CN1711660A - Nonaqueous electrolyte secondary battery - Google Patents

Nonaqueous electrolyte secondary battery Download PDF

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Publication number
CN1711660A
CN1711660A CNA2003801028979A CN200380102897A CN1711660A CN 1711660 A CN1711660 A CN 1711660A CN A2003801028979 A CNA2003801028979 A CN A2003801028979A CN 200380102897 A CN200380102897 A CN 200380102897A CN 1711660 A CN1711660 A CN 1711660A
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aforementioned
particle
lithium
active material
nonaqueous electrolytic
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CN1330046C (en
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志村奈緒
田中弘真
関野正宏
佐藤麻子
稲田周介
矢嶋亨
小口雅之
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Toshiba Corp
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0567—Liquid materials characterised by the additives
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

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  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

A nonaqueous electrolyte secondary battery comprising a positive electrode containing positive electrode active substance particles in which lithium double oxide particles are contained, a negative electrode and a nonaqueous electrolyte, wherein the lithium double oxide particles have a composition containing element (M) being at least one member selected from the group consisting of Ni and Co, having a particulate form containing secondary agglomerates, and exhibit a peak intensity ratio satisfying the following formula (1), wherein the content of lithium double oxide particles in the positive electrode active substance particles is 50 wt.% or more, wherein the molar ratio of positive electrode active substance particles satisfies the following formula (2) and the particle diameter of volume cumulative frequency 90% (D90) with respect to the positive electrode active substance particles is in the range of 10 to 25 mum, and wherein the nonaqueous electrolyte contains a sultone compound having at least one double bond in its ring: 2 <= (I003/I104) < 5 (1) 0.95 <= (YLi/YM) <= 1.02 (2).

Description

Rechargeable nonaqueous electrolytic battery
Technical field
The present invention relates to rechargeable nonaqueous electrolytic battery.
Background technology
In recent years, on the miniaturization of seeking electrical equipment such as mobile communication equipment, notebook computer, PDA, one-piece type video camera, pocket CD (MD) player, cordless telephone, light-weighted basis, as the power supply of these electrical equipment, people are pursuing compact and jumbo battery.
The primary cell that alkaline manganese battery and so on is arranged and the secondary cells such as nickel-cadmium cell, lead accumulator of the battery of having popularized as the power supply of these electrical equipment.Wherein, anodal lithium composite xoide, the negative pole of adopting adopts the rechargeable nonaqueous electrolytic battery that can occlusion discharges the carbon material of lithium ion, and small-sized, light weight, single battery voltage height and can obtain high-energy-density are so be subjected to gazing at of people.
As the positive active material of rechargeable nonaqueous electrolytic battery, put down in writing in the Japanese patent laid-open 10-69910 communique with general formula (1): Li V-x1Ni 1-x2M xO 2The diffraction peak of expression, (003) face of X-ray diffraction Miller index hk1 and (104) face than (003)/(104) be more than 1.2, average grain diameter D is 5～100 μ m, particle size distribution 10% more than the 0.5D, 90% lithium nickel composite oxide below 2D.
Yet, possess the secondary cell of the positive pole that contains this lithium nickel composite oxide, because the oxidative decomposition of nonaqueous electrolyte can take place, there is the short problem of charge and discharge circulation life.
The announcement of invention
The purpose of this invention is to provide the rechargeable nonaqueous electrolytic battery that charge and discharge circulation life increases.
The present invention 1 provides rechargeable nonaqueous electrolytic battery; This battery is the rechargeable nonaqueous electrolytic battery that possesses the positive pole, negative pole and the nonaqueous electrolyte that comprise the anodal active material that contains the lithium composite oxide power; Aforementioned lithium composite oxide power is the powder that contains the secondary aggregation grain; Mole more following than satisfying (A) formula; The peak intensity ratio satisfies following (B) formula; And the particle diameter of volume accumulated frequence 90% (D90) is in the scope of 10 μ m～25 μ m; Aforementioned nonaqueous electrolyte contains the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5?????????????(A)
0.95≤(X Li/X M)≤1.02?????????(B)
In the formula, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide powder, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, X LiBe the lithium molal quantity in the aforementioned lithium composite xoide powder, X MBe the molal quantity of the element M in the aforementioned lithium composite xoide powder, aforementioned elements M is be selected from Ni and Co at least a.
The present invention 2 provides rechargeable nonaqueous electrolytic battery, this battery is to possess the positive pole that comprises the positive active material particle that contains the lithium composite xoide particle, the rechargeable nonaqueous electrolytic battery of negative pole and nonaqueous electrolyte, aforementioned lithium composite xoide particle has the composition of the element M that comprises at least a formation that is selected from Ni and Co, has the particle shape that contains the secondary aggregation grain, and the peak intensity ratio satisfies following (C) formula, the content of the aforementioned lithium composite xoide particle in the aforementioned positive active material particle is more than 50 weight %, the mol ratio of aforementioned positive active material particle satisfies following (D) formula, the particle diameter (D90) of the volume accumulation frequency 90% in the aforementioned positive active material particle is in the scope of 10 μ m～25 μ m, aforementioned nonaqueous electrolyte contains the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5??????????(C)
0.95≤(Y Li/Y M)≤1.02??????(D)
In the formula, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide particle, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, Y LiBe the molal quantity of the lithium in the aforementioned positive active material particle, Y MBe the molal quantity of the element M in the aforementioned positive active material particle, aforementioned elements M is be selected from Ni and Co at least a.
The simple declaration of accompanying drawing
Fig. 1 is the stereogram of expression as the slim rechargeable nonaqueous electrolytic battery of an example of rechargeable nonaqueous electrolytic battery of the present invention.
Fig. 2 is the sectional view of part that the slim rechargeable nonaqueous electrolytic battery of Fig. 1 is cut off along the II-II line.
Fig. 3 is the stereogram of expression as the part incised notch of the square rechargeable nonaqueous electrolytic battery of an example of rechargeable nonaqueous electrolytic battery of the present invention.
Fig. 4 is the partial cross section figure of expression as the cylindrical shape rechargeable nonaqueous electrolytic battery of an example of rechargeable nonaqueous electrolytic battery of the present invention.
Fig. 5 is PRS's contained in the nonaqueous electrolyte of rechargeable nonaqueous electrolytic battery of expression embodiment 1 1The performance plot of H-NMR spectrum.
The best mode that carries out an invention
Below, the 1st, the 2nd rechargeable nonaqueous electrolytic battery of the present invention is described.
The 1st rechargeable nonaqueous electrolytic battery of the present invention is the rechargeable nonaqueous electrolytic battery that possesses the positive pole, negative pole and the nonaqueous electrolyte that comprise the anodal active material that contains the lithium composite oxide power; Aforementioned lithium composite oxide power is the powder that contains the secondary aggregation grain; Mole more following than satisfying (A) formula; The peak intensity ratio satisfies following (B) formula; And the particle diameter of volume accumulated frequence 90% (D90) is in 10 μ m～25 mu m ranges; Aforementioned nonaqueous electrolyte contains the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5?????????(A)
0.95≤(X Li/X M)≤1.02?????(B)
In the formula, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide powder, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, X LiBe the molal quantity of the lithium in the aforementioned lithium composite xoide powder, X MBe the molal quantity of the element M in the aforementioned lithium composite xoide powder, aforementioned elements M is selected from least a of Ni and Co.
Aforementioned sultone compound is when initial charge, because two key is opened, polymerization reaction take place is so can form lithium ion permeability protection tunicle on anodal surface.On the other hand; aforementioned lithium composite xoide powder is because that the expansion of following the occlusion of lithium to discharge is shunk is less, simultaneously not only on the surface of secondary aggregation grain; and form the protection tunicle in the gap between primary particle, so the protection tunicle can form complicated network configuration.Consequently, peel off from positive pole owing to can suppress the protection tunicle in the charge and discharge cycles, thus the oxidative decomposition of nonaqueous electrolyte can be suppressed, and can improve the charge and discharge circulation life of secondary cell.
