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    • 专利摘要:
    The present invention relates to a crosslinked copolymer comprising at least repeating units of poly (alkylene oxide) and at least recurring units of lithium polystyrene-sulfonyl (trifluoromethylsulfonyl) imide (PSTFSILi), the use of such a crosslinked copolymer for the preparation of a solid polymer electrolyte, a solid polymer electrolyte comprising said crosslinked copolymer, and a battery, for example Lithium Metal Polymer (LMP), comprising said solid polymer electrolyte Figure for the abstract: FIG. 6
    公开号:FR3088932A1
    申请号:FR1871953
    申请日:2018-11-27
    公开日:2020-05-29
    发明作者:Ekaterina Pavlenko；Phan TRANG；Adèle FERRAND；Didier Gigmes；Adrien Lassagne；Renaud Bouchet；Margaud LECUYER；Marc Deschamps
    申请人:Aix Marseille Universite；Institut Polytechnique de Grenoble；Blue Solutions SA；
    IPC主号:
    专利说明:

    Description
    Title of the invention: POLYMER ELECTROLYTE FOR LITHIUM METAL POLYMER BATTERY WITH IMPROVED PERFORMANCE The present invention relates to a crosslinked copolymer comprising at least repeating units of poly (alkylene oxide) and at least recurring units of polystyrene-sulfonyl (trifluoromethylsulfonyl) lithium imide (PSTFSILi), the use of such a crosslinked copolymer for the preparation of a solid polymer electrolyte, a solid polymer electrolyte comprising said crosslinked copolymer, and a battery, for example Lithium Metal Polymer (LMP) , comprising said solid polymer electrolyte.
    The invention applies typically and not exclusively to the field of Lithium Metal Polymer batteries, in particular for the production of electric vehicles and / or the storage of intermittent energies of the solar and / or wind type.
    Lithium Metal Polymer batteries currently on the market are in the form of a thin film wound several times or of several stacked thin films. This thin film wound or stacked has a thickness of the order of a hundred micrometers and comprises: a negative electrode (anode) ensuring the supply of lithium ions during discharge; a positive electrode (cathode) acting as a receptacle where the lithium ions are inserted; a solid polymer electrolyte conductive of lithium ions and situated between the positive electrode and the negative electrode; and a current collector connected to the positive electrode to provide the electrical connection. The negative electrode is generally made up of a sheet of metallic lithium or of a lithium alloy; the solid polymer electrolyte is generally composed of a polymer based on poly (ethylene oxide) (POE) and at least one lithium salt; the positive electrode usually comprises an active electrode material, for example based on metal oxide or based on phosphate of LiMPO 4 type where M represents a metal cation selected from the group Fe, Mn, Co, Ni and Ti , and one of the combinations of these cations, and possibly of carbon; moreover the current collector generally consists of a sheet of metal. The conductivity of the ions is ensured by the dissolution of the lithium salt in the POE. However, POE does not have sufficient mechanical strength at the temperatures usually used in an LMP battery (60-80 ° C) since it becomes a viscous liquid and loses its dimensional stability at these temperatures.
    Other (co) polymers based on POE have been described, such as random copolymers of poly (ethylene oxide-stat-propylene oxide) type (ie POE-stat-PPO), copolymers with polystyrene-b-POE type block (ie PS-b-POE), crosslinked POEs or copolymers comprising acrylate or methacrylate chains to which POE are connected, in particular in order to reinforce the mechanical properties. It has also been proposed to add to the POE-based polymer inorganic or organic particles, possibly nanometric, such as particles of aluminum oxide, titanium oxide or nanofibrils of cellulose. However, the ionic conductivities at 60 ° C. of the electrolytes based on such polymers remain low. Only the use of positive electrodes with a low grammage of active material (low surface capacity) and low currents (<C / 15) can recover a capacity at this temperature. The operating temperature of the batteries currently on the market is therefore 80 ° C. to obtain performance in accordance with the intended applications.
    In addition, attempts to improve the conductivity of POE by adding plasticizers have led to deterioration of the mechanical properties.
    Finally, in solid polymer electrolytes consisting of a lithium salt dissolved in a polyether polymer matrix such as POE doped with lithium salt, the fraction of the charge carried by lithium ions (also called cation transport number ) is weak (of the order of 0.2), due to the strong interaction between the lithium cation and the POE chains, which limits the electrical performance. The value of the cation transport number determines the share of current transported by the cation. A low cation transport number results in the formation of a salt concentration gradient in the thickness of the electrolyte during battery operation. This behavior generates a depletion of salt at the electrode, inducing an increase in the resistance of the electrolyte and reduced power performance, and promotes the formation of lithium dendrites, causing a decrease in faradic yield and ultimately, short -circuits.
    In order to remedy this problem, international application WO 2013/034848 describes di-block copolymers of type AB or tri-blocks of type BAB, in which block A is an unsubstituted poly (ethylene oxide) chain having a number average molecular mass less than or equal to 100 kDa and the block B is an anionic polymer capable of being prepared from one or more monomers chosen from vinyl monomers and derivatives, said monomers being substituted with T anion of a lithium sulfonyl (trifluoromethylsulfonyl) imide salt (TESILi) of the following formula:
    [Chem.l]
    Z / . u
    in which * represents the attachment point of the anion of said salt to said monomer via a covalent bond or a linear alkyl chain having from 1 to 5 carbon atoms. However, the AB type di-block or BAB type tri-block copolymers based on POE above, although having a transport number equal to 1, have a lower ionic conductivity than POE alone. Furthermore, their mechanical strength is not optimized.
    The object of the present invention is to overcome all or part of the drawbacks of the aforementioned prior art and to provide a polymer material, which can be used in a battery, in particular an LMP battery, in particular in a solid polymer electrolyte, said polymer material exhibiting good properties in terms of ionic conduction, in particular at a temperature greater than or equal to 60 ° C., number of cationic transport, and mechanical strength. It is also desirable to reduce or eliminate dendritic growth within a battery, in particular an LMP battery, and to guarantee good electrochemical performance, in particular in terms of resistance to cycling, faradic yield, said battery being able to be used in any security.
    These objects are achieved by the invention which will be described below.
    The first object of the invention is a crosslinked copolymer, characterized in that it comprises at least recurring units of lithium polystyrenesulfonyl (trifluoromethylsulfonyl) imide (PSTESILi) and at least recurring units of poly (alkylene oxide) chosen from poly (ethylene oxide) units, poly (propylene oxide) units, poly (ethylene and propylene oxide) units, and a mixture thereof, and in that said crosslinked copolymer is obtained by crosslinking of a tri-block copolymer of BAB type, in which:
    - block A is a crosslinkable poly (alkylene oxide) capable of being obtained from:
    * of at least one monomer chosen from ethylene glycol, propylene glycol, and their mixture, or from at least one oligomer of poly (alkylene oxide) chosen from poly (ethylene oxide), poly (propylene oxide), poly (ethylene and propylene oxide), and one of their mixtures, and * of at least one compound comprising at least one crosslinkable alkene or alkyne function, and
    each of the blocks B is an anionic polystyrene substituted by the anion of a lithium sulfonyl (trifluoromethylsulfonyl) imide salt (TFSILi) and corresponding to the following formula (I):
    [Chem. 2]
    in which n denotes the number of units of lithium styrenesulfonyl (trifluoromethylsulfonyl) imide for each of the blocks B.
