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    • 专利摘要:
    The present invention relates to the field of organic lithium batteries with high energy and power densities. In particular, the present invention relates to an organic lithium battery comprising a positive electrode based on organic redox compounds and an electrolyte comprising a high concentration of lithium salt, and its manufacturing process.
    公开号:FR3029360A1
    申请号:FR1461704
    申请日:2014-12-01
    公开日:2016-06-03
    发明作者:Margaud Lecuyer；Marc Deschamps；Joel Gaubicher；Philippe Poizot；Dominique Guyomard；Bernard Lestriez
    申请人:Centre National de la Recherche Scientifique CNRS；Universite de Nantes；Blue Solutions SA；
    IPC主号:
    专利说明:

    [0001] The present invention relates to the field of organic lithium batteries with high energy and power densities. In particular, the present invention relates to an organic lithium battery comprising a positive electrode based on organic redox compounds and an electrolyte comprising a high concentration of lithium salt, and its manufacturing process. Lithium batteries have become indispensable components in many devices that include portable devices, such as mobile phones, computers and light equipment, or heavier devices such as two-wheeled vehicles (bicycles). , mopeds) or four-wheeled vehicles (electric or hybrid motor vehicles). They are also widely studied for use in the field of stationary energy storage. A lithium metal battery comprises at least one negative electrode and at least one positive electrode between which is placed a separator impregnated with a liquid electrolyte or a solid polymer electrolyte ensuring by itself both the physical separation of the electrodes and the transport of the electrodes. lithium ions. The negative electrode is made of a sheet of lithium metal or a lithium alloy, possibly supported by a current collector; and the positive electrode is constituted by a current collector supporting an electrode material containing at least one positive electrode active material capable of reversibly inserting lithium ions, optionally a polymer which acts as a binder (eg poly (vinylidene fluoride) or PVdF) and / or optionally an agent generating an electronic conductivity (eg carbon black). The liquid electrolyte is for example composed of a lithium salt (e.g. LiBF4, LiC104, LiPF6, etc.) in solution in a solvent chosen to optimize the transport and dissociation of the ions. Conventional electrolyte solvents (eg propylene carbonate, rbutyrolactone, sulfolane, dimethoxyethane, tetrahydrofuran, 1,3-dioxolane, etc.) are saturated under normal conditions at about 1-1.5 mol / l of sodium salt. lithium. The separator is generally made of an electronically non-conductive porous material, for example a polymer material based on polyolefins (e.g., polyethylene) or fibers (e.g., glass fibers or wood fibers). During the operation of the battery, lithium ions pass from one to the other of the electrodes through the electrolyte. Upon discharge of the battery, an amount of lithium reacts with the positive electrode active material from the electrolyte, and an equivalent amount is introduced into the electrolyte from the active material of the negative electrode. , the lithium concentration thus remaining constant in the electrolyte. The insertion of the lithium into the positive electrode is compensated by supplying electrons from the negative electrode via an external circuit. During charging, the reverse phenomena take place. The various components of a lithium battery are chosen so as to produce, at the lowest possible cost, batteries which have a high energy density, good cycling stability and function safely. For historical reasons but also for electrochemical performance, currently commercialized technologies rely on the almost exclusive use of inorganic electrode materials, mainly based on transition metals such as Co, Mn, Ni or Fe. However, these 20 Inorganic electrode materials (eg LiCoO2, LiMnO4, LiFePO4, LiNi0.8Coo, i5A10.0502, LiNiv3Mni / 3C01 / 302, LiNi0.01111.504, etc.) have many disadvantages such as the risk of battery explosion. , their high toxicity, their difficulty of recycling, their high cost and / or their low specific capacity. In addition, these inorganic materials are generally made from resources of geological origin (i.e., non-renewable) and energy-consuming in their process. Given the volumes of battery production announced (several billion units per year for Li-ion technology), these inorganic electrode materials may no longer be available in large quantities over time. On the other hand, none of the existing technologies 30 meets the needs perfectly, while new environmental standards are emerging at European level (see http://ec.europa.eu/environment/waste/batteries/, Directive 2006/66 / EC).
    [0002] In this context, the development of organic lithium batteries comprising as a positive electrode active material a redox organic structure (eg nitroxide derivatives, polyaromatic compounds), that is to say an organic structure capable of implementing a or several reversible oxidation-reduction reactions, in particular by exchanging electrons with an electrode and simultaneously by associating with lithium ions, suggests certain potentialities. First of all, these organic redox structures have the advantage of including chemical elements (C, H, N, O, S, in particular) potentially derived from renewable resources, thus making them more abundant. Then, they destroy themselves quite easily by simple combustion at a relatively moderate temperature. In addition, their electrochemical properties (ionic and electronic conduction properties, oxidation potential value, specific capacity) can be modulated by appropriate functionalization (e.g. integration of attracting groups close to the redox center). Finally, organic redox structures generally have a relative density of the order of 1 g / cm3, they are therefore lighter than inorganic electrode materials, and therefore lead to lithium batteries having a reduced weight.
