Patent Application
20200067139
An embodiment of the present invention relates to a separator and a secondary battery including the separator. For example, an embodiment of the present invention relates to a separator capable of being used in a nonaqueous electrolyte-solution secondary battery and a nonaqueous electrolyte-solution secondary battery including the separator.
As a typical example of a nonaqueous electrolyte-solution secondary battery, a lithium ion secondary battery is represented. Since a lithium-ion secondary battery has a high energy density, it has been widely used in electronic devices such as a personal computer, a mobile phone, and a mobile information terminal. A lithium ion secondary battery includes a positive electrode, a negative electrode, an electrolyte solution charged between the positive electrode and the negative electrode, and a separator. The separator separates the positive electrode and the negative electrode from each other and also functions as a film transmitting the electrolyte solution and carrier ions. For example, patent literature 1 to 5 disclose a separator including a polyolefin.
Patent Literature 1: Japanese Patent Application Publication No. H10-298325
Patent Literature 2: Japanese Patent Application Publication No. 2011-233245
Patent Literature 3: Japanese Patent Application Publication No. 2014-118515
Patent Literature 4: Japanese Patent Application Publication No. 2014-182875
Patent Literature 5: Japanese Patent Application Publication No. 2012-227066
An object of the present invention is to provide a separator capable of being used in a secondary battery such as a nonaqueous electrolyte-solution secondary battery and a secondary battery including the separator.
An embodiment of the present invention is a separator including a first layer which consists of a porous polyolefin. The first layer has a parameter X, defined by the following equation, equal to or more than 0 and equal to or less than 20, and a minimum height of a ball in a falling-ball test of the first layer is equal to or more than 50 cm and equal to or less than 150 cm.
Here, MD tan δ and TD tan δ are respectively a loss tangent in a flow direction and a loss tangent in a width direction obtained by a viscoelasticity measurement of the first layer at a temperature of 90° C. and a frequency of 10 Hz. The minimum height is the lowest height of the ball placed over the first layer and having a diameter of 14.3 mm and a weight of 11.9 g, the lowest height causing a split in the first layer when the ball freely falls on the first layer.
According to the present invention, it is possible to provide a separator which not only possesses an excellent slip property and trimming processability but also enables production of a secondary battery in which an increase in an internal resistance can be suppressed when charging/discharging is repeated.
Hereinafter, the embodiments of the present invention are explained with reference to the drawings and the like. The invention can be implemented in a variety of different modes within its concept and should not be interpreted only within the disclosure of the embodiments exemplified below.
The drawings may be illustrated so that the width, thickness, shape, and the like are illustrated more schematically compared with those of the actual modes in order to provide a clearer explanation. However, they are only an example, and do not limit the interpretation of the invention.
In the specification and the claims, unless specifically stated, when a state is expressed where a structure is arranged “on” another structure, such an expression includes both a case where the substrate is arranged immediately above the “other structure” so as to be in contact with the “other structure” and a case where the structure is arranged over the “other structure” with an additional structure therebetween.
In the specification and the claims, an expression “substantially including only A” or an expression “consisting of A” includes a state where no substance is included other than A, a state where A and an impurity are included, and a state misidentified as a state where a substance other than A is included due to a measurement error. When this expression means the state where A and an impurity are included, there is no limitation to the kind and concentration of the impurity.
A schematic cross-sectional view of a secondary battery 100 according to an embodiment of the present invention is shown in
Although not illustrated, the secondary battery 100 possesses an electrolyte solution 140. The electrolyte solution 140 mainly exists in apertures of the positive electrode 110, the negative electrode 120, and the separator 130 as well as in the gaps between these members. The positive electrode 110 may include a positive-electrode current collector 112 and a positive-electrode active-substance layer 114. Similarly, the negative electrode 120 may include a negative-electrode current collector 122 and a negative-electrode active-substance layer 124. Although not illustrated in
The separator 130 is disposed between the positive electrode 110 and the negative electrode 120 and serves as a film having a role of separating the positive electrode 110 and the negative electrode 120 and transporting the electrolyte solution 140 in the secondary battery 100. A schematic cross-sectional view of the separator 130 is shown in
The first layer 132 has internal pores linked to each other. This structure allows the electrolyte solution 140 to permeate the first layer 132 and enables carrier ions such as lithium ions to be transported via the electrolyte solution 140. At the same time, physical contact between the positive electrode 110 and the negative electrode 120 is inhibited. On the other hand, when the secondary battery 100 has a high temperature, the first layer 132 melts and the pores disappear, thereby stopping the transportation of the carrier ions. This behavior is called shutdown. This behavior prevents heat generation and ignition caused by a short-circuit between the positive electrode 110 and the negative electrode 120, by which high safety is secured.
The first layer 132 includes a porous polyolefin. Alternatively, the first layer 132 may be structured with a porous polyolefin. Namely, the first layer 132 may be configured so as to include only a porous polyolefin or substantially include only a porous polyolefin. The porous polyolefin may contain an additive. In this case, the first layer 132 may be structured only with the polyolefin and the additive or substantially only with the polyolefin and the additive. When the porous polyolefin contains the additive, the polyolefin may be included in the porous polyolefin at a composition equal to or higher than 95 wt % or equal to or higher than 97 wt %. Furthermore, the polyolefin may be included in the first layer 132 at a composition equal to or higher than 95 wt % or equal to or higher than 97 wt %. As the additive, an organic compound (organic additive) is represented, and the organic compound may be an antioxidant (organic antioxidant) or a lubricant.
As the polyolefin structuring the porous polyolefin, a homopolymer obtained by polymerizing an α-olefin such as ethylene, propylene, 1-butene, 4-methyl-1-pentene, and 1-hexene or a copolymer thereof is represented. A mixture of these homopolymers and copolymers or a mixture of the homopolymers or copolymers having different molecular weights may be included in the first layer 132. That is, the molecular-weight distribution of the polyolefin may have a plurality of peaks. The organic additive may have a function to prevent oxidation of the polyolefin, and phenols or phosphoric esters may be employed as the organic additive, for example. Phenols having a bulky substituent such as a t-butyl group at an α-position and/or a β-position of a phenolic hydroxy group may be also used.
As a typical polyolefin, a polyethylene-based polymer is represented. When a polyethylene-based polymer is used, a low-density polyethylene or a high-density polyethylene may be used. Alternatively, a copolymer of ethylene with an α-olefin may be used. These polymers or copolymers may be a high-molecular weight polymer with a weight-average molecular weight equal to or higher than 100,000 or an ultrahigh-molecular weight polymer with a weight-average molecular weight of equal to or higher than 1,000,000. The use of a polyethylene-based polymer enables the shutdown function to be realized at a lower temperature, thereby providing high safety to the secondary battery 100.