    Thanks to the combination of repeating units of poly (alkylene oxide) and of recurring units of lithium polystyrene-sulfonyl (trifluoromethylsulfonyl) imide, and to crosslinking, said crosslinked copolymer has good properties in terms of number cation transport, ion conduction and mechanical strength, to be able to be used in a solid polymer electrolyte and / or in a composite electrode, in particular for an LMP battery.
    According to the invention, each block B preferably comprises from 4 to 31 units of lithium styrene-sulfonyl (trifluoromethylsulfonyl) imide (STFSILi), and even more preferably from 5 to 12 units of STFSILi. A particularly preferred value is 8 STFSILi patterns for each of the B blocks.
    The number-average molecular mass of a block B preferably ranges from 1.6 to 3.8 kDa.
    The lithium salt LiTFSI is directly grafted onto the polystyrene, which makes it possible to have a transport number of Li + cations equal to 1, while guaranteeing good mechanical strength and good ionic conduction, in particular by the crosslinking and the presence of poly (alkylene oxide) uniformly distributed in the copolymer.
    The crosslinked copolymer can comprise from 10 to 50% by mass approximately of PSTFSILi, and preferably from 13 to 28% by mass approximately of PSTFSILi, relative to the total mass of the crosslinked copolymer. A particularly preferred value is
    Approximately 22% by mass of PSTFSILi.
    The number average molecular weight of block A preferably ranges from 10 to 50 kDa, and even more preferably from 15 to 30 kDa. A particularly preferred value is 20 kDa.
    Block A preferably has a number average molecular weight less than or equal to 25 kDa.
    According to the invention, the block A preferably comprises from 227 to 1136 units of alkylene oxide, and even more preferably from 340 to 681 units of alkylene oxide. A particularly preferred value is 454 alkylene oxide units.
    Block A is preferably a poly (ethylene oxide) or a poly (ethylene and propylene oxide), and more preferably a poly (ethylene oxide).
    Block A preferably comprises a functional polymer of formula (II) below: [Chem. 3]
    - [COA-fUK- (H) in which R 1 is a substituent comprising at least one crosslinkable alkene or alkyne function; COA is a poly (alkylene oxide) chain chosen from the poly (ethylene oxide), poly (propylene oxide), poly (ethylene and propylene oxide) chains, and one of their mixtures, and preferably chosen from poly (ethylene oxide) and poly (ethylene and propylene oxide) chains, and more preferably still chosen from poly (ethylene oxide) chains; and p is between 10 and 50, preferably between 6 and 33, and more preferably between 12 and 15.
    Block A thus comprises crosslinkable functions uniformly distributed within said block A.
    The poly (alkylene oxide) COA chains are preferably linear.
    The substituent R 1 can be chosen from alkyl radicals containing at least one alkene or alkyne function, said substituent R 1 comprising from 4 to 10 carbon atoms, and preferably from 4 to 6 carbon atoms.
    According to a preferred embodiment of the invention, the functional polymer of formula (II) corresponds to the following formula (ΙΙ-a):
    [Chem. 4]
    in which y is between 11 and 91, preferably 17 and 75, and more preferably 23 and 45; and p is as defined in the invention.
    According to a particularly preferred embodiment of the invention, the block A corresponds to the following formula (Π-b):
    [Chem. 5]
    in which y and p are as defined in the invention; M is a substituent comprising a radical initiator capable of initiating the polymerization of the lithium styrene-sulfonyl (trifluoromethylsulfonyl) imide monomers of block B and of allowing the formation of a covalent bond between block A and block B.
    The radical initiator in the substituent M can be chosen from alkoxyamines, and controlled radical initiators based on nitroxides.
    Thanks to the radical initiator, for example of alkoxyamine type, the polymerization of lithium styrene-sulfonyl (trifluoromethylsulfonyl) imide monomers is ensured in a controlled manner, thus making it possible to form the block B while binding it with the block AT.
    The substituent M can be chosen from alkoxyamines. The C-0 bond of the alkoxyamine can break homolytically under the action of temperature, and generate a nitroxide acting as a controller of the polymerization reaction and an initiating radical which adds to the monomer.
    In particular, the substituent M corresponds to the following formula (III):
    [Chem. 6]
    in which * denotes the point of attachment of M to the terminal oxygen in block A of formula (ΙΙ-b), and SGI denotes a nitroxide radical of the following formula:
    [Chem. 7]
    in which ** denotes the point of attachment of SGI to the radical -CH- of M of formula (III).
    In the crosslinked copolymer according to the invention, the ratio of the number of moles of alkylene oxide to the number of moles of STFSILi (OA / Li) [respectively the ratio of the number of moles of oxide of ethylene on the number of moles of STFSILi (OE / Li)], preferably ranges from 7 to 65, more preferably from 10 to 50, and very particularly preferably from 15 to 25.
    The compound comprising a crosslinkable alkene or alkyne function can be chosen from the compounds of formula (IV) below:
    [Chem. 8]
    XR,: t -X '(IV) in which R' 1 is an alkyl group containing at least one alkene or alkyne function, said alkyl group comprising from 4 to 10 carbon atoms, and preferably from 4 to 6 carbon atoms ; and X and X ′, which are identical or different, are chosen independently of one another, from the halogen, carboxylic acid, acid chloride, ester and aldehyde functions.
    X and X ’are preferably identical.
    According to a particularly preferred embodiment, X and X ’are halogens, and more preferably chlorine atoms.
    For example, the compound comprising a crosslinkable alkene or alkyne function is 3-chloro-2-chloro-l-propene.
    Block A is capable of being obtained from at least one monomer chosen from ethylene glycol, propylene glycol, and their mixture, or from at least one oligomer of poly (alkylene oxide) chosen from poly (ethylene oxide), poly (propylene oxide), poly (ethylene and propylene oxide), and one of their mixtures, and at least one compound comprising at least one crosslinkable function alkene or alkyne, preferably by polycondensation.
    The poly (alkylene oxide) oligomer may include terminal groups of hydroxyl (-OH), thiol (-SH), primary (-NH 2 ) or secondary (-NHR 2 , R 2 = -) type. CH 3 on -C 2 H 5 ), and preferably of the hydroxyl or primary amine type.
    The oligomer of (alkylene oxide) may have a molar mass less than or equal to approximately 5000 g / mol, preferably ranging from 700 to 4000 g / mol approximately, and even more preferably ranging from 1000 at around 2000 g / mol.