    [0003] The studies carried out on organic lithium batteries since the beginning of the 1980s have focused exclusively on the search for new organic redox structures and have shown that the fundamental properties required for an organic redox structure to be implemented as an active ingredient of positive electrode are the electroactivity, the reversibility and a quasi insolubility in the electrolyte. By way of example, 7u-conjugated conductive polymers such as polypyrrole, polythiophene, polyaniline, polyacetylene or polyacryloxy (TEMPO) (with TEMPO: 2,2,6,6-tetramethylpiperidine-1-N- oxyl) have been used in lithium batteries as a positive electrode material. However, these organic redox structures generally have low specific capacities of the order of 100 mAh / g, in particular because they do not make it possible to exchange more than 0.5 electron with PP000523EN 4 monomer during the reactions. of oxidoreductions. The use of quinone derivatives as a positive electrode active material, a quinone generally characterized by two carbonyl functions present on an aromatic ring, has also attracted increasing interest. By way of example, 1,4-benzoquinone and 9,10-phenanthrenequinone (which have two carbonyl functions) respectively have high theoretical specific capacities of the order of 500 mAh / g and 256 mAh / g. In addition, they can theoretically undergo a two-electron oxidation-reduction reaction. In particular, JPS5686466 discloses an organic lithium battery comprising a negative electrode made of lithium metal; a positive electrode comprising 9,10-phenanthrenequinone as the active ingredient; a liquid electrolyte consisting of LiC104 in solution in propylene carbonate; and a separator impregnated with said liquid electrolyte. The battery has good stability with respect to its discharge capacity. However, the reversibility of oxidation-reduction reactions is insufficient and the average discharge voltage is relatively low (i.e. of the order of 2-2.5 volts). Similar results were obtained with anthraquinone. Thus, quinones having a greater number of carbonyl functions (e.g. three or four carbonyl functions) have been proposed to improve the electrochemical performance of organic lithium batteries. For example, Yao et al. [Int. J. of Electrochem. Sci., 2011, 6, 2905] have described an organic lithium battery comprising a negative electrode made of a lithium metal sheet; a positive electrode constituted by an aluminum current collector supporting an electrode material comprising 5,7,12,14-pentacenetetretone (PT) as the active material, acetylene black as an electronic conductivity generating agent and polytetrafluoroethylene as binder; a liquid electrolyte consisting of lithium bis (trifluoromethanesulfonyl) imide (LiTFSI) in 1 mol / l solution in rbutyrolactone; and a fiberglass separator impregnated with said liquid electrolyte. However, the cycling resistance of such a battery remains low since the initial specific capacitance is of the order of 300 mAh / g PP000523FR and drops to 170 mAh / g after 10 cycles. This poor cycling stability is mainly related to the solubility of the positive electrode active material (PT) in the solvent of the liquid electrolyte (see rbutyrolactone). Indeed, most organic redox structures of low molecular weight (i.e. molar mass less than 3000 g / mol) are soluble in the solvent of the liquid electrolyte. Also, when an organic redox structure is used as the electrode active material, the electronic conductivity between the current collector and said active material becomes insufficient and the reactivity is reduced. In addition, the concentration of active material that can be engaged in a redox reaction is decreased, which causes a drop in the capacity of the battery. Other redox organic structures based on indolin-3-one, such as the Indigo dye, also called Indigotine or 2- (1,3-dihydro-3-oxo-2Hindol-2-ylidene) -1,2- dihydro-3H-indole-3-one have also been proposed. In particular, Yao et al. [Chem. Letters, 2010, 39, 950] have described an organic lithium battery comprising a negative electrode consisting of a lithium metal sheet; a positive electrode constituted by an aluminum current collector supporting an electrode material comprising Indigotine as an active material, acetylene black as an electronic conductivity generating agent and polytetrafluoroethylene as a binder; a liquid electrolyte consisting of lithium hexafluorophosphate (LiPF6) in a 1 mol / l solution in a mixture of propylene carbonate and diethyl carbonate; and a separator impregnated with said liquid electrolyte. Here again, the specific capacity drops from 200 mAh / g to 20 mAh / g after about ten cycles, revealing a poor cycling stability. In order to avoid the dissolution of the active substance in the electrolyte, patent application EP 2546907 A1 describes the manufacture of an organic lithium battery comprising a negative electrode consisting of a lithium metal sheet; a positive electrode constituted by an aluminum current collector 30 supporting an electrode material comprising a pyrene-4,5,9,10-tetraone type organic redox structure having the following formula (1): PP000523EN 6 R5 (1) ) acetylene black as an electronic conductivity generating agent and polytetrafluoroethylene as a binder; a liquid electrolyte consisting of lithium hexafluorophosphate (LiPF 6) in 1 mol / l solution in a mixture of ethylene carbonate and methyl and ethyl carbonate; and a porous polyethylene separator impregnated with said liquid electrolyte. The performance of the organic lithium battery is improved in terms of cycling resistance and average discharge voltage. However, the preparation of the organic redox structure of formula (1) is complex (i.e. it comprises a large number of steps) and long. Thus, the object of the present invention is to overcome the disadvantages of the aforementioned prior art and to provide an economical organic lithium battery, which uses inexpensive raw materials, recyclable and non-toxic, and having good electrochemical performance in particular In terms of resistance to cycling. These objects are achieved by the invention which will be described below. The invention therefore has as its first object an organic lithium battery comprising: a negative electrode comprising lithium metal or a lithium metal alloy; a positive electrode possibly supported by a current collector, said positive electrode comprising at least one structure organic redox, at least one polymeric binder P1 and at least one agent generating an electronic conductivity, said organic redox structure being different from the sulfur-containing agents chosen from elemental sulfur S8 and sulfur-containing organic compounds comprising at least one SS bond, PP000523EN 7 said organic lithium battery being characterized in that it further comprises an electrolyte comprising at least one lithium salt L1 and at least one low molecular weight liquid linear polyether, it being understood that: when the electrolyte is a liquid electrolyte, the concentration of L1 lithium salt in said liquid electrolyte is at least about 1.6 mol / l, and the liquid electrolyte impregnates a porous separator, and * when the electrolyte is a gelled polymer electrolyte, it further comprises at least one polymeric binder P2, and the lithium salt concentration L1 in said gelled polymer electrolyte is such that the ratio 0 / Li is at most about 15, it being understood that in the ratio 0 / Li, "0" designates the number of oxygen atoms provided by the ether units of the low molecular weight linear polyether, and optionally by the ether units of the polymeric binder P2 if it contains them, and "Li" denotes the number of lithium ions provided by the lithium salt L1. The inventors of the present application have thus discovered that the use of a high concentration of lithium salt associated with the presence of a linear low molecular weight polyether in the electrolyte of the organic lithium battery makes it possible to significantly improve the electrochemical performance of said battery, particularly in terms of the stability of the specific capacitance during the discharge over a large number of cycles. This is quite surprising in that an increase in the concentration of lithium salt in a conventional electrolyte is generally accompanied by a decrease in ionic conductivity, an increase in viscosity and a decrease in mobility. lithium ions, inducing a decrease in the specific capacity and a limitation as to the current regime that can be used. By using such an electrolyte, the dissolution and diffusion of the organic redox structure of the positive electrode into the battery is greatly limited.
