• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A method of manufacturing a fully solid thin-film battery comprising the following successive steps: a) depositing a layer comprising at least one anode material on its conductive substrate, b) depositing a layer comprising at least one cathode material on its conductive substrate, c) depositing a layer comprising at least one solid electrolyte material on at least one layer obtained in step a) and / or b); d) depositing a layer of a crosslinked polymeric material comprising ionic groups: ○ either on the layer of anode material coated with a layer of solid electrolyte material and / or on the layer of coated cathode material or not a layer of solid electrolyte material; Either on the layer of cathode material coated with a layer of solid electrolyte material and / or on the layer of anode material coated or not with a layer of solid electrolyte material; e) successively facing a layer of anode material obtained in step a), c) or d) with a layer of cathode material obtained in step b), c) or d) being understood that the stack comprises at least one layer of solid electrolyte material obtained in step c) and at least one layer of a crosslinked polymer material obtained in step d); f) heat treatment and / or mechanical compression of the stack obtained in step e) to obtain a fully solid thin-film battery.
    公开号:FR3023417A1
    申请号:FR1456272
    申请日:2014-07-01
    公开日:2016-01-08
    发明作者:Fabien Gaben
    申请人:I TEN；
    IPC主号:
    专利说明:

    [0001] TECHNICAL FIELD The present invention relates to the field of batteries and in particular lithium ion batteries. It relates more particularly to lithium ion batteries ("Li-ion batteries") entirely solid, and a new method of manufacturing such batteries. State of the art There are known methods of manufacturing lithium ion batteries ("Li-ion batteries") presented in numerous articles and patents; Advances in Lithium-ion Batteries (W. van Schalkwijk and B. Scrosati), published in 2002 (Kluever Academic / Plenum Publishers) gives a good inventory. The electrodes of Li-ion batteries may be manufactured using printing or deposition techniques known to those skilled in the art, and in particular by roll coating ("roll coating"), doctor blade ("doctor blade"). ), or by tape casting. More recently, other architectures of Li-ion batteries have appeared. These are mainly thin-film, fully solid batteries. These batteries are of planar architectures, that is to say that they consist essentially of a set of three layers forming an elementary cell battery: anode layer and a cathode layer separated by a layer of 'electrolyte. These fully solid battery architectures use lithium metal anodes, and lithiated phosphate oxynitride films as the electrolyte. However, the large volume variations of the lithium anode during the charging and discharging steps make it extremely difficult to correctly encapsulate the battery without the risk of loss of sealing of the encapsulation. More recently, new fully solid battery architectures consisting of thin film stacking have been proposed. These batteries consist of a rigid and one-piece assembly of a set of elementary cells connected in parallel. These batteries use dimensionally stable anodes in order to guarantee the efficiency of encapsulation, and allow the realization of three-dimensional structures, with much better densities of surface energy than the planar architectures. Such batteries are described in WO 2013/064779 A1 or WO 2012/064777 A1. The batteries described in these documents do not contain liquid electrolyte based on organic solvent, their structure is in thin layers entirely solid, without porosity. in the electrode layers to ensure good stability properties of the battery over time. This manufacturing method has many advantages because it allows for multilayer assemblies, thin layers and therefore low resistive, which allows to maintain performance in terms of power. However, in some cases, the method of manufacturing such batteries may have some limitations depending on the materials used, especially for the electrolyte. Indeed, the use of ionic conductive glasses can be difficult to implement. For example, solid electrolytes, such as LiPON or lithiated borates have a relatively low glass transition temperature, generally between about 250 and 300 ° C: thus during the step of assembling the battery by annealing under pressure of different layers, the electrolyte materials can partially crystallize, which can change their ionic conduction property. In the same way, when the solid electrolyte based on lithiated phosphates is used, it may be advantageous to differentiate the chemical compositions of the electrolytes in contact with the anodes and the cathodes in order to optimize the performance of the electrolytes. However, the use of two formulations of lithiated phosphates on each of the faces of the electrodes may give rise to the appearance of new phases at the interface between the two electrolyte layers to be assembled and may therefore modify the conduction properties. In the same way, the solid electrolytes of Li7La3Zr2012 type (called LLZO) are good ionic conductors and are very stable in contact with the anodes and cathodes, but their very refractory nature makes it sometimes difficult to weld the electrodes at low temperature. without inducing interdiffusion phenomenon at the interfaces with the electrodes. A first object of the present invention is to provide a method for manufacturing batteries in thin layers entirely solid, not inducing the appearance of phases at the interface between the two layers of electrolytes to be assembled.
    [0002] Another object of the present invention is to provide a battery manufacturing method at low temperature without inducing interdiffusion phenomenon at the interfaces with the electrodes. Another object of the invention is to manufacture batteries in thin layers by a process that can be implemented industrially in a fairly simple manner.
    [0003] OBJECTS OF THE INVENTION A first object of the invention relates to a method of manufacturing a fully solid thin-film battery comprising the following successive steps: a) depositing a layer comprising at least one anode material (here called " layer of anode material ") on its conductive substrate, preferably selected from the group consisting of a metal sheet, a metal strip, a metallized insulating sheet, a metallized insulating strip, a metallized insulating film, said conductive substrates, or their conductive elements, which can serve as anode current collector; b) depositing a layer comprising at least one cathode material (here called "layer of cathode material") on its conductive substrate, preferably selected from the group consisting of a metal sheet, a metal strip, a metallized insulating sheet, a metallized insulating strip, a metallized insulating film, said conductive substrates, or their conductive elements, being able to serve as a cathode current collector, it being understood that the steps a) and b) can be reversed; c) depositing a layer comprising at least one solid electrolyte material (here called "layer of electrolyte material") on at least one layer obtained in step a) and / or b); d) depositing a layer of a crosslinked polymeric material having ionic groups: o either on the layer of anode material coated with a layer of solid electrolyte material and / or on the layer of coated cathode material or not a layer of solid electrolyte material; o either on the layer of cathode material coated with a layer of solid electrolyte material and / or on the layer of anode material coated or not with a layer of solid electrolyte material; e) successively facing a layer of anode material obtained in step a), c) or d) with a layer of cathode material obtained in step b), c) or d) being understood that the stack comprises at least one layer of solid electrolyte material obtained in step c) and at least one layer of a crosslinked polymer material obtained in step d); f) heat treatment and / or mechanical compression of the stack obtained in step e) to obtain a fully solid thin-film battery.
    [0004] The crosslinked polymeric material is preferably selected from polymethyl methacrylates, polyamines, polyimides, or polysiloxanes. Preferably, the ionic groups are chosen from the following cations: imidazolium, pyrazolium, tetrazolium, pyridinium, pyrrolidinium, such as n-propyl-n-methylpyrrolidinium (also called PYR13) or n-butyl-n- methylpyrrolidinium (also called PYR14), ammonium, phosphonium or sulfonium; and / or among the following anions: bis (trifluoromethane) sulfonimide, bis (fluorosulfonyl) imide, or n (nonafluorobutanesulfonyl) -n- (trifluoromethanesulfonyl) imide. In a particular embodiment, the crosslinked polymer material is obtained by a step of polymerizing a mixture of monomers and / or oligomers and / or prepolymers comprising one or more groups that can be polymerized thermally or photochemically, said monomer mixture and / or oligomers and / or pre-polymers comprising one or more reactive groups for grafting said ionic groups.
