POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, METHOD FOR PREPARING SAME, AND LITHIUM SECONDARY BATTERY INCLUDING SAME

Abstract

A positive electrode active material for a secondary battery according to an embodiment of the present invention comprises a lithium composite oxide represented by chemical formula 1 and containing a layer-structured lithium excess oxide, wherein the lithium composite oxide comprises a secondary particle; the secondary particle comprises at least one primary particle; the primary particle comprises at least one crystallite; at least one selected from the secondary particle, the primary particle, and the crystallite comprises a core and a shell occupying at least a portion of the surface of the core; and when the number of moles of at least one element having an oxidation number, selected from among nickel (Ni), cobalt (Co) and manganese (Mn) relative to the total number of moles of M1 and M2 in chemical formula 1 is Mp+/M, the Mp+/M in the core differs from that in the shell in the secondary particle: [Chemical formula 1] rLi2M1O3(1-r) LiaM2O2.

Description

TECHNICAL FIELD

The present disclosure relates to a cathode active material for a secondary battery, containing lithium composite oxide containing a layered structure of overlithiated oxide.

BACKGROUND ART

devices, such as a smartphone, an MP3 player, and a tablet PC, the demand for secondary batteries capable of storing electric energy is explosively increasing. In particular, with the advent of electric vehicles, medium and large energy storing systems, and portable devices requiring high energy density, the demand for lithium secondary batteries is increasing.

A material mostly favored recently as a cathode active material is a lithium-nickel-manganese-cobalt oxide, Li (Ni_xCo_yMn_z) O₂ (herein, x, y, and z are each independently an atomic fraction of oxide-composition elements, and 0<x≤1, 0<y≤1, 0≤z<1, and 0<x+y+z≤1). This material has the advantage of high capacity since the material is used at a higher voltage than LiCoO₂ that has been actively studied and used as a cathode active material, and has the advantage of low price due to a relatively small Co content therein. However, this material has disadvantages of unsatisfactory rate capability and poor cycle life characteristics at high temperatures.

Hence, research has been conducted to apply overlithiated layered oxide, which exhibits higher reversible capacity than conventional Li (Ni_xCo_yMn_z)O₂, to a lithium secondary battery.

However, there are problems of decreased discharge capacity (cycle life) and voltage decay during life cycling, which is due to phase transition from a spinel-like structure to a cubic structure due to transition metal migration during life cycling. These decreased discharge capacity (cycle life) and voltage decay are problems that must be solved in order to realize practical application to a lithium secondary battery.

DISCLOSURE OF INVENTION

Technical Problem

The present disclosure is intended to increase the charge/discharge capacity and solve the problems of life cycle deterioration and voltage decay by suppressing phase transition during life cycling in a cathode active material for a secondary battery.

Furthermore, the present disclosure is intended to increase the lithium ion mobility and improve the rate capability in a cathode active material for a secondary battery.

Furthermore, the present disclosure is intended to improve surface kinetic and structural stability of a cathode active material for a secondary battery.

Solution to Problem

The above problems are not solved by the following.

In accordance with an aspect of the present disclosure, there is provided a cathode active material for a secondary battery, including a lithium composite oxide represented by Formula 1 below and containing a layered structure of overlithiated oxide, wherein the lithium composite oxide includes a secondary particle, the secondary particle includes at least one primary particle, and the primary particle includes at least one crystallite, at least one selected from the secondary particle, the primary particles, and the crystallites includes a core and a shell occupying at least a part of the surface of the core, and, when the number of moles of at least one element, selected from the group consisting nickel (Ni), cobalt (Co), and manganese (Mn), in a predetermined oxidation state to the total number of moles of M1 and M2 in Formula 1 is M^p+/M, the M^p+/M in the core is different than in the shell of the secondary particle:

rLi₂M1O₃·(1-r)Li_aM2O₂  [Formula 1]

• • where, 0<r<1 and 0<a≤1; M1 is at least one of Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi; and M2 is at least one of Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi.

The M^p+/M in the core may be different than in the shell of the primary particle.

The M^p+/M in the core may be different than in the shell of the crystallite.

At least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which the M^p+/M has a gradient toward the center from the surface of the selected at least one.

In at least one selected from the secondary particle, the primary particle, and the crystallite, the Ni²⁺/Ni³⁺ may be higher in the shell than in the core.

At least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which the Ni²⁺/M decreases toward the center from the surface of the selected at least one.

At least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Ni³⁺/M increases toward the center from the surface of the selected at least one.

In at least one selected from the secondary particle, the primary particle, and the crystallite, the Ni²⁺/Ni³⁺ may be higher than 1 in the shell.

In at least one selected from the secondary particle, the primary particle, and the crystallite, the Mn³⁺/Mn⁴⁺ may be higher in the shell than in the core.

At least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which the Mn³⁺/M decreases toward the center from the surface of the selected at least one.

At least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which the Mn⁴⁺/M increases toward the center from the surface of the selected at least one.

In at least one selected from the secondary particle, the primary particle, and the crystallite, the Mn³⁺/Mn⁴⁺ may be higher than 1 in the shell.

The cathode active material may contain cobalt (Co) or contain no cobalt (Co).

In accordance with another aspect of the present disclosure, there is provided a secondary battery including the cathode active material.

