MULTILAYER ELECTRODE-ELECTROLYTE COMPONENTS AND THEIR PRODUCTION METHODS

Abstract

Described are multilayer components comprising a solid electrolyte layer and a solid electrode layer, both comprising ceramic particles while being polymer-free as well as electrochemical cells comprising them. The processes for preparing these multilayer components, which use a hot-pressing step, are also described.

Claims

1. A process for preparing a multilayer component comprising a solid electrode layer and a solid electrolyte layer, said process being selected from processes A and B: A: comprising at least the steps of: a) preparing the solid electrolyte layer by compressing ceramic particles; b) preparing a mixture comprising at least an electrochemically active material, ceramic particles, and an electron conductive material, the mixture being free of solvent; c) applying the mixture prepared in (b) on the solid electrolyte layer prepared in (a) to obtain a bilayer material; and d) pressing the bilayer material obtained in (c) at a pressure of at least 50 kg/cm.sup.2 and a temperature within the range of about 400° C. to about 900° C.; or B: comprising at least the steps of: a) preparing an electrolyte composition layer by applying a mixture of ceramic particles and a polymer on a first support; b) preparing a mixture comprising at least an electrochemically active material, ceramic particles, an electron conductive material, and optionally a polymer; c) applying the electrode material mixture prepared in step (b): i. on the electrolyte composition layer prepared in (a); or ii. on a second support followed by contacting a surface of the applied electrode material mixture with a surface of the electrolyte composition layer;  to afford a bilayer material; d) pressing the bilayer material obtained in (c) at a pressure of at least 50 kg/cm.sup.2 and a temperature within the range of about 400° C. to about 900° C.; wherein the solid electrolyte layer and the electrode layer are preferably free of polymer after step (d).

2. The process of claim 1, wherein step (a) excludes the addition of a solvent and/or excludes the addition of a lithium salt.

3-4. (canceled)

5. The process of claim 1, wherein the ceramic of step (a) of formula and/or the ceramic particles of step (b) comprise a ceramic of formula Li .sub.1+zAl.sub.zM.sub.2-z)(PO.sub.4).sub.3, wherein M is Ti, Ge, or a combination thereof, and z is such that 0<z<1, preferably M is Ge or M is Ti.

6-7. (canceled)

8. The process of claim 1, wherein step (a) of process A is carried out in the presence of oxygen (e.g., in air) and/or is carried out at a pressure within the range of 100 kg/cm.sup.2 to 5000 kg/cm.sup.2; or step (a) of process B further comprises pressing the mixture in the presence of oxygen (e.g., under air), preferably at a pressure within the range of 100 kg/cm.sup.2 to 5000 kg/cm.sup.2.

9. (canceled)

10. The process of claim 1, wherein step (d) is carried out: in an inert atmosphere (such as argon or nitrogen); and/or at a pressure in the range of 50 kg/cm.sup.2 to 5000 kg/cm.sup.2, or of 100 kg/cm.sup.2 to 5000 kg/cm.sup.2, or of 300 kg/cm.sup.2 to 2000 kg/cm.sup.2; and/or at a temperature of within the range of about 450° C. to about 850° C., preferably from about 600° C. to about 700° C. for process A, or preferably from about 600° C. to about 750° C. for process B; and/or for a period of more than 0 hour and less than 10 hours, or between 30 minutes and 5 hours, or between 30 minutes and 2 hours.

11-13. (canceled)

14. The process of claim 1, wherein the preparation of the mixture in step (b) is carried out by ball milling.

15. The process of claim 1, wherein the electrode is a positive electrode, preferably the electrochemically active material is selected from phosphates (e.g. LiM.sup.aPO.sub.4 where M.sup.a is Fe, Ni, Mn, Co, or a combination thereof), oxides and complex oxides such as LiMn.sub.2O.sub.4, LiM.sup.bO.sub.2 (M.sup.b being Mn, Co, Ni, or a combination thereof), and Li(NiM.sup.c)O.sub.2 (M.sup.c being Mn, Co, Al, Fe, Cr, Ti, Zr, or a combination thereof), elemental sulfur, elemental selenium, iron(III) fluoride, copper(II) fluoride, lithium iodide, and iodine, preferably the electrochemically active material is a phosphate of formula LiM.sup.aPO.sub.4 where M.sup.a is Fe, Mn, Co or a combination thereof (e.g., LiFePO.sub.4), wherein said electrochemically active material is made of particles optionally further coated with carbon.