    [0005] Preferably, the thermal and / or photochemical polymerization is carried out directly on the layer (s) of anodes, cathodes and / or electrolytes. Advantageously, the deposition of the crosslinked polymer material comprising ionic groups is carried out among at least one of the following techniques: dip-coating, spin-coating, roll coating ), doctor blade, electrospray, or electrophoresis. The thickness of the layer of polymeric material is less than 10 μm, preferably less than 5 μm, and even more preferably less than 2 μm. The anode, cathode and solid electrolyte layers are deposited among at least one of the following techniques: (i) physical vapor phase deposition (PVD), and more particularly by evaporation under vacuum, by laser ablation, by ion beam, by sputtering; (ii) chemical vapor deposition (CVD), and more particularly plasma assisted (PECVD), laser assisted (LACVD), or aerosol assisted (AA-CVD); (iii) electrospray; (iv) electrophoresis; (v) aerosol deposition; (vi) sol-gel; (vii) soaking, more particularly by dip-coating, spin-coating, or by the Langmuir-Blodgett process.
    [0006] Preferably, the anode, cathode and electrolyte layers are deposited by electrospray, electrophoresis, aerosol deposition, dipping, and are preferably all electrophoretically deposited. In a particular embodiment, the layers of anode material and / or cathode further comprise electronically conductive materials, and in particular graphite, and / or nanoparticles of lithium ion conductive materials, of the type used. for producing the electrolyte films, or crosslinked solid polymer materials comprising ionic groups. Preferably, the anode and / or cathode and / or electrolyte layers are produced by deposition of nanoparticles respectively anode material, cathode or electrolyte in at least one of the following techniques: electrospray , electrophoresis, aerosol deposition, soaking. More particularly, the nanoparticle layers of anode material, cathode and electrolyte are all deposited by electrophoresis.
    [0007] According to the invention, the heat treatment is carried out at a temperature of between 50 ° C. and 300 ° C., preferably between 100 ° C. and 200 ° C. and / or in that the mechanical compression of the layers to be assembled is carried out at a temperature of pressure between 10 and 100 MPa, preferably between 20 and 50 MPa. The anode material layer a) is made from material chosen from: (i) tin oxynitrides (of typical formula SnOxNy); (ii) lithium iron phosphate (of typical formula LiFePO4); (iii) mixed oxynitrides of silicon and tin (of typical formula SiaSnbOyNz with a> 0, b> 0, a-FLK2, 0 <y4, 0 <z3) (also known as SiTON), and in particular SiSno, 8701, 2N, 1.72; as well as oxynitrides in the form SiaSnbCcOyNz with a> 0, b> 0, a-FLK2, 0 <c <10, 0 <y <24, 0 <z <17; SiaSnbCcOyNzX, and SiaSnbOyNzXa with Xn at least one of F, Cl, Br, I, S, Se, Te, P, As, Sb, Bi, Ge, Pb; (iv) the nitrides of the type SixNy (in particular with x = 3 and y = 4), SnxNy (in particular with x = 3 and y = 4), ZnxNy (in particular with x = 3 and y = 4), Li3_xMxN (with M = Co, Ni, Cu); (v) the oxides SnO2, Li4Ti5012, SnBo, 6P0, 402.9. The cathode material layer b) is made from cathode material selected from: (i) LiMn 2 O 4, LiCoO 2, LiNiO 2, LiMn 1, 5 Ni 0, 504, LiMn 1, 5NiO 5, xxx O 4 (where x is selected from Al, Fe , Cr, Co, Rh, Nd, other rare earths, and where 0 <x <0.1), LiFeO2, LiMn1i3Ni1i3C01 / 304; (ii) LiFePO4, LiMnPO4, LiCoPO4, LiNiPO4, Li3V2 (PO4) 3 phosphates; phosphates of formula LiMM'PO4, with M and M '(M # M') selected from Fe, Mn, Ni, Co, V; (iii) all the lithiated forms of the following chalcogenides: V205, V308, TiS2, titanium oxysulfides (TiOyS), tungsten oxysulfides (VVOySz), CuS, CuS2. The electrolyte material layer c) is made from electrolyte material chosen from: o lithiated phosphates, preferably chosen from: Li3PO4; Li3 (Sc2_ xMx) (PO4) 3 with M = A1 or Y and 0 x 1; Li 1 + xMx (Sc) 2-x (PO 4) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Li 1 + xMx (Ga 1-y Sn y) 2-x (PO 4) 3 with O x 0.8; 0 y 1 and M = Al or Y; Li 1 + xMx (Ga) 2-x (PO 4) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; 0 y 1; Li 1, Al x -Ri 2-x (PO 4) 3 with O x 1, or Li 1, Al x Ge 2-x (PO 4) 3 with O x 1; or the Lii.x.zMx (Gei_yTiy) 2_xSizP3_z012 with 0x <_0.8 and & 0z <_0.6 and M = Al, Ga or Y or a mixture of two or three of these compounds o the lithiated borates, preferably chosen among: Li3 (Sc2, (Mx) (B03) 3 with M = A1 or Y and 0 x 1, Li1 + xMx (Sc) 2_x (B03) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Li 1 + x M x (Ga 1-y BcO 2-x (B0 3) 3 with 0 x 0.8; 0 y 1 and M = Al or Y; Li 1 + x M x (Ga) 2-x (B03) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; the oxynitrides, preferably selected from Li3PO4_xN2x / 3, Li4SiO4_xN2x / 3, Li4Ge04_xN2x / 3 with 0 <x <4 or Li3B03_xN2x / 3 with 0 <x <3, materials based on phosphorus or boron lithium oxynitrides (called LiPON and LIBON) which may also contain silicon, sulfur, zirconium, lithium aluminum, or a combination of aluminum, boron, sulfur and / or silicon, and boron for lithium phosphorus o the lithiated oxides, preferably selected from Li7La3Zr2012 or e Li5 + xLa3 (Zrx, A2_x) 012 with A = Sc, Y, Al, Ga and 1.4 x 2 or Li0.35La0.55TiO3. In a particular embodiment, the method further comprises a step of encapsulating the battery obtained in step f) by depositing at least one encapsulating layer of ceramic material, vitreous or vitroceramic. Advantageously, anodic and cathodic terminations are carried out by metallization of the cut sections, preferably by deposition of a layer of tin optionally deposited on a first sub-layer of nickel and / or epoxy resin loaded with metal particles. Preferably, the size of the nanoparticles of electrolyte materials is less than 100 nm, preferably less than 30 nm.
    [0008] The conductive substrates are made of aluminum, copper or nickel, preferably nickel, and optionally coated with a noble metal selected from the following metals: gold, platinum, palladium, vanadium, cobalt, nickel , manganese, niobium, tantalum, chromium, molybdenum, titanium, palladium, zirconium, tungsten or any alloy comprising at least one of these metals.