    According to one embodiment of the invention, the oligomer of (alkylene oxide) is chosen from the oligomers of the following formulas:
    * H- [O- (CH 2 ) x ] y -OH, in which 2 <x <4, and preferably x = 2; and 10 <y '<91, preferably 17 <y'<75, and more preferably 23 <y '<45, * H- [O-CH 2 -CHR 3 ] y -OH, in which R 3 is a alkyl group having from 1 to 3 carbon atoms, and preferably a methyl group; and 7 <y ”<69, preferably 10 <y” <34, and more preferably 17 <y ”<27, * H- [O- (CH 2 ) z -O- (CH 2 -CHR 4 ) u ] w-OH, in which 1 <z <4, and preferably z = 1 or 2; 1 <u <2, and preferably u = 1; w being such that the molar mass of the oligomer ranges from 700 to 4000 g / mol approximately, and preferably from 1000 to 2000 g / mol approximately, and more preferably 2 <w <23; and R 4 is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and preferably a hydrogen atom or a methyl group; it being understood that the aliphatic chains - (CH2) Z - and - (CH 2 -CHR 3 ) u - are different, * NH 2 -CHR 5 -CH2- [O-CH2-CHR 5 ] w -NH 2 , in which R 5 is an alkyl group having 1 to 3 carbon atoms, and preferably a methyl group; and 5 <w '<69, preferably 12 <w'<52, and more preferably 17 <w '<35, these oligomers can be marketed under the name Jeffamines® in a wide range of w when R 5 is a methyl, and * NH 2 -CHR 6 -CH2-O- [CH2-CH2-O] W -CH2-CHR 6 -NH2, wherein R 6 is an alkyl group having 1 to 3 carbon atoms, and preferably a methyl group; and 7 <w ”<91, preferably 17 <w” <68, and more preferably 23 <w ”<45.
    The oligomer of (alkylene oxide) is preferably chosen from the oligomers of formula H- [O- (CH 2 -CH 2 )] y -OH as defined in the invention.
    The oligomer of (alkylene oxide) is preferably an oligomer of (ethylene oxide), in particular of molar mass ranging from 750 to 4000 g / mol approximately, and more preferably ranging from 1000 to 2000 g / mol approximately.
    The crosslinked copolymer according to the invention can be prepared by a process comprising the following steps:
    i) the preparation of a crosslinkable poly (alkylene oxide) as defined in the invention, and ii) the copolymerization of the crosslinkable poly (alkylene oxide) of step i) with a styrene-sulfonyl monomer ( trifluoromethylsulfonyl) lithium imide (STFSILi).
    [0040]
    Step i) can in particular include the following sub-steps:
    ia) the polycondensation of an oligomer of (alkylene oxide) as defined in the invention with at least one compound comprising a crosslinkable alkene or alkyne function as defined in the invention, and ib) the functionalization of the poly (crosslinkable alkylene oxide) obtained in substep ia), with a substituent M as defined above.
    According to a particularly preferred embodiment of the invention, sub-step ia) implements 3-chloro-2-chloro-1-propene and the oligomer of formula H- [O- (CH 2 ) x ] y -OH as defined in the invention, 3-chloro-2-chloro-1-propene being in default with respect to the oligomer, to form a crosslinkable poly (alkylene oxide) of the following formula:
    [Chem.9]
    [0042]
    M in which y and p are as defined in the invention.
    Polycondensation is generally carried out in a solvent such as THF, in the presence of a strong base such as potassium hydroxide.
    Sub-step i-b) may include replacing the terminal hydroxyl functions with acrylate functions, in particular in the presence of excess acryloyl chloride and triethylamine, in a solvent such as THF; followed by the radical addition of an oxy-SGI alkoxyamine of the following formula:
    [Chem. 10]

    In particular in a solvent such as ethanol.
    Substep i-b) can thus make it possible to form the crosslinkable poly (alkylene oxide) of formula (ΙΙ-b) as defined in the invention.
    Stage ii) of copolymerization can be carried out by controlled radical polymerization, in particular by NMP polymerization ("nitroxide-Mediated Radical Poly10 merization").
    Step ii) is preferably carried out in a polar solvent such as N, N-dimethylformamide (DML), dimethylsulfoxide (DMSO), or water, in particular at a temperature ranging from 90 to 120 ° C. , especially for a period of 2 to 20 hours.
    The second object of the invention is the use of at least one crosslinked copolymer as defined in the first subject of the invention, for the preparation of a solid polymer electrolyte, in particular in a lithium battery, and especially in a lithium metal battery.
    The use of the crosslinked copolymer according to the present invention for the preparation of a solid polymer electrolyte, in particular in a lithium metal battery, leads to an energy storage device having excellent performance at low temperature (approximately 60 ° C), in particular a transport number of lithium ions of the order of 1, and an ionic conductivity greater than or equal to 10 5 S.cm 1 at 60 ° C. The high transport number makes it possible to limit the formation of a concentration gradient in the electrolyte during the discharge (respectively of the charge) making it possible to increase the performance in power (respectively the speed of the charge). The use of this crosslinked copolymer also makes it possible to limit the dendritic growth of lithium, and thus to envisage rapid and safe recharges. In fact, the problem with lithium metal battery technology is the formation of heterogeneous electro-deposits of lithium (including dendrites) during recharging, which reduces cyclability and can cause short circuits. The crosslinked copolymer according to the present invention also has good mechanical strength, high thermal stability (which ensures the safety of the energy storage devices comprising them), and improved potential stability (eg stability up to 4.5 V vs Li + / Li).
    The third object of the invention is a solid polymer electrolyte, characterized in that it comprises at least one crosslinked copolymer as defined in the first object, and at least one plasticizer.
    The solid polymer electrolyte of the invention has an optimized mechanical strength, notably facilitating its implementation and handling. Furthermore, it has a cation transport number equal to 1 and a good ionic conductivity, inducing good resistance to dentritic growth.
    The plasticizer can be chosen from linear and cyclic carbonates such as propylene carbonate, ethylene carbonate or dimethylcarbonate; fluorinated carbonates such as fluoroethylene carbonate; nitriles such as succinonitrile; lactones such as γ-butyrolactone; linear or cyclic liquid polyethers; fluorinated polyethers; and one of their mixtures.
    Indeed, the crosslinked copolymer of the invention is capable of absorbing a plasticizer, while retaining good mechanical strength and remaining solid. Furthermore, the presence of the plasticizer makes it possible to obtain a solid polymer electrolyte having an improved ionic conductivity (eg conductivity of at least 1x10 5 S / cm at 60 ° C).
    The linear or cyclic liquid polyether preferably has a molar mass less than or equal to approximately 10,000 g-mol 1 , preferably less than or equal to approximately 2000 g-mol 1 , and more preferably less than or equal to 600 g -mol · 1 approximately.