    [0004] In addition, the organic lithium battery of the invention has the advantage of being able to be implemented with various organic redox structures without having to modify their structures, in particular by adding new functional groups.
    [0005] In the present invention, "a low molecular weight liquid linear polyether" means a liquid linear polyether of molar mass less than or equal to about 10 000 g-mo1-1, preferably less than or equal to about 2000 g-mo1-1, and more preferably less than or equal to about 600 g-mo1-1.
    [0006] The low molecular weight liquid linear polyether of the electrolyte of the battery of the invention may be chosen from: polyethylene glycols of formula H- [O-CH 2 -CH 2] m-OH in which m is between 1 and 13, the glycol ethers of formula R- [O-CH 2 -CH 2] pOR 'in which p is between 1 and 13 and R and R', which are identical or different, are linear, branched or cyclic alkyl groups, comprising 1 to 20 carbon atoms, the ethers of formula R 1 - [CH 2 -O], 1-R 1 'in which q is between 1 and 13, R 1 and R 1', which are identical or different, are alkyl groups 20 linear, branched or cyclic, which may comprise from 1 to 20 carbon atoms and optionally heteroatoms, the cyclic ethers may comprise from 2 to 20 carbon atoms, the cyclic polyethers may comprise from 3 to 40 carbon atoms, and 25 * one of their mixtures. The polyether (s) used in the electrolyte of the invention is (are) particularly stable with respect to lithium and organic redox structures, thus making it possible to limit reactions as much as possible. parasites. In a preferred embodiment, the low molecular weight liquid linear polyether is tetraethylene glycol dimethyl ether (TEGDME) of the formula CH30- (CH2-CH2) 4-OCH3 (ie R, R '= CH3 and p = 4) or tetraethylene glycol (TEG) of formula H- (O-CH 2 -CH 2) 4 -OH (ie m = 4). The lithium salt L1 may be chosen from lithium fluoride (LiF03), lithium bis (trifluoromethanesulfonyl) imide (LiTFSI), lithium hexafluorophosphate (LiPF6), lithium fluoroborate (LiBF4), lithium metaborate (LiB02), lithium perchlorate (LiC104), lithium nitrate (LiNO3), lithium bis (fluorosulfonyl) imide (LiFSI), lithium bis (oxalato) borate (L1B (C204) 2 or LiBOB) and mixtures thereof . LiTFSI is the preferred lithium L1 salt.
    [0007] It goes without saying that the electrolyte of the battery of the invention is non-aqueous, that is to say that it does not include water or aqueous solvents. Indeed, an aqueous electrolyte is not compatible with a negative electrode lithium metal. The electrolyte preferably does not comprise carbonate-type organic solvents, the latter being unstable in the presence of a long-term lithium electrode and leading to consumption of the latter by the formation of a lithium foam. . According to a first variant, the electrolyte is a liquid electrolyte. It then thoroughly soaks the porous separator to impregnate the porosity. The choice of the porous separator is not limiting and this is well known to those skilled in the art. The porous separator may be of a non-conductive, electronically porous material, typically a polyolefin (e.g., polyethylene) -based polymeric material or fibers (e.g., glass fiber or wood fiber). According to this first variant, the concentration of lithium salt 1-1 in the liquid electrolyte ranges from about 1.6 to 8 mol / l, preferably from 1.8 to 6 mol / l, and more preferably from 2 to About 1 to 5 mol / l.
    [0008] The liquid electrolyte may consist of a lithium salt L1 dissolved in a solvent comprising at least one low molecular weight liquid linear polyether. The liquid electrolyte may consist solely of a lithium salt L1 and a liquid linear polyether of low molecular weight. The liquid electrolyte is preferably a solution comprising 4.5 mol / l LiTFSI in TEGDME. According to a second variant, the electrolyte is a gelled polymer electrolyte. The ratio 0 / Li of the gelled polymer electrolyte can range from about 2 to about 15, preferably from about 3 to about 10, and more preferably from about 4 to about 8. The polymer binder P2 of the gelled polymer electrolyte must be soluble in the low molecular weight liquid linear polyether. The polymer binder P2 may make it possible to solubilize the lithium salt 1-1 present in high concentration in the gelled polymer electrolyte and to ensure the mechanical strength of said gelled polymer electrolyte. The gelled polymer electrolyte can then be used alone, that is to say without a porous separator, and thus form a self-supporting dry electrolyte film. The polymer binder P2 of the gelled polymer electrolyte may be selected from: polyolefins such as homopolymers or copolymers of ethylene, propylene homopolymers or copolymers (e.g., ethylene-propylene copolymer); Polymers comprising several ether units such as polyethers, polyetherimides or polyvinyl ethers; * halogenated polymers such as homopolymers or copolymers of vinyl chloride, vinylidene fluoride (PVdF), vinylidene chloride, ethylene tetrafluoride or chlorotrifluoroethylene PP000523FR or copolymers of vinylidene fluoride and hexafluoropropylene ( PVdF-co-HFP); non-conducting electronic polymers of the anionic type such as poly (styrene sulphonate), poly (acrylic acid), poly (glutamate), alginate, gelatin or pectin; polyacrylates; elastomers such as homopolymers or copolymers of ethylene, propylene, styrene, butadiene or chloroprene; and * one of their mixtures. In the present text, the term "copolymer" means a polymer compound obtained from at least two different monomers. The polymeric binder P2 may have a molecular weight of substantially greater than about 10,000 g-mol, preferably substantially greater than about 50,000 g-mol, and more preferably substantially greater than 100,000 g-mol-1. about. Polyethers may have a linear, comb or block structure. Examples of polyethers that may be mentioned are homopolymers or copolymers of ethylene oxide (eg POE, POE copolymer), methylene oxide, propylene oxide, epichlorohydrin or allylglycidylether. The gelled polymer electrolyte may comprise from 40 to 80% by weight of polymer binder P2, and preferably from 50 to 70% by weight of polymer binder P2, relative to the total weight of the gelled polymer electrolyte. According to a particularly preferred embodiment of the invention, the polymer binder P2 is a mixture of a P2-A polymer and a P2-B polymer, said P2-A polymer making it possible to solubilize the present lithium L1 salt. in high concentration in the gelled polymer electrolyte and said P2_13 polymer for ensuring the mechanical strength of said gelled polymer electrolyte.
