WO2012137375A1 - 非水系二次電池用セパレータおよび非水系二次電池 - Google Patents
非水系二次電池用セパレータおよび非水系二次電池 Download PDFInfo
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- WO2012137375A1 WO2012137375A1 PCT/JP2011/074258 JP2011074258W WO2012137375A1 WO 2012137375 A1 WO2012137375 A1 WO 2012137375A1 JP 2011074258 W JP2011074258 W JP 2011074258W WO 2012137375 A1 WO2012137375 A1 WO 2012137375A1
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- separator
- secondary battery
- porous layer
- polyvinylidene fluoride
- adhesive
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/44—Fibrous material
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/46—Separators, membranes or diaphragms characterised by their combination with electrodes
- H01M50/461—Separators, membranes or diaphragms characterised by their combination with electrodes with adhesive layers between electrodes and separators
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/446—Composite material consisting of a mixture of organic and inorganic materials
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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
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/411—Organic material
- H01M50/414—Synthetic resins, e.g. thermoplastics or thermosetting resins
- H01M50/417—Polyolefins
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/411—Organic material
- H01M50/414—Synthetic resins, e.g. thermoplastics or thermosetting resins
- H01M50/426—Fluorocarbon polymers
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/409—Separators, membranes or diaphragms characterised by the material
- H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
- H01M50/451—Separators, membranes or diaphragms characterised by the material having a layered structure comprising layers of only organic material and layers containing inorganic material
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/489—Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
- H01M50/491—Porosity
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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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
- 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
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/403—Manufacturing processes of separators, membranes or diaphragms
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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
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/489—Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
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- 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
Definitions
- the present invention relates to a separator for a non-aqueous secondary battery and a non-aqueous secondary battery.
- Non-aqueous secondary batteries such as lithium ion secondary batteries are widely used as power sources for portable electronic devices such as notebook computers, mobile phones, digital cameras, and camcorders. Further, in recent years, these batteries have been studied for application to automobiles and the like because of their high energy density.
- a technique is known that uses a separator in which a porous layer made of a polyvinylidene fluoride resin (hereinafter also referred to as an adhesive porous layer) is formed on a polyolefin microporous film, which is a conventional separator (for example, see Patent Document 1).
- an adhesive porous layer made of a polyvinylidene fluoride resin (hereinafter also referred to as an adhesive porous layer) is formed on a polyolefin microporous film, which is a conventional separator (for example, see Patent Document 1).
- the adhesive porous layer is hot-pressed over the electrode in a state containing the electrolytic solution, the electrode and the separator can be satisfactorily bonded and can function as an adhesive. Therefore, the cycle life of the soft pack battery can be improved.
- a battery element is manufactured by winding the electrode and the separator in an overlapped state, and the element is enclosed in the metal can exterior together with an electrolytic solution. Is made.
- a battery element is produced in the same manner as the battery with the above metal can, and this is put together with the electrolyte in the soft pack exterior.
- a battery is produced by encapsulating and finally adding a hot press process. Therefore, in the case of using the separator having the adhesive porous layer as described above, a battery element can be produced in the same manner as the battery with the above metal can outer case. There is also an advantage that no change is required.
- a positive electrode or a negative electrode of a general non-aqueous secondary battery includes a current collector, and an active material layer including an electrode active material and a binder resin formed on the current collector.
- the adhesive porous layer mentioned above adhere attaches with respect to the binder resin in an electrode, when making it join with an electrode by hot press. Therefore, in order to ensure better adhesiveness, it is preferable that the amount of the binder resin in the electrode is large.
- the binder resin used for the electrode is generally a polyvinylidene fluoride resin, but in recent years, the use of styrene-butadiene rubber is increasing. For an electrode using such a styrene-butadiene rubber, it has been difficult to obtain sufficient battery characteristics while achieving both ion permeability and adhesiveness in a separator having a conventional adhesive porous layer.
- the porosity of the porous layer made of polyvinylidene fluoride resin is 50 to 90%, which is a very high porosity.
- an adhesive porous layer having a high porosity has a problem that when subjected to a hot press process under severe bonding conditions, the porous structure is crushed due to insufficient mechanical properties. .
- pores having a pore diameter of 0.05 to 10 ⁇ m are scattered on the surface of the adhesive porous layer.
- both electrode adhesion, ion permeability and battery cycle characteristics are compatible. Is difficult.
- the present invention is superior in adhesion to the electrode compared to the prior art, can ensure sufficient ion permeability even after being bonded to the electrode, and can withstand a mechanical press sufficiently. It aims at providing the separator for non-aqueous secondary batteries provided with the adhesive porous layer which has a physical property and a uniform porous structure.
- a separator for a non-aqueous secondary battery comprising a porous substrate and an adhesive porous layer containing a polyvinylidene fluoride-based resin formed on at least one surface of the porous substrate, the adhesive The porous layer has a porosity of 30% to 60%, and an average pore size of 1 nm to 100 nm. 2.
- the separator for non-aqueous secondary batteries as described. 4). 4. The separator for a non-aqueous secondary battery according to any one of 1 to 3 above, wherein the adhesive porous layer is formed on both front and back surfaces of the porous substrate. 5. The total weight of both surfaces of the adhesive porous layer formed on both surfaces of the porous substrate is 1.0 g / m 2 or more and 3.0 g / m 2 or less, and one surface side of the adhesive porous layer 5.
- the adhesion to the electrode is superior to that of the prior art, sufficient ion permeability can be secured even after bonding with the electrode, and further, the mechanical properties are uniform and uniform enough to withstand hot pressing.
- a separator for a nonaqueous secondary battery provided with an adhesive porous layer having a porous structure can be provided. By using such a separator of the present invention, it is possible to provide a non-aqueous secondary battery having a high energy density and a high performance aluminum laminate pack exterior.
- a separator for a non-aqueous secondary battery according to the present invention includes a porous substrate and an adhesive porous layer containing a polyvinylidene fluoride-based resin formed on at least one surface of the porous substrate.
- the numerical value range indicated by “ ⁇ ” means a numerical range including an upper limit value and a lower limit value.
- the porous substrate means a substrate having pores or voids therein.
- a substrate include a microporous film, a porous sheet made of a fibrous material such as a nonwoven fabric and a paper sheet, or one or more other porous layers laminated on the microporous film or the porous sheet.
- the composite porous sheet etc. which were made to be mentioned can be mentioned.
- a microporous membrane is a membrane that has a large number of micropores inside and a structure in which these micropores are connected, and allows gas or liquid to pass from one surface to the other. Means.
- the material constituting the porous substrate can be either an organic material or an inorganic material having electrical insulation.
- a thermoplastic resin as a constituent material of the base material.
- the shutdown function is a function to prevent the thermal runaway of the battery by blocking the movement of ions by melting the thermoplastic resin and closing the pores of the porous substrate when the battery temperature rises.
- the thermoplastic resin a thermoplastic resin having a melting point of less than 200 ° C. is suitable, and polyolefin is particularly preferable.
- a polyolefin microporous membrane is suitable as a porous substrate using polyolefin.
- a polyolefin microporous membrane having sufficient mechanical properties and ion permeability and applied to a conventional separator for a non-aqueous secondary battery can be used.
