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Composite separator for lithium secondary battery and method for manufacturing same

A lithium secondary battery and composite diaphragm technology, which is applied in the field of composite diaphragm and its manufacturing, can solve the problems of battery capacity and output power drop, unsuitable for battery miniaturization, weak mechanical strength, etc., to achieve improved wettability, low thermal shrinkage, The effect of increasing the surface area

Pending Publication Date: 2022-04-01
G MATERIALS CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the severe heat shrinkage of the above-mentioned polyolefin separator at high temperature and weak mechanical strength, when the temperature of the battery rises sharply, as the edge of the separator shrinks, the positive and negative electrodes may contact each other and short circuit, resulting in heat release, fire, explosion
[0006] The easiest way to improve the stability of the battery is to increase the thickness of the diaphragm. However, as the thickness of the diaphragm increases, although the mechanical strength will increase, the battery capacity and output power will decrease, and it is not suitable for the battery. miniaturization

Method used

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  • Composite separator for lithium secondary battery and method for manufacturing same
  • Composite separator for lithium secondary battery and method for manufacturing same
  • Composite separator for lithium secondary battery and method for manufacturing same

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0066] Preparation example 1. Preparation of organic-inorganic composite sol

[0067] Alumina sol was prepared by adding 30 g of boehmite powder to 260 ml of distilled water, stirring, then adding 3.3 g of acetic acid, stirring at room temperature for 1 hour, then heating to about 70° C., and keeping at this temperature for 2 hour, then cooled to room temperature, and then added distilled water to bring the total weight to 300 g, thereby preparing a 10% by weight alumina sol.

[0068]Add 39 g of 5% by weight acetic acid solution to 130 g of 3-glycidoxypropyltrimethoxysilane (GPS), stir at room temperature for 1 hour, then add 377.2 g of the above-mentioned alumina sol and heated for 4 hours. When the reaction was complete, 2.71 g of a 5% by weight acetic acid solution was added, followed by 21.79 g of methyltriethoxysilane dropwise while heating for 4 hours. After cooling the heated mixture to room temperature, 2.74 g of Y(NO 3 ) 3 ·6H 2 O and stirred to prepare an organi...

preparation example 2

[0069] Preparation example 2. Preparation of organic polymer binder PM (PVA / MA)

[0070] Transparent solutions were prepared by dispersing polyvinyl alcohol (PVA) (saponification >88%, average molecular weight <200000) powder in distilled water to a concentration of 5-10 wt%, followed by heating at about 90°C. Maleic acid (MA) was added to the PVA solution at a weight ratio (PVA:MA) of 8:2, followed by heating to prepare a clear solution and called PM. Tetraethoxysilane (TEOS) diluted with ethanol is added to this PM solution in an amount of 5 to 10% by weight relative to the amount of PVA, calculated as silica, to obtain a stable silica-containing modification PM solution, and named PMs. A stable PMa solution was also prepared by using 10 wt% boehmite powder with an average particle size of 4.5 nm instead of TEOS as described in the PMs procedure.

Embodiment 1

[0072] The coating slurry of the composite diaphragm is prepared by adding the organic-inorganic composite sol prepared in Preparation Example 1 to the boehmite slurry, which is prepared by adding boehmite (dispersion 10F4, Sasol, average The particle size is 40nm) powder is dispersed in distilled water and stirred at room temperature for 60 minutes. Add PVA and stir according to the components shown in Table 1. After immersing a porous PE substrate with a thickness of 9 μm into the coating slurry, pulled up by two glass rods, dried at room temperature for 30 min or more, and then dried in an oven at 90 °C for 30 min to obtain Composite separator with a heat-resistant coating formed on the surface of a polymer substrate.

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Abstract

The invention relates to a composite separator for a lithium secondary battery and a water-based manufacturing method thereof. The composite separator comprises a porous polymer base material; a heat-resistant coating layer containing an inorganic material formed on the surface of the porous polymer substrate; the composite adhesive or the organic polymer adhesive is used for bonding the porous polymer base material and the heat-resistant coating and is formed by mixing organic-inorganic composite sol and an organic polymer; and a nonionic surfactant. Therefore, the present invention exhibits high air permeability, low thermal shrinkage, and excellent electrochemical properties.

Description

technical field [0001] The invention relates to a composite separator for lithium secondary batteries with high air permeability and low heat shrinkage rate and a manufacturing method thereof. Background technique [0002] In recent years, with the trend toward high capacity and high output of secondary batteries, separators with high strength, high air permeability, and thermal shrinkage rate are increasingly required in order to achieve electrical stability of lithium secondary batteries during charge and discharge. [0003] In the case of lithium secondary batteries, lithium secondary batteries are required to have high mechanical strength in order to improve the stability during battery manufacturing and use, and high gas permeability is required in order to increase capacity and output power. and high thermal stability. For example, in the separator of a lithium secondary battery, the problem of thermal stability is very important. If the thermal stability of the separ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M50/446H01M50/449H01M50/403
CPCY02E60/10H01M10/4235H01M50/451H01M50/446H01M50/461H01M50/417H01M50/423H01M50/414H01M50/434H01M50/403H01M10/0525H01M50/449H01M50/411H01M10/052H01M50/431
Inventor 林昌燮林景兰郑舜溶
Owner G MATERIALS CO LTD