A thickness of the first layer 132 may be equal to or larger than 4 μm and equal to or smaller than 40 μm, equal to or larger than 5 μm and equal to or smaller than 30 μm, or equal to or larger than 6 μm and equal to or smaller than 15 μm.
A weight per unit area of the first layer 132 is appropriately determined in view of its strength, thickness, weight, and handleability. For example, the weight per unit area may be equal to or more than 4 g/m2 and equal to or less than 20 g/m2, equal to or more than 4 g/m2 and equal to or less than 12 g/m2, or equal to or more than 5 g/m2 and equal to or less than 10 g/m2, by which a weight-energy density and a volume-energy density of the secondary battery 100 can be increased. Note that a weight per unit area is a weight per unit area.
With respect to gas permeability of the first layer 132, its Gurley value may be selected from a range equal to or higher than 30 s/100 mL and equal to or lower than 500 s/100 mL or equal to or higher than 50 s/100 mL and equal to or lower than 300 s/100 mL so that sufficient ion-permeability can be obtained.
A porosity of the first layer 132 may be selected from a range equal to or more than 20 vol % and equal to or less than 80 vol % or equal to or more than 30 vol % and equal to or less than 75 vol % so that a retention volume of the electrolyte solution 140 is increased and the shutdown function is surely realized. A diameter of the pore (average pore diameter) in the first layer 132 may be selected from a range equal to or larger than 0.1 μm and equal to or smaller than 0.3 μm or equal to or larger than 0.1 μm and equal to or smaller than 0.14 μm so that a sufficient ion-permeability and a high shutdown function can be obtained.
The first layer 132 has a parameter X, defined by the following equation, equal to or more than 0 and equal to or less than 20 and a minimum height of a ball in a falling-ball test equal to or more than 50 cm and equal to or less than 150 cm. Here, MD tan δ and TD tan δ are respectively a loss tangent in a flow direction (also called a machine direction MD) and a loss tangent in a width direction (also called a transverse direction TD) obtained by a viscoelasticity measurement of the first layer at a temperature of 90° C. and a frequency of 10 Hz.
A loss tangent obtained by a dynamic viscoelasticity measurement of a substance (hereinafter, referred to as a tan δ) is represented by an equation
tan δ=E″/E′
using a storage modulus E′ and a loss modulus E″. The loss modulus indicates irreversible deformability to a stress, while the storage modulus indicates reversible deformability to a stress. Thus, the tan δ indicates deformation conformability of a substance to a change of a force applied from the exterior. A decrease in anisotropy of the tan δ in a plane direction of a substrate makes the deformation conformability of the substance with respect to the change of a force applied from the exterior isotropic and allows the substance to uniformly deform in the plane direction.
In the secondary battery such as a nonaqueous electrolyte-solution secondary battery, a pressure and a shearing force in a plane direction are applied to the separator because the electrodes (positive electrode 110 and the negative electrode 120) expand and shrink during charging/discharging. At this time, if the deformation compatibility of the first layer 132 structuring the separator is isotropic, the separator uniformly deforms. Hence, anisotropy of the stress generated in the first layer 132 due to the periodic deformation of the electrodes in a charging/discharging cycle is reduced. Accordingly, separation of the positive-electrode active-substance layer 114 and the negative-electrode active-substance layer 124 hardly occurs, an increase in internal resistance of the secondary battery is prevented, and the cycle characteristics are improved.
In addition, it is expected from the time-temperature conversion rule relating to the stress-relaxation process of a polymer that the frequency obtained by converting the dynamic viscoelasticity measurement at a frequency of 10 Hz and a temperature of 90° C. into a measurement using, as a standard, a temperature range ranging from approximately 20 to 60° C., which corresponds to a temperature at which a secondary battery is normally operated, is much lower than 10 Hz and close to a time scale of the expansion-shrink motion of the electrodes caused by the charging/discharging cycle of a secondary battery. Therefore, a dynamic viscoelasticity measurement at 10 Hz and 90° C. enables rheology evaluation so as to correspond to the time scale of the charging/discharging cycle in the temperature range in which a secondary battery is used.
The anisotropy of the tan δ is evaluated by the parameter X defined by the above equation. When this parameter X is equal to or more than 0 and equal to or less than 20 or equal to or more than 2 and equal to or less than 20, it is possible to suppress an increase in internal resistance of a secondary battery during a charging/discharging cycle.
When the secondary battery is fabricated using the separator 130 including the first layer 132, the separator 130 is trimmed into a predetermined size. If a split occurs in an unintended direction during trimming, the yield of the secondary battery decreases. In addition, when a wound secondary battery is fabricated using the separator 130, the separator 130 and the electrodes (the positive electrode 110 and the negative electrode 120) are wound on a columnar member (hereinafter, referred to as a pin), and then the pin is extracted. At this time, if friction between the separator 130 and the pin is large, the pin cannot be readily extracted, thereby destroying the separator 130, the electrodes, or the pin. As a result, the manufacturing process is affected, and the yield is decreased. The inventors found that the minimum height of the ball in the falling-ball test has a relationship with trimming processability as well as friction between the first layer 132 and other members and greatly influences the yield. More specifically, it was proven that the separator 130 can be selectively cut in an intended direction and the friction with the pin can be reduced by configuring the first layer 132 so that the minimum height of the ball in the falling-ball test is equal to or more than 50 cm and equal to or less than 150 cm.
In the specification and claims, the falling-ball test is an evaluation test conducted as follows. A mirror-surface ball with a diameter of 14.3 mm and a weight of 11.9 g is subjected to a free fall on the first layer 132 from a height h. The height h is a distance between the ball immediately prior to the free fall and the first layer 132. The minimum height value of h which causes a split in the first layer 132 when the ball falls on the first layer 132 is the lowest value of the ball.
As described below, the first layer 132 is obtained by a rolling process. A hard and brittle skin layer is formed at a surface in the rolling process. In addition, a difference in orientation is generated in a rolling direction, depending on the rolling conditions. Specifically, an orientation difference arises between the MD and TD in the rolling process. Rolling in only the TD leads to an increase in an orientation in TD, while rolling in only the MD results in an increase in an orientation in the MD. A proportion of the skin layer and a MD-TD orientation balance relate to the split in the first layer 132. That is, the first layer 132 tends to become fragile to impact and to be readily split in an unintended direction with increasing proportion of the skin layer. Furthermore, when the orientation is biased in one of the MD and TD, a split readily occurs along the more strongly biased direction, and the friction in a direction perpendicular to the more strongly biased direction increases. Hence, the proportion of the skin layer and the orientation balance between the MD and TD influence the trimming processability and the friction of the first layer 132.
