JP2015156341A - battery separator - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a battery separator for a lithium secondary battery that suppresses characteristic deterioration at heat aging.

SOLUTION: The separator for a lithium secondary battery is formed by combining a support body and a porous ceramic layer containing ceramic fine particles. The ceramic fine particle is a layered compound represented by a chemical formula Mg6Al2(OH)16CO3 4H2O, and is a synthetic hydrotalcite sintered body that, when being sintered, becomes granular after water and carbonic acid are desorbed to block an interlayer.

COPYRIGHT: (C)2015,JPO&INPIT

Description

  The present invention relates to a battery separator.

  Conventionally, as a battery separator (hereinafter sometimes abbreviated as “separator”) used in a lithium secondary battery, a polyolefin porous film having fine pores that have penetrated has been used. These separators suppress heat generation by increasing the internal resistance of the battery when the battery malfunctions and generate heat, and the through-holes are melted and closed. It has been responsible for suppressing battery explosion due to runaway.

  However, in applications that require charging and discharging with a large current, such as batteries for hybrid vehicles and uninterruptible power supplies, recent research has made it possible to suppress thermal runaway explosion of electrode materials. Due to the increase in temperature, in order to avoid contact between electrodes due to thermal contraction of the separator, there is an increasing demand for a separator having high heat resistance and low internal resistance.

  In response to this demand, Patent Document 1 discloses that the battery is thermally runaway by combining a porous ceramic layer containing porous ceramic fine particles with a porous support such as a nonwoven fabric. There has been proposed a method capable of suppressing electrode contact without causing thermal contraction of the separator even in the case of occurrence of heat. This method is an excellent method because the porous ceramic layer can permeate the surface and the inside of the separator, and can provide high electrolyte retention and heat resistance.

  On the other hand, Patent Documents 2 and 3 propose a method of providing heat resistance by providing a porous ceramic layer containing ceramic fine particles on one side of a porous film. In particular, in Patent Document 2, titanium oxides such as alumina, zirconia, silica, titania, barium titanate, lead titanate, strontium titanate, and composite oxides thereof are effective as ceramic fine particles used in the porous ceramic layer. It is described that there is.

  In particular, silica having a high insulating property and alumina that forms a unique aggregate structure are very promising materials (see, for example, Patent Document 4). There was a problem, such as the deterioration of was observed.

Japanese Patent No. 4594098 Special table 2008-503049 gazette Japanese Patent No. 4499851 International Publication No. 2008/114727 Pamphlet

  An object of the present invention is to provide a battery separator in which deterioration of characteristics over time is suppressed.

  As a result of intensive studies, the present inventor has found that the above-described problems can be solved by the present invention described below.

  A battery separator in which a porous ceramic layer containing ceramic fine particles and a support are combined, wherein the ceramic fine particles are a synthetic hydrotalcite sintered body.

  In the present invention, it is possible to obtain a battery separator in which deterioration of characteristics over time is suppressed.

  The battery separator of the present invention is a battery separator in which a porous ceramic layer containing ceramic fine particles and a support are combined, wherein the ceramic fine particles are a synthetic hydrotalcite sintered body.

Synthetic hydrotalcite is a layered compound represented by the chemical formula Mg ₆ Al ₂ (OH) ₁₆ CO ₃ .4H ₂ O. When sintered, water and carbonic acid are desorbed and the layers are clogged and become granular. Since the surface is a layer rich in magnesium oxide, it is a basic oxide. In a lithium secondary battery, when a trace amount of water remains or invades, when the supporting electrolyte is lithium hexafluorophosphate (LiPF ₆ ), the supporting electrolyte is decomposed by this water, and hydrogen fluoride and phosphorus An acid ester form is formed. Hydrogen fluoride deteriorates the particle surface of the current collector and the positive electrode agent, and the phosphoric acid ester body deteriorates the particle surface of the negative electrode agent to deteriorate the battery characteristics and also cause gas generation.

  The produced hydrogen fluoride or phosphate ester is fixed on the surface of the synthetic hydrotalcite. In particular, hydrogen fluoride is fixed on the surface as MgF, and the generated hydroxyl group is also adsorbed and captured at the desorbed portion of carbonic acid. Thus, synthetic hydrotalcite is a highly preferred material.

  The synthetic hydrotalcite is used after being sintered at 600 to 800 ° C. and then pulverized. The particle size is preferably 0.3 μm or more and 5.0 μm or less, and more preferably 0.4 μm or more and 1.5 μm or less. The particle size is determined by sufficiently diluting the ceramic fine particles with water, and measuring this with a laser scattering type particle size measuring device (trade name: 3300EX2 manufactured by Microtrac Co., Ltd.). The resulting center particle size (D50, volume average) It is.

  In the present invention, the porous ceramic layer can contain a water-soluble cellulose derivative. The ceramic fine particles are dispersed in water to form a coating liquid for forming a porous ceramic layer. In this case, if a water-soluble cellulose derivative is contained, the water-soluble cellulose derivative becomes a dispersibility aid in water, and the coating liquid is thickened to improve the setting property of the coating liquid on the support. be able to. As the dispersing agent at the time of dispersion, various surfactants such as nonionic, anionic, and cationic, and salts for imparting electric charge to the ceramic fine particles can be used in combination.