    [0009] The polymer P2-A may be a polymer comprising several ether units as defined above. The polymer P2-B may be a halogenated polymer as defined above.
    [0010] The gelled polymer electrolyte may comprise from 5 to 30% by weight of polymer P2-A, and preferably from 10 to 25% by weight of polymer P2-Af relative to the total weight of the gelled polymer electrolyte. The preferred P2_A polymers are the ethylene oxide / propylene oxide copolymer and the ethylene oxide / butylene oxide copolymer. The gelled polymer electrolyte may comprise from 20 to 50% by weight of polymer P2-B, and preferably from 30 to 45% by weight of polymer P2-B, relative to the total weight of the gelled polymer electrolyte. . The preferred P2-13 polymers are polyvinylidene fluoride (PVdF) and the copolymer of vinylidene fluoride and hexafluoropropylene (PVd F-co-H FP). The gelled polymer electrolyte may comprise from 18 to 50% by weight of lithium salt L1, more preferably from 25 to 50% by weight of lithium salt L1, and more preferably from 30 to 45% by weight. about L1 lithium salt relative to the total weight of the gelled polymer electrolyte. The gelled polymer electrolyte may comprise from 1 to 35% by weight of linear low molecular weight liquid polyether, preferably from 2 to 30% by weight of linear liquid polyether of low molar mass, and more preferably from 2 to 30% by weight. at about 15% by weight of low molecular weight liquid linear polyether, based on the total weight of the gelled polymer electrolyte. The battery according to the invention can operate between 0 and 110 ° C, and preferably between 20 and 100 ° C.
    [0011] In a particular embodiment of the invention, the positive electrode of the battery of the invention comprises at least about 50% by weight of organic redox structure, and preferably at least about 65% by weight of organic structure. redox, with respect to the total mass of said positive electrode. In the present invention, the expression "organic redox structure" means an electroactive organic structure capable of reacting reversibly with Li, that is to say an organic structure capable of carrying out one or more reversible oxidation-reduction reactions, by exchanging electrons with an electrode and simultaneously by associating with lithium ions. The organic redox structure represents the active material of the positive electrode (i.e. the positive electrode material) of the organic lithium battery of the invention.
    [0012] In the present invention, the organic redox structure being different from the sulfur-containing agents chosen from elemental sulfur 58 and sulfur-containing organic compounds comprising at least one SS bond, this is not a positive electrode active material such as those generally used as a positive electrode active material of a lithium sulfur battery. The sulfur-containing organic compounds comprising at least one SS bond may be organic polysulfides, in particular those of general formula R2-SS, -, -R3 in which R2 and R3, which may be identical or different, represent a linear, branched or cyclic alkyl chain, which may be comprise from 1 to 20 carbon atoms, and n being from 1 to 50; and disulfide polymers having a sequence of S-S bonds that can be broken during the discharge cycle of a lithium sulfur battery, and reformed during the charge cycle. According to a particularly preferred form of the invention, the organic redox structure comprises at least two C = O carbonyl functions, two C = S thionic functions or two C = N imine functional groups, optionally present on at least one aromatic ring. Carbonyl functions are preferred. According to a particularly preferred form of the invention, the organic redox structure belongs to any of the following families: quinones, anthraquinones, benzoquinones, naphthoquinones, oxoindolylidenes, compounds derived from the C606 skeleton (ie derivatives rhodizonate), compounds comprising at least one tetracyclic pyracene, and compounds derived from the calix [4] arene backbone. The organic redox structure comprising at least two C thS thiones functional groups can be chosen from the sulfur equivalents of these compounds, for example cyclohexadienediethiones, compounds derived from the C252 (C6H4) 2 backbone, thioindolylidenes and skeletal derivatives. C6OnS6-No. The positive electrode may comprise from about 1 to about 30 weight percent, and preferably from about 2 to about 20 weight percent of electronically conductive generating agent, based on the total weight of the positive electrode. The agent generating an electronic conductivity that is suitable for the present invention is preferably chosen from carbon black, SP carbon, acetylene black, carbon fibers and nanofibers, carbon nanotubes, graphene, graphite, particles and metal 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 the conduction, in particular in the direction perpendicular to the positive electrode (ie in the direction of its thickness) and thus to promote the electrochemical processes within the electrode. In fact, the spherical electron-generating agent particles have a propensity to form three-dimensional conductive networks. As an example of carbon black, mention may be made of the carbon blacks marketed under the references: Ketjenblack 600JD®, Ketjenblack 7003D® PP000523FR 15 and Timcal Ensaco 350G®. According to a particular embodiment, the positive electrode comprises from 2 to 30% by weight of polymer binder P1, and preferably from 5 to 20% by weight of polymer binder P1, relative to the total mass of the positive electrode. The polymer binder P1 may be chosen from copolymers and homopolymers of ethylene; copolymers and homopolymers of propylene; homopolymers and copolymers of ethylene oxide (e.g. POE, POE copolymer), methylene oxide, propylene oxide, epichlorohydrin, allyl glycidyl ether, and mixtures thereof; halogenated polymers such as homopolymers and copolymers of vinyl chloride, vinylidene fluoride (PVdF), vinylidene chloride, ethylene tetrafluoride, or chlorotrifluoroethylene, copolymers of vinylidene fluoride and hexafluoropropylene (PVdF). co-HFP) or their mixtures; polyacrylates such as polymethyl methacrylate; polyalcohols such as polyvinyl alcohol (PVA); electron-conducting polymers such as polyaniline, polypyrrole, polyfluorenes, polypyrenes, polyazulenes, polynaphthalenes, polyacetylenes, poly (p-phenylenevinylene), polycarbazoles, polyindoles, polyazepines, polythiophenes, p-phenylene polysulfide or mixtures thereof; cationic type polymers such as polyethyleneimine (PEI), polyaniline in the form of emeraldine salt (ES), poly (N-vinylimidazole quaternized), poly (acrylamide-co-diallyldimethyl ammonium chloride) (AMAC) or their mixtures; and one of their mixtures. The polymer binder P1 is preferably a copolymer of POE or a copolymer of vinylidene fluoride and hexafluoropropylene. The positive electrode may further comprise at least one low molecular weight liquid linear polyether as defined in the present invention. The presence of the linear low molecular weight polyether in the positive electrode makes it possible to improve its ionic conductivity.