The inventors found that an increase in the minimum height of the ball in the falling-ball test results in a decrease in the proportion of the skin layer and in the orientation difference between the MD and TD. It was also found that, in the case where the minimum height is equal to or more than 50 cm, the split in an unintended direction is suppressed in trimming the first layer 132, and the friction with other members is decreased. Note that it is necessary to thicken the first layer 132 or reduce porosity in order to increase the minimum height to be more than 150 cm. However, an increase in thickness reduces energy density of the secondary battery, and a decrease in porosity causes a decrease in battery performance. Hence, it is preferred that the minimum height be equal to or less than 150 cm.
As experimentally proven by the following Examples, the use of the separator 130 including the first layer 132 satisfying the aforementioned parameters suppresses an increase in an internal resistance of the secondary battery in a charging/discharging cycle. Furthermore, it was found that the secondary battery can be manufactured in a good yield by using this separator 130.
Note that a piercing strength of the first layer 132 is preferred to be equal to or larger than 3 N and equal to or smaller than 10 N or equal to or larger than 3 N and equal to or smaller than 8 N. This range suppresses a break of the separator 130 including the first layer 132 when a pressure is applied to the secondary battery from the exterior during the fabrication process, thereby preventing a short-circuit between the positive and negative electrodes.
As described above, the positive electrode 110 may include the positive-electrode current collector 112 and the positive-electrode active-substance layer 114. Similarly, the negative electrode 120 may include the negative-electrode current collector 122 and the negative-electrode active-substance layer 124 (see
A metal such as nickel, copper, titanium, tantalum, zinc, iron, and cobalt or an alloy such as stainless including these metals can be used for the positive-electrode current collector 112 and the negative-electrode current collector 122, for example. The positive-electrode current collector 112 and the negative-electrode current collector 122 may have a structure in which a plurality of layers including these metals is stacked.
The positive-electrode active-substance layer 114 and the negative-electrode active-substance layer 124 respectively include a positive-electrode active substance and a negative-electrode active substance. The positive-electrode active substance and the negative-electrode active substance have a role to release and absorb carrier ions such as lithium ions.
As a positive-electrode active substance, a material capable of being doped or de-doped with carrier ions is represented, for example. Specifically, a lithium-based composite oxide containing at least one kind of transition metals such as vanadium, manganese, iron, cobalt, and nickel is represented. As such a composite oxide, a lithium-based composite oxide having an α-NaFeO2-type structure, such as lithium nickelate and lithium cobalate, and a lithium-based composite oxide having a spinel-type structure, such as lithium manganese spinel, are given. These composite oxides have a high average discharge potential.
The lithium-based composite oxide may contain another metal element and is exemplified by lithium nickelate (composite lithium nickelate) including an element selected from titanium, zirconium, cerium, yttrium, vanadium, chromium, manganese, iron, cobalt, copper, silver, magnesium, aluminum, gallium, indium, tin, and the like, for example. These metals may be adjusted to be equal to or more than 0.1 mol % and equal to or less than 20 mol % to the metal elements in the composite lithium nickelate. This structure provides the secondary battery 100 with an excellent rate property when used at a high capacity. For example, a composite lithium nickelate including aluminum or manganese and containing nickel at 85 mol % or more or 90 mol % or more may be used as the positive-electrode active substance.
Similar to the positive-electrode active substance, a material capable of being doped and de-doped with carrier ions can be used as the negative-electrode active substance. For example, a lithium metal or a lithium alloy is represented. Alternatively, it is possible to use a carbon-based material such as graphite exemplified by natural graphite and artificial graphite, cokes, carbon black, and a sintered polymeric compound exemplified by carbon fiber; a chalcogen-based compound capable of being doped and de-doped with lithium ions at a potential lower than that of the positive electrode, such as an oxide and a sulfide; an element capable of being alloyed or reacting with an alkaline metal, such as aluminum, lead, tin, bismuth, and silicon; an intermetallic compound of cubic system (AlSb, Mg2Si, NiSi2) undergoing alkaline-metal insertion between lattices; lithium-nitride compound (Li3-xMxN (M: transition metal)); and the like. Among the negative-electrode active substances, the carbon-based material including graphite such as natural graphite and artificial graphite as a main component provides a large energy density due to high potential uniformity and a low average discharge potential when combined with the positive electrode 110. For example, it is possible to use, as the negative-electrode active substance, a mixture of graphite and silicon with a ratio of silicon to carbon equal to or larger than 5 mol % and equal to or smaller 10 mol %.
The positive-electrode active-substance layer 114 and the negative-electrode active-substance layer 124 may each further include a conductive additive and binder other than the aforementioned positive-electrode active substance and the negative-electrode active substance.
As a conductive additive, a carbon-based material is represented. Specifically, graphite such as natural graphite and artificial graphite, cokes, carbon black, pyrolytic carbons, and a sintered polymeric compound such as carbon fiber are given. A plurality of materials described above may be mixed to use as a conductive additive.
As a binder, poly(vinylidene fluoride) (PVDF), polytetrafluoroethylene, poly(vinylidene fluoride-co-hexafluoropropylene), poly(tetrafluoroethylene-co-hexafluoropropylene), poly(tetrafluoroethylene-co-perfluoroalkyl vinyl ether), poly(ethylene-co-tetrafluoroethylene), a copolymer in which vinylidene fluoride is used as a monomer, such as a poly(vinylidene fluoride-co-hexafluoropropylene-co-tetrafluoroethylene), a thermoplastic resin such as a thermoplastic polyimide, polyethylene, and polypropylene, an acrylic resin, styrene-butadiene rubber, and the like are represented. Note that a binder may further have a function as a thickener.
The positive electrode 110 may be formed by applying a mixture of the positive-electrode active substance, the conductive additive, and the binder on the positive-electrode current collector 112, for example. In this case, a solvent may be used to form or apply the mixture. Alternatively, the positive electrode 110 may be formed by applying a pressure to the mixture of the positive-electrode active substance, the conductive additive, and the binder to process the mixture and arranging the processed mixture on the positive electrode 110. The negative electrode 120 can also be formed with a similar method.
The electrolyte solution 140 includes the solvent and an electrolyte, and at least a part of the electrolyte is dissolved in the solvent and electrically dissociated. As the solvent, water and an organic solvent can be used. In the case where the secondary battery 100 is utilized as a nonaqueous electrolyte-solution secondary battery, an organic solvent is used. As an organic solvent, carbonates such as ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, and 1,2-di(methoxycarbonyloxy)ethane; ethers such as 1,2-dimethoxyethane, 1,3-dimethoxypropane, tetrahydrofuran, and 2-methyltetrahydrofuran; esters such as methyl formate, methyl acetate, and γ-butyrolactone; nitriles such as acetonitrile and butyronitrile; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; carbamates such as 3-methyl-2-oxazolidone, sulfur-containing compounds such as sulfolane, dimethyl sulfoxide, and 1,3-propanesultone, a fluorine-containing organic solvent in which fluorine is introduced to the aforementioned organic solvent; and the like are represented. A mixed solvent of these organic solvents may also be employed.