  The water-soluble cellulose derivative in the present invention is a cellulose derivative synthesized by modifying a part of hydroxyl groups of β-glucose molecules bonded linearly by glycosidic bonds so as to be water-soluble. , A compound modified with a carboxymethoxy group, a methoxy group, a hydroxyethoxy group, or a hydroxyproxy group. A derivative substituted with a carboxymethoxy group is called carboxymethylcellulose (CMC), and can be water-solubilized with sodium salt or ammonium salt. Methylcellulose containing only methoxy groups dissolves only in low-temperature water and has a thermal gel property that gels an aqueous solution when the temperature rises. Moreover, it is excellent in foaming property and foaming property, and can behave like a nonionic polymer surfactant. In general, solubility and thermal gel properties can be controlled by combining a hydroxyethoxy group or a hydroxypropoxy group with a methoxy group. In addition, water-soluble cationized cellulose can also be used. However, cellulose derivatives such as cellulose acetate and ethyl cellulose cannot be used because they are water-insoluble cellulose derivatives that do not dissolve in water. The water-soluble cellulose derivative can be used in combination with ceramic fine particles to form a porous ceramic layer and reduce internal resistance. If the content of the water-soluble cellulose derivative is too large, a film is formed around the voids in the drying step to form independent voids, so that it is preferably 5% by mass or less of the porous ceramic layer, more preferably 3 It is below mass%.

  Various polymer binders can be used in combination in order to improve the adhesion between the ceramic particles and the adhesion between the support and the ceramic particles. In particular, when polyester or polypropylene, which is difficult to bond, is used for the support, it is preferable to use a latex polymer binder as the polymer binder. As the polymer binder, polyolefin, styrene-butadiene, acrylic, or the like can be used. The content of the polymer binder is preferably 0.5 to 20% by mass of the porous ceramic layer, and more preferably 1 to 8% by mass.

  In the present invention, a porous ceramic layer is combined with a support in order to improve the strength as a battery separator. Examples of the support include a porous film, a woven fabric, a nonwoven fabric, and a knitted fabric. Examples of the material for the support include polyester, polyolefin, polyamide, aramid, and cellulose. The support is a non-woven fabric using fibers such as polyester, polyolefin, polyamide, aramid, cellulose, etc., and is particularly excellent in heat resistance and easy to obtain fine fibers, using non-woven fabric using polyester or polyolefin fibers. Is preferred. The nonwoven fabric can be produced by various methods such as a wet method, a dry method, and an electrostatic spinning method. As a support body, it is preferable that it is 10-25 micrometers in thickness, and it is preferable that a porosity is 30-80%. More preferably, the thickness is 12 to 18 μm and the porosity is 40 to 70%.

The porous ceramic layer can be obtained by applying or casting a coating liquid containing ceramic fine particles on a support, gelling in some cases, and then drying. As an application or casting method, an air doctor coater, blade coater, knife coater, rod coater, squeeze coater, impregnation coater, gravure coater, kiss roll coater, die coater, reverse roll coater, transfer roll coater, spray coater, etc. The method used can be used. The coating amount of the porous ceramic layer is preferably 0.5 to 50 g / ^{m 2} by dry weight, more preferably from 1 to 30 g / ^{m 2.} It is also possible to adjust the thickness of the obtained battery separator by performing another heat calendering process after drying. The preferable thickness of the battery separator having a support is 10 to 30 μm, more preferably 12 to 25 μm.

  The obtained battery separator is cut and sandwiched between electrode materials for a lithium secondary battery, an electrolyte is injected, the battery is sealed, and a lithium secondary battery is obtained. The material constituting the positive electrode is mainly an active material and a conductive agent such as carbon black, a binder such as polyvinylidene fluoride and styrene-butadiene rubber, and as the active material, lithium cobaltate, lithium nickelate, lithium manganate In addition, lithium manganese composite oxides such as lithium nickel manganese cobaltate (NMC) and lithium aluminum manganate (AMO), and lithium iron phosphate are used. These are mixed and applied onto an aluminum foil as a current collector to form a positive electrode.

The material constituting the negative electrode is mainly an active material, a conductive agent, and a binder. As the active material, graphite, amorphous carbon material, silicon, lithium, lithium alloy and the like are used. These are mixed and applied onto a copper foil as a current collector to form a negative electrode. In a lithium secondary battery, a separator is sandwiched between a positive electrode and a negative electrode, and an electrolytic solution is impregnated therein to provide ionic conductivity and conduct. In the lithium secondary battery, a non-aqueous electrolyte solution is used. Generally, this is composed of a solvent and a supporting electrolyte. As the solvent, for example, ethylene carbonate (EC), propylene carbonate (PC), diethyl carbonate (DEC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC) and vinylene carbonate having an additive function, vinyl Carbonate type such as ethylene carbonate. Dimethoxymethane and dimethoxyethane (DME) can also be used. As the supporting electrolyte, in addition to lithium hexafluorophosphate and lithium tetrafluoroborate (LiBF ₄ ), an organic lithium salt such as LiN (SO ₂ CF ₃ ) ₂ is also used. Ionic liquids can also be used. Further, a gel electrolyte in which a lithium salt is dissolved in a gel polymer such as polyethylene glycol or a derivative thereof, polymethacrylic acid derivative, polysiloxane or a derivative thereof, or polyvinylidene fluoride can also be used.

