JP6250998B2 - Nonaqueous electrolyte battery and battery pack - Google Patents

Description

  Embodiments described herein relate generally to a nonaqueous electrolyte battery and a battery pack.

  In order to obtain excellent battery characteristics, it is known to optimize the porosity and balance of the positive electrode and the negative electrode. For example, in a battery using a positive electrode having an olivine structure, the porosity of the positive electrode and the negative electrode is set to 30 to 50% and 20 to 30%, respectively. However, since the appropriate range of the porosity range of the positive electrode and the negative electrode and the balance between the positive electrode porosity and the negative electrode porosity differ depending on the battery material and the battery structure, the battery characteristics are not sufficiently improved.

JP 2010-225366 A

  The problem to be solved by the present invention is to provide a nonaqueous electrolyte battery excellent in input characteristics and a battery pack having the nonaqueous electrolyte battery.

According to the embodiment, a nonaqueous electrolyte battery including a positive electrode, a negative electrode, and an exterior member is provided. The positive electrode is Li _1-x Ni _1-abc Co _a Mn _b M 1 _c O ₂ (M 1 is at least one selected from the group consisting of Mg, Al, Si, Ti, Zn, Zr, Ca, W, Nb and Sn) metal, containing a positive electrode active material made of -0.2 ≦ x ≦ 0.5,0 <a ≦ 0.5,0 <b ≦ 0.5,0 ≦ c ≦ 0.1). The positive electrode has a pore volume of 0.03 to 0.15 ml / g by mercury intrusion method, a pore surface area of 2.8 to 4.8 m ² / g by mercury intrusion method, and a porosity of 16 to 28 by mercury intrusion method. %. The negative electrode includes a negative electrode active material made of a lithium titanium composite oxide . The negative electrode has a pore volume of 0.08 to 0.2 ml / g by the mercury intrusion method, a pore surface area of 5.5 to 7.5 m ² / g by the mercury intrusion method, and a porosity of 18 to 30 by the mercury intrusion method. %. The exterior member accommodates at least a positive electrode and a negative electrode. The positive electrode is smaller than the negative electrode in terms of pore volume, pore surface area, and porosity.

It is a disassembled perspective view of the nonaqueous electrolyte battery which concerns on embodiment. It is a partial expansion perspective view of the electrode group used for the nonaqueous electrolyte battery of FIG. It is a block diagram which shows the electric circuit of the battery pack which concerns on embodiment.

(First embodiment)
According to the first embodiment, a nonaqueous electrolyte battery is provided that includes a positive electrode, a negative electrode, a nonaqueous electrolyte, and an exterior member that houses at least the positive electrode, the negative electrode, and the nonaqueous electrolyte. The positive electrode is Li _1-x Ni _1-abc Co _a Mn _b M 1 _c O ₂ (M 1 is at least one selected from the group consisting of Mg, Al, Si, Ti, Zn, Zr, Ca, W, Nb and Sn) And an active material containing -0.2≤x≤0.5, 0 <a≤0.5, 0 <b≤0.5, 0≤c≤0.1). The positive electrode has a pore volume of 0.03 to 0.15 ml / g by mercury intrusion method, a pore surface area of 2.8 to 4.8 m ² / g by mercury intrusion method, and a porosity of 16 to 28 by mercury intrusion method. %. The negative electrode includes a compound containing Ti. The negative electrode has a pore volume of 0.08 to 0.2 ml / g by the mercury intrusion method, a pore surface area of 5.5 to 7.5 m ² / g by the mercury intrusion method, and a porosity of 18 to 30 by the mercury intrusion method. %. The pore volume, pore surface area, and porosity of the positive electrode are smaller than the pore volume, pore surface area, and porosity of the negative electrode.

Li _{1 -x} Ni _{1 -abc} Co _a Mn _b M1 _c O ₂ Lithium nickel cobalt manganese composite oxide which is an example of the positive electrode active material and lithium titanium composite oxide which is an example of a compound containing Ti The nonaqueous electrolyte battery used for the negative electrode active material has a problem that it is difficult to exhibit good input characteristics because the electric conductivity of the negative electrode is lower than that of a battery using a carbon-based material for the negative electrode. In order to solve this problem, the inventors conducted intensive studies focusing on the porosity of the positive electrode and the negative electrode, and as a result, identified the pore volume, pore surface area, and porosity of each of the positive electrode and the negative electrode by mercury porosimetry. In addition, it has been found that excellent input / output characteristics can be obtained by making the positive electrode smaller than the negative electrode with respect to the pore volume, pore surface area, and porosity.

Since the negative electrode using a compound containing Ti such as a lithium titanium composite oxide has low electrical conductivity, it is important to improve the contact between particles in the active material-containing layer by lowering the porosity. The porosity is preferably in the range of 18-30%. When it exceeds 30%, contact between particles in the active material-containing layer becomes insufficient, so that it is difficult to obtain good input characteristics. On the other hand, if it is less than 18%, the non-aqueous electrolytic mass in the active material-containing layer is insufficient, and Li ^{+ on} the active material surface at the time of input tends to be insufficient, so that it is difficult to obtain good output characteristics. A more preferable range of the negative electrode porosity is in the range of 20 to 26%. On the other hand, by lowering the _{Li 1-x Ni 1-abc} Co a Mn b M1 using _c O ₂ positive electrode also negative electrode and porosity so likewise is low electrical conductivity, such as lithium-nickel-cobalt-manganese composite oxide active material It is important to improve the contact between the particles in the containing layer. The porosity of the positive electrode is preferably in the range of 16 to 28%. When it exceeds 28%, contact between particles in the active material-containing layer becomes insufficient, so that it is difficult to obtain good input characteristics. On the other hand, if it is less than 16%, the non-aqueous electrolytic mass in the active material-containing layer is insufficient, and Li ^{+ on} the active material surface at the time of input tends to be insufficient, so that it is difficult to obtain good output characteristics. A more preferable range of the positive electrode porosity is in the range of 18 to 24%. Here, the porosity is a value obtained by dividing the volume of pores when mercury is injected into pores having a diameter of about 60 μm corresponding to the initial pressure by the volume of the sample.