16-17. (canceled)

18. The process of claim 1, wherein the conductive electron material is selected from the group consisting of carbon black, Ketjen™ black, acetylene black, graphite, graphene, carbon fibers or nanofibers, carbon nanotubes, and a combination thereof, preferably the electron conductive material comprises carbon fibers (such as VGCF) or the electron conductive material comprises graphite.

19-22. (canceled)

23. The process of claim 1, wherein the ceramic of step (a) and the ceramic particles of step (b) are identical.

24-25. (canceled)

26. The process of claim 1, wherein step (a) of process B further comprises a solvent and comprises drying the mixture after application and/or further comprises removing the first support.

27-28. (canceled)

29. The process of claim 1, wherein in process B the polymer of step (a) and of step (b) if present is, independently in each occurrence, selected from a fluorinated polymer (such as le polyvinylidene fluoride (PVDF), or poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)), a poly(alkylene carbonate) (such poly(ethylene carbonate) or poly(propylene carbonate)), a polyvinyl butyral (PVB), or a polyvinyl alcohol (PVA), preferably the polymer is a poly(alkylene carbonate) (such as poly(ethylene carbonate) or poly(propylene carbonate)).

30-36. (canceled)

37. The process of claim 1, wherein said process B comprises step (c) (ii) and the process comprises removing the first support and the second support before contacting; or said process B comprises step (c) (ii) and the process comprises removing the first support and the second support after contacting and before step (d).

38. (canceled)

39. The process of claim 1, wherein the process B further comprises a step of laminating the bilayer material between rolls before step (d).

40. The process of claim 1, wherein step (b) of process B further comprises a solvent and step (c) further comprises drying the applied electrode material; or step (b) of process B comprises dry mixing the electrochemically active material, ceramic particles, and electron conductive material, suspending the resulting mixture with a polymer in a solvent, and step (c) further comprises drying the applied electrode material.

41-56. (canceled)

57. A multilayer component obtained by a process as defined in claim 1.

58. A multilayer component comprising a solid electrode layer and a solid electrolyte layer, wherein: the solid electrolyte layer comprises ceramic particles; the solid electrode layer comprises an electrochemically active material, ceramic particles, and an electron conductive material; and the solid electrode layer and the solid electrolyte layer are free of electrolyte polymer and polymer binder.

59. The multilayer component of claim 58, wherein the ceramic in the solid electrolyte layer is of formula and/or the ceramic particles of step (b) comprise a ceramic of formula Li.sub.1+zAl.sub.zM.sub.2-z(PO.sub.4).sub.3, wherein M is Ti, Ge, or a combination thereof, and 0<z<1 , preferably M is Ge or M is Ti.

60-61. (canceled)

62. The multilayer component of claim 58, wherein the electrode layer is a positive electrode layer, preferably the electrochemically active material is selected from phosphates (e.g. LiM.sup.aPO.sub.4 where M.sup.a is Fe, Ni, Mn, Co, or a combination thereof), oxides and complex oxides such as LiMn.sub.2O.sub.4, LiM.sup.bO.sub.2 (M.sup.b being Mn, Co, Ni, or a combination thereof), and Li(NiM.sup.c)O.sub.2 (M.sup.c being Mn, Co, Al, Fe, Cr, Ti, Zr, or a combination thereof), elemental sulfur, elemental selenium, iron(III) fluoride, copper(II) fluoride, lithium iodide, and iodine, preferably the electrochemically active material is a phosphate of formula LiM.sup.aPO.sub.4 where M.sup.a is Fe, Mn, Co or a combination thereof (such as LiFePO.sub.4), wherein said electrochemically active material is made of particles optionally coated with carbon.