    The linear or cyclic liquid polyether can be chosen from:
    * polyethylene glycols of formula H- [O-CH 2 -CH 2 ] q -OH, in which q is between 1 and 13, * glycol ethers of formula R 7 - [O-CH 2 -CH 2 ] q -OR 7 , in which q 'is between 1 and 13 and R 7 and R 7 ', identical or different, are linear, branched or cyclic alkyl groups, which can contain from 1 to 10 carbon atoms, * ethers of formula R 8 - [CH 2 -O] q -R 8 , in which q ”is between 1 and 13, R 8 and R 8 ', identical or different, are linear, branched or cyclic alkyl groups, which can comprise from 1 to 10 carbon atoms and optionally heteroatoms, * the cyclic ethers can comprise from 2 to 20 carbon atoms, the cyclic polyethers can comprise from 3 to 40 carbon atoms, and * one of their mixtures.
    The polyether (s) used in the electrolyte of the invention is (are) particularly stable with regard to lithium.
    In a preferred embodiment, the plasticizer is a linear or cyclic liquid polyether, and preferably is chosen from tetra ethylene glycol dimethyl ether (TEGDME) of formula CH 3 O- (CH 2 -CH 2 ) 4 - OCH 3 (ie R 7 , R 7 = CH 3 and q '= 4) or tetraethylene glycol (TEG) of formula H- (O-CH 2 CH 2 ) 4 -OH (ie q = 4).
    The solid polymer electrolyte according to the present invention can in particular be in any suitable form, for example in the form of a sheet, a film or a membrane. The solid polymer electrolyte according to the invention can be prepared by any technique known to those skilled in the art, such as for example by coating or by extrusion.
    The solid polymer electrolyte according to the present invention may comprise from 6 0 to 90% by mass approximately of crosslinked copolymer, and preferably from 75 to 85% by mass approximately of crosslinked copolymer, relative to the total mass of the solid polymer electrolyte.
    The solid polymer electrolyte according to the present invention may comprise from 10 to 40% by mass approximately of plasticizer, and preferably from 15 to 25% by mass approximately of plasticizer, relative to the total mass of the electrolyte solid polymer.
    This thus makes it possible to guarantee an operation of the LMP battery implementing such an electrolyte, with an optimal ionic conductivity.
    Finally, the invention has as a fourth object a battery, in particular an LMP battery, comprising:
    - a negative electrode comprising lithium metal or a lithium metal alloy,
    - a positive electrode, possibly supported by a current collector, and
    - a solid polymer electrolyte positioned between the positive electrode and the negative electrode, characterized in that the solid polymer electrolyte is as defined in the third object of the invention.
    The composite positive electrode can include:
    - at least one active material with a positive electrode,
    - at least one polymeric binder,
    - optionally at least one electronic conduction agent, and
    - optionally at least one plasticizer.
    The composite positive electrode may comprise at least 50% by mass approximately of active material of positive electrode, and preferably from 55 to 85% by mass approximately of active material of positive electrode, relative to the total mass of said composite positive electrode.
    The active material of positive electrode can be chosen from lithium phosphates, and in particular LiEePO 4 , Li 3 V 2 (PO 4 ) 3 , LiCoPO 4 , LiMnPO 4 , LiNiPO 4 ; lithium oxides such as for example LiNiO 2 , LiCoO 2 and LiMn 2 O 4 and their mixtures.
    Among these active materials, LiLePO 4 is very particularly preferred.
    According to a particular embodiment, the composite positive electrode comprises from 10 to 40% by mass approximately of polymeric binder, and preferably from 13 to 20% by mass approximately of polymeric binder, relative to the total mass of the composite positive electrode.
    The polymeric binder can be a tri-block copolymer of BAB type as defined in the invention (i.e. without crosslinking), or a material chosen from homopolymers and copolymers of ethylene; propylene homopolymers and copolymers; homopolymers and copolymers of ethylene oxide (e.g. POE, copolymer of POE), methylene oxide, propylene oxide, epichlorohydrin, allyl glycidyl ether, and mixtures thereof; halogenated polymers such as homopolymers and copolymers of vinyl chloride, vinylidene fluoride (PVdE), vinylidene chloride, ethylene tetrafluoride, or chlorotrifluoroethylene, copolymers of vinylidene fluoride and hexafluoropropylene (PVdE- co-HEP) or mixtures thereof; non-conductive anionic type electronic polymers such as poly (styrene sulfonate), poly (acrylic acid), poly (glutamate), alginate, pectin, gelatin or mixtures thereof; cationic type polymers such as polyethyleneimine (PEI), polyaniline in the form of emeraldine salt (ES), poly (quaternized N-vmylimidazole), poly (acrylamide-diallyldimethyl ammonium chloride) (AMAC) or their mixtures; polyacrylates; and one of their mixtures.
    According to a particularly preferred embodiment of the invention, the polymeric binder is a tri-block copolymer of BAB type as defined in the invention (i.e. without crosslinking). Thanks to the tri-block copolymer of the BAB type as defined in the invention present in the composite positive electrode, the formation of a concentration gradient in the thickness of the positive electrode during cycling, can be reduced, or even removed, leading to an improvement in battery power performance or the possibility of increasing the grammage of the positive electrode.
    The composite positive electrode can comprise from 0.05 to 10% by mass approximately of agent generating an electronic conductivity, and preferably from 0.2 to 5% approximately by mass of agent generating an electronic conductivity, by relative to the total mass of the composite positive electrode.
    The agent generating an electronic conductivity suitable for the present invention is preferably chosen from carbon black, SP carbon, acetylene black, carbon fibers and nanofibers, carbon nanotubes, graphene, graphite, metallic particles and fibers, and one of their mixtures.
    The agent generating an electronic conductivity is preferably carbon black. Preferably, the agent generating an electronic conductivity is in the form of spherical particles (ie in the form of beads) in order to promote conduction in particular in the direction perpendicular to the composite positive electrode (ie in the direction of its thickness ) and thus to favor the electrochemical processes within the electrode. Indeed, the agent particles generating electronic conductivity in spherical form have a propensity to form three-dimensional conductive networks.
    As an example of carbon black, mention may be made of the carbon blacks sold under the references: Ketjenblack 600JD®, Ketjenblack 700JD® and Timcal Ensaco 350G®.
    The composite positive electrode may further comprise at least one plasticizer, said plasticizer may be as defined in the present invention. The plasticizer of the positive electrode is preferably a linear or cyclic liquid polyether as defined in the invention or a linear, cyclic or fluorinated carbonate as defined in the invention.
    The composite positive electrode may comprise from 2 to 10% by mass approximately of plasticizer, and preferably from 3 to 5% by mass approximately of plasticizer, relative to the total mass of the composite positive electrode.
