COMPOSITION FOR HEAT-RESISTANT POROUS LAYER, SEPARATOR COMPRISING THE SAME AND ELECTROCHEMICAL BATTERY USING THE SAME
专利汇可以提供COMPOSITION FOR HEAT-RESISTANT POROUS LAYER, SEPARATOR COMPRISING THE SAME AND ELECTROCHEMICAL BATTERY USING THE SAME专利检索，专利查询，专利分析的服务。并且Disclosed herein is a composition for a heat resistant porous layer, a separator including the heat resistant porous layer formed from said composition, and an electrochemical battery including the separator. The composition for the heat resistant porous layer includes:
at least one selected from the group consisting of a monomer, oligomer, and polymer represented by Formula 1, and a mixture thereof;
at least one selected from the group consisting of a polyvinylidene fluoride (PVdF)-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof;
an initiator; and
a solvent,
wherein a unit originating from hexafluoropropylene is present in an amount of >0 wt% to ≤ 15 wt% based on the total weight of the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and the polyvinylidene fluoride-hexafluoropropylene-based copolymer has a weight average molecular weight of ≥ 600,000 g/mol.
Furthermore disclosed herein is a separator comprising a porous substrate and a heat resistant porous layer
wherein the heat resistant porous layer comprises polymers of PVdF and/or PVdF-HFP and a crosslinkable binder and the separator has a tensile strength of 50 kgf/cm 2 to 350 kgf/cm 2 , as measured after being left at 200°C for 10 minutes.
Furthermore disclosed is an electrochemical battery, comprising: an anode; a cathode; said separator; and an electrolyte.，下面是COMPOSITION FOR HEAT-RESISTANT POROUS LAYER, SEPARATOR COMPRISING THE SAME AND ELECTROCHEMICAL BATTERY USING THE SAME专利的具体信息内容。
The present invention relates to a heat resistant porous layer composition having high heat resistance, a separator including the heat resistant porous layer composition and having excellent fracture resistance at high temperature, an electrochemical battery using the separator, and a method for fabricating the separator.
A separator for an electrochemical battery refers to an intermediate film which isolates an anode from a cathode in a battery and consistently maintains ionic conductivity, thereby allowing charging/discharging of the battery.
Upon short circuit of a battery, high current flows therethrough while generating heat, thereby causing increase in temperature of the battery and thermal runaway. As a result, an electrolyte evaporates or is heated, causing a safety valve to be operated or the battery to catch fire. To prevent these problems, there has been proposed a method using a separator including a porous structure formed of a heat-meltable resin, in which the separator provides shutdown properties, i.e. melts, at a predetermined temperature or more to allow pores to be blocked, thereby stopping reactions in a battery and suppressing heat generation.
However, a large rechargeable battery has poor heat dissipation as compared with a smaller one and thus generates an increased amount of heat, which causes the internal temperature of the battery to be increased to a temperature of 200°C or more in a few seconds. In this case, a separator formed of a heat-meltable resin not only melts to allow pores to be blocked, but also suffers meltdown (see Korean Patent Publication No.
Therefore, there is a need for a separator which can maintain a form thereof without being fractured even in an environment in which the internal temperature of the battery is increased to a temperature of 200°C or more in a few seconds, as in a large rechargeable battery, while exhibiting excellent adhesion.
Korean Patent Publication No.
It is an aspect of the present invention to provide a separator which can maintain a form thereof without being fractured even in an environment in which the internal temperature of a battery is increased to 200°C or more in a few seconds while exhibiting excellent adhesion, and an electrochemical battery using the same.
In accordance with one aspect of the present invention, a heat resistant porous layer composition for a separator of an electrochemical battery includes: at least one selected from the group consisting of a monomer, oligomer, and polymer represented by Formula 1, and a mixture thereof; at least one selected from the group consisting of a polyvinylidene fluoride (PVdF)-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof; an initiator; and a solvent, wherein a unit originating from hexafluoropropylene is present in an amount of >0 wt% to ≤15 wt% based on the total weight of the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and the polyvinylidene fluoride-hexafluoropropylene-based copolymer has a weight average molecular weight of ≥600,000 g/mol;
where X1 to X3 are each independently an oxyethylene group; X4 is an oxyethylene group or a C1 to 10 alkyl group; R1 to R4 are each independently any one selected from the group consisting of a (meth)acrylate group, a hydroxy group, a carboxyl group, an ester group, a cyanate group, an isocyanate group, an amino group, a thiol group, a C1 to C10 alkoxy group, a vinyl group, and a heterocyclic group; a1 to a4 are each independently an integer from 1 to 10; n1 to n3 are each independently an integer from 0 to 10; and at least one of n1 to n4 is an integer from 1 to 10 (when X4 is an oxyethylene group, n4 is an integer from 1 to 10 and m is 1, and when X4 is a C1 to C10 alkyl group, n4 is 1 and m is 0).
In accordance with another aspect of the present invention, a separator of an electrochemical battery includes: a porous substrate; and a heat resistant porous layer formed on one or both surfaces of the porous substrate, wherein the heat resistant porous layer includes a crosslinkable binder and a non-crosslinkable binder, the non-crosslinkable binder including at least one selected from the group consisting of a polyvinylidene fluoride-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof, and the separator has a tensile strength of ≥ 50 kgf/cm2 to 350 kgf/cm2, as measured after being left at 200°C for 10 minutes.
In accordance with a further aspect of the present invention, a method for fabricating a separator of an electrochemical battery includes coating the heat resistant porous layer composition as set forth above onto one or both surfaces of a porous substrate, followed by curing the composition to form a heat resistant porous layer.
In accordance with yet another aspect of the present invention, there is provided an electrochemical battery, particularly a lithium rechargeable battery, including the separator of an electrochemical battery as set forth above.
A separator according to embodiments of the present invention can maintain a form thereof without being fractured even in an environment in which the internal temperature of a battery is increased to 200°C or more in a few seconds. Specifically, the separator exhibits excellent properties in terms of fracture resistance at high temperature, tensile strength after being left at 200°C for 10 minutes, and thermal shrinkage. Thus, the separator is not fractured even when charged/discharged for a long time, and a battery fabricated using the separator can exhibit high-efficiency charge/discharge properties and can avoid deterioration in performance. In addition, the separator can have excellent air permeability and adhesion to a substrate, thereby enhancing battery performance, such as battery reliability.
Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings. In addition, descriptions of details apparent to those skilled in the art will be omitted for clarity.
A separator according to one embodiment of the present invention includes a porous substrate and a heat resistant porous layer formed on one or both surfaces of the porous substrate.