  As the exterior body, a metal cylindrical can such as aluminum or stainless steel, a rectangular can, a sheet-type exterior body using a laminate film obtained by laminating aluminum foil with polypropylene, polyethylene, polyethylene terephthalate, polybutylene terephthalate, or the like can be used. Further, it can be used by stacking and stacking, or it can be used by rotating in a cylindrical shape.

  EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited to these at all.

Example 1
Next, the following material was stirred for 3 hours with a homogenizer (manufactured by Primex, trade name: TK HODISPER Model 2.5, rotation speed 2500 rpm) to prepare dispersion (1).

Synthetic hydrotalcite sintered body (Kyowa Chemical Industry, trade name: KW-2200) 40 parts by mass Special carboxylic acid type polymer activator (Kao, trade name: Poise 520) 0.5 parts by weight distilled water 100 parts by weight Part

  To 100 parts by mass of the obtained dispersion (1), a sodium carboxymethylcellulose aqueous solution having a concentration of 0.6% by mass (made by Nippon Paper Industries Co., Ltd., trade name: MAC500LC) and an acrylic resin (manufactured by JSR, trade name: TRD-202A) 4.0 parts by mass of 40.2% by mass) was added to prepare a coating liquid (1).

Next, 75 parts by mass of stretched regular polyethylene terephthalate (PET) fibers (0.1 dtex, length 3 mm) and 25 parts by mass of unstretched PET fibers (0.2 dtex, length 4 mm), and a basis weight of 8 by a wet method. A web of 0.0 g / m ² was prepared. The drying temperature at this time was 130 ° C. Next, a thermal calendering process was performed on the web at 220 ° C. to prepare a support that was a nonwoven fabric having a thickness of 15 μm. The obtained coating liquid (1) was impregnated into a support and dried at 100 ° C. to produce a separator (1) having a thickness of 22 μm.

(Comparative Example 1)
In place of the synthetic hydrotalcite sintered body in Example 1, a comparative separator (1) having a thickness of 22 μm was similarly used except that synthetic hydrotalcite (manufactured by Kyowa Chemical Industry Co., Ltd., trade name: DHT-6) was used. Produced.

(Comparative Example 2)
A comparative separator (2) having a thickness of 22 μm was prepared in the same manner except that alumina (manufactured by Daimei Chemical Co., Ltd., granular boehmite, trade name: C06) was used instead of the synthetic hydrotalcite sintered body in Example 1. .

[Evaluation of battery characteristics]
On the aluminum foil, 200 g / m ^{2 of} lithium manganate, acetylene black, and polyvinylidene fluoride were applied at a mass ratio of 100/5/3, the solvent was dried, and further pressed to produce a positive electrode. On the other hand, spherical artificial graphite, acetylene black, and polyvinylidene fluoride were coated at a mass ratio of 85/15/5 on a copper foil at a rate of 100 g / m ² , dried and pressed to prepare a negative electrode.

  A separator was sandwiched between the obtained electrodes, heated at 95 ° C. under a reduced pressure of 0.01 MPa or less for 12 hours, and then an electrolyte for a lithium secondary battery manufactured by Ube Industries (trade name: Purelyte, solvent) : EC / DEC / DME = 1/1/1 (volume ratio), supporting electrolyte: lithium hexafluorophosphate 1 mol / l) was dropped and sealed in an aluminum foil laminate film under reduced pressure. A secondary battery was produced. Next, the produced lithium secondary battery was charged to 4.2 V at 0.2 C, and then discharged at 0.2 C. At this time, the ratio of the discharge capacity initially performed under the condition of 0.2 C to the charge capacity was measured. Further, the internal resistance was measured with the voltage drop value taken as the voltage 30 minutes after the start of discharge under the condition of 0.2 C (discharge time of 300 minutes). The results are given in Table 1. Next, after the battery was left to heat at 90 ° C. for 24 hours, the shape was observed, charge / discharge was performed under the condition of 0.2 C, and the ratio of the discharge capacity to the charge capacity was measured.

  From a comparison between Example 1 and Comparative Examples 1 and 2, the battery using the synthetic hydrotalcite sintered body was able to maintain good characteristics over time.

  The battery separator of the present invention can be used as a capacitor separator in addition to a lithium secondary battery separator.

Claims (1)

  A battery separator in which a porous ceramic layer containing ceramic fine particles and a support are combined, wherein the ceramic fine particles are a synthetic hydrotalcite sintered body.