    [0013] The positive electrode may then comprise from 2 to 30% by weight of linear low molecular weight polyether liquid, and preferably from 8 to 20% by weight of liquid linear low molecular weight polyether, relative to the total mass of the positive electrode.
    [0014] The positive electrode may further comprise at least one lithium salt L2. The positive electrode may then comprise from 1 to 25% by weight of lithium salt L 2, preferably from 1 to 15% by weight approximately of lithium salt L 2, and more preferably from 1 to 10% by weight approximately of lithium salt L2, based on the total mass of the positive electrode. The lithium salt L2 may be chosen from lithium fluoride (LiF03), lithium bis (trifluoromethanesulfonyl) imide (LiTFSI), lithium hexafluorophosphate (LiPF6), lithium fluoroborate (LiBF4), lithium metaborate (LiBO2), lithium perchlorate (LiClO4), lithium nitrate (LiNO3), lithium bis (fluorosulfonyl) imide (LiFSI), lithium bis (oxalato) borate (L1B (C204) 2 or LIBOB) and their mixtures. LiTFSI is the preferred lithium L2 salt. The positive electrode of the invention may have a porosity of less than or equal to about 40% by volume, and preferably less than or equal to about 30% by volume, based on the total volume of the positive electrode. This makes it possible to improve the energy density of the battery. It should be noted that the total mass of the positive electrode comprises the mass of the organic redox structure, the mass of the polymeric binder P1, the mass of the agent generating an electronic conductivity, possibly the mass of the low linear liquid polyether. molar mass if it is present and possibly the mass of the lithium salt L2 if it is present. The positive electrode may be prepared by: a) mixing at least one organic redox structure with at least one agent generating an electronic conductivity, at least one polymer binder P1, optionally at least one lithium salt L2, optionally with PP000523FR 17 minus a low molecular weight liquid linear polyether, and optionally at least one solvent of said polymer binder P1, to obtain an electrode paste, b) by applying said electrode paste to at least one support, c) by drying said electrode paste. electrode to obtain a positive electrode in the form of a supported film. The polymer binder P1, the lithium salt L2 and the low molecular weight liquid linear polyether are as defined in the present invention. Step a) may be carried out by extrusion or grinding. Extrusion is very advantageous since it makes it easy to obtain low 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, and adversely affect the quality of the electronic percolating network. Finally, the calendering step has the disadvantage of increasing the number of steps to obtain the electrode and thus its cost of production. The solvent of the polymer binder P1 of step a) makes it possible to solubilize said polymeric binder P1. When present, said solvent preferably represents less than about 30% by weight of the total weight of the mixture of organic redox structure, electronic conductivity generating agent, polymeric binder P1, optionally lithium salt L2. and optionally linear liquid polyether of low molecular weight. The use during manufacture of the positive electrode of a small amount of solvent of the polymeric binder P1 leads to a positive electrode of low porosity (i.e. 40% by volume approximately). This low porosity makes it possible to control and optimize the amount of organic redox structure present in the positive electrode, and thus to achieve optimal energy density densities. The solvent of step a) may be chosen from water, N-methylpyrrolidone and carbonate-type solvents, such as ethylene carbonate, propylene carbonate, dimethyl carbonate and carbonate. diethyl or methyl and ethyl carbonate, acetone, alcohols such as methanol, ethanol or propanol, and mixtures thereof. The solvent is preferably selected from water, acetone, alcohols, and mixtures thereof. Step b) can be carried out by rolling or coating. The support may 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 (anticorrosive layer). As an example of a support film, there may be mentioned a plastic film of the polyethylene terephthalate (PET) silicone type. The supported positive electrode film obtained at the end of step c) may have a thickness of about 2 to 100 μm, and preferably about 10 to about 60 μm. Step c) can be performed at a temperature sufficient to allow removal of the solvent from step a). The second subject of the invention is a method of manufacturing an organic lithium battery as defined in the first subject of the invention, characterized in that it comprises the following steps: A) a step of preparing a liquid electrolyte or a gelled polymer electrolyte as defined in the present invention, in particular by mixing at least one linear low molecular weight liquid polyether with at least one lithium salt, said process further comprising one or more other sequences B1 or B2 following: B1) a step of assembling a positive electrode, a negative electrode, as defined in the present invention, and a gelled polymer electrolyte prepared in step A) , or PP000523FR 19 B2-i) a step of assembling a positive electrode, a negative electrode and a porous separator, as defined in the present invention, and B2-ii) a step of impregnation of assembly as obtained in step B2-i) by the liquid electrolyte prepared in step A). The low molecular weight liquid linear polyether, the lithium salt L1 and the polymeric binder P2 are as defined in the first subject of the invention. The liquid electrolyte of step A) is preferably prepared by dissolving with stirring at least one lithium salt L1 in a low molecular weight liquid linear polyether, optionally at a temperature ranging from 20 to 120 ° C. The gelled polymer electrolyte of step A) can be obtained by extrusion of at least one polymeric binder P2 with a solution comprising at least one low molecular weight liquid linear polyether and at least one lithium salt L1 to obtain a electrolyte paste, then by rolling the electrolyte paste, especially between two support films to obtain a gelled polymer electrolyte film. The extrusion can be carried out at a temperature of from about 60 to 170 ° C. The two support films may be silicone PET plastic films. The present invention is illustrated by the following examples, to which it is however not limited. EXAMPLES The starting materials used in the examples are listed below: - carbon black "Ketjen black 6003D®", AkzoNobel, PP000523EN 20 - Indigotine, 2- (1,3-dihydro-3-oxo-2H-indole) 2-ylidene) -1,2-dihydro-3H-indol-3-one, 95% purity, Sigma Aldrich, copolymer of POE (co-POE), Mw 105 g.mol1-1, "ZSN 8100", Zeospan - copolymer of vinylidene fluoride and hexafluoropropylene (PVdF-co-HFP), Mw = 6.105 g.mol1-1, "Solex", Solvay, LiTFSI, 3M, Silicone PET film, Mitsubishi, Tetraethylene glycol dimethyl ether ( TEGDME) of 99% purity, Sigma Aldrich, Polypropylene monolayer separator, Celgard 2500, N-methylpyrrolidone (NMP), 99.5% purity, Sigma Aldrich. Unless otherwise indicated, all materials have been used as received from manufacturers.
