Granted Patent B2

US 12,338,136 · App. 18/400,498 · Granted Jun 24, 2025

Inventors: Hang Zhang (Beijing, CN); Yafei Liu (Beijing, CN); Yuqiang Jin (Beijing, CN); Xuequan Zhang (Beijing, CN); Yanbin Chen (Beijing, CN)

Assignee: Beijing Easpring Material Technology Co., Ltd.

C01G53/42H01M10/0525C01P2004/03C01P2004/61C01P2004/62C01P2004/84C01P2006/11C01P2006/16C01P2006/40

Abstract

Claims (81)

1. A cathode material, wherein the cathode material is composed of secondary particles agglomerated by primary particles; wherein individual secondary particle comprises an inner core structure, a middle layer, and a shell layer, in this order, along a direction from a center to a surface of the individual secondary particle; wherein the middle layer is distributed in a circular ring shape, and an inner radius r1 of the circular ring-shaped middle layer and a radius R of the secondary particle satisfy the following relation:

r1/R is more than 0.35 and less than 1;

wherein the secondary particle has a structure of close packing of an inner core structure, loose and porous middle layer, and close packing of the shell layer;

wherein a porosity of the middle layer is greater than or equal to 20%;

wherein an average pore diameter of the middle layer is less than or equal to 1 μm; and

the porosity of the middle layer is determined by a ratio of a pore area in an annular area of the middle layer to a circular ring area of the middle layer in the scanning electron microscope (SEM) image showing a cross-section of the secondary particles of the cathode material;

wherein the cathode material has a composition represented by formula I:

Li 1+a Ni x M y M′ z O 2   formula I,

wherein −0.1≤a≤0.2, 0.5≤x≤1, 0≤y≤0.5, 0≤z≤0.1, and x+y+z=1; M is at least one element selected from the group consisting of Mn, Al, Fe, and Mg; M′ is at least one element selected from the group consisting of B, Mg, Al, Ca, Sr, Ba, Zr, Ti, Ce, Y, W, La, Nb, Ta, Zn, Co, and Mo; and

wherein the cathode material is a lamellar cobalt-free cathode material.

2. The cathode material of claim 1 , wherein the r1/R is within a range of 0.4-0.7;

and/or, the middle layer exhibits a reticulate loose and porous structure;

and/or, the porosity of said middle layer is within a range of 25-35%;

and/or, the average pore diameter of said middle layer is within a range of 300-500 nm.

3. The cathode material of claim 1 , wherein an outer radius r2 of the circle ring-shaped middle layer and the radius R of the secondary particles satisfy the following relation:

0.5< r 2/ R< 1;

and/or, r2/R−r1/R is within a range of 0.1-0.5.

4. The cathode material of claim 3 , wherein the r2/R is within a range of 0.7-0.9;

and/or, r2/R−r1/R is within a range of 0.2-0.4.

5. The cathode material of claim 1 , wherein the secondary particles have an average particle diameter D 50 within a range of 8-20 μm;

and/or, the primary particles of the inner core structure are closely packed in a spherical and/or spheroidal shape;

and/or, a length-diameter ratio L1 of the primary particles of the inner core structure satisfies: 1≤L1≤2;

and/or, the primary particles of the shell layer are radially and closely packed;

and/or, a length-diameter ratio L2 of the primary particles of the shell layer satisfies: 2.5≤L2≤5.

6. The cathode material of claim 1 , wherein a length-diameter ratio L1 of the primary particles of the inner core structure satisfies: 1.2≤L1≤1.8;

and/or,

wherein a length-diameter ratio L2 of the primary particles of the shell layer satisfies: 3≤L2≤4.

7. The cathode material of claim 1 , wherein the primary particles of the cathode material have an average particle size within a range of 300-700 nm;

and/or, wherein a tap density TD of the cathode material is more than or equal to 2.5 g/cm 3 .

8. The cathode material of claim 7 , wherein the primary particles of the cathode material have an average particle size within a range of 400-600 nm;

and/or, wherein the tap density TD of the cathode material is within a range of 2.5-3 g/cm 3 .

9. A method for preparing the cathode material of claim 1 , comprising the following steps:

(1) mixing a nickel salt, an optional M salt, and an optional M′ element-containing compound with a solvent to prepare a mixed salt solution, preparing a precipitant solution with a precipitant, and preparing a complexing agent solution with a complexing agent;

(2) introducing the mixed salt solution into a reaction kettle containing the precipitant solution and the complexing agent solution to carry out a co-precipitation reaction, in the presence of a protective atmosphere;

the co-precipitation reaction comprising the following steps:

(2-1) controlling a temperature of the reaction system to be T1, carrying out a first-stage co-precipitation reaction until the median particle diameter D 50 of the co-precipitated particles reaches D 1 , then stopping the introduction of the mixed salt solution;