The input / output performance is a performance governed not only by the electric conductivity of the negative electrode active material-containing layer but also by the nonaqueous electrolytic mass. In the case of a battery using Li _1-x Ni _1-abc Co _a Mn _b M1 _c O ₂ such as lithium nickel cobalt manganese composite oxide for the positive electrode and Ti containing compound such as lithium titanium composite oxide for the negative electrode Since the input / output characteristics are controlled by the negative electrode, it is preferable that more nonaqueous electrolyte is held in the negative electrode than in the positive electrode when the nonaqueous electrolytic mass of the whole battery is viewed. Therefore, in the positive electrode, the pore volume by the mercury intrusion method is 0.03 to 0.15 ml / g, the pore surface area by the mercury intrusion method is 2.8 to 4.8 m ² / g, and in the negative electrode by the mercury intrusion method. The pore volume is 0.08 to 0.2 ml / g, and the pore surface area by mercury intrusion method is within the range of 5.5 to 7.5 m ² / g. In addition, the pore volume, the pore surface area, and the porosity are made smaller for the positive electrode than for the negative electrode. This makes it possible to hold more nonaqueous electrolyte in the negative electrode than in the positive electrode.

Here, when only lithium cobaltate is used as the positive electrode active material, if the non-aqueous electrolysis mass of the negative electrode is larger than that of the positive electrode, the depth of discharge of the positive electrode during the charge / discharge cycle is deepened, which may increase the resistance. Concerned. Further, when only the spinel type lithium manganate is used as the positive electrode active material, the elution of Mn during the charge / discharge cycle is remarkable when the pore surface area of the positive electrode is in the range of 2.8 to 4.8 m ² / g. Therefore, there is a concern that the resistance increase will become large. Therefore, by providing a positive electrode containing Li _1-x Ni _1-abc Co _a Mn _b M1 _c O ₂ and a negative electrode containing a compound containing Ti, and by defining the pore distribution of the positive electrode and the negative electrode, A nonaqueous electrolyte battery having excellent output performance can be realized.

  Further, as compared with the case where an electrode group having a binding force of an electrode group such as a metal can is used as the battery outer member, the outer member includes a metal foil having a thickness of 5 to 1000 μm and the inner surface is made of a resin layer. The improvement in input / output performance is more remarkable when the electrode group lacking the binding force is used. Here, the thickness of the metal foil is preferably in the range of 5 to 1000 μm. If it is less than 5 μm, the function as an exterior member may be insufficient from the point of strength, and if it exceeds 1000 μm, This is because the bonding with the resin layer has insufficient bonding strength and may have an insufficient function as an exterior member.

  The primary particle diameter of the positive electrode active material is preferably in the range of 0.1 to 1 μm. If the primary particle size of the positive electrode active material is small, the resistance increase due to the side reaction between the active material surface and the non-aqueous electrolyte is large, and thus there is a concern that the input / output performance may not be improved. On the other hand, when the primary particle diameter of the positive electrode active material is large, the diffusion of lithium ions in the positive electrode active material in the solid becomes reaction-controlled, and thus there is a possibility that the input / output performance cannot be improved. When the primary particle size of the positive electrode active material is in the range of 0.1 to 1 μm, an increase in resistance due to side reaction is suppressed and the influence on the input / output performance of the diffusion of lithium ions in the positive electrode active material in the solid is reduced. Therefore, it is easy to obtain excellent input / output performance. A more preferable range is in the range of 0.2 to 0.8 μm.

  The methods for measuring the pore volume by the mercury intrusion method, the pore surface area by the mercury intrusion method, and the porosity by the mercury intrusion method are described below.

As a measuring apparatus, Shimadzu Autopore 9520 (Autopore 9520 model manufactured by Shimadzu Corporation) is used. For the sample, the electrode is cut to a size of about 25 × 25 mm ² and folded to take a measuring cell. The initial pressure is 20 kPa (the initial pressure of 20 kPa corresponds to about 3 psia, and the pore diameter is about 60 μm). And a maximum pressure of 414 Mpa (the maximum pressure of 414 Mpa corresponds to about 59986 psia and corresponds to the pressure applied to a sample having a pore diameter of about 0.003 μm). The average value of the three samples is used as the measurement result. In organizing the data, the pore specific surface area is calculated assuming that the pore shape is cylindrical.

  The analysis principle of the mercury intrusion method is based on Washburn's formula (B).

D = −4γcos θ / P (B) where P is the pressure to be applied, D is the pore diameter, γ is the surface tension of mercury (480 dyne · cm ⁻¹ ), and θ is the contact angle between mercury and the pore wall surface. °. Since γ and θ are constants, the relationship between the applied pressure P and the pore diameter D is obtained from the Washburn equation, and the mercury intrusion volume at that time is measured to derive the pore diameter and its volume distribution. Can do. For details of the measurement method and principle, refer to Jinbo Motoni et al .: “Fine Particle Handbook” Asakura Shoten, (1991), Hayakawa Sohachiro Edition: “Powder Physical Property Measurement Method” Asakura Shoten (1978).

  In addition, taking out the positive electrode and the negative electrode from the battery, immersing them in ethyl methyl carbonate to remove the Li salt, and then drying them are used as measurement samples.