According to one aspect the unit originating from hexafluoropropylene is present in an amount of > 0 wt% to ≤ 15 wt% based on the total weight of the polyvinylidene fluoride-hexafluoropropylene-based copolymer, wherein the total weight is calculated on a polyvinylidene fluoride-hexafluoropropylene-based copolymer having a weight average molecular weight of ≥ 600,000 g/mol to ≤ 1,700,000 g/mol, specifically, ≥ 700,000 g/mol to ≤ 1,200,000 g/mol.
The term "weight average molecular weight" herein may be determined from a polystyrene equivalent value by using GPC (Gel Permeation Chromatography).
The term "unit" especially means and/or includes repeating unit or not repeating unit in a homopolymer and/or copolymer.
According to one aspect, a heat resistant porous layer composition for a separator of an electrochemical battery, comprising:
- at least one selected from the group consisting of a monomer, oligomer, and polymer represented by Formula 1, and a mixture thereof;
- at least one selected from the group consisting of a polyvinylidene fluoride (PVdF)-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof;
- ≥ 1 wt% to ≤ 15 wt% of an initiator, based on the total weight of at least one selected from the group consisting of the monomer, the oligomer, and the polymer represented by Formula 1, and the mixture thereof; and
- ≥ 60 wt% to ≤ 98 wt% of a solvent, based on the total weight of at least one selected from the group consisting of the monomer, the oligomer, and the polymer represented by Formula 1, and the mixture thereof;
- wherein the unit originating from hexafluoropropylene is present in an amount of > 0 wt% to ≤ 15 wt%, wherein the wt% range is based on the total weight of a polyvinylidene fluoride-hexafluoropropylene-based copolymer having a weight average molecular weight of ≥ 600,000 g/mol to ≤ 1,700,000 g/mol, specifically, ≥ 700,000 g/mol to ≤ 1,200,000 g/mol;
where X1 to X3 are each independently an oxyethylene group; X4 is an oxyethylene group or a C1 to C10 alkyl group; R1 to R4 are each independently any one selected from the group consisting of a (meth)acrylate group, a hydroxy group, a carboxyl group, an ester group, a cyanate group, an isocyanate group, an amino group, a thiol group, a C1 to C10 alkoxy group, a vinyl group, and a heterocyclic group; a1 to a4 are each independently an integer from 1 to 10; n1 to n3 are each independently an integer from 0 to 10; and at least one of n1 to n4 is an integer from 1 to 10, and when X4 is an oxyethylene group, n4 is an integer from 1 to 10 and m is 1, and when X4 is a C1 to C10 alkyl group, n4 is 1 and m is 0.
The porous substrate may include any suitable porous substrate so long as the porous substrate has numerous pores and can be used in typical electrochemical devices. The porous substrate may be a polymer film formed of at least one selected from the group consisting of polyethylene, polypropylene, polyethylene terephthalate, polybutylene terephthalate, polyester, polyacetal, polyamide, polyimide, polycarbonate, polyether ether ketone, polyaryl ether ketone, polyetherimide, polyamideimide, polybenzimidazole, polyethersulfone, polyphenylene oxide, a cyclic olefin copolymer, polyphenylene sulfide, polyethylene naphthalene, or mixtures thereof, without being limited thereto. Alternatively, the porous substrate may take the form of a non-woven fabric. By way of example, the porous substrate may be a polyolefin-based substrate, which has excellent shutdown properties, thereby enhancing battery stability. The polyolefin-based substrate may be selected from the group consisting of a polyethylene monolayer, a polypropylene monolayer, a polyethylene/polypropylene bilayer, a polypropylene/polyethylene/polypropylene trilayer, and a polyethylene/polypropylene/polyethylene trilayer. By way of another example, the polyolefin-based resin may include a non-olefin resin in addition to an olefin resin, or may include a copolymer of olefin and non-olefin monomers. The porous substrate may have a thickness of ≥ 1 µm to ≤ 40 µm, specifically ≥ 5 µm to ≤ 15 µm, more specifically ≥ 5 µm to ≤ 10 µm. Within this range of thickness of the porous substrate, it is possible to fabricate a separator which has an appropriate thickness, that is, is thick enough to prevent short circuit between an anode and a cathode of a battery and is not so thick as to increase internal resistance of the battery.
The heat resistant porous layer may include a crosslinkable binder and a non-crosslinkable binder, and be formed of a heat resistant porous layer composition. In one embodiment, the heat resistant porous layer composition may include: at least one selected from the group consisting of a monomer, oligomer, and polymer represented by Formula 1, and a mixture thereof; a non-crosslinkable binder; an initiator; and a solvent.
where X1 to X3 are each independently an oxyethylene group; X4 is an oxyethylene group or a C1 to C10 alkyl group; R1 to R4 are each independently any one selected from the group consisting of a (meth)acrylate group, a hydroxy group, a carboxyl group, an ester group, a cyanate group, an isocyanate group, an amino group, a thiol group, a C1 to C10 alkoxy group, a vinyl group, and a heterocyclic group; a1 to a4 are each independently an integer from 1 to 10; n1 to n3 are each independently an integer from 0 to 10; and at least one of n1 to n4 is an integer from 1 to 10 (when X4 is an oxyethylene group, n4 is an integer from 1 to 10 and m is 1, and when X4 is a C1 to C10 alkyl group, n4 is 1 and m is 0).
The ester group may be represented by -COOR; and the amino group may be represented by -NRaRb, where R, Ra and Rb may be each independently any one selected from the group consisting of a C1 to C20 alkyl group, a C2 to C20 alkenyl group, a C2 to C20 alkynyl group, a C3 to C20 cycloalkyl group, a C3 to C20 cycloalkenyl group, a C4 to C20 cycloalkynyl group, and a C6 to C30 aryl group. In addition, the heterocyclic group may be any one selected from the group consisting of a C2 to C20 heterocyclo alkyl group, a C3 to C20 heterocyclo alkenyl group, a C3 to C20 heterocyclo alkynyl group, and a C6 to C20 heteroaryl group and may include a heteroatom selected from N, O, and S. For example, the heterocyclic group may include an epoxy group, an oxetane group, and the like. Specifically, the monomer, oligomer, or polymer represented by Formula 1 may be a compound represented by Formula 2 or Formula 3:
where R5 may be a C1 to C10 alkyl group; n5 to n7 may be each independently an integer from 1 to 5; and a5 to a12 may be each independently an integer from 1 to 10.
Examples of a compound represented by Formula 1 may include ethoxylated pentaerythritol tetraacrylate and ethoxylated trimethylolpropane triacrylate, without being limited thereto.
The heat resistant porous layer may include a crosslinkable binder formed by heat curing or photocuring at least one selected from the group consisting of the monomer, the oligomer, the polymer, and a mixture thereof. The crosslinkable binder can enhance dimensional stability of the heat resistant porous layer and heat resistance of the separator. In addition, the separator has excellent wettability to an electrolyte and thus can improve charging/discharging properties of a battery when used in the battery.
