JP2021018974A - Positive electrode active material with uniform dispersion of aluminum - Google Patents

Abstract

To provide a positive electrode active material in which the dispersion of aluminum is uniform.SOLUTION: A positive electrode active material is a crystalline oxide containing lithium, nickel and aluminum, and the dispersion of aluminum within a primary particle in the oxide is uniform.SELECTED DRAWING: Figure 2

Description

The present invention relates to a positive electrode active material containing lithium, nickel and aluminum.

It is known that various materials are used as the positive electrode active material of the lithium ion secondary battery. Among them, the lithium nickel oxide represented by LiNiO ₂ was widely used as a positive electrode active material at the beginning of the development of the lithium ion secondary battery as described in Patent Document 1.

In addition, a lithium nickel metal oxide in which a part of nickel in LiNiO ₂ is replaced with another metal has been developed, and research on a lithium ion secondary battery using the lithium nickel metal oxide as a positive electrode active material has been energetically studied. It has been done. In particular, in recent years, many lithium ion secondary batteries have been reported in which lithium nickel cobalt aluminum oxide having a layered rock salt structure in which a part of nickel of LiNiO ₂ is replaced with cobalt and aluminum is used as a positive electrode active material.

Patent Document 2 specifically describes a lithium ion secondary battery using LiNi _0.81 Co _0.15 Al _0.04 O ₂ as a positive electrode active material.

In Patent Document 3, Lithium ion using LiNi _0.8 Co _0.16 Al _0.04 O ₂ or LiNi _0.8 Co _0.15 Al _0.04 O _1.9 F _0.1 as the positive electrode active material is adopted. The secondary battery is specifically described.

Patent Document 4 specifically describes a lithium ion secondary battery that employs LiNi _0.8 Co _0.15 Al _0.05 O ₂ as the positive electrode active material.

Patent Document 5 describes Li _1.013 Ni _0.831 Co _0.119 Al _0.050 O ₂ , Li _1.013 Ni _0.858 Co _0.123 Al _0.020 O ₂ or Li ₁ as the positive electrode active material. _.013 A lithium ion secondary battery _using Ni _0.867 Co _0.098 Al _0.035 O ₂ is specifically described.

Japanese Unexamined Patent Publication No. 63-12126 Japanese Unexamined Patent Publication No. 2006-128119 Japanese Unexamined Patent Publication No. 2006-278341 Japanese Unexamined Patent Publication No. 2014-139926 JP-A-2017-195020

In general, lithium nickel cobalt aluminum oxide is obtained by co-precipitating nickel, cobalt and aluminum as hydroxides from an aqueous solution in which nickel, cobalt and aluminum are dissolved to obtain a hydroxide containing nickel, cobalt and aluminum. It is produced by isolating and then mixing the hydroxide with a lithium compound and firing. Then, the lithium nickel cobalt aluminum oxide produced by the above-mentioned production method is used as a positive electrode active material.
However, the present inventor has found that the distribution of aluminum is biased in the positive electrode active material produced by the above-mentioned production method.

The present invention has been made in view of such circumstances, and an object of the present invention is to provide a positive electrode active material having a uniform dispersion of aluminum.

The present inventor considered that the bias of the distribution of aluminum in the positive electrode active material manufactured by the conventional general manufacturing method is that aluminum is more likely to precipitate in the coprecipitation step than other transition metals. .. As a result of diligent studies, by adding a chelate compound to a metal aqueous solution in which aluminum and other transition metals are dissolved to improve the solubility of aluminum in water, and then controlling the pH of the metal aqueous solution, aluminum and others The present inventor has developed a technique for co-precipitating all transition metals in the same pH range. Then, the present inventor has succeeded in producing a positive electrode active material in which aluminum is uniformly dispersed in the primary particles by using such a technique.

The positive electrode active material of the present invention is a crystalline oxide containing lithium, nickel and aluminum, and is characterized in that the dispersion of aluminum in the primary particles in the oxide is uniform.

According to the present invention, it is possible to provide a positive electrode active material having a uniform dispersion of aluminum.

It is a STEM image of the positive electrode active material of Example 1. It is a STEM-EDX image which made Al of the positive electrode active material of Example 1 a measurement target.

The best mode for carrying out the present invention will be described below. Unless otherwise specified, the numerical range "x to y" described in the present specification includes the lower limit x and the upper limit y. Then, a numerical range can be constructed by arbitrarily combining these upper and lower limit values and the numerical values listed in the examples. Further, the numerical value arbitrarily selected from the numerical range can be set as the upper limit value and the lower limit value.

The positive electrode active material of the present invention is a crystalline oxide containing lithium, nickel and aluminum, and is characterized in that the dispersion of aluminum in the primary particles in the oxide is uniform.

In the present specification, "uniform dispersion of aluminum in primary particles" means that when the aluminum concentration in the cross section of the primary particles is analyzed, the relative standard deviation of the aluminum concentration per 400 nm ² cross section in the cross section is 20%. It means that it is as follows.
The relative standard deviation for the aluminum concentration is calculated by the following formula.
The relative standard deviation (%) = 100 × (standard deviation for aluminum concentration per cross-sectional area of 400 nm ²⁾ / (average value for the aluminum concentration per cross-sectional area of 400 nm ²⁾

The relative standard deviation for the aluminum concentration is preferably small. Examples of the range of relative standard deviations for the aluminum concentration include 0.1% to 20%, 0.5% to 15%, 1% to 12%, and 2% to 10%.

The primary particles are particles as a single crystal structure showing the same crystal orientation, and mean particles that are recognized as one particle when observed with an electron microscope.

The particle size of the primary particles is preferably small. This is because it can be expected that the charge transfer resistance when functioning as the positive electrode active material is reduced, and as a result, charging / discharging at a high rate and charging / discharging at a low temperature can be expected to proceed smoothly. However, primary particles having an excessively small particle size are not preferable. The reason is that an inconvenient reaction is likely to occur.

The average particle size of the primary particles is preferably in the range of 20 nm to 500 nm, more preferably in the range of 30 nm to 300 nm, further preferably in the range of 50 nm to 200 nm, and particularly preferably in the range of 70 nm to 150 nm. When the constituent metal species of the positive electrode active material of the present invention are the same, the particle size of the primary particles tends to decrease as the aluminum content increases.

In the present specification, the particle size of the primary particle is defined by analyzing an electron microscope image of the cross section of the primary particle to calculate the cross-sectional area of the primary particle, and here, it is assumed that the cross section of the primary particle is a circle. It means the diameter calculated from the cross-sectional area. Further, the average particle size of the primary particles means an arithmetic mean value of the particle size of the primary particles.

The particle size of the primary particles is preferably uniform to some extent. The relative standard deviation of the particle size of the primary particles is preferably 50% or less. Examples of the range of relative standard deviations of the particle diameters of the primary particles are 1% to 50%, 5% to 40%, and 10% to 35%.

The positive electrode active material of the present invention is produced as secondary particles, which are aggregates of a plurality of primary particles. The average particle size of the positive electrode active material of the present invention is preferably in the range of 1 to 30 μm, more preferably in the range of 3 to 20 μm, and even more preferably in the range of 5 to 15 μm.
The average particle size of the positive electrode active material of the present invention means D ₅₀ in the measurement by the laser scattering diffraction type particle size distribution meter.

In the particle size distribution of the positive electrode active material of the present invention as measured by a laser scattering diffraction type particle size distribution meter, the value of D _90- D ₁₀ is 10 μm or more, or the value of (D _90- D ₁₀ ) / D ₅₀ is. It is preferably 0.6 or more. These parameters mean that the particle size distribution of the secondary particles in the positive electrode active material of the present invention is broad. When the particle size distribution is broad, the shape of the frequency distribution of particle size may show a single peak, but it may also show multimodality.

The positive electrode active material having a broad particle size distribution is suitable for producing with good reproducibility even when the scale of the manufacturing equipment and the conditions of the manufacturing method are changed. Further, in the process of forming the positive electrode active material layer on the positive electrode current collector during the positive electrode production, small positive electrode active material particles can enter between the large positive electrode active material particles, so that the positive electrode has a broad particle size distribution. By using the active material, it becomes possible to form a high-density positive electrode active material layer.