    It should be noted that the total mass of the composite positive electrode includes the mass of the active material, the mass of the polymer binder, possibly the mass of the agent generating an electronic conductivity and possibly the mass of the plasticizer s' they are present.
    According to a preferred embodiment of the invention, the grammage of the positive electrode (that is to say the amount of active material of positive electrode / cm 2 / face) ranges from 1 to 3 mAh / cm 2 .
    The composite positive electrode can be prepared as follows:
    a) by mixing the active material of the positive electrode with the polymeric binder, optionally the agent generating an electronic conductivity, optionally the plasticizer, and optionally at least one solvent for the said polymeric binder, in order to obtain an electrode paste,
    b) by applying said electrode paste to at least one support,
    c) drying said electrode paste to obtain a composite positive electrode in the form of a supported film.
    Step a) can be carried out by extrusion or by grinding.
    Extrusion is very advantageous since it makes it possible to easily obtain non-porous electrodes while using little solvent. It also makes it possible to avoid a calendering step on the dry electrode which can cause changes in the structure of the electrode, adversely affect the good coating of the grains of the agent generating electronic conductivity and thus can induce collapse of the electrode during cycling. Finally, the calendering step has the disadvantage of increasing the number of steps to obtain the electrode and thus its production cost.
    The solvent for the polymeric binder of step a) makes it possible to dissolve said polymeric binder.
    When it is present, said solvent preferably represents less than 50% by mass approximately of the total mass of the mixture of the active material of positive electrode, of polymeric binder, optionally of agent generating an electronic conductivity, and possibly plasticizer.
    The use during the manufacture of the positive composite electrode of a small amount of solvent of the polymer binder makes it possible to lead to a positive electrode of low porosity (i.e. <10% by volume approximately). This low porosity makes it possible to control and optimize the amount of active material present in the composite positive electrode, and thus to achieve optimal energy density densities.
    The solvent of step a) can be chosen from water; A-methylpyrrolidone; carbonates such as ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate or methyl and ethyl carbonate; acetone; alcohols such as methanol, ethanol or propanol; and one of their mixtures.
    Step b) can be carried out by rolling or by coating.
    The support can be a current collector and / or a support film.
    As an example of a current collector, there may be mentioned an aluminum current collector covered with a carbon-based layer (anticorrosion layer).
    As an example of a support film, mention may be made of a plastic film of the silicone polyethylene terephthalate (PET) type.
    The positive electrode supported film obtained in Tissue from step c) can have a thickness ranging from 2 to 100 μm approximately, and preferably from 10 to 60 μm approximately.
    Step c) can be carried out at a temperature sufficient to allow the solvent from step a) to be removed.
    The operating temperature of the battery is approximately 60 to 100 ° C.
    Thanks to the use of a crosslinked copolymer according to the invention at least in the solid polymer electrolyte, the operating temperature of the battery can be lowered.
    The performance of the battery of the invention at 60 ° C. is superior, at high speed (eg (> C / 2)), and similar at low speed (eg (c / io)), to that of batteries available on the market with an operating temperature of 80 ° C, a gain of 20 ° C for equal or even better performance.
    The present invention is illustrated by the following exemplary embodiments, to which it is not however limited.
    Brief description of the drawings The accompanying drawings illustrate the invention:
    [Fig.l] represents the Young's modulus (in MPa), as a function of the mass rate of PSTFSILi of materials conforming and not conforming to the invention.
    [Fig-2] represents the variation of the ionic conductivity (in S / cm) as a function of the 1000 / T ratio, T being the temperature in Kelvin for materials conforming and not conforming to the invention.
    [Fig. 3] represents the glass transition temperature (in ° C) as a function of the mass rate of PSTFSILi of materials conforming and not conforming to the invention.
    [Fig-4] represents the melting temperature (in ° C) as a function of the mass rate of
    PSTFSILi of materials conforming and not conforming to the invention.
    [Fig.5] represents the voltage of a positive composite electrode according to the invention (in volts) as a function of the discharge capacity (in mAh) at 60 ° C and at different speeds (from D / 9 , 4 at D / 0.9), the charge always being C / 9.4.
    [Fig.6] represents the curve of the discharge capacity (in mAh) and the coulombic efficiency (in%), as a function of the number of cycles, at 60 ° C. and at different discharge regimes (from D / 9.4 to D / 0.9), the charge still being C / 9.4.
    [0101] [fig-7] shows the power performance of two LMP batteries compliant and [0102] not in accordance with the invention.
    Description of examples
    The raw materials used in the examples are listed below:
    - carbon black Ketjenblack EC600JD, AkzoNobel,
    - LiFePO 4 , Pulead,
    - PVDF-co-HFP, Solvay,
    - homo-POE, Sumitomo Seika,
    - LiTFSI, Solvay,
    - aluminum current collector covered with a carbon layer, Armor,
    - lithium metal sheet, Blue Solutions,
    - POE oligomer, PEG2000, sigma-aldrich,
    - 3-chloro-2-chloro-l-propene,
    - TEGDME, sigma-aldrich,
    - potassium hydroxide (KOH),
    - tetrahydrofuran (THF),
    - diethyl ether,
    - acetonitrile,
    - water,
    - acryloyl chloride,
    - triethylamine,
    - dimethylformamide (DMF),
    - 2-Hydroxy-4 '- (2-hydroxyethoxy) -2-methylpropiophenone: Irgacure 2959 photoinitiator,
    - SGI nitroxide and alkoxyamine ΜΑΜΑ-SGI of the following formulas:
    [Chem. 11]
    MÂMÂ-SGt
    Unless otherwise indicated, all materials have been used as received from the manufacturers.
    EXAMPLE 1 Preparation of Crosslinked Copolymers in Accordance with the First Object [0103] of the Invention [0104] Preparation of a Crosslinkable Poly (Ethylene Oxide) Precursor of Block A [0105] Preparation of a Poly (Ethylene Oxide) ) crosslinkable: sub-step ia) as defined in the invention [Chem. 12]

    127.6 g of a 1.5 kDa POE oligomer and 9.5 g of KOH are dissolved in 200 ml of tetrahydrofuran (THF) at 40 ° C. When the solution is homogeneous, 10 g of 3-chloro-2-chloro-1-propene dissolved in 20 ml of THF are added to the POE oligomer solution previously prepared. The polycondensation reaction was carried out at 40 ° C for 3 days. 3-chloro-2-chloro-l-propene being in default, the crosslinkable poly (ethylene oxide) obtained is terminated by hydroxyl functions.
    The reaction medium was then cooled, centrifuged, then the supernatant was precipitated in diethyl ether. The purification is completed by an ultrafiltration to remove the low molecular weight polymers and the salts which have not been removed in the centrifugation step. The water is removed by rotary evaporation and the product is dried under vacuum.
