JP4639573B2 - Method for producing positive electrode active material for non-aqueous secondary battery - Google Patents

Description

[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for producing a positive electrode active material for a non-aqueous secondary battery, a positive electrode active material for a non-aqueous secondary battery by the production method, and a non-aqueous secondary battery using the same.
[0002]
[Prior art]
A positive electrode active material is used for the non-aqueous secondary battery.
With the rapid progress of portable and cordless electronic devices, development of non-aqueous secondary batteries that are smaller, lighter, and have a larger capacity than conventional secondary batteries is underway. Among them, lithium secondary batteries have already been put into practical use as power sources for mobile phones, notebook computers, etc., and further studies have been made on increasing the size and increasing output as power sources for automobiles and communication power backup.
[0003]
As a positive electrode active material for a non-aqueous secondary battery, for example, spinel type lithium manganese oxide has been conventionally used, but a positive electrode active material capable of producing a larger capacity non-aqueous secondary battery is demanded. It was.
[0004]
In such a situation, the composition formula LiCo _1/3 Ni _1/3 Mn _1/3 O ₂ [Ohzuku et al., Chemistry Letters, 642 (2001)] and LiNi ₁ having a layered structure containing nickel and manganese. _{/ 2} Mn _1/2 O ₂ [Ohzuku et al., Chemistry Letters, 744 (2001)] and Li [Ni _x Li _{(1 / 3-2x / 3)} Mn _{(2 / 3-x / 3)} ] O ₂ ( 0 ≦ x ≦ 1/2) , Li [Ni x Co 1-2x Mn x] O 2 (0 <x ≦ 1/2) represented by [Lu et al., 42nd battery Symposium Proceedings, Lecture No. 2I12, 42 (2001)] A new compound has been proposed and attracted attention as a positive electrode active material for a non-aqueous secondary battery capable of solving the above-mentioned problems.
[0005]
As a nickel source and a manganese source for synthesizing these compounds, it is conventionally considered that the compound having a layered structure cannot be obtained even if a nickel compound and a manganese compound are mixed and used. Composite hydroxide was used. However, since divalent manganese in the composite hydroxide is easily oxidized and becomes trivalent, the synthesis conditions of the composite hydroxide and the atmosphere for the subsequent handling are strictly controlled. Therefore, it was difficult to produce the composite hydroxide. There has been a demand for a method for easily producing a positive electrode active material for a non-aqueous secondary battery comprising the above compound having a layered structure without using the composite hydroxide.
[0006]
[Problems to be solved by the invention]
An object of the present invention, the composition formula _{Li [Ni (xy) Li (} 1 / 3-2x / 3) Mn (2/3-x / 3-y) Co 2y] O 2 ··· (I)
(0 <x ≦ 0.5, 0 ≦ y ≦ 1/6, x> y)
A positive electrode active material for a non-aqueous secondary battery comprising a compound represented by formula (1) and having a layered structure, a positive electrode active material for a non-aqueous secondary battery obtained by using the same, and a non-aqueous electrode using the same It is to provide a water secondary battery.
[0007]
[Means for Solving the Problems]
As a result of intensive studies on a method for producing an active material for a non-aqueous secondary battery comprising a compound having a layered structure and containing nickel and manganese and represented by the composition formula (I), the nickel source By using dinickel trioxide as the above, it was found that the active material for a non-aqueous secondary battery can be easily obtained, and the present invention has been completed.
[0008]
That is, the present invention relates to the composition formula Li [Ni _(xy) Li _{(1 / 3-2x / 3)} Mn _{(2 / 3-x / 3-y)} Co _2y ] O ₂ (0 <x < 0.5, 0 ≦ y ≦ 1/6, x> y) A method for producing a positive electrode active material for a non-aqueous secondary battery comprising a compound having a layered structure, comprising dinickel trioxide, and calcining the above compound Provided is a method for producing a positive electrode active material for a non-aqueous secondary battery, comprising firing a configurable mixture. Moreover, this invention provides the positive electrode active material for non-aqueous secondary batteries obtained by the manufacturing method of the said description. Furthermore, this invention provides the non-aqueous secondary battery using the positive electrode active material for non-aqueous secondary batteries described above.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
Next, the present invention will be described in detail.
