• 专利附录
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    • 专利摘要:
    PURPOSE: To provide a positive electrode active material and a nonaqueous electrolyte secondary battery utilizing it which is excellent in a high-discharge capacity and high-temperature stability having both advantages of nickel acid lithium and an olivine compound. CONSTITUTION: Related to the positive electrode active material, the surface of a nickel acid lithium particle 11 expressed by a formula LiyNi1-zM'zO2 (where 0.05<=y<=1.2 and 0<=z<=0.5. M' is at least one kind selected from among Fe, Co, Mn, Cu, Zn, Al, Sn, B, Ga, Cr, V, Ti, Mg, Ca, and Sr) is covered with an olivine compound 12 which is expressed by a formula LixMPO4 (where 0.05<=x<=1.2. M is at least one kind selected from among Fe, Mn, Co, Ni, Cu, Zn, and Mg) having an olivine type crystal structure.
    公开号:KR20040018963A
    申请号:KR1020030058820
    申请日:2003-08-25
    公开日:2004-03-04
    发明作者:이자야 오카에；케이조 코가；타케히코 타나카
    申请人:소니 가부시키가이샤；
    IPC主号:
    专利说明:

    Positive active material and non-aqueous electrolyte secondary battery {POSITIVE ACTIVE MATERIAL AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY}
    [13] The present invention relates to a positive active material capable of reversibly doping and undoping lithium, and to a nonaqueous electrolyte secondary battery using the positive active material.
    [14] General formula Li y Ni 1-z M ' z O 2 (0.05 ≤ y ≤ 1.2, 0 ≤ z ≤ 0.5, M' is Fe, Co, Mn, Cu, Zn, Al, Sn, B, Ga, Cr Lithium nickelate, represented by one or more species selected from the group consisting of V, Ti, Mg, Ca, and Sr), is widely used as a positive active material for lithium ion secondary batteries. It is known that active materials can obtain greater charge / discharge capacities.
    [15] The discharge capacity of lithium cobalt acid is about 150 mAh / g, while the lithium nickelate has a discharge capacity of about 180 to 200 mAh / g. Since nickel, a raw material of lithium nickelate, is cheaper than cobalt, lithium nickelate is superior to lithium cobalt in terms of cost. Further, since nickel is superior to cobalt in terms of supply stability of ore, lithium nickelate is superior to lithium cobalt in terms of supply stability of raw materials.
    [16] However, lithium nickelate having such an advantage has a disadvantage in that the stability of the state of charge is lower than that of lithium cobalt acid. This is because the stability of the lithium nickelate crystal structure is low due to the instability of tetravalent Ni ions generated during charging, and thus, the reactivity with the electrolyte solution is high, and the thermal decomposition initiation temperature of lithium nickelate is also lower than that of lithium cobalt acid. Therefore, a problem arises in that the degradation of lithium nickelate increases when the charge / discharge cycle at a high temperature or the high temperature is maintained in a charged state.
    [17] On the other hand, a polyaniline (polyaniline) as a basic skeleton, and the general formula Li x MPO 4 (0.05 ≤ x ≤ 1.2, M is Fe, Mn, Co, Ni, Cu, Zn, Mg, Cr, V, Mo, Ti And olivine compounds represented by one or more species selected from the group consisting of Al, Nb, B, and Ga) are known as positive materials for lithium ion secondary batteries.
    [18] When these olivine compounds are used as positive active materials for secondary batteries, since the crystal structure changes of the olivine compounds due to charging / discharging are small, the olivine compounds can effectively improve the cycle characteristics, and the oxygen atoms in the crystals are phosphorus atoms of the crystals. Since it is covalently bonded to and thus stably present in the crystal, it is unlikely to release oxygen even when the battery is exposed to a high temperature environment, which is an advantage of improving safety.
    [19] The olivine compound having the above-described advantages is used in the form of particles, in which case the olivine compound has a disadvantage of low energy density. The discharge capacity per weight of lithium cobalt acid generally used in lithium ion secondary batteries is about 150 mAh / g, and the discharge capacity per weight of lithium nickel acid is about 180 to 200 mAh / g, while the olivine compound discharge capacity per weight (olivine compound Is included in the case of a type having a large charge / discharge capability) is less than or equal to the discharge capacity of lithium cobaltate. In addition, the true density of lithium cobalt acid is 5. lg / cm 3, and the true density of lithium nickel acid is 4.8 g / cm 3, while the true density of the olivine compound is about 3.5 g / cm 3. That is, the true density of the olivine compound is about 30% less than the true density of lithium cobalt and lithium nickelate respectively.
    [20] Thus, when the olivine compound is used alone in the cell, the energy density per volume is small, which cannot satisfy the desire of consumers who want a larger capacity. Olivine compounds have another disadvantage of low electronic conductivity. As a result, when the olivine compound is used alone as a positive active material, there arises a problem that the load characteristic is lower than that of each of the lithium cobalt and lithium nickelate.
    [21] It is conceivable to use a mixture of lithium nickelate and olivine compounds as positive materials in order to effectively use the advantages of both materials, but in order to obtain stability at high temperature in a battery using lithium nickelate, a considerable amount, for example, For example, since 50% by weight or more of the olivine compound needs to be mixed with lithium nickelate, a large charge / discharge capacity which is an advantage of lithium nickelate cannot be obtained.
    [22] It is an object of the present invention to provide a plus active material having the advantages of lithium nickelate and olivine compound, that is, having a large discharge capacity and very high temperature stability, and to provide a non-aqueous electrolyte secondary battery using such a plus active material. will be.
    [23] In order to solve the above problems, the inventors have found through investigation that it is effective to cover the particle surface of lithium nickelate with olivine compounds to maximize the characteristics of the lithium nickelate and olivine compounds.
    [24] Therefore, in order to achieve the above object, according to the first aspect of the present invention, the general formula Li y Ni 1-z M ' z O 2 (0.05 ≤ y ≤ 1.2, 0 ≤ z ≤ 0.5, M' is Fe, Particles of lithium nickel acid represented by Co, Mn, Cu, Zn, Al, Sn, B, Ga, Cr, V, Ti, Mg, Ca, and Sr); An olivine compound having a olivine type crystal structure represented by Li x MPO 4 (0.05 ≦ x ≦ 1.2, M is one or more species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, and Mg) A positive active material is provided, wherein the particle surface of lithium nickelate is covered with an olivine compound.
