TW201444162A - Lithium-ion battery positive electrode active material, lithium-ion battery positive electrode, and lithium-ion battery - Google Patents

Abstract

Provided is a lithium-ion battery positive electrode active material with which particle cracks are effectively suppressed, thereby improving battery characteristics such as, for example, battery life, and a positive electrode mixture using the positive active material becomes excellent in coating properties and fixing properties during battery fabrication. The lithium-ion battery positive electrode active material is represented by a composition formula of LixNi1-yMyO2+[alpha], where, M is a metal, 0.9 ≤ x ≤ 1.2, 0 < y ≤ 0.7, and -0.1 ≤ [alpha] ≤ 0.1. The lithium-ion battery positive electrode active material has an average particle diameter (D50) of 7 [mu]m to 12 [mu]m, inclusive. In a micro-compression test, the lithium-ion battery positive electrode active material has an average mechanical strength of 10 MPa to 60 Mpa, inclusive, and an average displacement of 0.2 [mu]m to 1 [mu]m, inclusive, said average mechanical strength being obtained when one of the secondary particles of the positive electrode active material is loaded by a diamond indenter at a loading rate of 2.67 mN/s up to a set load of 49 mN, said average displacement being obtained when the distance of the indenter moving from a position where the indenter touches the particle and starts pressing to a position where pressure cracks have occurred is defined as displacement.

Description

Positive electrode active material for lithium ion battery, positive electrode for lithium ion battery, and lithium ion battery

The present invention relates to a positive electrode active material for a lithium ion battery, a positive electrode for a lithium ion battery, and a lithium ion battery.

A lithium-containing transition metal oxide is generally used as a positive electrode active material of a lithium ion battery. Specifically, it is lithium cobaltate (LiCoO ₂ ), lithium nickelate (LiNiO ₂ ), lithium manganate (LiMn ₂ O ₄ ), etc., in order to improve characteristics (high capacity, cycle characteristics, storage characteristics, internal resistance reduction, The rate characteristic) or the improvement of security is developing the combination of these. Lithium-ion batteries for large-scale applications such as vehicle use or load leveling are required to have different characteristics from those used in mobile phones or personal computers to date.

The above-mentioned lithium cobaltate (LiCoO ₂ ), lithium nickelate (LiNiO ₂ ), or lithium manganate (LiMn ₂ O ₄ ), as disclosed in, for example, Patent Document 1, is a representative material for a positive electrode active material, and each other Each has its own advantages and disadvantages. Lithium cobaltate is a material that achieves a balance between capacity and safety. However, cobalt is a very rare metal called a rare metal, and therefore has a high cost. Lithium nickelate has a very large battery capacity but lacks safety. Lithium manganate is extremely thermally stable, but it has reports of low capacity.

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2006-004724

Recently, a ternary positive electrode active material represented by NiMnCo or NiCoAl is used in terms of high capacity, safety, and cost, and it is said that, for example, when the positive electrode active material of the ternary system is high in nickel ratio, it is used. The lithium ion secondary battery produced therefrom may cause cracks (cracks) in the particles of the positive electrode active material due to charge and discharge, thereby causing deterioration in battery life. Further, in general, a positive electrode mixture is prepared by mixing a positive electrode active material, a conductive auxiliary agent, and a binder, and is applied to one surface or both surfaces of a current collector made of an aluminum foil or the like to prepare a positive electrode. . When the positive electrode mixture is applied to the current collector, pressure is applied to the particles of the positive electrode active material, and the particles are elastically or plastically deformed. Therefore, the deformation of the particles of the positive electrode active material causes a problem that the coatability of the positive electrode mixture using the positive electrode active material to the current collector is deteriorated.

An object of the present invention is to provide a positive electrode active material for a lithium ion battery, which is excellent in battery characteristics such as battery life by suppressing cracking of particles, and coating of a positive electrode mixture using a positive electrode active material in the production of a battery. Good sex and fixation.

In order to suppress cracking in the particles of the positive electrode active material caused by charge and discharge of the lithium ion secondary battery, and to improve the coating property and fixability of the positive electrode mixture, the present inventors focused on the strength of the particles of the positive electrode active material, and further studied In addition, it is found that the hardness of one unit particle of the positive electrode active material, that is, the micro-compression hardness is controlled to a specific range, and the particle of the positive electrode active material is suppressed from being cracked after the charge and discharge, and the particle of the positive electrode active material is applied when the positive electrode mixture is applied. The deformation is very effective. Also, it was found that the composition of the positive electrode active material was set. These characteristics become better as a specific composition and the particle diameter of the positive electrode active material is uniform.