Advantageous Effects of Invention

In the cathode active material for a secondary battery according to the present disclosure, the phase transition during life cycling is suppressed to increase the charge/discharge capacity and solve the problems of life cycle deterioration and voltage decay.

Furthermore, the cathode active material for a secondary battery according to the present disclosure has increased lithium ion mobility and improved rate capability.

Furthermore, the cathode active material for a secondary battery according to the present disclosure has improved surface kinetic and structural stability.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows XPS analysis results of Ni 2p oxidation state of a comparative example and examples.

FIG. 2 shows XPS analysis results of Mn 2p oxidation state of a comparative example and examples.

FIG. 3 shows XPS analysis results of Mn 3s oxidation state of a comparative example and examples.

FIG. 4 shows XPS analysis results of transition metals of examples.

FIG. 5 shows SEM analysis results of a comparative example and an example.

FIG. 6 shows TEM-EDS and concentration gradient analysis results of Example 1.

FIG. 7 shows TEM-EDS and concentration gradient analysis results of Example 1.

FIG. 8 shows TEM-EDS and concentration gradient analysis results of Example 5.

FIG. 9 shows initial voltage profile analysis results of the comparative examples and examples.

FIG. 10 shows rate capability analysis results of the comparative examples and the examples.

FIG. 11 shows rate capability analysis results of the comparative examples and the examples.

FIG. 12 shows life cycle analysis results of the comparative examples and the examples.

FIG. 13 shows life cycle analysis results of the comparative examples and the examples.

FIG. 14 shows voltage analysis results of the comparative examples and the examples.

FIG. 15 shows voltage analysis results of the comparative examples and the examples.

MODE FOR CARRYING OUT THE INVENTION

As used herein, terms such as “comprising” should be understood as open-ended terms that do not preclude the inclusion of other technical features.

As used herein, the terms “as an example”, “as an example”, and “preferably” refer to embodiments of the present disclosure that may afford certain benefits, under certain circumstances, and are not intended to exclude other embodiments from the scope of the disclosure.

As used herein, the term “as a preferable example” refers to a preferable embodiment as a means for technical problems to be solved by the present disclosure, that is, effects of suppressing phase transition, increasing charge and discharge capacity, solving life cycle deterioration and voltage decay, increasing lithium mobility, and improving rate capability and structural stability.

A cathode active material for a secondary battery according to an embodiment of the present disclosure contains a lithium composite oxide represented by Formula 1 below and containing a layered structure of overlithiated oxide.

rLi₂M1O₃·(1-r)Li_aM2O₂  [Formula 1]

In Formula 1, 0<r<1 and 0<a≤1; M1 and M2 are each independent; M1 is at least one selected from Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi; and M2 is at least one selected from Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi.

As a preferable example, M1 is at least one selected from Mn, Cr, Fe, Co, Ni, Mo, Ru, W, Ti, Zr, Sn, V, Al, Mg, Ta, B, P, Nb, Cu, La, Ba, Sr, and Ce; and M2 is at least one selected from Ni, Co, Mn, Cr, Fe, Mo, Ru, W, Ti, Zr, Sn, V, Al, Mg, Ta, B, P, Nb, Cu, La, Ba, Sr, and Ce.

As an example, in Formula 1, the overlithiated oxide may be a solid solution phase in which monoclinic-structured Li₂M1O₃ and rhombohedral-structured Li_aM2O₂ are present in a mixed state.

As a more preferable example, the average valence of M1 may be 3.5 to 4.5 or may be 4.

As a more preferable example, the average valence of M2 may be 2.5 to 3.5 or may be 3.

As a preferable example, Formula 1 may be expressed as Formula 1-1 below.

rLi₂Mn_pMd1_1-pO₃·(1-r)Li_aNi_xCo_yMn_zMd2_1-(x+y+z)O₂  [Formula 1-1]

In Formula 1-1, 0<r<1, 0<p≤1, 0<a≤1, 0≤x≤1, 0≤y≤1, 0<z≤1, and 0<x+y+z≤1; Md1 and Md2 are each independent; Md1 is at least one selected from Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi; and Md2 is at least one selected from Mo, Nb, Fe, Cr, V, Cu, Zn, Sn, Mg, Ru, Al, Ti, Zr, B, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi.

Md1 and Md2 may be each independently an element, a dopant, or a coating material, and desired effects of the present disclosure can be obtained regardless of the types of Md1 and Md2.

As a more preferable example, Md1 is at least one selected from Cr, Fe, Co, Ni, Mo, Ru, W, Ti, Zr, Sn, V, Al, Mg, Ta, B, P, Nb, Cu, La, Ba, Sr, and Ce; and Md2 is at least one selected from Cr, Fe, Mo, Ru, W, Ti, Zr, Sn, V, Al, Mg, Ta, B, P, Nb, Cu, La, Ba, Sr, and Ce.

As an example, in Formula 1-1, the overlithiated oxide may be a solid solution phase in which monoclinic-structured Li₂Mn_pMd1_1-pO₃ and rhombohedral-structured Li_aNi_xCo_yMn_zMd_1-(x+y+z)O₂ are present in a mixed state.

As an example, the overlithiated oxide may have a layered structure in which a lithium atomic layer alternately overlaps an atomic layer of nickel, cobalt, manganese, or Md via an oxygen atomic layer interposed therebetween.