As a typical electrolyte, a lithium salt is represented. For example, LiClO4, LiPF6, LiAsF6, LiSbF6, LiBF4, LiCF3SO3, LiN(CF3SO2)2, LiC(CF3SO2)3, Li2B10Cl10, a lithium salt of a carboxylic acid having 2 to 6 carbon atoms, LiAlCl4, and the like are represented. Just one kind of the lithium salts mentioned above may be used, and more than two kinds of lithium salts may be combined.
Note that, in a broad sense, an electrolyte may mean a solution of an electrolyte. However, in the present specification and claims, a narrow sense is employed. That is, an electrolyte is a solid and is electrically dissociated upon dissolving in a solvent to provide an ion conductivity to the resulting solution.
As shown in
In the present embodiment, a method for preparing the first layer 132 described in the First Embodiment is described. An explanation of the structures the same as those of the First Embodiment may be omitted.
A method for preparing the first layer 132 includes (1) a process for obtaining a polyolefin composite by kneading an ultrahigh-molecular weight polyethylene, a low-molecular weight hydrocarbon, and a pore-forming agent, (2) a process for forming a sheet by rolling the polyolefin composite with a rolling roll (rolling process), (3) a process for removing the pore-forming agent from the sheet obtained in the process (2), and (4) a process for processing into a film state by stretching the sheet obtained in the process (3).
A shape of the ultrahigh-molecular weight polyolefin is not limited, and a polyolefin processed into a powder state may be used. As the low-molecular weight hydrocarbon, a low-molecular weight polyolefin such as polyolefin wax and a low-molecular weight polymethylene such as Fisher-Tropsh wax are represented. A weight-average molecular weights of the low-molecular weight polyolefin and the low-molecular weight polymethylene are equal to or higher than 200 and equal to or lower than 3000, for example, by which the low-molecular weight hydrocarbon can be prevented from being volatilized and can be homogeneously mixed with the ultrahigh-molecular weight polyolefin. Note that a polymethylene is defined as a kind of polyolefin in the present specification and claims.
In the process (1), the ultrahigh-molecular weight polyolefin and the low-molecular weight polyolefin may be mixed with a mixer (first-step mixing), and the mixture may be mixed again (second-step mixing) after adding the pore-forming agent into the mixture, for example. In the first-step mixing, an organic compound such as an antioxidant may be added. The ultrahigh-molecular weight polyolefin and the low-molecular weight polyolefin can be uniformly mixed, and the ultrahigh-molecular weight polyolefin, the low-molecular weight polyolefin, and the pore-forming agent can also be uniformly mixed by performing the two-step mixing. The uniform mixing of these materials, especially that of the ultrahigh-molecular weight polyolefin and the low-molecular weight polyolefin can be confirmed by an increase in bulk density of the mixture. The uniform mixing promotes uniform crystallization, which results in uniform crystal distribution and reduced anisotropy of the tan δ. It is preferred that there be an interval equal to or more than 1 minute between the first-step mixing and the addition of the pore-forming agent.
As the pore-forming agent used in the process (1), an organic filling agent and an inorganic filling agent are represented. As an organic filling agent, a plasticizer may be used, for example, and a low-molecular weight hydrocarbon such as a liquid paraffin is represented.
As the inorganic filling agent, an inorganic material soluble in a neutral, acidic, or alkaline solvent is represented, and calcium carbonate, magnesium carbonate, barium carbonate, and the like are exemplified. Other than these materials, an inorganic compound such as calcium chloride, sodium chloride, and magnesium sulfate is represented. Just one kind of the pore-forming agent may be used, or two or more kinds of pore-forming agents may be combined. Calcium carbonate is represented as a typical pore-forming agent.
In the process (3) in which the pore-forming agent is removed, a solution of water or organic solvent to which an acid or a base is added, or the like is used as a cleaning solution. A surfactant may be added to the cleaning solution. An addition amount of the surfactant can be arbitrarily selected from a range equal to or more than 0.1 wt % to 15 wt % or equal to or more than 0.1 wt % and equal to or less than 10 wt %. It is possible to secure a high cleaning efficiency and prevent the surfactant from being left by selecting the addition amount from this range. A cleaning temperature may be selected from a temperature range equal to or higher than 25° C. and equal to or lower than 60° C., equal to or higher than 30° C. and equal to or lower than 55° C., or equal to or higher than 35° C. and equal to or lower than 50° C., by which a high cleaning efficiency can be obtained and evaporation of the cleaning solution can be avoided.
In the process (3), water cleaning may be further conducted after removing the pore-forming agent with the cleaning solution. The temperature in the water cleaning may be selected from a temperature range equal to or higher than 25° C. and equal to or lower than 60° C., equal to or higher than 30° C. and equal to or lower than 55° C., or equal to or higher than 35° C. and equal to or lower than 50° C.
The stretched first layer 132 may be annealed (thermal fixation) in the process (4). An oriented and crystallized region formed by being stretched and an amorphous region are mixed in the stretched first layer 132. The amorphous region is reconstructed (clustered) by the annealing treatment, by which dynamic nonuniformity in a microregion disappears.
In view of molecular motion of the polyolefin molecules to be used, an annealing temperature can be selected from a range equal to or higher than (Tm−30° C.) and lower than Tm, equal to or higher than (Tm−20° C.) and lower than Tm, or equal to or higher than (Tm−10° C.) and lower than Tm where Tm is a melting point of the ultrahigh-molecular weight polyolefin. Selection from these temperature ranges dispels the dynamic nonuniformity and prevents the pores from closing.
In the present embodiment, an embodiment in which the separator 130 has the porous layer 134 in addition to the first layer 132 is explained.
As described in the First Embodiment, the porous layer 134 may be disposed on one side or both sides of the first layer 132 (see
The porous layer 134 is insoluble in the electrolyte solution 140 and is preferred to include a material chemically stable in a usage range of the second battery 100. As such a material, it is possible to represent a polyolefin such as polyethylene, polypropylene, polybutene, poly(ethylene-co-propylene); a fluorine-containing polymer such as poly(vinylidene fluoride), polytetrafluoroethylene, poly(vinylidene fluoride-co-hexafluoropropylene), poly(vinylidene fluoride-co-hexafluoropropylene-co-tetrafluoroethylene), and poly(ethylene-co-tetrafluoroethylene), an aromatic polyimide (aramide); rubber such as poly(styrene-co-butadiene) and a hydride thereof, a copolymer of methacrylic esters, a poly(acrylonitrile-co-acrylic ester), a poly(styrene-co-acrylic ester), ethylene-propylene rubber, and poly(vinyl acetate); a polymer having a melting point and a glass-transition temperature of 180° C. or more, such as poly(phenylene ether), a polysulfone, a poly(ether sulfone), polyphenylenesulfide, a poly(ether imide), a polyamide-imide, a polyether-amide, and a polyester; a water-soluble polymer such as poly(vinyl alcohol), poly(ethylene glycol), a cellulose ether, sodium alginate, poly(acrylic acid), polyacrylamide, poly(methacrylic acid); and the like.