  Hereinafter, the nonaqueous electrolyte battery of the embodiment will be described in detail for each member.

1) Negative electrode The negative electrode includes a current collector and a negative electrode material layer (negative electrode active material-containing layer) that is supported on one or both surfaces of the current collector and includes a negative electrode active material, a conductive agent, and a binder. In this negative electrode, for example, a conductive agent and a binder are added to a powdered negative electrode active material, these are suspended in an appropriate solvent, and this suspension (slurry) is applied to a current collector, dried, pressed Then, it is manufactured by forming a strip electrode. The pore distribution and porosity of the negative electrode can be controlled by adjusting the slurry stirring conditions (for example, stirring method, rotation speed, and bead diameter). For example, when using a thin-film swirl type high-speed mixer (Primics Filmmix 40-40), increasing the peripheral speed or lengthening the residence time reduces the particle size and sharpens the distribution. The pore diameter decreases and the porosity tends to increase because it is less likely to be crushed by the electrode press. In addition, for example, when using a horizontal bead mill (IMH RMH-03) and the bead diameter is small, the particle size becomes smaller and the distribution becomes sharper when the disk rotational speed is increased or the flow velocity is lowered. Tends to increase because the pore diameter becomes smaller and the porosity becomes difficult to be crushed by the electrode press. On the other hand, when the bead diameter is large, the particle size becomes smaller and the distribution becomes broader when the disk rotational speed is increased or the flow rate is lowered. Therefore, the pore diameter becomes smaller and the porosity is easily crushed by the electrode press. Therefore, it tends to be smaller. For example, when using a wet micronizer (Starburst Lab manufactured by Sugino Machine), increasing the pressure or decreasing the processing amount reduces the particle size and sharpens the distribution, so the pore size is small. Therefore, the porosity tends to increase because it becomes difficult to be crushed by the electrode press.

  A metal foil or an alloy foil is used for the current collector. Aluminum foil or aluminum alloy foil is particularly preferable. The aluminum foil and aluminum alloy foil desirably have an average crystal grain size of 50 μm or less, more preferably 30 μm or less, and still more preferably 5 μm or less. By setting the average crystal grain size of the aluminum foil or aluminum alloy foil to 50 μm or less, the strength of the aluminum foil or aluminum alloy foil can be dramatically increased. For this reason, it is possible to increase the negative electrode capacity by increasing the pressure during pressing to increase the density of the negative electrode material layer. Further, it is possible to prevent the current collector from being dissolved and corroded in an overdischarge cycle under a high temperature environment (40 ° C. or higher). For this reason, an increase in negative electrode impedance can be suppressed. Furthermore, output performance, rapid charge, and charge / discharge cycle performance can also be improved.

The average crystal grain size is determined as follows. The structure of the current collector surface is observed with an optical microscope, and the number n of crystal grains existing within 1 mm × 1 mm is determined. Using this n, the average crystal grain area S is determined from S = 1 × 10 ⁶ / n (μm ² ). The average crystal particle diameter d (μm) is calculated from the obtained S value by the following formula (A).

d = 2 (S / π) ^1/2 (A)
The average crystal grain size of the aluminum foil or aluminum alloy foil changes under complex influences from a plurality of factors such as material structure, impurities, processing conditions, heat treatment history, and annealing conditions. The crystal grain size can be adjusted by combining the above-mentioned factors in the production process of the current collector.

  The thickness of the current collector is desirably 20 μm or less, more preferably 15 μm or less. The aluminum foil preferably has a purity of 99% by mass or more. The aluminum alloy is preferably an alloy containing elements such as magnesium, zinc, and silicon. Transition metals such as iron, copper, nickel and chromium contained as alloy components are preferably 1% by mass or less.

The negative electrode active material includes a compound containing Ti. Examples of Ti-containing compounds include spinel type lithium titanium composite oxides (for example, Li _{4 + y} Ti _5-d M2 _d O ₁₂ (M2 is Mg, Al, Si, Ti, Zn, Zr, Ca, W, Nb). And at least one metal selected from the group consisting of Sn, −1 ≦ y ≦ 3, 0 ≦ d ≦ 0.1, ramsdellite-type lithium titanium composite oxide (for example, Li _{2 + x} Ti ₃ O ₇ ( x varies in the range of −1 ≦ x ≦ 3 due to charge / discharge reaction), metal composite oxidation containing at least one element selected from the group consisting of Ti and P, V, Sn, Cu, Ni and Fe Examples of the metal composite oxide containing at least one element selected from the group consisting of Ti and P, V, Sn, Cu, Ni and Fe include TiO ₂ —P ₂ O _{5. , TiO 2 -V 2 O 5,} TiO 2 -P 2 O 5 -SnO 2, T _{O 2 -P 2 O 5 -MeO (} Me is at least one element selected from the group consisting of Cu, Ni and Fe) can be cited. The metal composite oxide, the crystallinity is low, the crystal phase It is preferable that the amorphous phase coexist or the amorphous phase exists alone, and the metal composite oxide having such a microstructure can greatly improve the cycle performance. When lithium is inserted by charging, it changes to a lithium titanium composite oxide.

As other active materials, metal sulfides and metal nitrides can be used as the metal compound. As the metal sulfide, titanium sulfide such as TiS ₂ , molybdenum sulfide such as MoS ₂ , iron sulfide such as FeS, FeS ₂ , and Li _x FeS ₂ can be used. Metal nitrides can be used, for example, lithium cobalt nitride (e.g. _{Li s Co t N, 0 <} s <4,0 <t <0.5).

  The type of the negative electrode active material can be one type or two or more types.