The production method of the present invention is a method for producing a positive electrode active material for a non-aqueous secondary battery composed of a compound represented by the composition formula (I) and having a layered structure. It is characterized by containing nickel. Here, dinickel trioxide does not strictly mean a compound represented by the composition formula Ni ₂ O ₃ , and the nickel content is lower than 78.6% by weight (Ni / O molar ratio Ni / O It means O <1.) It contains nickel oxide. Dinickel trioxide is commercially available, and among the commercially available dinickel trioxide, the X-ray diffraction measurement result is JCPDS card no. Unlike Ni ₂ O ₃ shown in 14-04-81, the same card no. Although there is what gives a powder X-ray diffraction pattern close to NiO shown in 4-0835, if the nickel content is less than 78.6% by weight, it is dinickel trioxide in the production method of the present invention.
[0010]
The positive electrode active material for a non-aqueous secondary battery in the present invention has a layered structure, and is composed of a compound represented by the composition formula (I). When y> 0 in the composition formula (I), that is, Co is contained, This is preferable because the discharge capacity and cycle characteristics at room temperature are improved. In addition, it is more preferable to include Li in the transition metal site with x <0.5, that is, Ni content <Mn content in the composition formula (I), because cycle characteristics at high temperature are improved. Since the discharge capacity may be reduced when x is 0.4 or less, the range of x is more preferably 0.4 <x <0.5, and more preferably y> 0. Further, each site of lithium, nickel, manganese, and cobalt is changed from Na, K, Mg, Ca, Sr, Ba, B, Al, Ga, In, Si, Zr, You may substitute by Sn, Ti, V, Cr, Fe, Cu, Ag, Zn etc. in the range within 50 mol% of each site. Further, oxygen may be substituted with halogen, sulfur, or nitrogen within a range of 5 mol% or less.
[0011]
Here, the layered structure refers to, for example, Electrochemical and Solid-State Letters, Vol. 4 (2001), pages A200 to A203, which refers to a structure identified by X-ray diffraction as having a crystal structure of α-NaFeO ₂ type.
[0012]
In the production method of the present invention, as long as dinickel trioxide is contained in the mixture, the combination of the lithium compound, the manganese compound, the cobalt compound, and the compound containing the element contained as necessary is not particularly limited. . Examples of compounds containing metal elements other than nickel include oxides, hydroxides, oxyhydroxides, carbonates, nitrates, acetates, chlorides, organometallic compounds, and alkoxides, but are not limited thereto. Is not to be done. The nickel source is preferably substantially all dinickel trioxide. The mixture in the production method of the present invention can be produced by mixing the aforementioned compounds.
[0013]
In the production method of the present invention, a known method can be used as a method for mixing raw materials. Mixing can be carried out either dry or wet, but simpler dry mixing is preferred. As dry mixing, V-type mixer, W-type mixer, ribbon mixer, drum mixer, dry ball mill, etc. Can be carried out by known methods.
[0014]
After the mixture is compression-molded as necessary, it is maintained at a temperature range of 600 ° C. or higher and 1200 ° C. or lower, preferably 800 ° C. or higher and 1100 ° C. or lower, more preferably 900 ° C. or higher and 1050 ° C. or lower for 2 hours to 30 hours. By baking, a positive electrode active material for a non-aqueous secondary battery made of a compound represented by the composition formula (I) and having a layered structure can be produced. At that time, it is preferable to rapidly reach the holding temperature as long as the baking container is not damaged. As the firing atmosphere, air, oxygen, nitrogen, argon, or a mixed gas thereof can be used, but an atmosphere containing oxygen is preferable. After firing, the particle size can be adjusted to a predetermined particle size by a publicly known method such as a vibration mill, a jet mill, or a dry ball mill.