63-64. (canceled)

65. The multilayer component of claim 58, wherein the conductive material is selected from the group consisting of carbon black, Ketjen™ black, acetylene black, graphite, graphene, carbon fibers or nanofibers, carbon nanotubes, and a combination thereof, preferably the electron conductive material comprises carbon fibers (such as VGCF) or comprises graphite.

66-70. (canceled)

71. The multilayer component of claim 58, wherein the ceramic particles in the solid electrolyte layer and the ceramic particles in the solid electrode layer are identical.

72. The multilayer component of claim 58, comprising a high contact at the interface between the solid electrolyte layer and the solid electrode layer and/or wherein at least one layer of the multilayer component has a density of at least 90% of the theoretical density.

73. (canceled)

74. Electrochemical cell comprising a negative electrode, a positive electrode and an electrolyte, wherein the electrolyte and positive electrode together form a multilayer component as defined in claim 58, preferably the negative electrode comprises a lithium or lithium alloy film and a polymer interlayer between the lithium or lithium alloy film and the solid electrolyte layer, the polymer interlayer preferably comprising a polyether polymer and a lithium salt, such as an optionally crosslinked PEO-based polymer and a lithium salt (e.g. LiTFSI).

75-76. (canceled)

77. Process for preparing an electrochemical cell comprising the steps of: (i) preparing a multilayer component according to a process as defined in claim 1; and (ii) assembling the multilayer component of step (i) with a negative electrode layer.

78. The process of claim 77, wherein the negative electrode layer comprises a lithium or lithium alloy film and a polymer interlayer between the lithium or lithium alloy film and the solid electrolyte layer, the polymer interlayer preferably comprising a polyether polymer and a lithium salt, such as an optionally crosslinked PEO-based polymer and a lithium salt (such as LiTFSI

79. (canceled)

80. A battery comprising at least one electrochemical cell as defined in claim 74, said battery preferably being a lithium battery or a lithium-ion battery.

81. (canceled)

82. The multilayer component of claim 57, comprising a high contact at the interface between the solid electrolyte layer and the solid electrode layer and/or wherein at least one layer of the multilayer component has a density of at least 90% of the theoretical density.

83. Electrochemical cell comprising a negative electrode, a positive electrode and an electrolyte, wherein the electrolyte and positive electrode together form a multilayer component as defined in claim 57, preferably the negative electrode comprises a lithium or lithium alloy film and a polymer interlayer between the lithium or lithium alloy film and the solid electrolyte layer, the polymer interlayer preferably comprising a polyether polymer and a lithium salt, such as an optionally crosslinked PEO-based polymer and a lithium salt (e.g. LiTFSI).

84. A battery comprising at least one electrochemical cell as defined in claim 83, said battery preferably being a lithium battery or a lithium-ion battery.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0059] FIG. 1 schematically illustrates an embodiment of the present process.

[0060] FIG. 2 displays the X-ray diffraction pattern of (a) LAGP before sintering and (b) LAGP after sintering at 1000° C.

[0061] FIG. 3 displays the first two charge/discharge curves of a cell prepared according to an embodiment of the present process when cycled at a current of 100 μA.

[0062] FIG. 4 shows charge/discharge curves of a cell prepared according to the embodiment described in Example 2.

DETAILED DESCRIPTION

[0063] The following detailed description and examples are illustrative and should not be interpreted as further limiting the scope of the invention.

[0064] All technical and scientific terms and expressions used herein have the same definitions as those commonly understood by the person skilled in the art when relating to the present technology. The definition of some terms and expressions used is nevertheless provided below for clarity purposes.

[0065] When the term “about” is used herein, it means approximately, in the region of, and around. When the term “about” is used in relation to a numerical value, it modifies it, for example, above and below its nominal value by a variation of 10%. This term may also take into account the probability of random errors in experimental measurements or rounding of a number.

[0066] The expressions “free of polymer”, “free of polymer binder”, “excluding a polymer”, or “excluding a polymer binder” are equivalents and mean that the characterised material, being either the electrolyte or an electrode, does not contain a polymer commonly used in electrolytes or as electrode material binder (for example, a PEO-based polymer, fluorinated polymer, poly(alkylene carbonate), polyvinyl butyral, polyvinyl alcohol, etc.). The expression does not, however, intend to exclude carbon-based macromolecules (such as graphene, carbon nanotubes, carbon fibers, etc.) which would serve as electronically conductive materials in electrode materials.