  Examples of the binder include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), polyacrylic acid, fluorine rubber, and styrene butadiene rubber.

  Examples of the conductive agent include carbon black, graphite (graphite), graphene, fullerenes, coke and the like. Among these, carbon black and graphite are preferable, and examples of the carbon black include acetylene black, ketjen black, and furnace black.

  The blending ratio of the negative electrode active material, the conductive agent and the binder is preferably in the range of 73 to 96% by weight of the negative electrode active material, 2 to 20% by weight of the conductive agent, and 2 to 7% by weight of the binder.

2) Positive electrode The positive electrode includes a positive electrode current collector and a positive electrode material layer (positive electrode active material-containing layer) that is supported on one or both surfaces of the current collector and includes an active material, a conductive agent, and a binder.

  For this positive electrode, for example, a conductive agent and a binder are added to the positive electrode active material, these are suspended in an appropriate solvent, and this suspension is applied to a current collector such as an aluminum foil, dried and pressed. It is produced by forming a strip electrode. The pore distribution and porosity of the positive electrode can be controlled by adjusting the stirring conditions (for example, the stirring method, the number of rotations, and the bead diameter) of the slurry. Examples of the control method are the same as those described for the negative electrode.

The positive electrode active material includes Li _1-x Ni _1-abc Co _a Mn _b M1 _c O ₂ . The positive electrode active material may include only this oxide or may contain other types of active materials.

Other positive electrode active materials include various oxides and sulfides. For example, manganese dioxide (MnO ₂ ), iron oxide, copper oxide, nickel oxide, lithium manganese composite oxide (eg, Li _x Mn ₂ O ₄ or Li _x MnO ₂ ), lithium nickel composite oxide (eg, Li _x NiO ₂₎ ), Lithium cobalt composite oxide (Li _x CoO ₂ ), lithium nickel cobalt composite oxide {for example, Li _x Ni _1-yz Co _y M _z O ₂ (M is selected from the group consisting of Al, Cr and Fe) At least one element), 0 ≦ y ≦ 0.5, 0 ≦ z ≦ 0.1}, lithium manganese cobalt composite oxide {for example, Li _x Mn _1-yz Co _y M _z O ₂ (M is At least one element selected from the group consisting of Al, Cr and Fe), 0 ≦ y ≦ 0.5, 0 ≦ z ≦ 0.1}, a lithium manganese nickel composite compound (for example, Li _x Mn _1/2 Ni _1/2 O ₂ ), Spinel type lithium-manganese-nickel composite oxide _{(e.g., Li x Mn 2-y Ni} y O 4), lithium phosphates having an olivine structure _{(e.g., Li x FePO 4, Li x} Fe 1-y Mn y PO ₄ , Li _x CoPO ₄ ), iron sulfate (eg, Fe ₂ (SO ₄ ) ₃ ), vanadium oxide (eg, V ₂ O ₅ ), and the like. In addition, conductive polymer materials such as polyaniline and polypyrrole, disulfide-based polymer materials, organic materials such as sulfur (S) and carbon fluoride, and inorganic materials are also included. In addition, about x, y, and z which do not have the description of the preferable range above, it is preferable that it is the range of 0 or more and 1 or less.

  The type of the positive electrode active material can be one type or two or more types.

  Examples of the conductive agent include carbon black, graphite (graphite), graphene, fullerenes, coke and the like. Among these, carbon black and graphite are preferable, and examples of the carbon black include acetylene black, ketjen black, and furnace black.

  Examples of the binder include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), polyacrylic acid, and fluorine rubber.

  The compounding ratio of the positive electrode active material, the conductive agent and the binder is preferably in the range of 80 to 95% by weight of the positive electrode active material, 3 to 20% by weight of the conductive agent, and 2 to 7% by weight of the binder.

  The positive electrode current collector is preferably formed from an aluminum foil or an aluminum alloy foil. The average crystal grain size of the aluminum foil and the aluminum alloy foil is preferably 50 μm or less. More preferably, it is 30 μm or less. More preferably, it is 5 μm or less. When the average crystal grain size is 50 μm or less, the strength of the aluminum foil or aluminum alloy foil can be dramatically increased, the positive electrode can be densified with a high press pressure, and the battery capacity is increased. Can be made.

  The thickness of the current collector is 20 μm or less, more preferably 15 μm or less. The purity of the aluminum foil is preferably 99% by mass or more. As the aluminum alloy, an alloy containing elements such as magnesium, zinc, and silicon is preferable. On the other hand, the content of transition metals such as iron, copper, nickel and chromium is preferably 1% by mass or less.

3) Nonaqueous electrolyte This nonaqueous electrolyte contains a nonaqueous solvent and an electrolyte salt dissolved in the nonaqueous solvent. Further, the non-aqueous solvent may contain a polymer. However, it is preferable that a Li salt having B is contained as an electrolyte salt.

Examples of the electrolyte salt include LiPF ₆ , LiBF ₄ , Li (CF ₃ SO ₂ ) ₂ N (bistrifluoromethanesulfonylamide lithium; commonly known as LiTFSI), LiCF ₃ SO ₃ (commonly known as LiTFS), Li (C ₂ F ₅ SO _{2) 2} N (bis pentafluoroethanesulfonyl amide lithium; called _{LiBETI), LiClO 4, LiAsF 6} , LiSbF 6, bisoxalato Lato lithium borate _{(LiB (C 2 O 4)} 2 ( known as LiBOB)), difluoro (oxalato) Lithium borate (LiF ₂ BC ₂ O ₄ ), difluoro (trifluoro-2-oxide-2-trifluoro-methylpropionate (2-)-0,0) lithium borate (LiBF ₂ (OCOOC (CF ₃ ) ₂ ) (commonly known as LiBF ₂ (HHIB))). These electrolyte salts may be used alone or in combination of two or more. In particular, LiPF ₆ , LiBF ₄ , lithium bisoxalatoborate (LiB (C ₂ O ₄ ) ₂ (common name LiBOB)), difluoro (oxalato) lithium borate (LiF ₂ BC ₂ O ₄ ), difluoro (trifluoro-2-trifluoro Oxide-2-trifluoro-methylpropionate (2-)-0,0) lithium borate (LiBF ₂ (OCOOC (CF ₃ ) ₂ ) (commonly known as LiBF ₂ (HHIB))) is preferred.