Below, positive pole, negative pole and nonaqueous electrolyte are described.
1) positive pole
This positive pole comprises collector body and is carried on the anodal layer that contains aforementioned positive active material, adhesive and conductive agent of the one or both sides of collector body.
After lithium composite xoide for example can mix by the compound (for example oxide, oxygen oxide) that each is constituted element, in air or under the oxygen atmosphere, calcine and synthesize.
Below explanation will be with the lithium (X in the lithium composite xoide Li) and element M (X M) mol ratio (X Li/ X M) be set in the reason in 0.95～1.02 the scope.Mol ratio (X Li/ X M) if less than 0.95, then crystallinity can obviously reduce, so the possibility of the occlusion release that lithium takes place is hardly arranged.On the other hand, mol ratio (X Li/ X MIf) surpass 1.02, though then crystallinity is good, promote particle to grow up during owing to calcining, so the ratio of single-particle raises.Consequently, not only follow the expansion of the occlusion release of lithium to shrink increase, and the protection tunicle of lining primary particle is isolated fully, can not get network configuration, so the protection tunicle is peeled off easily in charge and discharge cycles, charge and discharge circulation life probably can shorten.Mol ratio (X Li/ X M) comparatively ideal scope be 0.97～1.02, better scope is 0.99～1.02.
As lithium composite xoide, can exemplify lithium nickel composite oxide, lithium cobalt composite oxide, lithium/nickel/cobalt composite oxide etc.Also can contain lithium and element M element in addition in the aforementioned lithium composite xoide.This element can exemplify Mn, Al, Sn, Fe, Cu, Cr, Zn, Mg, Si, P, F, Cl, B etc.The kind of adding element can be a kind, also can be more than 2 kinds.
Aforementioned lithium composite xoide preferably accounts for more than 50% of positive active material.
Below explanation is with the peak intensity I of (003) face in the powder x-ray diffraction 003(104) the peak intensity I of face 104Ratio (I 003/ I 104) be limited to the reason of aforementioned range.Peak intensity I 104Ratio (I 003/ I 104If) more than 5; though then crystallinity is good; but grow up owing to promoted grain; so show tabular property; the ratio that is the high single-particle of crystal orientation raises; therefore follow the expansion of the occlusion release of lithium to shrink increase, and the protection tunicle of each primary particle that is covered is isolated fully, can not obtain network configuration.Consequently, because charge and discharge cycles is peeled off the protection tunicle easily, so charge and discharge circulation life probably can shorten.By with peak intensity than (I 003/ I 104) be set in more than 2 and less than 5, can improve the ratio of secondary aggregation grain, the expansion shrinkage that can reduce simultaneously to follow the occlusion of lithium to discharge.In addition, crystallization does not have directionality, is that peak intensity is than (I under isotropic situation fully 003/ I 104) be 2 by the value that calculates.Peak intensity is than (I 003/ I 104) better scope be greater than 2 and below 4.95.
Below explanation is defined in the particle diameter (D90) of the volume accumulation frequency 90% of lithium composite xoide powder the reason of aforementioned range.If D90 is less than 10 μ m, then because the quantity of the primary particle of formation secondary aggregation grain is on the low side, so the contact area deficiency between secondary aggregation grain and the protection tunicle, the protection tunicle is peeled off easily, and charge and discharge circulation life probably can shorten.On the other hand, if D90 surpasses 25 μ m, then because the quantity of the primary particle of formation secondary aggregation grain is more, so the protection tunicle can not be penetrated into the inside of secondary aggregation grain, the state that the surperficial protected tunicle of approaching only secondary aggregation grain covers.Therefore, peeling off appears in protection tunicle easily in the charge and discharge cycles, and charge and discharge circulation life probably can shorten.The better scope of D90 is 10 μ m～20 μ m.
As aforementioned conductive agent, can exemplify acetylene black, carbon black, graphite etc.
The aforementioned adhesion agent has makes active material remain on the collector body and the function of bonding active material.As the aforementioned adhesion agent, can use for example polytetrafluoroethylene (PTFE), poly-inclined to one side vinylidene fluoride (PVdF), polyether sulfone, ternary ethylene-propylene copolymer (EPDM), styrene butadiene rubbers (SBR) etc.
The proportioning of aforementioned positive active material, conductive agent, adhesive is preferably in the scope of positive active material 80～95 weight %, conductive agent 3～20 weight %, adhesive 2～7 weight %.
As aforementioned collector body, can use the conductive board of porous matter structure or the conductive board of atresia.These conductive boards can be made by for example aluminium, stainless steel or nickel.
Aforementioned positive pole for example can be suspended in the appropriate solvent by positive active material, conductive agent and adhesive, should hang absurd creature and be coated on collector body, and dry back forms lamellar and makes.
2) negative pole
Aforementioned negative pole comprises collector body and is carried on the negative electrode layer of the one or both sides of collector body.
Aforementioned negative electrode layer comprises carbonaceous thing and the adhesive that occlusion discharges lithium ion.
As aforementioned carbonaceous thing, can exemplify graphite material or carbon materials such as graphite, coke, carbon fiber, spherical carbon, thermal decomposition gas-phase carbon pledge, resin calcined material; By being that carbon, mesophase pitch based carbon fiber, mesophasespherule etc. (the mesophase pitch based carbon fiber can the raising capacity and charge, and is desirable especially) are in 500～3000 ℃ of graphite materials of heat-treating and obtaining or carbon material etc. to thermosetting resin, isotropic pitch, mesophase pitch.Wherein, the more satisfactory face d at interval that is to use with (002) face 002Graphite material for the graphite crystallization below the 0.34nm.Possess and comprise this graphite material and can be improved significantly as the battery capacity and the heavy-current discharge characteristic of the rechargeable nonaqueous electrolytic battery of the negative pole of carbonaceous thing.Aforementioned interval d 002Even more ideal below 0.337nm.
For example can adopt polytetrafluoroethylene (PTFE), poly-inclined to one side vinylidene fluoride (PVdF), ternary ethylene-propylene copolymer (EPDM), styrene butadiene rubbers (SBR), carboxymethyl cellulose (CMC) etc. as the aforementioned adhesion agent.
The proportioning of aforementioned carbonaceous thing and aforementioned adhesion agent is preferably in the scope of carbonaceous thing 90～98 weight %, adhesive 2～20 weight %.
As aforementioned collector body, can use the conductive board of porous matter structure or the conductive board of atresia.These conductive boards can be by making such as copper, stainless steel or nickel.
Aforementioned negative pole for example can be by occlusion being discharged lithium ion carbonaceous thing and the adhesive outstanding absurd creature that obtains that in the presence of solvent, mixes be coated on the collector body, dry back is with desirable pressure compacting 1 time or divide and carry out the multistage for 2～5 times and suppress and make.
Make electrode group with above-described positive pole and negative pole.
This electrode group for example can sandwich dividing plate by (i) between positive pole and negative pole, be rolled into swirl shape; (ii) between positive pole and negative pole, sandwich dividing plate, be rolled into flat pattern; (iii) between positive pole and negative pole, sandwich dividing plate, be rolled into swirl shape after, to radially the compression; (iv) sandwich dividing plate between positive pole and negative pole, bending is more than 1 time; (carry out stacked method when v) between positive pole and negative pole, sandwiching dividing plate and make.
It is also passable that electrode group is not pressurizeed, but in order to improve the integrated intensity of positive pole, negative pole and dividing plate, also can pressurize.Can when pressurization, heat simultaneously.
Contain the adhesiveness macromolecule in the electrode group in order to improve the integrated intensity of positive pole, negative pole and dividing plate, can to make.Have a fusible macromolecule as aforementioned, can exemplify polyacrylonitrile (PAN), polyacrylate (PMMA), poly-inclined to one side vinylidene fluoride (PVdF), polyvinyl chloride (PVC) or poly(ethylene oxide) (PEO) etc.
As the dividing plate that is used for this electrode group, can adopt little porous membrane, weave cotton cloth, the sandwich of nonwoven fabrics and identical or different material wherein etc.Material as forming dividing plate can exemplify polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-butene copolymer etc.As the formation material of dividing plate, can adopt to be selected from more than a kind or 2 kinds of aforesaid kind.