Examples of the range of D _{90 to} D ₁₀ include ₁₀ μm to 30 μm, 12 μm to 25 μm, and 14 μm to 20 μm. Examples of the range of (D _90- D ₁₀ ) / D ₅₀ include 0.6 to 2, 0.8 to 1.8, and 1 to 1.6.

The crystal structure exhibited by the positive electrode active material of the present invention can be exemplified by a rock salt structure, a layered rock salt structure, and a spinel structure, although it depends on the contents of lithium, nickel, aluminum, oxygen, and other elements. A rock salt structure is preferred.

In the positive electrode active material of the present invention, lithium is a charge carrier. Lithium separates from the lithium sites in the crystal structure during charging and is inserted into the lithium sites in the crystal structure during discharge. Nickel is thought to contribute preferentially to the redox reaction during charge and discharge, and aluminum is thought to contribute to the maintenance of the crystal structure.

As a suitable oxide in the positive electrode active material of the present invention, an oxide represented by the following general formula (1) showing a layered rock salt structure can be exemplified.
Formula _{(1) Li a Ni b Al} c M d D e O f F g
In the general formula (1), a, b, c, d, e, f, g are 0.5 ≦ a ≦ 2, 0 <b <1, 0 <c ≦ 0.2, 0 ≦ d <1, It satisfies 0 ≦ e ≦ 0.2, b + c + d + e = 1, 1.8 ≦ f ≦ 2.2, and 0 ≦ g ≦ 0.2. M is selected from Co, Mn, W and Zr. D is a doping element.

The value of b in the general formula is a value that greatly affects the capacity of the positive electrode active material.
In the general formula, b preferably satisfies 0.85 ≦ b ≦ 0.99, more preferably 0.9 ≦ b ≦ 0.98, and satisfies 0.93 ≦ b ≦ 0.97. It is more preferable to do so.

In the general formula, c preferably satisfies 0.001 ≦ e ≦ 0.1, more preferably 0.001 ≦ e ≦ 0.09, and 0.001 ≦ c ≦ 0.05. Satisfaction is even more preferable, 0.001 ≦ c ≦ 0.03 is even more preferable, and 0.002 ≦ c ≦ 0.01 is particularly preferable.

In the general formula, d preferably satisfies 0 ≦ d ≦ 0.2, more preferably 0.001 ≦ d ≦ 0.1, and more preferably 0.003 ≦ d ≦ 0.07. Is more preferable, and 0.005 ≦ d ≦ 0.05 is particularly preferable.
M _d can also be expressed as (Co _d1 , Mn _d2 , W _d3 , Zr _d4 ). d = d1 + d2 + d3 + d4.

Examples of the range of d1 include 0 ≦ d1 ≦ 0.2, 0.001 ≦ d1 ≦ 0.1, 0.01 ≦ d1 ≦ 0.08, and 0.03 ≦ d1 ≦ 0.06.
Examples of the range of d2 include 0 ≦ d2 ≦ 0.1, 0.001 ≦ d2 ≦ 0.08, 0.005 ≦ d2 ≦ 0.05, and 0.01 ≦ d2 ≦ 0.03.
Examples of the range of d3 include 0 ≦ d3 ≦ 0.1, 0.001 ≦ d3 ≦ 0.05, 0.003 ≦ d3 ≦ 0.03, and 0.004 ≦ d3 ≦ 0.01.
Examples of the range of d4 include 0 ≦ d4 ≦ 0.1, 0.001 ≦ d4 ≦ 0.05, 0.002 ≦ d4 ≦ 0.01, and 0.002 ≦ d4 ≦ 0.008.

The values of a, e, f, and g may be values within the range specified by the general formula, and preferably 0.5 ≦ a ≦ 1.5, 0 ≦ e ≦ 0.1, 1.8 ≦ f ≦ 2. .1, 0 <g ≦ 0.15, more preferably 0.8 ≦ a ≦ 1.3, 0 <e ≦ 0.01, 1.9 ≦ f ≦ 2.1, 0 <g ≦ 0.1 It can be exemplified.

D in the general formula is a doping element, which is an element capable of improving the characteristics of the positive electrode active material. F in the general formula is also an element capable of improving the characteristics of the positive electrode active material.

As D, Na, Ca, V, Cu, Sn, Tl, Fe, Sr, Ti, Ba, Y, rare earth elements, Os, Ir, Cd, Re, Bi, Rh, Cr, Zn, In, Pb, Ru , Nb, P, S can be exemplified.

The method for producing the positive electrode active material of the present invention, which is characterized in that the dispersion of aluminum in the primary particles is uniform, will be described.

The method for producing a positive electrode active material of the present invention (hereinafter, may be simply referred to as "the production method of the present invention") is
Precipitation step of mixing an aqueous solution in which nickel, aluminum and a chelate compound are dissolved and a basic substance to precipitate a transition metal hydroxide containing nickel and aluminum.
A precursor forming step of heating the transition metal hydroxide to remove adhering water or forming a precursor as a transition metal oxide.
It has a firing step of mixing the precursor and a lithium salt and firing.

In the production method of the present invention, coprecipitation of nickel and aluminum in the precipitation step is a technical key.

The precipitation step will be described. Unless otherwise specified, the pH specified in the present specification refers to a value measured at 25 ° C.

In order to prepare an aqueous solution in which nickel, aluminum and a chelate compound are dissolved (hereinafter, may be referred to as a transition metal-containing aqueous solution), the nickel compound has a metal composition ratio in the transition metal hydroxide to be precipitated. And aluminum compounds may be added to water in appropriate proportions, and chelate compounds may be added to dissolve these compounds in water.

Examples of the nickel compound include nickel sulfate, nickel carbonate, nickel nitrate, nickel acetate, and nickel chloride. Examples of the aluminum compound include aluminum sulfate, aluminum carbonate, aluminum nitrate, and aluminum chloride.

The chelate compound is an amino group, an amide group, an imide group, an imino group, a cyano group, an azo group, a hydroxyl group, an alkoxy group, a carboxyl group, an ester group, an ether group, a carbonyl group, or a phosphate group that can be coordinated with a metal ion. , Phosphate group, phosphonic acid group, phosphonic acid ester group, phosphinic acid group, phosphinic acid ester group, phosphenic acid group, phosphenic acid ester group, phosphenic acid group, phosphenic acid ester group, thiol group, sulfide group, It is a compound having a plurality of sulfinyl groups, sulfonyl groups, sulfonic acid groups, thiocarboxyl groups, thioester groups or thiocarbonyl groups, and having a structure capable of coordinating to metal ions with the plurality of the groups.

Specific examples of chelate compounds include polyamine compounds such as ethylenediamine and diethylenetriamine, amino acids such as glycine, alanine, cysteine, glutamine, arginine, aspartic acid, aspartic acid, serine and ethylenediaminetetraacetic acid, malonic acid, succinic acid, glutaric acid and maleine. Examples thereof include dicarboxylic acids such as acids and phthalic acids, and hydroxycarboxylic acids.

As the chelating compound, hydroxycarboxylic acid is particularly preferable. Examples of the hydroxycarboxylic acid having a hydroxyl group and a carboxylic acid group in the molecule include an aliphatic hydroxycarboxylic acid and an aromatic hydroxycarboxylic acid.

The aliphatic hydroxycarboxylic acids include glycolic acid, lactic acid, tartronic acid, glyceric acid, 2-hydroxybutyric acid, 3-hydroxybutyric acid, γ-hydroxybutyric acid, malic acid, tartaric acid, citramalic acid, citric acid, isocitric acid, and leucine acid. , Mevalonic acid, pantoic acid, quinic acid, shikimic acid can be exemplified.

Examples of the aromatic hydroxycarboxylic acid include o-hydroxybenzoic acid derivatives such as salicylic acid, gentisic acid and orsellinic acid, mandelic acid, benzylic acid and 2-hydroxy-2-phenylpropionic acid.

All of the above-mentioned specific hydroxycarboxylic acids can form a conformation in which an OH group and a CO ₂ H group can be coordinated with the same metal ion.