[0067] The term “support” as used herein defines a material, generally in the form of a film or foil, on which a mixture, such as a slurry, is applied. The support material is unreactive to the mixture applied thereon. Examples of materials used as support include polymer supports such as polypropylene, polyethylene and other inert polymers.

[0068] The term “lithium salt” as used herein refers to any lithium salt that can be used in solid electrolytes of electrochemical cells. Non-limiting examples of lithium salts comprise lithium hexafluorophosphate (LiPF.sub.6), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), lithium bis(fluorosulfonyl)imide (LiFSI), lithium 2-trifluoromethyl-4,5-dicyano-imidazolate (LiTDI), lithium 4,5-dicyano-1,2,3-triazolate (LiDCTA), lithium bis(pentafluoroethylsulfonyl)imide (LiBETI), lithium tetrafluoroborate (LiBF.sub.4), lithium bis(oxalato)borate (LiBOB), lithium nitrate (LiNO.sub.3), lithium chloride (LiCl), lithium bromide (LiBr), lithium fluoride (LiF), lithium perchlorate (LiClO.sub.4), lithium hexafluoroarsenate (LiAsF.sub.6), lithium trifluoromethanesulfonate (LiSO.sub.3CF.sub.3) (LiTf), lithium fluoroalkylphosphate Li[PF.sub.3(CF.sub.2CF.sub.3).sub.3] (LiFAP), lithium tetrakis(trifluoroacetoxy)borate Li[B(OCOCF.sub.3).sub.4] (LiTFAB), or lithium bis(.sub.1,2-benzenediolato(2-)-O,O′)borate Li[B(C.sub.6O.sub.2).sub.2] (LBBB).

[0069] The present document relates to the preparation of solid multilayer electrode-electrolyte components. This process avoids the use of a polymer in the electrolyte or as a binder in the electrode of the final material. Two variations of this process are described here. The first variant does not include a polymer during the preparation of the multilayer, while the second eliminates the polymer used during a hot pressing step. Solvents are generally not required with the first variant of the process. FIG. 1 illustrates one embodiment of the process, showing that the solid electrode and electrolyte layers are hot-pressed together.

[0070] While sintering of cathode materials at high temperatures under oxygen may cause part of the cathode material to burn, it was found that LAGP and LATP are strongly affected when sintered under inert atmosphere. For these ceramics, gaseous oxygen would then be easily lost thereby forming germanium (II) or titanium (II) oxide and lithium phosphate impurities (see FIG. 2).

[0071] This document therefore presents a new process for the preparation of component comprising at least two layers including ceramic-based electrolyte and electrode layers for use in electrochemical applications. The process is simple and rather short. One of the variants also avoids the use of toxic and/or flammable solvents. It also ensures good contact at the interface between the electrolyte and electrode solid layers, where the two layers are intimately bonded (fused) to each other. The electrode-electrolyte solid component also possesses a density appropriate for its use in electrochemical cells.

[0072] An example of such a process for the preparation of a multilayer component comprises at least the steps of: [0073] a) preparing a solid electrolyte layer by compressing particles comprising a ceramic; [0074] b) preparing a mixture comprising at least an electrochemically active material, ceramic particles, and an electron conductive material, the mixture being free of solvent; [0075] c) applying the mixture prepared in (b) on the solid electrolyte layer prepared in (a) to obtain a bilayer material; [0076] d) pressing the bilayer material obtained in (c) at a pressure of at least 50 kg/cm.sup.2, or between 50 kg/cm.sup.2 and 5000 kg/cm.sup.2, and at a temperature in the range of about 400° C. to about 900° C., or about 450° C. to about 850° C., or about 600° C. to about 700° C.

[0077] For instance, step (a) of the present process avoids the use of a solvent and/or lithium salt. The solid electrolyte layer and the solid electrode layer of the component are free of polymer (i.e., polymer of solid polymer electrolyte or polymer binder).