The present invention, which is completed based on the above findings, is a positive electrode active material for a lithium ion battery, which is represented by a composition formula: Li _x Ni _1-y M _y O _2+α (in the above formula, M is Metal, 0.9≦x≦1.2, 0<y≦0.7, -0.1≦α≦0.1), average particle diameter D50 is 7 μm or more and 12 μm or less, in the micro compression test, the positive electrode active material is made by a diamond indenter One particle of the secondary particles is applied at a load speed of 2.67 mN/sec until the load is 49 mN, and the average mechanical strength is 10 MPa or more and 60 MPa or less, and the pressure is pressed against the position at which the particles start to be pressed against the pressure head. When the indenter moving distance from the position of the crack is set to be displaced, the average displacement is 0.2 μm or more and 1 μm or less.

In one embodiment, the positive electrode active material for a lithium ion battery of the present invention has a better average mechanical strength of 15 MPa or more and 60 MPa or less.

In another embodiment, the positive electrode active material for a lithium ion battery of the present invention is one or more selected from the group consisting of Mn, Co, Cu, Al, Zn, Mg, and Zr.

In still another embodiment of the positive electrode active material for a lithium ion battery of the present invention, the M is one or more selected from the group consisting of Mn and Co.

In still another embodiment of the positive electrode active material for a lithium ion battery of the present invention, the average mechanical strength and the average displacement are in a micro-compression test, and one of the secondary particles of the positive electrode active material is made of a diamond-made indenter. The particles were loaded at a load speed of less than 2.67 mN/sec until the set load was 49 mN.

In another aspect, the present invention provides a positive electrode for a lithium ion battery using the positive electrode active material for a lithium ion battery of the present invention.

In still another aspect of the present invention, a lithium ion battery is used The positive electrode for a lithium ion battery of the invention.

According to the present invention, it is possible to provide a positive electrode active material for a lithium ion battery, which is excellent in battery characteristics such as battery life by suppressing cracking of particles, and coating of a positive electrode mixture using a positive electrode active material in the production of a battery. Good sex and fixation.

Figure 1 is a graph showing the relationship between mechanical strength (CS) and displacement of the micro-compression test of Example 3.

Fig. 2 is a graph showing the relationship between mechanical strength (CS) and displacement of the micro compression test of Comparative Example 2.

(Composition of positive active material for lithium ion battery)

As a material of the positive electrode active material for a lithium ion battery of the present invention, a compound useful as a positive electrode active material for a positive electrode for a general lithium ion battery can be widely used, and it is particularly preferable to use lithium cobaltate (LiCoO ₂ ) or lithium nickelate ( A lithium-containing transition metal oxide such as LiNiO ₂ ) or lithium manganate (LiMn ₂ O ₄ ). The positive electrode active material for a lithium ion battery of the present invention produced using such a material is represented by the following composition formula: composition formula: Li _x Ni _1-y M _y O _{2+ α}

(In the above formula, M is a metal, 0.9≦x≦1.2, 0<y≦0.7, -0.1≦α≦0.1).

Further, M is preferably one or more selected from the group consisting of Mn, Co, Cu, Al, Zn, Mg, and Zr, and more preferably one or more selected from the group consisting of Mn and Co.

The positive electrode active material for a lithium ion battery of the present invention is composed of a primary particle, a secondary particle formed by agglomeration of primary particles, or a mixture of primary particles and secondary particles. The primary particles, the secondary particles formed by agglomeration of the primary particles, or the mixture of the primary particles and the secondary particles have an average particle diameter D50 of 7 μm or more and 12 μm or less. When the average particle diameter D50 is 7 μm or more and 12 μm or less, the powder having unevenness is suppressed, and when the electrode of the lithium ion battery is produced, the positive electrode mixture containing the positive electrode active material can be uniformly applied, and the electrode composition can be suppressed. Uneven. Therefore, when used in a lithium ion battery, battery characteristics such as rate characteristics and cycle characteristics become good. The average particle diameter D50 is preferably 7 μm or more and 9 μm or less.

