SOLID-STATE BATTERY AND METHOD FOR MANUFACTURING SAME BY DEPROTONATION

Abstract

A solid-state battery (20) with a solid electrolyte (8) and to the method for producing same. The method includes: protonating a body (11) made of, a protonatable ceramic material, to form a protonated layer (12, 13) on the body (11); deprotonating the protonated layer (13) to obtain a porous layer provided with mini-cavities (18); depositing a metal element forming an anode (14) on the deprotonated layer (13) on a first side (7) of the body (11), and infiltrating mini-cavities (18) of the porous layer by the metal element, and assembling a cathode (15) on a second side (9) of the body (11), preferably opposite the first side (7) of the anode (14).

Claims

1. A method for producing a solid-state battery with a solid electrolyte, wherein the method comprises the following successive steps: a step of protonating a body containing, preferably being entirely made of, a protonatable ceramic material, to form a protonated layer on the body, a step of deprotonating the protonated layer so as to obtain a porous layer provided with mini-cavities, a step of depositing a metal element forming an anode on the deprotonated layer on a first side of the body, and of infiltrating the mini-cavities of the porous layer by the metal element, and a step of assembling a cathode on a second side of the body, preferably opposite the first side of the anode.

2. The production method according to claim 1, wherein the ceramic material is selected from: doped or undoped lithium and/or lanthanum zirconium oxide, of the LLZO type, a doped or undoped beta-alumina solid electrolyte material of the Na-b″-Al.sub.2O.sub.3 type, a ternary, quaternary or higher order sulphide-based solid electrolyte material, for example of the Li.sub.6PS.sub.5X type (where X is selected from the elements Cl, Br or I) or of the Li.sub.2S—P.sub.2S.sub.5 type, a ternary, quaternary or higher order halogen-based solid electrolyte material, for example of the Li.sub.3MX.sub.6 type (where M is a metal or a metal alloy, and X is a halogen), a lithium ion-conducting solid electrolyte material of the LISICON (lithium super ionic conductor) type, for example of the Li.sub.4±xSi.sub.1-xX.sub.xO.sub.4 type (where X is selected from the elements P, Al, or Ge), and a sodium ion-conducting solid electrolyte material of the NASICON (sodium super ionic conductor) type, for example of the Na.sub.xMM′(XO.sub.4).sub.3 type (where M and M′ are metals and X is selected from the elements Si, P or S).

3. The production method according to claim 1, wherein in the protonation step, the body is immersed in a protic solvent, such as water, acetone or ethanol.

4. The production method according to claim 1, wherein in the deprotonation step, the body is heated to a predefined temperature, preferably of at least 750° C., to separate the protons from the protonated layer.

5. The production method according to claim 1, wherein the metal element is melted onto the body during the metal element deposition step.

6. The production method according to claim 1, wherein the metal element contains a material to be selected from: alkali-metals, such as lithium, sodium, potassium, rubidium, caesium or francium, alkaline-earth metals, such as beryllium, magnesium, calcium, strontium, barium or radium, all transition metals, which make up columns 3 to 11 of the periodic table, including lanthanides and actinides, and alloys of these metals.

7. The production method according to claim 1, wherein it comprises an additional step of removing a part of the protonated layer from the body in order to deposit the cathode directly onto the unprotonated part of the body.

8. The production method according to claim 7, wherein the additional step of removing a part of the protonated layer from the body is carried out by polishing the second side of the body.

9. The production method according to claim 1, wherein the cathode contains a material to be selected from: a lithium-nickel-manganese-cobalt oxide of the NMC type, such as LiNi.sub.xMn.sub.yCo.sub.zO.sub.2 or Li.sub.2-x-y-zNi.sub.xMn.sub.yCo.sub.zO.sub.2 where x+y+z≤1, a lithium-nickel-manganese oxide of the LNMO type, such as LiNi.sub.0.5Mn.sub.1.5O.sub.4, a lithium iron phosphate oxide of the LFP type, such as LiFePO.sub.4, a lithium manganese oxide of the LMO type, such as LiMn.sub.2O.sub.4, and a lithium-nickel-cobalt-aluminium oxide of the NCA type, such as LiNiCoAlO.sub.2.

10. A solid-state battery (20) with a solid electrolyte (8) comprising an anode, a cathode and a solid ceramic electrolyte, wherein the solid electrolyte is provided with a porous, deprotonated layer provided with mini-cavities, and an unprotonated part superimposed on one another, the cathode being deposited on the body, the anode comprising a metal element deposited on the protonated layer of the body opposite the cathode, the metal element having infiltrated the mini-cavities in the porous, deprotonated layer.