As an example, r may be not greater than 1, not greater than 0.9, not greater than 0.8, not greater than 0.7, or not greater than 0.6.

As an example, p may be greater than 0, may be not smaller than 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, or 0.9, or may be 1.0.

As a more preferable example, in the lithium composite oxide of the present disclosure, the number of moles of lithium to the total number of moles of M1 and M2, Li/M, may be not lower than 1.01, 1.05, or 1.1 and may be not higher than 1.7, 1.6, 1.5, 1.4, or 1.3.

As a more preferable example, in the lithium composite oxide, the number of moles of lithium (Li) to the total number of moles of M1 and M2, Li/M, may be not lower than 0.1, 0.2, or 0.3 and may be not higher than 0.7, 0.6, or 0.5.

As a more preferable example, in the lithium composite oxide, the number of moles of cobalt (Co) to the total number of moles of M1 and M2, Co/M, may be not lower than 0.0, 0.05, or 0.1 and may be not higher than 0.3, 0.2, or 0.1.

As a more preferable, a cathode active material according to an embodiment of the present disclosure may not contain Co.

As a more preferable example, in the lithium composite oxide, the number of moles of manganese (Mn) to the total number of moles of M1 and M2, Mn/M, may be not lower than 0.1, 0.2, or 0.3 and may be not higher than 0.8 or 0.7.

As a more preferable example, in the lithium composite oxide, the number of moles of Md2 to the total number of moles of M1 and M2, Md2/M, may be not lower than 0.0 and may be not higher than 0.2 or 0.1.

The lithium composite oxide includes a secondary particle, the secondary particle includes at least one primary particle, and the primary particle includes at least one crystallite.

As used herein, “at least one” refers to one or two or more.

As an example, the secondary particle may include one primary particle and may be formed by aggregation of two or more primary particles.

As an example, the primary particle may include one crystallite or may be formed by aggregation of two or more crystallites.

In the cathode active material according to an embodiment of the present disclosure, at least one selected from the secondary particle, the primary particle, and the crystallite includes a core and a shell occupying at least a part of the surface of the core.

As an example, the secondary particle may be a particle having a core-shell structure including a core and a shell occupying at least a part of the surface of the core.

In particular, the “at least a part” may mean being more than 0%, or not less than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the total surface area of the secondary particle.

The average diameter (D50) of the secondary particle may be 0.5 to 20 μm.

As an example, the thickness of the shell of the secondary particle may be more than 0 and not more than 10 μm, more than 0 and not more than 1 μm, more than 0 and not more than 500 nm, more than 0 and not more than 400 nm, more than 0 and not more than 300 nm, more than 0 and not more than 200 nm, more than 0 and not more than 150 nm, more than 0 and not more than 100 nm, more than 0 and not more than 90 nm, more than 0 and not more than 80 nm, more than 0 and not more than 70 nm, more than 0 and not more than 60 nm, or more than 0 and not more than 50 nm.

As an example, the thickness of the shell of the secondary particle may be more than 0.0% or not less than 1, 10, 20, 30, 40, 50, 60, 70, 80, or 90% and may be less than 100% or not more than 90, 80, 70, 60, 50, 40, 30, 20, 10, or 1%.

As an example, the primary particle may include a core and a shell occupying at least a part of the surface of the core.

In particular, the “at least a part” may mean being more than 0% or not less than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the total surface area of the primary particle.

As an example, the thickness of the shell of the primary particle may be more than 0 and not more than 10 μm, more than 0 and not more than 1 μm, more than 0 and not more than 500 nm, more than 0 and not more than 400 nm, more than 0 and not more than 300 nm, more than 0 and not more than 200 nm, more than 0 and not more than 150 nm, more than 0 and not more than 100 nm, more than 0 and not more than 90 nm, more than 0 and not more than 80 nm, more than 0 and not more than 70 nm, more than 0 and not more than 60 nm, or more than 0 and not more than 50 nm.

As an example, the thickness of the shell of the primary particle may be more than 0.0% or not less than 1, 10, 20, 30, 40, 50, 60, 70, 80, or 90% and may be less than 100% or not more than 90, 80, 70, 60, 50, 40, 30, 20, 10, or 1%.

As an example, the crystallite may include a core and a shell occupying at least a part of the surface of the core.

In particular, the “at least a part” may mean being more than 0% or not less than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the total surface area of the crystallite.

As an example, the thickness of the shell of the crystallite may be more than 0 and not more than 10 μm, more than 0 and not more than 1 μm, more than 0 and not more than 500 nm, more than 0 and not more than 400 nm, more than 0 and not more than 300 nm, more than 0 and not more than 200 nm, more than 0 and not more than 150 nm, more than 0 and not more than 100 nm, more than 0 and not more than 90 nm, more than 0 and not more than 80 nm, more than 0 and not more than 70 nm, more than 0 and not more than 60 nm, or more than 0 and not more than 50 nm.

As an example, the thickness of the shell of the crystallite may be more than 0.0% or not less than 1, 10, 20, 30, 40, 50, 60, 70, 80, or 90% and may be less than 100% or not more than 90, 80, 70, 60, 50, 40, 30, 20, 10, or 1%.

The “core” of the secondary particle, the primary particle, or the crystallite means a region that is present inside the secondary particle, the primary particle, or the crystallite and is close to the center of the particle excluding the surface of the particle.