The micro compression test of the present invention can be carried out using a micro compression test apparatus. The micro-compression test apparatus includes a platform for carrying particles to be tested, and a diamond-made indenter having a pressure-sensitive surface having a diameter of 50 to 500 μm for compressing the particles supported on the platform. The micro-compression test apparatus can apply a load of, for example, 9.8 to 4903 mN to the particles by electromagnetic force from the indenter, whereby, for example, particles each having a particle diameter of 1 to 500 μm, that is, each particle can be compressed. The sample was confirmed to be a secondary particle of the positive electrode active material by a microscope, and this was used as a particle to be measured. In the micro compression test, the positive electrode active material for a lithium ion battery of the present invention has a load of 49 mN when a load of a load of 49 mN is applied to a particle of a secondary particle of a positive electrode active material at a load speed of 2.67 mN/sec. The above is 60 MPa or less, and the average displacement is 0.2 μm or more and 1 μm or less. In the micro-compression test of the present invention, tens to hundreds of secondary particles of the positive electrode active material to be tested are used, and each of the particles is tested, and the mechanical strength and displacement are measured to obtain an average value of the measurement results. As the average mechanical strength and average displacement. Apply a load to the particles at a load speed of 2.67 mN/sec until the load is set to 49 mN, so that the particles are compressed and displaced, and the displacement is increased sharply. (The test force required for compression is fixed) The point at which the particle is fractured is determined, and the mechanical strength and displacement at the point are obtained.

That is, the displacement system indicates the moving distance of the indenter of the micro compression test apparatus, and more specifically, it is obtained by the fact that the self-indenter is in contact with the position where the particles mounted on the stage start to be pressed, and the particles are displaced by displacement. The moving distance of the indenter up to the position of the increase (the position of the fracturing).

Further, the mechanical strength (CS) is determined according to JIS R 1639-5 according to the following formula (1).

CS(MPa)=2.48×P/π d ² (1)

[P: test force (N), d: particle size (nm)]

The secondary particles of the positive electrode active material are aggregated by the fine particles (primary particles). Therefore, in the micro compression test apparatus, if the load is increased sharply, sudden deformation occurs, and it becomes difficult to accurately measure the target. The average mechanical strength and average displacement of the positive active material. Therefore, in the present invention, accurate average mechanical strength and average displacement are measured by loading a load of one particle of the secondary particles of the positive electrode active material at a slow speed of 2.67 mN/sec. Further, the average mechanical strength and the average displacement of the positive electrode active material for a lithium ion battery of the present invention may be such that, in the micro compression test, one particle of the secondary particle of the positive electrode active material is made by a diamond indenter. The load was applied at a load speed of 2.67 mN/s until the set load was 49 mN. Further, in the present invention, it was confirmed that the minimum load speed in the range of the above average mechanical strength and average displacement was 0.446 mN/sec.

When the mechanical strength of one particle of the secondary particles of the positive electrode active material is 10 MPa or more and 60 MPa or less, and the average displacement is 0.2 μm or more and 1 μm or less, the positive electrode active material caused by charging and discharging of the lithium ion secondary battery is suppressed. Cracks occur within the particles. Again, use this The coating properties and fixability of the positive electrode mixture of the positive electrode active material are improved. When the mechanical strength is less than 10 MPa, the strength of the positive electrode active material is insufficient, and the rupture of the particles after charging and discharging increases. In addition, when the mechanical strength exceeds 60 MPa, there is a possibility that it is hard as the AS resin, and it is likely to be broken (the impact strength is weak). When the displacement is less than 0.2 μm, the strength of the positive electrode active material is insufficient, and the cracking of the particles after charging and discharging increases. In addition, when the displacement exceeds 1 μm, the following particles may be formed: soft particles, insufficient firing and sintering, and loosely broken, and crystal defects such as breaking strength cannot be obtained. The present invention is based on the fact that the strength of the entire positive electrode active material is not controlled, and further, the mechanical strength and displacement of one unit particle of the positive electrode active material are controlled to the above range, and the particle breakage after charging and discharging is reduced. It is very effective to suppress deformation of the positive electrode active material particles when the positive electrode mixture is applied. By controlling the mechanical strength and displacement of one particle of such secondary particles, a positive electrode active material having good crystallinity and battery characteristics can be produced. The average mechanical strength is preferably 10 MPa or more and 60 MPa or less, and the average mechanical strength is preferably 15 MPa or more and 60 MPa or less.

(Construction of a positive electrode for a lithium ion battery and a lithium ion battery using the same)

The positive electrode for a lithium ion battery according to the embodiment of the present invention has a structure in which a positive electrode mixture is provided on one surface or both surfaces of a current collector made of an aluminum foil or the like, and the positive electrode mixture is a positive electrode active material for a lithium ion battery having the above configuration. It is prepared by mixing conductive additives and adhesives. Moreover, the lithium ion battery of the embodiment of the present invention includes the positive electrode for a lithium ion battery having such a configuration.

