparation method of lithium-ion battery electrode material, specifically as follows:

[0050] 3g of sucrose, ethylphenylboronic acid, and thiophene were sequentially added into deionized water with a total mass of 30g according to the C:B:S molar ratio of 1:0.01:0.01, and stirred uniformly in the reactor to form the first mixture. Add 0.5 g of lithium nitrate, ferrous acetate, and ammonium phosphate to the first mixture in sequence according to the molar ratio of Li:Fe:P of 0.9:1:1, and stir to form a second mixture. The second mixture was heated at 70°C and stirred at 200 rpm until the solution evaporated to dryness to form a solid. Then vacuum-dried at 70°C for 8h, then heated to 250°C for 3h under an argon atmosphere at a rate of 1°C per minute and then calcined for 3h, cooled and ground. Then, it is heated to 700° C. for 8 hours at a heating rate of 1° C. per minute and calcined for 8 hours. The obtained solid product is ...

Embodiment 3

[0052] The present embodiment provides a kind of preparation method of lithium-ion battery electrode material, specifically as follows:

[0053] Add 3 g of glucose, 4-aminophenylboronic acid, and sulfonated polystyrene into deionized water with a total mass of 150 g in sequence according to the C:B:S molar ratio of 1:0.1:0.1, and stir evenly in the reactor to form the first mixture . Add 0.5 g of lithium hydroxide, iron phosphate, and diammonium hydrogen phosphate to the first mixture in sequence according to the molar ratio of Li:Fe:P of 1.1:1:1, and stir evenly to form the second mixture. The second mixture was heated at 90°C and stirred at 400 rpm until the solution evaporated to dryness to form a solid. Then vacuum dry at 100°C for 12h, then heat to 450°C for 5h under nitrogen atmosphere at a rate of 20°C per minute for calcination, then cool and grind. Then, it is heated to 1000° C. for 30 hours at a heating rate of 20° C. per minute and calcined for 30 hours. The obtai...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention provides a preparation method of a lithium ion battery electrode material. The preparation method comprises the following steps: adding a carbon source and any two of a boron source, a sulfur source and a nitrogen source of a nonmetallic doping raw material as dispersoids into a dispersant, and uniformly stirring the materials to form a first mixture; adding a lithium source, an ironsource and a phosphorus source to the first mixture, or adding a lithium source, an iron source, a manganese source and a phosphorus source, or adding a lithium source and a titanium source to form asecond mixture; stirring and heating the second mixture until the solution is evaporated to form a solid to obtain a precursor of a nonmetallic co-doped carbon-coated electrode material; drying the solid in vacuum, heating the solid to 250-450 DEG C under an inert gas atmosphere, heating the solid at a constant temperature for 3-5h, and cooling and grinding the solid to obtain a reaction precursor; and heating the reaction precursor to 700-1000 DEG C under an inert gas atmosphere, calcining the reaction precursor at a constant temperature for 8-30h, and carrying out grinding and sieving aftercooling to obtain the lithium ion battery electrode material.

Description

technical field [0001] The invention relates to the technical field of lithium-ion battery electrode materials, in particular to a preparation method of a non-metallic element co-doped carbon-coated lithium-ion battery electrode material and an electrode material prepared by the method. Background technique [0002] At present, lithium-ion batteries are widely used in various mobile electronic products and new energy vehicles. Lithium cobalt oxide (LiCoO 2 ), lithium nickelate (LiNiO 2 ), lithium manganate (LiMn 2 o 4 ), lithium iron manganese phosphate (LiFe 0.5 +xMn 0.5 -xPO 4 ), lithium iron phosphate (LiFePO 4 ) cathode materials and graphite, lithium titanate (Li 4 Ti 5 o 12 ) is the most common negative electrode application. where LiCoO 2 The price is expensive, the cost is high, the Co resource is poor, and the toxicity is high; LiNiO 2 Poor thermal stability and poor safety; LiMn 2 o 4 Although the safety performance is good, the capacity decays quick...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/13H01M4/36
CPCH01M4/13H01M4/362Y02E60/10
Inventor 沈伟申兰耀张振宇王胜彬周恒辉
Owner PULEAD TECH IND
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products