[0015]
A preferred configuration for producing a battery will be described below by taking as an example the case where the positive electrode active material for a non-aqueous secondary battery of the present invention is used for the positive electrode of a lithium secondary battery.
A positive electrode of a lithium secondary battery which is one embodiment of the present invention includes a positive electrode mixture containing the active material for a non-aqueous secondary battery of the present invention, and further containing a carbonaceous material, a binder and the like as a conductive material. It can be produced by carrying it on a current collector.
[0016]
Examples of the carbonaceous material include natural graphite, artificial graphite, cokes, and carbon black. As the conductive material, each may be used alone, for example, artificial graphite and carbon black may be mixed and used.
[0017]
As the binder, a thermoplastic resin is usually used. Specifically, polyvinylidene fluoride (hereinafter sometimes referred to as PVDF), polytetrafluoroethylene (hereinafter sometimes referred to as PTFE), and tetrafluoroethylene. -Hexafluoropropylene / vinylidene fluoride copolymer, hexafluoropropylene / vinylidene fluoride copolymer, tetrafluoroethylene / perfluorovinyl ether copolymer, and the like. These may be used alone or in combination of two or more.
[0018]
Further, a fluororesin and a polyolefin resin are used as binders, so that the ratio of the fluororesin in the positive electrode mixture is 1 to 10% by weight and the ratio of the polyolefin resin is 0.1 to 2% by weight. Use in combination with the positive electrode active material of the invention is preferable because it has excellent binding properties with the current collector and can further improve the safety against external heating.
[0019]
As the positive electrode current collector, Al, Ni, stainless steel, or the like can be used, but Al is preferable because it is easily processed into a thin film and is inexpensive. Examples of the method of supporting the positive electrode mixture on the positive electrode current collector include a method of pressure molding, or a method of pasting using a solvent or the like, and applying and drying and pressing on the positive electrode current collector. .
[0020]
As a negative electrode of a lithium secondary battery which is one of the embodiments of the present invention, for example, a lithium metal, a lithium alloy, or a material capable of being doped / undoped with lithium ions can be used. Materials that can be doped / undoped with lithium ions include carbonaceous materials such as natural graphite, artificial graphite, cokes, carbon black, pyrolytic carbons, carbon fibers, and fired organic polymer compounds; lower potential than the positive electrode And chalcogen compounds such as oxides and sulfides capable of doping and dedoping lithium ions.
[0021]
The shape of the carbonaceous material may be, for example, a flake shape such as natural graphite, a spherical shape such as mesocarbon microbeads, a fibrous shape such as graphitized carbon fiber, or an aggregate of fine powder. A thermoplastic resin can be added as a binder. Examples of the thermoplastic resin include PVDF, polyethylene, and polypropylene.
[0022]
Examples of the chalcogen compounds such as oxides and sulfides used as the negative electrode include oxides of Group 13, 14, and 15 elements of the periodic table. Also in these cases, a carbonaceous material can be added as a conductive material and a thermoplastic resin can be added as a binder, if necessary.
[0023]
As the negative electrode current collector, Cu, Ni, stainless steel, or the like can be used. In particular, in a lithium secondary battery, Cu is preferable because it is difficult to form an alloy with lithium and it can be easily processed into a thin film. The negative electrode current collector is loaded with a mixture containing the negative electrode active material by pressure molding, or pasted using a solvent, and fixed on the negative electrode current collector by coating, drying and pressing. The method of doing is mentioned.
[0024]
Examples of the separator used in the lithium secondary battery according to one embodiment of the present invention include a porous film, a nonwoven fabric, a woven fabric made of a material such as polyolefin resin such as polyethylene and polypropylene, fluororesin, nylon, and aromatic aramid. A material having a form such as cloth can be used. The thickness of the separator is preferably as thin as possible as long as the mechanical strength is maintained in that the volume energy density of the battery is increased and the internal resistance is reduced, and is preferably about 10 to 200 μm.