It is generally known that when the pH of an aqueous metal solution is made basic, metal hydroxides are precipitated. The pH at which the metal hydroxide is precipitated differs depending on the type of metal. Therefore, when a basic substance is added to a metal aqueous solution in which a plurality of types of metal ions are dissolved to make the pH of the metal aqueous solution basic, the type of metal hydroxide precipitated at each pH is different. It will be. As a result, it is expected that the composition of the metal hydroxide will vary.

However, in the production method of the present invention, the chelate compound is dissolved in the transition metal-containing aqueous solution. Here, since the chelate compound coordinates with the metal ion to form a stable complex, the solubility of the metal ion in water is improved. Therefore, even if the metal is precipitated at a relatively low pH under the condition that the chelate compound is not present, the precipitation pH becomes high in the transition metal-containing aqueous solution in which the chelate compound is dissolved. As a result, nickel and aluminum are both precipitated as hydroxides in the same pH range.

Comparing the solubility of nickel and aluminum in basic water, aluminum is inferior in solubility. In the production method of the present invention, the chelate compound is added to the transition metal-containing aqueous solution in order to improve the solubility of aluminum.

The molar ratio of the chelate compound to aluminum in the transition metal-containing aqueous solution is preferably 1 or more, preferably in the range of 1 to 10, more preferably in the range of 1.5 to 8, and even more preferably in the range of 2 to 6. ..

In order to prepare the transition metal-containing aqueous solution, it is preferable to use a reaction tank equipped with a stirrer, and it is preferable to use a reaction tank equipped with a device capable of introducing an inert gas such as nitrogen or argon. Further, it is more preferable to use a reaction vessel equipped with an apparatus under constant temperature conditions.

The transition metal-containing aqueous solution is preferably heated in the range of 40 to 90 ° C, more preferably 40 to 80 ° C.

In order to mix the transition metal-containing aqueous solution and the basic substance while appropriately controlling the pH, it is rational to use the basic aqueous solution as the basic substance.
To prepare a basic aqueous solution, the basic compound may be dissolved in water.

In order to prepare a basic aqueous solution, it is preferable to use a reaction tank equipped with a stirrer, and it is preferable to use a reaction tank equipped with a device capable of introducing an inert gas such as nitrogen or argon. Further, it is more preferable to use a reaction vessel equipped with an apparatus under constant temperature conditions.

The pH of the basic aqueous solution is preferably in the range of 11 to 14, more preferably in the range of 11 to 13, and even more preferably in the range of 11 to 12. The basic compound that can be used may be one that dissolves in water and exhibits basicity. For example, alkali metal hydroxides such as ammonia, sodium hydroxide, potassium hydroxide, and lithium hydroxide, sodium carbonate, and carbonic acid. Alkali metal carbonates such as potassium and lithium carbonate, alkali metal phosphates such as trisodium phosphate, tripotassium phosphate and trilithium phosphate, and alkali metal acetates such as sodium acetate, potassium acetate and lithium acetate. Can be done. The basic compound may be used alone or in combination of two or more.
Since the pH of the reaction solution is preferably kept in a suitable range in the precipitation step, it is preferable that the basic aqueous solution contains at least a basic compound having a buffering ability. Examples of the basic compound having a buffering ability include ammonia, alkali metal carbonate, alkali metal phosphate, and alkali metal acetate.

The basic aqueous solution is preferably heated in the range of 40 to 90 ° C, more preferably 40 to 80 ° C.

In the precipitation step, by mixing a transition metal-containing aqueous solution and a basic substance, metal ions and hydroxide ions react to form transition metal hydroxides containing nickel and aluminum, which have low solubility in water. Produces and precipitates. The precipitated transition metal hydroxide particles form the basis of the primary particles of the positive electrode active material of the present invention. Therefore, if the precipitation step is performed under a condition in which the precipitation rate of the transition metal hydroxide is extremely high, that is, a condition in which nuclei of the transition metal hydroxide are generated everywhere, irregular transition metal hydroxide particles are formed. As a result, unfavorable crystallization of the primary particles of the positive electrode active material of the present invention may occur. Therefore, in the precipitation step, it is preferable to precipitate the transition metal hydroxide particles under the mildest possible conditions.

In the precipitation step, it is preferable to keep the reaction solution in which the transition metal-containing aqueous solution and the basic substance are mixed at a constant pH. The pH value here means the value itself obtained by measuring the reaction solution with a pH meter. The pH is preferably in the range of 10 to 14, more preferably in the range of 10 to 12, and particularly preferably in the range of 10 to 11.

The precipitation step is preferably carried out in a reaction vessel equipped with a stirrer, and more preferably carried out in a reaction vessel equipped with an apparatus capable of introducing an inert gas such as nitrogen or argon. Further, a reaction vessel provided with an apparatus under constant temperature conditions is more preferable.

In the precipitation step, it is preferable that the amount of dissolved oxygen present in the reaction system is small. If the amount of dissolved oxygen present in the reaction system is large, an inconvenient oxidation reaction may occur, or suitable crystallization of the transition metal hydroxide accompanying precipitation of the transition metal hydroxide may be hindered.

In order to reduce the amount of dissolved oxygen present in the reaction system, the precipitation step is performed under heating, while introducing an inert gas into the reaction system, oxygen scavenger, reducing agent, and antioxidant. It is preferable to carry out in the presence of an agent or the like.

As the heating condition, the range of 40 to 90 ° C. and 60 to 80 ° C. can be exemplified.
Examples of the inert gas include nitrogen, argon and helium.
Deoxidizers, reducing agents, antioxidants include ascorbic acid and its salts, glioxylic acid and its salts, hydrazine, dimethylhydrazine, hydroquinone, dimethylamine borane, NaBH ₄ , NaBH ₃ CN, KBH ₄ , sulfite and its salts. , Thiosulfate and its salt, pyrosulfite and its salt, phosphorous acid and its salt, hypophosphorous acid and its salt can be exemplified.

After the precipitation step, the transition metal hydroxide is separated by filtration or the like. The transition metal hydroxide can be obtained by the above method. Considering that the transition metal hydroxide produced in the precipitation step becomes a production intermediate for the positive electrode active material of the present invention, the following invention can be grasped.
A nickel-aluminum-containing hydroxide which is a particulate hydroxide containing nickel and aluminum, wherein the dispersion of aluminum in the particles is uniform.

A compound containing a metal M (that is, a metal selected from Co, Mn, W, and Zr) other than lithium, nickel, and aluminum, and a compound containing a doping element are added to the transition metal-containing aqueous solution in the precipitation step. The transition metal hydroxide containing the metal M or the doping element may be produced.

Next, the precursor forming step will be described. The precursor forming step is a step of heating a transition metal hydroxide to form a transition metal hydroxide from which adhering water has been removed, or heating a transition metal hydroxide to form a transition metal oxide. Is. The transition metal hydroxide from which the adhering water has been removed or the transition metal oxide is a precursor of the positive electrode active material.

The heating temperature is preferably in the range of 100 to 800 ° C, more preferably in the range of 200 to 700 ° C, and particularly preferably in the range of 300 to 600 ° C. The precursor forming step may be carried out under normal pressure or under reduced pressure.

Considering that the transition metal oxide produced in the precursor forming step becomes a production intermediate for the positive electrode active material of the present invention, the following invention can be grasped.
A nickel-aluminum-containing oxide which is a particulate oxide containing nickel and aluminum, and is characterized in that the dispersion of aluminum in the particles is uniform.

Next, the firing process will be described. The firing step is a step of mixing the precursor and the lithium salt and firing.

Examples of the lithium salt include lithium carbonate, lithium hydroxide, lithium nitrate, lithium acetate, lithium oxalate, and lithium halide. The blending amount of the lithium salt may be appropriately determined so as to obtain a positive electrode active material having a desired lithium composition.

Examples of the mixing device include a mortar and pestle, a stirring mixer, a V-type mixer, a W-type mixer, a ribbon-type mixer, a drum mixer, and a ball mill.

In the firing step, a compound other than the lithium salt may be mixed. In particular, it is preferable that a compound selected from Na compound, F compound and P compound is mixed. Due to the presence of Na, F, and P, improvement in the rate characteristics and / or capacity retention rate of the lithium ion secondary battery including the positive electrode active material of the present invention can be expected.