- the polyolefin microporous membrane preferably contains polyethylene from the viewpoint of having the shutdown function described above, and the polyethylene content is preferably 95% by weight or more.
- a polyolefin microporous film containing polyethylene and polypropylene is preferable from the viewpoint of imparting heat resistance that does not easily break when exposed to high temperatures.
- a polyolefin microporous membrane include a microporous membrane in which polyethylene and polypropylene are mixed in one sheet.
- Such a microporous membrane preferably contains 95% by weight or more of polyethylene and 5% by weight or less of polypropylene from the viewpoint of achieving both a shutdown function and heat resistance.
- the polyolefin microporous membrane has a structure of at least two layers, and one of the two layers includes polyethylene and the other layer includes polypropylene.
- a polyolefin microporous membrane having a structure is also preferred.
- the weight average molecular weight of polyolefin is preferably 100,000 to 5,000,000. If the weight average molecular weight is less than 100,000, it may be difficult to ensure sufficient mechanical properties. On the other hand, if it exceeds 5 million, the shutdown characteristics may be deteriorated or molding may be difficult.
- Such a polyolefin microporous membrane can be produced, for example, by the following method. That is, (i) a step of extruding a molten polyolefin resin from a T-die to form a sheet, (ii) a step of subjecting the sheet to crystallization treatment, (iii) a step of stretching the sheet, and (iv) heat treatment of the sheet A method of forming the microporous film by sequentially performing the steps is performed.
- a step of melting a polyolefin resin together with a plasticizer such as liquid paraffin, extruding it from a T-die and cooling it to form a sheet (ii) a step of stretching the sheet, (iii) Examples include a method of forming a microporous film by sequentially performing a step of extracting a plasticizer from the sheet, and (iv) a step of heat-treating the sheet.
- a plasticizer such as liquid paraffin
- porous sheets made of fibrous materials include polyesters such as polyethylene terephthalate, polyolefins such as polyethylene and polypropylene, heat-resistant polymers such as aromatic polyamides and polyimides, polyethersulfone, polysulfone, polyetherketone, and polyetherimide. Or a porous sheet made of a mixture of these fibrous materials.
- the composite porous sheet a structure in which a functional layer is laminated on a porous sheet made of a microporous film or a fibrous material can be adopted. Such a composite porous sheet is preferable in that a further function can be added by the functional layer.
- a porous layer made of a heat resistant resin or a porous layer made of a heat resistant resin and an inorganic filler can be used.
- the heat resistant resin include one or more heat resistant polymers selected from aromatic polyamide, polyimide, polyethersulfone, polysulfone, polyetherketone, and polyetherimide.
- a metal oxide such as alumina or a metal hydroxide such as magnesium hydroxide can be suitably used.
- the composite method include a method of coating a functional sheet on a porous sheet, a method of bonding with an adhesive, and a method of thermocompression bonding.
- the film thickness of the porous substrate is preferably in the range of 5 to 25 ⁇ m from the viewpoint of obtaining good mechanical properties and internal resistance.
- the Gurley value (JIS P8117) of the porous substrate is preferably in the range of 50 to 800 seconds / 100 cc from the viewpoint of preventing short circuit of the battery and obtaining sufficient ion permeability.
- the puncture strength of the porous substrate is preferably 300 g or more from the viewpoint of improving the production yield.
- Polyvinylidene fluoride resin A polyvinylidene fluoride resin is applied to the separator for a non-aqueous secondary battery of the present invention.
- a polyvinylidene fluoride-based resin a homopolymer of vinylidene fluoride (that is, polyvinylidene fluoride), a copolymer of vinylidene fluoride and another copolymerizable monomer, or a mixture thereof can be used.
- the monomer copolymerizable with vinylidene fluoride for example, one kind or two or more kinds such as tetrafluoroethylene, hexafluoropropylene, trifluoroethylene, trichloroethylene, or vinyl fluoride can be used.
- a polyvinylidene fluoride resin can be obtained by emulsion polymerization or suspension polymerization.
- the polyvinylidene fluoride resin used for the separator for a non-aqueous secondary battery of the present invention preferably contains 98 mol% or more of vinylidene fluoride as a structural unit. When 98 mol% or more of vinylidene fluoride is contained, sufficient mechanical properties and heat resistance can be secured even under severe hot press conditions.
- the polyvinylidene fluoride resin used in the present invention preferably has a weight average molecular weight in the range of 300,000 to 3,000,000.
- the range of 300,000 to 2,000,000 is more preferable, and the range of 500,000 to 1,500,000 is more preferable. If the weight average molecular weight is less than 300,000, the adhesive porous layer may not have sufficient mechanical properties to withstand the adhesion process with the electrode, and sufficient adhesion may not be obtained. Further, when the weight average molecular weight is larger than 3 million, the viscosity of the slurry containing the resin is increased, so that it is difficult to form the adhesive porous layer, or good crystals are formed in the adhesive porous layer. This is not preferable because it may be difficult to obtain a suitable porous structure.
- the porous structure of the adhesive porous layer is an important technical element.
- the porous structure has a porosity of 30 to 60% and an average pore diameter of 1 to 100 nm.
- the adhesive porous layer is composed of a polyvinylidene fluoride-based resin, has a number of micropores inside, and has a structure in which these micropores are connected. It means a porous layer in which gas or liquid can pass from one side to the other side.
- the average pore diameter is calculated by using the pore surface area S of the adhesive porous layer calculated from the nitrogen gas adsorption amount and the pore volume V of the adhesive porous layer calculated from the porosity. Is calculated from the following formula 1, assuming that is cylindrical.
- the specific surface area (m 2 / g) of the porous substrate applied by the nitrogen gas adsorption method and the composite film formed with the adhesive porous layer The specific surface area (m 2 / g) is measured. Then, the specific surface area is multiplied by the basis weight (g / m 2 ) to obtain the pore surface area per unit area of the sheet, and the pore surface area of the porous substrate is subtracted from the pore surface area of the composite membrane. Thus, the pore surface area S of the adhesive porous layer is calculated.
- the porosity of the adhesive porous layer is 30 to 60%.
- the porosity of the adhesive porous layer is 30% or more, good ion permeability can be obtained, and sufficient battery characteristics can be obtained.
- the porosity of the adhesive porous layer is 60% or less, sufficient mechanical properties can be obtained to such an extent that the porous structure is not crushed when adhered to the electrode in the hot press step.
- the porosity is 60% or less, the surface porosity becomes low and the area occupied by the polyvinylidene fluoride resin having an adhesive function increases, so that sufficient adhesive force can be secured.
- the porosity of the adhesive porous layer is more preferably 30 to 50%.
- the average pore size of the adhesive porous layer is 1 to 100 nm. If the average pore size of the adhesive porous layer is 100 nm or less, it becomes easy to have a porous structure in which uniform pores are uniformly dispersed, and the adhesion points with the electrode are uniformly dispersed, so that good adhesion can be obtained. Can do. In that case, since the movement of ions becomes uniform, sufficient cycle characteristics can be obtained, and even better load characteristics can be obtained. On the other hand, the average pore diameter is preferably as small as possible from the viewpoint of uniformity, but it is practically difficult to form a porous structure smaller than 1 nm.
- the polyvinylidene fluoride-based resin swells.