The “shell” means a region that is close to the surface excluding the center of the particle or the inside of the particle.

In the cathode active material according to an embodiment of the present disclosure, a transition metal, such as nickel, cobalt, and/or manganese, may be diffused into the secondary particle, the primary particle, and/or the crystallite, to form the shell distinguishable from the core.

In the cathode active material according to an embodiment of the present disclosure, when the number of moles of at least one element, selected from the group consisting nickel (Ni), cobalt (Co), and manganese (Mn), in a predetermined oxidation state, to the total number of moles of M1 and M2 in Formula 1 is M^p+/M, the M^p+/M in the core is different than in the shell of the secondary particle.

In the present disclosure, the number of moles of at least one element, selected from the group consisting nickel (Ni), cobalt (Co), and manganese (Mn), in a predetermined oxidation state, to the total number of moles of M1 and M2 in Formula 1 is designated as M^p+/M.

In the cathode active material according to an embodiment of the present disclosure, the M^p+/M in the core is different than in the shell of the secondary particle.

In the lithium composite oxide having the above-described composition in the present disclosure, the M^p+/M in the core is controlled to be different than in the shell of the secondary particle, so that the surface kinetic improvement can be attained to increase the lithium mobility in the surface and the irreversible reaction can be reduced in the particle surface to increase structural stability and efficiency.

As a more preferable example, the M^p+/M in the core may be different than in the shell of the primary particle.

In the lithium composite oxide having the above-described composition in the present disclosure, the M^p+/M in the core is controlled to be different than in the shell of the primary particle, so that the surface kinetic improvement can be attained to increase the lithium mobility in the surface and the irreversible reaction can be reduced in the particle surface to increase structural stability and efficiency.

As a more preferable example, the M^p+/M in the core may be different than in the shell of the crystallite.

In the lithium composite oxide having the above-described composition in the present disclosure, the M^p+/M in the core is controlled to be different than in the shell of the crystallite, so that the surface kinetic improvement can be attained to increase the lithium mobility in the surface and the irreversible reaction can be reduced in the particle surface to increase structural stability and efficiency.

As one example, when the number of moles of nickel (Ni) in an oxidation state of +2 to the total number of moles of M1 and M2 in Formula 1 is Ni²⁺/M, the Ni²⁺/M in the core may be different than in the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As one example, when the number of moles of nickel (Ni) in an oxidation state of +3 to the total number of moles of M1 and M2 in Formula 1 is Ni³⁺/M, the Ni³⁺/M in the core may be different than in the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As one example, when the number of moles of cobalt (Co) in an oxidation state of +2 to the total number of moles of M1 and M2 in Formula 1 is Co²⁺/M, the Co²⁺/M may be different in the core and the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As one example, when the number of moles of cobalt (Co) in an oxidation state of +3 to the total number of moles of M1 and M2 in Formula 1 is Co³⁺/M, the Co³⁺/M the core may be different than in the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As one example, when the number of moles of manganese (Mn) in an oxidation state of +3 to the total number of moles of M1 and M2 in Formula 1 is Mn³⁺/M, the Mn³⁺/M in the core may be different than in the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As one example, when the number of moles of manganese (Mn) in an oxidation state of +4 to the total number of moles of M1 and M2 in Formula 1 is Mn⁴⁺/M, the Mn⁴⁺/M in the core may be different than in the shell of at least one selected from the secondary particle, the primary particle, and the crystallite.

As a more preferable example, the secondary particle may include an oxidation state gradient portion in which M^p+/M has a gradient toward the center from the surface of the secondary particle.

As a more preferable example, the primary particle may include an oxidation state gradient portion in which M^p+/M has a gradient toward the center from the surface of the primary particle.

As a more preferable example, the crystallite may include an oxidation state gradient portion in which M^p+/M has a gradient toward the center from the surface of the crystallite.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Ni²⁺/M has a gradient.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Ni³⁺/M has a gradient.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Co²⁺/M has a gradient.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Co³⁺/M has a gradient.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Mn³⁺/M has a gradient.

As an example, at least one selected from the secondary particle, the primary particle, and the crystallite may include an oxidation state gradient portion in which Mn⁴⁺/M has a gradient.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher in the shell than in the core of the secondary particle.

In the secondary particle, the Ni²⁺/Ni³⁺ in the shell may be more than 1 time, not less than 1.1 times, not less than 1.2 times, or not less than 1.3 times and may be not more than 3.0 times or not more than 2.0 times the Ni²⁺/Ni³⁺ in the core.

The secondary particle may include an oxidation state gradient portion in which the Ni²⁺/M decreases toward the center from the surface of the secondary particle.

The secondary particle may include an oxidation state gradient portion in which the Ni³⁺/M increases toward the center from the surface of the secondary particle.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher than 1 in the shell of the secondary particle.

The Ni²⁺/Ni³⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the secondary particle.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher in the shell than in the core of the secondary particle.

In the secondary particle, the Mn³⁺/Mn⁴⁺ in the shell may be more than 1 time, not less than 1.1 times, or not less than 1.2 times, or may be not more than 3.0 times or not more than 2.0 times the Mn³⁺/Mn⁴⁺ in the core.

The secondary particle may include an oxidation state gradient portion in which the Mn³⁺/M decreases toward the center from the surface of the secondary particle.

