Method for producing surface-treated oxide particles, and oxide particles produced by said production method
US-2016301063-A1 · Oct 13, 2016 · US
US12074325B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12074325-B2 |
| Application number | US-202117365644-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 1, 2021 |
| Priority date | Dec 21, 2020 |
| Publication date | Aug 27, 2024 |
| Grant date | Aug 27, 2024 |
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An all-solid-state battery includes: an anode current collector; a lithium storage layer including a first layer located at an electrolyte-layer side and a second layer located at an anode current collector side, having a higher porosity than the first layer, and including an interface portion and a core portion, which is a remaining portion other than the interface portion; an electrolyte layer; and a cathode layer, wherein the anode current collector, the lithium storage layer, the electrolyte layer, and the cathode layer are sequentially laminated, and the interface portion is in contact with the first layer and has a higher binder content per unit volume than the core portion.
Opening claim text (preview).
What is claimed is: 1. An anodeless all-solid-state battery, comprising: an anode current collector; a lithium storage layer comprising: a first layer located at an electrolyte-layer side, and a second layer located at an anode current collector side, having a higher porosity than the first layer, and including an interface portion and a core portion, which is a remaining portion other than the interface portion; an electrolyte layer; and a cathode layer, wherein the anode current collector, the lithium storage layer, the electrolyte layer, and the cathode layer are sequentially laminated, and wherein the interface portion is in contact with the first layer and has a higher binder content per unit volume than the core portion. 2. The anodeless all-solid-state battery of claim 1 , wherein the lithium storage layer comprises a carbon material and a metal powder. 3. The anodeless all-solid-state battery of claim 2 , wherein the carbon material comprises at least one selected from a group consisting of a particulate carbon material, a fibrous carbon material, and combinations thereof. 4. The anodeless all-solid-state battery of claim 3 , wherein the particulate carbon material comprises at least one selected from a group consisting of carbon black, graphitizable carbon, non-graphitizable carbon, and combinations thereof. 5. The anodeless all-solid-state battery of claim 3 , wherein the fibrous carbon material comprises at least one selected from a group consisting of carbon nanofibers, carbon nanotubes, vapor-grown carbon fibers, and combinations thereof. 6. The anodeless all-solid-state battery of claim 2 , wherein the metal powder comprises at least one selected from a group consisting of aluminum (Al), zinc (Zn), indium (In), silver (Ag), gold (Au), magnesium (Mg), silicon (Si), bismuth (Bi), germanium (Ge), platinum (Pt), antimony (Sb), and combinations thereof. 7. The anodeless all-solid-state battery of claim 1 , wherein a thickness ratio of the first layer and the second layer is 1:0.5-2. 8. The anodeless all-solid-state battery of claim 1 , wherein the first layer has a porosity of 5% or less. 9. The anodeless all-solid-state battery of claim 1 , wherein the second layer has a porosity of 5% to 50%. 10. The anodeless all-solid-state battery of claim 1 , wherein the first layer comprises a polyvinylidene fluoride (PVDF) binder. 11. The anodeless all-solid-state battery of claim 1 , wherein the second layer comprises a polyvinylidene fluoride (PVDF) binder and a nitrile butadiene rubber (NBR) binder. 12. The anodeless all-solid-state battery of claim 1 , wherein the interface portion has a higher nitrile butadiene rubber binder content per unit volume than the core portion. 13. The anodeless all-solid-state battery of claim 1 , wherein a thickness of the interface portion is 0.1% to 10% of a thickness of the second layer. 14. A method of manufacturing an anodeless all-solid-state battery, the method comprising: preparing a first binder solution comprising a polyvinylidene fluoride (PVDF) binder and a first solvent; preparing a second binder solution comprising a nitrile butadiene rubber (NBR) binder and a second solvent different from the first solvent; preparing a first slurry comprising a carbon material, a metal powder, and the first binder solution; preparing a second slurry by adding the second binder solution to the first slurry; forming a second layer by applying the second slurry on a substrate; forming a first layer by applying the first slurry on the second layer and obtaining a lithium storage layer comprising the first layer and the second layer; and forming an all-solid-state battery by sequentially laminating an anode current collector, the lithium storage layer, an electrolyte layer, and a cathode layer, wherein: the first layer of the lithium storage layer is located at an electrolyte-layer side and the second layer, which has a higher porosity than the first layer, is located at an anode-current-collector side, the second layer comprises an interface portion, which is in contact with the first layer, and a core portion, which is a remaining portion other than the interface portion, and the interface portion has a higher binder content per unit volume than the core portion. 15. The method of claim 14 , wherein the second solvent has a lower density than the first solvent, has a higher solubility of a nitrile butadiene rubber (NBR) binder than a solubility of a polyvinylidene fluoride (PVDF) binder, or has a higher vapor pressure than the first solvent. 16. The method of claim 14 , wherein the first solvent comprises N-methyl-2-pyrrolidone (NMP) and the second solvent comprises hexyl butyrate. 17. The method of claim 14 , wherein the second slurry has a lower solid content than the first slurry. 18. The method of claim 14 , wherein a solid content of the first slurry is 4 wt % to 10 wt %. 19. The method of claim 14 , wherein a solid content of the second slurry is 3 wt % or less. 20. The method of claim 14 , further comprising, after applying the second slurry on the substrate, drying or standing the second layer, and allowing the second binder solution to rise to a surface of the second layer.
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