  The electrolyte salt concentration is preferably in the range of 1M or more and 3M or less. Thereby, the performance when a high load current is passed can be improved.

  The non-aqueous solvent is not particularly limited, but examples thereof include propylene carbonate (PC), ethylene carbonate (EC), 1,2-dimethoxyethane (DME), γ-butyrolactone (GBL), tetrahydrofuran. (THF), 2-methyltetrahydrofuran (2-MeHF), 1,3-dioxolane, sulfolane, acetonitrile (AN), diethyl carbonate (DEC), dimethyl carbonate (DMC), methyl ethyl carbonate (MEC), dipropyl carbonate ( DPC) and the like. These solvents may be used alone or in combination of two or more. When two or more kinds of solvents are combined, it is preferable to select from all solvents having a dielectric constant of 20 or more.

  The non-aqueous electrolyte may contain an additive. The additive is not particularly limited, but examples thereof include vinylene carbonate (VC), fluorovinylene carbonate, methyl vinylene carbonate, fluoromethyl vinylene carbonate, ethyl vinylene carbonate, propyl vinylene carbonate, butyl vinylene carbonate, Examples thereof include dimethyl vinylene carbonate, diethyl vinylene carbonate, dipropyl vinylene carbonate, vinylene acetate (VA), vinylene butyrate, vinylene hexanate, vinylene crotonate, catechol carbonate, propane sultone, and butane sultone. The type of additive can be one type or two or more types.

4) Separator The separator is not particularly limited as long as it has insulating properties, but a porous film or a nonwoven fabric made of a polymer such as polyolefin, cellulose, polyethylene terephthalate, and vinylon can be used. Inorganic particles may be contained in the porous film or nonwoven fabric. One type of separator material may be used, or two or more types may be used in combination.

5) Exterior member As the exterior member, a laminate film having a thickness of 0.5 mm or less or a metal container having a thickness of 3 mm or less is used. The metal container is more preferably 0.5 mm or less in thickness. A resin container made of a polyolefin resin, a polyvinyl chloride resin, a polystyrene resin, an acrylic resin, a phenol resin, a polyphenylene resin, a fluorine resin, or the like may be used.

  Examples of the shape of the exterior member, that is, the battery shape, include a flat type (thin type), a square type, a cylindrical type, a coin type, and a button type. In addition, the battery can be applied to, for example, a small application loaded on a portable electronic device or the like, or a large application loaded on a two-wheel to four-wheel automobile or the like.

  Examples of the laminate film include a multilayer film including a resin layer and a metal layer interposed between the resin layers. The metal layer is preferably an aluminum foil or an aluminum alloy foil for weight reduction. For the resin layer, for example, a polymer material such as polypropylene (PP), polyethylene (PE), nylon, polyethylene terephthalate (PET) can be used. The laminate film can be formed into the shape of an exterior member by sealing by heat sealing.

  The metal container is made of aluminum or an aluminum alloy. As the aluminum alloy, an alloy containing elements such as magnesium, zinc and silicon is preferable. When transition metals such as iron, copper, nickel and chromium are contained in the alloy, the amount is preferably 100 ppm or less.

  An example of the nonaqueous electrolyte battery of the embodiment is shown in FIG. The battery shown in FIG. 1 is a sealed square nonaqueous electrolyte battery. The nonaqueous electrolyte battery includes an outer can 1, a lid 2, a positive external terminal 3, a negative external terminal 4, and an electrode group 5. An exterior member is composed of the exterior can 1 and the lid 2.

  The outer can 1 has a bottomed rectangular tube shape, and is formed of a metal such as aluminum, an aluminum alloy, iron, or stainless steel, for example.

  As shown in FIG. 2, the flat electrode group 5 has a positive electrode 6 and a negative electrode 7 wound in a flat shape with a separator 8 therebetween. The positive electrode 6 is a positive electrode except for, for example, a strip-shaped positive electrode current collector made of a metal foil, a positive electrode current collector tab 6a having one end parallel to the long side of the positive electrode current collector, and at least the positive electrode current collector tab 6a. And a positive electrode material layer (positive electrode active material-containing layer) 6b formed on the current collector. On the other hand, the negative electrode 7 excludes, for example, a strip-shaped negative electrode current collector made of a metal foil, a negative electrode current collector tab 7a having one end parallel to the long side of the negative electrode current collector, and at least a portion of the negative electrode current collector tab 7a. And a negative electrode material layer (negative electrode active material-containing layer) 7b formed on the negative electrode current collector.

  In the positive electrode 6, the separator 8, and the negative electrode 7, the positive electrode current collecting tab 6 a protrudes from the separator 8 in the winding axis direction of the electrode group, and the negative electrode current collecting tab 7 a protrudes from the separator 8 in the opposite direction. Thus, the positive electrode 6 and the negative electrode 7 are wound while being shifted in position. As a result of such winding, as shown in FIG. 2, the electrode group 5 has the positive electrode current collecting tab 6a wound in a spiral shape from one end face and is wound in a spiral form from the other end face. The negative electrode current collection tab 7a protrudes. An electrolytic solution (not shown) is impregnated in the electrode group 5.