The thickness of aforementioned separator plate with below the 30 μ m for well, better scope is below the 25 μ m.Simultaneously, for well, better lower limit is 8 μ m to the lower limit of thickness with 5 μ m.
Aforementioned separator plate with 120 ℃, 1 hour percent thermal shrinkage below 20% for well, the aforementioned hot shrinkage is serving as better below 15%.
For well, better scope is 35～50% to the vesicularity of aforementioned separator plate in 30～60% scope.
The air transmission coefficient of aforementioned separator plate was with 600 seconds/100cm 3Below for well.Air transmission coefficient is meant 100cm 3Air see through the desired time of dividing plate (second).The upper limit of air transmission coefficient was with 500 seconds/100cm 3Even more ideal.Simultaneously, the lower limit of air transmission coefficient was with 50 seconds/100cm 3For good, even more ideal lower limit is 80 seconds/100cm 3
The width of dividing plate cans be compared to anodal most and negative pole is wideer slightly.By such structure, can prevent from not insert dividing plate between positive pole and negative pole and directly contact.
3) nonaqueous electrolyte
Nonaqueous electrolyte can use the electrolyte that has aqueous or gelatinous form in fact.
Below nonaqueous solvents and electrolyte contained in aqueous nonaqueous electrolyte and the gel nonaqueous electrolyte are explained.
Nonaqueous solvents comprises the sultone compound that has at least one two key in the ring.
Here, as the sultone compound that has at least one two key in the ring, the sultone compd B that can adopt at least one H of sultone compd A that the general formula shown in followingization 1 represents or sultone compd A to be replaced by alkyl.Among the application, both sultone compd A or B can be adopted separately, also sultone compd A and B can be used simultaneously.
(changing 1)
Change in 1 C mH nBe straight chain shape alkyl, m and n are the integers more than 2 that satisfies 2m＞n.
The sultone compound that has at least one two key in the ring, owing to opening two keys with the reaction of positive pole, polymerization reaction take place is so can form lithium ion permeability protection tunicle on anodal surface.In the sultone compound, comparatively ideal is the m=3 in the sultone compd A, the compound of n=4, promptly 1, and 3-propylene sultone (1,3-propene sultone, PRS) or the compound of m=4, n=6, promptly 1, the 4-butene sultone (1,4-butylene sultone, BTS).As the sultone compound, both can adopt 1 separately, 3-propylene sultone (PRS) or 1,4-butene sultone (BTS) also can and be used PRS and BTS.
The ratio of sultone compound is preferably below the 10 volume %.This is that then aforementioned protection tunicle can become very thick because if the ratio of sultone compound surpasses 10% volume, and the lithium ion permeability reduces, and the discharge capacity that is lower than under the temperature of normal temperature can reduce.And for example under the low temperature of-20 ℃ of grades, in order to keep high discharge capacity, the contained ratio of sultone compound is preferably below 4% volume.In addition, in order to ensure the formation amount of protection tunicle, the ratio of sultone compound should guarantee to be 0.01 volume % at least.The ratio of sultone compound is if more than 0.1 volume %, even for example under higher temperature such as 65 ℃ of grades, also can fully manifest the defencive function of protecting tunicle.
Preferably also contain ethylene carbonate (EC) in the nonaqueous solvents.The content of EC in the nonaqueous solvents is more fortunately in the scope of 25 volume %～50 volume %.The nonaqueous electrolyte that can obtain the conductance height and have appropriate viscosity thus.Better EC content range is 25 volume %～45 volume %.
Can and use sultone compound and EC and other solvent in the nonaqueous solvents.As other solvent, can exemplify linear carbonate { for example, carbonic acid methyl ethyl ester (MEC), diethyl carbonate (DEC), dimethyl carbonate (DMC) etc. }, vinylene carbonate (VC), ethylene thiazolinyl ethyl (VEC), carbonic acid phenyl ethyl (phEC), propylene carbonate (PC), gamma-butyrolacton (GBL), gamma-valerolactone (VL), methyl propionate (MP), ethyl propionate (EP), 2-methylfuran (2Me-F), furans (F), thiophene (TIOP), catechol carbonic ester (CATC), glycol sulfite (ES), 12-crown ether-4, tetraethylene glycol dimethyl ether etc.Other solvent types is more than a kind or 2 kinds.
As the electrolyte that dissolves in the aforementioned nonaqueous solvents, can exemplify lithium perchlorate (LiClO 4), phosphorus hexafluoride acid lithium (LiPF 6), tetrafluoride lithium borate (LiBF 4), arsenic hexafluoride lithium (LiAsF 6), the inclined to one side sulfonic acid lithium of trifluoro (LiCF 3SO 3), two three fluoridize sulfonyloxy methyl imonium lithium [LiN (CF 3SO 2) 2] and LiN (C 2F 5SO 2) 2Deng lithium salts.Used electrolytical kind can be more than a kind or 2 kinds.
The meltage of aforesaid electrolyte in aforementioned nonaqueous solvents, comparatively ideal is 0.5～2.5 mole/L.Better scope is 1～2.5 mole/L.
In order to improve the wetability with dividing plate, preferably contain the surfactant of trioctyl phosphate (TOP) and so in the aforementioned aqueous nonaqueous electrolyte.The addition of surfactant is comparatively ideal to be below 3%, and better is in 0.1～1% scope.
The amount of aforementioned aqueous nonaqueous electrolyte, comparatively ideal is to be 0.2～0.6g corresponding to battery unit capacity 100mAh, better scope is 0.25～0.55g/100mAh.
The container of taking in above-mentioned electrode group and nonaqueous electrolyte is described.
The shape of container for example can have been made the round-ended cylinder type, end rectangle cartridge type has been arranged, bag shape, cup-shaped etc.
This container for example can be made by the film that contains resin bed, metallic plate, metallic film etc.
Resin bed contained in the aforementioned film for example can be made by polyolefin (for example polyethylene, polypropylene), polyamide etc.Contain in the film of resin bed, preferably adopt the laminated film of the metal level and the integrated formation of protective layer on the two sides that is disposed at the aforementioned metal layer.The aforementioned metal layer plays the effect of blocks moisture and the effect that keeps container shapes.The aforementioned metal layer for example can exemplify aluminium, stainless steel, iron, copper, nickel etc.Wherein, light weight, aluminum ratio that the blocks moisture ability is strong are more satisfactory.The aforementioned metal layer can be made by a kind of metal, also can be integrated into by the metal level more than 2 kinds.In aforementioned 2 layers of protective layer, the protective layer that joins with the outside works to prevent aforementioned metal layer damaged.This outer protection layer is made of a kind of resin bed or the resin bed more than 2 kinds.On the other hand, the internal protection layer works to prevent that the aforementioned metal layer is subjected to the nonaqueous electrolyte corrosion.This internal protection layer by a kind of resin bed or more than 2 kinds resin bed constitute.And, can dispose the thermoplastic resin of using with heat seal mode airtight container on the surface of this internal protection layer.
Contain resin bed film thickness with below the 0.3mm for well, comparatively ideal scope is below the 0.25mm, better scope is below the 0.15mm, optimal scope is below the 0.12mm.If thickness, then causes distortion and damaged easily less than 0.05mm, thus the lower limit of film thickness with 0.05mm for well.
Aforementioned metal plate and aforementioned metal film can be made by for example iron, stainless steel, aluminium.
The thickness of aforementioned metal plate and aforementioned metal film with below the 0.4mm for well, comparatively ideal scope is below the 0.3mm, optimal scope is below the 0.25mm.If thickness less than 0.05mm, then may not obtain full intensity, so, the lower limit of the thickness of metallic plate and metallic film with 0.05mm for well.