(Method for producing positive electrode active material for lithium ion battery)

Next, a method for producing a positive electrode active material for a lithium ion battery according to an embodiment of the present invention will be described in detail.

First, a metal salt solution is prepared. The metal is Ni and metal M. As the metal M, it is preferred It is one or more selected from the group consisting of Mn, Co, Cu, Al, Zn, Mg, and Zr, and more preferably one or more selected from the group consisting of Mn and Co. Further, the metal salt is a sulfate, a chloride, a nitrate, an acetate or the like, and particularly preferably a nitrate. The reason for this is that even if it is mixed as an impurity into the calcined raw material, it can be directly calcined, so that the washing step is omitted, and the nitrate functions as an oxidizing agent, thereby promoting the oxidation of the metal in the calcining raw material. Each metal contained in the metal salt is adjusted in advance so as to have a desired molar ratio. Thereby, the molar ratio of each metal in the positive electrode active material is determined.

Next, lithium carbonate was suspended in pure water, and then a metal salt solution of the above metal was introduced to prepare a metal carbonate slurry. At this time, the lithium carbonate containing fine particles was precipitated in the slurry. Further, when the lithium compound does not react during the heat treatment as a sulfate or a chloride of a metal salt, it is washed with a saturated lithium carbonate solution, and then subjected to filtration separation. On the other hand, when a lithium compound reacts as a lithium raw material in a heat treatment like a nitrate or an acetate, it can be used as a baking precursor without washing, directly filtering and separating, and drying.

Next, a powder of a lithium salt composite (precursor for a lithium ion battery positive electrode material) is obtained by drying the filtered lithium-containing carbonate.

Next, a firing container having a specific size capacity is prepared, and the firing container is filled with a powder of a precursor for a lithium ion battery positive electrode material. Next, the firing container filled with the powder of the precursor for the positive electrode material for a lithium ion battery is transferred to a firing furnace and fired. In the calcination step, the temperature is raised to 850 to 1000 ° C at a heating rate of 140 to 170 ° C / h, and then maintained at this temperature for a specific period of time. Cooling step, cooling 70 ~ 90 ℃ / h of cooling rate from the holding temperature to 300 ℃, and further, this time to feed the supply air amount or more of 10m ³ / h, or to supply an amount of more than 10m ³ / h feed oxygen. According to such a firing condition, heat is uniformly introduced in the temperature increasing step, and the thermal conductivity of the particles becomes good. Further, in the cooling step, cooling to a specific temperature at an appropriate temperature decreasing rate, and supplying appropriate air or oxygen, thereby promoting the rearrangement of atoms in the transition metal layer or the structural change of the transition metal layer to produce lamination defects, oxygen defects, and the like. Further, the average mechanical strength of the secondary particles can be controlled to 10 MPa or more and 60 MPa or less, and the average displacement can be controlled to 0.2 μm or more and 1 μm or less.

Further, when the firing is carried out under a pressure of 101 to 202 kPa, the amount of oxygen in the composition is further increased, which is preferable.

In the method for producing a positive electrode active material for a lithium ion battery of the present invention, the crystallization is promoted by increasing the firing temperature, and the average particle diameter D50 is controlled to be 7 μm or more and 12 μm or less.

[Examples]

The embodiments for better understanding of the invention and its advantages are provided below, but the invention is not limited to the embodiments.

(Examples 1 to 11)

First, a specific input amount of lithium carbonate was suspended in 3.2 liters of pure water, and then a metal salt solution of 4.8 liters was charged. Here, in the metal salt solution, the nitrate hydrate of each metal was adjusted so that each metal became the composition ratio shown in Table 1, and the total metal molar number was adjusted to 14 mol.

By this treatment, the lithium carbonate containing fine particles was precipitated in the solution, and the precipitate was separated by filtration using a filter press.

Then, the precipitate was dried to obtain a lithium-containing carbonate (precursor for a positive electrode material for a lithium ion battery).

Next, a baking container is prepared, and the firing container is filled with a lithium-containing carbonate. Second, in the table The firing was carried out under the firing conditions shown in 2. Then, after cooling to room temperature, it was crushed to obtain a powder of a positive electrode material of a lithium ion secondary battery.

(Comparative examples 1 to 3)

In Comparative Examples 1 to 3, each metal of the raw material was set to the composition shown in Table 1, and fired under the firing conditions shown in Table 2, and the same treatments as in Examples 1 to 11 were carried out.

(Evaluation) - Evaluation of the composition of the positive electrode material -

The metal content in each positive electrode material was measured by an inductively coupled plasma emission spectrometer (ICP-OES), and the composition ratio (mol ratio) of each metal was calculated. The composition of each metal was confirmed as shown in Table 1. Further, the oxygen content was measured by the LECO method to calculate α.