The non-crosslinkable binder may be selected from among polyvinylidene fluoride (PVdF)-based polymers. The polyvinylidene fluoride-based polymer may be a polyvinylidene fluoride-based homopolymer, a polyvinylidene fluoride-based copolymer, or a mixture thereof. The polyvinylidene fluoride-based homopolymer refers to a polymer obtained by polymerization of a vinylidene fluoride (VDF) monomer alone or by polymerization of a vinylidene fluoride monomer and ≥ 0 wt% to ≤ 5 wt% of a monomer other than the vinylidene fluoride monomer. Here, the polyvinylidene fluoride-based homopolymer does not include a hexafluoropropylene (HFP) monomer as the monomer other than the vinylidene fluoride monomer. Specifically, the polyvinylidene fluoride-based homopolymer may include a unit originating from the vinylidene fluoride monomer alone, or may further include ≥ 0 wt% to ≤ 5 wt% of the unit originating from the monomer other than the vinylidene fluoride monomer, wherein the unit originating from the monomer other than the vinylidene fluoride monomer does not include a unit originating from a hexafluoropropylene HFP monomer. The polyvinylidene fluoride copolymer refers to a copolymer obtained by polymerization of a vinylidene fluoride monomer and a monomer other than the vinylidene fluoride monomer, for example, a copolymer including the unit originating from a hexafluoropropylene monomer in addition to the unit originating from a vinylidene fluoride monomer or a copolymer including greater than 5 wt% of a unit originating from a monomer other than the vinylidene fluoride monomer and the hexafluoropropylene monomer. The polyvinylidene fluoride copolymer may include a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer including a unit originating from vinylidene fluoride and a unit originating from hexafluoropropylene. The polyvinylidene fluoride-hexafluoropropylene copolymer may include a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based binary polymer or a ter- or more polymer further including units other than a unit originating from a vinylidene fluoride monomer and a unit originating from a hexafluoropropylene monomer. Although the above units are described as originating from monomers, the present invention is not limited thereto and the units may originate from oligomers and the like.
Specifically, the non-crosslinkable binder may be a polyvinylidene fluoride-based homopolymer. The polyvinylidene fluoride-based homopolymer can improve adhesion of the heat resistant porous layer formed of the heat resistant porous layer composition to the porous substrate and can enhance fracture resistance at high temperature or tensile strength of the separator when used together with the monomer, oligomer, or polymer represented by Formula 1. The polyvinylidene fluoride-based homopolymer may have a weight average molecular weight (Mw) of ≥ 400,000 g/mol to ≤ 1,700,000 g/mol. Specifically, the polyvinylidene fluoride-based homopolymer may have a weight average molecular weight (Mw) of ≥ 400,000 g/mol to ≤ 1,500,000 g/mol, more specifically ≥ 400,000 g/mol to ≤ 1,200,000 g/mol. When a polyvinylidene fluoride-based homopolymer having a weight average molecular weight in the above range is used, it is possible to fabricate a battery which exhibits enhanced adhesion between the separator and the porous substrate even after charge/discharge of the battery, thereby providing efficient electrical output.
Alternatively, the non-crosslinkable binder may be a polyvinylidene fluoride-hexafluoropropylene-based copolymer which has a weight average molecular weight (Mw) of ≥ 600,000 g/mol to ≤ 1,700,000 g/mol and in which the unit originating from hexafluoropropylene is present in an amount of > 0 wt% to ≤ 15 wt%. When a polyvinylidene fluoride-hexafluoropropylene-based copolymer having a weight average molecular weight and a content of the unit originating from hexafluoropropylene in the above range is used, it is possible to enhance fracture resistance at high temperature or tensile strength of the separator and to fabricate a battery which exhibits enhanced adhesion between the separator and the porous substrate even after charge/discharge of the battery, thereby providing efficient electrical output.
A weight ratio of at least one selected from the group consisting of the monomer, oligomer, and polymer represented by Formula 1, and a mixture thereof to at least one selected from the group consisting of the polyvinylidene fluoride-based homopolymer, the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof may range from 8:2 to 2:8, specifically from 6.5:3.5 to 3.5:6.5. Within this range of weight ratio, desired heat resistance and adhesion of the heat resistant porous layer can be advantageously satisfied.
The initiator serves to initiate crosslinking of at least one selected from the group consisting of the monomer, the oligomer, the polymer, and a mixture thereof to form crosslinks. The initiator may be properly selected depending upon the kind of a terminal reactive group of at least one selected from the group consisting of the monomer, the oligomer, the polymer, and a mixture thereof. For example, the initiator may include a thermal polymerization initiator such as peroxide, azo, amine, imidazole, or isocyanate initiators, or a photopolymerization initiator such as onium salts or organic metal salts. Examples of the peroxide initiator may include t-butyl peroxy laurate, 1,1,3,3-t-methylbutylperoxy-2-ethylhexanoate, 2,5-dimethyl-2,5-di(2-ethylhexanoylperoxy)hexane, 1-cyclohexyl-1-methylethylperoxy-2-ethylhexanoate, 2,5-dimethyl-2,5-di(m-toluoylperoxy)hexane, t-butyl peroxy isopropyl monocarbonate, t-butyl peroxy-2-ethylhexyl monocarbonate, t-hexyl peroxy benzoate, t-butyl peroxy acetate, dicumyl peroxide, 2,5,-dimethyl-2,5-di(t-butyl peroxy) hexane, t-butyl cumyl peroxide, t-hexyl peroxy neodecanoate, t-hexyl peroxy-2-ethyl hexanoate, t-butyl peroxy-2-2-ethylhexanoate, t-butyl peroxy isobutyrate, 1,1-bis(t-butyl peroxy)cyclohexane, t-hexyl peroxyisopropyl monocarbonate, t-butyl peroxy-3,5,5-trimethyl hexanoate, t-butyl peroxy pivalate, cumyl peroxy neodecanoate, di-isopropyl benzene hydroperoxide, cumene hydroperoxide, isobutyl peroxide, 2,4-dichloro benzoyl peroxide, 3,5,5-trimethyl hexanoyl peroxide, octanoyl peroxide, lauryl peroxide, stearoyl peroxide, succinic acid peroxide, benzoyl peroxide, 3,5,5-trimethyl hexanoyl peroxide, benzoyl peroxy toluene, 1,1,3,3-tetramethyl butyl peroxy neodecanoate, 1-cyclohexyl-1-methylethyl peroxy neodecanoate, di-n-propyl peroxy dicarbonate, di-isopropyl peroxy carbonate, bis(4-t-butyl cyclohexyl) peroxy dicarbonate, di-2-ethoxy methoxy peroxy dicarbonate, di(2-ethyl