    [0015] EXAMPLE 1 Manufacture of batteries B-1, B-2 and B-3 1.1 Preparation of the positive electrode 3 g of Ketjenblack carbon black, 21 g of Indigotine, 4.8 g of co-POE copolymer, 1, 2 g of lithium salt (LiTFSI) and 5 g of water were mixed at 80 ° C. for 20 minutes in a mixer sold under the trade name Plastograph® EC by Brabender®. The amount of water used was about 16.6% by weight of the total mass of carbon black, Indigotine, co-POE copolymer and LiTFSI lithium salt.
    [0016] The resulting slurry was then rolled at 95 ° C onto an aluminum current collector coated with a carbon-based layer.
    [0017] The film thus obtained was dried at 110 ° C. for 20 minutes in an oven to obtain a positive electrode E-1 in the form of a film in accordance with the invention. Table 1 below shows the mass composition of the positive electrode E-1 obtained: TABLE 1 Black Co-POE Salt Electrode Indigo positive lithium carbon (0/0) (0/0) (0/0) (0/0) E-1 10 4 16 70 1.2 Preparation of gelled polymeric electrolytes Lithium salt (LiTFSI) was dissolved in TEGDME with magnetic stirring at 50 ° C. Then, to the resulting mixture was added a copolymer of Zeospan® POE and a copolymer of vinylidene fluoride and hexafluoropropylene (PVdF-co-HFP). The resulting mixture was kneaded in the Plastograph® EC mixer as described in Example 1.1, at 130 ° C for 40 minutes. The resulting electrolyte paste was laminated at 125 ° C between two silicone PET plastic films. Table 2 below shows the mass composition of two gelled polymeric electrolytes obtained: TABLE 2 Electrolyte TEGDME Co-POE salt PVdF-co-HFP Polymer (0/0) lithium ratio (0/0) (0/0) 0 Gel / Li (0/0) PG-1 6 39 20 35 4 PG-2 24.7 13.3 22 40 22 20 1.3 Preparation of a solid polymer electrolyte The solid polymer electrolyte was prepared by extrusion of a mixture of lithium salt (LiTFSI), copolymer of POE Zeospan® and PVDF-co-PP000523FR 22 HFP, and then rolling the electrolyte paste obtained at 125 ° C between two plastic films of silicone PET. Table 3 below shows the mass composition of the solid polymer electrolyte obtained: TABLE 3 Electrolyte TEGDME Co-POE salt PVdF-co-HFP Polymer (0/0) lithium (0/0) (0/0) solid (0/0) PS-1 0 12 48 40 The solid polymer electrolyte not according to the invention and as prepared above, comprises a concentration of lithium salt such as the ratio 0 / Li of the number of atoms Oxygen supplied by the ethers units of 10 co-POE on the number of lithium ions provided by the lithium salt is 22. 1.4 Manufacture of organic lithium batteries Three batteries B-1, B-2 and B-3 have were prepared by assembling under an anhydrous atmosphere (air with a dew point <-40 ° C) by manual rolling at room temperature: - the positive electrode E-1 obtained in Example 1.1 above, - a negative electrode comprising lithium metal in the form of a lithium metal film approximately 100 μm thick, and - the gelled polymer electrolyte PG-1 ob taken in Example 1.2 above, or the gelled polymer electrolyte PG-2 obtained in Example 1.2 above, or the solid polymer electrolyte PS-1 obtained in Example 1.3 above. The battery B-1 is in accordance with the invention since it comprises a positive electrode, a negative electrode and a gelled polymer electrolyte as defined in the present invention.
    [0018] On the other hand, batteries B-2 and B-3 are not in accordance with the invention since they do not comprise a liquid or gelled polymer electrolyte as defined in the present invention. The specific capacity (in mAh / g) of battery B-1 (curve with solid circles), battery B-2 (curve with solid triangles), and battery B-3 (curve with solid squares) ) as a function of the number of cycles at a current regime of C / 10 and at a temperature of 100 ° C. is shown in FIG. 1. These results show that the use of a gelled polymer electrolyte as defined herein The invention makes it possible to maintain an initial specific capacity of the same order of magnitude as that obtained with a solid polymer electrolyte (battery B-3) in organic lithium batteries. The relative capacity corresponding to the ratio of the discharge capacity of cycle n to the discharge capacity of the first cycle, batteries B-1 (curve with solid circles), B-2 (curve with solid triangles) and B-3 (curve with solid squares) as a function of the number of cycles at a current regime of C / 10 and a temperature of 100 ° C is shown in FIG. 2.