- the average pore diameter is preferably 1 nm or more.
- the average pore size of the adhesive porous layer is more preferably 20 to 100 nm.
- the above-described swelling due to the electrolytic solution varies depending on the type of polyvinylidene fluoride resin and the composition of the electrolytic solution, and the degree of failure associated with the swelling also varies.
- the polyvinylidene fluoride resin for example, when a copolymer containing a large amount of a copolymer component such as hexafluoropropylene is used, the polyvinylidene fluoride resin tends to swell. Therefore, in the present invention, it is preferable to select a polyvinylidene fluoride-based resin that does not cause the above-mentioned problems associated with swelling in the range of an average pore diameter of 1 to 100 nm. From such a viewpoint, it is preferable to use a polyvinylidene fluoride resin containing 98 mol% or more of vinylidene fluoride.
- the polyvinylidene fluoride resin When attention is paid to the electrolytic solution, for example, when an electrolytic solution having a high cyclic carbonate content such as ethylene carbonate or propylene carbonate having a high dielectric constant is used, the polyvinylidene fluoride resin easily swells. As a result, problems associated with the above-mentioned swelling are likely to occur. In this regard, if a polyvinylidene fluoride-based resin containing 98 mol% or more of vinylidene fluoride is used, sufficient ion permeability can be obtained even when an electrolytic solution consisting only of a cyclic carbonate is applied, and good battery performance is obtained. Since it is obtained, it is preferable.
- the adhesive porous layer according to the present invention is characterized in that its average pore diameter is very small as compared with the conventional one, although it has an appropriate porosity as a separator for non-aqueous secondary batteries. Is. This means that a fine porous structure is developed and uniform. According to such a porous structure, since the movement of ions at the interface between the separator and the electrode becomes more uniform as described above, a uniform electrode reaction can be obtained. Therefore, the effect of improving the load characteristics and cycle characteristics of the battery can be obtained. In addition, since the polyvinylidene fluoride resin is uniformly distributed on the separator surface, the adhesion with the electrode becomes better.
- the porous structure of the present invention also improves ion migration at the interface between the porous substrate and the adhesive porous layer.
- the laminated separator is likely to be clogged at the interface between the two layers, and the ion migration is likely to be lowered. Therefore, it may be difficult to obtain good battery characteristics.
- the adhesive porous layer in the present invention has a fine porous structure, is uniform, and has a relatively large number of pores. Therefore, since the probability that the hole of the porous substrate and the hole of the adhesive porous layer can be satisfactorily connected increases, clogging at the interface can be remarkably suppressed.
- the adhesive porous layer has sufficient mechanical properties that can sufficiently withstand hot pressing and a uniform porous structure. Therefore, even when the amount of binder resin in the electrode is reduced and the hot press conditions are relaxed, superior adhesion is obtained compared to the conventional technology, and sufficient ion permeability is ensured even after bonding to the electrode. it can. Therefore, if such a separator is used, it is possible to provide a non-aqueous secondary battery having a high energy density and a high performance aluminum laminate pack exterior.
- a method of applying a polyvinylidene fluoride resin having a high weight average molecular weight can be mentioned, and specifically, a polyfluoride having 600,000 or more, preferably 1,000,000 or more is used. It is preferable to apply a vinylidene chloride resin.
- Another example is a method of increasing the content of vinylidene fluoride in the polyvinylidene fluoride resin. Specifically, it is preferable to use a polyvinylidene fluoride resin containing 98 mol% or more of vinylidene fluoride.
- the method etc. which make the temperature of a coagulation bath lower and form a fine void
- the adhesive porous layer can be mixed with fillers or other additives made of inorganic or organic substances within a range that does not impair the effects of the present invention.
- a filler By mixing such a filler, it is possible to improve the slipperiness and heat resistance of the separator.
- the inorganic filler for example, a metal oxide such as alumina or a metal hydroxide such as magnesium hydroxide can be used.
- the organic filler for example, an acrylic resin or the like can be used.
- the separator for a non-aqueous secondary battery of the present invention comprises a porous substrate and an adhesive porous layer containing a polyvinylidene fluoride resin formed on at least one surface of the porous substrate.
- the adhesive porous layer is an adhesive layer that adheres to the electrode by hot pressing in a state containing the electrolytic solution, it needs to exist as the outermost layer of the separator.
- it is preferable to adhere both the positive electrode and the negative electrode to the separator from the viewpoint of cycle life it is preferable to form an adhesive porous layer on the front and back of the porous substrate.
- the adhesive porous layer preferably has a sufficiently porous structure from the viewpoint of ion permeability.
- the difference between the Gurley value of the porous substrate used and the Gurley value of the composite separator after forming the adhesive porous layer is 300 seconds / 100 cc or less, more preferably 150 seconds / 100 cc or less, More preferably, it is 100 seconds / 100 cc or less.
- this difference is higher than 300 seconds / 100 cc, the adhesive porous layer is too dense to inhibit ion permeation, and sufficient battery characteristics may not be obtained.
- the Gurley value of the separator for a non-aqueous secondary battery of the present invention is preferably in the range of 50 seconds / 100 cc to 800 seconds / 100 cc from the viewpoint of obtaining sufficient battery performance.
- the porosity of the non-aqueous secondary battery separator is suitably in the range of 30% or more and 60% or less from the viewpoint of obtaining the effects of the present invention and good mechanical properties of the separator.
- the weight of the polyvinylidene fluoride resin is preferably in the range of 0.5 g / m 2 or more and 1.5 g / m 2 or less on one surface from the viewpoint of adhesion to the electrode, ion permeability and battery load characteristics. It is.
- the total weight of the polyvinylidene fluoride-based resin is preferably 1.0 g / m 2 or more and 3.0 g / m 2 or less.
- the weight difference between the front and back surfaces is also important.
- the total weight of both surfaces of the adhesive porous layer formed on the front and back of the porous substrate is 1.0 to 3.0 g / m 2
- the weight of one surface side of the adhesive porous layer is The weight difference on the other side is preferably 20% or less with respect to the total weight of both sides. If this exceeds 20%, curling may become prominent, which may hinder handling and may reduce cycle characteristics.
- the curvature of the separator for a non-aqueous secondary battery is preferably in the range of 1.5 to 2.5 from the viewpoint of ensuring good ion permeability.
- the film thickness of the non-aqueous secondary battery separator is preferably 5 to 35 ⁇ m from the viewpoint of mechanical strength and energy density.
- the film thickness on one side of the adhesive porous layer is preferably in the range of 0.5 to 5 ⁇ m from the viewpoint of ensuring adhesion and good ion permeability.
- the fibril diameter of the polyvinylidene fluoride resin in the adhesive porous layer is preferably in the range of 10 to 1000 nm from the viewpoint of cycle characteristics.
- the membrane resistance of the non-aqueous secondary battery separator is preferably in the range of 1 to 10 ohm ⁇ cm 2 from the viewpoint of securing sufficient battery load characteristics.
- the membrane resistance is a resistance value when the separator is impregnated with the electrolytic solution, and is measured by an alternating current method.
- the above numerical values are values measured at 20 ° C. using 1M LiBF 4 propylene carbonate / ethylene carbonate (1/1 weight ratio) as the electrolytic solution.