hexyl peroxy) dicarbonate, dimethoxy butyl peroxy dicarbonate, di(3-methyl-3-methoxy butyl peroxy) dicarbonate, 1,1-bis(t-hexyl peroxy)-3,3,5-trimethylcyclohexane, 1,1-bis(t-hexyl peroxy)cyclohexane, 1,1-bis(t-butyl peroxy)-3,3,5-trimethylcyclohexane, 1,1-(t-butyl peroxy)cyclododecane, 2,2-bis(t-butyl peroxy)decane, t-butyl trimethyl silyl peroxide, bis(t-butyl) dimethyl silyl peroxide, t-butyl triallyl silyl peroxide, bis(t-butyl) diallyl silyl peroxide, tris(t-butyl)allyl silyl peroxide, and the like. Examples of the azo initiator may include 2,2'-azobis(4-methoxy-2,4-dimethyl valeronitrile), dimethyl 2,2'-azobis(2-methyl propionate), 2,2'-azobis(N-cyclohexyl-2-methyl propionamide), 2,2-azobis(2,4-dimethyl valeronitrile), 2,2'-azobis(2-methyl butyronitrile), 2,2'-azobis[N-(2-propenyl)-2-methylpropionamide], 2,2'-azobis(N-butyl-2-methyl propionamide), 2,2'-azobis[N-(2-propenyl)-2-methyl propionamide], 1,1'-azobis(cyclohexane-1-carbonitrile), 1-[(cyano-1-methylethyl)azo]formamide, and the like. Examples of the isocyanate initiator may include polyisocyanates, such as an aliphatic polyisocyanate, alicyclic polyisocyanate, araliphatic polyisocyanate, aromatic polyisocyanate, and derivatives or modifiers thereof, and the like. For example, the isocyanate initiator may include trimethylenediisocyanate, tetramethylenediisocyanate, hexamethylenediisocyanate, pentamethylenediisocyanate, 1,2-propylenediisocyanate, 1,2-butylenediisocyanate, 2,3-butylenediisocyanate, 1,3-butylenediisocyanate, 2,4,4- or 2,2,4-trimethylhexamethylenediisocyanate, 2,6-diisocyanatemethylcaproate, lysine ester triisocyanate, 1,4,8-triisocyanateoctane, 1,6,11-triisocyanateundecane, 1,8-diisocyanate-4-isocyanatemethyloctane, 1,3,6-triisocyanatehexane, 2,5,7-trimethyl-1,8-diisocyanate-5-isocyanatemethyloctane, and the like. Examples of other thermal polymerization initiators may include benzophenone (BZP, Aldrich), 2,6-bis(azidobenzylidene)-4-methyl cyclohexanone (bisazido, Aldrich), 2,2-dimethoxy-2-phenylacetophenone, 1-benzoyl-1-hydroxycyclohexane, 2,4,6-trimethyl benzoyldiphenylphosphine oxide, 3-methyl-2-butenyltetramethylene sulfonium hexafluoroantimonate salt, ytterbium trifluoromethanesulfonate salt, samarium trifluoromethanesulfonate salt, erbium trifluoromethanesulfonate salt, dysprosium trifluoromethanesulfonate salt, lanthanum trifluoromethanesulfonate salt, tetrabutylphosphonium methanesulfonate salt, ethyltriphenylphosphonium bromide salt, benzyl dimethylamine, dimethylaminomethyl phenol, triethanolamine, 2-methyl imidazole, 2-ethyl-4-methyl imidazole, 1,8-diaza-bicyclo(5,4,0)undecene-7, triethylenediamine, tri-2,4-6-dimethyl aminomethyl phenol, and the like.
Examples of the photopolymerization initiator may include aryl sulfonium hexafluoroantimonate salt, diphenyl diiodonium hexafluorophosphate salt, diphenyl diiodonium hexaantimonium salt, ditolyliodonium hexafluorophosphate salt, 9-(4-hydroxyethoxyphenyl)thianthrenium hexafluorophosphate salt, and the like.
The initiator may be present in an amount of ≥ 1 wt% to ≤ 15 wt%, specifically ≥ 3 wt% to ≤ 10 wt% based on the total weight of at least one selected from the group consisting of the monomer, the oligomer, the polymer, and a mixture thereof. Within this range, the initiator can provide a desired crosslinking degree or curing degree.
In one embodiment, the composition may further include a crosslinking agent to adjust a degree of crosslinking, as needed. Examples of the crosslinking agent may include m- or p-divinylbenzene such as 1,4-cyclohexanediobismethacrylate, and ethylene glycol dimethacrylate, without being limited thereto.
The solvent is not particularly limited so long as the solvent can dissolve at least one selected from the group consisting of the monomer, the oligomer, the polymer, and a mixture thereof and/or dissolve or disperse the polyvinylidene fluoride-based homopolymer and the polyvinylidene fluoride-hexafluoropropylene-based copolymer. Examples of the solvent may include: C1 to C15 alcohols; hydrocarbon solvents such as aliphatic hydrocarbons, alicyclic hydrocarbons, and aromatic hydrocarbons; halogenated hydrocarbon solvents; ethers such as aliphatic ethers and alicyclic ethers; and mixtures thereof. For example, the solvent may include: ketones such as acetone, methylethyl ketone, methylbutyl ketone, methylisobutyl ketone, and cyclohexanone; ethers such as ethyl ether, dioxane, and tetrahydrobutane; esters such as methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, isobutyl acetate, pentyl acetate, and isopentyl acetate; alcohols such as butanol, 2-butanol, isobutyl alcohol, isopropyl alcohol, ethanol, and methanol; halogenated hydrocarbons such as dichloromethane, chloroform, dichloroethane, trichloroethane, tetrachloroethane, dichloroethylene, trichloroethylene, tetrachloroethylene, and chlorobenzene; or hydrocarbons such as n-hexane, cyclohexanol, methylcyclohexanol, benzene, and toluene, and the like.
Next, a separator according to another embodiment of the present invention will be described. Since a separator according to this embodiment includes substantially the same components as the separator according to one embodiment of the invention as set forth above, except that the heat resistant porous layer or the heat resistant porous layer composition further includes inorganic particles, the inorganic particles will be mainly described herein. The separator can have further enhanced heat resistance by further including the inorganic particles.
The inorganic particles are not particularly limited and may include any suitable inorganic particles generally used in the art. Examples of the inorganic particles may include Al2O3, SiO2, B2O3, Ga2O3, TiO2, and SnO2, without being limited thereto. These may be used alone or as a mixture thereof. In one embodiment, the inorganic particles may include, for example, Al2O3 (alumina). Although the size of the inorganic particles is not particularly limited, the inorganic particles may have an average particle diameter of ≥ 1 nm to ≤ 2,000 nm, for example, ≥ 100 nm to ≤ 1,000 nm, more specifically ≥ 300 nm to ≤ 600 nm. Within this range, the inorganic particles can be prevented from suffering deterioration in dispersibility and processability in the heat resistant porous layer composition, and the thickness of the heat resistant layer can be properly adjusted, thereby preventing deterioration in mechanical properties and increase in electrical resistance. In addition, the size of pores generated in the heat resistant porous layer can be properly adjusted, thereby reducing probability of occurrence of internal short circuit during charge/discharge of a battery.