Examples of Na compounds include sodium salts such as NaF, NaCl, NaCl, NaI, Na ₃ PO ₄ , Na ₂ HPO ₄ , NaH ₂ PO ₄ , Na ₂ SO ₄ , NaHSO ₄ , NaNO ₃ , and CH ₃ CO ₂ Na. it can.
Examples of the F compound include metal fluorides such as LiF, NaF, KF, MgF ₂ , CaF ₂ , BaF ₂ , and AlF ₃ .
The P _{compounds, H 3 PO 4, LiH 2} PO 4, Li 2 HPO 4, Li 3 PO 4, NaH 2 PO 4, Na 2 HPO 4, Na 3 PO 4, KH 2 PO 4, K 2 HPO 4, Phosphoric acid and phosphate such as K ₃ PO ₄ can be exemplified.

The firing may be carried out in an atmospheric atmosphere or an oxygen gas atmosphere, or in the presence of an inert gas such as helium or argon. The heating temperature at the time of firing can be exemplified in the range of 400 to 1100 ° C, 500 to 1000 ° C, and 600 to 800 ° C. The heating time at the time of firing can be exemplified by 1 to 50 hours.

The firing may be carried out under a single temperature condition, may be carried out by combining a plurality of firing steps having different temperature conditions, or may be carried out by setting a specific temperature raising program.

As a method of combining a plurality of firing steps having different temperature conditions, a first firing step of heating at 400 to 800 ° C. to form a first fired body and a second method of heating the first fired body at 550 to 1000 ° C. The firing process can be mentioned. By combining a plurality of firing steps, a suitable positive electrode active material can be produced.

The temperature of the first firing step can be exemplified in the range of 400 to 800 ° C. and 650 to 750 ° C. The heating time of the first firing step can be exemplified in the range of 3 to 30 hours, 5 to 20 hours, and 5 to 15 hours.

The second firing step is a step of heating the first fired body at 550 to 1000 ° C.
Here, from the viewpoint of crystal formation of the positive electrode active material, it is easier to form crystals having a uniform shape when heated at a low temperature as much as possible. Therefore, the temperature in the second firing step can be exemplified in the range of 550 to 950 ° C, 550 to 900 ° C, 550 to 850 ° C, and 550 to 800 ° C.

The heating time of the second firing step can be exemplified in the range of 3 to 30 hours, 5 to 20 hours, and 5 to 15 hours.

The fired body obtained in the firing step is preferably used as a positive electrode active material having a constant particle size distribution through a crushing step and a classification step.

The production method of the present invention may have a coating step of coating the precursor with a metal compound before the firing step. That is, there is a production method in which a firing step is performed after the coating step of coating the precursor with a metal compound is performed after the precursor forming step (hereinafter, referred to as the second production method of the present invention). ), The positive electrode active material of the present invention may be produced.

The coating process will be described. The coating step is a step of coating a precursor "transition metal hydroxide from which adhering water has been removed" or "transition metal oxide" with a metal compound to form a coated body.
Hereinafter, a case where the “transition metal oxide” is coated with a metal compound will be described. In the case of coating the "transition metal hydroxide from which the adhering water has been removed" with a metal compound, in the following description, the "transition metal oxide" is appropriately appropriate for the "transition metal hydroxide from which the adhering water has been removed". It should be read as.

Specific examples of the metal compound include ZrO ₂ , CaVO ₃ , MnO ₂ , La ₂ CuO ₄ , La ₂ NiO ₄ , SnO ₂ , Tl ₂ Mn ₂ O ₇ , EuO, Fe ₂ O ₃ , CamnO ₃ , SrMnO ₃ , and so on. (Sr, La) TiO ₃ , La TIM ₃ , SrFeO ₃ , BaMoO ₃ , CaMoO ₃ , Ln ₂ Os ₂ O ₇ (Ln is an element selected from Y and rare earth elements), Tl ₂ Ir ₂ O ₇ , Cd ₂ Re ₂ O ₇ , Lu ₂ Ir ₂ O ₇ , Bi ₂ Rh ₂ O ₇ , Bi ₂ Ir ₂ O ₇ , Ti ₂ O ₃ , WO ₂ , VO, V ₂ O ₃ , LaMnO ₃ , CaCrO ₃ , LaCoO _{3, (ZnO) 5, SrCrO} 3, In 0.97 Y 0.03 O 3, Zn x Al y O (x + y = 1), LiV 2 O 4, Na 1-x CoO 2 (0 <x <1) , LiTi ₂ O ₄ , SrMoO ₃ , BaPbO ₃ , Tl ₂ Os ₂ O ₇ , Pb ₂ Os ₂ O ₇ , Pb ₂ Ir ₂ O ₇ , Lu ₂ Ru ₂ O ₇ , Bi ₂ Ru ₂ O ₇ , Sr RuO ₃ , CaRuO ₃ , CrO ₂ , MoO ₂ , ReO ₂ , TiO, LaO, SmO, LaNiO ₃ , SrVO ₃ , ReO ₃ , IrO ₂ , RuO ₂ , RhO ₂ , OsO ₂ , NdO, NbO, La ₂ O _{3 LaSr x Co y O 3 (x} + y = 1), NaCoO 3, NaNiO 3, LiCoO 3, metal oxide selected from LiNiO ₃ or can be exemplified metal hydroxides of these precursors.
Among the metal compounds, the metal oxide preferably has a crystal structure such as a perovskite type.

In order to coat the transition metal oxide with a metal compound, a method of spraying a precursor of each metal compound or an aqueous solution in which each metal is dissolved on the transition metal oxide and then / or simultaneously drying the transition metal oxide may be adopted. .. Further, the transition metal oxide is immersed in the precursor of each metal compound or the aqueous solution in which each metal is dissolved, and the precursor of each metal compound or the hydroxide of each metal is adhered to the surface of the transition metal oxide. After that, a method of heating and drying may be adopted. In particular, a dispersion of a transition metal oxide is mixed with a precursor of each metal compound or an aqueous solution in which each metal is dissolved to precipitate a hydroxide of each metal on the surface of the transition metal oxide, and then dried. (Hereinafter, it may be referred to as a precipitation method) is preferably adopted.

Hereinafter, a suitable precipitation method when the metal of the metal compound is Zr will be described in detail. The precipitation method has the following coat-1) step, coat-2) step and coat-3) step. When the metal of the metal compound is a metal other than Zr, the zirconium in the steps 1), coat-2) and coat-3) may be read as the metal. When the metal of the metal compound is a plurality of metals, an aqueous solution containing the plurality of metals may be used in the coat-2) step, or while changing the metal type of the metal aqueous solution, coat-1) The step, the coat-2) step and the coat-3) step may be repeated.

coat-1) Dispersion solution preparation step for dispersing transition metal oxides in water,
coat-2) A zirconium precipitation step of mixing a zirconium aqueous solution containing a chelate compound with the dispersion to precipitate zirconium hydride on the surface of a transition metal oxide.
coat-3) A step of drying a transition metal oxide in which zirconium hydride is precipitated on the surface to form a coated body.

It is preferable to pulverize the transition metal oxide before the coat-1) step. Further, it is preferable to adjust the pH so that the pH of the dispersion liquid is in the range of about 9 to 12.

Next, the coat-2) step will be described.
The zirconium aqueous solution containing the chelate compound is produced by dissolving the zirconium compound and the chelate compound in water. The zirconium aqueous solution containing the chelate compound is usually an acidic solution. The molar ratio of the chelate compound to zirconium in the zirconium aqueous solution is preferably 1 or more, preferably in the range of 1 to 10, more preferably in the range of 1.5 to 8, and even more preferably in the range of 2 to 6.

Examples of the zirconium compound include zirconium oxide, zirconium hydride, zirconium sulfate, zirconium nitrate, zirconium phosphate, and zirconium halide.

For the explanation of the chelate compound, the explanation in the precipitation step is incorporated.