(2-2) controlling the temperature of the reaction system to be T2, continuously introducing the mixed salt solution to perform a second-stage co-precipitation reaction until the median particle diameter D 50 of the co-precipitated particles reaches D 2 , then stopping the introduction of the mixed salt solution;

(2-3) controlling the temperature of the reaction system to be T3, continuously introducing the mixed salt solution to perform a third-stage co-precipitation reaction until the median particle diameter D 50 of the co-precipitated particles reaches D 3 , then stopping the introduction of the mixed salt solution;

(2-4) aging, separating, washing, and drying the co-precipitation slurry obtained in step (2-3) to obtain a cathode material precursor;

(3) blending a lithium source, the cathode material precursor, and an optional M′ element-containing compound to obtain a mixture, sintering the mixture in the presence of an oxygen-containing atmosphere, then cooling, crushing, sieving the sintered product and removing iron thereof to prepare a cathode material;

wherein T1>T2, and/or 0.35<D1/D3<1.

10. The method of claim 9 , wherein T1−T2 is larger than or equal to 15° C.;

and/or, D1/D3 is within a range of 0.4-0.7;

and/or, |T1−T3|≤5° C.;

and/or, 0.5<D2/D3<1;

and/or, D2/D3-D1/D3 is within a range of 0.1-0.5.

11. The method of claim 10 , wherein T1−T2 is within a range of 15-40° C.;

and/or, |T1−T3| is within a range of 2-5° C.;

and/or, D2/D3 is within a range of 0.7-1;

and/or, D2/D3−D1/D3 is within a range of 0.2-0.4.

12. The method of claim 9 , wherein the temperature T1 is within a range of 60-80° C.; the particle diameter D1 is within a range of 4-10 μm;

and/or, the temperature T2 is within a range of 40-60° C.; the particle diameter D2 is within a range of 6-18 μm;

and/or, the temperature T3 is within a range of 60-80° C.; the particle diameter D3 is within a range of 8-20 μm.

13. The method of claim 12 , wherein the T1 is within a range of 65-75° C.; the particle diameter D1 is within a range of 5-9 μm;

and/or, the temperature T2 is within a range of 45-55° C.; the particle diameter D2 is within a range of 7-14 μm;

and/or, the temperature T3 is within a range of 65-75° C.; the particle diameter D3 is within a range of 9-16 μm.

14. The method of claim 9 , wherein the nickel salt, the M salt, and the M′ element-containing compound are used in an amount such that a molar ratio of n(Ni):n(M):n(M′) is (0.5-1):(0-0.5):(0-0.1);

and/or,

wherein the nickel salt and the M salt are each independently selected from the group consisting of sulfate salt, chloride salt, nitrate salt, acetate, and a combination thereof;

and/or,

wherein the M′ element-containing compound in step (1) is selected from the group consisting of sulfate of M′, chloride of M′, nitrate of M′, acetate of M′, and a combination thereof;

and/or,

wherein the M′ element-containing compound in step (3) is selected from the group consisting of oxide of M′, hydroxide of M′, oxyhydroxide of M′, and a combination thereof;

and/or,

wherein the solvent is selected from the group consisting of water, inorganic acid, alcohol, ether, amine, and a combination thereof;

and/or,

wherein the precipitant is selected from the group consisting of sodium hydroxide, sodium carbonate, sodium bicarbonate, sodium oxalate, potassium hydroxide, potassium carbonate, potassium bicarbonate, potassium oxalate, and a combination thereof;

and/or,

wherein the complexing agent is selected from the group consisting of ammonium hydroxide, ammonium sulfate, ammonium nitrate, ammonium chloride, salicylic acid, sulfosalicylic acid, ethylenediaminetetraacetic acid, and a combination thereof;

and/or,

wherein the protective atmosphere is selected from the group consisting of nitrogen gas, argon gas, air, oxygen gas, and a combination thereof;

and/or,

wherein pH values of the first-stage co-precipitation reaction, the second-stage co-precipitation reaction, and the third-stage co-precipitation reaction are independently within a range of 9-13;

and/or,

wherein the lithium source, the cathode material precursor, and the M′ element-containing compound are used in an amount such that n(Li)/[n(Ni)+n(M)+n(M′)] is within a range of (1-1.2):1;

and/or, the M′ element-containing compound in step (1) and the M′ element-containing compound in step (3) are used in an amount such that n(M′)/[n(Ni)+n(M)+n(M′)] in said lamellar cobalt-free electrode material is within a range of 0-0.1;

and/or,

wherein the oxygen-containing atmosphere is selected from oxygen gas and/or air;

and/or,

wherein the sintering conditions comprising: a sintering temperature within a range of 600-1,000° C. and a sintering time within a range of 6-20 h.

15. A lithium ion battery comprising the cathode material of claim 1 .

Assignments (1)

Priority Claims (1)

Continuity (3)

References Cited (24)