Lithium transition metal composite oxide as a positive electrode active material for rechargeable lithium secondary batteries

Patent metadata

Field	Value
Publication number	US-12002952-B2
Application number	US-201917041266-A
Country	US
Kind code	B2
Filing date	Mar 6, 2019
Priority date	Mar 28, 2018
Publication date	Jun 4, 2024
Grant date	Jun 4, 2024

Abstract

A powderous positive electrode material for lithium ion batteries, comprising crystalline lithium transition metal-based oxide particles having a general formula Li1+a ((Niz (Ni0.5Mn0.5)y Cox)1−k Ak)1−a O2, wherein A is a dopant, −0.030≤a≤0.025, 0.10≤x≤0.40, 0.25≤z≤0.52, x+y+z=1 and k≤0.01, wherein the crystalline powder has a crystallite size less than 33 nm as determined by the Scherrer equation based on the peak of the (104) plane obtained from the X-ray diffraction pattern using a Cu K α radiation source, and wherein the molar ratio MR(Ni) of Ni versus the total transition metal content in a cross section of a particle is higher in the surface area than in the center area of the particle, as determined by EDS analysis.

First claim

The invention claimed is:

1. A powderous positive electrode material for lithium ion batteries, comprising crystalline lithium transition metal-based oxide particles having a general formula Li 1+a ((Ni z (Ni 0.5 Mn 0.5 ) y Co x ) 1−k A k ) 1−a O 2 , wherein A is a dopant, −0.030≤a≤0.025, 0.10≤x≤0.40, 0.25≤z≤0.52, x+y+z=1 and k≤0.01, wherein the crystalline powder has a crystallite size less than 33 nm as determined by the Scherrer equation based on the peak of the (104) plane obtained from the X-ray diffraction pattern using a CuKα radiation source, and wherein MR(SC—Ni) is between 1.04 and 1.10, MR(SC—Ni) being a normalized molar ratio MR(Ni) of a particle, wherein EDS analysis is performed at sample locations having the same volume and being located along an EDS scan line crossing a center of the particle on a cross-section of the particle, wherein a first sample location (D1) is at a surface of a first particle edge, a second sample location (D3) is at a center of the particle, and a third sample location (D5) is at a surface of a second particle edge, opposite the first particle edge, and wherein MR(SC—Ni) is obtained by dividing the sum of the value of MR(Ni) measured in a volume at the first sample location and the value of MR(Ni) measured in a volume at the third sample location, by two times the value of MR(Ni) measured in a volume at the second sample location.

2. The powderous positive electrode material of claim 1 , wherein 0.18≤x≤0.22, 0.42≤z≤0.52 and 1.075<z/y<1.625.

3. The powderous positive electrode material of claim 1 , having a crystallite size between 25.0 and 30.5 nm.

4. The powderous positive electrode material of claim 1 , having a carbon content ≤400 ppm.

5. The powderous positive electrode material of claim 1 , comprising particles having a coating comprising a LiNaSO 4 secondary phase, wherein the LiNaSO 4 secondary phase is present in a content between 0.15 and 5 wt % with respect to the total weight of the powder and the secondary phase further comprises up to 1 wt % of one or more of Al 2 O 3 , LiAlO 2 , LiF, Li 3 PO 4 , MgO or Li 2 TiO 3 .

6. The powderous positive electrode material of claim 1 , wherein the dopant A is selected from the group consisting of one or more of Al, Ca, W, B, Si, Ti, Mg and Zr.

7. The powderous positive electrode material of claim 1 , wherein the powder has a particle size distribution with a D50 of 8 to 12 μm.

8. A method for preparing the powderous positive electrode material of claim 1 , the method comprising the steps of:
providing a M′-based precursor prepared from the co-precipitation of metal salts with a base; wherein the M′-based precursor comprises particles having a molar ratio MR(Ni) of Ni versus the total transition metal content in a cross section of a particle that is higher in a surface area than in a center area of the particle, as determined by EDS analysis,
mixing the M′-based precursor with one of LiOH, Li 2 O or LiOH·H 2 O, thereby obtaining a first mixture, whereby the Li to transition metal ratio in the first mixture is between 0.65 and 0.97,
sintering the first mixture in an oxidizing atmosphere in a rotary kiln at a temperature between 650 and 850° C., for a time between ⅓ and 3 hrs, thereby obtaining a lithium deficient precursor powder,
mixing the lithium deficient precursor powder with one of LiOH, Li 2 O or LiOH·H 2 O, thereby obtaining a second mixture, and
sintering the second mixture in an oxidizing atmosphere at a temperature between 750 and 800° C., for a time between 6 and 36 hrs.

9. The method according to claim 8 , wherein the M′-based precursor has a particle size distribution with a D50 of 10 to 15 μm.

Assignees

• Umicore Nv
• Umicore Korea Ltd

Inventors

• Kim Jihye
• Paulsen Jens
• Park Areum
• Gil Hee-Sung

Classifications

• H01M4/525 Primary

  of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title

• H01M4/0471 Primary

  involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title

• H01M4/133

  Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx · CPC title

• H01M4/505

  of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title

• H01M10/0525

  Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title