    [0009] Another object of the invention relates to a battery that can be obtained by the method according to the invention. Advantageously, the surface capacitance of the cathode is greater than or equal to the surface capacitance of the anode. In a preferred embodiment, the stack of cathode and anode layers is shifted laterally. Advantageously, the battery comprises at least one encapsulation layer, preferably a ceramic, glass or glass-ceramic layer. Even more advantageously, the battery comprises a second encapsulation layer deposited on said first encapsulation layer, said second encapsulation layer preferably being silicone. Preferably, said at least one encapsulation layer completely covers four of the six faces of said battery and partially the two remaining faces, located under the metallizations used for the connection of the battery. In a particular embodiment, the battery comprises terminations at the level where the cathode current collectors, respectively anodic, are apparent. Advantageously, the anode connections and the cathode connections are on the opposite sides of the stack. DETAILED DESCRIPTION OF THE INVENTION 1. Definitions In the context of the present invention, the term "electrophoretic deposition" or "electrophoretic deposition" means a layer deposited by a process for deposition of particles previously suspended in a liquid medium, on a preferably conductive substrate, the displacement of the particles towards the surface of the substrate being generated by the application of an electric field between two electrodes placed in the suspension, one of the electrodes constituting the conductive substrate on which the deposit is made, the other electrode ("counter-electrode") being placed in the liquid phase. A so-called "dense" deposit of particles is formed on the substrate, if the zeta potential of the suspension of the particles has an appropriate value, and / or following a specific densification treatment of thermal and / or mechanical nature. This deposit has a particular structure and recognizable by the skilled person that distinguishes it from the deposits obtained by any other technique. For the purpose of this paper, the size of a particle is its largest dimension. Thus, a "nanoparticle" is a particle of which at least one of the dimensions is less than 100 nm. The "particle size" or "average particle size" of a powder or set of particles is given in D50. Battery means "any solid" (also called here battery "fully solid"), a battery does not include liquid phase material. The term "surface capacitance" of an electrode is the amount of lithium ion that can be inserted into an electrode (expressed in mA.h / cm 2). 2. Detailed Description In order to meet the drawbacks mentioned above, the inventor has developed a new process for manufacturing all-solid batteries that do not contain organic solvents so that they can be heated without risk of combustion. The objectives are achieved by the implementation of a method for manufacturing a thin-film battery comprising at least one layer of a crosslinked polymer material comprising ionic groups. The batteries obtained by the method according to the invention are of multilayer structure, in opposition to planar structures of conventional thin film batteries, to obtain batteries having a good density of energy and power. In addition, the method of obtaining these batteries makes it possible to assemble the layers of the battery at a relatively low temperature, ie at a temperature below 300 ° C., without reducing the surface capacitances of the electrodes constituting the battery. resultant. The realization of a "all solid" battery requires the use of dimensionally stable materials, in order to make the behavior of the battery more reliable, particularly as regards the limitation of deformation stresses on the encapsulation, or on the electrodes. The layers of the anode, cathode and solid electrolyte layers are deposited in at least one of the following techniques: i) physical vapor phase deposition (PVD), and more particularly by evaporation under vacuum, by laser ablation, by ion beam, by sputtering; ii) chemical vapor deposition (CVD), and more particularly plasma assisted (PECVD), laser assisted (LACVD), or aerosol assisted (AA-CVD); iii) electrospray; iv) electrophoresis; v) aerosol deposition; vi) sol-gel; vii) soaking, more particularly by dip-coating, spin-coating, or by the Langmuir-Blodgett process. According to the invention, the anode, cathode and solid electrolyte layers are advantageously deposited by electrophoresis. The electrophoretic deposition of particles is done by the application of an electric field between the substrate on which the deposit is made and a counterelectrode, allowing the particles charged with the colloidal suspension to move, and to deposit them on the substrate. The absence of binders and other solvents deposited on the surface with the particles makes it possible to obtain very compact deposits. The compactness obtained thanks to the electrophoretic deposition limits or even avoids the risk of cracks or appearance of other defects in the deposit during the drying steps. In addition, the deposition rate can be very high depending on the applied electric field and the electrophoretic mobility of the particles of the suspension.
    [0010] According to the invention, the method of manufacturing an all-solid battery according to the invention comprises a step a) of depositing a layer of anode material. The materials chosen for the layer of anode material are preferably selected from the following materials: (i) tin oxynitrides (of typical formula SnOxNy); (ii) lithium iron phosphate (of typical formula LiFePO4); (iii) mixed oxynitrides of silicon and tin (of typical formula SiaSnbOyNz with a> 0, b> 0, a-FLK2, 0 <y4, 0 <z3) (also known as SiTON), and in particular SiSno, 8701, 2N, 1.72; as well as oxynitrides in the form SiaSnbCcOyNz with a> 0, b> 0, a-FLK2, 0 <c-10, 0 <y <24, 0 <z <17; SiaSnbCcOyNzX, and SiaSnbOyNzXa with Xn at least one of F, Cl, Br, I, S, Se, Te, P, As, Sb, Bi, Ge, Pb. (Iv) SixNy nitrides (especially with x = 3 and y = 4), SnxNy (in particular with x = 3 and y = 4), ZnxNy (in particular with x = 3 and y = 4), Li3_xMxN (with M = Co, Ni, Cu); (v) the oxides SnO2, Li4Ti5012, SnBo, 6P0, 402.9.
    [0011] Li4Ti5O12 for producing an anode layer is particularly preferred. In addition, Li4Ti5O12 is a lithium insertion material reversibly inserting lithium ions without inducing deformation of the host material. According to the invention, the method of manufacturing an all-solid battery comprises a step b) of depositing a layer of cathode materials. The cathode material layer is preferably made by electrophoresis. The materials chosen for the layer of anode material are preferably selected from the following materials: (i) LiMn 2 O 4, LiCoO 2, LiNiO 2, LiMn 1.5 TiO, 504, LiMnt 5 NiO 5, xxx O 4 (where X is selected from Al, Fe, Cr, Co, Rh, Nd, other rare earths, and where 0 <x <0.1), LiFeO2, LiMn113Ni113C01 / 304; (ii) LiFePO4, LiMnPO4, LiCoPO4, LiNiPO4, Li3V2 (PO4) 3 phosphates; (iii) all the lithiated forms of the following chalcogenides: V205, V308, TiS2, titanium oxysulfides (TiOyS), tungsten oxysulfides (VVOyS), CuS, CuS2.
    [0012] The cathode electrode, consisting of a LiMn 2 O 4 thin film deposited on a metal substrate, preferably nickel, is advantageously produced without resorting to vacuum techniques or dry rooms, which are very expensive equipment to implement. . Indeed, LiMn2O4, such as LiMn1,5Ni0,504 are not spontaneously sensitive to air, however it is recommended to avoid prolonged exposure.
    [0013] The impact of exposures of cathode materials to the air during the manufacture of the electrodes remains negligible compared to the relatively short implementation times. For the production of the anode or the cathode, it is possible to add nanoparticles of electronically conductive materials, and in particular graphite, and / or nanoparticles of ionically conductive materials, of the type used to produce the nanoparticles, to the materials mentioned above. electrolyte films (described hereinafter), or crosslinked solid polymer materials having ionic groups. Advantageously, the deposits of the layer of anode material and cathode are made by electrophoretic deposition of nanoparticles of anode material and cathode respectively.
    [0014] Advantageously, the deposits of the nanoparticle layer of anode material and cathode are made directly on their metal substrate. For small nanoparticle sizes, i.e. less than 100 nm, deposition of the anode, cathode and electrolyte layers are achieved by electrospray, electrophoresis, aerosol deposition, or dipping. Advantageously, the anode, cathode and electrolyte layers are all deposited by electrophoresis. This particular embodiment of the method according to the invention makes it possible to obtain a dense and compact layer of nanoparticles, in particular by self-densification (called "self-sintering") of the nanoparticle layer during the electrophoretic deposition step, drying and / or heat treatment at low temperature. Moreover, the electrophoretic deposition of the nanoparticle layer of anode material or cathode being compact, the risk of cracking of the layer after drying is reduced, and this, unlike the layers of nanoparticles made from inks or fluids, having low solids and for which the deposits contain solvent in large quantities, which after drying gives rise to the appearance of cracks in the deposit, harmful to the operation of a battery. According to the invention, the deposition of the layer of anode material or cathode is carried out directly on its conductive substrate, preferably a metal conductive substrate selected from the following materials: nickel, aluminum or copper. In a preferred embodiment, the deposition of the anode material or cathode layer is performed on a nickel substrate. The thickness of the substrate is less than 10 μm, preferably less than 5 μm.
    [0015] The conductive substrates may be made in the form of sheets, possibly sheets comprising the patterns of the pre-cut electrodes or in the form of strips. In order to improve the quality of the electrical contacts with the electrodes, the substrates may advantageously be coated with a metal or a metal alloy, preferably chosen from gold, chromium, stainless steel, palladium, molybdenum, titanium, tantalum, or silver. According to the invention, the deposition of a layer of nanoparticles of anode material or of cathode directly on its conducting substrate, for example by electrophoresis, makes it possible to obtain a dense layer of nanocrystalline structure. However, the formation of grain boundaries is possible, leading to the formation of a particular layer of structure, between that of an amorphous and crystallized material, which can in certain cases limit the diffusion kinetics of the lithium ions in the thickness of the electrode. Thus, the power of the battery electrode and the life cycle can be affected.