    [0106] Preparation of a crosslinkable poly (ethylene oxide): substep i-b) as defined in the invention [Chem. 13]
    26.5 g of crosslinkable poly (ethylene oxide) as prepared above were reacted, at room temperature, for 15 h, with 7.4 g of acryloyl chloride in the presence of 8 g of triethylamine in 200 ml tetrahydrofuran. The terminal hydroxyl functions have thus been functionalized by acrylate functions. The residue obtained was precipitated in diethyl ether, filtered and then dried under vacuum.
    Then, 2 g of alkoxyamine of formula ΜΑΜΑ-SGI was added to the diacrylate as obtained above, at 80 ° C in 50 ml of ethanol under an inert atmosphere. After 4 hours of reaction, the product obtained was precipitated in diethyl ether, filtered, then dried under vacuum.
    Copolymerization of crosslinkable poly (ethylene oxide), precursor of block A, with lithium styrene-sulfonyl (trifluoromethylsulfonyl) imide (STFSILi) to form the tri-block copolymer BAB: step ii) as defined in l invention [Chem. 14]
    g of crosslinkable poly (ethylene oxide) containing an initiator as prepared in point 1.1.2 in 30 ml of DMF were reacted with 1 g of lithium styrenesulfonyl (trifluoromethylsulfonyl) imide (STFSILi) and 7 mg of nitroxide SGI under an inert atmosphere at 120 ° C. After 16 hours of reaction, approximately 80% of the STFSILi monomer has reacted.
    Styrene-sulfonyl (trifluoromethylsulfonyl) lithium imide (STFSILi) can be prepared as described in international application WO 2013/034848 A1. The copolymer obtained was precipitated in diethyl ether and then purified by dialysis in water (cutoff threshold at 3 kg.mol ') before being dried by lyophilization.
    A tri-block copolymer B AB CP-1 was obtained in accordance with the invention comprising 13.1% by mass of PSTFSILi, relative to the total mass of the copolymer. This copolymer has an OE / Li ratio of 48.4.
    Crosslinking and shaping of the copolymer [0109] 100 mg of copolymer as prepared in point 1.2 above was dissolved in 5 ml of an acetonitrile / water mixture (5/1 by volume). 0.9 mg of UV photoinitiator (2-Hydroxy-4 '- (2-hydroxyethoxy) -2-methylpropiophenone) was introduced into the solution. The resulting solution was then poured into a polypropylene petri dish (6 cm in diameter) placed on a flat surface. Most of the solvent was evaporated in an oven at 40 ° C for 24 hours, then at 60 ° C for 12 hours.
    Then the polymer film obtained was crosslinked under a UV mercury lamp sold under the trade name P300 MT Power supply by Fusion UV system Inc. for 30 seconds at 15 mW / cm 2 under ambient atmosphere. The film obtained was dried in the glove box to form a crosslinked copolymer in accordance with the invention CP r -1 comprising 13.1% by mass of PSTFSILi, relative to the total mass of the copolymer, and an OE / Li ratio 48.4.
    Obtaining other copolymers [0111] By modifying the amount of STFSILi monomer, other crosslinked copolymers CP r -2 and CP r -3; and non-crosslinked CP-2 and CP-3 were obtained.
    Table 1 below lists the composition of the copolymers obtained:
    [Tables 1]
    Copolymer % PSTFSILi OE / Li report crosslinking CP-1 13.1 48.4 no CP r -l 13.1 48.4 Yes CP-2 22 25.9 no CP r -2 22 25.9 Yes CP-3 28.4 18.4 no CPr-3 28.4 18.4 Yes
    Example 2: Preparation of solid polymer electrolytes in accordance with the third subject of the invention [0114] The crosslinked copolymers CP r -1, CP r -2 and CP r -3 in the form of films were soaked in TEGDME as a plasticizer for 1 hour in a dry room (dew point at -45 ° C), then the films obtained were collected, and the excess plasticizer was removed with a Kimtech tissue. The films were weighed before and after the absorption of the plasticizer, which makes it possible to deduce the percentage of plasticizer in the films.
    The thicknesses of the films range on average from 30 to 60 μm.
    Table 2 below represents the composition of the solid polymer electrolytes obtained:
    [Tables2]
    Solid polymer electrolyte % by mass TEGDME Copolymer OE / Li report E-la 14 CP r -l 59 E-lb 12.3 CP r -l 57 E-2a 22.8 CP r -2 40 E-2b 17.4 CPr-2 35 E-2c 14.5 CP r -2 33 E-3a 23.4 CP r -3 30 E-3b 21.3 CPr-3 28 E-3c 16 CP r -3 24 E-3d 18.7 CP r -3 26
    Example 3: Physico-chemical characterizations [0118] Young's modulus [0119] The Young's modulus (elasticity modulus) was calculated from the stress vs elongation curves obtained using a dynamic mechanical analyzer sold under the trade name Dynamic Mechanical Analyzer DMA Q800, by the company TA Instruments, and this at 50 ° C., with a sweep of dry air. FIG. 1 appended shows the Young's modulus (in MPa), as a function of the mass content of PSTFSILi in the crosslinked copolymer (in%) (curve with the empty circles, copolymers CP r -1, CP r -2 and CP r -3), in the non-crosslinked copolymer (curve with solid circles, CP-1, CP-2 and CP-3 copolymers) and in a mixture of crosslinked copolymer and TEGDME plasticizer (curve with solid squares, electrolytes E-lb, E-2b and E-3b). FIG. 1 shows first of all that the crosslinking of block A in the tri-block copolymer BAB has a significant impact on the Young's modulus since an increase of a factor 3 to 5 is obtained for the same mass rate of PSTFSILi (eg from 0.46 MPa to 1.7 MPa for the copolymer comprising 28.4% by weight of PSTFSILi). Furthermore, this crosslinking provides sufficient mechanical strength to be able to combine the crosslinked copolymer according to the invention with a plasticizer. In particular, the plasticization increases the ionic conductivity, while guaranteeing a completely acceptable Young's modulus. This gives a good compromise between ionic conductivity and mechanical strength at 50 ° C for the solid polymer electrolytes E-lb, E-2b and E-3b. Finally, the mechanical strength of the copolymer can be modulated as a function of the mass content of PSTFSILi in the crosslinked copolymer.
    Ionic conductivity [0122] The ionic conductivity was calculated according to the following formula:
    [Math.l]
    where S and 1 are respectively the surface and the thickness of the solid polymer electrolyte or of the copolymer. R e i is the resistance of the solid polymer electrolyte or of the copolymer determined at high frequency by impedance spectroscopic (VMP300, BioLogic) on a symmetrical cell Li / solid polymer electrolyte or copolymer / Li. The temperature is fixed by means of a climatic chamber between 10 and 80 ° C.
