Cathode active material for lithium secondary battery

1. A cathode active material for a lithium secondary battery, comprising:

a nickel-based lithium metal oxide particle doped with Zr and Al,

wherein, the nickel-based lithium metal oxide particle comprises:

a core portion having a constant molar content of nickel; and

a shell portion surrounding an outer surface of the core portion and having a concentration gradient in which a molar content of nickel gradually decreases in a direction from an interface with the core portion to an outermost periphery,

wherein the core portion and the shell portion are doped with Al and Zr, and

wherein an average composition of the nickel-based lithium metal oxide particles is represented by the following formula 4:

Li m [Ni 1-w4-x4-y4-z4 Co w4 M1 x4 M2 y4 M3 z4 ] n O 2-p4 X p4   [Formula 4]

in the formula 4:

M1 is selected from the group consisting of Mn, Mg, Sn, Ca, Ge, Ga, B, Mo, and

M2 is Zr,

M3 is Al,

X is selected from the group consisting of F, N, and P,

w4, x4, y4, z4, and p4 meet 0<w4≤0.2, 0<x4≤0.2, 0<y4≤0.006, 0<z4≤0.006, 0<w4+x4+y4+z4≤0.4, and 0≤p4≤0.1,

m is 0.95≤m≤1.1, and

n is 0.95≤n≤1.1.

2. The cathode active material of claim 1 ,

wherein a molar ratio of Zr:Al in the nickel-based lithium metal oxide particle is 15:1 to 0:4:1.

3. The cathode active material of claim 1 ,

wherein a doping amount of Zr in the nickel-based lithium metal oxide particle is 2,000 to 5,000 ppm.

4. The cathode active material of claim 1 ,

wherein an amount of Al doped in the nickel-based lithium metal oxide particle is 100 to 1,500 ppm.

5. The cathode active material of claim 1 ,

wherein the nickel-based lithium metal oxide particle has a primary particle shape in the form of a rod.

6. The cathode active material of claim 5 ,

wherein the nickel-based lithium metal oxide particle is a large-particle having a D50 diameter of 10 to 30 μm, and has a lattice parameter of an axis from 2.85 to 2.88 Å.

7. The cathode active material of claim 5 ,

wherein the nickel-based lithium metal oxide particle is a large-particle having a D50 diameter of 10 to 30 μm, and has a lattice parameter of c axis from 14.13 to 14.37 Å.

8. The cathode active material of claim 5 ,

wherein the nickel-based lithium metal oxide particle has a crystallite size of 60 nm to 200 nm.

9. The cathode active material of claim 1 ,

wherein the nickel-based lithium metal oxide particles are plural and a mixture of two kinds of the nickel-based lithium metal oxide particles having different particle diameters.

10. The cathode active material of claim 9 ,

wherein the mixture comprises a large-particle having a D50 diameter of 10 to 30 μm and a small-particle having a D50 particle size of 1 to 6 μm.

11. The cathode active material of claim 10 ,

wherein the weight ratio of the large-particles: the small-particles is in a range of 50:50 to 90:10.

12. The cathode active material of claim 1 ,

wherein the nickel-based lithium metal oxide particle has 50% or more of a value of the follow equation 3:

R2/(R2+D2)*100%  [Equation 3]

in the equation 3, R2 is a radius of the core portion in the nickel-based metal oxide particle, and D2 is a thickness of the shell portion in the nickel-based metal oxide particle.

13. The cathode active material of claim 1 ,

wherein the core portion composition of the nickel-based lithium metal oxide particle is represented by the following formula 5:

Li m [Ni 1-w5-x5-y5-z5 Co w5 M1 x5 M2 y5 M3 z5 ] n O 2-p5 X p5   [Formula 5]

in the formula 5:

M1 is selected from the group consisting of Mn, Mg, Sn, Ca, Ge, Ga, B, Mo, and

M2 is Zr,

M3 is Al,

X is selected from the group consisting of F, N, and P,

w5, x5, y5, z5, and p5 meet 0≤w5≤0.1, 0≤x5≤0.1, 0<y5≤0.005, 0<z5≤0.006, 0≤w5+x5+y5+z5≤0.2, and 0≤p5≤0.1,

m is 0.95≤m≤1.1, and

n is 0.95≤n≤1.1.