    [0016] Advantageously, in order to improve the performance of the battery, a recrystallization heat treatment may be performed to improve the crystallinity, and possibly the consolidation of the electrode to enhance the power of the electrodes (anode and / or cathode).
    [0017] The recrystallization heat treatment of the anode and / or cathode layer is carried out at a temperature of between 300 ° C. and 1000 ° C., preferably between 400 ° C. and 800 ° C., and even more preferentially between 500 ° C. and 700 ° C. The heat treatment must be performed after step a) and / or b) deposition of the anode layer and / or cathode, but before step c) of deposition of the electrolyte layer. According to the invention, the method of manufacturing a battery comprises a step c) of depositing a layer of electrolyte material. The deposition of the electrolyte material layer is performed on the anode material layer, and / or on the cathode material layer. The deposition of a solid electrolyte layer on the anode and / or cathode layer makes it possible to protect the electrochemical cell from an internal short circuit. It also allows for a fully solid battery with a long service life, and simple to manufacture. The deposition of the layer of electrolyte material is preferably carried out by electrophoresis. More particularly, the materials chosen as electrolyte materials are preferably chosen from the following materials: on the layer of material obtained in step a) and / or b): the lithiated phosphates, preferably chosen from : Li3PO4; Li3 (Sc2_ xMx) (PO4) 3 with M = A1 or Y and 0 x 1; Li 1 + xMx (Sc) 2-x (PO 4) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Li 1 + xMx (Ga 1-y Sn y) 2-x (PO 4) 3 with O x 0.8; 0 y 1 and M = Al or Y; Li 1 + xMx (Ga) 2-x (PO 4) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; 0 y 1; Li 1, Al x -Ri 2-x (PO 4) 3 with O x 1, or Li 1, Al Ge 2 -X (PO 4) 3 with O x 1; or Li1.x.zMx (Gei_yTi02_xSizP3_z012 with 0x <1.8 and 0y1.0 & 0z0.6 and M = Al, Ga or Y or a mixture of two or three of these compounds or lithiated borates, preferably selected from Li3 (Sc2, (Mx) (B03) 3 with M = A1 or Y and 0 x 1, Li1 + xMx (Sc) 2 - x (B03) 3 with M = Al, Y, Ga or a mixture of the three Compounds and 0 x 0.8; 0 y 1; Li 1 + x M x (Ga 1-y BcO 2-x (B0 3) 3 with 0 x 0.8; 0 y 1 and M = Al or Y; Lit + xMr (Ga) 2X (B03) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; 0 <y 1 o oxynitrides, preferably selected from Li3PO4_xN2x / 3, Li4SiO4_xN2x / 3, Li4Ge04_xN2x / 3 with 0 < x <4 or Li3B03_xN2x / 3 with 0 <x <3, materials based on phosphorus or boron lithium oxynitrides (called LiPON and LIBON) which may also contain silicon, sulfur, zirconium, aluminum or a combination of aluminum, boron, sulfur and / or silicon, and boron for lithium phosphorus o the lithiated oxides, preferably selected from Li7La3Zr2012 or Li5 + xLa3 (Zrx, A2_x) 012 with A = Sc, Y, Al, Ga and 1.4 x 2. Preferably, when a layer of electrolyte material is deposited only on the layer obtained at step b), depositing a layer of electrolyte material chosen from: Li3 (Sc2_xMx) (PO4) 3 with M = A1 or Y and 0 x; or Lii + xMx (Sc) 2, (PO4) 3 with M = Al, Y, Ga or a mixture of two or three of the compounds and 0 x 0.8; 0 <_y <_ 1.0; or Li 1 + xMx (Ga) 2-x (PO 4) 3 with M = Al, Y or a mixture of the two compounds M and 0 x 0.8; 0 <_y <_ 1.0; or Li 1 · x M x (Ga 1 -B 2 O 2-x (PO 4) 3 with 0 x 0.8; 0 y 1.0 and M = Al or Y, or a mixture of the two compounds; or o Li 1, Al x-ri 2-x (PO4) 3 with 0 x 1, where Li1, AlxGe2-x (PO4) 3 with 0 x 1, or where Li1, Mx (Gei-y-riy) 2-xBizP3_z012 with 0x <1.8 and 0y1 , 0, 0, 0, 0,6, and M = Al, Ga or Y, or a mixture of two or three of these compounds, or o Lithiated oxides selected from Li7La3Zr2012 or Li5, La3 (Zrx, A2,) O12 with A = Sc, Y, Al, Ga and 1.4 x 2 Li0.35La0.55TiO3 or Li0.51_a0.5TiO3; the lithiated borates, preferably selected from: Li3 (Sc2 _, (Mx) (B03) 3 with M = A1 or Y and 0 x 1, Li1 + xMx (Sc) 2_x (B03) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Lii + xMx (Ga1-yBcO2-x (B03) 3 with 0 x 0.8; 0 y 1 and M = Al or Y; Li1 + xMx (Ga) 2-x (B03) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; 0 <y 1; oxynitrides, preferably selected from Li3PO4_xN2x / 3, Li4SiO4_xN2x / 3, Li4Ge04_xN2x / 3 with 0 <x <4 or Li3B03_xN2x / 3 with 0 <x <3 the material x based on lithium oxynitrides of phosphorus or boron (called LiPON and LIBON) which may also contain silicon, sulfur, zirconium, aluminum, or a combination of aluminum, boron, sulfur and / or silicon , and boron for lithium phosphorus. Advantageously, the solid electrolyte layer is produced by electrophoretic deposition of nanoparticles of electrolyte material, electrically insulating. The layers obtained are completely covering, without localized defects. The deposition current densities focusing on the less insulating areas, especially localized where a defect is possibly present. The absence of defects in the electrolyte layer, prevents the appearance of creeping short-circuit, excessive self-discharge, or even failure of the battery cell. The performance of the batteries obtained by the process according to the invention is partly due to the crystalline structure of the electrolyte material (s). To obtain a good performance of the battery, it is advantageous to obtain an electrolyte made of amorphous glass, or nanocrystalline structures. Thus, in order to avoid the growth of the particle size of the electrolyte materials after their deposition, and to avoid creating reactions at the interfaces, the assembly of the battery must not be carried out at a high temperature, ie at a temperature not exceeding 300 ° C.
    [0018] According to the invention, after the deposition of the layer of electrolyte material, a layer of a crosslinked polymeric material comprising ionic groups is produced: o either on the layer of anode material coated with a layer of electrolyte material; solid electrolyte and / or on the layer of cathode material coated or not with a layer of solid electrolyte material; or on the layer of cathode material coated with a layer of solid electrolyte material and / or on the layer of anode material coated or not with a layer of solid electrolyte material. Preferably the crosslinked polymeric material is selected from polymethyl methacrylates, polyimides, polysiloxanes, polyamines. Preferably, the ionic groups are chosen from the following cations: imidazolium, pyrazolium, tetrazolium, pyridinium and pyrrolidinium, such as n-propyl-n-methylpyrrolidinium (also known as PYR13) or n-butyl-n-methylpyrrolidinium. (also known as PYR14), ammonium, phosphonium or sulfonium; and / or among the following anions: bis (trifluoromethane) sulfonimide, bis (fluorosulfonyl) imide, or n (nonafluorobutanesulfonyl) -n- (trifluoromethanesulfonyl) imide (of empirical formula C5F12NO4S2, also called IM14). The use of such anions makes it possible to retain good properties of resistance to exposure to air and moisture, which simplifies industrial implementation and guarantees better performance in terms of battery life. . In addition, the layer of crosslinked polymer material comprising ionic groups makes it possible to guarantee the safety and the service life of the battery by protecting it against the risks of short-circuiting and solvent ignition. Indeed, these polymeric materials are completely solid and do not include any liquid electrolyte, or dissolved in a solvent. In addition, these crosslinked polymer materials are resistant to high temperatures, without the risk of evaporation or inflammation of an organic solvent.