The 2nd rechargeable nonaqueous electrolytic battery of the present invention is to possess the positive pole that comprises the positive active material particle that contains the lithium composite xoide particle, the rechargeable nonaqueous electrolytic battery of negative pole and nonaqueous electrolyte, aforementioned lithium composite xoide particle has the composition of the element M that comprises at least a kind of formation that is selected from Ni and Co, has the particle shape that contains the secondary aggregation grain, and the peak intensity ratio satisfies following (C) formula, the content of the aforementioned lithium composite xoide particle in the aforementioned positive active material particle is more than the 50 weight %, the mol ratio of aforementioned positive active material particle satisfies following (D) formula, the particle diameter (D90) of the volume accumulation frequency 90% in the aforementioned positive active material particle is in the scope of 10 μ m～25 μ m, aforementioned nonaqueous electrolyte comprises the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5?????????????(C)
0.95≤(Y Li/Y M)≤1.02?????????(D)
In the formula, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide particle, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, Y LiBe the molal quantity of the lithium in the aforementioned positive active material particle, Y MBe the molal quantity of the element M in the aforementioned positive active material particle, aforementioned elements M is be selected from Ni and Co at least a.
In the 2nd rechargeable nonaqueous electrolytic battery of the present invention, except that positive pole, other formation is described identical with aforementioned the 1st rechargeable nonaqueous electrolytic battery.Below positive pole is explained.
This positive pole possesses collector body and is carried on the one or both sides of collector body, contains the anodal layer of aforementioned positive active material particle, adhesive and conductive agent.
The peak intensity of the lithium composite xoide particle by will containing element M is than (I 003/ I 104) be set in more than 2 below 5, can improve the ratio of secondary aggregation grain, the expansion shrinkage that can reduce to follow the occlusion of lithium to discharge simultaneously.In addition, crystallization does not have directionality, is that peak intensity is than (I under isotropic situation fully 003/ I 104) be 2 by the value of calculating gained.Peak intensity is than (I 003/ I 104) better scope be greater than 2 and below 4.95.
Because peak intensity is than (I in the positive active material particle 003/ I 104) more than 2 less than the content of 5 lithium composite xoide particle more than 50 weight %, so the mol ratio (Y of positive active material particle Li/ Y M) with the mol ratio of lithium composite xoide particle about equally.Therefore, if mol ratio (Y Li/ Y M) less than 0.95, then owing to the reasons such as crystallinity reduction of lithium composite xoide particle, the occlusion of lithium discharges and might take place hardly in the positive active material.On the other hand, if mol ratio (Y Li/ Y M) greater than 1.02; though then the crystallinity of lithium composite xoide particle is good,,, the expansion of not only following the occlusion of lithium to discharge increases so shrinking because the ratio of the single-particle in the lithium composite xoide particle raises; and the protection tunicle of lining primary particle is isolated fully, is difficult to obtain network configuration.Consequently, because the protection tunicle is peeled off easily in the charge and discharge cycles, so charge and discharge circulation life probably can shorten.Mol ratio (Y Li/ Y M) more satisfactory scope be 0.97～1.02, better scope is 0.99～1.02.
Because the content of the lithium composite xoide particle in the positive active material particle is more than 50 weight %, so reflect in the particle size distribution of positive active material particle that the particle size distribution of lithium composite xoide particle is big.If the particle diameter (D90) of the volume accumulation frequency 90% of positive active material particle is less than 10 μ m; the quantity of primary particle of secondary aggregation grain that then constitutes the lithium composite xoide particle is on the low side; so the contact area between secondary aggregation grain and the protection tunicle diminishes, the protection tunicle is peeled off easily.Therefore, may can not get long charge and discharge circulation life.On the other hand; if D90 is greater than 25 μ m; the quantity of primary particle of secondary aggregation grain that then constitutes the lithium composite xoide particle is on the high side, and the infiltration of protection tunicle in most cases is the surperficial protected by the state of membrane cover of only secondary aggregation grain less than the inside of secondary aggregation grain.Therefore, the protection tunicle is peeled off easily in charge and discharge cycles, may can not get long charge and discharge circulation life.The better scope of D90 is 10 μ m～20 μ m.
The content of the lithium composite xoide particle in the positive active material particle can improve the adhesiveness between anodal and the protection tunicle more for a long time.Therefore, in order to obtain longer charge and discharge circulation life, comparatively ideal is that the content of the lithium composite xoide particle in the positive active material particle is more than the 60 weight %, and better is more than the 70 weight %.
As the lithium composite xoide that contains element M, can exemplify lithium nickel composite oxide, lithium cobalt composite oxide, lithium/nickel/cobalt composite oxide etc.In the aforementioned lithium composite xoide,, can add the element of other kind from improving viewpoints such as characteristic.This dvielement can exemplify Mn, Al, Sn, Fe, Cu, Cr, Zn, Mg, Si, P, F, Cl, B etc.The kind of adding element both can be a kind, also can be more than 2 kinds.
Wherein, with following (E) formula or (F) consisting of of representing of formula,
Li aCo bM1 cO 2???????????(E)
In the formula, aforementioned M1 is the element more than a kind that is selected from Ni, Mn, B, Al and Sn, aforementioned molar ratio a, b, c satisfy 0.95≤a≤1.05,0.95≤b≤1.05,0≤c≤0.05,0.95≤b+c≤1.05 respectively, and the better scope of mol ratio is respectively 0.97≤a≤1.03,0.97≤b≤1.03,0.001≤c≤0.03.
Li xNi yCo zM2 wO 2?????????????(F)
In the formula, aforementioned M2 is the element more than a kind that is selected from Mn, B, Al and Sn, aforementioned molar ratio x, y, z, w satisfy 0.95≤x≤1.05,0.7≤y≤0.95,0.05≤z≤0.3,0≤w≤0.1,0.95≤y+z+w≤1.05 respectively, the better scope of mol ratio x, y, z is 0.97≤x≤1.03,0.75≤y≤0.9,0.1≤z≤0.25, the comparatively ideal scope of mol ratio w is 0≤w≤0.07, better scope is 0≤w≤0.05, and optimal scope is 0≤w≤0.03.In order fully to obtain the additive effect of element M 2, the lower limit of mol ratio w with 0.001 for well.
In the aforementioned lithium composite xoide particle, all particles can not have identical composition, peak intensity such as the fruit more than 2 less than 5, then can constitute by forming the different particles more than 2 kinds.
In addition, aforementioned positive active material particle can be made of aforementioned lithium composite xoide particle, also can contain this lithium composite xoide particle other particle in addition.
As other particle, can exemplify peak intensity than (I 003/ I 104) lithium-contained composite oxide particle greater than 5.This lithium-contained composite oxide particle has very high activity under charged state, thus if containing the positive pole of aforementioned lithium-contained composite oxide particle is under the hot environment, then can be rapidly and the sultone compound in the nonaqueous electrolyte react.Consequently, be stored in hot environment following time, can form the protection tunicle by the sultone compound rapidly on anodal surface, so can suppress the oxidative decomposition of nonaqueous electrolyte with charged state.Therefore, can reduce secondary cell and be stored in the generation of the gas in hot environment following time with charged state, thus the expansion of battery can be suppressed, thus the secondary cell that the expansion when obtaining the long and charging high temperature of charge and discharge circulation life and preserving is inhibited.Peak intensity is than (I 003/ I 104) comparatively ideal scope be more than 7.In addition owing to do not detect peak intensity than might having the crystal structure of not occlusion lithium greater than 500 particle with from the particle at the peak of (104) face, so peak intensity than the upper limit with 500 for good.
In order to obtain charge and discharge circulation life and all good secondary cells of charging high temperature preservation characteristics, peak intensity is than (I 003/ I 104) greater than 5 the ratio of lithium-contained composite oxide particle in the positive active material particle with more than the 0.1 weight %, less than 50 weight % for well.Better scope is 0.5～48 weight %.
As lithium-contained composite oxide, can exemplify lithium cobalt composite oxide etc.Can add at least a kind and the different types of element of formation element in the aforementioned lithium-contained composite oxide.As adding element, can exemplify Ni, Mn, Al, Sn, Fe, Cu, Cr, Zn, Mg, Si, P, F, Cl, B etc.In addition, the composition of aforementioned lithium-contained composite oxide can be aforementioned (E) formula or (F) the represented composition of formula.