- the separator for a non-aqueous secondary battery of the present invention described above is an adhesive porous material in which a solution containing a polyvinylidene fluoride resin is directly applied onto a porous substrate to solidify the polyvinylidene fluoride resin. It can be manufactured by a method in which the layer is formed integrally on the porous substrate.
- a polyvinylidene fluoride resin is dissolved in a solvent to prepare a coating solution.
- This coating solution is applied onto the porous substrate and immersed in an appropriate coagulation solution.
- the layer made of polyvinylidene fluoride resin has a porous structure.
- the coagulating liquid is removed by washing with water, and the adhesive porous layer can be integrally formed on the porous substrate by drying.
- a good solvent that dissolves the polyvinylidene fluoride resin can be used.
- a good solvent for example, a polar amide solvent such as N-methylpyrrolidone, dimethylacetamide, dimethylformamide, dimethylformamide and the like can be suitably used.
- a phase separation agent that induces phase separation in addition to the good solvent.
- phase separation agent include water, methanol, ethanol, propyl alcohol, butyl alcohol, butanediol, ethylene glycol, propylene glycol, and tripropylene glycol.
- Such a phase separation agent is preferably added in a range that can ensure a viscosity suitable for coating.
- what is necessary is just to mix or melt
- the composition of the coating solution preferably includes a polyvinylidene fluoride resin at a concentration of 3 to 10% by weight.
- a solvent it is preferable to use a mixed solvent containing 60% by weight or more of a good solvent and 40% by weight or less of a phase separation agent from the viewpoint of forming an appropriate porous structure.
- the coagulation liquid water, a mixed solvent of water and the good solvent, or a mixed solvent of water, the good solvent, and the phase separation agent can be used.
- a mixed solvent of water, a good solvent, and a phase separation agent is preferable.
- the mixing ratio of the good solvent and the phase separation agent should be adjusted to the mixing ratio of the mixed solvent used for dissolving the polyvinylidene fluoride resin.
- the concentration of water is preferably 40 to 90% by weight from the viewpoint of forming a good porous structure and improving productivity.
- the conventional coating methods such as Meyer bar, die coater, reverse roll coater, and gravure coater can be applied to the porous substrate.
- the adhesive porous layer is formed on both sides of the porous substrate, it is possible to solidify, wash and dry after coating the coating solution one side at a time. From the viewpoint of productivity, it is preferable to solidify, wash and dry after coating.
- the separator of this invention can be manufactured also with the dry-type coating method besides the wet coating method mentioned above.
- the dry coating method is a method in which a coating liquid containing a polyvinylidene fluoride resin and a solvent is applied onto a porous substrate, and the solvent is removed by volatilization by drying the coating liquid. How to get.
- the coating film tends to be a dense film compared to the wet coating method, and it is almost impossible to obtain a porous layer unless a filler or the like is added to the coating liquid.
- a filler or the like is added to the coating liquid.
- the separator of the present invention can also be produced by a method in which an adhesive porous layer and a porous substrate are prepared separately, and these sheets are superposed and combined by thermocompression bonding or an adhesive.
- a method of obtaining the adhesive porous layer as an independent sheet the coating liquid is applied onto the release sheet, and the adhesive porous layer is formed by using the wet coating method or the dry coating method described above. Examples include a method of peeling only the porous layer.
- Non-aqueous secondary battery of the present invention is characterized by using the separator of the present invention described above.
- the non-aqueous secondary battery has a configuration in which a separator is disposed between a positive electrode and a negative electrode, and these battery elements are enclosed in an exterior together with an electrolytic solution.
- a lithium ion secondary battery is suitable as the non-aqueous secondary battery.
- the structure which formed the electrode layer which consists of a positive electrode active material, binder resin, and a conductive support agent on a positive electrode collector can be employ
- the positive electrode active material include lithium cobaltate, lithium nickelate, spinel structure lithium manganate, and olivine structure lithium iron phosphate.
- the adhesive porous layer of the separator is disposed on the positive electrode side, since the polyvinylidene fluoride resin has excellent oxidation resistance, LiMn 1/2 Ni 1 1 that can operate at a high voltage of 4.2 V or higher.
- a positive electrode active material such as 2 O 2 or LiCo 1/3 Mn 1/3 Ni 1/3 O 2 can be easily applied.
- binder resin examples include polyvinylidene fluoride resin.
- conductive assistant examples include acetylene black, ketjen black, and graphite powder.
- current collector examples include aluminum foil having a thickness of 5 to 20 ⁇ m.
- the negative electrode a structure in which an electrode layer made of a negative electrode active material and a binder resin is formed on the negative electrode current collector can be adopted, and a conductive additive may be added to the electrode layer as necessary.
- a negative electrode active material for example, a carbon material that can occlude lithium electrochemically, a material that forms an alloy with lithium such as silicon or tin, and the like can be used.
- the binder resin include polyvinylidene fluoride resin and butylene-stadiene rubber.
- the separator for a non-aqueous secondary battery since the adhesiveness is good, sufficient adhesiveness can be ensured even when not only polyvinylidene fluoride resin but also a butylene-stadiene rubber is used as the negative electrode binder.
- the conductive assistant include acetylene black, ketjen black, and graphite powder.
- the current collector include copper foil having a thickness of 5 to 20 ⁇ m. Moreover, it can replace with said negative electrode and can also use metal lithium foil as a negative electrode.
- the electrolytic solution has a structure in which a lithium salt is dissolved in an appropriate solvent.
- the lithium salt include LiPF 6 , LiBF 4 , LiClO 4, and the like.
- the solvent include cyclic carbonates such as ethylene carbonate, propylene carbonate, fluoroethylene carbonate, and difluoroethylene carbonate, chain carbonates such as dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, and fluorine-substituted products thereof, ⁇ -butyrolactone, ⁇ -Cyclic esters such as valerolactone or a mixed solvent thereof can be suitably used.
- the separator provided with the conventional adhesive porous layer it may be difficult to exhibit the adhesion to the electrode depending on the type of the electrolytic solution used, but according to the separator of the present invention, the type of the electrolytic solution However, there is a great advantage in that good adhesiveness can be exhibited.
- the separator for a non-aqueous secondary battery of the present invention can be applied to a battery with a metal can exterior, but it is suitably used for a soft pack battery with an aluminum laminate film exterior because of its good adhesiveness to the electrode.
- the positive electrode and the negative electrode are joined via a separator, impregnated with an electrolytic solution, and enclosed in an aluminum laminate film.
- a non-aqueous secondary battery can be obtained by hot-pressing it.
- an electrode and a separator can be bonded well, and a non-aqueous secondary battery excellent in cycle life can be obtained.
- the adhesion between the electrode and the separator is good, the battery is excellent in safety.
- the void volume V per 1 m 2 of sheet is calculated from the porosity. Assuming that all the holes are cylindrical, the average hole diameter (diameter) d is calculated from the hole surface area S and the hole volume V according to the following formula 2.
- d 4 ⁇ V / S (Formula 2) d: average pore diameter of the adhesive porous layer V: pore volume of the adhesive porous layer S: pore surface area of the adhesive porous layer This d is the average pore diameter of the adhesive porous layer made of polyvinylidene fluoride resin It was.