The secondary particle may include an oxidation state gradient portion in which the Mn⁴⁺/M increases toward the center from the surface of the secondary particle.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher than 1 in the shell of the secondary particle.

The Mn³⁺/Mn⁴⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the secondary particle.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher in the shell than in the core of the primary particle.

In the primary particle, the Ni²⁺/Ni³⁺ in the shell may be more than 1 time, not less than 1.1 times, not less than 1.2 times, or not less than 1.3 times and may be not more than 3.0 times or not more than 2.0 times the Ni²⁺/Ni³⁺ in the core.

The primary particle may include an oxidation state gradient portion in which Ni²⁺/M decreases toward the center from the surface of the primary particle.

The primary particle may include an oxidation state gradient portion in which Ni³⁺/M increases toward the center from the surface of the primary particle.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher than 1 in the shell of the primary particle.

The Ni²⁺/Ni³⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the primary particle.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher in the shell than in the core of the primary particle.

In the primary particle, the Mn³⁺/Mn⁴⁺ in the shell may be more than 1 time, not less than 1.1 times, or not less than 1.2 times and may be not more than 3.0 times or not more than 2.0 times the Mn³⁺/Mn⁴⁺ in the core.

The primary particle may include an oxidation state gradient portion in which the Mn³⁺/M decreases toward the center from the surface of the primary particle.

The primary particle may include an oxidation state gradient portion in which Mn⁴⁺/M increases toward the center from the surface of the primary particle.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher than 1 in the shell of the primary particle.

The Mn³⁺/Mn⁴⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the primary particle.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher in the shell than in the core of the crystallite.

In the crystallite, the Ni²⁺/Ni³⁺ in the shell may be more than 1 time, not less than 1.1 times, not less than 1.2 times, or not less than 1.3 times and may be not more than 3.0 times or not more than 2.0 times the Ni²⁺/Ni³⁺ in the core.

The crystallite may include an oxidation state gradient portion in which the Ni²⁺/M decreases toward the center from the surface of the crystallite.

The crystallite may include an oxidation state gradient portion in which the Ni³⁺/M increases toward the center from the surface of the crystallite.

As a more preferable example, the Ni²⁺/Ni³⁺ may be higher than 1 in the shell of the crystallite.

The Ni²⁺/Ni³⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the crystallite.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher in the shell than in the core of the crystallite.

In the crystallite, the Mn³⁺/Mn⁴⁺ in the shell may be more than 1 time, not less than 1.1 times, or not less than 1.2 times and may be not more than 3.0 times or not more than 2.0 times the Mn³⁺/Mn⁴⁺ in the core.

The crystallite may include an oxidation state gradient portion in which the Mn³⁺/M decreases toward the center from the surface of the crystallite.

The crystallite may include an oxidation state gradient portion in which the Mn⁴⁺/M increases toward the center from the surface of the crystallite.

As a more preferable example, the Mn³⁺/Mn⁴⁺ may be higher than 1 in the shell of the crystallite.

The Mn³⁺/Mn⁴⁺ may be not lower than 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, or 2.0 in the shell of the crystallite.

As a more preferable example, the cathode active material may contain cobalt (Co).

As a more preferable, the cathode active material according to an embodiment of the present invention may not contain cobalt (Co). In particular, by controlling the oxidation state of a transition metal of the core and the shell in the secondary particle, the primary particle, or the crystallite while not using expensive cobalt, the phase transition during life cycling of the cathode active material for a secondary battery can be suppressed to increase the charge and discharge capacity and solve the problems of life cycle deterioration and voltage decay.

The cathode active material according to an embodiment of the present disclosure may further include a separate coating layer. The coating layer may contain at least one coating material selected from P, Nb, Si, Sn, Al, Pr, Al, Ti, Zr, Fe, Al, Fe, Co, Ca, Mn, Ti, Sm, Zr, Fe, La, Ce, Pr, Mg, Bi, Li, W, Co, Zr, B, Ba, F, K, Na, V, Ge, Ga, As, Sr, Y, Ta, Cr, Mo, W, Mn, Ir, Ni, Zn, In, Na, K, Rb, Cs, Fr, Sc, Cu, Ru, Rh, Pd, Ag, Cd, Sb, Hf, Ta, Re, Os, Pt, Au, Pb, Bi, and Po, but is not particularly limited thereto.

The coating layer blocks the contact between the cathode active material and an electrolyte included in the lithium secondary battery to suppress the occurrence of side reactions, thereby improving the life cycle and increasing packing density. In some embodiments, the coating layer can act as a lithium ion conductor.

The coating layer may be formed on the entire surface of the cathode active material or the entire surface of the primary particle, or may be partially formed thereon.

In addition, the coating layer may be in a single-layer coating, double-layer coating, grain boundary coating, uniform coating, or island coating form.

In the cathode active material according to an embodiment of the present disclosure, a lithium ion diffusion path may be formed inside the primary particle.

In the cathode active material according to an embodiment, a surface that constitutes a layer of the layered structure may have crystal orientation in a direction perpendicular to a C-axis inside the primary particle, and the lithium ion diffusion path may be formed inside or outside the primary particle in a direction toward the center of the particle of the cathode active material.

As a more preferable example, the secondary particle may include a concentration gradient portion in which at least one element selected from nickel (Ni), cobalt (Co), and manganese (Mn) has a concentration gradient.

