FUNCTIONAL COATING MATERIAL FOR LITHIUM ION BATTERY SEPARATOR AND PREPARATION METHOD THEREFOR

Abstract

Provided are a functional coating material for a lithium ion battery separator and a preparation method therefor. The functional coating material for a lithium ion battery separator comprises 1-15% mass fraction of inorganic nanoparticles, 8-30% mass fraction of nanofibers and 1-5% mass fraction of an adhesive, and the remainder being a solvent. The preparation method therefor comprises the following steps: (1) preparing the nanofibers as a spinning precursor liquid; (2) preparing a dispersion liquid with the inorganic nanoparticles and the spinning precursor liquid; and (3) adding the adhesive to the dispersion liquid, and mixing same until uniform to obtain the functional coating material for a lithium ion battery separator.

Claims

1. A functional coating material for lithium ion battery separator, the functional coating material comprising inorganic nanoparticles in a mass fraction of 1% to 15%, nanofibers in a mass fraction of 8% to 30%, and an adhesive in a mass fraction of 1% to 5%, with the balance being a solvent.

2. The functional coating material for lithium ion battery separator according to claim 1, wherein the inorganic nanoparticles have an average particle size of 5 nm to 50 nm.

3. The functional coating material for lithium ion battery separator according to claim 1, wherein the inorganic nanoparticles have an average particle size of 20 nm to 30 nm.

4. The functional coating material for lithium ion battery separator according to claim 1, wherein the inorganic nanoparticles are one or more selected from the group consisting of SiO.sub.2, TiO.sub.2, and Al.sub.2O.sub.3.

5. The functional coating material for lithium ion battery separator according to claim 1, wherein the inorganic nanoparticles are SiO.sub.2 and/or TiO.sub.2.

6. The functional coating material for lithium ion battery separator according to claim 1, wherein the nanofibers are one or more selected from the group consisting of aramid nanofibers, cellulose acetate nanofibers, and polyimide nanofibers.

7. The functional coating material for lithium ion battery separator according to claim 1, wherein the adhesive is one or more selected from the group consisting of polymethyl methacrylate (PMMA), carboxymethyl cellulose (CMC), polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP), polyvinylidene fluoride (PVDF), polyacrylic acid, and chitosan.

8. The functional coating material for lithium ion battery separator according to claim 1, wherein the solvent is one or more selected from the group consisting of ethanol, water, and N-methylpyrrolidone (NMP).

9. A method for preparing the functional coating material for lithium ion battery separator according to claim 1, comprising step of: (1) preparing the nanofibers into a spinning precursor liquid; (2) preparing a dispersion liquid using the inorganic nanoparticles and the spinning precursor liquid; (3) adding the adhesive to the dispersion liquid with well mixing to obtain a functional coating material for lithium ion battery separator, wherein the preparing the dispersion liquid in step (2) is selected from one of: a. adding the inorganic nanoparticles to the spinning precursor liquid for electrospinning to obtain an inorganic nanoparticle/nanofiber composite membrane; dispersing the inorganic nanoparticle/nanofiber composite membrane in the solvent to obtain a dispersion liquid; or b. electrospinning the spinning precursor liquid to obtain a nanofiber membrane, dispersing the nanofiber membrane in the solvent, adding the inorganic nanoparticles, and performing dispersing again to obtain the dispersion liquid.

10. The method according to claim 9, wherein in step (1) or (2), the spinning precursor liquid is one or more selected from the group consisting of a spinning precursor liquid of aramid nanofibers, a spinning precursor liquid of cellulose acetate nanofibers, or a spinning precursor liquid of polyimide nanofibers.

11. The method according to claim 9, wherein in step (1) or (2), the nanofibers are in a mass fraction of 15% in the spinning precursor liquid.

12. The method according to claim 9, wherein the electrospinning is performed under a condition of a voltage of 10 kV to 20 kV, a solvent base rate of 0.2 mL/h to 1 mL/h, and a receiving distance of 12 cm to 18 cm.

13. The method according to claim 9, wherein the dispersing in any one of steps a and b is performed in manners including ultrasonic dispersion and mill beating treatment.

14. A lithium ion battery separator coated with the functional coating material according to claim 1.

15. The lithium ion battery separator according to claim 14, wherein the functional coating material is coated in a thickness of 0.5 to 3 μm.

Description

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0037] In order to make the technical means, features, realized objects and technical effects of the present disclosure easy to understand, the present disclosure will be further illustrated below in conjunction with specific embodiments. However, the following embodiments are only preferred, but not all of, embodiments of the present disclosure. Based on the embodiments in the implementations, other embodiments obtained by those skilled in the art without creative work shall fall within the protection scope of the present disclosure.