The inorganic particles may be present in an amount of ≥ 50 wt% to ≤ 95 wt%, specifically 60 wt% to 95 wt%, more specifically 75 wt% to 95 wt%, even more specifically 75 wt% to 90 wt%, based on the total weight of the heat resistant porous layer in terms of solid content. Within this range, the inorganic particles can exhibit sufficient heat dissipation properties, thereby effectively suppressing thermal shrinkage of the separator when the separator is coated with the inorganic particles.
In preparation of the heat resistant porous layer composition, the inorganic particles may be added in the form of an inorganic dispersion in which the inorganic particles are dispersed in an appropriate solvent. Such a solvent is not particularly limited and may include any suitable solvent generally used in the art. For example, the solvent, in which the inorganic particles are dispersed, may include acetone. The inorganic dispersion may be prepared by any typical method, for example, by adding an appropriate amount of Al2O3 to acetone, followed by dispersion using a bead mill.
Next, a separator according to a further embodiment of the present invention will be described. A separator according to this embodiment includes substantially the same components as the separator according to the above embodiment except that a heat resistant porous layer further includes a non-crosslinkable binder other than at least one selected from the group consisting of the polyvinylidene fluoride-based homopolymer, the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and combinations thereof. Thus, such a non-crosslinkable binder other will be mainly described herein.
The heat resistant porous layer composition can exhibit further enhanced adhesion and heat resistance by further including the non-crosslinkable binder. For example, the non-crosslinkable binder may include at least one selected from the group consisting of other polyvinylidene fluoride polymers, polymethylmethacrylate, polyacrylonitrile, polyvinylpyrrolidone, polyvinylacetate, polyethylene oxide, cellulose acetate, cellulose acetate butyrate, cellulose acetate propionate, cyanoethylpullulan, cyanoethylpolyvinylalcohol, cyanoethylcellulose, cyanoethylsucrose, pullulan, carboxymethyl cellulose, acrylonitrile-butadiene-styrene copolymer, and combinations thereof. Here, other polyvinylidene fluoride polymers refer to polyvinylidene fluoride polymers other than the polyvinylidene fluoride-based homopolymer and the polyvinylidene fluoride-hexafluoropropylene-based copolymer according to the present invention.
In accordance with another aspect of the present invention, a separator includes a porous substrate; and a heat resistant porous layer formed on one or both surfaces of the porous substrate, wherein the heat resistant porous layer includes a crosslinkable binder and a non-crosslinkable binder, and the non-crosslinkable binder includes at least one selected from the group consisting of a polyvinylidene fluoride-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof, and wherein the separator has a tensile strength of 50 kgf/cm2 to 350 kgf/cm2, for example, 100 kgf/cm2 to 350 kgf/cm2, as measured after being left at 200°C for 10 minutes.
When the separator has a tensile strength of 50 kgf/cm2 to 350 kgf/cm2, as measured after being left at 200°C for 10 minutes, the separator cannot be fractured even when the internal temperature of a battery exceeds 200°C, thereby preventing deterioration in performance and stability of the battery.
The tensile strength may be measured by the following method, without being limited thereto. First, the separator is cut to a size of 5 cm×5 cm in the MD and the TD, and all sides of the separator are fixed to a plate using an imide tape. Then, the plate is placed in an oven at 200°C for 10 minutes, followed by stretching the separator using a tensile strength tester (3343, Instron Corporation) and measuring the tensile strength.
The separator can avoid being fractured after being left at 200°C for 10 minutes with all sides thereof fixed, as the method described above. Although such a method is an exemplary method for measuring fracture resistance at high temperature, the present invention is not limited thereto. The fracture resistance at high temperature refers to a property which allows the separator, all sides of which are fixed, to be resistant to being fractured without shrinking at high temperature. For example, the fracture resistance at high temperature may be evaluated by cutting the separator to a size of 5 cm×5 cm in the MD and the TD, fixing all sides of the separator to a plate using an imide tape, leaving the plate in an oven at 200°C for 10 minutes, and checking whether the separator is fractured with the naked eye. The fracture resistance at high temperature refers to a property which allows the separator, all sides of which are fixed, to be resistant to being fractured without shrinking at high temperature. Since the separator is fixedly interposed between an anode and a cathode in a battery, unlike typical indexes of heat resistance, such as a thermal shrinkage rate, the fracture resistance at high temperature may be usefully used as an index of heat resistance of the fixed separator. In the present invention, the crosslinkable binder may be formed by heat curing or photocuring at least one selected from the group consisting of the monomer, oligomer, polymer represented by Formula 1, and a mixture thereof.
The separator according to embodiments of the present invention or a separator fabricated by a method for fabricating a separator according to the present invention may have an air permeability of 300 sec/100 cc or less, specifically 200 sec/100 cc or less, more specifically from ≥ 100 sec/100 cc to ≤ 200 sec/100 cc. The air permeability of the separator refers to the time (unit: sec) that it takes 100 cc of air to pass through the separator, and may be measured using an instrument such as EG01-55-1MR (Asahi Seiko Co., Ltd.).
The separator including the heat resistant porous layer according to embodiments of the present invention may have a thermal shrinkage of 7% or less in the machine direction (MD) or the transverse direction (TD), specifically 6% or less, more specifically 5% or less, for example > 0% to ≤ 3% as measured after being left at 150°C for 60 minutes. The thermal shrinkage of the separator may be measured by any suitable method generally used in the art. The thermal shrinkage of the separator may be measured by the following method, without being limited thereto. The separator is cut into a specimen having a size of 5 cm×5 cm (width (MD)×length (TD)), and the specimen is left in a chamber at 150°C for 60 minutes, followed by measuring the degree to which the separator shrinks in the MD and the TD and calculating the thermal shrinkage based on the measured values.
The separator including the heat resistant porous layer according to embodiments of the present invention may have an adhesive strength to a porous substrate (hereinafter, "adhesive strength to a substrate") of 0.5 N or more, specifically 0.7 N or more, more specifically from ≥ 1 N to ≤ 10 N. When the separator has an adhesive strength to a substrate of 0.5 N or more, the heat resistant porous layer can exhibit excellent adhesion to a porous substrate, thereby maintaining battery performance for a long time. The adhesive strength to a substrate may be measured by a typical method (for example, ASTM-D903) generally used in the art without limitation. An example of the method for measuring the adhesive strength to a substrate of the separator is as follows: The separator is cut into a specimen having a size of 1.2 cm×5 cm (MD×TD), and the specimen is attached to a tape (Scotch, 3M Co., Ltd.) excluding about 5 mm of both ends thereof. Then, the specimen is grasped by an upper action grip of a UTM (Mode3343, Instron Corporation) at one end thereof not attached to the tape and is grasped by a lower action grip at a taped portion of the other end, followed by measuring a force required to peel the heat resistant porous layer off of the porous substrate, thereby finding the adhesive strength to a substrate.
