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Transition metal phosphate-clad composite lithium ion battery anode material

A composite positive electrode material and lithium-ion battery technology, applied in the direction of non-aqueous electrolyte battery electrodes, etc., can solve the problems of no electrochemical activity, poor rate performance, unsafe and other problems, achieve good cycle performance and rate performance, and improve cycle performance And magnification performance, the effect of simple and easy to control the production process

Inactive Publication Date: 2010-10-13
HUAZHONG UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The cathode material that has been commercialized at this stage is LiCoO 2 , due to the lack of cobalt resources, toxicity and unsafety, it is not suitable for electric vehicle batteries
Because Ni 3+ Unstable, difficult to prepare stoichiometric LiNiO 2
Spinel LiMn 2 o 4 Due to the electrolyte decomposition at high charge potential, the Jahn-Teller effect at low discharge potential, and the easy dissolution of manganese ions in the electrolyte, its cycle performance is poor, which hinders its large-scale commercial application.
The lithium-rich composite material nLi 2 MnO 3 .(1-n)LiMO 2 Li in (02 MnO 3 It is an insulator, which leads to poor cycle performance, poor rate performance, and low coulombic efficiency for the first charge and discharge.
People use Mg, Al, Ti, V, Cr, Co, Ni and other metal ions to do modification research, but the effect is not ideal
In addition, Al, which is not easy to dissolve and has a stable structure, is widely used. 2 o 3 , MgO, SiO 2 Surface treatment and coating of other oxides can improve the cycle performance, but because these oxides are not electrochemically active, the specific capacity is lost, and the lithium ion transport channel is hindered, which affects the rate performance.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0011] Embodiment 1 core is lithium manganese oxide LiMn 2 o 4 , the shell is iron phosphate FePO 4 Composite electrode material

[0012] Lithium manganese oxide LiMn prepared by solid-state sintering 2 o 4 Fine powder dispersed in ferrous sulfate FeSO 4 In the aqueous solution, after stirring for a period of time, the Fe 2+ with PO 4 3- Ammonium dihydrogen phosphate NH with a molar ratio of 1:1 4 h 2 PO 4 The aqueous solution was slowly added to the above suspension, and after mechanical stirring for a period of time, the obtained product was separated by filtration, dried at 130°C, and then sintered at 550°C. The outer shell iron phosphate FePO in the resulting composite electrode material 4 Lithium manganese oxide LiMn 2 o 4 1% of the mass ratio. Using a lithium sheet as the negative electrode, the uncoated lithium manganate LiMn at room temperature was measured 2 o 4 and iron phosphate FePO 4 Coated lithium manganese oxide LiMn 2 o 4 The magnification pe...

Embodiment 2

[0016] Example 2 The core is lithium manganate LiAl doped with aluminum 0.02 mn 1.98 o 4 , the shell is titanium phosphate TiPO 4 composite electrode materials.

[0017] Al-doped lithium manganate LiAl prepared by sol-gel method 0.02 mn 1.98 o 4 fine powder dispersed in titanium nitrate Ti(NO 3 ) 3 In the aqueous solution, after ultrasonic stirring for a period of time, the Ti 3+ with PO 4 3- Ammonium dihydrogen phosphate NH with a molar ratio of 1:1 4 h 2 PO 4 The aqueous solution is slowly added to the above suspension, and after reacting and aging for a period of time, the obtained product is separated by filtration, dried at 80°C, and then sintered at 300°C. Titanium phosphate TiPO in the obtained composite electrode material 4 LiAl 0.02 mn 1.98 o 4 0.01% of the mass ratio.

Embodiment 3

[0018] Embodiment 3 core is lithium nickelate LiNiO 2 , the shell is vanadium phosphate VPO 4 Composite electrode material

[0019] Lithium nickelate LiNiO prepared by hydrothermal / solvothermal method 2 Fine powder dispersed in vanadium chloride VCl 3 In the aqueous solution, after a period of magnetic stirring, the V 3+ with PO 4 3- Ammonium dihydrogen phosphate NH with a molar ratio of 1:1 4 h 2 PO 4 The aqueous solution is slowly added to the above suspension, and after reacting and aging for a period of time, the obtained product is separated by filtration, dried at 90°C, and then sintered at 350°C. The shell vanadium phosphate VPO in the resulting composite electrode material 4 Occupying core lithium nickelate LiNiO 2 0.1% of the mass ratio.

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Abstract

The invention discloses a transition metal phosphate-clad composite lithium ion battery anode material with lithium-storing active material as a main core and electrochemically active transition metal phosphate as a cladding layer. The active material core mainly carries out electrochemical reaction, and provides battery capacity; and the cladding layer not only can protect the lithium-storing active material and reduce the dissolution and erosion of the active material by electrolyte, but also can increase the battery capacity and improve the rate capability of the active material.

Description

technical field [0001] The invention belongs to the technical fields of electrochemistry, material chemistry and chemical power supply products, and in particular relates to a lithium-ion battery composite cathode material Background technique [0002] Energy is the basic support of the national economy and one of the five elements for human survival. Energy security directly affects national security, sustainable development and social stability, and mineral energy provides 90% of the world's energy. According to scientific calculations, the proven reserves of oil, coal, and natural gas are 140 billion tons, 1,031.6 billion tons, and 152m 3 According to the current mining level, they can still be mined for 30 years, 200 years, and 60 years. The depletion of fossil energy resources urgently requires the development of new renewable energy and efficient clean energy. Lithium-ion batteries have attracted widespread attention because of their high operating voltage, high ener...

Claims

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Application Information

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IPC IPC(8): H01M4/13
CPCY02E60/122Y02E60/10
Inventor 黄云辉杨泽夏圣安李爽张五星袁利霞胡先罗
Owner HUAZHONG UNIV OF SCI & TECH
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