In this lithium-contained composite oxide particle, all particles can not have identical composition, as long as peak intensity also can constitute by forming the different particles more than 2 kinds than greater than 5.
Aforementioned conductive agent, aforementioned adhesion agent, aforementioned collector body can exemplify and the described identical example of the aforementioned the 1st rechargeable nonaqueous electrolytic battery.
Aforementioned positive pole for example can should hang absurd creature and be coated on the collector body by positive active material, conductive agent and adhesive are suspended in appropriate solvent, and dry back forms lamellar and makes.
Used positive active material particle contains the above lithium composite xoide particle that contains element M of 50 weight % in above-described the 2nd rechargeable nonaqueous electrolytic battery of the present invention, and the peak intensity of aforementioned lithium composite xoide particle is than (I 003/ I 104) more than 2 less than 5, have the particle shape that contains the secondary aggregation grain simultaneously, the mol ratio (Y of aforementioned positive active material particle Li/ Y M) in 0.95～1.02 scope, and the particle diameter (D90) of the volume of aforementioned positive active material particle accumulation frequency 90% is in the scope of 10 μ m～25 μ m, so, can with the reaction of sultone compound, form lithium ion permeability protection tunicle on anodal surface.This protects tunicle not only on the surface of secondary aggregation grain, and forms in the gap between primary particle, so can have complicated network configuration.Consequently, can in charge and discharge cycles, suppress the protection tunicle and peel off,, improve the charge and discharge circulation life of secondary cell so can suppress the oxidative decomposition of nonaqueous electrolyte from positive pole.
With reference to Fig. 1～Fig. 4 slim, square, cylindrical shape rechargeable nonaqueous electrolytic battery as an example of rechargeable nonaqueous electrolytic battery of the present invention are elaborated.
Fig. 1 is the stereogram of expression as the slim rechargeable nonaqueous electrolytic battery of an example of rechargeable nonaqueous electrolytic battery of the present invention.Fig. 2 is the sectional view of part that the slim rechargeable nonaqueous electrolytic battery of Fig. 1 is cut off along short side direction.Fig. 3 is the stereogram of expression as the part incised notch of the square rechargeable nonaqueous electrolytic battery of an example of rechargeable nonaqueous electrolytic battery of the present invention.Fig. 4 is the partial cross section figure of cylindrical shape rechargeable nonaqueous electrolytic battery of an example of expression rechargeable nonaqueous electrolytic battery of the present invention.
At first, slim rechargeable nonaqueous electrolytic battery is explained.
As shown in Figure 1, the electrode group 2 of in the container body 1 of making rectangular cup, packing into.Electrode group 2 possesses the structure that the sandwich that comprises positive pole 3, negative pole 4 and be configured in the dividing plate 5 between positive pole 3 and the negative pole 4 is rolled into flat pattern.Nonaqueous electrolyte is held in electrode group 2.A part of broadening at container body 1 edge plays the effect of cover plate 6.Container body 1 and cover plate 6 are made of laminated film respectively.This laminated film comprises outer protection layer 7, contains the internal protection layer 8 of thermoplastic resin, is configured in the metal level 9 between outer protection layer 7 and the internal protection layer 8.In the container body 1, lid 6 adopts the thermoplastic resin of internal protection layer 8 to be fixed by heat seal, by this electrode group 2 is sealed in the container.Anodal 3 are connected with positive terminal 10, and negative pole 4 is connected with anode connector 11, is led to external container respectively, plays the effect of positive terminal and negative terminal.
Below, the square rechargeable nonaqueous electrolytic battery is explained.
As shown in Figure 3, the electrode group 13 of in the such metal of for example aluminium is shaped on end rectangle cylindrical container 12, packing into.Electrode group 13 is the parts that are rolled into flat behind the order lamination according to anodal 14, dividing plate 15 and negative pole 16.Near the partition 17 that peristome is arranged the central authorities be configured in electrode group 13 above.
Nonaqueous electrolyte is held in electrode group 13.Possess explosion-protection equipment 18a and near central authorities, have the hush panel 18b in circular open hole to be welded on the peristome of container 12 by method of laser welding.Negative terminal 19 is configured in the circular port of hush panel 18b by sealing.The anode connector 20 of drawing from negative pole 16 is welded in the lower end of negative terminal 19.On the other hand, positive terminal (not having diagram) is connected in the container 12 of double as positive terminal.
Below, the cylindrical shape rechargeable nonaqueous electrolytic battery is explained.
The bottom that is shaped on the container 21 of round-ended cylinder shape at stainless steel has disposed insulator 22.Electrode group 23 is loaded in the aforementioned container 21.Former electrodes group 23 is that the ribbon that will form behind positive pole 24, dividing plate 25, negative pole 26 and dividing plate 25 laminations is rolled into gyrate structure, makes dividing plate 25 be positioned at the outside.
The nonaqueous electrolyte of having packed in the aforementioned container 21.The insulating paper 27 of central portion opening is configured in the top of the former electrodes group 23 in the aforementioned container 21.Insulator seal oralia 28 is configured in the upper opening portion of aforementioned container 21, and by to adopting inboard ca(u)lk processing method near the aforementioned upper opening portion aforementioned hush panel 28 being fixed in aforementioned container 21.Positive terminal 29 is entrenched in the central authorities of aforementioned dielectric hush panel 28.One end of anodal reed 30 is connected in aforementioned anodal 24, and the other end is connected in aforementioned positive terminal 29.Aforementioned negative pole 26 is connected in aforementioned container 21 as negative terminal by not shown anode reed.
Below, describe embodiments of the invention in detail with reference to aforementioned figures.
(embodiment 1)
＜anodal manufacturing 〉
Preparation has composition shown in the following table 1 and volume accumulation frequency 90% particle diameter D90 and peak intensity than (I 003/ I 104) by following table 1 the lithium composite xoide particle of indicating value.The result who observes with scanning electron microscope is can confirm to contain the secondary aggregation grain in this lithium composite xoide particle.In addition, volume accumulation frequency 90% particle diameter D90 and peak intensity are than (I 003/ I 104) measure with following described method.
The mensuration of＜D90 〉
That is, measure the possessive volume of the particle of the particle diameter of lithium composite xoide particle and each grain size intervals by the laser diffraction and scattering method.The volume of grain size intervals is accumulated the particle diameter that reaches overall at 90% o'clock accumulate frequency 90% particle diameter as volume.
The mensuration of＜peak intensity ratio 〉
X-ray diffraction is measured the RINT 2000 that uses Electric Co., Ltd of science to make.Measure under the appointed condition below the line source use Cu-K of X ray α 1 (wavelength 1.5405 ) reach.Tube voltage 40kV, electric current 40mA, 0.5 ° of divergent slit, 0.5 ° of scatter slit, be subjected to optical slits width 0.15mm.In addition, used the monochromatic light instrument.Be determined under the condition of 2 °/minute of sweep speeds, 0.01 ° of sweep spacing, scan axis 2 θ/θ and carry out.With the peak value of 2 θ=45.0 ° ± 0.5 ° peak value, with the peak value of 2 θ=18.8 ° ± 0.2 ° peak value as (003) face as (104) face.In addition, peak intensity (cps) is that the measured value of the diffraction sample represented with 2 θ axles deducts the value that backstage value (background) obtains.
N-N-methyl-2-2-pyrrolidone N-(NMP) solution that adds acetylene black 5 weight % and poly-inclined to one side vinylidene fluoride (PVdF) 5 weight % in aforementioned lithium composite xoide powder 90 weight % mixes, and is modulated into slurry.With the two sides of aforementioned slurry coating,, make the positive pole of structure that anodal layer is supported on the two sides of collector body then by dry, die mould at the aluminium foil system collector body of thick 15 μ m.The thickness of anodal layer is single face 60 μ m.