    [0019] In one embodiment of the process according to the invention, the crosslinked polymeric material containing ionic groups is directly deposited by dip-coating, spin-coating, roll coating. , doctor blade, electrospray, or electrophoresis. For this purpose, the polymer material is first dissolved in a suitable solvent, the dissolved polymer material is deposited on the layer (s) of the anode, cathode and / or electrolyte and then the layer of material is dried. polymer to remove the solvent. Advantageously, the deposition of the crosslinked polymer material is carried out by electrophoresis in order to limit the defects in the layer which could cause short circuits on the final battery. Electrophoresis deposition provides a dense and compact layer. Moreover, the electrophoretic deposition makes it possible to reduce the risk of cracking of the layer after drying, and this, unlike layers made from inks or fluids, having low solids and for which the deposits contain solvent in large amounts. quantity, which after drying gives rise to the appearance of cracks in the deposit, detrimental to the operation of a battery. In another embodiment of the process according to the invention, a monomer and / or an oligomer and / or a pre-polymer comprising one or more polymerizable groups are deposited. Preferably, a prepolymer is deposited comprising one or more reactive groups allowing the grafting of the ionic groups. The polymerization is carried out thermally and / or photochemically directly on the layer (s) of anode, cathode or electrolyte. Typically, the polymerization is carried out in the presence of a thermal initiator, for example selected from benzoyl peroxide, acetyl peroxide or azoisobutyronitrile, and / or a photochemical initiator, for example selected from benzoin, an acetophenone such as 2,2-dimethoxy-2-phenylacetophenone or 2,2-diethoxyacetophenone.
    [0020] The deposition of a crosslinked polymer material comprising ionic groups makes it possible to considerably increase the ionic conductivity of the electrolyte. In addition, these materials are difficult to ignite, resistant to high temperature, and have negligible vapor pressure. The layer of crosslinked polymer material comprising ionic groups then makes it possible to manufacture a battery in thin layers of three-dimensional structure without resorting to a heat treatment and / or a severe mechanical compression during the step of assembling said battery . Indeed, the production of at least one layer of crosslinked polymer material comprising ionic groups makes it possible to assemble the electrodes at a low temperature, ie a temperature not exceeding 300 ° C., preferably 200 ° C. and even more preferentially 150 ° C. According to a particular embodiment of the method of the invention, the electrodes (anode and cathode) are "punched" in a cutting pattern to make cuts to the dimensions of the battery to achieve. The punching of the electrodes may be performed after step c) of depositing the electrolyte layer, or after step d) of depositing the layer of crosslinked polymer material comprising ionic groups. These patterns comprise three cutouts which are adjacent (for example U-shaped) and which define the size of the battery. A second slot can be made on the uncut side to be able to ensure the passage of products necessary for the encapsulation of the component. The anode and cathode electrodes are then stacked alternately to constitute a stack of several elementary cells. The cutting patterns of the anodes and cathodes are placed in "head-to-tail" configuration.
    [0021] In another particular embodiment of the process according to the invention, the electrodes are cut before step c) of depositing the layer or layers of electrolyte, allowing the electrode edges to be covered by a film of electrolyte. electrolyte, thus protecting the contact of the electrodes with the atmosphere, and making it possible to improve the calendar life of the battery. In an alternative embodiment, the cuts are made on the substrates before the steps a) and b) of deposition of the anode and cathode layer, allowing the edges of the electrodes to be covered by an electrolyte film. This particular embodiment has the advantage of covering the electrode edges before the deposition of the layer of electrolyte material, which subsequently makes it possible to easily produce an encapsulation film around the electrodes, especially when the layer Electrolyte is composed of moisture-stable materials. The overlapping of the lateral edges of the electrodes also makes it possible to reduce the risk of short circuit in the cell. Finally, an essential step of the method according to the invention comprises a heat treatment and / or mechanical compression of the stack obtained previously to obtain a fully solid thin-film battery. The heat treatment is carried out at a temperature of between 50 and 300 ° C., preferably 100 and 200 ° C. Advantageously, the temperature of the heat treatment does not exceed 200 ° C. Advantageously, the mechanical compression of the layers to be assembled is carried out at a pressure of between 10 and 100 MPa, preferably between 20 and 50 MPa. In a particular embodiment, it is advantageous, after the stacking step and before the addition of the terminations, to encapsulate the stack by depositing a thin layer of encapsulation to ensure the protection of the cell of the battery. vis-à-vis the atmosphere. The encapsulation layer must be chemically stable, withstand high temperature and be impermeable to the atmosphere to play its barrier layer function. For example, the thin encapsulation layer consists of either a polymer, or a ceramic, glass or glass ceramic, which may be for example in the form of oxide, nitride, phosphates, oxynitride, or of siloxane. Advantageously, this encapsulation layer comprises a ceramic, glass or glass-ceramic layer coated with an epoxy resin or silicone. The encapsulation layer may advantageously be deposited by chemical vapor deposition (CVD), which makes it possible to have an overlap of all the surfaces of the accessible stack. Thus, the encapsulation can thus be carried out directly on the stacks, the coating being able to penetrate all the available cavities. Advantageously, a second encapsulation layer may be deposited on the first encapsulation layer to increase the protection of the battery cells of their external environment. Typically, the deposition of this second layer can be achieved by a silicone impregnation. The choice of such a material comes from the fact that it withstands high temperatures and the battery can thus be easily assembled by soldering on electronic cards without appearance of glass transitions. Advantageously, encapsulation of the battery is performed on four of the six faces of the stack. The encapsulation layers surround the periphery of the stack, the rest of the protection to the atmosphere being provided by the layers obtained by the terminations.
    [0022] Preferably, the cathodic and anodic connections are offset laterally, which allows the encapsulation layer to function as a dielectric to avoid the presence of a short circuit on these ends.
    [0023] Once the stacking has been completed, and after the step of encapsulation of the stack if the latter is carried out, terminations (electrical contacts) are added at the level where the cathodic current collectors, respectively anodic, are apparent (uncoated). insulating electrolyte). These contact areas may be on opposite sides of the stack to collect current but also or on adjacent sides.
    [0024] To achieve the endings, the stack, possibly embedded, is cut according to section planes to obtain unitary battery components, with the bare on each of the cutting plane connections (+) and (-) of drums. The connections can then be metallized using plasma deposition techniques known to those skilled in the art and / or by immersion in a conductive epoxy resin (loaded with silver) and / or a molten tin bath. The terminations make it possible to resume the alternately positive and negative electrical connections on each of the ends. These terminations make it possible to make the electrical connections in parallel between the different battery elements. For this, only the connections (+) go out on one end, and the (-) are available on the other ends.
    [0025] This battery being entirely solid, and using a lithium-insertion material as anode material, the risks of formation of lithium metal dendrites during the charging steps are zero and the insertion capacity of the lithium anode becomes limited. .
    [0026] Also, in order to guarantee good cycling performance of the battery according to the invention, the battery architecture for which the surface capacitance of the cathodes is greater than or equal to the surface capacitance of the anodes is preferred. The layers of the battery being completely solid, the risk of lithium dendrite formation no longer exists when the anode is fully charged. Thus, such a battery architecture avoids the creation of battery cell overload. Also, the production of such a battery with surface capacities of cathodes greater than or equal to those of the anodes makes it possible to increase the performance in terms of service life, expressed in number of cycles. Indeed, the electrodes are dense and completely solid, the risk of loss of electrical contact between the particles is zero. In addition, there is no longer any risk of deposition of lithium metal in the electrolyte or in the pores of the electrodes, and finally the risk of deterioration of the crystalline structure of the cathode material is non-existent.