As an aromatic polyamide, poly(paraphenylene terephthalamide), poly(metaphenylene isophthalamide), poly(parabenzamide), poly(metabenzamide), poly(4,4′-benzanilide terephthalamide), poly(paraphenylene-4,4′-biphenylenecarboxylic amide), poly(metaphenylene-4,4′-biphenylenecarboxilic amide), poly(paraphenyelnee-2,6-natphthalenedicarboxlic amide), poly(metaphenyelnee-2,6-natphthalenedicarboxlic amide), poly(2-chloroparaphenylene terephthalamide), a copolymer of paraphenylene terephthalamide with 2,6-dichloroparaphenylene terephthalamide, a copolymer of metaphenylene terephthalamide with 2,6-dichloroparaphenylene terephthalamide, and the like are represented, for example.
The porous layer 134 may include a filler. A filler consisting of an organic substance or an inorganic substance is represented as a filler. A filler called a filling agent and consisting of an inorganic substance is preferred. A filler consisting of an inorganic oxide such as silica, calcium oxide, magnesium oxide, titanium oxide, alumina, mica, zeolite, aluminum hydroxide, boehmite, and the like is more preferred, at least one kind of filler selected from a group consisting of silica, magnesium oxide, titanium oxide, aluminum hydroxide, boehmite, and alumina is further preferred, and alumina is especially preferred. Alumina has a number of crystal forms such as α-alumina, β-alumina, γ-alumina, θ-alumina, and the like, and any of the crystal forms can be appropriately used. Among them, α-alumina is most preferable due to its particularly high thermal stability and chemical stability. Just one kind of filler may be used, or two or more kinds of filler may be combined in the porous layer 134.
No limitation is provided to a shape of the filler, and the filler may have a sphere shape, a cylindrical shape, an elliptical shape, a gourd shape, and the like. Alternatively, a filler in which these shapes are mixed may be used.
When the porous layer 134 includes the filler, an amount of the filler to be included may be equal to or larger than 1 vol % and equal to or smaller than 99 vol % or equal to or larger than 5 vol % and equal to or smaller than 95 vol % with respect to the porous layer 134. The aforementioned range of the amount of the filler to be included prevents the space formed by contact between the fillers from being closed by the material of the porous layer 134, which leads to sufficient ion permeability and allows its weight per unit area to be adjusted.
A thickness of the porous layer 134 can be selected from a range equal to or larger than 0.5 μm and equal to or smaller than 15 μm or equal to or larger than 2 μm and equal to or smaller than 10 μm. Hence, when the porous layers 134 are formed on both sides of the first layer 132, a total thickness of the porous layers 134 may be selected from a range equal to or larger than 1.0 μm and equal to or smaller than 30 μm or equal to or larger than 4 μm and equal to or smaller than 20 μm.
When the total thickness of the porous layers 134 is arranged to be equal to or larger than 1.0 μm, internal short-circuits caused by damage to the secondary battery 100 can be more effectively prevented. The total thickness of the porous layers 134 equal to or to smaller than 30 μm prevents an increase in permeation resistance of the carrier ions, thereby preventing deterioration of the positive electrode 110 and a decrease in battery performance and a cycle property resulting from an increase in permeation resistance of the carrier ions. Moreover, it is possible to avoid an increase in distance between the positive electrode 110 and the negative electrode 120, which contributes to miniaturization of the secondary battery 100.
The weight per unit area of the porous layer 134 may be selected from a range equal to or more than 1 g/m2 and equal to or less than 20 g/m2 or equal to or more than 2 g/m2 and equal to or less than 10 g/m2. This range increases an energy density per weight and energy density per volume of the secondary battery 100.
A porosity of the porous layer 134 may be equal to or more than 20 vol % and equal to or less than 90 vol % or equal to or more than 30 vol % and equal to or less than 80 vol %. This range allows the porous layer 134 to have sufficient ion permeability. An average porous diameter of the pores included in the porous layer 134 may be selected from a range equal to or larger than 0.01 μm and equal to or smaller than 1 μm or equal to or larger than 0.01 μm and equal to or smaller than 0.5 μm, by which a sufficient ion permeability is provided to the secondary battery 100 and the shutdown function can be improved.
A gas permeability of the separator 130 including the aforementioned first layer 132 and the porous layer 134 may be equal to or higher than 30 s/100 mL and equal to or lower than 1000 s/100 mL or equal to or higher than 50 s/100 mL and equal to or lower than 800 s/100 L in a Gurley value, which enables the separator 130 to have sufficient strength, maintain a high shape stability at a high temperature, and possess sufficient ion permeability.
When the porous layer 134 including the filler is prepared, the aforementioned polymer or resin is dissolved or dispersed in a solvent, and then the filler is dispersed in this mixed liquid to form a dispersion (hereinafter, referred to as a coating liquid). As a solvent, water; an alcohol such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, and t-butyl alcohol; acetone, toluene, xylene, hexane, N-methylpyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide; and the like are represented. Just one kind of solvent may be used, or two or more kinds of solvents may be used.
When the coating liquid is prepared by dispersing the filler to the mixed liquid, a mechanical stirring method, an ultrasonic dispersing method, a high-pressure dispersion method, a media dispersion method, and the like may be applied. In addition, after the filler is dispersed in the mixed liquid, the filler may be subjected to wet milling by using a wet-milling apparatus.
An additive such as a dispersant, a plasticizer, a surfactant, or a pH-adjusting agent may be added to the coating liquid.
After the preparation of the coating liquid, the coating liquid is applied on the first layer 132. For example, the porous layer 134 can be formed over the first layer 132 by directly coating the first layer 132 with the coating liquid by using a dip-coating method, a spin-coating method, a printing method, a spraying method, or the like and then removing the solvent. Instead of directly applying the coating liquid over the first layer 132, the porous layer 134 may be transferred onto the first layer 132 after being formed on another supporting member. As a supporting member, a film made of a resin, a belt or drum made of a metal may be used.
Any method selected from natural drying, fan drying, heat drying, and vacuum drying may be used to remove the solvent. Drying may be conducted after substituting the solvent with another solvent (e.g., a solvent with a low boiling point). When heating, drying may be carried out at 10° C. or higher and 120° C. or lower or at 20° C. or higher and 80° C. or lower. This temperature range avoids a reduction in gas permeability caused by shrinkage of the pores in the first layer 132.