The manufacturing of＜negative pole 〉
Will as the carbon material down (face of (002) face of trying to achieve with powder x-ray diffraction is (d at interval through heat treated mesophase pitch based carbon fibers at 3000 ℃ 002) be 0.336nm) and powder 95 weight % and dimethyl formamide (DMF) solution of poly-inclined to one side vinylidene fluoride (PVdF) 5 weight % mix, be modulated into slurry.With the two sides of aforementioned slurry coating,, make the negative pole that negative electrode layer is supported on the structure of collector body by dry, die mould at the Copper Foil system collector body of thick 12 μ m.The thickness of negative electrode layer is single face 55 μ m.
In addition, the face of (002) face of carbonaceous thing interval d 002By powder x-ray diffraction spectrum, try to achieve respectively by the half breadth mid-point method.At this moment, do not carry out the scattering correction of Lorenz scattering etc.
＜dividing plate 〉
Prepared little porous polyethylene film system dividing plate of thick 25 μ m.
The modulation of＜nonaqueous electrolytic solution 〉
Ethylene carbonate (EC), gamma-butyrolacton (GBL), 3-propylene sultone (PRS) are mixed, make their volume ratio (EC: GBL: PRS) reach 33: 66: 1, be modulated into nonaqueous solvents.Then, make tetrafluoride lithium borate (LiBF 4) be dissolved in the gained nonaqueous solvents, make its concentration reach 1.5 moles/L, be modulated into aqueous nonaqueous electrolyte.
The manufacturing of＜electrode group 〉
With ultrasonic bonding the anodal reed of banded aluminium foil (thick 100 μ m) system is welded on the collector body of aforementioned positive pole, banded nickel foil (thick 100 μ m) system anode reed is welded on the collector body of aforementioned negative pole.Then, sandwich dividing plate between aforementioned positive pole and aforementioned negative pole, being rolled into the swirl shape postforming is flat, makes electrode group.
The laminate film of the thick 100 μ m that the two sides of aluminium foil covered with polyethylene and form is a rectangular cup by press forming, and the former electrodes group is packed in the gained container.
Then, the electrode group in the container in 80 ℃, vacuumize 12 hours, is removed moisture contained in electrode group and the laminate film with this.
Then, inject aqueous nonaqueous electrolyte in the electrode group in container, its injection rate is that battery capacity 1Ah is 4.8g, adopts the sealing of heat seal method, is assembled into the slim rechargeable nonaqueous electrolytic battery with the structure shown in the earlier figures 1,2, thick 3.6mm, wide 35mm, high 62mm.
(embodiment 2～8)
Except with the change shown in the composition according to the form below 2 of nonaqueous electrolyte, adopt and previous embodiment 1 described same method, assemble slim rechargeable nonaqueous electrolytic battery.
In the table 2, DEC represents diethyl carbonate, and MEC represents carbonic acid methyl ethyl ester, and PC represents propylene carbonate, and BTS represents the 4-butene sultone.
(embodiment 9～17)
Remove the mol ratio (X of Li and element M Li/ X M), peak intensity is than (I 003/ I 104) and volume accumulation frequency 90% particle diameter D90 change as shown in table 1 below outside, adopt and previous embodiment 1 described same method, assemble slim rechargeable nonaqueous electrolytic battery.
(comparative example 1～5)
Except change shown in the composition according to the form below 4 of nonaqueous electrolyte, adopt and previous embodiment 1 described same method, assemble slim rechargeable nonaqueous electrolytic battery.
In the table 4, EC represents that ethylene carbonate, MEC represent that carbonic acid methyl ethyl ester, PRS represent 1, and 3-propylene sultone, DEC represent that diethyl carbonate, GBL represent that gamma-butyrolacton, PC represent that propylene carbonate, PS represent propane sultone.
(comparative example 6～10)
Remove the mol ratio (X of Li and element M Li/ X M), peak intensity is than (I 003/ I 104) and volume accumulation frequency 90% particle diameter D90 change as shown in table 3 below outside, adopt and previous embodiment 1 described same method, assemble slim rechargeable nonaqueous electrolytic battery.
Under the following conditions, the charge of the secondary cell of the embodiment 1～17 that obtains and comparative example 1～10 is estimated, it the results are shown in down tabulation 2, table 4.
(charge)
For each secondary cell, as discharging and recharging step for the first time, at room temperature carry out 15 hours constant-current constant-voltage charging to 4.2V with 0.2C (130mA), at room temperature be discharged to 3.0V then with 0.2C.
Then, as charge, discharge and recharge the test that discharges and recharges of ratio 1C, end of charge voltage 4.2V, final discharging voltage 3.0V, obtain the discharge capacity sustainment rate (is 100% with the 1st time discharge capacity) after the repeated charge in the environment of 20 ℃ of temperature 500 times.
Table 1
The composition of lithium composite xoide Mol ratio (the X of Li and element M Li/X M) Peak intensity is than (I 003/I 104) ??D90 ??(μm)
Embodiment 1 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 2 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 3 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 4 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 5 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 6 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 7 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 8 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Embodiment 9 ??LiCoO 2 ??1.00 ??2.43 ??13.96
Embodiment 10 ??LiCoO 2 ??1.00 ??2.65 ??14.07
Embodiment 11 ??Li 0.996CoO 2 ??0.996 ??2.8 ??18.5
Embodiment 12 ??Li 1.01CoO 2 ??1.01 ??2.4 ??11.9
Embodiment 13 ??Li 1.01CoO 2 ??1.01 ??2.17 ??23.5
Embodiment 14 ??Li 0.998Ni 0.2Co 0.8O 2 ??0.998 ??3.87 ??16.2
Embodiment 15 ??LiNi 0.2Co 0.8O 2 ??1.00 ??2.55 ??15.06
Embodiment 16 ??LiNi 0.5Co 0.5O 2 ??1.00 ??4.23 ??12.87
Embodiment 17 ??LiNi 0.8Co 0.2O 2 ??1.00 ??3.88 ??14.93
Table 2
The kind of main solvent and mixing ratio (% represents volume %) Electrolytical kind and concentration The kind of sultone compound and proportioning The capacity sustainment rate (%) of 500 circulation times
Embodiment 1 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??87
Embodiment 2 ??49.5％EC，49.5％PC ??1.0M-LiPF 6 PRS-1 volume % ??85
Embodiment 3 ??33％EC，66％MEC ??1.0M-LiPF 6 PRS-1 volume % ??88
Embodiment 4 ??33％EC，33％MEC， ??33％DEC ??1.0M-LiPF 6 PRS-1 volume % ??92
Embodiment 5 ??33％EC，66％GBL ??1.5M-LiBF 4 BTS-1 volume % ??86
Embodiment 6 ??49.5％EC，49.5％PC ??1.0M-LiPF 6 BTS-1 volume % ??84
Embodiment 7 ??33％EC，66％MEC ??1.0M-LiPF 6 BTS-1 volume % ??87
Embodiment 8 ??33％EC，33％MEC， ??33％DEC ??1.0M-LiPF 6 BTS-1 volume % ??91
Embodiment 9 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??88
Embodiment 10 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??88
Embodiment 11 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??87
Embodiment 12 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??86
Embodiment 13 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??78
Embodiment 14 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??89
Embodiment 15 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??88
Embodiment 16 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??85
Embodiment 17 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??84
Table 3
The composition of lithium composite xoide Mol ratio (the X of Li and element M Li/X M) Peak intensity is than (I 003/I 104) ??D90 ??(μm)
Comparative example 1 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Comparative example 2 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Comparative example 3 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Comparative example 4 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Comparative example 5 ??LiCoO 2 ??1.00 ??3.4 ??15.25
Comparative example 6 ??Li 0.994CoO 2 ??0.994 ??5.1 ??7.25
Comparative example 7 ??Li 1.03CoO 2 ??1.03 ??250 ??10.25
Comparative example 8 ??Li 1.04CoO 2 ??1.04 ??16 ??5.76
Comparative example 9 ??Li 1.01CoO 2 ??1.01 ??2.4 ??26
Comparative example 10 ??Li 1.01Ni 0.2Co 0.8O 2 ??1.01 ??10 ??6.8
Table 4
The kind of main solvent and mixing ratio (% represents volume %) Electrolytical kind and concentration The kind of sultone compound and proportioning The capacity sustainment rate (%) of 500 circulation times
Comparative example 1 ??33.4％EC，66.6％GBL ??1.5M-LiBF 4 Do not have and add ??42
Comparative example 2 ??50％EC，50％PC ??1.0M-LiPF 6 Do not have and add ??20
Comparative example 3 ??33.4％EC，66.6％MEC ??1.0M-LiPF 6 Do not have and add ??36
Comparative example 4 ??33.4％EC，33.3％MEC ??33.3％DEC ??1.0M-LiPF 6 Do not have and add ??42
Comparative example 5 ??33％EC，66％GBL ??1.5M-LiBF 4 PS-1 volume % ??35
Comparative example 6 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??66
Comparative example 7 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??62
Comparative example 8 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??58
Comparative example 9 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??38
Comparative example 10 ??33％EC，66％GBL ??1.5M-LiBF 4 PRS-1 volume % ??23
Can obviously find out mol ratio (X from table 1 to table 4 Li/ X M) in 0.95～1.02 scope, peak intensity is than (I 003/ I 104) more than 2 less than 5 and D90 in 10 μ m～25 mu m ranges, the secondary cell that contains the embodiment 1～17 of the sultone compound that has at least one two key in lithium composite xoide and the ring compares with the secondary cell of comparative example 1～10, the appearance electricity sustainment rate of 500 circulation times is higher.Wherein, the secondary cell of embodiment 1～12,14～17 is compared with the secondary cell that D90 surpasses the embodiment 13 of 20 μ m, and the appearance electricity sustainment rate of 500 circulation times increases.