- Frm thickness It measured using the contact-type thickness meter (made by LITEMATIC Mitutoyo).
- the measurement terminal was a cylindrical one having a diameter of 5 mm, and was adjusted so that a load of 7 g was applied during the measurement.
- Weight A sample was cut into 10 cm ⁇ 10 cm and its weight was measured. The basis weight was determined by dividing the weight by the area.
- Weight of polyvinylidene fluoride resin The weight of the polyvinylidene fluoride resin was measured from the spectrum intensity of FK ⁇ using an energy dispersive X-ray fluorescence analyzer (EDX-800HS Shimadzu Corporation). In this measurement, the weight of the polyvinylidene fluoride resin on the surface irradiated with X-rays is measured. Therefore, when a porous layer made of polyvinylidene fluoride resin is formed on both the front and back surfaces, the weight of each polyvinylidene fluoride resin on the front and back surfaces is measured by measuring the front and back surfaces. The weight can be measured.
- Wa weight per unit area of the base material (g / m 2)
- Wb weight of polyvinylidene fluoride resin (g / m 2)
- t represents the thickness ([mu] m).
- Table 1 shows the measurement results of average pore diameter and weight (total weight on both surfaces, surface weight, back surface weight, ratio of weight difference between the front surface side and back surface side to the total weight on both surfaces), and the Gurley value of the separator.
- the separators of the following examples and comparative examples are also collectively shown in Table 1.
- Examples 2 to 5 Using the same coating liquid as in Example 1 and a polyethylene microporous membrane, the coating amount was changed as shown in Table 1 by the same method to obtain a separator for a non-aqueous secondary battery of the present invention.
- Examples 6 and 7 Using the same coating liquid as in Example 1 and a polyethylene microporous membrane, by the same method, only the coating amount on the front and back sides was changed as shown in Table 1 to obtain the non-aqueous secondary battery separator of the present invention. It was.
- Example 8 Except that a polyolefin microporous membrane (M824 Celgard) having a film thickness of 12 ⁇ m, a Gurley value of 425 seconds / 100 cc, and a porosity of 38% consisting of a three-layer structure of polypropylene / polyethylene / polypropylene was used as the polyolefin microporous membrane.
- the separator for non-aqueous secondary batteries of this invention was obtained like 1.
- a separator for a non-aqueous secondary battery of the present invention was obtained in the same manner as in Example 1 except that the polyvinylidene fluoride was used and the coating amount on both sides was 0.8 g / m 2 .
- Comparative Example 2 The separator for the non-aqueous secondary battery was the same as Comparative Example 1 except that the concentration of the polyvinylidene fluoride resin was 8% by weight and the dimethylacetamide / tripropylene glycol was 55/45 weight ratio. Got.
- Example 3 A non-aqueous secondary battery separator was obtained in the same manner as in Example 1 except that the temperature of the coagulation liquid was 0 ° C.
- Example 1 the polyvinylidene fluoride resin of Example 1 is relatively difficult to swell in the electrolyte solution. From this, it is preferable to select an appropriate polyvinylidene fluoride resin for the porous structure of the adhesive porous layer. I know it ’s good.
- Example 1 is significantly smaller.
- the curvature is the polyolefin microporous membrane. It is presumed to reflect the clogging of the interface between the adhesive and the adhesive porous layer. In other words, it can be said that the higher the curvature, the greater the degree of clogging.
- the system of the comparative example uses a polyvinylidene fluoride resin that easily swells in the electrolyte, it is necessary to consider clogging due to this swelling. Based on the above-described contents, it is considered that the system having a large average pore diameter in Comparative Example 2 is less affected by swelling, but the curvature is significantly high even in such a system. This seems to reflect the fact that the adhesive porous layer in the present invention is fine and uniform porous and therefore is not prone to clogging stochastically. Accordingly, the porous structure as in the present invention can prevent clogging of the interface, and the configuration of the present invention is considered suitable from the viewpoint of ion migration.
- the porosity of the porous layer made of the polyvinylidene fluoride resin is small, but in such a configuration, there are few pores formed in the porous layer made of the polyvinylidene fluoride resin.
- the formation of an interface with the polyolefin microporous film is not preferable, and clogging becomes remarkable, and therefore the curvature is high. Therefore, the membrane resistance is high at 20 ° C. or ⁇ 20 ° C., and sufficient ion permeability is not obtained. This tendency is more remarkable at ⁇ 20 ° C.
- a lead tab was welded to the positive electrode and the negative electrode, the positive and negative electrodes were joined via a separator, an electrolyte solution was impregnated, and sealed in an aluminum pack using a vacuum sealer.
- the electrolyte used here was 1M LiPF 6 ethylene carbonate / ethyl methyl carbonate (3/7 weight ratio).
- a test battery was produced by applying a load of 20 kg per 1 cm 2 of electrode with a hot press machine and performing hot pressing at 90 ° C. for 2 minutes.
- Load characteristic test The load characteristic test was performed using the produced non-aqueous secondary battery. The load characteristics of the battery were determined by measuring a relative discharge capacity of 2C with reference to a discharge capacity of 0.2C at 25 ° C., and using this as an index. This test was performed on batteries using the separators of Examples 1 to 9 and Comparative Examples 1 to 4. The results are shown in Table 3.
- porous layer Most of the porous layer is attached to the electrode surface, but the one that is partially damaged is judged to have a medium uniformity ( ⁇ ), and most of the adhesive porous layer is attached to the electrode surface. Those that were severely damaged were judged to have poor uniformity (x).
- thermomechanical property measurement TMA
- each separator was cut out to a width of 4 mm, and both ends thereof were pressed with a chuck, and set so that the distance between chucks was 10 mm.
- the applied load was 10 mN, the temperature was raised at a rate of temperature rise of 10 ° C./min, and the temperature at which the separator broke was measured.
- the separator of Example 1 was confirmed to break at 155 ° C., whereas the separator of Example 8 was confirmed to break at 180 ° C. It can be seen that applying polypropylene is preferable from the viewpoint of heat resistance.
- Example 1 and Comparative Examples 1 to 4 were tested for adhesion to electrodes using various electrolytes in the same manner as described above.
- 1M LiPF 6 ethylene carbonate / ethyl methyl carbonate (3/7 weight ratio) is used as the electrolytic solution A
- 1M LiPF 6 ethylene carbonate / propylene carbonate / ethyl methyl carbonate (3/2/5 weight ratio) is used as the electrolytic solution B
- 1M LiPF 6 ethylene carbonate / propylene carbonate (1/1 weight ratio) was used as the electrolytic solution C.
- Table 4 The results are shown in Table 4.
- Table 4 shows the relative peel strength when the peel strength obtained for each of the positive electrode and negative electrode of the separator of Example 1 is 100, and the average peel strength between the positive electrode and the negative electrode is 70 or more. Is described as ⁇ , those of 50 or more and less than 70 are described as ⁇ , and those of less than 50 are described as ⁇ .
- the non-aqueous secondary battery separator of the present invention can be suitably used for a non-aqueous secondary battery, and is particularly suitable for a non-aqueous secondary battery having an aluminum laminate exterior, which is important for bonding with an electrode.