    [25] In order to achieve the above object, according to the second aspect of the present invention, a positive electrode comprising a positive active material, and capable of doping or undoping lithium metal, lithium alloy, and lithium A nonaqueous electrolyte secondary battery comprising a negative electrode including one substance selected from the group consisting of materials and a nonaqueous electrolyte is provided. The positive active material is represented by the general formula Li y Ni 1-z M ' z O 2 (0.05 ≦ y ≦ 1.2, 0 ≦ z ≦ 0.5, and M ′ is Fe, Co, Mn, Cu, Zn, Al, Sn, Particles of lithium nickelate represented by one or more species selected from the group consisting of B, Ga, Cr, V, Ti, Mg, Ca, and Sr, and a general formula Li x MPO 4 (0.05 ≦ x ≦ 1.2, M comprises an olivine compound having an olivine type crystal structure represented by at least one species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, and Mg), and particles of lithium nickelate The surface is covered with olivine compound.
    [26] The above-described positive active material according to the present invention can suppress the reaction between the electrolyte and lithium nickel nitrate, which is the surface of lithium nickel nitrate covered with excellent stability of olivine compound, thereby improving the stability of lithium nitrate at high temperature. Because it improves.
    [27] More specifically, by maintaining the large charge / discharge capacity of lithium nickelate and adding the olivine compound, it is possible to improve the stability of lithium nickelate at high temperature while suppressing the decrease in energy density, thereby increasing the charge / discharge capacity and high temperature stability, For example, cycle features and maintenance features can be combined at high levels.
    [28] According to the present invention, by covering the particle surface of lithium nickelate with the olivine compound, that is, by intensively arranging the olivine compound on the surface of the lithium nickelate particle, the reaction between the lithium nickelate and the electrolyte solution with a small amount of the olivine compound is suppressed. The effect can be obtained effectively. Accordingly, the amount of the olivine compound can be reduced in comparison with the amount of the olivine compound simply mixed with lithium nickelate, and as a result, the decrease in energy density due to the addition of the olivine compound can be suppressed.
    [29] Since the olivine compound adheres to the particle surface of lithium nickelate, the low electronic conductivity of the olivine compound is compensated by the high electronic conductivity of lithium nickelate. As a result, it is possible to sufficiently obtain the characteristics of the olivine compound without reducing the energy density as compared with the case of using one olivine compound as the positive active material.
    [30] An important point of the present invention lies in the fact that the olivine compound is provided not just to adhere to the particle surface of lithium nickelate, but to cover the particle surface of lithium nickelate. When the olivine compound is provided to be randomly attached to the particle surface of lithium nickelate by simply mixing the olivine compound with particles of lithium nickelate, the above-described effect cannot be obtained. That is, the above-mentioned effect can be obtained only by uniformly covering the particle surface of lithium nickelate with an olivine compound.
    [31] Since the non-aqueous electrolyte secondary battery of the present invention uses the above-described positive active material, it is possible to combine high level of high temperature stability and charge / discharge capacity.
    [32] Hereinafter, the present invention will be described in detail with reference to the drawings. In addition, this invention is not limited to the following description, It can change suitably within the range which does not deviate from the summary of this invention.
    [1] 1 is a longitudinal sectional view showing one configuration example of a coin-shaped nonaqueous electrolyte secondary battery to which the present invention is applied.
    [2] 2 is a schematic view showing the form of a disk mill which is a kind of high speed rotary impact grinder used in Example 1. FIG.
    [3] 3 shows a typical view of a material treated with a disk mill.
    [4] Fig. 4 is a longitudinal sectional view showing a configuration example of a cylindrical nonaqueous electrolyte secondary battery to which the present invention is applied.
    [5] 5 is a characteristic diagram showing the relationship between the discharge capacity and the number of cycles for the battery produced in Example 1. FIG.
    [6] 6 is a schematic diagram showing the form of a mixer / crusher used in Example 2. FIG.
    [7] 7 is a schematic diagram showing the form of the high speed stirrer / mixer used in Example 3. FIG.
    [8] <Explanation of symbols for the main parts of the drawings>
    [9] 1: non-aqueous electrolyte secondary battery 2: positive electrode
    [10] 3: plus can 4: negative electrode
    [11] 5: minus can 6: separator
    [12] 7: insulation gasket
    [33] The invention will now be described in detail with reference to the drawings.
    [34] The following will be described through the coin-shaped non-aqueous electrolyte secondary battery shown in FIG. As shown in FIG. 1, the coin-shaped nonaqueous electrolyte secondary battery 1 includes a positive electrode 2, a positive can 3 containing the positive electrode 2, and a positive electrode 2. A negative can 4 for accommodating the negative electrode 4 and the negative electrode 4, and a separator 6 arranged between the positive electrode 2 and the negative electrode 4. ) And an insulating gasket 7. In the case of using an electrolyte solution as the electrolyte, both the positive can 3 and the negative can 5 are filled with a nonaqueous electrolyte solution. When using a solid electrolyte or gel electrolyte, a solid electrolyte layer or gel electrolyte layer is formed on the active material of the positive electrode 2 and the negative electrode 4. Each of the positive active material and the negative active material is selected as a material for doping or undoping lithium.
    [35] The positive electrode 2 is manufactured by forming a layer of the positive active material including the positive active material in the positive current collector. Aluminum foil is used as a positive current collector.
    [36] The plus active material used is prepared by covering the particle surface of lithium nickelate with an olivine compound having a olivine type crystal structure. Lithium nickelate is represented by the general formula Li y Ni 1-z M ' z O 2 , where 0.05 ≦ y ≦ 1.2, 0 ≦ z ≦ 0.5, and M ′ is Fe, Co, Mn, Cu, Zn, At least one species selected from the group consisting of Al, Sn, B, Ga, Cr, V, Ti, Mg, Ca, and Sr. The olivine compound is represented by the general formula Li x MPO 4 , wherein 0.05 ≦ x ≦ 1.2, and M is one or more species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, and Mg.