In the coat-2) step, it is preferable to control the pH of the mixed solution in the coat-2) step in order to efficiently precipitate zirconium. Here, it is assumed that zirconium hydride having low solubility is deposited on the surface of the transition metal oxide by setting the pH of the mixed solution to the alkaline side. For example, it is preferable to add a basic aqueous solution so that the pH of the solution in step 2) is in the range of 9 to 13, 11 to 13 or 12 to 13. As the basic aqueous solution, the one described in the precipitation step may be adopted.

The transition metal oxide that has undergone the coat-2) step is separated by a method such as filtration and subjected to the coat-3) step.

The drying in the coat-3) step is preferably carried out under heating and / or under reduced pressure. The heating temperature can be exemplified in the range of 100 to 500 ° C. and 200 to 400 ° C.
The main purpose of the drying in the coat-3) step is to remove the water adhering to the transition metal oxide in which zirconium hydride is precipitated on the surface. However, by raising the heating temperature, zirconium hydride existing on the surface of the transition metal oxide may be dehydrated and changed to zirconium oxide. That is, the coated body may be a transition metal oxide coated with zirconium hydride or a transition metal oxide coated with zirconium hydride.

In the second production method of the present invention, since the transition metal oxide particles are coated with a metal compound in the coating step, the coated metal compound acts as a barrier in the firing step, and nickel forms a layered rock salt structure or the like. It is considered that the movement to the lithium site of the crystal structure is suppressed.

The positive electrode active material of the present invention is used as the positive electrode active material of a lithium ion secondary battery. The lithium ion secondary battery provided with the positive electrode active material of the present invention (hereinafter, may be referred to as the lithium ion secondary battery of the present invention) will be described below. Specifically, the lithium ion secondary battery of the present invention includes a positive electrode, a negative electrode, a solid electrolyte or an electrolytic solution and a separator including the positive electrode active material of the present invention.

The positive electrode has a current collector and a positive electrode active material layer bonded to the surface of the current collector.

A current collector is a chemically inert electron conductor that keeps current flowing through the electrodes during the discharge or charging of a lithium-ion secondary battery. Collectors include at least one selected from silver, copper, gold, aluminum, tungsten, cobalt, zinc, nickel, iron, platinum, tin, indium, titanium, ruthenium, tantalum, chromium, molybdenum, and stainless steel. Metallic materials can be exemplified. The current collector may be covered with a known protective layer. A current collector whose surface is treated by a known method may be used as the current collector.

The current collector can take the form of foil, sheet, film, linear, rod, mesh or the like. Therefore, as the current collector, for example, a metal foil such as a copper foil, a nickel foil, an aluminum foil, or a stainless steel foil can be preferably used. When the current collector is in the form of a foil, a sheet, or a film, the thickness thereof is preferably in the range of 1 μm to 100 μm.

The positive electrode active material layer contains a positive electrode active material and, if necessary, a conductive auxiliary agent and / or a binder.

As the positive electrode active material, only the positive electrode active material of the present invention may be adopted, or the positive electrode active material of the present invention and a known positive electrode active material may be used in combination.

The conductive auxiliary agent is added to increase the conductivity of the electrode. Therefore, the conductive auxiliary agent may be arbitrarily added when the conductivity of the electrode is insufficient, and may not be added when the conductivity of the electrode is sufficiently excellent. The conductive auxiliary agent may be a chemically inert electron high conductor, and examples thereof include carbon black, which are carbonaceous fine particles, graphite, Vapor Grown Carbon Fiber, and various metal particles. To. Examples of carbon black include acetylene black, Ketjen black (registered trademark), furnace black, and channel black. These conductive auxiliary agents can be added to the active material layer alone or in combination of two or more.

The mixing ratio of the conductive auxiliary agent in the active material layer is preferably 1: 0.005 to 1: 0.5, and 1: 0.01 to 1: 0 in terms of mass ratio. It is more preferably .2, and even more preferably 1: 0.03 to 1: 0.1. This is because if the amount of the conductive auxiliary agent is too small, an efficient conductive path cannot be formed, and if the amount of the conductive auxiliary agent is too large, the moldability of the active material layer is deteriorated and the energy density of the electrode is lowered.

The binder serves to anchor the active material or the conductive auxiliary agent to the surface of the current collector and maintain the conductive network in the electrode. Examples of the binder include fluororesins such as polyvinylidene fluoride, polytetrafluoroethylene and fluororubber, thermoplastic resins such as polypropylene and polyethylene, imide resins such as polyimide and polyamideimide, alkoxysilyl group-containing resins and poly ( Examples thereof include acrylic resins such as meta) acrylic acid, styrene-butadiene rubber (SBR), and carboxymethyl cellulose. These binders may be used alone or in combination of two or more.

The mixing ratio of the binder in the active material layer is preferably 1: 0.001 to 1: 0.3, preferably 1: 0.005 to 1: 0, in terms of mass ratio. It is more preferably .2, and even more preferably 1: 0.01 to 1: 0.15. This is because if the amount of the binder is too small, the moldability of the electrode is lowered, and if the amount of the binder is too large, the energy density of the electrode is lowered.

The negative electrode has a current collector and a negative electrode active material layer bonded to the surface of the current collector. As the current collector, the one described in the positive electrode may be appropriately adopted. The negative electrode active material layer contains a negative electrode active material and, if necessary, a conductive auxiliary agent and / or a binder.

As the negative electrode active material, a known material may be used, and examples thereof include a carbon-based material capable of occluding and releasing lithium, an element capable of alloying with lithium, and a compound having an element capable of alloying with lithium. ..

Examples of the carbon-based material include graphitizable carbon, graphite, cokes, graphites, glassy carbons, calcined organic polymer compound, carbon fibers, activated carbon, and carbon blacks. Here, the calcined organic polymer compound refers to a material obtained by calcining a polymer material such as phenols or furans at an appropriate temperature to carbonize it.

Specific elements that can be alloyed with lithium include Na, K, Rb, Cs, Fr, Be, Mg, Ca, Sr, Ba, Ra, Ti, Ag, Zn, Cd, Al, Ga, In, and Si. , Ge, Sn, Pb, Sb, Bi can be exemplified, and Si or Sn is particularly preferable.

Specific examples of the compound having an element that can be alloyed with lithium include ZnLiAl, AlSb, SiB ₄ , SiB ₆ , Mg ₂ Si, Mg ₂ Sn, Ni ₂ Si, TiSi ₂ , MoSi ₂ , CoSi ₂ , and NiSi ₂ . _{CaSi 2, CrSi 2, Cu 5} Si, FeSi 2, MnSi 2, NbSi 2, TaSi 2, VSi 2, WSi 2, ZnSi 2, SiC, Si 3 N 4, Si 2 N 2 O, SiO v (0 <v ≦ 2), SnO _w (0 <w ≦ 2), SnSiO ₃ , LiSiO or LiSnO can be exemplified, and in particular, SiO _x (0.3 ≦ x ≦ 1.6 or 0.5 ≦ x ≦ 1.5). Is preferable.

The negative electrode active material preferably contains a Si-based material having Si. The Si-based material is preferably composed of silicon and / or a silicon compound capable of occluding and releasing lithium ions, and for example, SiO _x (0.5 ≦ x ≦ 1.5) is preferable. Although silicon has a large theoretical charge / discharge capacity, silicon has a large volume change during charge / discharge. Therefore, by using SiO _x containing silicon as the negative electrode active material, it is possible to alleviate the volume change of silicon.

As the negative electrode active material, a Si material obtained by heating layered polysilane obtained by treating CaSi ₂ with an acid such as hydrochloric acid or hydrofluoric acid at 300 to 1000 ° C. may be adopted. Further, the Si material may be heated together with a carbon source and carbon-coated to be used as the negative electrode active material.

As the negative electrode active material, one or more of the above can be used.

As the conductive auxiliary agent and the binder used for the negative electrode, those described for the positive electrode may be appropriately and appropriately adopted in the same blending ratio.

In order to form an active material layer on the surface of the current collector, a conventionally known method such as a roll coating method, a die coating method, a dip coating method, a doctor blade method, a spray coating method, or a curtain coating method is used to collect current. The active material may be applied to the surface of the body. Specifically, the active material, the solvent, and if necessary, the binder and / or the conductive auxiliary agent are mixed to prepare a slurry. Examples of the solvent include N-methyl-2-pyrrolidone, methanol, methyl isobutyl ketone, and water. The slurry is applied to the surface of the current collector and then dried. In order to increase the electrode density, the dried one may be compressed.