[0078] The present process may use any ceramic known to the person skilled art, the selected ceramic being suitable as an electrolyte ceramic and being stable under the present process conditions. For instance, the ceramic in the solid electrolyte layer may be of formula Li.sub.1+zAl.sub.zM.sub.2-z(PO.sub.4).sub.3, wherein M is Ti, Ge, or a combination thereof, and 0<z<1. According to one example, M is Ge. According to another example, M is Ti. For instance, z is in the range of 0.25 to 0.75, or of 0.1 to 0.9, or of 0.3 to 0.7, or of 0.4 to 0.6, or of about 0.5. The ceramic may have a NASICON-like structure.

[0079] The solid electrolyte layer may have a final thickness (after step (d)) below 1 mm, or in the range of 50 μm to 1 mm, or 50 μm to 500 μm, or 50 μm to 200 μm.

[0080] The solid electrolyte layer is preferably compressed in step (a) without external heating and in the presence of oxygen (e.g., in air). The bilayer material after addition of the electrode layer mixture is preferably hot-pressed in step (d) in an inert atmosphere (e.g., under argon nitrogen).

[0081] For example, step (a) may be carried out at a pressure in the range of 100 kg/cm.sup.2 to 5000 kg/cm.sup.2.

[0082] The hot-pressing step (d) may be carried for a period of more than 0 hour and less than 10 hours, or between 30 minutes and 5 hours, or between 30 minutes and 2 hours. The hot-pressing step may be performed in a heating chamber such as ovens, furnaces, etc. while applying pressure on at least one side of the bilayer material. Preferably, the hot-pressing step is carried out using a hot-pressing furnace, hot-press die, and the like. The bilayer material is generally included in a mold, and the pressure is applied uniaxially.

[0083] The mixing step (b) in the present process may be performed by any method known in the art such as ball milling, planetary mixer, etc. For instance, the mixing step may be carried out by ball milling using zirconia (zirconium dioxide) balls.

[0084] Alternatively, the process for preparing a multilayer component comprising a solid electrode layer and a solid electrolyte layer comprises at least the steps of: [0085] a) preparing a solid electrolyte layer by the application of a mixture of ceramic particles and a polymer on a first support; [0086] b) preparing a mixture comprising at least an electrochemically active material, ceramic particles, an electron conductive material, and optionally a polymer; [0087] c) applying the electrode material mixture prepared in step (b): [0088] i. on the solid electrolyte layer prepared in (a); or [0089] ii. on a second support followed by contacting a surface of the applied electrode material mixture with a surface of the solid electrolyte layer;;  to afford a bilayer material; [0090] d) pressing the bilayer material obtained in (c) at a pressure of at least 50 kg/cm.sup.2 and a temperature of between about 400° C. and about 900° C.

[0091] Step (a) of the process may exclude the addition of a solvent. Alternatively, step (a) of the process further comprises a solvent and a step of drying the mixture after application. In one example, step (a) further comprises removing the first support. Preferably, step (a) excludes the addition of a lithium salt.

[0092] Non-limiting examples of polymers that may be used in step (a) and optionally step (b) (if present) comprise, independently in each occurrence, a fluorinated polymer (such as le polyvinylidene fluoride (PVDF), or poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)), a poly(alkylene carbonate) (such poly(ethylene carbonate) or poly(propylene carbonate)), a polyvinyl butyral (PVB), or a polyvinyl alcohol (PVA), for example, the polymer is a poly(alkylene carbonate) (such as poly(ethylene carbonate) or poly(propylene carbonate)). The solid electrolyte layer and the electrode layer are free of polymer after step (d).

[0093] The ceramic of step (a) is, for instance, of formula Li.sub.1+zAl.sub.zM.sub.2-z(PO.sub.4).sub.3, wherein M is Ti, Ge, or a combination thereof, and z is such that 0<z<1. Step (a) may further comprise pressing the mixture in the presence of oxygen (like oxygen from air), for instance, at a pressure of between 100 kg/cm.sup.2 and 5000 kg/cm.sup.2.