    [0019] In particular, Figure 2 shows for battery B-3 (solid polymer electrolyte) a very rapid drop in discharge capacity during the first cycles and the lack of stabilization in subsequent cycles, probably related to a dissolution of the Indigotine in the solid polymer electrolyte and thus, its diffusion. On the other hand, the use of a gelled polymer electrolyte as defined in the present invention makes it possible to significantly improve the cyclability of the organic lithium battery. The use of a solid polymer electrolyte having a lithium salt concentration such as the 0 / Li ratio of the number of oxygen atoms provided by the ether units of the co-POE on the number of lithium ions supplied by the The lithium salt is less than 15 is also not suitable since it would generate a significant increase in the viscosity of the electrolyte, and thus a significant lowering of the capacity restored and therefore the energy density. EXAMPLE 2 Manufacture of Batteries B-4 and B-5 2.1 Preparation of the Positive Electrode 1.75 g of Ketjenblack Carbon Black, 24.5 g of Indigotine, 4.53 g of TEGDME, 1.42 g of salt of lithium (LiTFSI), 2.8 g of PVDF-co-HFP polymer and 5 g of N-methylpyrrolidone (NMP) were mixed at 120 ° C. for 20 minutes in a mixer sold under the trade name Plastograph® EC by the Brabender® company. The amount of NMP used accounted for about 14% by weight of the total mass of carbon black, Indigotine, TEGDME, LiTFSI lithium salt and PVDF-co-HFP. The resulting slurry was then rolled at 80 ° C onto an aluminum current collector coated with a carbon-based layer.
    [0020] The film thus obtained was dried at 110 ° C. for 20 minutes in an oven to obtain a positive electrode E-2 in the form of a film according to the invention. Table 4 below shows the mass composition of the positive electrode E-2 obtained: TABLE 4 TEGDME PVDF-co-Indigo positive lithium carbon (0/0) HFP (0/0) black electrode (0 / 0) (0/0) (0/0) E-2 5 4.06 12.94 8 70 2.2 Preparation of two liquid electrolytes Two liquid electrolytes L-1 and L-2 were prepared by dissolving a sodium salt. lithium LiTFSI in TEGDME with magnetic stirring for 10 minutes at 50 ° C. The liquid electrolyte L-1, according to the invention, had a concentration of lithium salt equal to 2.27 mol / l. The liquid electrolyte L-2, not in accordance with the invention, had a concentration of 0.9 mol / l. 2.3 Manufacture of Organic Lithium Batteries Two B-4 and B-5 batteries were prepared by assembling under an anhydrous atmosphere (air with a dew point <-40 ° C) by manual lamination at room temperature: - the positive electrode E -2 obtained in Example 2.1 above, - a negative electrode comprising lithium metal in the form of a lithium metal film approximately 100 μm thick, and 10 - a Celgard 2500 separator impregnated with the liquid electrolyte L-1 obtained in Example 2.2 above, or a Celgard 2500 separator impregnated with the liquid electrolyte L-2 obtained in Example 2.2 above. The specific capacity (in mAh / g) of the battery B-4 (curve with the solid black diamonds) and the battery B-5 (curve with the empty circles) as a function of the number of cycles at a current regime of C / 20-D / 20 (a charge or discharge in 20 hours) and a temperature of 40 ° C is shown in Figure 3. This figure 3 shows a slower fall in the discharge capacity for the battery B-4 according to the invention (curve with solid black diamonds), which shows the effectiveness of a high lithium salt content to slow the diffusion of the active ingredient in the liquid electrolyte.
    权利要求:
    Claims (17)
    [0001]
    REVENDICATIONS1. An organic lithium battery comprising: a negative electrode comprising lithium metal or a lithium metal alloy; a positive electrode optionally supported by a current collector, said positive electrode comprising at least one organic redox structure, at least one polymer binder P1 and at least one agent generating an electronic conductivity, said organic redox structure being different from the sulfur-containing agents chosen from elemental sulfur S8 and sulfur-containing organic compounds comprising at least one SS bond, said organic lithium battery being characterized in that it further comprises an electrolyte comprising at least one lithium salt L1 and at least one low molecular weight liquid linear polyether, it being understood that: when the electrolyte is a liquid electrolyte, the concentration of lithium salt L1 in said liquid electrolyte is at least 1.6 mol / I, and the liquid electrolyte impregnates a and when the electrolyte is a gelled polymer electrolyte, it further comprises at least one polymeric binder P2 and the concentration of lithium salt L1 in said gelled polymer electrolyte is such that the ratio 0 / Li is from plus 15, it being understood that in the ratio 0 / Li, "0" designates the number of oxygen atoms provided by the ether units of the low molecular weight liquid linear polyether, and possibly by the ether units of the polymeric binder P2 s it contains it, and "Li" denotes the number of lithium ions provided by the lithium salt L1.
    [0002]
    2. Battery according to claim 1, characterized in that the low molecular weight liquid linear polyether is a liquid linear polyether of molar mass less than or equal to 10 000 g-mo1-1.
    [0003]
    3. Battery according to claim 1 or 2, characterized in that the lithium salt L1 is chosen from lithium fluoride (LiF03), lithium PPB (lithium trifluoromethanesulfonyl) imide (LiTFSI), lithium hexafluorophosphate (LiF03) and lithium hexafluorophosphate (LiF03). LiPF6), lithium fluoroborate (LiBF4), lithium metaborate (LiB02), lithium perchlorate (LiClO4), lithium nitrate (LiNO3), lithium bis (fluorosulfonyl) imide (LiFSI), lithium bis ( oxalato) borate (L1B (C204) 2 or LiBOB) and mixtures thereof.