A thickness of the porous layer 134 can be controlled by a thickness of the coating film in a wet state after coating, an amount of the filler included, a concentration of the polymer and the resin, and the like.
An example for preparing the separator 130 is described below. In the following Examples, the prepared first layers 132 were used as the separator 130.
To a mixture of 68 wt % of ultrahigh-molecular weight polyethylene powder (GUR2024 manufactured by Ticona) and 32 wt % of polyethylene wax (FNP-0115, manufactured by Nippon Seiro Co. Ltd.) having a weight-average molecular weight of 1000, 0.4 weight portions of an antioxidant (Irg1010, manufactured by CIBA Speciality Chemicals), 0.1 weight portions of an antioxidant (P168 manufactured by CIBA Speciality Chemicals®), and 1.3 weight portions of sodium stearate with respect to 100 weight portions of the summation of the ultrahigh-molecular weight polyethylene and the polyethylene wax were added, and these materials were mixed in a power state with a Henschel mixer at a rotation rate of 440 rpm for 70 seconds. Next, calcium carbonate (manufactured by Maruo Calcium Co. LTD.) with an average particle diameter of 0.1 μm was added so that its proportion to the entire volume is 38 vol %, and these materials were mixed in a Henschel mixer at a rotation rate of 440 rpm for 80 seconds. At this time, a light-duty bulk density of the powder was approximately 500 g/L. The obtained mixture was rolled using three rolling rollers R1, R2, and R3 having a surface temperature of 150° C., where a first rolling was carried out using the rollers R1 and R2 while a second rolling was carried out using the rollers R2 and R3. The mixture was cooled stepwise while being drawn with a winding roller different in speed from the rolling rollers (drawing ratio (winding speed/rolling speed)=1.4), resulting in a sheet with a thickness of approximately 64 μm. This sheet was dipped in hydrochloric acid (4 mol/L) including 0.5 wt % of a nonionic surfactant to remove calcium carbonate, sequentially stretched to 6.2 times in a lateral direction at 100° C., and annealed at 126° C. (134° C. of a melting point of the polyolefin-resin composite−8° C.) to obtain the separator 130.
The separator 130 was obtained with the same method as the Example 1 except that 71.5 wt % of GUR4032 manufactured by Ticona was used as the ultrahigh-molecular weight polyethylene powder, 28.5 wt % of the polyethylene wax was used, a sheet with a thickness of approximately 70 μm was prepared using the three rolling rollers R1, R2, and R3 having a surface temperature of 150° C., the sheet was stretched to 7.0 times, and the annealing was carried out at 123° C. (a melting point of the polyolefin-resin composite 133° C.−10° C.).
The separator 130 was obtained with the same method as the Example 2 except that 70 wt % of the ultrahigh-molecular weight polyethylene powder was used, 30 wt % of the polyethylene wax was used, the calcium carbonate was used at 37 vol %, a sheet with a thickness of approximately 41 μm was prepared by rolling the mixture with a pair of rolling rollers having a surface temperature of 150° C., followed by cooling the mixture stepwise while being drawn with a winding roller different in speed from the rolling rollers (drawing ratio (winding speed/rolling speed)=1.4), the sheet was stretched to 6.2 times, and the annealing was carried out at 120° C. (a melting point of the polyolefin-resin composite 133° C.−13° C.).
An example for preparing separators used as Comparative Examples is described below. In the following Comparative Examples, the prepared first layers 132 were used as the separator 130.
To a mixture of 70 wt % of ultrahigh-molecular weight polyethylene powder (GUR4032 manufactured by Ticona) and 30 wt % of polyethylene wax (FNP-0115, manufactured by Nippon Seiro Co. Ltd.) having a weight-average molecular weight of 1000, 0.4 weight portions of an antioxidant (Irg1010, manufactured by CIBA Speciality Chemicals), 0.1 weight portions of an antioxidant (P168 manufactured by CIBA Speciality Chemicals®), and 1.3 weight portions of sodium stearate with respect to 100 weight portions of the summation of the ultrahigh-molecular weight polyethylene and the polyethylene wax were added, and calcium carbonate (manufactured by Maruo Calcium Co. LTD.) with an average particle diameter of 0.1 μm was simultaneously added so that its proportion to the entire volume is 36 vol %. These materials were mixed with a Henschel mixer at a rotation rate of 440 rpm for 150 seconds. At this time, a light-duty bulk density of the powder was approximately 350 g/L. The obtained mixture was rolled with a pair of rolling rolls having a surface temperature of 150° C., cooled stepwise while being drawn with a winding roller different in speed from the rolling rollers (drawing ratio (winding speed/rolling speed)=1.4), resulting in a sheet with a thickness of approximately 29 μm. This sheet was dipped in hydrochloric acid (4 mol/L) including 0.5 wt % of a nonionic surfactant to remove calcium carbonate, sequentially stretched to 6.2 times in a lateral direction at 100° C. and annealed at 115° C. (133° C. of a melting point of the polyolefin-resin composite−12° C.) to obtain the first layer 132.
A commercially available polyolefin porous film (polyolefin separator) was used as the separator of the Comparative Example 2.
A method for fabricating the secondary batteries including the separators of the Examples 1 to 3 and Comparative Examples 1 and 2 is described below.
A commercially available positive electrode manufactured by applying a stack of LiNi0.5Mn0.3Co0.2O2/conductive material/PVDF (weight ratio of 92/5/3) on an aluminum foil was processed. Here, LiNi0.5Mn0.3Co0.2O2 is an active-substance layer. Specifically, the aluminum foil was cut so that a size of the positive-electrode active-substance layer is 45 mm×30 mm and that a portion with a width of 13 mm, in which the positive-electrode active-substance layer is not formed, was left in a periphery and was used as a positive electrode in the following fabrication process. A thickness, a density, and a positive-electrode capacity of the positive-electrode active-substance layer were 58 μm, 2.50 g/cm3, and 174 mAh/g, respectively.
A commercially available negative electrode manufactured by applying graphite/poly(styrene-co-1,3-butadiene)/carboxymethyl cellulose sodium salt (weight ratio of 98/1/1) on a copper foil was used. Here, the graphite functions as a negative-electrode active-substance layer. Specifically, the copper foil was cut so that a size of the negative-electrode active-substance layer is 50 mm×35 mm and that a portion with a width of 13 mm, in which the negative-electrode active-substance layer is not formed, was left in a periphery and was used as a negative electrode in the following fabrication process. A thickness, a density, and a negative-electrode capacity of the negative-electrode active-substance layer were 49 μm, 1.40 g/cm3, and 372 mAh/g, respectively.
The positive electrode, the separator, and the negative electrode were stacked in the order in a laminated pouch to obtain a stacked body. At this time, the positive electrode and the negative electrode were arranged so that the entire top surface of the positive-electrode active-substance layer overlaps with a main surface of the negative-electrode active-substance layer.