    [37] Lithium nickelate represented by the general formula Li y Ni 1-z M ′ z O 2 described above has the advantage of large discharge capacity. In particular, the discharge capacity of lithium cobalt acid is about 150 mAh / g, while the lithium nickelate is about 180 to 200 mAh / g. In addition, since nickel, which is a raw material of lithium nickelate, is cheaper than cobalt, lithium nickelate is superior to lithium cobaltate in terms of cost. Further, since nickel is superior to cobalt in terms of supply stability of ore, lithium nickelate is superior to lithium cobalt in terms of supply stability of raw materials. Therefore, when lithium nickelate is used, a positive active material having a large discharge capacity can be produced at a low price.
    [38] However, lithium nickelate having such an advantage has a disadvantage in that the stability of the state of charge is lower than that of lithium cobalt acid. This is because the stability of the lithium nickelate crystal structure is low due to instability of the tetravalent Ni ions generated during charging, and thus the reactivity with the electrolyte solution is high, and the thermal decomposition initiation temperature of lithium nickelate is also lower than that of lithium cobalt acid. Therefore, when only lithium nickelate is used as the positive active material, a problem arises in that the charge / discharge cycle at high temperature or the degradation of the positive active material at high temperature in the charged state increases.
    [39] When the secondary battery is used as a positive electrode material, because the change in crystal structure due to charge / discharge is small, the olivine compound is excellent in terms of cycle characteristics, and the oxygen atom is covalently bonded with the phosphorus atom of the crystal so that it exists stably in the crystal. Therefore, the olivine compound having the olivine type crystal structure represented by the general formula Li x MPO 4 is advantageous in that the release rate of oxygen is low even when the battery is exposed to a high temperature environment.
    [40] Therefore, when the olivine compound represented by the general formula Li x MPO 4 is used as a positive active material, a nonaqueous electrolyte secondary battery having excellent cycle characteristics and stability can be produced.
    [41] Formula LiMPO 4 (M is at least one species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, Mg, Cr, V, Mo, Ti, Al, Nb, B, and Ga), specifically LiFePO An olivine compound having a olivine type crystal structure represented by 4 (hereinafter sometimes referred to as “lithium iron phosphate”) is preferably used as the plus active material.
    [42] These lithium iron phosphates are made from iron, which is richer in natural resources and cheaper than manganese. Therefore, when lithium iron phosphate is used as a positive active material, a nonaqueous electrolyte secondary battery can be manufactured at low cost as compared with the case where lithium-manganese oxide is used as a positive active material.
    [43] However, the olivine compound having the advantages described above and represented by the general formula Li x MPO 4 is used in the form of particles, in which case the olivine compound has a disadvantage of low energy density. Generally, the discharge capacity per weight of lithium cobalt acid used in a lithium ion secondary battery is about 150 mAh / g, and the discharge capacity per weight of lithium nickel acid is about 180 to 200 mAh / g, while the discharge capacity per weight of the olivine compound is present. (Even when the olivine compound is a type having a high charge / discharge capability) is below the discharge capacity of lithium cobalt acid. In addition, the true density of lithium cobalt acid is 5. lg / cm 3, and the true density of lithium nickel acid is 4.8 g / cm 3, while the true density of the olivine compound is about 3.5 g / cm 3. That is, the true density of the olivine compound is about 30% less than the true density of lithium cobalt and lithium nickelate respectively.
    [44] Thus, when the olivine compound is used alone as a plus active material, the energy density per volume is small, making it impossible to satisfy the desire for larger doses. Olivine compounds have another disadvantage of low electronic conductivity. As a result, when the olivine compound is used alone as a positive active material, there arises a problem that the load characteristic is lower than that of each of lithium cobalt and lithium nickelate.
    [45] In order to solve the above-mentioned problems and to maximize the characteristics of lithium nickelate as a plus active material and of the olivine compound as a positive active material, according to the present invention, the surface of the particle of lithium nickel nitrate is covered with an olivine compound so that Are manufactured. In this form, since the particle surface of lithium nickelate is covered with an excellent olivine compound, the reaction between the electrolyte solution and lithium nickelate can be suppressed, thereby improving the stability of lithium nickelate in high temperature conditions. Can be. More specifically, by maintaining the large charge / discharge capacity of lithium nickelate and adding the olivine compound, it is possible to improve the stability of lithium nickelate at high temperature while suppressing the decrease in energy density, thereby increasing the charge / discharge capacity and high temperature stability, For example, cycle features and maintenance features can be combined at high levels.
    [46] An important point of the present invention lies in the fact that the olivine compound is provided not just to adhere to the particle surface of lithium nickelate, but to cover the particle surface of lithium nickelate. When the olivine compound is provided to be randomly attached to the particle surface of lithium nickelate by simply mixing the olivine compound with particles of lithium nickelate, the above-described effect cannot be obtained. That is, the above-mentioned effect can be obtained only by uniformly covering the particle surface of lithium nickelate with the olivine compound.
    [47] According to the present invention, by covering the particle surface of lithium nickelate with the olivine compound, that is, by intensively arranging the olivine compound on the surface of the lithium nickelate particle, the reaction between the lithium nickelate and the electrolyte solution with a small amount of the olivine compound is suppressed. The effect can be obtained effectively. Accordingly, the amount of the olivine compound can be reduced compared to the amount of the olivine compound simply mixed with lithium nickel nitrate, and as a result, the decrease in energy density due to the addition of the olivine compound can be suppressed.
    [48] Since the olivine compound adheres to the particle surface of lithium nickelate, the low electronic conductivity of the olivine compound is compensated by the high electronic conductivity of lithium nickelate. As a result, the characteristic of an olivine compound can fully be acquired compared with the case of using one olivine compound as a positive active material.
    [49] The content of the olivine compound based on the total weight of the plus active substance is preferably 5% to 50% by weight. When the content of the olivine compound is less than 5% by weight, the number of particles of the olivine compound covering the particle surface of lithium nickelate is too small. Accordingly, the effects of the present invention may not be sufficiently obtained.
    [50] In addition, when the content of the olivine compound is 50% by weight or more, a large charge / discharge capacity, which is an advantage of lithium nickelate, cannot be sufficiently obtained, and the advantage of energy density is lower than that of conventional active materials such as lithium cobalt acid.
    [51] Therefore, by adjusting the content of the olivine compound within the above-mentioned range, it is possible to greatly improve the high temperature stability without damaging the large charge / discharge capacity which is an advantage of lithium nickelate.