[0038] The experimental methods in the following examples are conventional methods unless otherwise specified. The materials and reagents used in the following examples can be commercially available unless otherwise specified.

[0039] The water in the following examples can be tap water, purified water, distilled water, drinking water, or the like.

[0040] In the following examples, SiO.sub.2 and Al.sub.2O.sub.3 particles were purchased from Aladdin (Cat. Nos. S139944 and A299287, respectively), and TiO.sub.2 particles were purchased from Degussa (Cat. No. P25).

[0041] In the following examples, ultrasonic dispersion is achieved by using an ultrasonic cell disruptor, but not limited thereto.

[0042] In the following examples, the spinning precursor liquid of aramid nanofibers, the spinning precursor liquid of cellulose acetate nanofibers, and the spinning precursor liquid of polyimide nanofibers are prepared as follows:

[0043] For preparing the spinning precursor liquid of aramid nanofibers, dimethylacetamide is added to an aramid fiber stock solution followed by stirring at 60° C., obtaining the spinning precursor liquid of aramid which is in a mass fraction of 15%.

[0044] For preparing the spinning precursor liquid of cellulose acetate nanofibers, cellulose acetate (secondary cellulose acetate with a degree of esterification of 240 to 260) is dissolved in a mixed solvent of acetone and other solvents, obtaining the spinning precursor liquid of cellulose acetate nanofibers which is in a mass fraction of 15%.

[0045] For preparing the spinning precursor liquid of polyimide nanofibers, pyromellitic dianhydride and 4,4-diaminodiphenyl ether (ODA) at a molar ratio of 1:1 are added to the N,N-dimethylformamide solvent followed by vigorous stirring for 12 hr in an ice bath at 0° C., finally obtaining a polyimide acid solution in a mass fraction of 15% as the spinning precursor liquid of polyimide nanofibers.

Example 1-4

[0046] (1) Inorganic nanoparticles were added to a spinning precursor liquid for electrospinning to obtain an inorganic nanoparticle/nanofiber composite membrane, and the composite membrane was cut into small pieces and added to a solvent for dispersing by beating using a sand mill at 5000 rpm for 1 hr, obtaining a dispersion liquid.

[0047] (2) An adhesive was added to the dispersion liquid and mixed well to obtain a functional coating material for lithium ion battery separator whose composition is shown in Table 1.

[0048] (3) The above functional coating material was coated on a PP membrane in a coating thickness of 2 μm with a scraper.

[0049] (4) The coated base membrane was put into an oven and dried at 100° C. for 5 hr.

[0050] The inorganic nanoparticles have an average particle size of 20 nm in Examples 1 and 2, and an average particle size of 50 nm in Examples 3 and 4.

TABLE-US-00001 TABLE 1 Composition of functional coating materials of Examples 1-4 Functional coating materials Composition of Mass Types and Types and inorganic fraction of mass mass nanoparticles inorganic fraction of fraction of Solvent Ex. SiO.sub.2 Al.sub.2O.sub.3 TiO.sub.2 nanoparticles nanofibers adhesive type 1 100% — —  1% Aramid PMMA Ethanol nanofiber 1%  8% 2  50% 50% — 10% Cellulose CMC Water acetate 3% nanofiber 25% 3 100% — — 10% Aramid PVDF- NMP nanofiber HFP 25% 3% 4  50% — 50%- 15% Cellulose PVDF Ethanol acetate 5% nanofiber 30%

Example 5-10

[0051] (1) The nanofiber membrane obtained by electrospinning the spinning precursor liquid was cut into small pieces and added to a solvent for well dispersing using an ultrasonic cell disruptor, and then the inorganic nanoparticles were added for another ultrasonic dispersing, obtaining a dispersion liquid.

[0052] (2) An adhesive was added to the dispersion liquid and mixed well to obtain a functional coating material for lithium ion battery separator whose composition is shown in Table 2.

[0053] (3) The above functional coating material was sprayed on a PE membrane in a coating thickness of 1.5 μm.

[0054] (4) The coated base membrane was put into an oven and dried at 50° C. for 24 hr.

[0055] The inorganic nanoparticles have an average particle size of 5 nm in Examples 5 and 6, and an average particle size of 30 nm in Examples 7-10.

TABLE-US-00002 TABLE 2 Composition of functional coating materials of Examples 5-10 Functional coating materials Composition of Mass Types and Types and inorganic fraction of mass mass nanoparticles inorganic fraction of fraction of Solvent Ex. SiO.sub.2 Al.sub.2O.sub.3 TiO.sub.2 nanoparticles nanofibers adhesive type  5 100% — —  1% Aramid PMMA Ethanol nanofiber 1%  8%  6  50% 50% — 10% Cellulose chitosan Water acetate 3% nanofiber 25%  7 100% — — 10% Aramid PVDF- NMP nanofiber HFP 25% 3%  8  50% — 50%- 15% Cellulose PVDF Ethanol acetate 5% nanofiber 30%  9 100% — 10% Aramid Poly- Water nanofiber acrylic 20% acid 5% 10 100% — — 15% Polyimide PVDF- NMP nanofiber HFP 25% 3%

Comparative Example 1

[0056] (1) The nanofiber membrane obtained by electrospinning was cut into small pieces and added to a solvent for well dispersing using an ultrasonic cell disruptor, obtaining a dispersion liquid.