Abstract
Description
1. 多孔質基材と、前記多孔質基材の少なくとも一方の面に形成されたポリフッ化ビニリデン系樹脂を含む接着性多孔質層と、を備えた非水系二次電池用セパレータであって、前記接着性多孔質層は、空孔率が30%以上60%以下であり、かつ、平均孔径が1nm以上100nm以下であることを特徴とする非水系二次電池用セパレータ。
2. 前記接着性多孔質層は空孔率が30%以上50%以下であり、前記ポリフッ化ビニリデン系樹脂はフッ化ビニリデンが98mol%以上含まれていることを特徴とする上記1に記載の非水系二次電池用セパレータ。
3. 前記多孔質基材の一方の面に形成されている前記接着性多孔質層の重量が、0.5g/m2以上1.5g/m2以下であることを特徴とする上記1または2に記載の非水系二次電池用セパレータ。
4. 前記接着性多孔質層は前記多孔質基材の表裏両面に形成されていることを特徴とする上記1~3のいずれかに記載の非水系二次電池用セパレータ。
5. 前記多孔質基材の両面に形成された前記接着性多孔質層の両面合計の重量が、1.0g/m2以上3.0g/m2以下であり、前記接着性多孔質層の一面側の重量と他面側の重量の差が、両面合計の重量に対して20%以下であることを特徴とする上記4に記載の非水系二次電池用セパレータ。
6. 前記多孔質基材がポリエチレンを含むポリオレフィン微多孔膜であることを特徴とする上記1~5のいずれかに記載の非水系二次電池用セパレータ。
7. 前記多孔質基材がポリエチレンとポリプロピレンとを含むポリオレフィン微多孔膜であることを特徴とする上記1~5のいずれかに記載の非水系二次電池用セパレータ。
8. 前記ポリオレフィン微多孔膜が少なくとも2層以上の構造となっており、当該2層のうち一方の層はポリエチレンを含み、他方の層はポリプロピレンを含むことを特徴とする上記7に記載の非水系二次電池用セパレータ。
9. 上記1~8のいずれかに記載のセパレータを用いた非水系二次電池。
本発明において、多孔質基材とは内部に空孔ないし空隙を有する基材を意味する。このような基材としては、微多孔膜や、不織布、紙状シート等の繊維状物からなる多孔性シート、あるいは、これら微多孔膜や多孔性シートに他の多孔性層を1層以上積層させた複合多孔質シート等を挙げることができる。なお、微多孔膜とは、内部に多数の微細孔を有し、これら微細孔が連結された構造となっており、一方の面から他方の面へと気体あるいは液体が通過可能となった膜を意味する。
本発明の非水系二次電池用セパレータには、ポリフッ化ビニリデン系樹脂を適用する。ポリフッ化ビニリデン系樹脂としては、フッ化ビニリデンの単独重合体(すなわちポリフッ化ビニリデン)、フッ化ビニリデンと他の共重合可能なモノマーとの共重合体、あるいはこれらの混合物を用いることができる。フッ化ビニリデンと共重合可能なモノマーとしては、例えばテトラフロロエチレン、ヘキサフロロプロピレン、トリフロロエチレン、トリクロロエチレンあるいはフッ化ビニル等の一種類又は二種類以上を用いることができる。このようなポリフッ化ビニリデン系樹脂は、乳化重合または懸濁重合により得ることが可能である。
本発明において、接着性多孔質層の多孔構造は重要な技術要素である。その多孔構造は、空孔率が30~60%であり、かつ、平均孔径が1~100nmである。ここで、接着性多孔質層とは、ポリフッ化ビニリデン系樹脂を含んで構成されており、内部に多数の微細孔を有し、これら微細孔が連結された構造となっており、一方の面から他方の面へと気体あるいは液体が通過可能となった多孔質層を意味する。また、平均孔径は、窒素ガス吸着量から算出される接着性多孔質層の空孔表面積Sと、空孔率から算出される接着性多孔質層の空孔体積Vを用いて、すべての孔が円柱状であることを仮定して、以下の式1から算出する。
d:接着性多孔質層の平均孔径
V:接着性多孔質層の空孔体積
S:接着性多孔質層の空孔表面積
本発明の非水系二次電池用セパレータは、上述したように、多孔質基材と、多孔質基材の少なくとも一方の面に形成されたポリフッ化ビニリデン系樹脂を含む接着性多孔質層とを備えている。ここで、接着性多孔質層は、電解液を含んだ状態で熱プレスによって電極と接着する接着層であるため、セパレータの最外層として存在する必要がある。当然、正極および負極の両方とセパレータを接着させた方がサイクル寿命の観点から好ましいので、多孔質基材の表裏に接着性多孔質層を形成させた方が好ましい。
上述した本発明の非水系二次電池用セパレータは、ポリフッ化ビニリデン系樹脂を含む溶液を多孔質基材上に直接塗工して、ポリフッ化ビニリデン系樹脂を固化させることで、接着性多孔質層を多孔質基材上に一体的に形成する方法で製造できる。
本発明の非水系二次電池は、上述した本発明のセパレータを用いたことを特徴とする。
本発明において、非水系二次電池は、正極および負極の間にセパレータが配置され、これらの電池素子が電解液と共に外装内に封入された構成となっている。非水系二次電池としてはリチウムイオン二次電池が好適である。
(接着性多孔質層の平均孔径)
ガス吸着法でBET式を適用することにより、ポリオレフィン微多孔膜の比表面積(m2/g)と、接着性多孔質層を形成した複合セパレータの比表面積(m2/g)を測定する。これら比表面積(m2/g)にそれぞれの目付(g/m2)を乗算して、シート1m2当たりの空孔表面積を算出する。ポリオレフィン微多孔膜の空孔表面積を複合セパレータの空孔表面積から減算することで、接着性多孔質層1m2当たりの空孔表面積Sを算出する。別途、空孔率からシート1m2当たりの空孔体積Vを算出する。ここですべての孔が円柱状であることを仮定すると、平均孔径(直径)dは空孔表面積Sおよび空孔体積Vから以下の式2で算出される。
d:接着性多孔質層の平均孔径
V:接着性多孔質層の空孔体積
S:接着性多孔質層の空孔表面積
このdをポリフッ化ビニリデン系樹脂からなる接着性多孔質層の平均孔径とした。
接触式の厚み計(LITEMATIC ミツトヨ社製)を用いて測定した。測定端子は直径5mmの円柱状のものを用い、測定中には7gの荷重が印加されるように調整して行った。
サンプルを10cm×10cmに切り出し、その重量を測定した。重量を面積で割ることで目付を求めた。
エネルギー分散型蛍光X線分析装置(EDX-800HS 島津製作所)を用いてFKαのスペクトル強度からポリフッ化ビニリデン系樹脂の重量を測定した。この測定ではX線を照射した面のポリフッ化ビニリデン系樹脂の重量が測定される。よって表裏両面にポリフッ化ビニリデン系樹脂からなる多孔質層を形成した場合、表裏各々の測定を行うことで表裏各々のポリフッ化ビニリデン系樹脂の重量が測定され、それを合計することで表裏合計の重量が測定できる。
複合セパレータの空孔率ε(%)は以下の式3から算出した。
ここで、Waは基材の目付(g/m2)、Wbはポリフッ化ビニリデン系樹脂の重量(g/m2)、tは膜厚(μm)である。
JIS P8117に従い、ガーレ式デンソメータ(G-B2C 東洋精機社製)にて測定した。