    [52] For example, when a positive active material of the present invention is prepared using lithium nickelate having a discharge capacity of 180 mAh / g and an olivine compound having a discharge capacity of 150 mAh / g, the discharge capacity of the positive active material is about 165 mAh / g. To a value in the range of 178.5 mAh / g. Thus, the reduction in the discharge effect of the positive active material can be suppressed to about 8% or less of the discharge capacity of the positive active material made only of lithium nickelate.
    [53] When the positive active material is prepared using lithium nickelate having a true density of 4.8 g / cm 3 and the olivine compound having a true density of 3.5 g / cm 3, the apparent density of the positive active material is from 4.15 g / cm 3 to The value falls within the range of 4.74 g / cm 3. Therefore, the density reduction can be suppressed to a value of about 14% or less.
    [54] As the olivine compound used in the present invention, it is preferable to use the olivine compound synthesized at a baking temperature of about 500 ° C to 700 ° C, as described in Japanese Patent Laid-Open No. 2001-250555. It has been found that the average particle size of the olivine compound synthesized at this baking temperature is generally smaller than the average particle size of lithium nickelate, and more specifically, at least 1/2 or less of the average particle size of lithium nickelate. For example, the average particle size of lithium nickelate is in the range of about 10 μm to 20 μm, while the average particle size of the olivine compound is in the range of about 5 μm or less.
    [55] As used herein, the term "average particle size" means a value measured in a mixed state of partial primary particles and secondary particles that are aggregates of primary particles. Since the secondary particles of the olivine compound are more likely to be pulverized into primary particles than the secondary particles of lithium nickelate, the particles of the olivine compound synthesized at the baking temperature described above are particles having a size about 1/10 of the lithium nickelate particles. Almost pulverized. That is, the particle size of the olivine compound can be reduced to an appropriate particle size by the size of the material covering the surface of the secondary particles of lithium nickelate. In contrast, when the olivine compound obtained by baking at a temperature of 700 ° C. or more is used, since the size of the primary particles becomes too large, such olivine compound is not preferable as a material for covering the particle surface of lithium nickelate.
    [56] The calculations make it clear that when the particle size of the olivine compound is less than half the particle size of lithium nickelate, more than 28 olivine compound particles may lie on the surface of one of the particles of lithium nickelate. This particle size relationship is important for obtaining the desired effect of the present invention.
    [57] According to the invention, the average particle size of the olivine compound is preferably at most 1/2, preferably at most 1/10 of the lithium nickelate average particle size. The lower limit of the average particle size of the olivine compound can be determined through various conditions of the olivine compound preparation process. In order to reliably obtain the effect of the present invention, the particles of the olivine compound are preferably finer. This is because it is easier for finer particles of the olivine compound to more densely cover the particle surface of lithium nickelate.
    [58] It is preferable that the coating thickness of the olivine compound on the surface of each lithium nickelate particle | grain is 0.1 micrometer-100 micrometers. If the coating thickness is thinner than 0.1 mu m, the effect of the present invention may not be obtained. When the thickness of the coating is thicker than 10 mu m, the content of the olivine particles in the plus active material becomes too large, which reduces the charge / discharge capacity per volume and the energy density per volume, which makes it impossible to obtain a large charge / discharge capacity. . Therefore, the effect of this invention can be reliably acquired by adjusting the coating thickness of the olivine compound on the surface of each lithium nickelate particle within the said range.
    [59] In this way, the plus active material of the present invention complements the shortcomings of lithium nickelate and olivine compounds and features a combination of large charge / discharge capacity, which is an advantage of lithium nickelate, and a high level of high temperature stability, which is an advantage of olivine compounds. It is done. Such plus active materials are superior to lithium cobalt acid, which is an active material of the related prior art. When such a plus active material is used, a nonaqueous electrolyte secondary battery having excellent charge / discharge capacity and excellent high temperature stability can be realized.
    [60] The binder to be included in the positive active material layer may be a known resin material commonly used as a binder of the positive active material layer of this kind of non-aqueous electrolyte secondary battery. The plus active material layer may comprise known additives such as conductive agents.
    [61] The plus can 3, which is adapted to contain the plus electrode 2, serves as an external terminal on the side of the non-aqueous electrolyte secondary battery 1 plus electrode.
    [62] The negative electrode 4 is manufactured by forming a negative active material layer containing a negative active material on the negative current collector. For negative current collectors, nickel foil is used.
    [63] The negative active material can be exemplified by any material that can do or undo lithium. Examples of such materials include, for example, non-graphitized carbon, artificial carbon, natural graphite, pyrolytic carbon, pitch coke, needle coke, coke such as petroleum coke, graphite, glassy carbon, phenolic resins, furan resins and the like at appropriate temperatures. Carbonized materials such as baked bodies, carbon fibers, and activated carbon of organic polymer compounds obtained by carbonization. In addition, metal lithium, metals or semiconductors capable of forming alloys or compounds with lithium, and alloys or compounds thereof may be used as the negative active material. Such metals, alloys or compounds are represented by the formula D s E t Li u , where D is at least one species selected from each of the metal elements allowed to form an alloy or compound with lithium, and E is other than lithium and D At least one species selected from metal elements and semiconductor elements of s, t and u are specified to satisfy s > 0, t &gt; In particular, the metal element or semiconductor element capable of forming an alloy or compound with lithium may be a metal element or semiconductor element of group IV, preferably silicon or tin, most preferably tin. Oxides capable of doping or undoping lithium at relatively low potentials, such as iron oxide, ruthenium oxide, molybdenum oxide, tungsten oxide, titanium oxide and tin oxide, and nitrides can likewise be used as negative active materials.
    [64] The binder to be included in the negative active material layer may be a known resin material commonly used as a binder of the negative active material layer of this kind of non-aqueous electrolyte secondary battery.
    [65] The negative can 5, which is adapted to contain the negative electrode 4, serves as an external terminal on the negative electrode side of the nonaqueous electrolyte secondary battery 1.
    [66] Examples of the nonaqueous electrolyte include a solid prepared by mixing or dissolving an electrolyte in a nonaqueous electrolyte solution prepared by dissolving an electrolyte salt in a nonaqueous solvent, a solid electrolyte (an inorganic electrolyte or a polymer electrolyte including an electrolyte salt) and a polymer compound, or the like. Electrolytes such as gels.