As the solid electrolyte, one that can be used as the solid electrolyte of the lithium ion secondary battery may be appropriately adopted.

The electrolytic solution contains a non-aqueous solvent and an electrolyte dissolved in the non-aqueous solvent.

As the non-aqueous solvent, cyclic carbonates, cyclic esters, chain carbonates, chain esters, ethers and the like can be used. Examples of the cyclic carbonate include ethylene carbonate, propylene carbonate, butylene carbonate, and vinylene carbonate, and examples of the cyclic ester include gamma-butyrolactone, 2-methyl-gamma-butyrolactone, acetyl-gamma-butyrolactone, and gamma-valerolactone. Examples of the chain carbonate include dimethyl carbonate, diethyl carbonate, dibutyl carbonate, dipropyl carbonate, and ethyl methyl carbonate, and examples of the chain ester include propionic acid alkyl ester, malonic acid dialkyl ester, and acetate alkyl ester. Examples of ethers include tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, 1,2-diethoxyethane, and 1,2-dibutoxyethane. As the non-aqueous solvent, a compound in which some or all of the chemical structure of the specific solvent is replaced with fluorine may be adopted.

Examples of the electrolyte include lithium salts such as LiClO ₄ , LiAsF ₆ , LiPF ₆ , LiBF ₄ , LiCF ₃ SO ₃ , LiN (FSO ₂ ) ₂ , and LiN (CF ₃ SO ₂ ) ₂ .

Examples of the electrolytic solution include a solution in which a lithium salt is dissolved in a non-aqueous solvent such as ethylene carbonate, dimethyl carbonate, propylene carbonate, and diethyl carbonate at a concentration of about 0.5 mol / L to 1.7 mol / L.

The separator separates the positive electrode and the negative electrode, and allows lithium ions to pass through while preventing a short circuit due to contact between the two electrodes. As the separator, polytetrafluoroethylene, polypropylene, polyethylene, polyimide, polyamide, synthetic resin such as polyaramid (Aromatic polyamide), polyester, polyacrylonitrile, polysaccharides such as cellulose and amylose, and natural products such as fibroin, keratin, lignin and suberin. Examples thereof include porous bodies, non-woven fabrics, and woven fabrics using one or more electrically insulating materials such as polymers and ceramics. Further, the separator may have a multi-layer structure.

Next, an example of a method for manufacturing a lithium ion secondary battery will be described.

A separator is sandwiched between the positive electrode and the negative electrode as needed to form an electrode body. The electrode body may be a laminated type in which a positive electrode, a separator and a negative electrode are stacked, or a wound type in which a positive electrode, a separator and a negative electrode are wound. After connecting from the positive electrode current collector and the negative electrode current collector to the positive electrode terminal and the negative electrode terminal leading to the outside using a current collector lead or the like, an electrolytic solution is added to the electrode body to add a lithium ion secondary. Use a battery. Further, the lithium ion secondary battery of the present invention may be charged and discharged in a voltage range suitable for the type of active material contained in the electrode.

The shape of the lithium ion secondary battery of the present invention is not particularly limited, and various shapes such as a cylindrical type, a square type, a coin type, and a laminated type can be adopted.

The lithium ion secondary battery of the present invention may be mounted on a vehicle. The vehicle may be a vehicle that uses electric energy from a lithium ion secondary battery for all or part of its power source, and may be, for example, an electric vehicle or a hybrid vehicle. When a lithium ion secondary battery is mounted on a vehicle, a plurality of lithium ion secondary batteries may be connected in series to form an assembled battery. In addition to vehicles, devices equipped with lithium-ion secondary batteries include various battery-powered home appliances such as personal computers and mobile communication devices, office devices, and industrial devices. Further, the lithium ion secondary battery of the present invention includes wind power generation, solar power generation, hydraulic power generation and other power storage devices and power smoothing devices for electric power systems, power supply sources for power and / or auxiliary machinery such as ships, aircraft, and aircraft. Power supply sources for spacecraft and / or auxiliary equipment, auxiliary power sources for vehicles that do not use electricity as power sources, power sources for mobile household robots, power sources for system backup, power sources for non-disruptive power supply devices, It may be used as a power storage device that temporarily stores the electric power required for charging in a charging station for an electric vehicle or the like.

Although the embodiments of the present invention have been described above, the present invention is not limited to the above embodiments. It can be carried out in various forms with modifications, improvements, etc. that can be made by those skilled in the art, without departing from the gist of the present invention.

Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples. The present invention is not limited to these examples.

(Example 1)
The positive electrode active material of Example 1 was produced as follows.

95 g (361.4 mmol) nickel sulfate hexahydrate, 4.3 g (11.46 mmol) aluminum nitrate nine hydrate, 0.62 g (1.88 mmol) sodium tungstate dihydrate, and chelate. 3.4 g (44.7 mmol) of glycolic acid as a compound was dissolved in 400 mL of pure water to prepare a transition metal-containing aqueous solution.
The molar ratio of nickel, aluminum and tungsten in the transition metal-containing aqueous solution is 96.5: 3: 0.5.

A basic aqueous solution was prepared by mixing sodium hydroxide, aqueous ammonia and pure water.

-Precipitation step In a constant temperature bath maintained at 60 ° C., a basic aqueous solution was supplied to a transition metal-containing aqueous solution under nitrogen gas introduction and stirring conditions to prepare a reaction solution. The pH of the reaction solution was maintained in the range of 10.3 to 0.85, and nickel, aluminum and tungsten were precipitated as transition metal hydroxides. The pH value here means the value itself obtained by measuring the reaction solution with a pH meter.

The transition metal hydroxide was separated by filtration. The transition metal hydroxide was washed with pure water using an ultrasonic cleaner, and then the transition metal hydroxide was isolated by filtration.

-Precursor formation step The transition metal hydroxide was heated at 300 ° C. for 5 hours in the atmosphere to obtain a transition metal oxide as a precursor.

-Coating step 30 g of transition metal oxide was added to 400 mL of pure water to prepare a dispersion of transition metal oxide.
0.15 g (0.42 mmol) of zirconium sulfate tetrahydrate and 0.12 g (1.58 mmol) of glycolic acid as a chelating compound were dissolved in water to prepare a coating solution.
The dispersion of the transition metal oxide and the coating solution were mixed to prepare a mixed solution. Then, an aqueous sodium hydroxide solution was added until the pH of the mixture reached 12.5 to obtain a coated body in which zirconium hydride was precipitated on the surface of the transition metal oxide. The coated body was separated by filtration, dried, and subjected to a firing step.

Firing step 10 g precursor coat, 3.0 g (125 mmol) lithium hydroxide anhydride, 0.475 g (1.25 mmol) Na ₃ PO ₄ 12 hydrate, 0.032 g (1.25 mmol) LiF was mixed in a mortar to prepare a mixture. Then, the mixture was heated at 600 ° C. for 10 hours in an air atmosphere to obtain a first fired body.

The first calcined product was crushed in a mortar to obtain a powder. The powdery first fired body was heated at 725 ° C. for 15 hours in an oxygen gas atmosphere to obtain a second fired body. The second fired body was crushed in a mortar to obtain the positive electrode active material of Example 1.
The theoretical composition of the positive electrode active material of Example 1 is Li ₁ Ni _0.965 Al _0.03 W _0.005 Zr _0.0011 Na _0.03 P _0.01 O ₂ F _0.01 .

The positive electrode and the lithium ion secondary battery of Example 1 were manufactured as follows.

