Solid State Battery System Usable at High Temperatures and Methods of Use and Manufacture Thereof
US-2020358086-A1 · Nov 12, 2020 · US
US11791465B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11791465-B2 |
| Application number | US-202217848627-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 24, 2022 |
| Priority date | Feb 19, 2019 |
| Publication date | Oct 17, 2023 |
| Grant date | Oct 17, 2023 |
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Methods of making a sintered electrode comprise forming a slurry including 40 wt % to 75 wt % of a powder comprising a chalcogenide and at least one of an alkali metal or an alkaline earth metal, 1 wt % to 10 wt % of a binder, and 30 wt % to 50 wt % of a solvent. Methods include casting the slurry into a green tape. Methods include drying the green tape to form a dried green tape by removing at least a portion of the solvent. The dried green tape includes at most 10 wt % of organic material in the dried green tape. Methods include sintering the dried green tape at a temperature from 500° C. to 1350° C. for no more than 60 minutes to form the sintered electrode.
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What is claimed is: 1. A method of making a sintered electrode comprising: forming a slurry, as wt % of the slurry, comprising: 40 wt % to 75 wt % of a powder comprising a chalcogenide and at least one of an alkali metal or an alkaline earth metal; 1 wt % to 10 wt % of a binder; and 30 wt % to 50 wt % of a solvent, wherein the solvent leaches less than 1 ng/L of the at least one of the alkali metal or the alkaline earth metal; casting the slurry into a green tape; drying the green tape to form a dried green tape by removing at least a portion of the solvent, the dried green tape comprising at most 10 wt % of organic material in the dried green tape; and sintering the dried green tape at a temperature from 500° C. to 1350° C. for no more than 60 minutes to form the sintered electrode comprising a first surface and a second surface opposite the first surface. 2. The method of claim 1 wherein the powder comprises lithium. 3. The method of claim 1 , wherein the solvent leaches less than 0.1 ng/L of the at least one of the alkali metal or the alkaline earth metal. 4. The method of claim 1 , wherein the solvent is a non-polar solvent comprising a dielectric constant at 20° C. of less than 20. 5. The method of claim 1 , wherein the solvent comprises 1-methoxy-2-propanyl acetate (MPA). 6. The method of claim 1 , wherein the sintered electrode comprises a lithium chalcogenide selected from a group consisting of: lithium cobaltite (LCO), lithium manganite spinel (LMO), lithium nickel cobalt aluminate (NCA), lithium iron phosphate (LFP), lithium cobalt phosphate (LCP), lithium titanate, lithium niobium tungstate, lithium nickel manganate, lithium titanium sulfide (LiTiS 2 ), and combinations thereof. 7. The method of claim 6 , wherein the slurry comprises an approximately stoichiometric amount of lithium for the lithium chalcogenide of the sintered electrode. 8. The method of claim 6 , wherein the slurry is approximately free of LiCO 3 . 9. The method of claim 1 , wherein the dried green tape comprises a component that undergoes an endothermic reaction from 200° C. to 300° C. during the sintering. 10. The method of claim 1 , wherein the binder comprises polyvinyl butyral, an acrylic polymer, polyvinyl alcohol, or combinations thereof. 11. The method of claim 1 , wherein the sintered electrode comprises a thickness between the first surface and the second surface from 2 micrometers to 100 micrometers. 12. The method of claim 1 , wherein a cross-sectional area of the first surface is at least 3 cm 2 . 13. The method of claim 1 , wherein the sintered electrode has an open porosity from 0.1% to 30%. 14. The method of claim 13 , wherein the open porosity comprises a pore phase that is continuous within a solid phase of the sintered electrode. 15. The method of claim 1 , wherein the drying comprises heating the green tape at a temperature of 60° C. to 80° C. 16. The method of claim 1 , wherein the sintering occurs for less than 45 minutes. 17. The method of claim 1 , wherein a charging capacity of a battery comprising the sintered electrode as a cathode is maintained at greater than 135 mA·hr/g after twenty charge-discharge cycles at a C/5 rate and 4.3 V charging potential, wherein the cathode is unground and unpolished. 18. The method of claim 1 , wherein the sintered electrode comprises an average grain size from 100 nanometers to 1000 nanometers. 19. A method of making a battery comprising: the method of claim 1 , the sintered electrode comprising a cathode, the sintered electrode is unground and unpolished; disposing a current collector on the first surface of the sintered electrode; contacting the sintered electrode with an electrolyte, the electrolyte penetrating a porous region of the sintered electrode; and disposing an anode on the electrolyte.
Chalcogenides or intercalation compounds thereof · CPC title
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
Solid materials · CPC title
Physical characteristics, e.g. porosity, surface area · CPC title
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