[0025]
As the electrolyte used in the lithium secondary battery which is one embodiment of the present invention, for example, a known one selected from a non-aqueous electrolyte solution in which a lithium salt is dissolved in an organic solvent or a solid electrolyte is used. Can do. Examples of the lithium salt include LiClO ₄ , LiPF ₆ , LiAsF ₆ , LiSbF ₆ , LiBF ₄ , LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiC (CF ₃ SO ₂ ) ₃ , Li ₂ B ₁₀ Cl ₁₀ , One or a mixture of two or more of lower aliphatic carboxylic acid lithium salts, LiAlCl _{4 and the} like can be mentioned.
[0026]
Examples of the organic solvent used in the lithium secondary battery which is one embodiment of the present invention include propylene carbonate, ethylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, 4-trifluoromethyl-1,3-dioxolane- Carbonates such as 2-one and 1,2-di (methoxycarbonyloxy) ethane; 1,2-dimethoxyethane, 1,3-dimethoxypropane, pentafluoropropyl methyl ether, 2,2,3,3-tetrafluoro Ethers such as propyldifluoromethyl ether, tetrahydrofuran, 2-methyltetrahydrofuran; esters such as methyl formate, methyl acetate, and γ-butyrolactone; nitriles such as acetonitrile and butyronitrile; N, N-dimethylform Amides such as amide, N, N-dimethylacetamide; carbamates such as 3-methyl-2-oxazolidone; sulfur-containing compounds such as sulfolane, dimethyl sulfoxide, 1,3-propane sultone, or the above organic solvents Although the thing which introduce | transduced the fluorine substituent can be used, normally 2 or more types of these are mixed and used. Among these, a mixed solvent containing carbonates is preferable, and a mixed solvent of cyclic carbonate and acyclic carbonate or cyclic carbonate and ether is more preferable.
[0027]
The mixed solvent of cyclic carbonate and non-cyclic carbonate has a wide operating temperature range, excellent load characteristics, and is hardly decomposable even when a graphite material such as natural graphite or artificial graphite is used as the negative electrode active material. In addition, a mixed solvent containing ethylene carbonate, dimethyl carbonate and ethyl methyl carbonate is preferable.
[0028]
Further, in view of particularly excellent safety improving effect is obtained, it is preferable to use an electrolyte containing an organic solvent having a lithium salt and / or fluorine substituent containing fluorine such as LiPF _6. A mixed solvent containing ethers having fluorine substituents such as pentafluoropropyl methyl ether and 2,2,3,3-tetrafluoropropyl difluoromethyl ether and dimethyl carbonate has excellent high-current discharge characteristics, preferable.
[0029]
As the solid electrolyte, for example, a polymer electrolyte such as a polyethylene oxide polymer compound, a polymer compound including at least one of a polyorganosiloxane chain or a polyoxyalkylene chain can be used. Moreover, what is called a gel type which hold | maintained the nonaqueous electrolyte solution in the polymer | macromolecule can also be used. Sulfide electrolytes such as Li ₂ S—SiS ₂ , Li ₂ S—GeS ₂ , Li ₂ S—P ₂ S ₅ , Li ₂ S—B ₂ S ₃ , or Li ₂ S—SiS ₂ —Li ₃ PO ₄ , When an inorganic compound electrolyte containing a sulfide such as Li ₂ S—SiS ₂ —Li ₂ SO ₄ is used, safety may be improved.
[0030]
The shape of the non-aqueous secondary battery of the present invention is not particularly limited, and may be any of a paper type, a coin type, a cylindrical type, a square type, and the like.
[0031]
Moreover, you may use the bag-shaped package which consists of a laminated sheet etc. which contain aluminum, without using the metal hard case which serves as a negative electrode or a positive electrode terminal as an exterior.