    The attached FIG. 2 shows the variation of the ionic conductivity (in S / cm) as a function of the ratio 1000 / T, T being the temperature in Kelvin, for the non-crosslinked copolymers CP-2 (curve with solid circles) and CP-3 (curve with solid triangles), for crosslinked copolymers CP r -2 (curve with empty circles) and CP r -3 (curve with empty triangles), and for solid polymer electrolytes E-2c ( curve with full squares) and E-3c (curve with empty squares).
    Figure 2 shows that the copolymers without plasticizer have a conductivity of 4 to 8 * 10 6 S / cm at 60 ° C, which is too low for use in batteries, especially at high speed and high grammage of l '' positive electrode (eg> 0.8 mAh / cm 2 ). Plasticizing with a small amount of plasticizer makes it possible to achieve a conductivity of 1.3 * 10 5 S / cm, without compromising the mechanical stability of the crosslinked copolymer.
    Figures 3 and 4 respectively show the glass transition temperature in ° C (Figure 3) and the melting temperature in ° C (Figure 4) as a function of the mass content of PSTLSILi, for the crosslinked copolymer (curve with the empty circles, copolymers CP r -1, CP r -2 and CP r -3), for the non-crosslinked copolymer (curve with solid circles, copolymers CP-1, CP-2 and CP-3), and for the solid polymer electrolyte (curve with solid squares, electrolytes E-la, E-2a and E-3a).
    The glass transition and melting temperatures were obtained by measuring the thermodynamic properties by DSC using a device sold under the trade name DSC3 by Mettler-Toledo. The measurements were carried out with the following parameters: 10 ° C / min between -110 ° C and 130 ° C.
    Figures 3 and 4 respectively show a sharp drop in the glass transition temperature and the melting temperature for the solid polymer electrolyte, compared to those of crosslinked and non-crosslinked copolymers. Such temperatures are suitable for obtaining an electrolyte having good ionic conduction at low temperature (less crystalline polymer), and which can be implemented in a battery at a lower temperature.
    Example 4: Electrochemical Characterizations [0129] Preparation of a Composite Positive Electrode [0130] A composite positive electrode in the form of a film was prepared as follows: a mixture of 46.3 g of LiLePO 4 , 1.2 g of carbon black, 17.5 g of CP-3 copolymer, 6.5 g of deionized water were introduced into a Plastograph brabender. The mixing was carried out at 60 ° C at 80 revolutions per minute.
    The paste thus obtained was then laminated at 60 ° C on a current collector made of aluminum coated with carbon. The film obtained was dried for 10 minutes at 100 ° C. before being used.
    The composite positive electrode obtained comprises 71.2% by mass of LLP active material, 26.9% by mass of CP-3 copolymer and 1.9% by mass of carbon black. It has a thickness of approximately 45 μm. The grammage obtained is 1.37 mAh / cm 2 .
    An LMP accumulator was prepared by assembly under a controlled atmosphere (dew point -50 ° C):
    - a film of solid polymer electrolyte E-3d as previously prepared with a thickness of 58.8 μm.
    a sheet of lithium metal with a thickness of approximately 50 μm, and
    - a composite positive electrode as previously prepared.
    To do this, the lithium sheet and the solid polymer electrolyte film are laminated at 70 ° C. and at 5 bars to ensure good Li / electrolyte contacts, then finally the composite positive electrode is laminated on the Li / electrolyte assembly to form the accumulator. The electrolyte film is disposed between the metallic lithium film and the composite positive electrode film. One lead wire is connected to lithium and another lead wire is connected to the current collector of the composite positive electrode.
    The accumulator obtained having a sandwich type structure is confined under vacuum in a pouch (well known according to the English term "coffee bag") to be tested in an uncontrolled atmosphere.
    An accumulator under a pressure of 1 bar and an area of 2.8 cm 2 was obtained.
    During operation of the accumulator, the TEGDME contained in the solid polymer electrolyte migrates at least partially into the composite positive electrode, in particular until the equilibrium is reached between the amount of TEGDME in l positive composite electrode, on the one hand, and in the solid polymer electrolyte, on the other hand.
    FIG. 5 shows the voltage of the positive composite electrode in volts as a function of the discharge capacity (in mAh) at 60 ° C. and at different speeds (from D / 9.4 to D / 0.9) , the charge still being C / 9.4. D represents the nominal capacity in mAh and D / n a discharge current corresponding to obtaining the capacity D in n hours. The polarization is proportional to the current density applied, which is typical for single-ion type polymers because the transport of the ions is ensured only by migration. Thus the capacitance values obtained are highly dependent on the low potential stop terminal.
    FIG. 6 represents the curve of the discharge capacity (in mAh) and the coulombic efficiency (in%), as a function of the number of cycles, at 60 ° C. and at different discharge regimes (from D / 9 , 4 at D / 0.9), the charge always being C / 9.4. Very good cycling resistance over more than 60 cycles associated with a faradic yield of 98.4% are obtained.
    FIG. 7 shows the comparison of the power performance of two LMP batteries:
    * a first LMP battery (curve with empty diamonds) operating at 60 ° C comprising a solid polymer electrolyte E-3d and a positive composite electrode as defined above, and * a second LMP battery currently used in industry (curve with circles full) operating at 80 ° C comprising a solid polymer electrolyte including
    48% by mass of homo-POE, 12% by mass of lithium salt LiTFSi, and 40% by mass of PVdF-co-HFP, and a positive electrode containing 68% by mass of active material LFP, 24% by mass homo-POE, 6% by mass of lithium salt LiTFSi, and 2% by mass of carbon black and having a thickness of approximately 60 μm and a grammage of 1.5 mAh / cm 2 .
    FIG. 7 shows the discharge capacity normalized by the nominal capacity (D / D o) as a function of the discharge regime (D / n) for the abovementioned batteries.
    The results obtained are remarkable, taking into account the thickness of the solid polymer electrolyte (58.8 μm), the very high grammage of the electrode (1.37 mAh / cm 2 ), for a positive electrode. composite not plasticized initially. They show that the solid polymer electrolytes of the invention have higher performances than those of commercial electrolytes at high speeds and equal at low cycling speeds.
    权利要求:
    Claims (2)
    [1" id="c-fr-0001]
    Claims [Claim 1] Crosslinked copolymer, characterized in that it comprises at least recurring units of lithium polystyrenesulfonyl (trifluoromethylsulfonyl) imide (PSTFSILi) and at least recurring units of poly (alkylene oxide) chosen from among units of poly (ethylene oxide), poly (propylene oxide) units, poly (ethylene and propylene oxide) units, and a mixture thereof, and in that said crosslinked copolymer is obtained by crosslinking d '' a tri-block copolymer of type B AB, in which:
    - block A is a crosslinkable poly (alkylene oxide) capable of being obtained from:
    * of at least one monomer chosen from ethylene glycol, propylene glycol, and their mixture, or from at least one oligomer of poly (alkylene oxide) chosen from poly (ethylene oxide), poly (propylene oxide), poly (ethylene and propylene oxide), and one of their mixtures, and * of at least one compound comprising at least one crosslinkable alkene or alkyne function, and
    each of the blocks B is an anionic polystyrene substituted by the anion of a lithium sulfonyl (trifluoromethylsulfonyl) imide salt (TFSILi) and corresponding to the following formula (I):
    [Chem.