  As shown in FIG. 1, the positive electrode current collecting tab 6a and the negative electrode current collecting tab 7a are each divided into two bundles with the vicinity of the winding center of the electrode group as a boundary. The conductive clamping member 9 includes first and second clamping parts 9a and 9b that are substantially U-shaped, and a connecting part that electrically connects the first clamping part 9a and the second clamping part 9b. 9c. In each of the positive and negative electrode current collecting tabs 6a and 7a, one bundle is sandwiched by the first sandwiching portion 9a, and the other bundle is sandwiched by the second sandwiching portion 9b.

  The positive electrode lead 10 includes a substantially rectangular support plate 10a, a through hole 10b opened in the support plate 10a, a bifurcated bifurcated branch from the support plate 10a, and a strip-shaped current collector 10c, 10d extending downward. Have On the other hand, the negative electrode lead 11 includes a substantially rectangular support plate 11a, a through hole 11b opened in the support plate 11a, a bifurcated branch from the support plate 11a, and a strip-shaped current collector 11c extending downward. 11d.

  The positive electrode lead 10 sandwiches the clamping member 9 between the current collectors 10c and 10d. The current collector 10 c is disposed in the first clamping part 9 a of the clamping member 9. The current collector 10d is disposed in the second clamping unit 9b. The current collectors 10c and 10d, the first and second clamping parts 9a and 9b, and the positive electrode current collector tab 6a are joined by, for example, ultrasonic welding. Thereby, the positive electrode 6 and the positive electrode lead 10 of the electrode group 5 are electrically connected via the positive electrode current collection tab 6a.

  The negative electrode lead 11 sandwiches the clamping member 9 between the current collectors 11c and 11d. The current collector 11 c is disposed in the first clamping part 9 a of the clamping member 9. On the other hand, the current collection part 11d is arrange | positioned at the 2nd clamping part 9b. The current collectors 11c and 11d, the first and second sandwiching portions 9a and 9b, and the negative electrode current collector tab 7a are joined by, for example, ultrasonic welding. Thereby, the negative electrode 7 and the negative electrode lead 11 of the electrode group 5 are electrically connected via the negative electrode current collection tab 7a.

  The materials of the positive and negative electrode leads 10 and 11 and the clamping member 9 are not particularly specified, but are preferably the same material as the positive and negative electrode external terminals 3 and 4. For the positive electrode external terminal 3, for example, aluminum or an aluminum alloy is used, and for the negative electrode external terminal 4, for example, aluminum, an aluminum alloy, copper, nickel, nickel-plated iron, or the like is used. For example, when the material of the external terminal is aluminum or an aluminum alloy, the lead material is preferably aluminum or an aluminum alloy. In addition, when the external terminal is copper, it is desirable that the material of the lead is copper.

  The rectangular plate-like lid 2 is seam welded to the opening of the outer can 1 by, for example, a laser. The lid 2 is made of a metal such as aluminum, aluminum alloy, iron or stainless steel, for example. The lid 2 and the outer can 1 are preferably formed from the same type of metal. The positive external terminal 3 is electrically connected to the support plate 10 a of the positive electrode lead 10, and the negative external terminal 4 is electrically connected to the support plate 11 a of the negative electrode lead 11. The insulating gasket 12 is disposed between the positive and negative external terminals 3 and 4 and the lid 2 and electrically insulates the positive and negative external terminals 3 and 4 and the lid 2. The insulating gasket 12 is preferably a resin molded product.

According to the nonaqueous electrolyte battery of the first embodiment described above, the battery includes a positive electrode containing Li _1-x Ni _1-abc Co _a Mn _b M1 _c O ₂ and a negative electrode containing a compound containing Ti, The pore volume, pore surface area, and porosity of the positive electrode and negative electrode by mercury porosimetry are specified, and the pore volume, pore surface area, and porosity are made smaller than those of the negative electrode. According to such a nonaqueous electrolyte battery, input / output performance can be improved.

(Second Embodiment)
According to the second embodiment, a battery pack including a nonaqueous electrolyte battery is provided. The nonaqueous electrolyte battery according to the first embodiment is used for the nonaqueous electrolyte battery. The number of nonaqueous electrolyte batteries (unit cells) included in the battery pack can be one or more. When a plurality of unit cells are provided, each unit cell is electrically connected in series or in parallel.

  Such a battery pack will be described in detail with reference to FIG. The plurality of unit cells 21 are electrically connected to each other in series to form an assembled battery 22. The positive electrode side lead 23 is connected to the positive electrode terminal of the assembled battery 22, and the tip thereof is inserted into the positive electrode side connector 24 and electrically connected thereto. The negative electrode side lead 25 is connected to the negative electrode terminal of the assembled battery 22, and the tip thereof is inserted into the negative electrode side connector 26 and electrically connected thereto. These connectors 24 and 26 are connected to a protection circuit 29 through wirings 27 and 28.

  The thermistor 30 detects the temperature of the unit cell 21, and the detection signal is transmitted to the protection circuit 29. The protection circuit 29 can cut off the plus side wiring 32a and the minus side wiring 32b between the protection circuit 29 and the terminal 31 for energizing the external device under a predetermined condition. The predetermined condition is, for example, when the temperature detected by the thermistor 30 is equal to or higher than a predetermined temperature. The predetermined condition is when the overcharge, overdischarge, overcurrent, etc. of the cell 21 are detected. This detection of overcharge or the like is performed for each single cell 21 or the entire single cell 21. When detecting each single cell 21, the battery voltage may be detected, or the positive electrode potential or the negative electrode potential may be detected. In the latter case, a lithium electrode used as a reference electrode is inserted into each unit cell 21. In the case of FIG. 3, a voltage detection wiring 33 is connected to each single cell 21, and a detection signal is transmitted to the protection circuit 29 through the wiring 33.

