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Preparation method for positive electrode material of secondary lithium battery

By first forming a phosphate coating layer in the secondary lithium battery cathode material and then adding the lithium source, the problem in the existing technology that the coating amount affects the capacity and the bonding is unstable is solved, and high specific capacity and cycle performance are achieved. and safety performance improvements.

Active Publication Date: 2017-01-04
NINGDE AMPEREX TECHNOLOGY LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the positive electrode materials prepared by the above coating materials and coating methods have the following defects: 1) when the coating amount is small, the coating effect is not obvious, and if the coating amount is too high, it will affect the material while improving the cycle performance. Capacity play; 2) The coating area cannot be controlled, and in many cases, a point-like or sheet-like coating state appears; 3) The coating often exists on the surface of the main material by physical adsorption, so the combination with the main material is not stable

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] The host material of the cathode material prepared in this example is Li 1.09 Ni 0.1 co 0.5 mn 0.4 o 2 , whose cladding material is Li 1.09 Ni 0.1 co 0.5 mn 0.4 PO 4 . Among them, Li 1.09 Ni 0.1 co 0.5 mn 0.4 o 2 Synthesized by precipitation method, the specific preparation steps are:

[0032] First, the intermediate product of the host material was synthesized by co-precipitation method: NiSO 4 、CoSO 4 , MnSO 4 Dissolve in deionized water according to the metal atomic ratio of 0.1:0.5:0.4, and configure a mixed solution with a total concentration of 1mol / L; then add the configured 1mol / L NaOH solution to the above solution, stir while adding, and the temperature Control at 75°C; after full reaction, evacuated secondary spherical particles are formed, with an average particle size of 20μm-21μm, and the resulting precipitate is washed with deionized water and ethanol several times; Sinter for 5 hours;

[0033] Then, by mass ratio 0.0024:1 P 2 o 5 Mix...

Embodiment 2

[0036] The host material of the cathode material prepared in this example is Li 1.10 Ni 1 / 3 co 1 / 3 mn 1 / 3 o 2 , whose cladding material Li 1.10 Ni 1 / 3 co 1 / 3 mn 1 / 3 PO 4 . Among them, Li 1.10 Ni 1 / 3 co 1 / 3 mn 1 / 3 o 2 Synthesized by precipitation method, the specific preparation steps are:

[0037] First, the precursor was synthesized by co-precipitation method: NiSO 4 、CoSO 4 , MnSO 4 Dissolve in deionized water according to the atomic ratio of 1.0:1.0:1.0, and configure a mixed solution with a total concentration of 1mol / L; then add the prepared 1mol / L NaOH solution to the above solution, stir while adding, and control the temperature At 75°C; after full reaction, evacuated secondary spherical particles are formed with an average particle size of 50 μm, and the resulting precipitate is washed with deionized water and ethanol several times;

[0038] Then, according to the mass ratio of 0.0001:1 (NH 4 ) 3 PO 4 Mix with the above resultant, and mix in a plan...

Embodiment 3

[0041] The host material of the cathode material prepared in this example is Li 1.08 Ni 0.5 co 0.2 mn 0.3 o 2 , whose cladding material Li 1.08 Ni 0.5 co 0.2 mn 0.3 PO 4 . Among them, Li 1.08 Ni 0.5 co 0.2 mn 0.3 o 2 It is synthesized by combustion method, and the specific preparation steps are as follows:

[0042] First, nickel nitrate, cobalt nitrate, and manganese nitrate are dissolved in ethanol at an atomic ratio of 0.50:0.20:0.30; after all substances are completely dissolved, glycerol is added, and the ratio of glycerol to total metal ions is 3:1; Put the above solution into a water bath at 80°C and stir to evaporate the ethanol; when the ethanol is completely evaporated, transfer the container to a resistance furnace for heating until it is fully burned; collect the obtained black matter and calcinate it at 750°C in an air atmosphere After 5 hours, particles with an average particle size of 0.5-0.8 μm are formed;

[0043] Then, by mass ratio 0.10:1 H 3...

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Abstract

The invention discloses a preparation method for a positive electrode material of a secondary lithium battery. An intermediate product of a host material Li<x>M<y>N<1-y>O<2-alpha>A<beta> is synthesized firstly; then a P source is added to the intermediate product to form a lithium-free phosphate; and then adding a Li source, and performing sintering to obtain the positive electrode material. Compared with the prior art, the preparation method for the positive electrode material of the secondary lithium battery has the advantages as follows: 1) the P source can be more uniformly dispersed on the surface of the host material; 2) the combination between a coating object and the host material becomes more tight; and 3) the positive electrode material has relatively high rate discharge performance.

Description

Technical Field [0001] This invention belongs to the field of secondary lithium battery technology, and more specifically, this invention relates to a method for preparing a high-performance secondary lithium battery cathode material. Background Technology [0002] Currently, lithium-containing transition metal oxides (LiMO2, where M represents Mn, Co, Ni, etc., and LiMO2 includes lithium cobalt oxide and various transition metal binary and ternary materials) are widely used in various commercially available secondary lithium batteries. Among them, multi-component cathode materials are considered to be the cathode materials for next-generation hybrid vehicle batteries. These materials have advantages such as low cost and simple synthesis processes. With the advancement of technology, the demand for battery energy density and electrochemical performance is increasing daily, which necessitates further improvements in the performance of cathode materials. [0003] Since dry coat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/58H01M4/505H01M4/525H01M4/48
CPCH01M4/48H01M4/505H01M4/525H01M4/5825H01M10/0525H01M4/366H01M2220/20Y02E60/10
Owner NINGDE AMPEREX TECHNOLOGY LTD