    [67] Non-aqueous electrolyte solutions are prepared by dissolving the electrolyte in an organic solvent. The organic solvent can be any species commonly used in batteries of this kind. Examples of such organic solvents are propylene carbonate, ethylene carbonate, diethyl carbonate, dimethyl carbonate, 1,2-dimethoxyethane, 1,2-diethoxyethane, γ-butyrolactone, tetrahydrofuran, 2-methyl tetrahydro Furan, 1,3-dioxolane, 4-methyl-1,3-dioxolane, diethyl ether, sulfolane, methylsulforan, acetonitrile, propionitrile, anisole, acetate, butyrate, and pro Cypionate. In particular, in view of voltage stability, it is preferable to use cyclic carbonates such as propylene carbonate or chain carbonates such as dimethyl carbonate and diethyl carbonate. These organic solvents may be used alone or in combination of two or more kinds thereof.
    [68] The solid electrolyte may also be an inorganic electrolyte or a polymer electrolyte as long as the material has lithium ion conductivity. Examples of the inorganic electrolytes include lithium nitride or lithium iodide. The polymer electrolyte consists of an electrolyte salt and a polymer compound in which the electrolyte salt is dissolved. Examples of the polymer compound used in the polymer electrolyte include polymers of ether raw materials such as polyethylene oxide and crosslinked polyethylene oxide, polymers of polymethacrylate ester raw material, and polymers of acrylate raw material. These polymers may be used alone or in the form of a mixture or copolymer of two or more kinds.
    [69] Once the non-aqueous electrolyte solution described above is absorbed to gel the polymer, the matrix of the gel electrolyte can be any polymer. Examples of the polymer used in the gel electrolyte include fluorocarbon polymers such as polyvinylidene fluoride and polyvinylidene-co-hexafluoropropylene.
    [70] Examples of polymers used in gel electrolytes also include polyacrylonitrile and polyacrylonitrile copolymers. Examples of the monomers (vinyl-based units) used in the copolymerization include vinyl acetate, methyl methacrylate, butyl methacrylate, methyl acrylate, butyl acrylate, itaconic acid, hydrogenated methyl acrylate, hydrogenated ethyl acrylate, acrylamide, vinyl chloride Vinylidene fluoride and vinylidene chloride. Examples of polymers used in gel electrolytes are acrylonitrile-butadiene copolymer rubbers, acrylonitrile-butadiene-styrene copolymer resins, acrylonitrile-polyethylene-propylene-diene-styrene copolymer resins, Acrylonitrile-vinyl chloride copolymer resin, acrylonitrile-methacrylate resin, and acrylonitrile-acrylate copolymer resin are further included.
    [71] Examples of polymers used in gel electrolytes include ether-based polymers such as polyethylene oxide, polyethylene oxide copolymers, and crosslinked polyethylene oxides. Examples of the unit used for the copolymerization include polypropylene oxide, methyl methacrylate, butyl methacrylate, methyl acrylate, and butyl acrylate.
    [72] In particular, in view of redox stability, the fluorocarbon polymer is preferably used in the matrix of the gel electrolyte.
    [73] The electrolyte salt used in the electrolyte may be any electrolyte salt commonly used in this type of cell. Examples of electrolyte salts include LiC10 4 , LiAsF 6 , LiPF 6 , LiBF 4 , LiB (C 6 H 5 ) 4 , CH 3 SO 3 Li, CF 3 SO 3 Li, LiCl, and LiBr.
    [74] The separator 6 is adapted to separate the positive electrode 2 and the negative electrode 4. The separator 6 may be a polymer membrane made of the same material as any membrane commonly used to form separators of this kind of non-aqueous electrolyte secondary battery, for example polypropylene. In addition, when a solid electrolyte or a gel electrolyte is used as the electrolyte of the battery 1, the separator 6 does not necessarily need to be provided.
    [75] The insulating gasket 7 is adapted to prevent leakage of the nonaqueous electrolyte solution filled in both the positive can 3 and the negative can 5, and is integrally assembled to the negative can 5.
    [76] In the coin-shaped non-aqueous electrolyte secondary battery 1 having the form as described above, the positive active material is prepared by covering the particle surface of lithium nickelate with an olivine compound having a olivine-type crystal structure. Formula Li y Ni 1-z M ' z O 2 (0.05 ≤ y ≤ 1.2, 0 ≤ z ≤ 0.5, M' is Fe, Co, Mn, Cu, Zn, A1, Sn, B, Ga, Cr , V, Ti, Mg, Ca, and Sr, one or more species selected from the group consisting of, the olivine compound is of the general formula LiM x PO 4 (0.05 ≤ x ≤ 1.2, M is Fe, Mn, Co, Ni , Cu, Zn, and Mg). Therefore, the disadvantages of lithium nitrate and olivine compounds can be compensated for each other, and a combination of the high charge / discharge capacity of lithium nickel nitrate and the high level of high temperature stability of olivine compound can be combined. Both high temperature stability can be improved.
    [77] The nonaqueous electrolyte secondary battery 1 configured as described above is manufactured according to the following manner when an electrolyte solution is used as the electrolyte.
    [78] First, the positive electrode 2 is manufactured as follows. Lithium nickelate (LiNiO 2 ) powder and lithium-manganese olivine compound (LiMnPO 4 ) powder as a raw material are lightly mixed in a specific ratio. In this case, the olivine compound content is adjusted to 20% by weight, for example.
    [79] As the olivine compound used in the present invention, it is preferable to use an olivine compound synthesized at a baking temperature of about 500 ° C to about 700 ° C, as described in Japanese Patent Laid-Open No. 2001-250555. It was confirmed that the average particle size of the olivine compound synthesized at this baking temperature is generally smaller than the average particle size of lithium nickelate, and more specifically, at least about 1/2 or less of the average particle size of lithium nickelate. The olivine compound particles synthesized at the baking temperatures described above can be pulverized into particles that are about 1/10 or less of the lithium nickelate particle size. That is, the particle size of the olivine compound can be reduced to the desired particle size with the material covering the secondary particle surface of lithium nickelate.
    [80] On the other hand, when the olivine compound prepared by baking at a temperature of 700 ° C. or more is used, since the size of the primary particles is too large, such olivine compound is not suitable as a material for covering the particle surface of lithium nickelate.