    权利要求:
    Claims (2)
    [0001]
    REVENDICATIONS1. A method of manufacturing a fully solid thin-film battery comprising the following steps: a) depositing a layer comprising at least one anode material (herein called "anode material layer") on its conductive substrate, preferably selected from the group consisting of a metal sheet, a metal strip, a metallized insulating sheet, a metallized insulating strip, a metallized insulating film, said conductive substrates, or their conductive elements, which can serve as anode current collector; b) depositing a layer comprising at least one cathode material (here called "layer of cathode material") on its conductive substrate, preferably selected from the group consisting of a metal sheet, a metal strip, a metallized insulating sheet, a metallized insulating strip, a metallized insulating film, said conductive substrates, or their conductive elements, being able to serve as a cathode current collector, it being understood that the steps a) and b) can be reversed; c) depositing a layer comprising at least one solid electrolyte material (here called "layer of electrolyte material") on at least one layer obtained in step a) and / or b); d) depositing a layer of a crosslinked polymeric material having ionic groups: o either on the layer of anode material coated with a layer of solid electrolyte material and / or on the layer of coated cathode material or not a layer of solid electrolyte material; o either on the layer of cathode material coated with a layer of solid electrolyte material and / or on the layer of anode material coated or not with a layer of solid electrolyte material; e) successively facing a layer of anode material obtained in step a), c) or d) with a layer of cathode material obtained in step b), c) or d) being understood that the stack comprises at least one layer of solid electrolyte material obtained in step c) and at least one layer of a crosslinked polymer material obtained in step d); f) heat treatment and / or mechanical compression of the stack obtained in step e) to obtain a fully solid thin-film battery.
    [0002]
    2. Method according to claim 1, characterized in that the crosslinked polymeric material is selected from polymethyl methacrylates, polyamines, polyimides, or polysiloxanes.3. 4. Process according to Claim 1 or 2, characterized in that the ionic groups are chosen from the following cations: imidazolium, pyrazolium, tetrazolium, pyridinium and pyrrolidinium. such as n-propyl-n-methylpyrrolidinium (also called PYR13) or n-butyl-n-methylpyrrolidinium (also called PYR14), ammonium, phosphonium or sulfonium; and / or among the following anions: bis (trifluoromethane) sulfonimide, bis (fluorosulfonyl) imide, or n- (nonafluorobutanesulfonyl) -n- (trifluoromethanesulfonyl) imide. Process according to any one of Claims 1 to 3, characterized in that the crosslinked polymer material is obtained by a step of polymerizing a mixture of monomers and / or oligomers and / or pre-polymers comprising one or more polymerizable groups by thermal or photochemical route, said mixture of monomers and / or oligomers and / or pre-polymers comprising one or more reactive groups for grafting said ionic groups. Process according to Claim 4, characterized in that the thermal and / or photochemical polymerization is carried out directly on the layer (s) of anodes, cathodes and / or electrolytes. Process according to any one of Claims 1 to 3, characterized in that the deposition of the crosslinked polymer material comprising ionic groups is carried out among at least one of the following techniques: dip-coating, dip-spinning (spin-coating), roll coating, doctor blade, electrospray, or electrophoresis. Process according to any one of Claims 1 to 5, characterized in that the thickness of the layer of polymer material is less than 10 μm, preferably less than 5 μm, and still more preferably less than 2 μm. Process according to any one of claims 1 to 7, characterized in that the anode, cathode and solid electrolyte layers are deposited among at least one of the following techniques: (i) physical vapor phase deposition ( PVD), and more particularly by evaporation in vacuo, by laser ablation, by ion beam, by sputtering; (ii) chemical vapor deposition (CVD), and more particularly plasma assisted (PECVD), laser assisted (LACVD), or aerosol assisted (AA-CVD); (iii) electrospray; (iv) electrophoresis; (v) aerosol deposition; (vi) sol-gel; (vii) soaking, more particularly by dip-coating, spin-coating, or by the Langmuir-Blodgett process. 9. Method according to any one of claims 1 to 8, characterized in that the anode, cathode and electrolyte layers are deposited by electrospray, electrophoresis, aerosol deposition, soaking, and are preferably all deposited by electrophoresis. 10. Method according to any one of claims 1 to 9, characterized in that the layers of anode material and / or cathode further comprise electronic conductive materials, and in particular graphite, and / or nanoparticles of conductive materials of lithium ions, of the type used to make the electrolyte films, or crosslinked solid polymer materials comprising ionic groups. 11. Method according to any one of claims 1 to 10, characterized in that the anode layers and / or cathode and / or electrolyte are produced by a deposition of nanoparticles respectively of anode material, cathode or electrolyte among at least one of the following techniques: electrospray, electrophoresis, aerosol deposition, dipping. 12. The method of claim 11, characterized in that the nanoparticle layers of anode material, cathode and electrolyte are all deposited by electrophoresis. Process according to any one of Claims 1 to 12, characterized in that the heat treatment is carried out at a temperature of between 50 ° C and 300 ° C, preferably between 100 ° C and 200 ° C and / or in that the mechanical compression of the layers to be assembled is carried out at a pressure of between 10 and 100 MPa, preferably between 20 and 50 MPa. 14. Process according to any one of claims 1 to 13, characterized in that the layer of anode material a) is made from material chosen from: (i) tin oxynitrides (of typical formula SnOxNy) ; (ii) lithium iron phosphate (of typical formula LiFePO4); (iii) mixed oxynitrides of silicon and tin (of typical formula SiaSnbOyNz with a> 0, b> 0, a-FLK2, 0 <y4, 0 <z3) (also known as SiTON), and in particular SiSno, 8701, 2N, 1.72; as well as oxynitrides in the form SiaSnbCcOyNz with a> 0, b> 0, a-FLK2, 0 <c <10, 0 <y <24, 0 <z <17; SiaSnbCcOyNzX, and SiaSnbOyNzXa with Xn at least one of F, Cl, Br, I, S, Se, Te, P, As, Sb, Bi, Ge, Pb; (iv) the nitrides of the type SixNy (in particular with x = 3 and y = 4), SnxNy (in particular with x = 3 and y = 4), ZnxNy (in particular with x = 3 and y = 4), Li3_xMxN (with M = Co, Ni, Cu); (y) the oxides SnO2, Li4Ti5012, SnBo, 6P0, 402.9. 