Battery separator with dielectric coating
US-2017062788-A1 · Mar 2, 2017 · US
US11588209B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11588209-B2 |
| Application number | US-201816479988-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2018 |
| Priority date | Aug 21, 2018 |
| Publication date | Feb 21, 2023 |
| Grant date | Feb 21, 2023 |
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Separators, high performance electrochemical devices, such as, batteries and capacitors, including the aforementioned separators, systems and methods for fabricating the same. In one implementation, a separator is provided. The separator comprises a polymer substrate (131), capable of conducting ions, having a first surface and a second surface opposing the first surface. The separator further comprises a first ceramic-containing layer (136), capable of conducting ions, formed on the first surface. The first ceramic-containing layer (136) has a thickness in arrange from about 1,000 nanometers to about 5000 nanometers. The separator further comprises a second ceramic-containing layer (138), capable of conducting ions, formed on the second surface. The second ceramic-containing layer (138) is a binder-free ceramic-containing layer and has a thickness in arrange from about 1 nanometer to about 1,000 nanometers.
Opening claim text (preview).
The invention claimed is: 1. A method of forming a separator for a battery, comprising: exposing a first material to be deposited on a microporous ion-conducting polymeric layer positioned in a processing region to an evaporation process, wherein the microporous ion-conducting polymeric layer has: a first surface; a second surface opposing the first surface; and a first ceramic-containing layer, capable of conducting ions, formed on the first surface, wherein the first ceramic-containing layer is prepared by a slot-die technique or a doctor blade technique and has a thickness in a range from about 1,000 nanometers to about 5,000 nanometers; reacting the evaporated first material with a reactive gas and/or plasma to deposit a second ceramic-containing layer, capable of conducting ions, on the second surface of the microporous ion-conducting polymeric layer, wherein the second ceramic-containing layer consists essentially of aluminum oxide and/or lithium aluminum oxide, is a binder-free ceramic-containing layer, and has a thickness in a range from about 1 nanometer to about 1,000 nanometers; and then reacting an evaporated second material with a second reactive gas and/or plasma to deposit a third ceramic-containing layer, capable of conducting ions, on the second ceramic-containing layer, wherein the third ceramic-containing layer comprises silicon oxide, is binder-free and has a thickness in a range from about 1 nanometer to about 100 nanometers. 2. The method of claim 1 , wherein the first ceramic-containing layer comprises a material selected from porous aluminum oxide, porous-ZrO 2 , porous-HfO 2 , porous-SiO 2 , porous-MgO, porous-TiO 2 , porous-Ta 2 O 5 , porous-Nb 2 O 5 , porous-LiAlO 2 , porous-BaTiO 3 , ion-conducting garnet, anti-ion-conducting perovskites, or combinations thereof. 3. The method of claim 1 , wherein the first ceramic-containing layer comprises a binder. 4. The method of claim 1 , wherein the first material to be deposited is a metallic material comprising aluminum. 5. The method of claim 1 , wherein the first material to be evaporated is a metal oxide comprising lithium aluminum oxide. 6. The method of claim 1 , further comprising reacting an evaporated third material with a third reactive gas and/or plasma to deposit a fourth ceramic-containing layer, capable of conducting ions, on the third ceramic-containing layer, wherein the fourth ceramic-containing layer comprises zirconium oxide, is binder-free and has a thickness in a range from about 1 nanometer to about 100 nanometers. 7. The method of claim 1 , further comprising exposing the microporous ion-conducting polymeric layer to a cooling process prior to exposing the first material to the evaporation process. 8. The method of claim 7 , wherein the cooling process cools the microporous ion-conducting polymeric layer to a temperature of about −20° C. to about 22° C. 9. The method of claim 8 , wherein the cooling process cools the microporous ion-conducting polymeric layer to a temperature of about −10° C. to about 0° C. 10. The method of claim 1 , wherein the reactive gas is an oxygen-containing gas selected from oxygen (O 2 ), ozone, oxygen radicals, or combinations thereof. 11. The method of claim 1 , wherein the plasma is an oxygen-containing plasma. 12. The method of claim 1 , wherein the evaporation process is a thermal evaporation process or an electron beam evaporation process. 13. The method of claim 1 , wherein the evaporation process comprises exposing the first material to be deposited to a temperature of about 1,300° C. to about 1,600° C. 14. The method of claim 1 , wherein the microporous ion-conducting polymeric comprises polyethylene or polypropylene. 15. The method of claim 1 , wherein the microporous ion-conducting polymeric has a thickness of about 1 μm to about 25 μm. 16. A method of forming a separator for a battery, comprising: exposing a microporous ion-conducting polymeric layer to a first cooling process; exposing a first material to be deposited on the microporous ion-conducting polymeric layer positioned in a processing region to an evaporation process, wherein the microporous ion-conducting polymeric layer has: a first surface; a second surface opposing the first surface; and a first ceramic-containing layer, capable of conducting ions, formed on the first surface, wherein the first ceramic-containing layer is prepared by a slot-die technique or a doctor blade technique and has a thickness in a range from about 1,000 nanometers to about 5,000 nanometers; reacting the evaporated first material with a reactive gas and/or plasma to deposit a second ceramic-containing layer, capable of conducting ions, on the second surface of the microporous ion-conducting polymeric layer, wherein the second ceramic-containing layer consists essentially of aluminum oxide and/or lithium aluminum oxide; exposing the microporous ion-conducting polymeric layer to a second cooling process after depositing the second ceramic-containing layer; and then reacting an evaporated second material with a second reactive gas and/or plasma to deposit a third ceramic-containing layer, capable of conducting ions, on the second ceramic-containing layer, wherein the third ceramic-containing layer comprises silicon oxide and is binder-free. 17. The method of claim 16 , wherein the second ceramic-containing layer has a thickness in a range from about 1 nanometer to about 1,000 nanometers and the third ceramic-containing layer has a thickness in a range from about 1 nanometer to about 100 nanometers. 18. The method of claim 16 , further comprising exposing the microporous ion-conducting polymeric layer to a third cooling process after depositing the third ceramic-containing layer. 19. The method of claim 18 , further comprising reacting an evaporated third material with a reactive gas and/or plasma to deposit a fourth ceramic-containing layer, capable of conducting ions, on the third ceramic-containing layer, wherein the fourth ceramic-containing layer comprises zirconium oxide, is binder-free, and has a thickness in a range from about 1 nanometer to about 100 nanometers. 20. A method of forming a separator for a battery, comprising: exposing a first material to be deposited on a microporous ion-conducting polymeric layer positioned in a processing region to an evaporation process, wherein the microporous ion-conducting polymeric layer has: a first surface; a second surface opposing the first surface; and a first ceramic-containing layer, capable of conducting ions, formed on the first surface, wherein the first ceramic-containing layer is prepared by a slot-die technique or a doctor blade technique and has a thickness in a range from about 1,000 nanometers to about 5,000 nanometers; reacting the evaporated first material with a reactive gas and/or plasma to deposit a second ceramic-containing layer, capable of conducting ions, on the second surface of the microporous ion-conducting polymeric layer, wherein the second ceramic-containing layer comprises porous aluminum oxide, is a binder-free ceramic-containing layer, and has a thickness in a range from about 1 nanometer to about 1,000 nanometers; then reacting an evaporated second material with a second reactive gas and/or plasma to deposit a third ceramic-containing layer, capable of conducting ions, on the second ceramic-containing layer, wherein the third ceramic-containing layer comprises porous silicon oxide, is binder-free and has a thickness in a range from about 1 nanometer to about
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