14. The cathode active material of claim 13 ,

wherein, the shell portion of the nickel-based lithium metal oxide particle is represented by the following formula 5 at the interface, and the following formula 6 at the outermost periphery, and a molar content of Ni, M1, M2, and M3 is gradually changed from the interface to the outermost periphery

Li m [Ni 1-w6-x6-y6-z6 Co w6 M1 x6 M2 y6 M3 z6 ] n O 2-p6 X p6   [Formula 6]

in the formula 6:

M1 is selected from the group consisting of Mn, Mg, Sn, Ca, Ge, Ga, B, Mo, and

M2 is Zr,

M3 is Al,

X is selected from the group of F, N, and P,

w6, x6, y6, z6, and p6 meets 0<w6≤0.3, 0<x6≤0.3, 0<y6≤0.007, 0<z6 ≤0.006, 0<w6+x6+y6+z6≤0.5, and 0≤p6≤0.1,

m is 0.95≤m≤1.1, and

n is 0.95≤n≤1.1.

15. The cathode active material of claim 1 ,

wherein the nickel-based lithium metal oxide particle has 75% or more of a value of the follow equation 3.

16. The cathode active material of claim 1 , further comprising:

a coating layer which surrounds an outer surface of the shell portion and contains at least one of an element which is B, Mg, Zr, Al, Mn, Co or a combination thereof, an oxide of the element, an amorphous compound, a lithium ion conductive oxide and polymer.

17. A method for producing cathode active material for lithium secondary battery, comprising:

preparing a first metal salt aqueous solution and a second metal salt aqueous solution each containing a nickel source material, a dissimilar metal source material, and water, and molar concentrations of the nickel source material being different from each other;

a first coprecipitation step of supplying the first metal salt aqueous solution at a constant rate to a reactor in which pH is kept constant and a chelating agent is supplied;

a second coprecipitation step of gradually decreasing the supply rate of the first metal salt aqueous solution and gradually increasing the supply rate of the second metal salt aqueous solution after the first coprecipitation step;

obtaining nickel-based metal hydroxide particles in the second coprecipitation step; and

obtaining nickel-based lithium metal oxide particles doped with Zr and Al by sintering a mixture of the nickel-based metal hydroxide particles, a lithium source material, a Zr supply material, and an Al supply material after the second coprecipitation step,

wherein an average composition of the nickel-based lithium metal oxide particles is represented by the following formula 4:

Li m [Ni 1-w4-x4-y4-z4 Co w4 M1 x4 M2 y4 M3 z4 ] n O 2-p4 X p4   [Formula 4]

in the formula 4:

M1 is selected from the group consisting of Mn, Mg, Sn, Ca, Ge, Ga, B, Mo, and

M2 is Zr

M3 is Al,

X is selected from the group consisting of F, N, and P,

w4, x4, y4, z4, and p4 is respectively, 0<w4≤0.2, 0<x4≤0.2, 0<y4≤0.006, 0 <z4≤0.006, 0<w4+x4+y4+z4≤0.4, and 0≤p4≤0.1,

m is 0.95≤m≤1.1, and

n is 0.95≤n≤1.1.

18. The method of claim 17 ,

wherein the first coprecipitation step and the second coprecipitation step are controlled so that a value of the following equation 1 for the obtained nickel-based metal hydroxide particle is not less than 50%:

R1/(R1+D1)*100%  [Equation 1]

in the above equation 1, R1 is a radius of a core portion in the nickel-based metal hydroxide particle, and D1 is a thickness of a shell portion in the nickel-based metal hydroxide particle.

19. The method of claim 18 ,

wherein the first coprecipitation step and the second coprecipitation step are controlled so as to satisfy the following equation 2:

log(T1)/log(T1+T2)≈R1/(R1+D1)  [Equation 2]

in the above equation 2, T1 is an execution time of the first coprecipitation step, and T2 is an execution time of the second coprecipitation step.