    [0004]
    4. Battery according to any one of the preceding claims, characterized in that the organic redox structure comprises at least two C = 0 carbonyl functions, two C = S thiones functions or two C = N imine functions.
    [0005]
    5. Battery according to any one of the preceding claims, characterized in that the positive electrode comprises at least 50% by weight of organic redox structure with respect to the total mass of said positive electrode.
    [0006]
    6. Battery according to any one of the preceding claims, characterized in that the positive electrode comprises from 1 to 30% by weight of agent generating an electronic conductivity with respect to the total mass of the positive electrode.
    [0007]
    7. Battery according to any one of the preceding claims, characterized in that the agent generating an electronic conductivity is chosen from carbon black, SP carbon, acetylene black, carbon fibers and nanofibers, carbon nanotubes, graphene, graphite, metal particles and fibers and one of their mixtures.
    [0008]
    8. Battery according to any one of the preceding claims, characterized in that the positive electrode comprises from 2 to 30% by weight of polymer binder P1 relative to the total mass of the positive electrode.
    [0009]
    9. Battery according to any one of the preceding claims, characterized in that the polymeric binder P1 is chosen from copolymers and homopolymers of ethylene; copolymers and homopolymers of propylene; homopolymers and copolymers of ethylene oxide, methylene oxide, propylene oxide, epichlorohydrin, allyl glycidyl ether and mixtures thereof; halogenated polymers; polyacrylates; polyalcohols; electronically conductive polymers; cationic type polymers; and one of their mixtures.
    [0010]
    10. Battery according to any one of the preceding claims, characterized in that the polymeric binder P2 is chosen from polyolefins, polymers comprising several ether units, halogenated polymers, nonconductive polymers of the anionic type, polyacrylates, elastomers and one of their mixtures.
    [0011]
    11. Battery according to any one of the preceding claims, characterized in that the gelled polymer electrolyte comprises from 40 to 80% by weight of polymer binder P2 relative to the total weight of the gelled polymer electrolyte.
    [0012]
    12. Battery according to any one of the preceding claims, characterized in that the polymeric binder P2 is a mixture of a P2-A polymer and a P2-B polymer, said polymer P2-A for solubilizing the salt of lithium L1 present in high concentration in the gelled polymer electrolyte and said P2-13 polymer for ensuring the mechanical strength of said gelled polymer electrolyte.
    [0013]
    13. Battery according to claim 12, characterized in that the P2_A polymer is a polymer comprising several ether units and the polymer P2-13 is a halogenated polymer.
    [0014]
    14. Battery according to any one of the preceding claims, characterized in that the 0 / Li ratio of the gelled polymer electrolyte ranges from 3 to 10.
    [0015]
    15. Battery according to any one of the preceding claims, characterized in that the gelled polymer electrolyte comprises from 1 to 35% by weight of liquid linear polyether of low molecular weight relative to the total mass of the gelled polymer electrolyte. PP000523EN 29
    [0016]
    16. Battery according to any one of claims 1 to 9, characterized in that the concentration of lithium salt L1 in the liquid electrolyte is from 1.8 to 6 mol / l.
    [0017]
    17. A method of manufacturing an organic lithium battery as defined in any one of claims 1 to 16, characterized in that it comprises the following steps: A) a step of preparation of a liquid electrolyte or d a gelled polymer electrolyte as defined in any one of claims 1 to 16, said process further comprising one or other of the following B1 or B2 sequences: B1) a step of assembling an electrode positive, a negative electrode, as defined in any one of claims 1 to 16, and a gelled polymer electrolyte prepared in step A), or B2-i) an assembly step of a positive electrode, a negative electrode and a porous separator, as defined in any one of claims 1 to 16, and B2-ii) a step of impregnating the assembly as obtained from the step B2-i) by the liquid electrolyte prepared in step A).
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    同族专利:
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    JP2017535927A|2017-11-30|
    CN107251287B|2020-10-23|
    SG11201704456PA|2017-06-29|
    WO2016087759A1|2016-06-09|
    CA2967918A1|2016-06-09|
    FR3029360B1|2019-04-26|
    EP3227944B1|2019-01-02|
    KR20170091703A|2017-08-09|
    US20170271677A1|2017-09-21|
    EP3227944A1|2017-10-11|
    ES2714080T3|2019-05-27|
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    法律状态:
    2015-12-21| PLFP| Fee payment|Year of fee payment: 2 |
    2016-06-03| PLSC| Publication of the preliminary search report|Effective date: 20160603 |
    2016-12-22| PLFP| Fee payment|Year of fee payment: 3 |
    2017-12-21| PLFP| Fee payment|Year of fee payment: 4 |
    2019-12-19| PLFP| Fee payment|Year of fee payment: 6 |
    2021-09-10| ST| Notification of lapse|Effective date: 20210806 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1461704A|FR3029360B1|2014-12-01|2014-12-01|ORGANIC LITHIUM BATTERY|
    FR1461704|2014-12-01|FR1461704A| FR3029360B1|2014-12-01|2014-12-01|ORGANIC LITHIUM BATTERY|
    US15/529,328| US10586986B2|2014-12-01|2015-11-30|Organic lithium battery|
    ES15810690T| ES2714080T3|2014-12-01|2015-11-30|Organic lithium battery|
    SG11201704456PA| SG11201704456PA|2014-12-01|2015-11-30|Organic lithium battery|
    CA2967918A| CA2967918A1|2014-12-01|2015-11-30|Organic lithium battery|
    JP2017528917A| JP2017535927A|2014-12-01|2015-11-30|Organic lithium battery|
    EP15810690.6A| EP3227944B1|2014-12-01|2015-11-30|Organic lithium battery|
    KR1020177018104A| KR20170091703A|2014-12-01|2015-11-30|Organic lithium battery|
    CN201580065015.9A| CN107251287B|2014-12-01|2015-11-30|Organic lithium battery|
    PCT/FR2015/053265| WO2016087759A1|2014-12-01|2015-11-30|Organic lithium battery|
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