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Nickel-cobalt lithium aluminate precursor preparation method

A technology of nickel cobalt lithium aluminate and precursor, which is used in chemical instruments and methods, nickel compounds, electrode manufacturing, etc. problems, to achieve the effect of facilitating large-scale industrial production, ensuring product quality, and simple process

Inactive Publication Date: 2017-06-30
OPTIMUM BATTERY CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] At present, the precursor of nickel-cobalt lithium aluminate is usually prepared by controlled crystallization method, but this method cannot guarantee the mixing uniformity of the three elements of nickel, cobalt and aluminum, and the performance of the prepared precursor is unstable

Method used

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  • Nickel-cobalt lithium aluminate precursor preparation method

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preparation example Construction

[0029] Please refer to figure 1 , The present invention provides a method for preparing a lithium nickel cobalt aluminate precursor, which includes the following steps:

[0030] 1) According to the molar ratio of Ni:Co:Al=(0.6-0.9):(0.05-0.3):(0.01-0.1), the nickel salt solution, cobalt salt solution and aluminum salt solution are mixed to form the first mixed solution;

[0031] 2) Adding the first mixed solution to ammonia water with a mass fraction of 5%-25%, and after stirring evenly, adjust the pH value with an alkaline solution to form a second mixed solution with pH ≥ 12;

[0032] 3) Add an appropriate amount of additives to the second mixed solution, stir evenly and then stand and age for 10-24 hours to form a precursor colloid;

[0033] 4) Wash the precursor colloid with distilled water first, then wash with alcohol liquid, and then concentrate by centrifugation to obtain a precursor gel;

[0034] 5) Dry the precursor gel at 200-300°C for 4-8 hours, and then calcinate at 1100-16...

Embodiment 1

[0037] In this embodiment, equal volumes of nickel chloride solution, cobalt chloride solution and aluminum chloride solution with concentrations of 0.9 mol / L, 0.3 mol / L and 0.1 mol / L are mixed to form a first mixed solution; The first mixed solution is added to ammonia water with a mass fraction of 25%, stirred evenly at a high speed of 4500r / min, and then the pH value is adjusted with NaOH solution to form a second mixed solution with pH=12; to the second mixed solution Add an appropriate amount of additives, where the added amount of the additives is 0.05% relative to the mass fraction of the second mixed solution, then stir evenly at a high speed of 4500r / min, then stand and age for 24h to form a precursor colloid; The precursor colloid is washed with distilled water and absolute ethanol in turn, and then concentrated by centrifugation to obtain a precursor gel; the precursor gel is dried at 300°C for 8 hours, and then calcined at 1600°C for 6 hours to obtain precursor powde...

Embodiment 2

[0039] In this embodiment, equal volumes of nickel chloride solution, cobalt chloride solution, and aluminum chloride solution with concentrations of 0.6 mol / L, 0.05 mol / L, and 0.01 mol / L are mixed to form a first mixed solution; The first mixed solution was added to ammonia water with a mass fraction of 5%, stirred uniformly at a high speed of 4500r / min, and then the pH value was adjusted by NaOH solution to form a second mixed solution with pH=12; to the second mixed solution Add an appropriate amount of additives, wherein the added amount of the additives is 0.01% relative to the mass fraction of the second mixed solution, and then stir evenly at a high speed of 4500r / min and then stand and age for 10 hours to form a precursor colloid; The precursor colloid was washed with distilled water and anhydrous ethylene glycol in turn, and then concentrated by centrifugation to obtain a precursor gel; the precursor gel was dried at 200°C for 4 hours, and then calcined at 1100°C for 3 ...

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Abstract

The present invention provides a nickel-cobalt lithium aluminate precursor preparation method, which comprises: 1) mixing a nickel salt solution, a cobalt salt solution and an aluminum salt solution according to a molar ratio of Ni to Co to Al is (0.6-0.9):(0.05-0.3)(0.01-0.1) to form a first mixing solution; 2) adding the first mixing solution into ammonia water, uniformly stirring, and adjusting the pH value with an alkali solution to form a second mixing solution with the pH value of more than or equal to 12; 3) adding an appropriate amount of an additive to the second mixing solution, uniformly stirring, and carrying out standing aging for 10-24 h to form a precursor colloid; 4) washing the precursor colloid by using distilled water, then washing with an alcohol liquid, and carrying out centrifugation concentration to obtain a precursor gel; and 5) drying the precursor gel for 4-8 h at a temperature of 200-300 DEG C, and calcining for 3-6 h at a temperature of 1100-1600 DEG C to obtain the precursor powder.

Description

[0001] 【Technical Field】 [0002] The invention relates to the technical field of lithium ion battery cathode materials, in particular to a method for preparing a lithium nickel cobalt aluminate precursor. [0003] 【Background technique】 [0004] Lithium-ion batteries, as a new generation of environmentally friendly batteries, have become one of the focus of the development of the battery industry, and the market has increasingly higher requirements for the energy density of lithium-ion batteries. Cathode material is a key factor restricting the improvement of the energy density of lithium-ion batteries. Therefore, ternary cathode materials with high discharge specific capacity, low temperature and good rate performance have received market attention. Especially nickel cobalt lithium aluminate is used as a cathode material for batteries. The capacity, mass energy density, and volume energy density have been greatly improved. The physical, chemical and electrochemical properties of t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/485H01M4/525H01M10/0525B82Y30/00
CPCB82Y30/00H01M4/364H01M4/485H01M4/525H01M10/0525C01G53/006C01P2004/03C01P2004/61Y02E60/10H01M4/0454H01M2004/028H01M4/463H01M4/0404H01M4/32
Inventor 唐超饶睦敏容亮斌邓昌源
Owner OPTIMUM BATTERY CO LTD