Next, a method for fabricating a separator according to one embodiment of the present invention will be described. A method for fabricating a separator according to one embodiment includes preparing a heat resistant porous layer composition and applying the heat resistant porous layer composition to one or both surfaces of a porous substrate, followed by curing the composition to form a heat resistant porous layer, wherein the heat resistant porous layer composition includes: at least one selected from the group consisting of the monomer, oligomer, polymer represented by Formula 1, and a mixture thereof; at least one selected from the group consisting of a polyvinylidene fluoride-based homopolymer, a polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof; an initiator; and a solvent, and the unit originating from hexafluoropropylene is present in an amount of >0 wt% to ≤ 15 wt% based on the total weight of the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and the polyvinylidene fluoride-hexafluoropropylene-based copolymer has a weight average molecular weight of ≥ 600,000 g/mol to ≤ 1,700,000 g/mol.
Preparing a heat resistant porous layer composition may include mixing at least one selected from the group consisting of the monomer, oligomer, polymer represented by Formula 1, and a mixture thereof; at least one selected from the group consisting of the polyvinylidene fluoride-based homopolymer, the polyvinylidene fluoride-hexafluoropropylene-based copolymer, and a mixture thereof; the initiator; and the solvent, followed by stirring at 10°C to 40°C for 30 min to 5 hours. Here, mixing may be performed using a ball mill, a bead mill, or a screw mixer.
The heat resistant porous layer composition may further include inorganic particles and/or other non-crosslinkable binders. The inorganic particles and/or other non-crosslinkable binders are as described above.
Then, a porous heat resistant layer is formed on one or both surfaces of the porous substrate using the heat resistant porous layer composition. Before forming the heat resistant porous layer, one or both surfaces of the porous substrate may be optionally subjected to post-treatment such as sulfonation treatment, graft treatment, corona discharge treatment, UV irradiation treatment, plasma treatment, or sputter etching treatment to enhance adhesion to the porous heat resistant layer. After post-treatment, the heat resistant porous layer may have, for example, an island shape or a thin-film shape.
Forming a heat resistant porous layer on the porous substrate using the heat resistant porous layer composition may be performed by any suitable method generally used in the art, for example, coating, lamination, and coextrusion, without being limited thereto. Examples of coating may include dip coating, die coating, roll coating, and comma coating. These methods may be used alone or in combination thereof. For example, the heat resistant porous layer of the separator may be formed by dip coating.
Then, the porous heat resistant layer may be optionally dried. This allows a solvent used in preparing the heat resistant porous layer composition to be volatilized. In drying, it is possible to minimize residues of the solvent in the heat resistant porous layer composition through adjustment of temperature and time. For example, drying may be performed at ≥ 80°C to ≤ 100°C, specifically ≥ 80°C to ≤ 90°C for ≥ 5 sec to ≤ 60 sec, specifically ≥ 10 sec to ≤ 40 sec.
Thereafter, the porous heat resistant layer may be subjected to photocuring or heat curing. Specifically, photocuring may include UV curing and infrared curing, for example, UV curing. Photocuring may include irradiation of the porous heat resistant layer at a fluence of ≥ 500 mJ/cm2 to ≤ 3000 mJ/cm2, specifically ≥ 500 mJ/cm2 to ≤ 2000 mJ/cm2 per one surface. Irradiation may be performed for ≥ 1 min to ≤ 15 hours. After photocuring, heat treatment may be performed at a temperature of about 50°C to about 180°C for ≥ 1 to ≤ 10 hours to achieve uniform curing density. In addition, when the porous heat resistant layer is subjected to heat curing, heat curing may be performed at ≥ 60°C to ≤ 120°C for ≥ 1 to ≤ 36 hours, specifically at ≥ 80°C to ≤ 110°C for ≥ 5 to ≤ 24 hours. Such a curing process allows terminal reactive groups of at least one selected from the group consisting of the monomer, oligomer, polymer represented by Formula 1, and a mixture thereof to be combined with one another to form a crosslinkable binder.
The heat resistant porous layer may have a thickness of ≥ 1 µm to ≤ 15 µm, specifically ≥ 2 µm to ≤ 10 µm, more specifically ≥ 2 µm to ≤ 8 µm. Within this range, the heat resistant porous layer has a suitable thickness to obtain good thermal stability and adhesive strength, and can prevent excessive increase in thickness of the entire separator, thereby suppressing increase in internal resistance of a battery.
In accordance with a further aspect of the present invention, there is provided a rechargeable battery including: an anode; a cathode; the separator as set forth above disposed between the anode and the cathode; and an electrolyte. The rechargeable battery is not particularly limited and may include any typical battery known in the art.
Specifically, the rechargeable battery may be a lithium rechargeable battery such as a lithium metal rechargeable battery, a lithium ion rechargeable battery, a lithium polymer rechargeable battery, or a lithium ion polymer rechargeable battery.
The rechargeable battery may be fabricated by any method generally used in the art without limitation. An example of a method for fabricating the rechargeable battery is as follows: A separator including the heat resistant layer according to the present invention is disposed between the anode and the cathode of the battery, followed by filling the battery with the electrolyte.
Referring to
The separator 30 is as described above.
The anode 10 may include an anode current collector and an anode active material layer formed on the anode current collector. The anode active material layer may include an anode active material, a binder, and optionally a conductive material.
The anode current collector may include aluminum (Al) and nickel (Ni), without being limited thereto.
The anode active material may include a compound into or from which lithium ions can be reversibly intercalated or deintercalated. Specifically, the anode active material may include at least one selected among complex oxides or complex phosphates of lithium and a metal such as cobalt, manganese, nickel, aluminum, iron, or a combination thereof. More specifically, the anode active material may include a lithium-cobalt oxide, a lithium-nickel compound, a lithium-manganese oxide, a lithium-nickel-cobalt-manganese oxide, a lithium-nickel-cobalt-aluminum oxide, a lithium-iron phosphate, or a combination thereof.
The binder serves to allow particles of the anode active material to easily adhere to one another and to allow the anode active material to adhere to the anode current collector. Examples of the binder may include polyvinylalcohol, carboxymethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, polyvinyl chloride, carboxylated chloride, polyvinyl fluoride, an ethylene oxide-containing polymer, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, a styrene-butadiene rubber, an acrylated styrene-butadiene rubber, an epoxy resin, and nylon, without being limited thereto. These may be used alone or as a mixture thereof.