- Evaluation of average particle size D50 -

The particle profile was cut out by FIB, and the SIM image was obtained in this state using a FIB device (SMI3050SE) manufactured by SII Nanotechnology. The average particle diameter D50 is calculated by measuring only the radial direction of the particles existing on an arbitrary straight line on the SIM image.

- Evaluation of average mechanical strength and average displacement -

A micro compression test using a micro compression test apparatus MCT-211 manufactured by Shimadzu Corporation was carried out. In the micro-compression test, first, one of the particles of the secondary particles is pressed by a diamond-made indenter at a load speed of 2.67 mN/sec and a set load of 49 mN to compress and deform, and the displacement is increased sharply. (The test force required for compression is fixed) The point at which the particle is fractured is determined, and the mechanical strength and displacement at the point are obtained.

The mechanical strength (CS) was determined according to JIS R 1639-5 by the following formula (1).

CS(MPa)=2.48×P/π d ² (1)

[P: test force (N), d: particle size (nm)]

This measurement was performed on 20 particles, and the average value thereof was determined.

- Evaluation of discharge capacity and charge and discharge efficiency -

The positive electrode active material, the conductive material, and the binder are weighed at a ratio of 90:5:5, and the positive electrode active material and the conductive material are mixed by dissolving the binder in an organic solvent (N-methylpyrrolidone). Slurry was formed to prepare a positive electrode mixture, which was applied to an Al foil and dried, followed by pressurization to prepare a positive electrode. Then, a 2032 type coin cell in which the counter electrode was used for the evaluation of Li was prepared, and the electrolytic solution was prepared by dissolving 1 M-LiPF ₆ in EC-DMC (1:1), and the current density was measured to be 0.2 C. The discharge capacity at that time. Further, the charge and discharge efficiency was calculated from the initial discharge capacity and the initial charge capacity obtained by the measurement of the battery.

The results of these are shown in Tables 1-3.

According to Table 3, the average particle diameter D50 of Examples 1 to 11 was 7 μm or more. Further, the average mechanical strength was 12 MPa or more and 60 MPa or less, and the average displacement was 0.2 μm or more and 1 μm or less, and the discharge capacity and charge and discharge efficiency of the produced battery were good. Further, the positive electrode mixture containing the positive electrode active material is also excellent in coatability to the current collector.

The average mechanical strength of Comparative Examples 1 to 3 was less than 10 MPa, and in Comparative Examples 1 and 3, the average displacement was more than 1 μm, and the charge and discharge efficiency of the produced battery was poor.

The relationship between the mechanical strength (CS) and the displacement of the micro-compression test of Example 3 and Comparative Example 2 is shown in Figs. 1 and 2, respectively.

Claims (7)

A positive active material for a lithium ion battery, which is represented by a composition formula: Li _x Ni _1-y M _y O _2+α (in the formula, M is a metal, 0.9≦x≦1.2, 0<y≦0.7, -0.1 ≦α≦0.1), the average particle diameter D50 is 7 μm or more and 12 μm or less. In the micro compression test, one particle of the secondary particles of the positive electrode active material is loaded at a load speed of 2.67 mN/sec by a diamond indenter. When the load is applied until the load is 49 mN, the average mechanical strength is 10 MPa or more and 60 MPa or less, and when the moving distance of the indenter from the position where the indenter abutting particles start to press to the position of the fracturing is shifted, The average displacement is 0.2 μm or more and 1 μm or less. The positive electrode active material for a lithium ion battery according to the first aspect of the invention, wherein the average mechanical strength is 15 MPa or more and 60 MPa or less. The positive electrode active material for a lithium ion battery according to the first aspect of the invention, wherein the M is one or more selected from the group consisting of Mn, Co, Cu, Al, Zn, Mg, and Zr. The positive electrode active material for a lithium ion battery according to the third aspect of the invention, wherein the M is one or more selected from the group consisting of Mn and Co. The positive electrode active material for a lithium ion battery according to the first aspect of the invention, wherein the average mechanical strength and the average displacement are in a micro-compression test, and one of the secondary particles of the positive electrode active material is made of a diamond-made indenter. The particles were loaded at a load speed of less than 2.67 mN/sec until the set load was 49 mN. A positive electrode for a lithium ion battery, which comprises the positive electrode active material for a lithium ion battery according to any one of claims 1 to 5. A lithium ion battery using a lithium ion battery having a patent application scope 6 pole.