15. Method according to any one of claims 1 to 14, characterized in that the cathode material layer b) is made from cathode material chosen from: (i) the LiMn 2 O 4, LiCoO 2, LiNiO 2 and LiMn 1 oxides, 5Ni, 504, LiMn1.5Ni0.5- xXx04 (where x is selected from Al, Fe, Cr, Co, Rh, Nd, other rare earths, and where 0 <x <0.1), LiFeO2, LiMn1i3Ni1i3C01 / 304; (ii) LiFePO4, LiMnPO4, LiCoPO4, LiNiPO4, Li3V2 (PO4) 3 phosphates; phosphates of formula LiMM'PO4, with M and M '(M # M') selected from Fe, Mn, Ni, Co, V; (iii) all lithiated forms of the following chalcogenides: V205, V308, TiS2, titanium oxysulfides (TiOySz), tungsten oxysulfides (VVOySz), CuS, CuS2. 16. Method according to any one of claims 1 to 15, characterized in that the electrolyte material layer c) is made from electrolyte material chosen from: o lithiated phosphates, preferably chosen from: Li3PO4; Li3 (Sc2_ xMx) (PO4) 3 with M = A1 or Y and 0 x 1; Li 1 + xMx (Sc) 2-x (PO 4) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Li 1 + xMx (Ga 1-y Sn y) 2-x (PO 4) 3 with O x 0.8; 0 y 1 and M = Al or Y; Li 1 + xMx (Ga) 2-x (PO 4) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; 0 y 1; Li 1, Al x -Ri 2-x (PO 4) 3 with O x 1, or Li 1, Al x Ge 2-x (PO 4) 3 with O x 1; or Lii.x.zMx (Gei_yTi02_xSizP3_z012 with 0x <_0.8 and, 0 & Oz <_0.6 and M = Al, Ga or Y or a mixture of two or three of these compounds o the lithiated borates, preferably chosen among: Li3 (Sc2, (Mx) (B03) 3 with M = A1 or Y and 0 x 1, Li1 + xMx (Sc) 2_x (B03) 3 with M = Al, Y, Ga or a mixture of the three compounds and 0 x 0.8; 0 y 1; Li 1 + x M x (Ga 1-y BcO 2-x (B0 3) 3 with 0 x 0.8; 0 y 1 and M = Al or Y; Li 1 + x M x (Ga) 2-x (B03) 3 with M = Al, Y or a mixture of the two compounds and 0 x 0.8; the oxynitrides, preferably selected from Li3PO4_xN2x / 3, Li4SiO4_xN2x / 3, Li4Ge04_xN2x / 3 with 0 <x <4 or Li3B03_xN2x / 3 with 0 <x <3, materials based on phosphorus or boron lithium oxynitrides (called LiPON and LIBON) which may also contain silicon, sulfur, zirconium, lithium aluminum, or a combination of aluminum, boron, sulfur and / or silicon, and boron for lithium phosphorus o the lithiated oxides, preferably selected from Li7La3Zr2012 or Li5 + xLa3 (Zrx, A2_x) 012 with A = Sc, Y, Al, Ga and 1.4 x 2 or Li0.35La0.55TiO3. 17. Method according to any one of claims 1 to 16, characterized in that it further comprises a step of encapsulation of the battery obtained in step f) by depositing at least one layer of encapsulation of ceramic, vitreous or vitroceramic material. 18. Process according to claim 17, characterized in that anodic and cathodic terminations are carried out by metallization of the cut sections, preferably by deposition of a layer of tin optionally deposited on a first sub-layer of nickel and / or epoxy resin loaded with metallic particles. Process according to any one of Claims 11 to 18, characterized in that the size of the nanoparticles of electrolyte materials is less than 100 nm, preferably less than 30 nm. 20. Method according to any one of claims 1 to 19, characterized in that the conductive substrates are aluminum, copper or nickel, preferably nickel, and optionally coated with a noble metal selected from the following metals: gold, platinum, palladium, vanadium, cobalt, nickel, manganese, niobium, tantalum, chromium, molybdenum, titanium, palladium, zirconium, tungsten or any alloy comprising minus one of these metals. 21. Battery obtainable by the method according to any one of claims 1 to 20. 22. Battery according to claim 21, characterized in that the surface capacitance of the cathode is greater than or equal to the capacitance per unit area. 'anode. 23. Battery according to claim 21 or 22, characterized in that the stack of the cathode and anode layers is shifted laterally. 24. Battery according to any one of claims 21 to 23, characterized in that it comprises at least one encapsulation layer, preferably a ceramic layer, glass or glass ceramic. 25. Battery according to claim 24, characterized in that it comprises a second encapsulation layer deposited on said first encapsulation layer, said second encapsulation layer preferably being silicone. 26. Battery according to claim 24 or 25, characterized in that said at least one encapsulation layer completely covers four of the six faces of said battery and partially the two remaining faces, located under the metallizations used for the connection of the battery. 27. Battery according to any one of claims 20 to 26 characterized in that it comprises terminations at the level where cathodic current collectors, respectively anodic, are apparent. Battery according to Claim 27, characterized in that the anode connections and the cathode connections are on the opposite sides of the stack.
    类似技术:
    公开号 | 公开日 | 专利标题
    EP3164904B1|2021-03-31|All-solid battery including a solid electrolyte and a layer of polymer material
    EP3398220B1|2021-09-22|All-solid-state battery including a solid electrolyte and a layer of ion-conducting material
    EP3164903B1|2021-04-28|Solid-state battery including an electrolyte made of a cross-linked solid polymer material
    US20200036000A1|2020-01-30|Solid-state batteries, separators, electrodes, and methods of fabrication
    FR3023302A1|2016-01-08|COMPLETELY SOLID BATTERY COMPRISING A LITHIA PHOSPHATE SOLID ELECTROLYTE, STABLE IN CONTACT WITH THE ANODE
    EP2962345B1|2020-06-24|Process for manufacturing a monolithic all-solid-state battery
    EP2543095B1|2013-11-20|Microbattery and method for manufacturing same
    US20210265613A1|2021-08-26|All-solid battery including a lithium phosphate solid electrolyte which is stable when in contact with the anode
    WO2018051048A1|2018-03-22|Method for the production of an electrochemical device
    FR3054727A1|2018-02-02|ELECTROCHEMICAL DEVICE, SUCH AS A MICROBATTERY OR ELECTROCHROME DEVICE, AND METHOD FOR PRODUCING THE SAME
    同族专利:
    公开号 | 公开日
    EP3164904A1|2017-05-10|
    EP3164904B1|2021-03-31|
    FR3023417B1|2016-07-15|
    JP6758199B2|2020-09-23|
    JP2017529645A|2017-10-05|
    KR20170028391A|2017-03-13|
    KR102350255B1|2022-01-13|
    US20170133711A1|2017-05-11|
    CN106537676A|2017-03-22|
    CN106537676B|2021-03-12|
    WO2016001588A1|2016-01-07|
    US10581113B2|2020-03-03|
    US20200176815A1|2020-06-04|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR2880198A1|2004-12-23|2006-06-30|Commissariat Energie Atomique|Device for the storage of energy using a nanostructured electrode, for the fabrication of micro- batteries with improved life and stability|
    FR2893623A1|2005-11-22|2007-05-25|Inst Nat Polytech Grenoble|Making crosslinked polymer film bearing ionic groups, useful as electrolyte for lithium battery, comprises extruding polymer material having prepolymer, polymerizing extruded polymer and grafting ionic groups|
    JP2008171588A|2007-01-09|2008-07-24|Sumitomo Electric Ind Ltd|Lithium battery|
    WO2013064779A1|2011-11-02|2013-05-10|Fabien Gaben|Method for manufacturing all-solid-state thin-film batteries|CN107275673A|2016-04-07|2017-10-20|中国科学院物理研究所|A kind of lithium battery solid electrolyte film and its preparation method and application|US6894143B2|2001-06-29|2005-05-17|Zeon Corporation|Polyether polymer, process for producing the same, composition for solid polymer electrolyte, and use thereof|
    JP4501052B2|2002-01-24|2010-07-14|東洋紡績株式会社|Thermally crosslinkable polymer solid electrolyte, polymer solid electrolyte membrane and method for producing the same|