    [81] Thus, the plus active material according to the invention can be reliably produced by using olivine compounds baked at the above-mentioned temperatures.
    [82] The mixture is then subjected to stirring with strong friction and impact to form a lithium and olivine compound complex, which covers the particle surface of lithium nickelate with the olivine compound.
    [83] A disk mill apparatus, a mixer / crusher, or a high speed stirrer / mixer, which is a kind of high speed rotary impact grinder, may be used to perform stirring accompanied by strong friction and impact forces. By using such a grinding / stirring apparatus, the mixture to be put into the apparatus is subjected to a grinding / stirring treatment accompanied by sufficient and uniform strong friction and impact, whereby the surface of the lithium nickelate particles is subjected to a strong friction and impact. Covered with olivine compounds.
    [84] The processing conditions of the grinding / stirring apparatus may be appropriately set according to the specifications of the apparatus, the amount of the mixture to be treated, and the like.
    [85] The positive electrode 2 is manufactured by using as a positive active material a mixture that has undergone grinding and stirring with strong friction and impact. More specifically, the positive active material mixed with the appropriate amount of the conducting agent and the binder is dispersed in a solvent to produce a positive mixture in the form of a slurry. This plus mixture is evenly applied to the plus current collector and dried to produce a plus electrode 2 with a layer of plus active material.
    [86] Next, the negative electrode 4 is manufactured as follows. First, the negative active material and the binder are dispersed in a solvent to prepare a negative mixture in the form of a slurry. This negative mixture is evenly applied to the negative current collector and dried to produce a negative electrode 4 with a layer of negative active material.
    [87] A nonaqueous electrolyte solution is prepared by dissolving an electrolyte salt in a nonaqueous solvent.
    [88] The positive electrode 2 is housed in a positive can 3, the negative electrode 4 is housed in a negative can 5, and a separator 6 is provided between the positive electrode 2 and the negative electrode 4. Are arranged. Both the positive can 3 and the negative can 5 are filled with a non-aqueous electrolyte solution, and the positive can 3 and the negative can 5 are fixed to each other by sandwiching the insulating gasket 7. The nonaqueous electrolyte secondary battery 1 is thus completed.
    [89] The shape of the nonaqueous electrolyte secondary battery is not particularly limited. For example, the secondary battery may be formed in any shape such as the shape of a cylinder, a square, a bottom, or a laminate sheet as well as the coin shape described above.
    [90] The method for producing the negative electrode and the positive electrode, respectively, is not limited to the above-described method and may be any known method. For example, known binders, conductive materials and the like are added to the active material, the mixture is added to the solvent, the resulting slurry is applied to the current collector, known additives and the like are added to the active material and the mixture Heating, applying this heated mixture to a current collector, and molding the active material only in the form of an electrode, or mixing the conductive material and the binder into the active material, and forming the mixture in the form of an electrode. Various known methods can be used.
    [91] More specifically, the binder and organic solvent are mixed with the active material to form a slurry, the slurry is applied to a current collector, the slurry is dried, and the active material and the binder are formed while applying heat and pressure (if necessary). Thus, a method of producing an electrode with high strength can be used.
    [92] The method of combining the components into the cell is not particularly limited and may be any method known in the art. For example, a stacking method in which electrodes and separators are laminated in sequence, and a sub-assembly of electrodes and separators inserted between the electrodes are manufactured, and the subassemblies are wound around a winding core. Various methods known in the art, such as the winding method, can be selected. In addition, the present invention can be effectively applied to a method of manufacturing a square-shaped battery by a winding method.
    [93] (Yes)
    [94] The invention will be more apparent from the following examples.
    [95] Each of these examples was performed by preparing the positive active material of the present invention and the non-aqueous electrolyte secondary battery using the positive active material, and evaluating the characteristics of the non-aqueous electrolyte secondary battery thus prepared.
    [96] (Example 1)
    [97] In this example, a positive active material and a cylindrical nonaqueous electrolyte secondary battery using the positive active material and having the form shown in Fig. 4 were prepared as follows.
    [98] (Production of plus electrode)
    [99] Firstly a plus active material was prepared. The olivine compound (LiMnPO 4 ) powder of lithium-manganese raw material was added to the lithium nickelate (LiNiO 2 ) powder in an amount of 20% by weight. These powders mixed slightly with each other. The mixture was placed in a disk mill (one kind of high speed rotary impact mill) and treated for 10 minutes. The grinding / stirring process was performed by rotating the disk-attached circular plate at a rotation speed of 10,000 rpm.
    [100] 2 is a schematic view showing the shape of a disk mill. In order to sufficiently pulverize and stir the material to be treated, the disk mill has a circulation structure that once feeds the material to the outer periphery and then returns the material back to the stirring section 9 through the rotation of the disk 8. By using such a disk mill, the material can be ground and stirred sufficiently uniformly.
    [101] The mixture of lithium nickelate and olivine compound introduced into the disk mill is pulverized and agitated by the strong impact force provided by the disk mill rotating at high speed, whereby the particle surface of lithium nickelate is covered with the olivine compound.
    [102] Cross sections of the milled (or powdered) and stirred materials with a disk mill were observed by scanning electron microscopy (SEM) and energy dispersive X-ray analyzer (EDS). Accordingly, small particles in which phosphorus (P) was clearly detected around each of the large particles (hereinafter referred to as base particles) having nickel (Ni) clearly detected and having a diameter of about 10 to 20 µm. It has been confirmed that {hereinafter, referred to as sub-particles} is densely attached in the form of a layer having a thickness of about 0.5 to 3 mu m. This state is schematically illustrated in FIG. 3. In FIG. 3, the blackened part of the center part is the basic particle 11, and the surrounding white part surrounding this basic particle 11 is the subparticle 12 layer. By examining the detected element type and the particle size of these particles, it was confirmed that the basic particles 11 were particles of lithium nickelate, and the secondary particles 12 were olivine compounds.
    [103] The battery was produced by using the material thus prepared as a positive active material.