  Although FIG. 3 shows a mode in which the unit cells 21 are connected in series, they may be connected in parallel in order to increase the battery capacity. The assembled battery packs can be connected in series or in parallel.

  Moreover, the aspect of a battery pack is changed suitably by a use. As the use of the battery pack, those in which cycle characteristics with large current characteristics are desired are preferable. Specific examples include a power source for a digital camera, a vehicle for a two- to four-wheel hybrid electric vehicle, a two- to four-wheel electric vehicle, an assist bicycle, and the like. In particular, the vehicle-mounted one is suitable.

  According to the battery pack of the second embodiment described in detail above, since the non-aqueous electrolyte battery of the first embodiment is included, a battery pack excellent in input / output performance can be provided.

  Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.

(Example A-1)
<Preparation of positive electrode>
LiNi _0.5 Co _0.2 Mn _0.3 O ₂ (primary particle size: 0.6 μm, center particle size: 6 μm) is used as the positive electrode active material, and the ratio is 2.5% by weight with respect to the whole positive electrode as a conductive agent. Acetylene black was added to graphite and 2.5% by weight with respect to the whole positive electrode, and PVdF was added as a binder to 5% by weight with respect to the whole positive electrode. These were dispersed in n-methylpyrrolidone (NMP) solvent to prepare a slurry. For dispersion, a horizontal bead mill (RMH-03, manufactured by IMEX Co., Ltd.) was used, zirconia beads 0.5 mmφ were used as beads, and the disk rotation speed was 1200 rpm. The obtained slurry was applied to an aluminum foil having a thickness of 15 μm, dried, and pressed to prepare a positive electrode having a pore volume of 0.07 mL / g, a pore surface area of 3.4 m ² / g, and a porosity of 22%.

<Production of negative electrode>
Li ₄ Ti ₅ O ₁₂ (center particle size 1 μm) is used as the negative electrode active material, and PVdF as the binder is 5% by weight with respect to the whole negative electrode so that graphite is 5% by weight with respect to the whole negative electrode. % To prepare a slurry by mixing in an N-methylpyrrolidone (NMP) solution. For dispersion, a horizontal bead mill (RMH-03 manufactured by IMEX Co., Ltd.) was used, zirconia beads 0.2 mmφ were used for the beads, and the disk rotation speed was 1800 rpm. The obtained slurry was applied to a current collector made of an aluminum foil having a thickness of 15 μm, dried and pressed to obtain a pore volume of 0.13 mL / g, a pore surface area of 6.8 m ² / g, and a porosity of 24. % Negative electrode was produced.

<Preparation of non-aqueous electrolyte>
A non-aqueous electrolyte composed of 33% by volume of PC and 67% by volume of DEC was mixed with 1.5M LiPF ₆ to obtain a non-aqueous electrolyte.

<Battery assembly>
After impregnating a 20 μm-thick separator made of cellulose non-woven electrolyte with a non-aqueous electrolyte, the positive electrode is covered with this separator, and the negative electrode is overlapped with the separator so as to face the positive electrode and wound into a spiral shape. Groups were made. The electrode group was pressed into a flat shape. A metal can made of an aluminum plate having a thickness of 20 μm was prepared as an exterior member. A flat non-aqueous electrolyte battery was produced by inserting a flat electrode group into the exterior member.

(Examples A-2 to A-3, Comparative Example A-1)
A battery was prepared in the same manner as in Example A-1, except that the dispersion conditions were changed and the physical properties of the positive electrode and the negative electrode were adjusted as shown in Table 1.

(Example B-1, Comparative Example B-1)
An exterior member made of a laminate film including an aluminum foil having a thickness of 0.2 mm (200 μm) and a resin layer covering both surfaces of the aluminum foil and having an inner surface formed of a polypropylene layer was prepared. A battery similar to Example A-1 or Comparative Example A-1 was produced except that this exterior member was used.

(Comparative Examples C-1, 2, D-1, 2)
A battery was prepared in the same manner as in Example A-1, except that the positive electrode active material and the dispersion conditions were changed and the physical properties of the positive electrode and the negative electrode were adjusted as shown in Table 1.

  Table 1 below shows the type of active material, pore volume, pore surface area and porosity, and type of exterior member of the positive and negative electrodes of the obtained battery.

The input value of the obtained battery was measured by the following method. The battery was charged at SOC of 50% and charged at a current of 10 C for 60 seconds in a 25 ° C. environment. When the pre-charge voltage is V _0sec and the post-charge voltage is V _60sec , the resistance is calculated by dividing the value of (V _60sec -V _0sec ) by the 10C current value, and when the battery voltage becomes 2.8V from the resistance value The current value of was calculated. The pre-cycle input value was obtained by multiplying the calculated current value by the battery voltage of 2.8V.

The battery whose input value before the cycle was measured was subjected to a cycle of 1C with a charge / discharge current value of 1000 times within a range of 1.2 V to 2.8 V in a battery voltage of 45 ° C. environment. The input value measurement similar to the above was performed on the battery after cycling, and the input value after cycling was measured. Table 2 below shows the input values before and after the cycle.