In addition, do not add the sultone compound comparative example 1～4 secondary cell and be that the peak intensity of secondary cell of comparative example 5 of additive is than greater than 5 with the PS that does not have two keys, and D90 is less than the comparative example 6 of 10 μ m and 10 secondary cell, mol ratio greater than 1.02, peak intensity is than the secondary cell greater than 5 comparative example 7, mol ratio greater than 1.02, peak intensity is than greater than 5 and the D90 secondary cell that surpasses the comparative example 9 of 25 μ m less than the secondary cell and the D90 of the comparative example 8 of 10 μ m, the appearance electricity sustainment rate of their 500 circulation times is all less than 70%.
(embodiment 18)
With D90 is that 15.25 μ m, peak intensity are than (I 003/ I 104) be 3.4 LiCoO 2Particle (the 1st active material particle) 70 weight % and D90 are that 14.93 μ m, peak intensity are than (I 003/ I 104) be 3.8 LiNi 0.8Co 0.2Mn 0.06O 2Particle (the 2nd active material particle) 30 weight % mix, and obtain the positive active material particle.The result that scanning electron microscope (SEM) is observed is to confirm that the part of the 1st active material particle has formed the form of secondary aggregation grain.
The D90 of the positive active material particle that obtains and mol ratio (Y Li/ Y M) as shown in table 5 below.
Except that the positive active material particle that uses gained, obtain slim rechargeable nonaqueous electrolytic battery with previous embodiment 1 described same formation.
(embodiment 19～24)
The composition, peak intensity that remove to adopt the 1st active material and the 2nd active material are than (I 003/ I 104) and D90, positive active material particle in the proportioning, the D90 and the mol ratio (Y of positive active material particle of the 1st active material Li/ Y M) outside the positive active material particle as shown in table 5 below, obtain slim rechargeable nonaqueous electrolytic battery with previous embodiment 1 described same formation.
With with previous embodiment 1 described same method, measure the appearance electricity sustainment rate of 500 circulation times of the secondary cell of gained embodiment 18～24, its result is as shown in table 6 below.Simultaneously, under the following conditions, estimate the charging high temperature preservation characteristics of the secondary cell of embodiment 18～24 and previous embodiment 1, its result is as shown in table 6 below.
(charging high temperature preservation characteristics)
To each secondary cell, with the charging of the condition of charge rate 1C, end of charge voltage 4.2V, be determined at the thickness of preserving the battery case after 120 hours in the environment of 80 ℃ of temperature, try to achieve the thickness change of the battery case in the preservation according to (I) formula.
{(t 1-t 0)/t 0}×100(％)???(I)
In the formula, t 0Be the battery case thickness before preserving, t 1For preserving the battery case thickness after 120 hours.
Table 5
The 1st active material The 2nd active material Positive active material (Y Li/Y M) ?D90 ?(μm)
Form Peak intensity is than (I 003/I 104) D90 (μm) Ratio (weight %) Form Peak intensity is than (I 003/I 104) D90 (μm)
Embodiment 1 ?LiCoO 2 3.4 ?15.25 ?100 ?- ?- ?- ?1.00 ?15.25
Embodiment 18 ?LiCoO 2 3.4 ?15.25 ?70 ?LiNi 0.8Co 0.2?Mn 0.06O 2 ?3.8 ?14.93 ?1.00 ?15.1
Embodiment 19 ?LiCoO 2 3.4 ?15.25 ?70 ?LiNi 0.8Co 0.2?Al 0.06O 2 ?3.8 ?14.93 ?1.00 ?15.1
Embodiment 20 ?LiCoO 2 3.4 ?15.25 ?80 ?Li 1.04CoO 2 ?30 ?16 ?1.01 ?15.5
Embodiment 21 ?LiCoO 2 3.4 ?15.25 ?80 ?Li 1.05Co 0.97?Sn 0.03O 2 ?50 ?6 ?1.02 ?13.0
Embodiment 22 ?LiCoO 2 3.4 ?15.25 ?80 ?Li 1.04Co ?Sn 0.0007O 2 ?10 ?16 ?1.00 ?15.5
Embodiment 23 ?LiNi 0.8Co 0.2?Mn 0.06O 2 3.8 ?14.93 ?80 ?Li 1.05Co 0.97?Sn 0.03O 2 ?50 ?6 ?1.02 ?12.5
Embodiment 24 ?LiNi 0.8CO 0.2?Al 0.06O 2 3.8 ?14.93 ?80 ?Li 1.05Co 0.97?Sn 0.03O 2 ?50 ?6 ?1.02 ?12.5
Table 6
The thickness change of battery case (%) The capacity sustainment rate (%) of 500 circulation times
Embodiment 1 ??1.82 ??87
Embodiment 18 ??1.78 ??90
Embodiment 19 ??1.69 ??91
Embodiment 20 ??1.29 ??88
Embodiment 21 ??1.12 ??88
Embodiment 22 ??1.59 ??89
Embodiment 23 ??1.38 ??88
Embodiment 24 ??1.32 ??89
Can clearly be seen that to possess the peak intensity of comprising than (I from table 5, table 6 003/ I 104) compare with embodiment 1 at the battery of the embodiment 18～19 of the positive pole of the positive active material that constitutes less than 52 kinds composite oxides that contain the lithium cobalt more than 2, the circulation sustainment rate is better, and how many thickness changes also makes moderate progress.
In addition, possesses the peak intensity of comprising than (I 003/ I 104) more than 2 less than 5 composite oxides that contain elemental lithium M and peak intensity than (I 003/ I 104) the appearance electricity sustainment rate of 500 circulation times of secondary cell of embodiment 20～24 of positive pole of lithium-contained composite oxide greater than 5 kept higher value, the expansion the when high temperature that charges is simultaneously preserved has been compared minimizing with embodiment 1.
In addition, in the previous embodiment, the molal quantity of the element M in the positive active material particle is the molal quantity of contained element when containing Ni or Co in the positive active material particle, is the molal quantity sum of Ni and Co when containing Ni and Co in the positive active material.