[0032]
【Example】
EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited at all by these. Unless otherwise specified, the electrode for charge / discharge test and the production of the flat battery and the powder X-ray diffraction measurement were performed by the following methods.
[0033]
(1) Production of flat battery for charge / discharge test A 1-methyl-2-pyrrolidone (hereinafter sometimes referred to as NMP) solution of PVDF as a binder is added to a mixture of a positive electrode active material and acetylene black of a conductive material. Active material: conductive material: binder = 86: 10: 4 (weight ratio) is added and kneaded to obtain a paste. The paste is applied to a # 100 stainless steel mesh as a positive electrode current collector and 150 Vacuum drying was performed at 0 ° C. for 8 hours to obtain a positive electrode.
[0034]
On the obtained positive electrode, ethylene carbonate (hereinafter may be referred to as EC), dimethyl carbonate (hereinafter may be referred to as DMC) and ethyl methyl carbonate (hereinafter may be referred to as EMC) as electrolytes. LiPF ₆ dissolved in a 30:35:35 (volume ratio) mixed solution so as to be 1 mol / liter (hereinafter sometimes referred to as LiPF ₆ / EC + DMC + EMC), a polypropylene porous membrane as a separator, A flat battery was prepared by combining metallic lithium as the negative electrode.
[0035]
(2) Powder X-ray diffraction measurement
For Reference Example 1 and Examples 2 to 4, RU200 type manufactured by Rigaku Corporation was used, and for Reference Example 5 and Example 6, RINT type manufactured by Rigaku Corporation was used, and measurement was performed under the following conditions. .
X-ray: CuKα
Voltage-current: 40 kV-30 mA (RU200), 140 mA (RINT)
Measurement angle range: 2θ = 10-90 °
Slit: DS-1 °, RS-0.3mm, SS-1 °
Step: 0.02 °
[0036]
Reference example 1
(1) Synthesis of positive electrode active material First, dinickel trioxide (manufactured by Hayashi Junyaku Kogyo Co., Ltd., nickel content 73.4% by weight, BET specific surface area 134 m ² / g; powder X-ray diffraction measurement result is shown in FIG. ), Manganese carbonate (manufactured by Wako Pure Chemical Industries, Ltd., reagent grade, manganese content 46.4% by weight), lithium hydroxide (manufactured by Honjo Chemical Co., Ltd.), and the molar ratio of each element is Li: Ni: Mn = 1.0: 0.5: After being weighed so as to be 0.5, it was mixed well in a mortar. The obtained mixed powder was placed in a box furnace and calcined by holding at 1000 ° C. for 15 hours in air, whereby positive electrode active material E1 for non-aqueous secondary battery (x = 0 in composition formula (I)) .5, y = 0, and Li [Ni _0.5 Mn _0.5 ] O ₂ ) was obtained. The powder X-ray diffraction measurement result of E1 is shown in FIG. E1 was confirmed to have a layered structure similar to the report by Ohzuku et al. (Chemistry Letters, 744 (2001)).
[0037]
(2) Charging / discharging performance evaluation when used as a positive electrode active material of a lithium secondary battery A flat battery was prepared using the obtained compound particles E1, and charging by constant current constant voltage charging and constant current discharging was performed under the following conditions. A discharge test was performed.
Charging maximum voltage 4.3V, charging time 8 hours, charging current 0.5mA / cm ²
Discharge minimum voltage 3.0V, discharge current 0.5mA / cm ²
Charge / discharge test temperature 25 ° C
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 123 and 117 mAh / g, respectively, which were higher than the spinel type lithium manganese oxide and showed good cycle characteristics.
[0038]
Example 2
(1) Synthesis of positive electrode active material Non-aqueous secondary battery in the same manner as in Reference Example 1 except that nimanganese trioxide (manufactured by Kojundo Chemical Laboratory Co., Ltd., purity 99.9 wt%) was used as the manganese raw material. A positive electrode active material E2 was obtained. The result of powder X-ray diffraction measurement of E2 is shown in FIG. It was confirmed that E2 also has the same layered structure as reported by Ohzuku et al.