[0094] In one example, the process comprises step (c) (ii) and the process comprises removing the first support and the second support before contacting the electrode material layer with the solid electrolyte layer. Alternatively, the process comprises step (c) (ii) and the process comprises removing the first support and the second support after contacting the electrode material layer with the solid electrolyte layer.

[0095] The process preferably further comprises laminating the bilayer material between rolls before step (d).

[0096] In other examples, step (b) further comprises a solvent and step (c) further comprises drying the applied electrode material. For instance, step (b) can comprise dry mixing of the electrochemically active material, ceramic particles, and electron conductive material, suspending the resulting mixture with a polymer in a solvent, followed by drying of the applied electrode material.

[0097] Step (d) may be carried out under inert atmosphere (for example under argon, nitrogen). This step may also be carried out at a pressure of between 50 kg/cm.sup.2 and 5000 kg/cm.sup.2, or between 100 kg/cm.sup.2 and 5000 kg/cm.sup.2, or between 300 kg/cm.sup.2 and 2000 kg/cm.sup.2. The temperature applied in step (d) may be within the range of about 450° C. to about 850° C., or about 600° C. to about 750° C. This step is preferably carried out for a period of more than 0 hour and less than 10 hours, or between 30 minutes and 5 hours, or between 30 minutes and 2 hours.

[0098] The solid electrolyte layer may have a final thickness below 1 mm, or in the range of 50 μm to 1 mm, or of 50 μm to 500 μm, or of 50 μm to 200 μm. The combined thickness of the bilayer material, comprising the electrode layer and electrolyte is preferably below 1 mm, or within the range of 50 μm to 1 mm, or of 50 μm to 600 μm, or of 100 μm to 400 μm.

[0099] In either of the present processes, the electrode layer of the multilayer component is preferably a positive electrode. For example, the electrode layer contains between about 25 wt % and about 60 wt % of electrochemically active material, between about 25 wt % and about 60 wt % of ceramic particles, and between about 5 wt % and about 15 wt % of electron conductive material, the total being of 100%.

[0100] Non-limiting examples of electrochemically active material comprise phosphates (e.g. LiM.sup.aPO.sub.4 where M.sup.a is Fe, Ni, Mn, Co, or a combination thereof), oxides and complex oxides such as LiMn.sub.2O.sub.4, LiM.sup.bO.sub.2 (M.sup.b being Mn, Co, Ni, or a combination thereof), and Li(NiM.sup.c)O.sub.2 (M.sup.c being Mn, Co, Al, Fe, Cr, Ti, Zr, or a combination thereof), elemental sulfur, elemental selenium, iron(III) fluoride, copper(II) fluoride, lithium iodide, and iodine. In some examples, the electrochemically active material of the positive electrode is a phosphate LiM.sup.aPO.sub.4 where M.sup.a is Fe, Mn, Co or a combination thereof (such as LiFePO.sub.4), wherein said electrochemically active material is made of particles optionally further coated with carbon.

[0101] The electron conductive material included in the electrode layer may be selected from carbon black, Ketjen™ black, acetylene black, graphite, graphene, carbon fibers or nanofibers (for example, VGCF), carbon nanotubes, and a combination thereof. For instance, the electron conductive material comprises carbon fibers (such as VGCF) or graphite.

[0102] For instance, the ceramic particles in the electrode layer comprise a compound of the formula Li.sub.1+zAl.sub.zM.sub.2-z(PO.sub.4).sub.3, wherein M is Ti, Ge, or a combination thereof, and 0<z<1. In one example, M is Ge. In another example, M is Ti. For instance, z is between 0.25 and 0.75, or z is about 0.5.

[0103] In some examples, the ceramic in the solid electrolyte layer and the ceramic particles in the solid electrode layer comprise the same compound.

[0104] Multilayer components obtainable or obtained by the present process are also contemplated herein. For instance, the multilayer components comprise an intimately fused interface between the solid electrolyte layer and solid electrode layer. The solid electrolyte layer and solid electrode layer each possess a high density. For instance, the density of each at least one of the two layers is of at least 90% of the theoretical density.