Next, the stacked body was arranged in an envelope-shaped housing formed by stacking an aluminum layer and a heat-seal layer, and 0.25 mL of an electrolyte solution was added into the housing. A mixed solution in which LiPF6 was dissolved at 1.0 mol/L in a mixed solvent of ethyl methyl carbonate, diethyl carbonate, and ethylene carbonate with a volume ratio of 50:20:30 was used as the electrolyte solution. The secondary battery was fabricated by heat-sealing the housing while reducing the pressure in the housing. A designed capacity of the secondary battery was 20.5 mAh.
The physical properties of the separators according to the Examples 1 to 3 and the Comparative Examples 1 and 2 as well as the evaluation results of the performance of the secondary batteries including the separators are described below.
The thicknesses were measured using a High-Resolution Digital Measuring Unit manufactured by Mitsutoyo Corporation.
The first layer 132 was trimmed into a square with a side length of 10 cm, and its weight W (g) was measured. The porosity (vol %) was calculated from the thickness D (μm) and the weight W (g) according to the following equation,
Porosity (vol %)=(1−(W/specific gravity)/(10×10×D/10000))×100
where the specific gravity is that of the ultrahigh-molecular weight polyethylene powder.
The light-duty bulk density was measured according to JIS R9301-2-3.
Approximately 50 mg of the separator was charged in a pan made of aluminum, and a DSC (Differential Scanning Calorimetry) thermogram was obtained at a temperature-elevating rate of 20° C./min using a differential scanning calorimeter EXSTAR 6000 manufactured by Seiko Instruments Inc. A melting peak top at around 140° C. was employed as the melting point Tm of the separator.
The dynamic viscoelasticity measurement of the separator was carried out using a dynamic viscoelastic analyzer itk DVA-225 manufactured by itk Inc. under the conditions of a measurement frequency of 10 Hz and a measurement temperature of 90° C.
Specifically, the tan δ in a flow direction (MD tan δ) was measured by applying a tensile strength of 30 cN to a test piece prepared by cutting the separators of Examples 1 to 3 and the Comparative Examples 1 and 2 into a rectangular stripe shape having a longitude in the flow direction and a width of 5 mm, while a distance between chucks was 20 mm. Similarly, the tan δ in the longitudinal direction (TD tan δ) was measured by applying a tensile strength of 30 cN to a test piece prepared by cutting the separators into a rectangular stripe shape having a longitude in the width direction and a width of 5 mm, while a distance between chucks was 20 mm. The measurements were carried out while increasing the temperature from a room temperature at a temperature-elevating rate of 20° C./min, and the parameter X was calculated using the value of tan δ when the temperature reached 90° C.
The tools used in the falling-ball test are illustrated in
In this state, a mirror-surface ball having a diameter of 14.3 mm, a weight of 11.9 g, and a surface roughness Ra of 0.016 μm was allowed to freely fall from over the opening, and then whether a break (split) occurred in the separator 130 was confirmed. This operation was carried out plural times, where a new separator 130 was used in every falling-ball test. Note that the surface roughness (Ra) of the ball was measured with a non-contact surface profiler system (VertScan™ 2.0 R5500GML manufactured by Ryoka Systems Inc.) under the following conditions.
Object lens: magnifying power of 5 (Michelson type)
Intermediate lens: magnifying power of 1 (Michelson type)
Wavelength filter: 530 nm
CCD camera: ⅓ inch
Measuring mode: wave
Data correction: spherical approximation with a radius of 7.15 mm
The height of the ball subjected to the free fall in the first falling-ball test, that is, the distance between the ball immediately prior to the free fall and the separator 130 was defined as h1. In the case where a break was observed in the separator 130 as a result of the first falling-ball test, the height of the ball h2 in the second falling-ball test was changed to (h1−5 cm), while the height of the ball h2 in the second falling-ball test was changed to (h1+5 cm) in the case where no break was observed in the separator 130. The falling-ball test was repeated by changing the height of the ball in this way. Namely, the height of the ball hk+1 in the (k+1)th falling-ball test was changed to (hk−5 cm) in the case where a break was observed in the separator 130 as an evaluation result of the kth (k is an integral equal to or larger than 1) falling-ball test performed by employing a distance hk between the separator 130 and the ball, while the height of the ball hk+1 was changed to (hk+5 cm) in the (k+1)th falling-ball test in the case where no break was observed. The falling-ball test was repeated until the number of the falling-ball tests in which the break was observed and the number of the falling-ball tests in which no break was observed each reached five, and the lowest height of the ball in the falling-ball test in which the break was observed was determined as the minimum height.
The separator 130 was cut into a tape shape into the MD×TD of 62 mm×30 cm, and one terminal of the MD was attached to a scale weight of 300 g, while the other terminal was wound on a stainless-steel scale (model 13131 manufactured by Shinwa Rules Co., Ltd.) five times. The stainless-steel scale has a bent knob at a terminal in the longitudinal direction, and the separator 130 was wound so that the TD of the separator and the longitudinal direction of the stainless-steel scale are parallel to each other. After that, the stainless-steel scale was extracted toward the side on which the bent knob is formed at a rate of approximately 8 cm/s, and a feeling of easiness of extraction (extraction feeling) was evaluated. Specifically, a case where the scale was smoothly extracted without feeling any resistance was evaluated as “+”, a case where a slight resistance was felt was evaluated as “±”, and a case where a resistance was sensed and a hardness of extraction was felt was evaluated as “−”.
The width of the portion of the TD of the separator 130 wound five times was measured with a caliper before and after extracting the stainless-steel scale, and a variation (mm) therebetween was calculated. This variation is an elongation of the separator in the extraction direction when the winding start of the separator moves in the extraction direction of the stainless-steel scale due to the friction between the stainless-steel scale and the separator 130 and the separator deforms into a helical shape.
As illustrated in
Next, the sledge 220 having a lower surface stuck with the separator 130 was placed on a plate 224 processed with a fluorine resin (a plate subjected to SILVERSTONE™ processing). A scale weight 226 was disposed on the sledge 220. A total weight of the scale weight 226 and the sledge 220 was 1800 g. As shown in
A string (Super Cast PE Tou No. 2 manufactured by SUNLINE CO, LTD.) was attached to the sledge 220, and the sledge 220 was pulled at a rate of 20 mm/min using an Autograph (model AG-I manufactured by Shimadzu Corporation) via a pully 228 to measure a tension thereof. This tension indicates the friction between the plate 224 and the separator 130. The pin-extracting resistance was calculated according to the following equation by using the tension F (N) at the 10 mm advanced point from the starting point of the measurement.
