Cathode active material for lithium secondary battery, method of manufacturing the same and lithium secondary battery including the same
US-2023187618-A1 · Jun 15, 2023 · US
US12489111B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12489111-B2 |
| Application number | US-202217708267-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 30, 2022 |
| Priority date | Apr 2, 2021 |
| Publication date | Dec 2, 2025 |
| Grant date | Dec 2, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A composite cathode active material for an all-solid-state battery including a sulfide solid electrolyte, a preparation method thereof, a cathode layer for an all-solid-state battery, and an all-solid-state battery including the cathode layer, the composite cathode active material including a secondary particle including a plurality of primary particles; and a buffer layer on a surface of the secondary particle, wherein the secondary particle includes a nickel lithium transition metal oxide represented by Formula 1 (Li a Ni 1-b M b O 2 ), the buffer layer includes a first buffer layer adjacent to a surface of the secondary particle and including an oxide represented by Formula 2 (Li x A y O z ); and a second buffer layer including an oxide represented by Formula 3 (Li x E y O z ).
Opening claim text (preview).
What is claimed is: 1 . A composite cathode active material for an all-solid-state battery that includes a sulfide solid electrolyte, the composite cathode active material comprising: a secondary particle including a plurality of primary particles; and a buffer layer on a surface of the secondary particle, wherein: the secondary particle includes a nickel lithium transition metal oxide represented by Formula 1, the buffer layer includes: a first buffer layer adjacent to a surface of the secondary particle and including an oxide represented by Formula 2-1; and a second buffer layer including an oxide represented by Formula 3, an amount of the oxide represented by Formula 2-1 is in a range of about 0.01 mol % to about 0.5 mol %, an amount of the oxide represented by Formula 3 is in a range of about 0.01 mol % to about 0.5 mol %, and a total amount of the oxide represented by Formula 2-1 and the oxide represented by Formula 3 is in a range of about 0.2 mol % to about 0.5 mol %, all mol % being based on 100 mol % of the composite cathode active material, Li a Ni 1-b M b O 2 Formula 1 in Formula 1, a and b satisfy the following relations: 0.95≤a≤1.10, 0<b<0.5, and M is cobalt (Co), manganese (Mn), aluminum (Al), or a combination thereof, Li x Ti y O z Formula 2-1 in Formula 2-1, x, y, and z satisfy the following relations: 0≤x≤3, 0<y≤2, 0<z≤4, and Li x E y O z Formula 3 in Formula 3, x, y, and z satisfy the following relations: 0≤x≤3, 0<y≤2, 0<z≤4, and E is Si, Zr, Nb, B, La, Mo, P, Mg, Al, Zn, or a combination thereof. 2 . The composite cathode active material as claimed in claim 1 , wherein: the oxide represented by Formula 3 is represented by Formula 3-1: Li x Zr y O z Formula 3-1 in Formula 3-1, x, y, and z satisfy the following relations: 0≤x≤3, 0<y≤2, and 0<z≤4. 3 . The composite cathode active material as claimed in claim 1 , wherein the oxide represented by Formula 2-1 is Li 2 TiO 3 , or a combination thereof. 4 . The composite cathode active material as claimed in claim 1 , wherein the oxide represented by Formula 3 is Li 2 ZrO 3 , ZrO 2 , La 2 O 3 , Nb 2 O 3 , B 2 O 3 , SiO 2 , MgO, Al 2 O 3 , ZnO, Li 3 PO 4 , or a combination thereof. 5 . The composite cathode active material as claimed in claim 1 , wherein: the nickel lithium transition metal oxide represented by Formula 1 has a layered crystal structure, and the oxide represented by Formula 2-1 and the oxide represented by Formula 3 each independently have a triclinic crystal structure or a monoclinic crystal structure. 6 . The composite cathode active material as claimed in claim 1 , wherein, according to inductively coupled plasma (ICP) analysis for the composite cathode active material, the composite cathode active material includes: Ti in an amount of about 0.01 mol % to about 0.5 mol %, and Zr in an amount of about 0.01 mol % to about 0.5 mol %, all mol % being based on 100 mol % of the composite cathode active material. 