As is apparent from the comparison between Examples A-1 to A-3 and Comparative Examples A-1, C-1, C-2, D-1 and D-2 in Tables 1 and 2, the Examples According to the batteries of A-1 to A-3, the decrease of the input value after the cycle is small as compared with the batteries of Comparative Examples A-1, C-1, C-2, D-1, and D-2. Further, as is clear from the comparison between Example B-1 and Comparative Example B-1, according to the battery of Example B-1, a decrease in the input value after the cycle was observed in the battery of Comparative Example B-1. Smaller than that. Further, as is clear from the comparison between the comparative examples C-1 and C-2 and the comparison between the comparative examples D-1 and D-2, the positive electrode active material contains Li _1-x Ni _1-abc Co _a Mn _b M1 _c O. _{When 2} is not included, it can be seen that the input characteristics are not improved even if the pore volume, pore surface area and porosity are specified. From the above, it can be seen that the input characteristics are improved regardless of the type of the exterior member by specifying the types of the positive and negative electrode active materials and the pore distribution.

According to the nonaqueous electrolyte battery of at least one embodiment and example described above, a positive electrode containing Li _1-x Ni _1-abc Co _a Mn _b M1 _c O ₂ , and a negative electrode containing a compound containing Ti Since the pore volume, pore surface area and porosity of the positive electrode are smaller than the pore volume, pore surface area and porosity of the negative electrode, the input / output performance can be improved.

Although several embodiments of the present invention have been described, these embodiments are presented by way of example and are not intended to limit the scope of the invention. These novel embodiments can be implemented in various other forms, and various omissions, replacements, and changes can be made without departing from the scope of the invention. These embodiments and modifications thereof are included in the scope and gist of the invention, and are included in the invention described in the claims and the equivalents thereof.
Hereinafter, the invention described in the scope of claims of the present application will be appended.
[1]
At least one metal _{Li 1-x Ni 1-abc} Co a Mn b M1 c O 2 (M1 are the Mg, Al, Si, Ti, Zn, Zr, Ca, W, selected from the group consisting of Nb and Sn, -0.2 ≦ x ≦ 0.5, 0 <a ≦ 0.5, 0 <b ≦ 0.5, 0 ≦ c ≦ 0.1), and pore volume by mercury porosimetry A positive electrode within a range of 0.03 to 0.15 ml / g, a pore surface area by a mercury intrusion method of 2.8 to 4.8 m ² / g, and a porosity of 16 to 28% by a mercury intrusion method;
Contains a compound containing Ti, pore volume by mercury intrusion method is 0.08 to 0.2 ml / g, pore surface area by mercury intrusion method is 5.5 to 7.5 m ² / g, pores by mercury intrusion method A negative electrode with a rate in the range of 18-30%;
Including at least an exterior member in which the positive electrode and the negative electrode are accommodated,
The non-aqueous electrolyte battery, wherein the positive electrode volume is smaller than the negative electrode in terms of the pore volume, the pore surface area, and the porosity.
[2]
The non-aqueous electrolyte battery according to [1], wherein the exterior member includes a resin layer that forms at least part of the inner surface and a metal foil having a thickness of 5 to 1000 μm.
[3]
The non-aqueous electrolyte battery according to [2], wherein the active material of the positive electrode includes a material having a primary particle diameter in the range of 0.1 to 1 μm.
[4]
The nonaqueous electrolyte battery according to [2], wherein the negative electrode active material is lithium titanate.
[5]
A battery pack comprising the nonaqueous electrolyte battery according to any one of [1] to [4].

  DESCRIPTION OF SYMBOLS 1 ... Exterior can, 2 ... Cover, 3 ... Positive electrode external terminal, 4 ... Negative electrode external terminal, 5 ... Electrode group, 6 ... Positive electrode, 6a ... Positive electrode current collection tab, 6b ... Positive electrode material layer, 7 ... Negative electrode, 7a ... Negative electrode Current collecting tab, 7b ... negative electrode material layer, 8 ... separator, 9 ... clamping member, 10 ... positive electrode lead, 11 ... negative electrode lead, 12 ... insulating gasket, 21 ... single cell, 22 ... assembled battery, 29 ... protection circuit, 30 ... Thermistor.

Claims (5)

At least one metal _{Li 1-x Ni 1-abc} Co a Mn b M1 c O 2 (M1 are the Mg, Al, Si, Ti, Zn, Zr, Ca, W, selected from the group consisting of Nb and Sn, -0.2 ≦ x ≦ 0.5,0 <contain a positive electrode active material consisting of a ≦ 0.5,0 <b ≦ 0.5,0 ≦ c ≦ 0.1), the pores by mercury porosimetry A positive electrode having a volume of 0.03 to 0.15 ml / g, a pore surface area of 2.8 to 4.8 m ² / g by mercury intrusion method, and a porosity of 16 to 28% by mercury intrusion method;
Contains a negative electrode active material made of lithium titanium composite oxide, has a pore volume of 0.08 to 0.2 ml / g by mercury porosimetry, and a pore surface area of 5.5 to 7.5 m ² / g by mercury porosimetry. A negative electrode having a porosity of 18 to 30% by mercury intrusion method,
Including at least an exterior member in which the positive electrode and the negative electrode are accommodated,
The pore volume, the pore surface area and the porosity, the positive electrode torquecontrol water electrolyte cell smaller than the negative electrode. The outer member is a non-aqueous electrolyte battery according a resin layer forming at least a portion of the inner surface, and a metal foil 5~1000μm thickness including請 Motomeko 1. The positive electrode active material, a non-aqueous electrolyte battery according to the primary particle diameter in the range of 0.1~1μm to including claim 1 or 2. The nonaqueous electrolyte battery according to any one of the lithium-titanium composite oxide according to claim 1 to 3 Ru der lithium titanate. Including batteries pack non-aqueous electrolyte cell according to any one of claims 1 to 4.

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