Pin-extracting resistance=F×1000/(9.80665/1800)
The increase in internal resistance of the secondary batteries, prepared according to the aforementioned method, after a charging/discharging cycle was obtained as follows. The secondary batteries were subjected to four-cycles of charging/discharging where one cycle is performed with a current of 0.2 C in a voltage range from 4.2 V to 2.7 V at 55° C. (A current which discharges a regulated capacity at a one-hour rate discharge capacity is defined as 1 C. The same definition is applied below). After that, a voltage with an amplitude of 10 mV was applied to the secondary batteries at 25° C. using an LCR meter (chemical impedance meter model 3532-80 manufactured by HIOKI E.E. CORPORATION) to measure alternating-current impedances of the secondary batteries.
An equivalent series resistance (Rs1: Ω) at a frequency of 10 Hz and an equivalent series resistance (Rs2: Ω) at a reactance of 0 were read from the measurement results, and a resistance (R1: Ω) corresponding to their difference was calculated according to the following equation:
R
1:(Ω)=Rs1−Rs2
where Rs1 mainly indicates a total resistance including a resistance (liquid resistance) when a Li+ ion permeates the separator, a conduction resistance in the positive and negative electrodes, and a resistance of an ion passing through an interface between the positive electrode and the electrolyte solution. Hence, R1 shows a summation of the resistance in the positive and negative electrodes and the resistance of the ion passing through the interfaces between the positive and negative electrodes and the electrolyte solution.
After measuring the resistance R1, the secondary batteries were subjected to the charging/discharging cycle test for 100 cycles where a constant current in a voltage range from 4.2 V to 2.7 V was applied at 55° C. with one cycle set at a charging current of 10 and a discharging current of 100. After that, a voltage with an amplitude of 10 mV was applied to the secondary batteries at 25° C. using an LCR meter (chemical impedance meter model 3532-80 manufactured by HIOKI E.E. CORPORATION) to measure the alternating-current impedances of the secondary batteries.
Similar to the calculation of the resistance R1, an equivalent series resistance (Rs3: Ω) at a frequency of 10 Hz and an equivalent series resistance (Rs4: Ω) at a reactance of 0 were read from the measurement results, and a resistance (R2: Ω) indicating a summation of the conduction resistance in the positive and negative electrodes and the resistance of the ion passing through the interfaces between the positive and negative electrodes and the electrolyte solution after the 100 cycles was calculated according to the following equation.
R
2:(Ω)=Rs3−Rs4
The properties of the separators of the Examples 1 to 3 and the Comparative Examples 1 and 2 as well as those of the secondary batteries fabricated using the separators are summarized in Table 1. As shown in Table 1, the light-duty bulk densities of the polyolefin-resin composites serving as raw materials of the Examples 1 to 3 are as high as 500 g/L. This is probably because calcium carbonate was added after the ultrahigh-molecular weight polyethylene powder, the polyethylene wax, and the antioxidants were uniformly mixed and then mixing was carried out again so that the ultrahigh-molecular weight polyethylene, calcium carbonate, the polyethylene wax, and the antioxidants were uniformly mixed. On the other hand, in the Comparative Example 1, the light-duty bulk density of the polyolefin-resin composite is as low as 350 g/L, which suggests that a uniform mixing was not achieved. It is considered that the polyethylene crystals isotropically grow on a microlevel by stretching the sheet prepared with the uniformly mixed polyolefin-resin composite, followed by annealing. Hence, it can be understood that the parameters X of the separators of the Examples 1 to 3 indicative of the anisotropy of the tan δ are as small as 20 or less. Note that the light-duty bulk density of the polyolefin-resins composite is unknown because the Example 2 is a commercially available product.
Moreover, it was confirmed that the separators 130 of the Examples 1 to 3 have the parameter X equal to or less than 20 and the minimum height of the falling-ball test equal to or more than 50 cm and equal to or less than 150 cm. In contrast, the separators of the Comparative Examples 1 and 2 have the parameter X more than 20, and the minimum height remains as low as 40 cm or less. It is considered that the proportion of the skin layer is low in the Examples 1 to 3 than that in the Comparative Examples 1 and 2 due to the large thicknesses of the first layers 132 at the time of rolling. It was also confirmed that the trimming processability and the extraction feeling are preferred and the variation in the width after the extraction is as small as 0.04 mm or less in the Examples 1 to 3. This is probably because, as described above, the separators 130 of the Examples 1 to 3 have a smaller proportion of the skin layer than the separators 130 of the Comparative Examples 1 and 2 so that the orientation balance between the MD and TD falls within an appropriate range. Moreover, it was proven that the pin-extracting resistance exceeds 0.1 N in the Comparative Examples 1 and 2. The pin-extracting resistance relates to the friction of the separator 130 and indicates the easiness of pin extraction when a wound secondary battery is fabricated. Hence, a decrease in the pin-extracting resistance improves the slip property with respect to the pin, which contributes to a reduction in a production takt time of a secondary battery.
It was also found that an increase in the internal resistance of the secondary battery is small when the separators of Example 1 to 3 are used. On the other hand, the use of the separators 130 of the Comparative Examples 1 and 2 was found to increase the internal resistance of the secondary battery. That is, it was proven that the increase in internal resistance remarkably changes when the parameter X reaches 20 and that excellent results are demonstrated in the Examples 1 to 3 in which the parameter X is equal to or less than 20 so that the increase in the internal resistance after the charging/discharging cycle is suppressed.
From the results mentioned above, it can be concluded that the use of the separator having the parameter X equal to or less than 20 and the minimum height in the falling-ball test equal to or more than 50 cm and equal to or less than 150 cm allows production of a secondary battery exhibiting a small increase in the internal resistance in a short manufacturing takt time in a high yield. Hence, implementation of the present embodiment enables high-productivity production of a highly reliable secondary battery.
The aforementioned modes described as the embodiments of the present invention can be implemented by appropriately combining with each other as long as no contradiction is caused. Furthermore, any mode which is realized by persons ordinarily skilled in the art through the appropriate addition, deletion, or design change of elements is included in the scope of the present invention as long as it possesses the concept of the present invention.
It is understood that another effect different from that provided by the modes of the aforementioned embodiments is achieved by the present invention if the effect is obvious from the description in the specification or readily conceived by persons ordinarily skilled in the art.
100: Secondary battery, 110: Positive electrode, 112: Positive-electrode current collector, 114: Positive-electrode active-substance layer, 120: Negative electrode, 122: Negative-electrode current collector, 124: Negative-electrode active-substance layer, 130: Separator, 132: First layer, 134: Porous layer, 140: Electrolyte solution, 200: Frame, 202: Opening, 204: Plate, 206: Clamp, 210: Tape, 232: Cutter Knife, 220: Sledge, 222: Protrusion, 224: Plate, 228: Pully
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2016/081480 | 10/24/2016 | WO | 00 |