The conductive material serves to impart conductivity to an electrode. Examples of the conductive material may include natural graphite, synthetic graphite, carbon black, carbon fibers, metal powder, and metal fibers, without being limited thereto. These may be used alone or as a mixture thereof. The metal powder and the metal fibers may include a metal such as copper, nickel, aluminum, silver, and the like.
The cathode 20 may include a cathode current collector and a cathode active material layer formed on the cathode current collector.
The cathode current collector may include copper (Cu), gold (Au), nickel (Ni), and a copper alloy, without being limited thereto.
The cathode active material layer may include a cathode active material, a binder, and optionally a conductive material.
The cathode active material may include a material into or from which lithium ions can be reversibly intercalated or deintercalated, metallic lithium, a metallic lithium alloy, a material capable of being doped with or dedoped from lithium, a transition metal oxide, or a combination thereof.
Examples of the material into or from which lithium ions can be reversibly intercalated or deintercalated may include carbon-based materials, for example, crystalline carbon, non-crystalline carbon, or a combination thereof. Examples of the crystalline carbon may include amorphous, plate-like, flake, spherical, or fibrous natural graphite or synthetic graphite. Examples of the non-crystalline carbon may include soft or hard carbon, mesophase pitch carbide, baked cokes, and the like. The metallic lithium alloy may include an alloy of lithium and a metal selected from the group consisting of Na, K, Rb, Cs, Fr, Be, Mg, Ca, Sr, Si, Sb, Pb, In, Zn, Ba, Ra, Ge, Al, and Sn. Examples capable of being doped with or dedoped from lithium may include Si, SiOx (0<x<2), a Si-C composite, a Si-Y alloy, Sn, SnO2, a Sn-C composite, Sn-Y, and a mixture of at least one thereof and SiO2. The elemental Y may be selected from the group consisting of Mg, Ca, Sr, Ba, Ra, Sc, Y, Ti, Zr, Hf, Rf, V, Nb, Ta, Db, Cr, Mo, W, Sg, Tc, Re, Bh, Fe, Pb, Ru, Os, Hs, Rh, Ir, Pd, Pt, Cu, Ag, Au, Zn, Cd, B, Al, Ga, Sn, In, Tl, Ge, P, As, Sb, Bi, S, Se, Te, Po and a combination thereof. Examples of the transition metal oxide may include a vanadium oxide, a lithium-vanadium oxide, and the like.
The kinds of the binder and conductive material used in the cathode are the same as those of the binder and conductive material used in the anode.
Each of the anode and the cathode may be fabricated by preparing an active material composition by mixing the active material, the binder, and optionally the conductive material in a solvent, and applying the composition to the current collector. Here, the solvent may include N-methyl pyrrolidone, without being limited thereto. Since such a method for fabricating an electrode is well known in the art, detailed description thereof will be omitted herein.
The electrolyte may include an organic solvent and a lithium salt.
The organic solvent serves as a medium through which ions involved in electrochemical reactions of a battery can be migrated. Examples of the organic solvent may include a carbonate solvent, an ester solvent, an ether solvent, a ketone solvent, an alcohol solvent, and a nonprotonic solvent.
Examples of the carbonate solvent may include dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), methylpropyl carbonate (MPC), ethylpropyl carbonate (EPC), ethylmethyl carbonate (EMC), ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), and the like. Specifically, a carbonate solvent capable of increasing dielectric constant while exhibiting low viscosity may be prepared by mixing a chain type carbonate and an annular carbonate. Here, the annular carbonate and the chain type carbonate may be mixed in a volume ratio of 1:1 to 1:9.
Examples of the ester solvent may include methyl acetate, ethyl acetate, n-propyl acetate, dimethyl acetate, methyl propionate, ethyl propionate, γ-butyrolactone, decanolide, valerolactone, mevalonolactone, caprolactone, and the like. Examples of the ether solvent may include dibutyl ether, tetraglyme, diglyme, dimethoxy ethane, 2-methyl tetrahydrofuran, tetrahydrofuran, and the like. Examples of the ketone solvent may include cyclohexanone, and examples of the alcohol solvent may include ethyl alcohol, isopropyl alcohol, and the like.
Such organic solvents may be used alone or as a mixture thereof. When a mixture of the organic solvents is used, a mixing ratio of the organic solvents may be adjusted depending upon desired battery performance.
The lithium salt is dissolved in the organic solvent to serve as a source for lithium ions, thereby allowing basic operation of the rechargeable battery while promoting migration of lithium ions between the anode and the cathode.
Examples of the lithium salt may include LiPF6, LiBF4, LiSbF6, LiAsF6, LiN(SO3C2F5)2, LiN(CF3SO2)2, LiC4F9SO3, LiClO4, LiAlO2, LiAlCl4, LiN(CxF2x+1SO2)(CyF2y+1SO2) (x and y being a natural number), LiCl, LiI, LiB(C2O4)2, or a combination thereof.
The concentration of the lithium salt may range from 0.1 M to 2.0 M. Within this range, the electrolyte can have an appropriate conductivity and viscosity, thereby exhibiting excellent performance to allow lithium ions to effectively migrate.
The rechargeable battery according to a further aspect of the present invention may have a capacity retention after 100 cycles of ≥ 70% to ≤ 100%, specifically ≥ 80% to ≤ 100%.
Next, the present invention will be described in more detail with reference to examples, comparative examples, and experimental examples. However, it should be noted that these examples, comparative examples, and experimental examples are provided for illustration only and should not be construed in any way as limiting the invention.
7 wt% of a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer (KF9300, Kureha Chemicals, weight average molecular weight: 1,000,000 g/mol, HFP: 1 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-1 solution.
7 wt% of a polyvinylidene fluoride (PVdF)-based homopolymer (KF1100, Kureha Chemicals, weight average molecular weight: 300,000 g/mol, HFP: 0 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-2 solution.
7 wt% of a polyvinylidene fluoride (PVdF)-based homopolymer (Solef 5130, Solvay Specialty Polymers, weight average molecular weight: 1,100,000 g/mol, HFP: 0 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-3 solution.
7 wt% of a polyvinylidene fluoride (PVdF)-based homopolymer (Solef 6020, Solvay Specialty Polymers, weight average molecular weight: 660,000 g/mol, HFP: 0 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-4 solution.
7 wt% of a polyvinylidene fluoride (PVdF)-based homopolymer (Kynar HSV900, Arkema Chemicals, weight average molecular weight: 900,000 g/mol, HFP: 0 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-5 solution.
7 wt% of a polyvinylidene fluoride (PVdF)-based homopolymer (Kynar HSV800, Arkema Chemicals, weight average molecular weight: 800,000 g/mol, HFP: 0 wt%) and 93 wt% of dimethyl acetamide (DMAc, Daejung Chemicals & Metals Co., Ltd.) were mixed, followed by stirring at 40°C for 3 hours, thereby preparing a 1-6 solution.