As a more preferable example, the primary particle may include a concentration gradient portion in which at least one element selected from nickel (Ni), cobalt (Co), and manganese (Mn) has a concentration gradient.

As a more preferable example, the crystallite may include a concentration gradient portion in which at least one element selected from nickel (Ni), cobalt (Co), and manganese (Mn) has a concentration gradient.

As a more preferable example, when the number of moles of nickel (Ni) to the total number of moles of M1 and M2 in Formula 1 is defined as Ni/M, the Ni/M may be higher in the shell than in the core in at least one selected from the secondary particle, the primary particle, and the crystallite.

As a more preferable example, when the number of moles of cobalt (Co) to the total number of moles of M1 and M2 in Formula 1 is defined as Co/M, the Co/M may be higher in the shell than in the core in at least one selected from the secondary particle, the primary particle, and the crystallite.

As a more preferable example, when the number of moles of manganese (Mn) to the total number of moles of M1 and M2 in Formula 1 is defined as Mn/M, the Mn/M may be lower in the shell than the core in at least one selected from the secondary particle, the primary particle, and the crystallite.

As a more preferable example, Mn/M>Ni/M>Co/M may be satisfied in the core of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example, the Ni/M may be not lower than 0.1, 0.2, or 0.3 and may be not higher than 1.0, 0.9, or 0.8 in the core of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example, the Co/M may be not higher than 0.3, 0.2, 0.1, or 0.05 and may be not lower than 0.0 in the core of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example, the Mn/M may be not lower than 0.4, 0.5, or 0.6 and may be not higher than 1.0, 0.9, or 0.8 in the core of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example of the present invention, the maximum Ni/M may be not less than 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, or 95 mol % and may be not more than 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 30, 25, 20, 15, or 10 mol % in the shell of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example of the present invention, the maximum Co/M may be not less than 1, 3, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, or 95 mol % and may be not more than 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 30, 25, 20, 15, or 10 mol % in the shell of the secondary particle, the primary particle, and/or the crystallite.

As a more preferable example of the present invention, the minimum Mn/M may be not less than 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, or 95 mol % and may be not more than 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 30, 25, 20, 15, or 10 mol % in the shell of the secondary particle, the primary particle, and/or the crystallite.

Hereinafter, a method for preparing a cathode active material for a secondary battery according to an embodiment of the present disclosure will be described in detail.

First, a step of forming precursor particles is performed.

As a more preferable example, the precursor particles may be manufactured by co-precipitation, and a complexing agent may be added for the manufacturing.

Then, a step of subjecting the formed precursor particles to first thermal treatment at 300 to 1000° C. followed by cooling is performed.

Then, a step of, after the first thermal treatment and then cooling, subjecting the precursor particles to wet coating with a compound containing at least one element selected from cobalt, nickel, and manganese may be performed.

Then, a step of mixing a first lithium compound with the first thermally treated and then cooled particles or the wet-coated particles and subjecting the mixture to second thermal treatment at 800 to 1000° C., followed by cooling is performed.

Then, a step of, after the second thermal treatment and then cooling, subjecting the precursor particles to wet coating with a compound containing at least one element selected from cobalt, nickel, and manganese may be performed.

Then, a step of mixing a second lithium compound with the second thermally treated and then cooled particles or the wet-coated particles and subjecting the mixture to third thermal treatment at 300 to 1000° C., followed by cooling is performed.

An embodiment of the present disclosure may include a step of subjecting the precursor particles to wet coating with a compound containing at least one element selected from cobalt, nickel, and manganese, after the step of forming the precursor particles before the step of first thermal treatment followed by cooling, between the step of first thermal treatment followed by cooling and the step of second thermal treatment followed by cooling, and between the step of second thermal treatment followed by cooling and the step of third thermal treatment followed by cooling.

As a more preferable example, in the step of wet coating, co-precipitation may be performed, and a complexing agent may be added.

A secondary battery according to an embodiment of the present disclosure includes the cathode active material.

The cathode active material is as described above, and a binder, a conductor, and a solvent are not particularly limited as long as these can be used on a cathode current collector for a secondary battery.

The lithium secondary battery may specifically include a cathode, an anode disposed to face the cathode, and an electrolyte between the cathode and the anode, and any battery that can be used as a secondary battery is not particularly limited thereto.

Hereinafter, examples of the present disclosure are specifically described.

EXAMPLES 1 TO 5

Preparation of Precursor

A spherical Ni_xCo_yMn_z(OH) precursor was synthesized using co-precipitation. In a 90-L reactor, 25 wt % of NaOH and 28 wt % of NH₄OH were added to an aqueous solution of 2.5 M complex transition-metal sulfates prepared by mixing NiSO₄·6H₂O, MnSO₄·H₂O, and COSO₄·7H₂O while the mole ratio of Ni:Co:Mn was adjusted. The pH in the reactor was maintained at 9.0-12.0, and the temperature in the reactor was maintained at 45 to 50° C. In addition, N2, an inert gas, was injected into the reactor to prevent the oxidation of the prepared precursor. After the completion of synthesis and stirring, washing and dehydration were performed using a filter press (F/P). Finally, the dehydrated product was dried at 120° C. for 2 days, and filtered through a 75-μm (200 mesh) sieve to obtain a Ni_xCo_yMn_z(OH) precursor of 4 μm.