    [0002]
    2]

    [Claim 2] in which n denotes the number of lithium styrenesulfonyl (trifluoromethylsulfonyl) imide units for each of the blocks B.
    Crosslinked copolymer according to claim 1, characterized in that it
    comprises from 10 to 50% by mass of PSTFSILi, relative to the total mass of the crosslinked copolymer. [Claim 3] Crosslinked copolymer according to claim 1 or 2, characterized in that the block A has a number average molecular weight less than or equal to 25 kDa. [Claim 4] Crosslinked copolymer according to any one of the preceding claims, characterized in that the block A comprises a functional polymer of the following formula (II): [Chem. 3] - [COA-fUb- (II) in which R 1 is a substituent comprising at least one crosslinkable alkene or alkyne function; COA is a poly (alkylene oxide) chain chosen from the poly (ethylene oxide), poly (propylene oxide), poly (ethylene and propylene oxide) chains, and one of their mixtures; and p is between 10 and 50. [Claim 5] Crosslinked copolymer according to claim 4, characterized in that the functional polymer of formula (II) corresponds to the following formula (II-a):[Chem. 4]"OL · T _THe pÎH-aïin which y is between 11 and 91. [Claim 6] Crosslinked copolymer according to any one of the preceding claims, characterized in that the ratio of the number of moles of alkylene oxide to the number of moles of STFSILi (OA / Li) ranges from 7 to 65. [Claim 7] Crosslinked copolymer according to any one of the preceding claims, characterized in that the compound comprising a crosslinkable alkene or alkyne function is chosen from the compounds of formula (IV) below: [Chem. 8] XmX '(IV) in which R' 1 is an alkyl group comprising at least one alkene or alkyne function, said alkyl group comprising from 4 to 10
    carbon atony; and X and X ’, identical or different, are chosen independently of one another, from the halogen, carboxylic acid, acid chloride, ester and aldehyde functions. [Claim 8] Crosslinked copolymer according to any one of the preceding claims, characterized in that the compound comprising a crosslinkable alkene or alkyne function is 3-chloro-2-chloro-l-propene. [Claim 9] Crosslinked copolymer according to any one of the preceding claims, characterized in that the oligomer of (alkylene oxide) has a molar mass ranging from 700 to 4000 g / mol. [Claim 10] Use of at least one crosslinked copolymer as defined in any one of the preceding claims, for the preparation of a solid polymer electrolyte. [Claim 11] Solid polymer electrolyte, characterized in that it comprises at least one crosslinked copolymer as defined in any one of claims 1 to 9, and at least one plasticizer. [Claim 12] Solid polymer electrolyte according to claim 11, characterized in that the plasticizer is chosen from linear and cyclic carbonates; fluorinated carbonates; nitriles; lactones; linear or cyclic liquid polyethers; fluorinated polyethers; and one of their mixtures. [Claim 13] Solid polymer electrolyte according to claim 11 or 12, characterized in that the plasticizer is a linear or cyclic liquid polyether with a molar mass less than or equal to 10,000 g-mol *, chosen from: * polyethylene glycols of formula H- [O -CH 2 -CH 2 ] q -OH, in which q is between 1 and 13, * the glycol ethers of formula R 7 - [O-CH 2 -CH 2 ] q -OR 7 , in which q 'is between 1 and 13 and R 7 and R 7 ', identical or different, are linear, branched or cyclic alkyl groups, * the ethers of formula R 8 - [CH 2 -O] q -R 8 , in which q ” is between 1 and 13, R 8 and R 8 ', identical or different, are linear, branched or cyclic alkyl groups, * cyclic ethers, cyclic polyethers, * one of their mixtures. [Claim 14] Solid polymer electrolyte according to any one of claims11 to 13, characterized in that it comprises from 10 to 40% by mass of plasticizer, relative to the total mass of the solid polymer electrolyte. [Claim 15] Battery including:- a negative electrode comprising lithium metal or a lithium metal alloy,
    - a positive electrode, possibly supported by a current collector, and
    - a solid polymer electrolyte positioned between the positive electrode and the negative electrode, characterized in that the solid polymer electrolyte is as defined in any one of claims 11 to 14.
    [Claim 16] Battery according to claim 15, characterized in that the composite positive electrode comprises:
    - at least one active material with a positive electrode,
    - at least one polymeric binder, and
    - optionally at least one electronic conduction agent, and
    - optionally at least one plasticizer, said polymeric binder being a tri-block copolymer BAB as defined in claim 1.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    EP0424827A1|1989-10-26|1991-05-02|Alcatel|Cross-linked polymeric electrolyte|
    US20150263382A1|2008-08-01|2015-09-17|Seeo, Inc.|High capacity cathode|
    WO2010083330A1|2009-01-16|2010-07-22|Seeo, Inc|Polymer compositions with oligomeric alkylene oxide pendants|
    FR2979630A1|2011-09-05|2013-03-08|Univ Provence Aix Marseille 1|BLOCK COPOLYMERS HAVING A POLYANIONIC BASED ON ANION MONOMER TYPE TFSILI AS ELECTROLYTE BATTERY.|
    WO2013034848A1|2011-09-05|2013-03-14|Universite D'aix-Marseille|Block copolymer including a polyanion based on a tfsili anion monomer as a battery electrolyte|
    FR3049114A1|2016-03-18|2017-09-22|Blue Solutions|POLYMER LITHIUM METAL BATTERY WITH HIGH ENERGY DENSITY|CN112510186A|2020-12-03|2021-03-16|珠海冠宇电池股份有限公司|Pre-lithiated silicon negative electrode material, silicon negative electrode piece, preparation method of silicon negative electrode piece and lithium battery|
    CN112786961A|2021-03-23|2021-05-11|上海电气集团股份有限公司|Biomass-based gel electrolyte, lithium ion battery, preparation method and application|
    法律状态:
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    PCT/FR2019/052802| WO2020109711A2|2018-11-27|2019-11-25|Polymer electrolyte for a lithium metal polymer battery having improved performance|
    US17/297,290| US20220029197A1|2018-11-27|2019-11-25|Polymer electrolyte for a lithium metal polymer battery having improved performance|
    CA3115556A| CA3115556A1|2018-11-27|2019-11-25|Polymer electrolyte for a lithium metal polymer battery having improved performance|
    JP2021524185A| JP2022508058A|2018-11-27|2019-11-25|Polyelectrolyte for lithium metal polymer batteries with improved performance|
    EP19868175.1A| EP3887415A2|2018-11-27|2019-11-25|Polymer electrolyte for a lithium metal polymer battery having improved performance|
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