    FR2853320B1|2003-04-03|2005-05-06|Rhodia Chimie Sa|RETICULABLE COMPOSITION FOR BATTERY ELECTROLYTE|
    JP4688406B2|2003-04-17|2011-05-25|セイコーインスツル株式会社|Electrochemical cell with terminal|
    WO2005085138A1|2004-03-06|2005-09-15|Werner Weppner|Chemically stable solid lithium ion conductors|
    DE102004010892B3|2004-03-06|2005-11-24|Christian-Albrechts-Universität Zu Kiel|Chemically stable solid Li ion conductor of garnet-like crystal structure and high Li ion conductivity useful for batteries, accumulators, supercaps, fuel cells, sensors, windows displays|
    CN100495801C|2004-12-13|2009-06-03|松下电器产业株式会社|Laminate including active material layer and solid electrolyte layer, and all solid lithium secondary battery using the same|
    US7776478B2|2005-07-15|2010-08-17|Cymbet Corporation|Thin-film batteries with polymer and LiPON electrolyte layers and method|
    DE102007030604A1|2007-07-02|2009-01-08|Weppner, Werner, Prof. Dr.|Ion conductor with garnet structure|
    US20090202899A1|2008-02-11|2009-08-13|Pyszczek Michael F|Electrical apparatus with integral thin film solid state battery and methods of manufacture|
    US8986895B2|2009-02-04|2015-03-24|Kabushiki Kaisha Toyota Chuo Kenkyusho|Garnet-type lithium ion-conducting oxide and all-solid-state lithium ion secondary battery containing the same|
    JP2010186626A|2009-02-12|2010-08-26|Sumitomo Bakelite Co Ltd|Secondary cell|
    AU2010271483A1|2010-01-22|2011-08-04|Toyota Jidosha Kabushiki Kaisha|Negative electrode structure for aqueous electrolyte batteries and aqueous electrolyte battery comprising the negative electrode structure|
    US20120281642A1|2010-11-08|2012-11-08|Qualcomm Incorporated|System and method for uplink multiple input multiple output transmission|
    EP2647066A1|2010-12-05|2013-10-09|Ramot at Tel Aviv University, Ltd.|Electrophoretic deposition of thin film batteries|
    CN102332579B|2011-02-21|2014-10-08|东莞新能源科技有限公司|Lithium ion battery and cathode active material thereof|
    US10001690B2|2011-04-05|2018-06-19|Acreo Swedish Ict Ab|Colloid electrolyte composition|
    JP6223725B2|2013-06-12|2017-11-01|新光電気工業株式会社|Battery and manufacturing method thereof|EP3436465A4|2016-04-01|2020-03-25|Nohms Tehcnologies, Inc.|Modified ionic liquids containing phosphorus|
    EP3518251A4|2016-09-21|2020-05-06|Murata Manufacturing Co., Ltd.|Solid electrolyte and all-solid battery|
    KR20180036410A|2016-09-30|2018-04-09|주식회사 엘지화학|All solid state battery|
    CN106532109A|2016-12-28|2017-03-22|上海航天电源技术有限责任公司|All-solid-state lithium-ion battery and manufacturing method thereof|
    CN110546786A|2017-04-27|2019-12-06|松下知识产权经营株式会社|Secondary battery|
    KR102075607B1|2017-06-01|2020-02-10|도요타 지도샤（주）|Positive electrode active material and fluoride ion battery|
    EP3656010A4|2017-07-17|2021-08-11|Nohms Technologies, Inc.|Phosphorus containing electrolytes|
    CN108232287B|2018-01-25|2020-07-03|成都特隆美储能技术有限公司|Lithium ion battery pole piece, manufacturing method and battery cell|
    CN110098430A|2018-01-30|2019-08-06|财团法人工业技术研究院|Solid electrolyte and solid state battery|
    CN110247105A|2018-03-07|2019-09-17|重庆市科学技术研究院|A kind of preparation method improving solid electrolyte consistency|
    KR20190124505A|2018-04-26|2019-11-05|주식회사 엘지화학|Electrolyte and Lithium Metal Electrode Comprising the Same|
    FR3080957B1|2018-05-07|2020-07-10|I-Ten|MESOPOROUS ELECTRODES FOR THIN FILM ELECTROCHEMICAL DEVICES|
    FR3080945A1|2018-05-07|2019-11-08|I-Ten|MESOPOROUS ELECTROLYTES FOR THIN-FILM ELECTROCHEMICAL DEVICES|
    FR3080952B1|2018-05-07|2020-07-17|I-Ten|ELECTROLYTE FOR THIN FILM ELECTROCHEMICAL DEVICES|
    FR3080862A1|2018-05-07|2019-11-08|I-Ten|METHOD FOR MANUFACTURING ANODES FOR LITHIUM ION BATTERIES|
    CN108832173B|2018-06-27|2020-11-03|东北大学|Gallium and molybdenum co-doped garnet type lithium ion solid electrolyte and preparation method thereof|
    CN108832174B|2018-06-28|2021-01-26|苏州清陶新能源科技有限公司|Preparation process of solid-state lithium ion battery|
    EP3591729A1|2018-07-03|2020-01-08|Renata AG|A multilayer packaging structure for a thin film battery and a method for manufacturing of such a structure|
    CN109524624B|2018-11-26|2021-09-03|中南大学|Preparation method of metal cathode coated with polymer protective film on surface and secondary battery|
    CN109728343B|2018-12-12|2021-04-27|南京师范大学|Preparation method of polyacid/high-molecular polymer hybrid nanowire and material obtained by preparation method|
    KR102175846B1|2018-12-20|2020-11-06|재단법인 포항산업과학연구원|Preparation method of solid state lithium ion secondary battery|
    CN111172545B|2019-01-15|2022-03-08|中国科学院海洋研究所|Photo-anode of ionic liquid modified semiconductor composite film and preparation method thereof|
    US11267707B2|2019-04-16|2022-03-08|Honeywell International Inc|Purification of bis imide|
    CN110137428B|2019-06-15|2021-11-26|河南固锂电技术有限公司|Preparation process of ultrathin lithium negative electrode film for all-solid-state lithium ion battery|
    US20210104738A1|2019-10-08|2021-04-08|Ulvac Technologies, Inc.|Multifunctional engineered particle for a secondary battery and method of manufacturing the same|
    FR3111741A1|2020-06-23|2021-12-24|Hfg|HIGH ENERGY AND POWER DENSITY ANODE FOR BATTERIES|
    FR3111740A1|2020-06-23|2021-12-24|I-Ten|HIGH ENERGY AND POWER DENSITY ANODE FOR BATTERIES|
    法律状态:
    2015-07-29| PLFP| Fee payment|Year of fee payment: 2 |
    2016-01-08| PLSC| Publication of the preliminary search report|Effective date: 20160108 |
    2016-07-28| PLFP| Fee payment|Year of fee payment: 3 |
    2017-07-12| PLFP| Fee payment|Year of fee payment: 4 |
    2018-07-30| PLFP| Fee payment|Year of fee payment: 5 |
    2019-07-31| PLFP| Fee payment|Year of fee payment: 6 |
    2020-07-27| PLFP| Fee payment|Year of fee payment: 7 |
    2021-07-26| PLFP| Fee payment|Year of fee payment: 8 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1456272A|FR3023417B1|2014-07-01|2014-07-01|COMPLETELY SOLID BATTERY COMPRISING SOLID ELECTROLYTE AND LAYER OF SOLID POLYMERIC MATERIAL|FR1456272A| FR3023417B1|2014-07-01|2014-07-01|COMPLETELY SOLID BATTERY COMPRISING SOLID ELECTROLYTE AND LAYER OF SOLID POLYMERIC MATERIAL|
    EP15745537.9A| EP3164904B1|2014-07-01|2015-07-01|All-solid battery including a solid electrolyte and a layer of polymer material|
    PCT/FR2015/051819| WO2016001588A1|2014-07-01|2015-07-01|All-solid battery including a solid electrolyte and a layer of polymer material|
    US15/323,711| US10581113B2|2014-07-01|2015-07-01|All-solid battery including a solid electrolyte and a layer of polymer material|
    CN201580036659.5A| CN106537676B|2014-07-01|2015-07-01|All-solid-state battery with solid electrolyte and polymer material layer|
    KR1020177002873A| KR102350255B1|2014-07-01|2015-07-01|All-solid battery including a solid electrolyte and a layer of polymer material|
    JP2016575464A| JP6758199B2|2014-07-01|2015-07-01|All-solid-state battery with layers of solid electrolyte and polymer material|
    US16/784,562| US20200176815A1|2014-07-01|2020-02-07|All-solid battery including a solid electrolyte and a layer of polymer material|
    [返回顶部]