[0105] The present document also relates to electrochemical cells comprising a negative electrode, a positive electrode and an electrolyte, wherein the electrolyte and positive electrode form a multilayer component as defined herein or obtained by the present process. For example, the negative electrode comprises a lithium or lithium alloy film and a polymer interlayer between the lithium or lithium alloy film and the solid electrolyte layer. The polymer interlayer may comprise, for instance, a polyether polymer and a lithium salt, such as an optionally crosslinked PEO-based polymer and a lithium salt (e.g. LiTFSI).

[0106] A process for preparing electrochemical cells as defined herein is also contemplated. Such a process comprises: [0107] (i) preparing a multilayer component according to a process as defined herein; and [0108] (ii) assembling the multilayer component of step (i) with a negative electrode layer.

[0109] For example, the negative electrode layer comprises a lithium or lithium alloy film and a polymer interlayer as described above between the lithium or lithium alloy film and the solid electrolyte layer.

[0110] The present description also describes a battery comprising at least one electrochemical cell as defined herein. For example, the battery is a lithium or lithium-ion battery.

[0111] The present technology also further relates to the use of the present electrochemical cells and batteries, for example, in mobile devices, such as mobile phones, cameras, tablets or laptops, in electric or hybrid vehicles, or in renewable energy storage.

EXAMPLES

[0112] The following non-limiting examples are illustrative embodiments and should not be construed as further limiting the scope of the present invention. These examples will be better understood with reference to the accompanying figures.

Example 1

[0113] (a) Solid Electrolyte-Cathode Component

[0114] Li.sub.1.5Al.sub.0.5Ge.sub.1.5(PO.sub.4).sub.3 (0.75 g, LAGP) powder is cold-pressed under air in a 16 mm titanium-zirconium-molybdenum (TZM) mold with 5 tons (5000 kg) of weight to form a LAGP electrolyte pellet. An amount of 0.75 g of a mixture containing carbon-coated LiFePO.sub.4 (45 wt %), LAGP (45 wt %), and vapor-grown carbon fibers (VGCF, 10 wt %), is added on the LAGP electrolyte pellet to form a bilayer material. This bilayer material is then pressed in a hot press at 650° C. for 1 hour with 2 tons (2000 kg) of pressure under inert atmosphere to give the solid electrolyte-cathode component.

[0115] (b) All Solid-State Electrochemical Cell

[0116] The solid electrolyte-cathode component obtained in (a) is assembled with a metallic lithium film and a protective layer comprising PEO and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) (with an O/Li molar ratio of 20:1) between the metallic lithium anode and the ceramic electrolyte.

[0117] The cell was cycled at 100 μA with charge/discharge results showing a 100% efficiency after 50 hours of cycling. FIG. 3 shows the potential as a function of capacity for the first two cycles.

Example 2

[0118] LAGP (85 wt.%) and QPAC®25 (poly(ethylene carbonate), 15 wt.%) were dispersed in N,N-dimethylformamide or a N,N-dimethylformamide:tetrahydrofuran (1:1) mixture. The obtained mixture was applied by Doctor blade on a polypropylene film. The film was then dried at 50° C. for 2 hours.

[0119] The cathode was prepared by mixing LAGP (45%), LiFePO.sub.4 (45%) and graphite (10%) using a SPEX® mixer to obtain a mixed positive electrode material. This mixed positive electrode material (85%) and QPAC®25 (15%) were dispersed in N,N-dimethylformamide or a N,N-dimethylformamide:tetrahydrofuran (1:1) mixture. The obtained mixture was applied as a film by Doctor blade on a polypropylene film. The cathode thus formed was dried at 50° C. for 2 hours.

[0120] The self standing LAGP electrolyte and cathode films were then separated from the polypropylene films and laminated together at 80° C. to reduce porosity and obtain a ceramic-cathode film having a thickness of between 100 and 400 μm. The film was then pounced and hot-pressed at 700° C. applying a pressure of 112 MPa for 1 hour. The hot-pressed solid ceramic electrolyte-cathode component was cycled with lithium metal and the results are shown in FIG. 4.

[0121] Numerous modifications could be made to any of the embodiments described above without departing from the scope of the present invention. All references, patents or scientific literature documents referred to in the present application are incorporated herein by reference in their entirety for all purposes.