(detection method of PRS)
To the secondary cell of embodiment 1 carry out aforementioned discharge and recharge step for the first time after, open electric circuit is more than 5 hours, make current potential fully stable after, Ar concentration 99.9% or more and dew point in the glove box below-50 ℃, decompose the taking-up electrode group.Then, the former electrodes group is contained in the centrifuge tube, adds methyl-sulfoxide (DMSO)-d 6The back sealing is taken out from aforementioned glove box, carries out centrifugation.Then, in aforementioned glove box, from aforementioned centrifuge tube, gather aforementioned electrolyte and aforementioned DMSO-d 6Mixed liquor.At the NMR of the 5mm φ aforementioned mixed liquor of about 0.5ml of packing in test tube, carry out NMR and measure.The device that is used for aforementioned NMR mensuration is the JNM-LA400WB of Jeol Ltd.'s system, and observing nuclear is 1H, observing frequency is 400MHz, with methyl-sulfoxide (DMSO)-d 6In contained little by little residual proton signal as interior mark utilization (2.5ppm).Measuring temperature is 25 ℃. 1In the H-NMR spectrum, near 4.5ppm, observe peak corresponding to EC, shown in the spectrum of Fig. 5, near (P 5.1ppm 1), near (the P 7.05ppm 2) and the near (P of 7.2ppm 3) observe peak corresponding to PRS.Contain PRS in the nonaqueous solvents that exists the secondary cell of embodiment 1 after these results can confirm to discharge and recharge for the first time step.
In addition, observing frequency is decided to be 100MHz, with methyl-sulfoxide (DMSO)-d 6(39.5ppm) carried out as interior mark 13C-NMR measures, near 66ppm, observe peak corresponding to the EC correspondence, at near near near the peak that observes the 74ppm, the 124ppm and the 140ppm corresponding to the PRS correspondence, contain PRS in the nonaqueous solvents that exists the secondary cell of the embodiment 1 after these results can confirm to discharge and recharge for the first time step.
In addition, exist 1In the H-NMR spectrum, tried to achieve the NMR integrated intensity of PRS and the ratio of the NMR integrated intensity of EC, can confirm to reduce to some extent before the ratio secondary cell for assembling of PRS in the nonaqueous solvents total amount.
The present invention is not limited to the foregoing description, is equally applicable to positive pole, negative pole, the dividing plate of other kind, the combination of container.
The possibility of utilizing on the industry
As mentioned above, the present invention can provide the rechargeable nonaqueous electrolytic battery that charge and discharge circulation life increases.

Claims (12)

1. rechargeable nonaqueous electrolytic battery, it is to possess the positive pole that comprises the positive active material particle that contains the lithium composite xoide particle, the rechargeable nonaqueous electrolytic battery of negative pole and nonaqueous electrolyte, it is characterized in that, aforementioned lithium composite xoide particle has the composition of the element M that comprises at least a kind of formation that is selected from Ni and Co, has the particle shape that contains the secondary aggregation grain, and the peak intensity ratio satisfies following (1) formula, the content of the aforementioned lithium composite xoide particle in the aforementioned positive active material particle is more than the 50 weight %, the mol ratio of aforementioned positive active material particle satisfies following (2) formula, the particle diameter (D90) of the volume accumulation frequency 90% of aforementioned positive active material particle is in the scope of 10 μ m～25 μ m, aforementioned nonaqueous electrolyte comprises the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5????????(1)
0.95≤(Y Li/ Y MIn (2) formulas of)≤1.02, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide particle, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, Y LiBe the molal quantity of the lithium in the aforementioned positive active material particle, Y MBe the molal quantity of the element M in the aforementioned positive active material particle, aforementioned elements M is selected from Ni and Co at least a kind.
2. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature are that also aforementioned peak intensity is than (I 003/ I 104) greater than 2 below 4.95.
3. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature also are, aforementioned molal quantity (Y Li/ Y M) more than 0.97 below 1.02.
4. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature are that also aforementioned volume accumulation frequency 90% particle diameter (D90) is below 20 μ m more than the 10 μ m.
5. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature are that also aforementioned lithium composite xoide particle also contains at least a kind of element that is selected from Mn, Al, Sn, Fe, Cu, Cr, Zn, Mg, Si, P, H, Cl and B.
6. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature are that also aforementioned positive active material particle is made of aforementioned lithium composite xoide particle.
7. rechargeable nonaqueous electrolytic battery as claimed in claim 1, its feature are that also aforementioned positive active material particle also contains the lithium-contained composite oxide particle that the peak intensity ratio satisfies following (3) formula.
(I 003/ I 104In (3) formulas of)＞5, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium-contained composite oxide particle, I 104Peak intensity (cps) for (104) face in the aforementioned powder x-ray diffraction.
8. rechargeable nonaqueous electrolytic battery as claimed in claim 7, its feature are that also the lithium-contained composite oxide particle that satisfies aforementioned (3) formula also contains Co.
9. rechargeable nonaqueous electrolytic battery as claimed in claim 7, its feature also be, the content of lithium-contained composite oxide particle in aforementioned positive active material particle that satisfies aforementioned (3) formula more than 0.1 weight % less than 50 weight %.
10. rechargeable nonaqueous electrolytic battery; It is the rechargeable nonaqueous electrolytic battery that possesses the positive pole, negative pole and the nonaqueous electrolyte that comprise the anodal active material that contains the lithium composite oxide power; It is characterized in that; Aforementioned lithium composite oxide power is the powder that contains the secondary aggregation grain; Mole more following than satisfying (4) formula; The peak intensity ratio satisfies following (5) formula; And the particle diameter of volume accumulated frequence 90% (D90) is in the scope of 10 μ m～25 μ m; Aforementioned nonaqueous electrolyte comprises the sultone compound that has at least one two key in the ring
2≤(I 003/I 104)＜5????????????????(4)
0.95≤(X Li/ X MIn (5) formulas of)≤1.02, I 003Be the peak intensity (cps) of (003) face in the powder x-ray diffraction of aforementioned lithium composite xoide powder, I 104Be the peak intensity (cps) of (104) face in the aforementioned powder x-ray diffraction, X LiBe the molal quantity of the lithium in the aforementioned lithium composite xoide powder, X MBe the molal quantity of the element M in the aforementioned lithium composite xoide powder, aforementioned elements M is selected from Ni and Co at least a kind.
11. rechargeable nonaqueous electrolytic battery as claimed in claim 10, its feature are that also the content of the aforementioned lithium composite xoide powder in the aforementioned positive active material is more than 50 weight %.
12. as claim 1 or 10 described rechargeable nonaqueous electrolytic batteries, its feature also is, aforementioned sultone compound is by 1,3-propylene sultone and 1, and at least one side of 4-butene sultone constitutes.
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Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0660887A (en) * 1992-08-06 1994-03-04 Sanyo Electric Co Ltd Nonaqueous battery
JPH1173966A (en) * 1997-07-01 1999-03-16 Matsushita Electric Ind Co Ltd Nonaqueous electrolyte secondary battery and manufacture of its positive electrode active material
JPH11154509A (en) * 1997-11-21 1999-06-08 Japan Storage Battery Co Ltd Nonaqueous electrolyte secondary battery
US6756153B1 (en) * 1999-01-28 2004-06-29 Zeon Corporation Binder composition for electrode for lithium-ion secondary battery and utilization thereof
JP2001297761A (en) * 2000-04-12 2001-10-26 Sumitomo Metal Mining Co Ltd Positive electrode activator for nonaqueous electrolyte secondary cell
JP2002083597A (en) * 2000-06-30 2002-03-22 Matsushita Electric Ind Co Ltd Lithium secondary battery
KR100357415B1 (en) * 2000-07-13 2002-10-18 새한에너테크 주식회사 Electrolyte for lithium ion polymer battery
JP5034136B2 (en) * 2000-11-14 2012-09-26 株式会社Ｇｓユアサ Cathode active material for non-aqueous electrolyte secondary battery and non-aqueous electrolyte secondary battery using the same
JP4190162B2 (en) * 2001-03-01 2008-12-03 三井化学株式会社 Nonaqueous electrolyte, secondary battery using the same, and additive for electrolyte
KR100342605B1 (en) * 2001-07-05 2002-06-29 이원재 Electrolyte for Lithium Rechargeable Batteries
JP3797197B2 (en) * 2001-11-01 2006-07-12 株式会社ジーエス・ユアサコーポレーション Nonaqueous electrolyte secondary battery

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