11. The solid-state battery with a solid electrolyte according to claim 10, wherein the metal element is blocked by the unprotonated part of the body.

12. The solid-state battery with a solid electrolyte according to claim 10, wherein the metal element contains a material to be selected from: alkali-metals, such as lithium, sodium, potassium, rubidium, caesium or francium, alkaline-earth metals, such as beryllium, magnesium, calcium, strontium, barium or radium, all of the so-called transition metals, which make up columns 3 to 11 of the periodic table, including lanthanides and actinides, and alloys of these metals.

13. The solid-state battery with a solid electrolyte according to claim 10, wherein the ceramic material is selected from: doped or undoped lithium and/or lanthanum zirconium oxide, of the LLZO type, a doped or undoped beta-alumina solid electrolyte material of the Na-b″-Al.sub.2O.sub.3 type, a ternary, quaternary or higher order sulphide-based solid electrolyte material, for example of the Li.sub.6PS.sub.5X type (where X is selected from the elements Cl, Br or I) or of the Li.sub.2S—P.sub.2S.sub.5 type, a ternary, quaternary or higher order halogen-based solid electrolyte material, for example of the Li.sub.3MX.sub.6 type (where M is a metal or a metal alloy, and X is a halogen), a lithium ion-conducting solid electrolyte material of the LISICON (lithium super ionic conductor) type, for example of the Li.sub.4±xSi.sub.1-xX.sub.xO.sub.4 type (where X is selected from the elements P, Al, or Ge), and a sodium ion-conducting solid electrolyte material of the NASICON (sodium super ionic conductor) type, for example of the Na.sub.xMM′(XO.sub.4).sub.3 type (where M and M′ are metals and X is selected from the elements Si, P or S).

14. The solid-state battery with a solid electrolyte according to claim 10, wherein the cathode is bonded to the unprotonated part of the body.

15. The solid-state battery with a solid electrolyte according to claim 10, wherein the cathode contains a material to be selected from: a lithium-nickel-manganese-cobalt oxide of the NMC type, such as LiNi.sub.xMn.sub.yCo.sub.zO.sub.2 or Li.sub.2-x-y-zNi.sub.xMn.sub.yCo.sub.zO.sub.2 where x+y+z≤1, a lithium-nickel-manganese oxide of the LNMO type, such as LiNi.sub.0.5Mn.sub.1.5O.sub.4, a lithium iron phosphate oxide of the LFP type, such as LiFePO.sub.4, a lithium manganese oxide of the LMO type, such as LiMn.sub.2O.sub.4, and a lithium-nickel-cobalt-aluminium oxide of the NCA type, such as LiNiCoAlO.sub.2.

16. An electronic system, for example a watch, a mobile phone, a laptop computer or a motor vehicle comprising a solid-state battery with a solid electrolyte, according to claim 10.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0066] Other specific features and advantages will be clearly observed in the following description, which is given as a rough guide and in no way as a limiting guide, with reference to the accompanying drawings, in which:

[0067] FIG. 1 is a block diagram showing the steps of the method according to the invention; and

[0068] FIGS. 2a) to 2f) are diagrammatic, cross-sectional views of the battery after each step of the method for producing the battery according to the invention.

DETAILED DESCRIPTION OF THE INVENTION

[0069] The invention relates to a method for producing 10 a solid-state battery 20. Such a battery 20 comprises an anode 14, a cathode 15 and an electrolyte arranged between the cathode 15 and the anode 14. A solid electrolyte 8 is understood to refer to an electrolyte that is not liquid.

[0070] The electrolyte 8 is formed from a body 11 containing a material capable of undergoing protonation. In other words, it is able to exchange H.sup.+ ions with the protons. Preferably, the body 11 is made entirely of this material.

[0071] The ceramic material used can be selected from: [0072] doped or undoped lithium and/or lanthanum zirconium oxide, of the LLZO type, [0073] a doped or undoped beta-alumina solid electrolyte material of the Na-b″-Al.sub.2O.sub.3 type, [0074] a ternary, quaternary or higher order sulphide-based solid electrolyte material, for example of the Li.sub.6PS.sub.5X type (where X is selected from the elements Cl, Br or I) or of the Li.sub.2S—P.sub.2S.sub.5 type, [0075] a ternary, quaternary or higher order halogen-based solid electrolyte material, for example of the Li.sub.3MX.sub.6 type (where M is a metal or a metal alloy, and X is a halogen), [0076] a lithium ion-conducting solid electrolyte material of the LISICON (lithium super ionic conductor) type, for example of the Li.sub.4±xSi.sub.1-xX.sub.xO.sub.4 type (where X is selected from the elements P, Al, or Ge), and [0077] a sodium ion-conducting solid electrolyte material of the NASICON (sodium super ionic conductor) type, for example of the Na.sub.xMM′(XO.sub.4).sub.3 type (where M and M′ are metals and X is selected from the elements Si, P or S).