ポリフッ化ビニリデン系樹脂としてクレハ化学社製のKFポリマー #9300(フッ化ビニリデン/ヘキサフロロプロピレン=98.9/1.1mol% 重量平均分子量195万)を用いた。該ポリフッ化ビニリデン系樹脂を5重量%の濃度でジメチルアセトアミド/トリプロピレングリコール=7/3重量比である混合溶媒に溶解し、塗工液を作製した。これを膜厚9μm、ガーレ値160秒/100cc、空孔率43%のポリエチレン微多孔膜(TN0901:SK社製)の両面に等量塗工し、水/ジメチルアセトアミド/トリプロピレングリコール=57/30/13重量比の凝固液(40℃)に浸漬することで固化させた。これを水洗、乾燥することでポリオレフィン系微多孔膜の表裏両面にポリフッ化ビニリデン系樹脂からなる接着性多孔質層が形成された本発明の非水系二次電池用セパレータを得た。このセパレータについて、セパレータの膜厚、ポリフッ化ビニリデン系樹脂中のVDFの含有量、セパレータ(全体)と接着性多孔質層(PVdF層)の空孔率、接着性多孔質層(PVdF層)の平均孔径と重量(両面の合計重量、表面の重量、裏面の重量、表面側の重量と裏面側の重量差の両面合計重量に対する割合)、セパレータのガーレ値の測定結果を表1に示す。なお、以下の実施例および比較例のセパレータについても同様に表1にまとめて示す。
実施例1と同様の塗工液、およびポリエチレン微多孔膜を用い、同様の方法で、表1に示すように塗工量のみ変化させて本発明の非水系二次電池用セパレータを得た。
実施例1と同様の塗工液、およびポリエチレン微多孔膜を用い、同様の方法で、表1に示すように表裏の塗工量のみ変化させて本発明の非水系二次電池用セパレータを得た。
ポリプロピレン/ポリエチレン/ポリプロピレンの3層構造からなる膜厚12μm、ガーレ値425秒/100cc、空孔率38%のポリオレフィン微多孔膜(M824 セルガード社)をポリオレフィン微多孔膜として用いた以外は、実施例1と同様にして本発明の非水系二次電池用セパレータを得た。
共重合組成がフッ化ビニリデン/ヘキサフロロプロピレン/クロロトリフロロエチレン=92.0/4.5/3.5重量比となるポリフッ化ビニリデン系樹脂を乳化重合にて作製した。このポリフッ化ビニリデン系樹脂の重量平均分子量は41万であった。該ポリフッ化ビニリデンを用い、両面の塗工量を0.8g/m2にしたこと以外は実施例1と同様にして、本発明の非水系二次電池用セパレータを得た。
共重合組成がフッ化ビニリデン/ヘキサフロロプロピレン/クロロトリフロロエチレン=92.0/4.5/3.5重量比となるポリフッ化ビニリデン系樹脂を乳化重合にて作製した。このポリフッ化ビニリデン系樹脂の重量平均分子量は41万であった。該ポリフッ化ビニリデンを12重量%の濃度でジメチルアセトアミド/トリプロピレングリコール=60/40重量比である混合溶媒に溶解し、塗工液を作製した。これを膜厚9μm、ガーレ値160秒/100cc、空孔率43%のポリエチレン微多孔膜(TN0901:SK社製)の両面に等量塗工し、水/ジメチルアセトアミド/トリプロピレングリコール=50/30/20重量比の凝固液(40℃)に浸漬することで固化させた。これを水洗、乾燥することでポリオレフィン系微多孔膜にポリフッ化ビニリデン系樹脂からなる多孔質層が形成された非水系二次電池用セパレータを得た。
塗工液の組成として、ポリフッ化ビニリデン系樹脂の濃度を8重量%とし、ジメチルアセトアミド/トリプロピレングリコール=55/45重量比とした以外、比較例1と同様にして非水系二次電池用セパレータを得た。
凝固液の温度を0℃とした以外は実施例1と同様の方法にて非水系二次電池用セパレータを得た。
ポリフッ化ビニリデン系樹脂としてクレハ化学社製のKFポリマー #9300(フッ化ビニリデン/ヘキサフロロプロピレン=98.9/1.1mol% 重量平均分子量195万)を用いた。該ポリフッ化ビニリデンを5重量%でNMPに溶解し塗工液を作製した。これを膜厚9μm、ガーレ値160秒/100cc、空孔率43%のポリエチレン微多孔膜(TN0901:SK社製)の両面に等量塗工し、100℃で12時間真空乾燥させた。しかし、得られたポリフッ化ビニリデン膜は緻密であり、接着性多孔質層を形成することはできなかった。
電解液に1M LiBF4 プロピレンカーボネート/エチレンカーボネート=1/1重量比を用い、この電解液をセパレータに含浸させた。これをリードタブ付きのアルミ箔電極に挟みアルミパックに封入して試験セルを作製した。この試験セルの抵抗を交流インピーダンス法(測定周波数:100kHz)により20℃、-20℃にて測定した。この測定を実施例1、比較例1~3及び上記のポリエチレン微多孔膜(TN0901:SK社製)について実施した。その結果を表2に示す。また、得られた20℃の抵抗値から以下の式4を適用することで曲路率を算出した。この結果も表2に示す。
τ:曲路率
R(ohm・cm2):電解液を含浸させたときのセパレータの抵抗
r(ohm・cm):電解液の比抵抗
ε(%):空孔率
t(cm):膜厚
-20℃の抵抗を20℃の抵抗で割った値については、実施例1、比較例2およびポリオレフィン微多孔膜では同等となっているのに対し、比較例1のものは著しく増大している。接着性多孔質層中に電解液が含浸した状態においては、膨潤した樹脂中に存在している電解液のイオンは、空孔中に存在している電解液のイオンに比べて移動速度が極めて遅く、その差は低温でより顕著となる。このことから、比較例1のものは実施例1のものに比べて、膨潤した樹脂が多量の電解液を含み、かつ、空孔に独立に存在している電解液量が少ないため、イオンの移動に差が生じ、低温における抵抗値が高くなったものと推定される。比較例1,2は実施例1に比べ電解液に膨潤しやすいポリフッ化ビニリデン系樹脂を適用しているが、このような樹脂を適用した場合は、孔径を小さくしていくと膨潤した樹脂中のイオンの量が増大していく。よって、このような樹脂を適用した場合は、ポリフッ化ビニリデン系樹脂からなる多孔質層の孔径を小さくしてしまうと、イオン透過性、特に低温におけるイオン透過性が低下してしまうため、好ましくない。それに対し、実施例1の場合は孔径が小さいにも関わらす、低温での抵抗増大が小さい。これは実施例1のポリフッ化ビニリデン系樹脂が比較的に電解液に膨潤し難いためであり、これより接着性多孔質層の多孔構造に対して適切なポリフッ化ビニリデン系樹脂を選定するのが良いことが分かる。
(負極の作製)
負極活物質である人造黒鉛(MCMB25-28 大阪ガス化学社製)300g、バインダーである日本ゼオン社製の「BM-400B」(スチレン-ブタジエン共重合体の変性体を40重量%含む水溶性分散液)7.5g、増粘剤であるカルボキシメチルセルロース3g、適量の水を双腕式混合機にて攪拌し、負極用スラリーを作製した。この負極用スラリーを負極集電体である厚さ10μmの銅箔に塗布し、得られた塗膜を乾燥し、プレスして負極活物質層を有する負極を作製した。