An aluminum foil having a thickness of 20 μm was prepared as a current collector for the positive electrode. As the positive electrode active material, 94 parts by mass of the positive electrode active material of Example 1, 3 parts by mass of acetylene black as a conductive auxiliary agent, and 3 parts by mass of polyvinylidene fluoride as a binder were mixed. This mixture was dispersed in an appropriate amount of N-methyl-2-pyrrolidone to prepare a slurry. The slurry was placed on the surface of the aluminum foil and applied using a doctor blade so that the slurry became a film. By heating and drying the aluminum foil coated with the slurry, N-methyl-2-pyrrolidone was removed by volatilization, and a positive electrode active material layer was formed on the surface of the aluminum foil. The aluminum foil having the positive electrode active material layer formed on the surface was compressed by using a roll press machine, and the aluminum foil and the positive electrode active material layer were firmly adhered to each other to form a bonded product. The joint was heated using a vacuum dryer and cut into a predetermined shape to obtain a positive electrode.

The negative electrode was manufactured as follows.
98.3 parts by mass of graphite was mixed with 1 part by mass of styrene-butadiene rubber and 0.7 parts by mass of carboxymethyl cellulose as a binder, and this mixture was dispersed in an appropriate amount of ion-exchanged water to prepare a slurry. This slurry was applied to a copper foil having a thickness of 20 μm, which is a current collector for a negative electrode, so as to form a film using a doctor blade, and the current collector to which the slurry was applied was dried and then pressed to form a bonded product. The joint was heated using a vacuum dryer and cut into a predetermined shape to obtain a negative electrode.

A laminated lithium ion secondary battery was manufactured using the above positive electrode and negative electrode. Specifically, a rectangular sheet having a thickness of 25 μm made of a resin film having a three-layer structure of polypropylene / polyethylene / polypropylene was sandwiched between the positive electrode and the negative electrode as a separator to form a group of electrode plates. The electrode plates were covered with a pair of laminated films, the three sides were sealed, and then the electrolytic solution was injected into the bag-shaped laminated film. As the electrolytic solution, a solution in which LiPF ₆ was dissolved at a volume ratio of 3: 3: 4 in a solvent obtained by mixing ethylene carbonate, ethyl methyl carbonate and dimethyl carbonate at a volume ratio of 3: 3: 4 was used. Then, by sealing the remaining one side, the laminated lithium ion secondary battery of Example 1 was obtained in which the four sides were hermetically sealed and the electrode plate group and the electrolytic solution were sealed.

(Example 2)
The positive electrode active material of Example 2 was produced as follows.

94 g (357.6 mmol) nickel sulfate hexahydrate, 4.2 g (14.94 mmol) cobalt sulfate heptahydrate, 0.6 g (1.82 mmol) sodium tungstate dihydrate, 0.35 g (0.93 mmol) aluminum nitrate nine hydrate and 0.28 g (3.68 mmol) of glycolic acid as a chelating compound were dissolved in 400 mL of pure water to prepare a transition metal-containing aqueous solution.
The molar ratio of nickel, cobalt, tungsten and aluminum in the transition metal-containing aqueous solution is 95.5: 4: 0.5: 0.25.

A basic aqueous solution was prepared by mixing sodium hydroxide, aqueous ammonia and pure water.

-Precipitation step In a constant temperature bath maintained at 60 ° C., a basic aqueous solution was supplied to a transition metal-containing aqueous solution under nitrogen gas introduction and stirring conditions to prepare a reaction solution. The pH of the reaction solution was maintained in the range of 10.8 to 10.85, and nickel, cobalt, tungsten and aluminum were precipitated as transition metal hydroxides. The pH value here means the value itself obtained by measuring the reaction solution with a pH meter.

The transition metal hydroxide was separated by filtration. The transition metal hydroxide was washed with pure water using an ultrasonic cleaner, and then the transition metal hydroxide was isolated by filtration.

-Precursor formation step The transition metal hydroxide was heated at 300 ° C. for 5 hours in the atmosphere to obtain a transition metal oxide as a precursor.

Firing step 10 g of precursor, 3.0 g (125 mmol) of lithium hydroxide anhydride, 0.475 g (1.25 mmol) of Na ₃ PO ₄ dodecahydrate, 0.032 g (1.25 mmol) of LiF. It was mixed in a mortar to prepare a mixture. Then, the mixture was heated at 600 ° C. for 10 hours in an air atmosphere to obtain a first fired body.

The first calcined product was crushed in a mortar to obtain a powder. The powdery first fired body was heated at 725 ° C. for 15 hours in an oxygen gas atmosphere to obtain a second fired body. The second fired body was crushed in a mortar to obtain a positive electrode active material of Example 2.
The theoretical composition of the positive electrode active material of Example 2 is Li ₁ Ni _0.955 Co _0.04 W _0.005 Al _0.0025 Na _0.03 P _0.01 O ₂ F _0.01 .

The lithium ion secondary battery of Example 2 was produced in the same manner as in Example 1 except that the positive electrode active material of Example 2 was used.

(Example 3)
The following coating step was carried out between the precursor forming step and the firing step, and the precursor in the firing step used after the coating step was the same method as in Example 2 except that the precursor of Example 3 was used. A positive electrode active material, a positive electrode, and a lithium ion secondary battery were manufactured.
The theoretical composition of the positive electrode active material of Example 3 is Li ₁ Ni _0.955 Co _0.04 W _0.005 Al _0.0025 Zr _0.002 Na _0.03 P _0.01 O ₂ F _0.01. Is.

-Coating step 30 g of transition metal oxide was added to 400 mL of pure water to prepare a dispersion of transition metal oxide.
0.3 g (0.84 mmol) of zirconium sulfate tetrahydrate and 0.25 g (3.29 mmol) of glycolic acid as a chelating compound were dissolved in water to prepare a coating solution.
The dispersion of the transition metal oxide and the coating solution were mixed to prepare a mixed solution. Then, an aqueous sodium hydroxide solution was added until the pH of the mixture reached 12.5 to obtain a coated body in which zirconium hydride was precipitated on the surface of the transition metal oxide. The coated body was separated by filtration, dried, and subjected to a firing step.

(Example 4)
The positive electrode active material of Example 4 was produced as follows.

94 g (357.6 mmol) nickel sulfate hexahydrate, 4.2 g (14.94 mmol) cobalt sulfate heptahydrate, 0.62 g (1.88 mmol) sodium tungstate dihydrate, 0.35 g 400 mL of pure (0.93 mmol) aluminum nitrate hexahydrate, 0.26 g (0.73 mmol) zirconium sulfate tetrahydrate, and 0.49 g (6.44 mmol) glycolic acid as the chelating compound. A transition metal-containing aqueous solution was prepared by dissolving it in water.
The molar ratio of nickel, cobalt, tungsten, aluminum and zirconium in the transition metal-containing aqueous solution is 95.5: 4: 0.5: 0.25: 0.25.

A basic aqueous solution was prepared by mixing sodium hydroxide, aqueous ammonia and pure water.

-Precipitation step In a constant temperature bath maintained at 60 ° C., a basic aqueous solution was supplied to a transition metal-containing aqueous solution under nitrogen gas introduction and stirring conditions to prepare a reaction solution. The pH of the reaction solution was maintained in the range of 10.8 to 10.85, and nickel, cobalt, tungsten, aluminum and zirconium were precipitated as transition metal hydroxides. The pH value here means the value itself obtained by measuring the reaction solution with a pH meter.

The transition metal hydroxide was separated by filtration. The transition metal hydroxide was washed with pure water using an ultrasonic cleaner, and then the transition metal hydroxide was isolated by filtration.

-Precursor formation step The transition metal hydroxide was heated at 300 ° C. for 5 hours in the atmosphere to obtain a transition metal oxide as a precursor.

Firing step 10 g of precursor, 3.0 g (125 mmol) of lithium hydroxide anhydride, 0.475 g (1.25 mmol) of Na ₃ PO ₄ dodecahydrate, 0.032 g (1.25 mmol) of LiF. It was mixed in a mortar to prepare a mixture. Then, the mixture was heated at 600 ° C. for 10 hours in an air atmosphere to obtain a first fired body.

The first calcined product was crushed in a mortar to obtain a powder. The powdery first fired body was heated at 725 ° C. for 15 hours in an oxygen gas atmosphere to obtain a second fired body. The second fired body was crushed in a mortar to obtain the positive electrode active material of Example 4.
The theoretical composition of the positive electrode active material of Example 4 is Li ₁ Ni _0.955 Co _0.04 W _0.005 Al _0.0025 Zr _0.002 Na _0.03 P _0.01 O ₂ F _0.01. Is.