[0057] (2) An adhesive was added to the dispersion liquid and mixed well to obtain a functional coating material for lithium ion battery separator whose composition is shown in Table 3.

[0058] (3) The above functional coating material was sprayed on a PE membrane in a coating thickness of 1.5 μm.

[0059] (4) The coated base membrane was put into an oven and dried at 50° C. for 24 hr.

Comparative Example 2 and 3

[0060] (1) The nanofiber membrane obtained by electrospinning was cut into small pieces and added to a solvent for well dispersing using an ultrasonic cell disruptor, obtaining a dispersion liquid. Then, the inorganic nanoparticles were added for another ultrasonic dispersing, obtaining a dispersion liquid.

[0061] (2) An adhesive was added to the dispersion liquid and mixed well to obtain a functional coating material for lithium ion battery separator whose composition is shown in Table 3.

[0062] (3) The above functional coating material was sprayed on a PE membrane in a coating thickness of 1.5 μm.

[0063] (4) The coated base membrane was put into an oven and dried at 50° C. for 24 hr.

[0064] The inorganic nanoparticles have an average particle diameter of 30 nm.

TABLE-US-00003 TABLE 3 Composition of functional coating materials of Comparative Examples 1-3 Functional coating materials Mass Types Types fraction and and Composition of of mass mass inorganic inorganic fraction fraction Comp. nanoparticles nano- of nano- of Solvent Ex. SiO.sub.2 Al.sub.2O.sub.3 TiO.sub.2 particles fibers adhesive type 1 — — — — Aramid PVDF- NMP nanofiber HFP 25% 3% 2 100% — 10% Aramid PMMA Ethanol nanofiber 40% 3% 3 100% — — 10% Aramid PVDF- nanofiber HFP  5% 3% NMP

[0065] Effect Measurement

[0066] Thermal stability (150° C., 1 hr), ionic conductivity, air permeability, and wettability (contact angle) of the coated separators prepared in the above examples were measured. The measurement results are shown in Table 4:

TABLE-US-00004 TABLE 4 Measurement results of Examples 1-10 and Comparative Examples 1-3 Membrane Air permeability shrinkage Ionic (s/sq.in .Math. Wettability (150°C., conductivity 100 mL .Math. (contact 1 hr) (mS/cm) 1.22 kpa) angle °) Example 1 10% 0.35 285 40 Example 2  5% 0.56 295 30 Example 3 0.5%  0.55 298 30 Example 4 0.3%  0.4 302 20 Example 5 12% 0.38 270 42 Example 6  6% 0.59 280 29 Example 7 0.8%  0.57 285 28 Example 8 0.5%  0.42 295 21 Example 9 0.3%  0.45 285 25 Example 10 0.8%  0.43 290 27 Comparative  5% 0.32 280 35 Example 1 Comparative 0.5%  0.35 360 25 Example 2 Comparative 15% 0.42 270 30 Example 3

[0067] The measurement results show that the separators coated with the functional coating material for lithium ion battery separator that is made of the inorganic nanoparticles and the nanofibers had significantly improved thermal stability, ionic conductivity, and wettability, and the air permeability thereof was not affected. In Examples 3 and 4, the membrane shrinkage at 150° C. for 1 hr decreased to 0.5% and 0.3%, and the thermal stability was better than that of Comparative Example 1 without the addition of inorganic nanoparticles. Comparative Examples 2 and 3 show that the aramid nanofiber, when used too much, would affect the dispersibility of the fiber and the wettability and air permeability of the membrane. On the contrary, the aramid nanofiber, when used too little, was not beneficial to thermal stability.

[0068] The functional coating material for separator in the present disclosure reduces the thickness of the separator while retaining inorganic nanoparticles. Through the hydrogen bond force between the fiber and the separator, the bonding force between the coating layer and the base membrane is strengthened. The thermal stability of the separator is improved. The wettability between the separator and the electrolyte is strengthened. The lithium ion transmission performance is improved. It has a good application prospect.

[0069] The above descriptions are only the preferred embodiments of the present disclosure and are not intended to limit the present disclosure. Any modification, equivalent replacement, improvement, and the like made within the spirit and principle of the present disclosure shall be included in the protection scope of the present disclosure.