First Thermal Treatment and Cooling

The precursor was maintained in an O₂ or air (50 L/min) atmosphere in a box furnace while the temperature was elevated at a rate of 2° C. per min and maintained at 300 to 1000° C. for 1-10 hours, followed by furnace cooling.

Wet Coating (if Performed after the First Thermal Treatment and Cooling)

The precursor was wet-coated using co-precipitation.

In a reactor in which the precursor was stirred, an aqueous solution of complex transition-metal sulfates, which was prepared by mixing COSO₄·7H₂O, NiSO₄·6H₂O, or MnSO₄·H₂O with an adjusted molar ratio and distilled water, 25 wt % of NaOH, and 28 wt % of NH₄OH were added. The coating amount of the transition metal was 1-10 mol % relative to the total number of moles of nickel (Ni), cobalt (Co), and manganese (Mn), and the pH in the reactor was maintained at 9.0-12.0. After the completion of synthesis and stirring, washing and dehydration were performed using a filter press (F/P). Finally, the dehydrated product was dried at 150° C. for 14 hours to obtain a precursor having a concentration gradient.

Second Thermal Treatment and Cooling

The precursor was mixed with LiOH or Li₂CO₃, which was weighed with an adjusted Li/M ratio, by using a manual mixer (MM). The mixture was maintained in an O₂ or air (50 L/min) atmosphere in a Box furnace while the temperature was elevated at a rate of 2° C. per min and maintained at 800 to 1000° C. for 7-12 hours, followed by furnace cooling.

Wet Coating (if Performed after the Second Thermal Treatment and Cooling)

The lithium composite oxide was wet-coated using co-precipitation. In a reactor in which the particles were stirred, an aqueous solution of complex transition-metal sulfates, which was prepared by mixing CoSO₄·7H₂O, NiSO₄·6H₂O, or MnSO₄·H₂O with an adjusted molar ratio and distilled water, 25 wt % of NaOH, and 28 wt % of NH₄OH were added. The coating amount of the transition metal was 1-10 mol % relative to the total number of moles of nickel (Ni), cobalt (Co), and manganese (Mn), and the pH in the reactor was maintained at 9.0-12.0. After the completion of synthesis and stirring, washing and dehydration were performed using a filter press (F/P). Finally, the dehydrated product was dried at 150° C. for 14 hours to obtain a lithium composite oxide having a concentration gradient.

Third Thermal Treatment and Cooling

The coated product was mixed with LiOH or Li₂CO₃, which was weighed with an adjusted Li/M ratio, by using a manual mixer (MM). The mixture was maintained in an O₂ or air atmosphere in a box furnace while the temperature was elevated at a rate of 4.4° C. per min and maintained at 300 to 1000° C. for 7-12 hours, followed by furnace cooling.

COMPARATIVE EXAMPLES 1 AND 2

Each cathode active material was prepared by the same method as in Examples 1 to 5 except that a step of wet coating with a transition metal as in the manufacturing of Examples 1 to 5 was not performed.

Table 1 below relates to the manufacturing methods of Examples 1 to 5 and Comparative Examples 1 to 2.

	TABLE 1
	Comparative	Comparative
	ITEM	Example 1	Example 2	Example 1	Example 2	Example 3	Example 4	Example 5
	Ni
	Co
	Mn
	Temperature	° C.
thermal
treatment
	N M		—	—			—	—
	Temperature	° C.
thermal
treatment
Lithium	Li/M	ratio
	N M		—	—	—	—			—
product
	Temperature	° C.	—	—	—	—			—
thermal
treatment
Lithium	Li/M	ratio	—	—	—	—			—
indicates data missing or illegible when filed

MANUFACTURING EXAMPLE

Manufacturing of Lithium Secondary Battery

Cathode slurries were prepared by dispersion of 90 wt % of the cathode active materials of the examples and comparative examples, 5.5 wt % of carbon black, and 4.5 wt % of a PVDF binder in 30 g of N-methyl-2 pyrrolidone (NMP). Each of the cathode slurries was applied to a 15 μm-thick aluminum (Al) thin film as a cathode current collector, dried, and then roll-pressed to manufacture a cathode.

For the cathode, metallic lithium was used as a counter electrode, and 1.15 M LiPF₆ in EC/DMC/EMC=2/4/4 (vol %) was used as an electrolyte.

A separator formed of a porous polyethylene (PE) film was interposed between the cathode and the anode to form a battery assembly, and the electrolyte was injected into the battery assembly to manufacture a lithium secondary battery (coin cell)

EXPERIMENTAL EXAMPLE 1

Table 2 below relates to characteristics of lithium secondary batteries of the examples and comparative examples.

	TABLE 2
	Comparative	Comparative
	ITEM	Example 1	Example 2	Example 1	Example 2	Example 3	Example 4	Example 5
	CH.	mAh/g
( 25° C.)	DCH.
0.1 C	Eff.	%
2.0-4.  V
rate capability	ate	%
5 C/0.1 C
life cycle	Cycle Life
( 25° C.)	(50 cy.)
1 C/1 C	Voltage Decay
2. -4.6 V	(50 cy.)
indicates data missing or illegible when filed

The XPS analysis results of FIGS. 1 to 3 can confirm Ni²⁺/Ni³⁺ and Mn³⁺/Mn⁴⁺ in the shell and the core of the comparative example and the examples.

