Separator for non-aqueous secondary battery, secondary battery, and manufacturing method of secondary battery
US-2022069413-A1 · Mar 3, 2022 · US
US12015170B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12015170-B2 |
| Application number | US-202318331272-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 8, 2023 |
| Priority date | Jun 9, 2022 |
| Publication date | Jun 18, 2024 |
| Grant date | Jun 18, 2024 |
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A separator, a method of manufacturing the separator, and an electrochemical device including the separator. The separator includes: a porous substrate; and an inorganic particle layer formed on at least one surface of the porous substrate, wherein a release rate of the inorganic particle layer is 70% or more when measured by immersing the separator in a water tank at room temperature and then subjecting the separator to sonication under conditions of a frequency of 40 kHz, an output of 1,000 W, and an application time of 60 seconds.
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What is claimed is: 1. A method of manufacturing a separator, the method comprising: (a1) preparing an acid aqueous solution including a silane compound represented by Chemical Formula 1 and an acid component; (a2) preparing an inorganic slurry by stirring inorganic particles, an acid component, and water; (a3) preparing a coating slurry by mixing the inorganic slurry and the acid aqueous solution; and (b) applying the prepared coating slurry on at least one surface of a porous substrate and drying the coating slurry to provide an inorganic particle layer: A a Si(OR) b Chemical Formula 1 wherein A is hydrogen, a polar functional group, or a C1-C10 alkyl group having a polar functional group, R is independently hydrogen or a C1-C5 alkyl group, a is 0 to 2, b is 2 to 4, and a+b is 4, and wherein the polar functional group of the silane compound includes one or two or more selected from an amino group, an epoxy group, a carboxyl group, a hydroxyl group, an amide group, a thiol group, a ketone group, an ester group, and an aldehyde group. 2. The method of claim 1 , wherein the process (a3) is performed in a weakly acidic atmosphere of more than pH 4 and pH 7 or less. 3. The method of claim 1 , wherein an absolute value of a difference in pH of the inorganic slurry prepared in the process (a2) and pH of the acid aqueous solution prepared in the process (a1) is 1 or less. 4. The method of claim 1 , wherein in the process (a2), the inorganic slurry is prepared by stirring the inorganic particles, acid component, and water at 50 to 500 rpm for 1 hour or longer. 5. The method of claim 1 , wherein the processes in (a1) to (a3) are performed in a weakly acidic environment of more than pH 4 and pH 7 or less. 6. The method of claim 1 , wherein the acid component is carbon dioxide, or an organic acid including one or two selected from acetic acid and lactic acid. 7. The method of claim 1 , wherein a weight ratio of the silane compound of Chemical Formula 1 to the inorganic particles in the coating slurry is 0.1 to 30:99.9 to 70. 8. The method of claim 1 , further comprising, after the process (b), (c) aging the porous substrate on which the inorganic particle layer is provided. 9. The method of claim 1 , wherein a surface of the porous substrate is subjected to a hydrophilic surface treatment. 10. The method of claim 9 , wherein the hydrophilic surface treatment includes one or more of a corona discharge treatment and a plasma discharge treatment.
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