[0039]
(2) Evaluation of Charging / Discharging Performance when Using as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles E2, and a charging / discharging test was conducted in the same manner as in Reference Example 1.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 115 and 108 mAh / g, respectively.
[0040]
Comparative Example 1
(1) Synthesis of positive electrode active material Non-aqueous secondary as in Reference Example 1, except that nickel hydroxide (made by Tanaka Chemical Research Co., Ltd., nickel content 61.8 wt%) was used as the nickel raw material. A positive electrode active material C1 for batteries was obtained. The result of powder X-ray diffraction measurement of C1 is shown in FIG. In addition to the layered structure similar to that reported by Ohzuku et al., Diffraction lines of NiO and Li ₂ MnO ₃ were observed in C1.
[0041]
(2) Evaluation of Charge / Discharge Performance when Using as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles C1, and a charge / discharge test was performed in the same manner as in Reference Example 1.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were as low as 84 and 83 mAh / g, respectively.
[0042]
Example 3
(1) Synthesis of positive electrode active material First, dinickel trioxide (manufactured by Hayashi Junyaku Kogyo Co., Ltd., nickel content 73.4% by weight, BET specific surface area 134 m ² / g; powder X-ray diffraction measurement result is shown in FIG. ), Cobalt trioxide (manufactured by Nippon Kagaku Sangyo Co., Ltd., product name PRM-73, cobalt content 72.8%), manganese dioxide (manufactured by High Purity Chemical Laboratory Co., Ltd., reagent 2N grade), hydroxylation Lithium (manufactured by Honjo Chemical Co., Ltd.) was weighed so that the molar ratio of each element was Li: Ni: Mn: Co = 1.04: 0.34: 0.42: 0.20, and then a mortar was sufficient. Mixed. The obtained mixed powder was placed in a box furnace and fired at 1000 ° C. for 15 hours in air, whereby positive electrode active material E3 for non-aqueous secondary battery (x = 0 in composition formula (I)). .44, y = 0.10, and Li [Ni _0.34 Li _0.04 Mn _0.42 Co _0.20 ] O ₂ ) was obtained. The powder X-ray diffraction measurement result of E3 is shown in FIG. E3 was also confirmed to have a layered structure similar to that reported by Ohzuku et al.
[0043]
(2) Evaluation of Charging / Discharging Performance when Used as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles E3, and a charging / discharging test was conducted in the same manner as in Reference Example 1.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 143 and 142 mAh / g, respectively.
[0044]
Example 4
(1) Synthesis of positive electrode active material A positive electrode active material E4 for a nonaqueous secondary battery was obtained in the same manner as in Example 3 except that the firing temperature was 950 ° C. The powder X-ray diffraction measurement result of E4 is shown in FIG. E4 was also confirmed to have a layered structure similar to that reported by Ohzuku et al.
[0045]
(2) Evaluation of Charge / Discharge Performance when Using as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles E4, and a charge / discharge test was performed in the same manner as in Reference Example 1.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 135 and 134 mAh / g, respectively.
[0046]
Reference Example 5
(1) Synthesis of positive electrode active material The same procedure as in Example 3 except that the molar ratio of each element was Li: Ni: Mn: Co = 1.00: 0.40: 0.40: 0.20. Thus, a positive electrode active material E5 for a non-aqueous secondary battery (in the composition formula (I), x = 0.50, y = 0.10, Li [Ni _0.40 Mn _0.40 Co _0.20 ] O ₂ ) was obtained. . The powder X-ray diffraction measurement result of E5 is shown in FIG. It was confirmed that E5 also has the same layered structure as reported by Ohzuku et al.