正極活物質であるコバルト酸リチウム(セルシードC 日本化学工業社製)粉末を89.5g、導電助剤のアセチレンブラック(デンカブラック 電気化学工業社製)4.5g、バインダーであるポリフッ化ビニリデン(KFポリマー W#1100 クレハ化学社製)を6重量%となるようにNMPに溶解した溶液をポリフッ化ビニリデンの重量が6重量%となるように双腕式混合機にて攪拌し、正極用スラリーを作製した。この正極用スラリーを正極集電体である厚さ20μmのアルミ箔に塗布し、得られた塗膜を乾燥し、プレスして正極活物質層を有する正極を作製した。
前記の正極と負極にリードタブを溶接し、セパレータを介してこれら正負極を接合させ、電解液をしみ込ませてアルミパック中に真空シーラーを用いて封入した。ここで電解液は1M LiPF6 エチレンカーボネート/エチルメチルカーボネート(3/7重量比)を用いた。これを熱プレス機により電極1cm2当たり20kgの荷重をかけ、90℃、2分の熱プレスを行うことで試験電池を作製した。
負荷特性試験は前記作製した非水系二次電池を用いて実施した。電池の負荷特性は25℃にて0.2Cの放電容量を基準にした2Cの相対放電容量を測定し、これを指標とした。この試験を実施例1~9、比較例1~4のセパレータを用いた電池について実施した。その結果を表3に示す。
充放電サイクル試験は前記作製した非水系二次電池を用いて実施した。充電条件は1C、4.2Vの定電流定電圧充電、放電条件は1C、2.75Vカットオフの定電流放電としサイクル特性試験を実施した。ここでサイクル特性の指標は100サイクル後の容量維持率とした。この試験を実施例1~9、比較例1~4のセパレータを用いた電池について実施した。その結果を表3に示す。
充放電サイクル試験後の電池を解体しセパレータと電極の接着性を確認した。接着性は接着力と均一性の観点から確認し、その結果を表3に示す。なお、接着力に関しては、正極側および負極側のそれぞれについて、実施例1のセパレータを用いた場合の剥離強度を100としたときの相対値で表3に示す。均一性に関しては、正極側および負極側のそれぞれについて剥離テストを行なった後に、接着性多孔質層がほぼ全て電極表面に付着していたものを均一性が良好(〇)と判断し、接着性多孔質層の大部分が電極表面に付着しているが一部破損しているものは均一性が中程度(△)と判断し、接着性多孔質層の大部分が電極表面に付着しておらず著しく破損していたものは均一性が不良(×)と判断した。
実施例1のセパレータと実施例8のセパレータ耐熱性を熱機械物性測定(TMA)により比較した。具体的には、それぞれのセパレータを幅4mmに切り出し、その両端をチャックで押さえ、チャック間距離が10mmとなるようにセットした。印加荷重10mNとし、昇温速度10℃/minで昇温させていき、セパレータが破断する温度を測定した。実施例1のセパレータは155℃で破断が確認されたの対し、実施例8のセパレータは180℃で破断が確認された。ポリプロピレンを適用することは耐熱性の観点からは好ましいことが分かる。
実施例1と比較例1~4のセパレータについて、各種電解液を用いて、上記と同様にして電極との接着性テストを実施した。なお、電解液Aとして1M LiPF6 エチレンカーボネート/エチルメチルカーボネート(3/7重量比)を用い、電解液Bとして1M LiPF6 エチレンカーボネート/プロピレンカーボネート/エチルメチルカーボネート(3/2/5重量比)を用い、電解液Cとして1M LiPF6 エチレンカーボネート/プロピレンカーボネート(1/1重量比)を用いた。結果を表4に示す。なお、表4には、実施例1のセパレータの正極、負極おのおので得られた剥離強度を100としたときの剥離強度の相対値で、正極と負極の剥離強度の平均値が70以上のものについては〇と記載し、50以上70未満のものについては△と記載し、50未満のものについては×と記載した。
Claims (9)
- 多孔質基材と、前記多孔質基材の少なくとも一方の面に形成されたポリフッ化ビニリデン系樹脂を含む接着性多孔質層と、を備えた非水系二次電池用セパレータであって、
前記接着性多孔質層は、空孔率が30%以上60%以下であり、かつ、平均孔径が1nm以上100nm以下であることを特徴とする非水系二次電池用セパレータ。 - 前記接着性多孔質層は空孔率が30%以上50%以下であり、
前記ポリフッ化ビニリデン系樹脂はフッ化ビニリデンが98mol%以上含まれていることを特徴とする請求項1に記載の非水系二次電池用セパレータ。 - 前記多孔質基材の一方の面に形成されている前記接着性多孔質層の重量が、0.5g/m2以上1.5g/m2以下であることを特徴とする請求項1または2に記載の非水系二次電池用セパレータ。
- 前記接着性多孔質層は前記多孔質基材の表裏両面に形成されていることを特徴とする請求項1~3のいずれかに記載の非水系二次電池用セパレータ。
- 前記多孔質基材の両面に形成された前記接着性多孔質層の両面合計の重量が、1.0g/m2以上3.0g/m2以下であり、
前記接着性多孔質層の一面側の重量と他面側の重量の差が、両面合計の重量に対して20%以下であることを特徴とする請求項4に記載の非水系二次電池用セパレータ。 - 前記多孔質基材がポリエチレンを含むポリオレフィン微多孔膜であることを特徴とする請求項1~5のいずれかに記載の非水系二次電池用セパレータ。
- 前記多孔質基材がポリエチレンとポリプロピレンとを含むポリオレフィン微多孔膜であることを特徴とする請求項1~5のいずれかに記載の非水系二次電池用セパレータ。
- 前記ポリオレフィン微多孔膜が少なくとも2層以上の構造となっており、当該2層のうち一方の層はポリエチレンを含み、他方の層はポリプロピレンを含むことを特徴とする請求項7に記載の非水系二次電池用セパレータ。
- 請求項1~8のいずれかに記載のセパレータを用いた非水系二次電池。
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Also Published As
Publication number | Publication date |
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TW201242136A (en) | 2012-10-16 |
US9065119B2 (en) | 2015-06-23 |
EP2696391B1 (en) | 2016-03-30 |
KR20130036043A (ko) | 2013-04-09 |
CN103155219A (zh) | 2013-06-12 |
EP2696391A4 (en) | 2014-02-12 |
JP5432417B2 (ja) | 2014-03-05 |
KR101297769B1 (ko) | 2013-08-20 |
EP2696391A1 (en) | 2014-02-12 |
TWI497790B (zh) | 2015-08-21 |
JPWO2012137375A1 (ja) | 2014-07-28 |
CN103155219B (zh) | 2016-01-06 |
US20130089770A1 (en) | 2013-04-11 |
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