10 wt% of a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer (Solef 21216, Solvay Specialty Polymers, weight average molecular weight: 570,000 g/mol, HFP: 12 wt%) and 90 wt% of acetone were mixed, followed by stirring at 40°C for 1 hour, thereby preparing a 2-1 solution.
10 wt% of a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer (Solef 21510, Solvay Specialty Polymers, weight average molecular weight: 300,000 g/mol, HFP: 15 wt%) and 90 wt% of acetone were mixed, followed by stirring at 40°C for 1 hour, thereby preparing a 2-2 solution.
10 wt% of a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer (Kynar Flex2801, Arkema Chemicals, weight average molecular weight: 300,000 g/mol, HFP: 10 wt%) and 90 wt% of acetone were mixed, followed by stirring at 40°C for 1 hour, thereby preparing a 2-3 solution.
10 wt% of a polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-based copolymer (Kynar Flex LBG, Arkema Chemicals, weight average molecular weight: 300,000 g/mol, HFP: 5 wt%) and 90 wt% of acetone were mixed, followed by stirring at 40°C for 1 hour, thereby preparing a 2-4 solution.
25 wt% of alumina having an average particle diameter (D50) of 500 nm (LS235, Nippon Light Metal Company Ltd.) was added to acetone, followed by dispersion at 25°C for 2 hours using a bead mill, thereby preparing an alumina dispersion. Then, 0.7 wt% of ethoxylated pentaerythritol tetraacrylate (PE-044, HANNONG Chemicals), 0.035 wt% of benzoyl peroxide, 6.6 wt% of the 1-1 solution prepared in Preparative Example 1-1, 55.4 wt% of the alumina dispersion, 37.265 wt% of acetone were mixed, thereby preparing a heat resistant porous layer composition. The prepared composition was dip-coated on both surfaces of a 7 µm thick polyethylene fabric (SKI Co., LTD.) to a thickness of 2 µm. Then, the coated layer was subjected to heat curing at 100°C for 24 hours, thereby fabricating a separator having an overall thickness of about 11 µm.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 1-2 solution prepared in Preparative Example 1-2 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 1-3 solution prepared in Preparative Example 1-3 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 1-4 solution prepared in Preparative Example 1-4 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 1-5 solution prepared in Preparative Example 1-5 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 1-6 solution prepared in Preparative Example 1-6 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that a heat resistant porous layer composition was prepared by mixing 82.665 wt% of acetone and 10 wt% of MeOH, which is a non-solvent (Daejung Chemicals & Metals Co., Ltd., purity: 99.9%) without using the alumina dispersion.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 2-1 solution prepared in Preparative Example 2-1 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 2-2 solution prepared in Preparative Example 2-2 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 2-3 solution prepared in Preparative Example 2-3 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
A separator was fabricated in the same manner as in Example 1 except that 6.6 wt% of the 2-4 solution prepared in Preparative Example 2-4 was used instead of 6.6 wt% of the 1-1 solution of Example 1.
The weight average molecular weights and contents (unit: wt%) of hexafluoropropylene (HFP) of the polyvinylidene fluoride-based homopolymers and the polyvinylidene fluoride-hexafluoropropylene-based copolymers used in Examples 1 to 7 and Comparative Examples 1 to 4 are shown in Table 1 and Table 2.
Compositions (unit: wt%) of each of the heat resistant porous layer compositions of Examples 1 to 7 and Comparative Examples 1 to 4 are shown in Table 3.
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was evaluated as to fracture resistance at high temperature, tensile strength after being left at 200°C for 10 minutes, air permeability, and adhesive strength. Results are shown in Table 4.
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was cut into a specimen having size of 5 cm×5 cm in the MD and TD. The specimens were fixed to a plate using an imide tape at all sides thereof, and the plate was placed in an oven (LO-FS050, Lk Lab Korea Co., Ltd.) at 200°C for 10 minutes, followed by checking whether the separator fractured. The specimen was rated as "fail" when suffering from fracture and rated as "pass" when not suffering from fracture.
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was cut into a specimen having size of 5 cm×5 cm in the MD and TD. The specimens were fixed to a plate using an imide tape at all sides thereof, and the plate was placed in an oven (LO-FS050, Lk Lab Korea Co., Ltd.) at 200°C for 10 minutes, followed by measuring tensile strength using a tensile strength tester (3343, Instron Corporation).
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was cut into a specimen having size of 100 mm×100 mm in the MD and TD, followed by measuring the time that it takes 100 cc of air to pass through the specimen using an air permeability tester (EG01-55-1MR, Asahi Seiko Co., Ltd.), thereby finding air permeability.
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was cut into a specimen having size of 1.2 cm (MD)×5 cm (TD), and the specimen was attached to a tape (Scotch, 3M Co., Ltd.) excluding about 5 mm of both ends thereof. Then, the specimen was grasped by an upper action grip of an UTM (Mode3343, Instron Corporation) at one of both ends thereof not attached to the tape and was grasped by a lower action grip at a taped portion of the other end, followed by measuring a force required to peel off the heat resistant porous layer from the porous substrate, thereby finding adhesive strength to a substrate.
Each of the separators fabricated in Examples 1 to 6 and Comparative Examples 1 to 4 was cut into a specimen having size of 10 cm×10 cm in the MD and TD, followed by marking dots at the center of the specimen and at points distanced 50 mm from the center in the MD and the TD, respectively. The specimens were left in an oven (LO-FS050, Lk Lab Korea Co., Ltd.) at 150°C for 1 hour, followed by measuring the distances between the marked dots, thereby calculating thermal shrinkage in the MD and the TD.
As shown in Table 4, it can be seen that the separators of Examples 1 to 6 including: the polyvinylidene fluoride-based homopolymer or the polyvinylidene fluoride-hexafluoropropylene-based copolymer having a weight average molecular weight of to 600,000 g/mol to ≤ 1,700,000 g/mol and comprising > 0 wt% to ≤ 15 wt% of the unit originating from hexafluoropropylene; and the crosslinkable binder according to the present invention had a tensile strength of 50 kgf/cm2 to 350 kgf/cm 2 as measured after being left at 200°C for 10 minutes, did not suffer from fracture even at a high temperature of 200°C, and exhibited a thermal shrinkage of 7%, for example > 0% to ≤ 3% and thus excellent heat resistance. Conversely, the separators of Comparative Examples 1 to 4 including: the polyvinylidene fluoride-hexafluoropropylene-based copolymer comprising > 0 wt% to ≤ 15 wt% of the unit originating from hexafluoropropylene on the total weight of the polyvinylidene fluoride-hexafluoropropylene-based copolymer having a weight average molecular weight of less than 600,000 g/mol; and the crosslinkable binder suffered from severe fracture, making measurement of tensile strength impossible, at a high temperature of 200°C and exhibited poor adhesive strength to a substrate as compared with those of Examples.
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