7 . The composite cathode active material as claimed in claim 1 , wherein: the nickel lithium transition metal represented by Formula 1 is represented by Formula 1-1, a compound represented by Formula 1-2, or a combination thereof: Li a Ni 1-b1-b2 Co b1 Mn b2 O 2 Formula 1-1 in Formula 1-1, a, b1, and b2 satisfy the following relations: 0.95≤a≤1.10, 0<b1+b2<0.5, 0<b1<0.2, and 0<b2<0.2, and Li a Ni 1-b1-b2 Co b1 Al b2 O 2 Formula 1-2 in Formula 1-2, a, b1, and b2 satisfy the following relations: 0.95≤a≤1.10, 0<b1+b2<0.5, 0<b1<0.2, and 0<b2<0.05. 8 . The composite cathode active material as claimed in claim 1 , wherein: a total thickness of the buffer layer is in a range of about 5 nm to about 50 nm, a thickness of the first buffer layer is in a range of about 1 nm to about 20 nm, a thickness of the second buffer layer is in a range of about 1 nm to about 20 nm, and a thickness ratio of the first buffer layer to the second buffer layer is in a range of about 0.1 to about 10. 9 . The composite cathode active material as claimed in claim 1 , wherein the first buffer layer and the second buffer layer are conformal coating layers. 10 . A cathode layer for an all-solid-state battery, the cathode layer comprising the composite cathode active material as claimed in claim 1 . 11 . An all-solid-state battery, comprising: a cathode layer; an anode layer; and a sulfide solid electrolyte layer therebetween, wherein the cathode layer includes the composite cathode active material as claimed in claim 1 . 12 . The all-solid-state battery as claimed in claim 11 , wherein the sulfide solid electrolyte is Li 2 S—P 2 S 5 , Li 2 S—P 2 S 5 —LiX, in which X is a halogen element, Li 2 S—P 2 S 5 —Li 2 O, Li 2 S—P 2 S 5 —Li 2 O—LiI, Li 2 S—SiS 2 , Li 2 S—SiS 2 —LiI, Li 2 S—SiS 2 —LiBr, Li 2 S—SiS 2 —LiCl, Li 2 S—SiS 2 —B 2 S 3 —LiI, Li 2 S—SiS 2 —P 2 S 5 —LiI, Li 2 S—B 2 S 3 , Li 2 S—P 2 S 5 -ZmSn, in which m and n are positive numbers, and Z is germanium (Ge), Zn, or gallium (Ga), Li 2 S—GeS 2 , Li 2 S—SiS 2 —Li 3 PO 4 , Li 2 S—SiS 2 -Li p M O q , in which p and q are positive numbers, and M is P, Si, Ge, B, Al, Ga, or indium (In), Li 7-x PS 6-x Cl x , in which 0≤x≤2, Li 7-x PS 6-x Br x , in which 0≤x≤2, and Li 7-x PS 6-x I x , in which 0≤x≤2. 13 . The all-solid-state battery as claimed in claim 11 , wherein the sulfide solid electrolyte is an argyrodite-type solid electrolyte including Li 6 PS 5 Cl, Li 6 PS 5 Br, or Li 6 PS 5 I. 14 . The all-solid-state battery as claimed in claim 11 , wherein: the anode layer includes an anode current collector and a first anode active material layer, a second anode active material layer is on the first anode active material layer, between the anode current collector and the first anode active material layer, or a combination thereof, and the second anode active material layer includes lithium or a lithium alloy. 15 . The all-solid-state battery as claimed in claim 11 , wherein: the anode layer includes an anode current collector and a first anode active material layer, and the all-solid-state battery further includes a carbon layer between the first anode active material layer and the solid electrolyte layer. 16 . A method of preparing a composite cathode active material for an all-solid-state battery as claimed in claim 1 , the method comprising: mixing a nickel lithium transition metal oxide represented by Formula 1, a precursor of an oxide represented by Formula 2-1, a lithium precursor, an organic solvent, and water to obtain a first mixture; adding, to the first mixture, a precursor of an oxide represented by Formula 3 and an organic solvent to obtain a second mixture and perform a reaction thereon; and drying and heat-treating the reaction product to obtain the composite cathode active material: Li a Ni 1-b M b O 2 Formula 1 wherein, in Formula 1, a and b satisfy the following relations: 0.95≤a≤1.10, 0<b<0.5, and M is cobalt (Co), manganese (Mn), aluminum (Al), or a combination thereof, Li x Ti y O z Formula 2-1 wherein, in Formula 2-1, x, y, and z satisfy the following relations: 0≤x≤3, 0<y≤2, 0<z≤4, and Li x E y O z Formula 3 wherein, in Formula 3, x, y, and z satisfy the following relations: 0≤x≤3, 0<y≤2, 0<z≤4, and E is Si, Zr, Nb, B, La, Mo, P, or a combination thereof. 17 . The method as claimed in claim 16 , wherein the heat-treating is performed at a temperature in a range of about 250° C. to about 500° C. 18 . The method as claimed in claim 16 , wherein the
Halides · CPC title
Solid materials · CPC title
Selection of inactive substances as ingredients for active masses, e.g. binders, fillers · CPC title
Alloys based on lithium · CPC title
Lithium (H01M4/405 takes precedence) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.