The lithium ion secondary battery of Example 4 was produced in the same manner as in Example 1 except that the positive electrode active material of Example 4 was used.

(Example 5)
The following coating step was carried out between the precursor forming step and the firing step, and the precursor in the firing step after the coating step was used in the same manner as in Example 4 in the same manner as in Example 5. A positive electrode active material, a positive electrode, and a lithium ion secondary battery were manufactured.
The theoretical composition of the positive electrode active material of Example 5 is Li ₁ Ni _0.955 Co _0.04 W _0.005 Al _0.0025 Zr _0.004 Na _0.03 P _0.01 O ₂ F _0.01. Is.

-Coating step 30 g of transition metal oxide was added to 400 mL of pure water to prepare a dispersion of transition metal oxide.
0.26 g (0.73 mmol) of zirconium sulfate tetrahydrate and 0.21 g (2.76 mmol) of glycolic acid as a chelating compound were dissolved in water to prepare a coating solution.
The dispersion of the transition metal oxide and the coating solution were mixed to prepare a mixed solution. Then, an aqueous sodium hydroxide solution was added until the pH of the mixture reached 12.5 to obtain a coated body in which zirconium hydride was precipitated on the surface of the transition metal oxide. The coated body was separated by filtration, dried, and subjected to a firing step.

(Comparative Example 1)
LiNi _0.85 Co _0.11 Al _0.04 O ₂ having a layered rock salt structure, which was produced by a conventional coprecipitation method without using a chelate compound in the precipitation step, was prepared. This was used as the positive electrode active material of Comparative Example 1.
The lithium ion secondary battery of Comparative Example 1 was produced in the same manner as in Example 1 except that the positive electrode active material of Comparative Example 1 was used.

(Evaluation example 1)
The positive electrode active material of Example 1 fixed with a resin was irradiated with an argon ion beam to produce a thin film having a thickness of about 100 nm. About the range of 20 nm in length × 20 nm in width in the cross section of the primary particles of the positive electrode active material of Example 1 formed on the thin film using STEM-EDX which is a combination of a scanning transmission electron microscope and an energy dispersive X-ray spectroscopic analyzer. , Ni, Al and W were analyzed. Then, the ratio (%) of Al to the total of Ni, Al and W was calculated.
The analysis was performed at five locations on the cross section of a particular primary particle. The analysis was also performed at 5 locations on the cross section of another primary particle and 5 locations on the cross section of yet another primary particle.

The positive electrode active material of Example 2 was also analyzed in the same manner. The measurement targets for the positive electrode active material of Example 2 are Ni, Co, W and Al. For the positive electrode active material of Example 2, the ratio (%) of Al to the total of Ni, Co, W and Al was calculated.
The positive electrode active material of Comparative Example 1 was also analyzed in the same manner. The measurement targets for the positive electrode active material of Comparative Example 1 are Ni, Co, and Al. For the positive electrode active material of Comparative Example 1, the ratio (%) of Al to the total of Ni, Co and Al was calculated.

The above results are shown in Table 1. The analytical values in Table 1 are atom% of Al.
Further, the STEM image of the positive electrode active material of Example 1 is shown in FIG. 1, and the STEM-EDX image of Al as a measurement target is shown in FIG.

It can be seen that in the positive electrode active materials of Examples 1 and 2, Al is uniformly dispersed and present in any of the primary particles. On the other hand, in the positive electrode active material of Comparative Example 1, it can be seen that Al is non-uniformly present in any of the primary particles.
From the above results, it can be said that the use of the chelate compound in the precipitation step contributed to the uniform dispersion of aluminum. Further, in the positive electrode active material of Comparative Example 1 in which the chelate compound was not used in the precipitation step, it is presumed that aluminum hydroxide was segregated in the precipitation step.
In the positive electrode active materials of Examples 1 and 2, the average value of Al fluctuated for each cross section of the primary particles because the apparent crystal plane (crystal orientation) appearing on the cross section of the primary particles was different. It is thought that it is due to the difference.

(Evaluation example 2)
The STEM image of the positive electrode active material of Example 1 obtained by the same method as that of Evaluation Example 1 was image-analyzed to calculate the cross-sectional area of the primary particles. Then, the diameter was calculated assuming that the cross section of the primary particle was a circle. This analysis was performed on 20 primary particles.
The positive electrode active materials of Example 2 and Comparative Example 1 were also analyzed in the same manner.
The above results are shown in Table 2. The particle diameter in Table 2 means the calculated diameter.

The particle size of the primary particles in the positive electrode active material of Example 1 is about 100 nm, and the particle size of the primary particles in the positive electrode active material of Example 2 is about 150 nm. Both can be said to have relatively small particle diameters.

(Evaluation example 3)
The particle size distribution of the positive electrode active material of Example 2 was measured using a laser scattering diffraction type particle size distribution meter. The positive electrode active material of Comparative Example 1 was also measured in the same manner. In Evaluation Example 3, the measurement target is mainly the secondary particles in the positive electrode active material.
Table 3 shows the results of D ₉₀ , D ₁₀ , D _50, etc. for each positive electrode active material. In Table 3, the units of D ₉₀ , D ₁₀ , D ₅₀ and D _90- D ₁₀ are μm.

From the results in Table 3, it can be said that the positive electrode active material of Example 2 has a relatively broad particle size distribution.

(Evaluation example 4)
The crystal structures of the positive electrode active materials of Examples 1 to 5 were analyzed by a powder X-ray diffractometer using Cu-κα.
It was confirmed that all the positive electrode active materials showed a diffraction pattern of a layered rock salt structure.

(Evaluation example 5)
The lithium ion secondary batteries of Examples 1 to 5 and Comparative Example 1 were repeatedly charged and discharged at a rate of 0.1 C by charging to 4.4 V and then discharging to 2.5 V.
Table 4 shows the discharge capacity in the initial charge / discharge cycle and the discharge capacity at the time when the charge / discharge cycle is repeated 20 times.

From the results in Table 4, it can be said that the lithium ion secondary batteries of Examples 1 to 5 have a larger discharge capacity and are superior in maintaining the discharge capacity as compared with the lithium ion secondary batteries of Comparative Example 1. ..

Claims (10)

A positive electrode active material which is a crystalline oxide containing lithium, nickel, and aluminum, and is characterized in that the dispersion of aluminum in the primary particles in the oxide is uniform. The positive electrode active material according to claim 1, wherein the oxide is represented by the following general formula (1).
Formula _{(1) Li a Ni b Al} c M d D e O f F g
In the general formula (1), a, b, c, d, e, f, g are 0.5 ≦ a ≦ 2, 0 <b <1, 0 <c ≦ 0.2, 0 ≦ d <1, It satisfies 0 ≦ e ≦ 0.2, b + c + d + e = 1, 1.8 ≦ f ≦ 2.2, and 0 ≦ g ≦ 0.2. M is selected from Co, Mn, W and Zr. D is a doping element. The positive electrode active material according to claim 1 or 2, wherein the relative standard deviation of the particle size of the primary particles is 50% or less. The positive electrode active material according to any one of claims 1 to 3, wherein the average particle size of the primary particles is in the range of 20 nm to 500 nm. The value of D _90- D ₁₀ in the particle size distribution measured using a laser scattering diffraction type particle size distribution meter is 10 μm or more, or the value of (D _90- D ₁₀ ) / D ₅₀ is 0.6 or more. The positive electrode active material according to any one of claims 1 to 4. A positive electrode comprising the positive electrode active material according to any one of claims 1 to 5. A lithium ion secondary battery comprising the positive electrode according to claim 6. A nickel-aluminum-containing hydroxide which is a particulate hydroxide containing nickel and aluminum, wherein the dispersion of aluminum in the particles is uniform. A nickel-aluminum-containing oxide which is a particulate oxide containing nickel and aluminum, wherein the dispersion of aluminum in the particles is uniform. The production intermediate of the positive electrode active material according to any one of claims 1 to 5, which comprises the nickel-aluminum-containing hydroxide according to claim 8 or the nickel-aluminum-containing oxide according to claim 9.