CATHODE ACTIVE MATERIAL PRECURSOR AND MANUFACTURING METHOD THEREOF, AND CATHODE ACTIVE MATERIAL
This proposes a minimum core radius for nickel-based metal hydroxide particles having a core-shell gradient (CSG) in which a concentration of nickel in a core portion is constantly maintained and a concentration of nickel in a shell portion is sharply decreased.
1 . A positive electrode active material precursor for a lithium rechargeable battery, the precursor comprising:
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 portion thereof,
wherein the positive electrode active material precursor includes a nickel-based metal hydroxide particle having a value of 50% or more of Formula 1:
R 1/( R 1+ D 1)*100% [Formula 1]
wherein, in Formula 1, R1 indicates a radius of the core portion in the nickel-based metal hydroxide particle, and D1 indicates a thickness of the shell portion in the nickel-based metal hydroxide particle.
2 . The positive electrode active material precursor of claim 1 , wherein
the nickel-based metal hydroxide particles
an angle formed by a curve representing the nickel molar content of the core portion and a curve representing the nickel molar content of the shell portion is in the range of 95.1° to 141.3°.
3 . The positive electrode active material precursor of claim 1 , wherein
a value of Formula 2 is greater than or equal to 75%.
4 . The positive electrode active material precursor of claim 1 , wherein
the nickel-based lithium metal oxide particle includes a plurality of nickel-based lithium metal oxide particles, and
a difference in Ni content between the nickel-based metal hydroxide particles is 3% or less.
5 . The positive electrode active material precursor of claim 1 , wherein
the positive electrode active material resulting from the nickel-based metal hydroxide particles has a heat generation amount of 650 J/g or less.
6 . The positive electrode active material precursor of claim 1 , wherein
the nickel-based metal hydroxide particle
is a large particle-diameter active material precursor particle having a D50 of 10 to 30 μm.
7 . The positive electrode active material precursor of claim 1 , wherein
an average composition of the nickel-based metal hydroxide particle
is represented by the following Chemical Formula 1:
Ni 1-w1-x1-y1-z1 Co w1 M1 x1 M2 y1 M3 z1 (OH) 2-p1 X p1 DeletedTexts [Chemical Formula 1]
wherein, in Chemical Formula 1,
each of M1, M2, and M3 is one element selected from the group consisting of Mn, Al, Mg, Zr, Sn, Ca, Ge, Ga, B, Ti, Mo, Nb, and W,
X is one element selected from the group consisting of F, N, and P, and
each of w1, x1, y1, z1, and p1 satisfies a following corresponding inequality: 0<w1≤0.2, 0<x1≤0.2, 0≤y1≤0.1, 0≤z1≤0.1, 0<w1+x1+y1+z1≤0.4, and 0≤p1≤0.1.
8 . A preparation method of a positive electrode active material precursor for a lithium rechargeable battery, the method comprising:
a preparation step of a first metal salt aqueous solution and a second metal salt aqueous solution, each of which contains a nickel source material, a dissimilar metal source material, and water, wherein molar concentrations of the nickel source material are different in the first metal salt aqueous solution and the second metal salt aqueous solution;
a first co-precipitation step of forming a core portion by supplying the first metal salt aqueous solution to a reactor having a pH that is constantly maintained, to which a chelating agent is supplied; and
a second co-precipitation step of forming a shell portion surrounding an outer surface of the core portion by gradually decreasing a supply rate of the first metal salt aqueous solution and by gradually increasing a supply rate of the second metal salt aqueous solution, after the first co-precipitation step,
wherein a nickel-based metal hydroxide particle including the core portion and the shell portion is obtained in the second co-precipitation step, and the first co-precipitation step and the second co-precipitation step are controlled to obtain a value of 50% or more of Formula 1 for the obtained nickel-based metal hydroxide particle:
R 1/( R 1+ D 1)*100% [Formula 1]
wherein, in Formula 1, R1 indicates a radius of the core portion in the nickel-based metal hydroxide particle, and D1 indicates a thickness of the shell portion in the nickel-based metal hydroxide particle.
9 . The preparation method of claim 8 , wherein
the first co-precipitation step and the second co-precipitation step are controlled to satisfy Formula 2:
log T 1/log( T 1+ T 2)≈ R 1/( R 1+ D 1) [Formula 2]
wherein, in Formula 2, T1 is an execution time of the first co-precipitation step, and T2 is an execution time of the second co-precipitation step.
10 . The preparation method of claim 9 , wherein
the first co-precipitation step
is performed for 10 hours or more.
11 . The preparation method of claim 10 , wherein
in the first co-precipitation step,
particles having a radius of R1 from a center and a constant molar content of nickel in the entire region are precipitated.
12 . The preparation method of any one of claim 8 to claim 11 , wherein
in the second co-precipitation step,
shell portions are formed by using the particles precipitated in the first co-precipitation step as core portions to have a thickness of R2 from surfaces of the core portions and a molar content of nickel that gradually decreases in a thickness direction from interfaces with the surfaces of the core portions, and
nickel-based metal hydroxide particles formed to include the core portion and the shell portion are obtained.
13 . A positive electrode active material for a lithium rechargeable battery, the material comprising:
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 portion thereof,
wherein the positive electrode active material precursor includes a nickel-based lithium metal oxide particle having a value of 50% or more of Formula 3:
R 2/( R 2+ D 2)*100% [Formula 3]
wherein, in Formula 3, R2 indicates a radius of the core portion in the nickel-based metal oxide particle, and D2 indicates a thickness of the shell portion in the nickel-based metal oxide particle.
14 . The positive electrode active material of claim 13 , wherein
an angle formed by a curve representing the nickel molar content of the core portion and a curve representing the nickel molar content of the shell portion is in the range of 95.1° to 141.3°.
15 . The positive electrode active material of claim 13 , wherein
a value of Formula 2 is greater than or equal to 75%.
16 . The positive electrode active material of claim 13 , wherein
the nickel-based lithium metal oxide particle
is a large particle-diameter active material particle having a D50 of 10 to 30 μm.
17 . The positive electrode active material of claim 13 , wherein
an average composition of the nickel-based lithium metal oxide particle
is represented by the following Formula 4:
Li 1+m [Ni 1-w4-x4-y4 Co w4 M1 x4 M2 y4 ] 1-z4 M3 z4 O 2-p4 X p4 [Chemical Formula 4]
wherein, in Chemical Formula 4,
each of M1, M2, and M3 is one element selected from the group consisting of Mn, Al, Mg, Zr, Sn, Ca, Ge, Ga, B, Ti, Mo, Nb, and W,
X is one element selected from the group consisting of F, N, and P,
each of w4, x4, y4, z4, and p4 satisfies a following corresponding inequality: 0<w4≤0.2, 0<x4≤0.2, 0≤y4≤0.1, 0≤z4≤0.1, 0<w4+x4+y4+z4≤0.4, and 0≤p1≤0.1, and
m satisfies an inequality: −0.05≤m≤0.25.
18 . The positive electrode active material of claim 13 , wherein
the nickel-based lithium metal oxide particle includes a plurality of nickel-based lithium metal oxide particles, and
a difference in Ni content between the nickel-based metal oxide particles is 3% or less.
19 . The positive electrode active material of claim 13 , wherein
the positive electrode active material has a heat generation amount of 650 J/g or less.
20 . The positive electrode active material of claim 13 , further comprising
a coating layer configured to surround an outer surface of the shell portion,
wherein the coating layer includes at least one of an element of B, Mg, Zr, Al, Mn, Co, or a combination thereof, an oxide of the element, an amorphous compound thereof, a lithium ion conductive oxide thereof, and a polymer thereof.