    [104] A positive mixture was prepared by mixing 90% by weight of the positive active material, 5% by weight of acetylene black as the conductive agent, and 5% by weight of polyvinylidene fluoride as the binder. This plus mixture was dispersed in solvent N-methyl-2-pyrrolidone to prepare a slurry. This positive mixture slurry was uniformly applied and dried on both surfaces of the strip-shaped aluminum foil (thickness 20 mu m), which is the positive current collector 30, and then subjected to compression molding by a roll press to form a strip-shaped positive electrode 22 )
    [105] (Production of Negative Electrodes)
    [106] A negative electrode mixture was prepared by mixing 90 parts by weight of the negative active material graphite and 10 parts by weight of the polyvinylidene fluoride (PVdF) binder. This negative mixture was dispersed in a solvent, N-methyl-2-pyrrolidone, to prepare a slurry. This negative mixture slurry was uniformly applied and dried on both surfaces of the strip-shaped copper foil (thickness 10 µm) used as the negative current collector 29, and then subjected to compression molding by a roll press to form a strip-shaped negative electrode. (21) was obtained.
    [107] (Battery assembly)
    [108] A strip-shaped negative electrode 21, a strip-shaped positive electrode 22, and a separator 23 (25 mu m thick) made of a polyethylene film with holes are stacked in this order, and a plurality of the stacks are wound spirally. The spiral electrode component shown in FIG. 4 was prepared.
    [109] This helical electrode component was housed in a nickel plated iron cell can 25 and an insulating plate 24 was disposed on the top and bottom surfaces of the electrode component. The positive lead 32 made of aluminum emerged from the positive current collector 30 and welded to the protrusion of the safety valve 28 electrically connected with the battery cover 27. The negative lead 31 made of nickel came out of the negative current collector 29 and was welded to the bottom surface of the battery can 25.
    [110] Also, a nonaqueous electrolyte solution was prepared by dissolving 0.5 mol / l of LiN (CF 3 SO 2 ) 2 and 0.5 mol / l of LiPF 6 in a mixed ratio of ethylene carbonate and dimethyl carbonate in a ratio of 1: 2.
    [111] The electrolyte solution is injected into a battery can 25 having a spiral electrode component assembled therein, and the battery can 25 is sandwiched with an insulating sealing gasket 26 of asphalt coating, thereby providing a safety valve 28 and a PTC device. And the battery cover 27 were fixed. A cylindrical non-aqueous electrolyte secondary battery shown in FIG. 4 having an outer diameter of 18 mm and a height of 65 mm was thus prepared.
    [112] (Comparative Example 1)
    [113] The same method as described in Example 1 except that a powder of lithium nickelate (LiNiO 2 ) and lithium-manganese olivine compound (LiMnPO 4 ) was mixed in a mortar for 30 minutes to produce a plus active material. Positive active material was prepared, and a non-aqueous electrolyte secondary battery was prepared.
    [114] (Comparative Example 2)
    [115] A non-aqueous electrolyte secondary battery was prepared in the same manner as described in Example 1, except that lithium nickelate (LiNiO 2 ) was used as the positive active material.
    [116] The nonaqueous electrolyte secondary batteries of Example 1, Comparative Example 1 and Comparative Example 2 were evaluated through high temperature cycle characteristics. The high temperature cycle characteristics were evaluated as follows.
    [117] (Evaluation of high temperature cycle characteristic)
    [118] Each of Examples 1, Comparative Example 1 and Comparative Example 2 was charged under the conditions of an ambient temperature of 50 ° C., a charging voltage of 4.2V, a charging current of 1,000 mA, and a charging time of 4 hours. After this constant current / constant voltage charging, the battery was discharged at a discharge current of 1,000 mA and an end voltage of 3.0 V. Charge / discharge were repeated on the same conditions as the above-mentioned, and the change of discharge capacity was tested. This result is shown in FIG.
    [119] As can be clearly seen in Fig. 5, for the battery of Example 1, when the number of cycles increases, the discharge capacity is stable and gradually decreases at a constant rate, and the discharge capacity decreases even after the charge / discharge is repeated by a large number of cycles. Is small. This means that the battery of Example 1 has a feature capable of ensuring a large discharge capacity.
    [120] For each of the batteries of Comparative Example 1 and Comparative Example 2, in the initial state of the cycle, the discharge capacity rapidly decreased, and in the state after repeated charging / discharging by a large number of cycles, the decrease in the discharge capacity of the battery of Example 1 Greater than the reduction in discharge capacity.
    [121] Accordingly, the present invention can realize a positive active material which is superior to the positive active material of the related art in terms of discharge capacity and stability, and by using such a positive active material, a non-aqueous solution having high discharge capacity, high stability, and stable high temperature cycle characteristics It becomes clear that the electrolyte secondary battery can be implemented.
    [122] (Example 2)
    [123] Powder of lithium-manganese olivine compound (LiMnPO 4 ) was added to the powder of lithium nickelate (LiNiO 2 ) in an amount of 20% by weight. These powders were mixed lightly with each other. This mixture was fed to a raw mixer / crusher comprising a combination of a mill rod 42 and a cylindrical vessel 41 shown in FIG. As the cylindrical vessel 41 rotates at high speed along the circumferential path, the mill is configured to mix the raw materials with each other, and the pulverized material is strong at the gap between the grinding rod 42 and the inner wall of the cylindrical vessel 41. Under friction, the outer surface of the lithium nickelate particles is covered with olivine compound particles. In this way, by using such a mixer / crusher as in Example 1, the large particle surface of lithium nickelate can be covered with small particles of the olivine compound.
    [124] The cross section of the material treated with the mixer / crusher was observed with a scanning electron microscope (SEM) and an energy dispersive X-ray analyzer (EDS). Accordingly, small particles in which phosphorus (P) was clearly detected around each of the large particles (hereinafter referred to as base particles) having nickel (Ni) clearly detected and having a diameter of about 10 to 20 µm. It has been confirmed that {hereinafter, referred to as sub-particles} is densely attached in the form of a layer having a thickness of about 0.5 to 3 mu m. By examining the detected element types and the particle sizes of these particles, it was confirmed that the basic particles were lithium nickelate particles, and the secondary particles were olivine compounds.
    [125] Using the plus active material thus prepared, a non-aqueous electrolyte secondary cell was prepared in the same manner as described in Example 1, and the high temperature cycle characteristics of the cell were evaluated in the same manner as described above. Therefore, as in Example 1, it was confirmed that when the number of cycles increased, the discharge capacity was stably and slowly decreased at a constant speed, and the decrease in the discharge capacity was small even after the charge / discharge was repeated by a large number of cycles. This means that the battery of Example 2 has a feature capable of ensuring a large discharge capacity.