[0047]
(2) Evaluation of Charge / Discharge Performance when Using as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles E5, and a charge / discharge test was conducted in the same manner as in Reference Example 1.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 147 and 144 mAh / g, respectively.
[0048]
Example 6
(1) Synthesis of positive electrode active material The same procedure as in Example 3 except that the molar ratio of each element was Li: Ni: Mn: Co = 1.06: 0.31: 0.43: 0.20. The positive electrode active material E6 for non-aqueous secondary battery (in the composition formula (I), x = 0.41, y = 0.10, Li [Ni _0.31 Li _0.06 Mn _0.43 Co _0.20 ] O ₂ ) Obtained. The powder X-ray diffraction measurement result of E6 is shown in FIG. E6 was also confirmed to have the same layered structure as reported by Ohzuku et al.
[0049]
(2) Evaluation of Charging / Discharging Performance when Used as Positive Electrode Active Material of Lithium Secondary Battery A flat battery was prepared using the obtained compound particles E6, and a charging / discharging test was conducted in the same manner as in Reference Example 1. The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were 137 and 137 mAh / g, respectively.
[0050]
Example 7
The charge / discharge behavior at 60 ° C. was examined for the compound particles E3, E5, and E6. A flat battery was prepared in the same manner as in Reference Example 1 except that a solution of LiPF ₆ dissolved in a 1: 1 (volume ratio) mixture of EC and EMC as an electrolyte was used in an amount of 1 mol / liter. It put in the thermostat and hold | maintained at 60 degreeC, and implemented the charging / discharging test.
The change in discharge capacity is shown in FIG. The discharge capacities at the 10th and 20th cycles were E3: 154, 151 mAh / g, E5: 155, 147 mAh / g and E6: 148, 145 mAh / g, respectively. Compared to E5 with x = 0.5, ie Ni content = Mn content, E <3 and E6 containing Li in transition metal sites with x <0.5, ie Ni content <Mn content, are even better. The cycle characteristics are shown.
[0051]
【The invention's effect】
According to the production method of the present invention, a positive electrode active material having a layered structure containing nickel and manganese can be easily produced, and a non-aqueous secondary battery using this has a large capacity. The present invention is extremely useful industrially.
[Brief description of the drawings]
FIG. 1 is a graph showing the results of powder X-ray diffraction measurement of dinickel trioxide used in Examples.
2 is a graph showing the results of powder X-ray diffraction measurement of the positive electrode active materials obtained in Reference Example 1, Example 2, and Comparative Example 1. FIG.
FIG. 3 is a diagram showing cycle changes in discharge capacity in Reference Example 1, Example 2 and Comparative Example 1;
4 is a graph showing the results of powder X-ray diffraction measurement in Examples 3 and 4. FIG.
FIG. 5 is a diagram showing cycle changes in discharge capacity in Examples 3 and 4.
6 is a graph showing the results of powder X-ray diffraction measurement in Reference Example 5 and Example 6. FIG.
7 is a graph showing cycle changes in discharge capacity in Reference Example 5 and Example 6. FIG.
FIG. 8 is a diagram showing a cycle change in discharge capacity in Example 3, Reference Example 5 and Example 6;

Claims (3)

Composition formula Li [Ni _(xy) Li _{(1 / 3-2x / 3)} Mn _{(2 / 3-x / 3-y)} Co _2y ] O ₂ (0 <x <0.5, 0 < y ≦ 1 / 6. A method for producing a positive electrode active material for a non-aqueous secondary battery comprising a compound having a layered structure of α-NaFeO ₂ represented by x> y), wherein the nickel content is 70.98 wt% or more A method for producing a positive electrode active material for a non-aqueous secondary battery, comprising: calcining a mixture containing dinickel trioxide of less than 78.6% by weight and capable of constituting the compound by firing.   A positive electrode active material for a non-aqueous secondary battery obtained by the production method according to claim 1.   A non-aqueous secondary battery comprising the positive electrode active material for a non-aqueous secondary battery according to claim 2.

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