The XPS analysis results of FIG. 4 can confirm the gradients of Ni, Mn, and Co in the shell and the core of the examples.

FIG. 5 can confirm SEM images of the comparative examples and the examples.

The TEM-EDS analysis results of FIGS. 6 to 8 can confirm metal concentration gradients in the cathode active material of the example.

FIG. 9 and Table 2 can confirm that the examples showed increased charge/discharge capacity and efficiency compared with the comparative examples. This is due to the results of increasing the lithium mobility in the surface by surface kinetic improvement, through a difference in the oxidation state of nickel and manganese in the core and the shell.

FIGS. 10 and 11 and Table 2 can confirm that the examples showed improved rate capability compared with the comparative examples. This is due to the results of reducing an irreversible reaction to increase efficiency, through a difference in the oxidation state of nickel and manganese in the core and the shell.

FIGS. 12 and 13 and Table 2 can confirm that the examples showed improved life cycle characteristics compared with the comparative examples. This is due to the result of solving the problems of cycle life deterioration and voltage decay resulting from phase transition during cycling of the overlithiated layered oxide, through a difference in the oxidation state of nickel and manganese in the core and the shell.

FIGS. 14 and 15 and Table 2 can confirm that the examples showed inhibited voltage decay compared with the comparative examples. This is due to the results of improving kinetic and structural stability in the particle surface, through a difference in the oxidation state of nickel and manganese in the core and the shell.

FIGS. 9 to 15 and Table 2 below could confirm that even the cathode active material of Example 5 containing no cobalt and employing wet coating with nickel (Ni) showed significantly improved performance of lithium secondary batteries.

Claims

1. A cathode active material for a secondary battery, comprising a lithium composite oxide represented by Formula 1 below and containing a layered structure of overlithiated oxide,

wherein the lithium composite oxide includes a secondary particle, the secondary particle includes at least one primary particle, and the primary particle includes at least one crystallite,

at least one selected from the secondary particle, the primary particles, and the crystallites comprises a core and a shell occupying at least a part of the surface of the core, and,

when the number of moles of at least one element, selected from the group consisting nickel (Ni), cobalt (Co), and manganese (Mn), in a predetermined oxidation state to the total number of moles of M1 and M2 in Formula 1 is Mp+/M, the Mp+/M in the core is different than in the shell of the secondary particle: rLi2M1O3·(1-r)LiaM2O2  [Formula 1]

where, 0<r<1 and 0<a 1; M1 is at least one of Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi; and M2 is at least one of Mo, Nb, Fe, Cr, V, Co, Cu, Zn, Sn, Mg, Ni, Ru, Al, Ti, Zr, B, Mn, Na, K, Y, P, Ba, Sr, La, Ga, Gd, Sm, W, Ca, Ce, Ta, Sc, In, S, Ge, Si, and Bi.

2. The cathode active material for a secondary battery of claim 1, wherein the Mp+/M in the core is different than in the shell of the primary particle.

3. The cathode active material for a secondary battery of claim 1, wherein the Mp+/M in the core is different than in the shell of the crystallite.

4. The cathode active material for a secondary battery of claim 1, wherein at least one selected from the secondary particle, the primary particle, and the crystallite includes an oxidation state gradient portion in which the Mp+/M has a gradient toward the center from the surface of the selected at least one.

5. The cathode active material for a secondary battery of claim 1, wherein in at least one selected from the secondary particle, the primary particle, and the crystallite, the Ni2+/Ni3+ is higher in the shell than in the core.

6. The cathode active material for a secondary battery of claim 1, wherein at least one selected from the secondary particle, the primary particle, and the crystallite includes an oxidation state gradient portion in which the Ni2+/M decreases toward the center from the surface of the selected at least one.

7. The cathode active material for a secondary battery of claim 1, wherein at least one selected from the secondary particle, the primary particle, and the crystallite includes an oxidation state gradient portion in which Ni3+/M increases toward the center from the surface of the selected at least one.

8. The cathode active material for a secondary battery of claim 1, wherein in at least one selected from the secondary particle, the primary particle, and the crystallite, the Ni2+/Ni3+ is higher than 1 in the shell.

9. The cathode active material for a secondary battery of claim 1, wherein in at least one selected from the secondary particle, the primary particle, and the crystallite, the Mn3+/Mn4+ is higher in the shell than in the core.

10. The cathode active material for a secondary battery of claim 1, wherein at least one selected from the secondary particle, the primary particle, and the crystallite includes an oxidation state gradient portion in which the Mn3+/M decreases toward the center from the surface of the selected at least one.

11. The cathode active material for a secondary battery of claim 1, wherein at least one selected from the secondary particle, the primary particle, and the crystallite includes an oxidation state gradient portion in which the Mn4+/M increases toward the center from the surface of the selected at least one.

12. The cathode active material for a secondary battery of claim 1, wherein in at least one selected from the secondary particle, the primary particle, and the crystallite, the Mn3+/Mn4+ is higher than 1 in the shell.

13. The cathode active material for a secondary battery of claim 1, wherein the cathode active material contains cobalt (Co) or contains no cobalt (Co).

14. A secondary battery comprising the cathode active material of claim 1.