    [126] Accordingly, even in Example 2, the present invention can realize a positive active material which is better than the positive active material of the related art in terms of discharge capacity and stability, and by using such a positive active material, the discharge capacity is large, the stability is high, and the stable high temperature cycle It becomes clear that a nonaqueous electrolyte secondary battery having characteristics can be implemented.
    [127] (Example 3)
    [128] Powder of lithium-manganese olivine compound (LiMnPO 4 ) was added to the powder of lithium nickelate (LiNiO 2 ) in an amount of 20% by weight. These powders were mixed lightly with each other. This mixture was fed to the high speed stirrer / mixer shown in FIG. The stirring blade 51 of the vessel 50 rotates at a blade tip speed of about 80 m / s to constitute such a high speed stirrer / mixer so that the raw material is in a high dispersion state while giving a strong impact to each particle of the raw material, This covers the outer surface of the lithium nickelate particles with particles of the olivine compound. In this way, by using a high speed stirrer / mixer as in Example 1, the large particle surface of lithium nickelate can be covered with small particles of the olivine compound. In addition, the processing time was set to 30 minutes.
    [129] The cross section of the material treated with the high speed stirrer / mixer was observed with a scanning electron microscope (SEM) and an energy dispersive X-ray analyzer (EDS). Accordingly, nickel (Ni) is clearly detected and large particles having a diameter of about 10 to 20 µm (hereinafter referred to as base particles) are small particles in which phosphorus (P) is clearly detected around each. It has been confirmed that {hereinafter, referred to as sub-particles} is densely attached in the form of a layer having a thickness of about 0.5 to 3 mu m. By examining the detected element types and the particle sizes of these particles, it was confirmed that the basic particles were lithium nickelate particles, and the secondary particles were olivine compounds.
    [130] Using the plus active material thus prepared, a non-aqueous electrolyte secondary cell was prepared in the same manner as described in Example 1, and the high temperature cycle characteristics of the cell were evaluated in the same manner as described above. Therefore, as in Example 1, when the number of cycles increases, the discharge capacity is stable and gradually decreases at a constant speed, and the decrease in the discharge capacity is small even after the charge / discharge is repeated by a large number of cycles. This means that the battery of Example 3 has a feature capable of ensuring a large discharge capacity.
    [131] Accordingly, even in Example 3, the present invention can realize a positive active material which is superior to the positive active material of the related art in terms of discharge capacity and stability, and by using such a positive active material, the discharge capacity is large, the stability is high, and the stable high temperature cycle It becomes clear that a nonaqueous electrolyte secondary battery having characteristics can be implemented.
    [132] While the preferred embodiments have been described using specific terms, such description is for illustrative purposes only and it is to be understood that changes and modifications may be made without departing from the spirit and scope of the following claims.
    [133] As described above, the present invention compensates for the drawbacks of lithium nitrate and olivine compounds to provide a positive active material having both high charge / discharge capacity which is an advantage of lithium nickel nitrate and high temperature stability which is an advantage of olivine compound. can do.
    权利要求:
    Claims (5)
    [1" claim-type="Currently amended] As a positive active material,
    General formula Li y Ni 1-z M ' z O 2 (0.05 ≤ y ≤ 1.2, 0 ≤ z ≤ 0.5, M' is Fe, Co, Mn, Cu, Zn, Al, Sn, B, Ga, Cr Lithium nickelate particles represented by one or more species selected from the group consisting of V, Ti, Mg, Ca, and Sr,
    Olivine having a olivine type crystal structure represented by the general formula Li x MPO 4 (0.05 ≦ x ≦ 1.2, M is one or more species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, and Mg) Olivine compound
    Including,
    The particle surface of the lithium nickelate is covered with the olivine compound, plus active material.
    [2" claim-type="Currently amended] The positive active material according to claim 1, wherein the olivine compound content in the positive active material is 5% by weight to 50% by weight.
    [3" claim-type="Currently amended] The positive active material according to claim 1, wherein the olivine compound is in particle form, and the average particle size of the particles of the olivine compound is 1/2 or less of the average particle size of the particles of the lithium nickelate.
    [4" claim-type="Currently amended] The positive active material of claim 1, wherein the coating thickness of the olivine compound is in the range of 0.1 μm to 10 μm.
    [5" claim-type="Currently amended] A non-aqueous electrolyte secondary battery,
    A positive electrode comprising a positive active material,
    A negative electrode comprising one material selected from the group consisting of lithium metal, lithium alloys and materials capable of doping or undoping lithium,
    Comprising a non-aqueous electrolyte,
    The plus active material,
    General formula Li y Ni 1-z M ' z O 2 (0.05 ≤ y ≤ 1.2, 0 ≤ z ≤ 0.5, M' is Fe, Co, Mn, Cu, Zn, Al, Sn, B, Ga, Cr Particles of lithium nickelate represented by one or more species selected from the group consisting of V, Ti, Mg, Ca, and Sr,
    Olivine having a olivine type crystal structure represented by the general formula Li x MPO 4 (0.05 ≦ x ≦ 1.2, M is one or more species selected from the group consisting of Fe, Mn, Co, Ni, Cu, Zn, and Mg) Olivine compound
    Including,
    The nonaqueous electrolyte secondary battery, wherein the lithium nickelate particle surface is covered with the olivine compound.
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    同族专利:
    公开号 | 公开日
    US20170155137A1|2017-06-01|
    JP2004087299A|2004-03-18|
    KR101059094B1|2011-08-25|
    CN1249833C|2006-04-05|
    CN1495945A|2004-05-12|
    US20040096743A1|2004-05-20|
    JP3632686B2|2005-03-23|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2002-08-27|Priority to JPJP-P-2002-00246848
    2002-08-27|Priority to JP2002246848A
    2003-08-25|Application filed by 소니 가부시키가이샤
    2004-03-04|Publication of KR20040018963A
    2011-08-25|Application granted
    2011-08-25|Publication of KR101059094B1
    优先权:
    申请号 | 申请日 | 专利标题
    JPJP-P-2002-00246848|2002-08-27|
    JP2002246848A|JP3632686B2|2002-08-27|2002-08-27|Positive electrode active material and non-aqueous electrolyte secondary battery|
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