Positive-electrode material for lithium ion secondary battery, method for producing the same, and lithium ion secondary battery
US-2017358799-A1 · Dec 14, 2017 · US
US11799078B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11799078-B2 |
| Application number | US-201815860901-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 3, 2018 |
| Priority date | Jun 30, 2017 |
| Publication date | Oct 24, 2023 |
| Grant date | Oct 24, 2023 |
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A composite cathode active material and a cathode and a lithium battery including the composite cathode active material. The composite cathode active material has a core including a plurality of primary particles including a nickel-containing first lithium transition metal oxide having a layered crystal structure; a grain boundary disposed between adjacent primary particles of the plurality of primary particles; and a shell on the core, the shell including a second lithium transition metal oxide having a spinel crystal structure, wherein the grain boundary includes a first composition having a spinel crystal structure.
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What is claimed is: 1. A composite cathode active material comprising: a core comprising a plurality of primary particles comprising a nickel-containing first lithium transition metal oxide having a layered crystal structure, and a grain boundary between adjacent primary particles of the plurality of primary particles; and a shell on the core, the shell comprising a second lithium transition metal oxide having a spinel crystal structure, wherein the grain boundary comprises a first composition having a spinel crystal structure, wherein a concentration of manganese in the grain boundary is greater than a concentration of manganese in the primary particles, wherein the second lithium transition metal oxide is represented by Formula 7: Li a Mn b Co c M5′ d O 4 Formula 7 wherein, in Formula 7, M5′ comprises vanadium, chromium, iron, zirconium, rhenium, aluminum, boron, germanium, ruthenium, tin, titanium, niobium, molybdenum, or platinum, 0.9≤a≤1.1, 0<b<2.0, 0<c<2.0, 0≤d<0.1, and b+c+d=2. 2. The composite cathode active material of claim 1 , wherein the first composition comprises at least one transition metal other than nickel, and wherein a concentration of the at least one transition metal other than nickel in the grain boundary is greater than a concentration of the at least one transition metal other than nickel within the plurality of primary particles. 3. The composite cathode active material of claim 2 , wherein the least one transition metal other than nickel comprises Mn, Co, Fe, or a combination thereof. 4. The composite cathode active material of claim 1 , wherein at least 50% of the grain boundaries between the adjacent primary particles of the plurality of primary particles comprise the first composition. 5. The composite cathode active material of claim 1 , wherein the grain boundary is substantially rectilinear in cross-section within the core. 6. The composite cathode active material of claim 1 , wherein the grain boundary is arranged in a direction which is parallel to a surface of an adjacent primary particle of the adjacent primary particles, and wherein the direction of the grain boundary is different from a direction of a tangent of a nearest surface of the core. 7. The composite cathode active material of claim 1 , wherein the core comprises a first grain boundary and a second grain boundary, wherein the first grain boundary and the second grain boundary are located directly on a same primary particle of the plurality of primary particles, and wherein the first grain boundary and the second grain boundary intersect at an angle determined by a shape of the same primary particle. 8. The composite cathode active material of claim 1 , wherein the core comprises a plurality of grain boundaries that are adjacent to the plurality of primary particles, wherein the plurality of grain boundaries are each arranged in a direction parallel to a surface of an adjacent primary particle, and wherein grain boundaries of the plurality of grain boundaries are arranged in different directions than each other. 9. The composite cathode active material of claim 1 , wherein a plurality of grain boundaries have an average length in a range of about 50 nanometers to about 1000 nanometers and an average thickness in a range of about 1 nanometers to about 200 nanometers, wherein a direction of the length is parallel to a surface of an adjacent primary particle, and wherein a direction of the thickness is perpendicular to the surface of the adjacent primary particle. 10. The composite cathode active material of claim 1 , wherein the spinel crystal structure has cubic symmetry. 11. The composite cathode active material of claim 10 , wherein the spinel crystal structure belongs to an Fd 3 m space group. 12. The composite cathode active material of claim 1 , wherein the grain boundary further comprises a second composition, and wherein the second composition comprises a lithium transition metal oxide, a lithium-free transition metal oxide, or a combination thereof. 13. The composite cathode active material of claim 12 , wherein the second composition has an amorphous structure, a layered structure, a spinel structure, a polyvalent anion crystal structure, or a combination thereof. 14. The composite cathode active material of claim 1 , wherein the nickel-containing first lithium transition metal oxide is represented by Formula 1: Li a MO 2 Formula 1 wherein, in Formula 1, M comprises nickel and at least one non-nickel Group 4 to Group 13 element, an amount of nickel is in a range of about 70 mole percent to less than about 100 mol percent, based on a total content of M, and 0.9≤a≤1.1. 15. The composite cathode active material of claim 1 , wherein the nickel-containing first lithium transition metal oxide is represented by Formula 2: Li a Ni b M1 c M2 d M3 e O 2 Formula 2 wherein, in Formula 2, M1, M2, and M3 are different and each independently comprises manganese, vanadium, chromium, iron, cobalt, zirconium, rhenium, aluminum, boron, germanium, ruthenium, tin, titanium, niobium, molybdenum, or platinum; and 0.9≤a≤1.1, 0.7<b<1.0, 0<c<0.3, 0<d<0.3, 0≤e<0.1, and b+c+d+e=1. 16. The composite cathode active material of claim 1 , wherein the nickel-containing first lithium transition metal oxide is represented by Formula 4c: a Li 2 MnO 3 .(1− a )LiM″O 2 Formula 4c wherein, in Formula 4c, M″ comprises nickel and cobalt, manganese, vanadium, chromium, iron, zirconium, rhenium, aluminum, boron, germanium, ruthenium, tin, titanium, niobium, molybdenum, platinum, or a combination thereof, and 0<a<1. 17. The composite cathode active material of claim 1 , wherein a thickness of the shell is about 300 nanometers or less. 18. The composite cathode active material of claim 1 , wherein a sum of an amount of the second lithium transition metal oxide and an amount of the first composition is about 10 weight percent or less, based on a total weight of the composite cathode active material. 19. The composite cathode active material of claim 1 , wherein a crack growth of a cross-section of the composite cathode active material after 50 charge/discharge cycles of a lithium battery comprising the composite cathode active material is about 6% or less, and wherein the crack growth is defined by Equation 1: Crack growth (%)=[(pore area of cross-section of composite cathode active material particles after 50 charge/discharge cycles−pore area of cross-section of composite cathode active material particles before charge/discharge cycles)/pore area of cross-section of composite cathode active material particles before charge/discharge cycles]×100% Equation 1. 20. A cathode comprising the composite cathode active material of claim 1 . 21. A lithium battery comprising: the cathode of claim 20 ; an anode; and an electrolyte between the cathode and the anode. 22. A method of preparing a composite cathode active material, the method comprising: providing a solution comprising a precursor of a second lithium transition metal oxide having a spinel crystal structure; mixing the solution and a nickel-containing first lithium transition metal oxide having a layered crystal structure to prepare a mixture; drying the mixture to prepare a dried product; and heat-treating the dried product to prepare the composite cathode active material of claim 1 . 23. The method of claim 22 , wherein an amount of the solution in the mix
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