[0078] The ceramic material is preferably made entirely of this material.

[0079] Preferably, the LLZO-type compound is selected, as it has a high ionic conductivity.

[0080] In order to produce the battery 20, a method is used which comprises a first step of protonating 1 the ceramic body 11. The body 11 is immersed in a protic or acidic solvent, such as water, acetone, mineral oil or ethanol, in order to replace atoms of the ceramic with a proton. Preferably, water is selected as the protic solvent.

[0081] The body 11 is immersed for a long period of time, at least for one day, preferably several days or even a week or more, depending on the size of the body 11 and the desired protonated layer.

[0082] The body is, for example, shaped like a pellet with a thickness of 0.7 mm to form a small battery 20. The body has preferably been previously polished to have parallel faces.

[0083] Preferably, in order to speed up the process, the liquid is heated to a predetermined temperature, for example 50° C.

[0084] In the case of the LLZO-type compound, the protonation formula with water is as follows:

LLZO+H.sub.2O.fwdarw.HLLZO+LiOH.

[0085] Regardless of the liquid used, the protonated compound of the HLLZO-type is obtained. The protonated HLLZO-type compound is more fragile than the unprotonated LLZO-type compound, which is a very hard ceramic.

[0086] At the end of this step, the body 11 comprises a protonated layer 12, 13 around the body 11. The layer 12, 13 is disposed around the entire body 11, if the body is fully immersed in the liquid.

[0087] The layer has a thickness of 20 μm for example. A first layer 13 is disposed on a first side 9 of the body 11, and a second layer 12 is disposed on a second side 7 of the body 11.

[0088] Optionally, the method 10 includes a second step of removing 2 the second protonated layer 12 from the second side 9 of the body 11 so that the cathode 15 can be deposited directly on an unprotonated part of the body 11 in a subsequent step. This is because the conductivity between the cathode 15 and an unprotonated part is better than between a cathode 15 and a protonated part.

[0089] Preferably, the second removal step 2 comprises polishing the second side 9 of the body 11. Polishing removes the protonated layer of material 12 to expose an unprotonated part of the body 11. For example, a 600 grit polishing tool is used to remove the HLLZO-type protonated layer.

[0090] Alternatively, the second protonated layer 12 is preserved on the second side 9 of the body 11, in order to deposit the cathode 15 thereon. Depending on the cathode 15 adhesion process, the second protonated layer 12 can be of use, in particular according to the adhesive used.

[0091] In a third step 3, the body 11 is heated to a predefined temperature in order to deprotonate the protonated layer 13. Deprotonation is understood to mean the removal of the protons from the protonated layer 13. Above a certain temperature, the protons separate from the rest of the compound. The deprotonation formula for a protonated material of the HLLZO type is as follows:

HLLZO.fwdarw.LZO+H.sub.2O.

[0092] The predefined temperature is preferably greater than 750°. This minimum temperature allows the preceding chemical reaction to take place in the case of the protonated material of the HLLZO type. The deprotonated layer 13 becomes porous as a result of the mini-cavities 18, which are created by the decomposition of the deprotonated layer 13. The porous layer 13 nonetheless remains solid. The heating time is, for example, equal to three hours.

[0093] The fourth step 4 consists of depositing a metal element forming an anode 14 on the protonated part on the first side 7 of the body 11. The first side 7 is selected such that it is opposite the second side 9 of the body 11. Thus, the cathode 15 and the anode 14 are arranged on either side of the body 11.

[0094] The metal element contains a material to be selected from: [0095] alkali-metals, such as lithium, sodium, potassium, rubidium, caesium or francium, [0096] alkaline-earth metals, such as beryllium, magnesium, calcium, strontium, barium or radium, [0097] all transition metals, which make up columns 3 to 11 of the periodic table, including lanthanides and actinides, and [0098] alloys of these metals.

[0099] The metal element is preferably made entirely of this material.

[0100] Preferably, lithium is selected for its physical and chemical properties that are conducive to use as an anode 14.

[0101] The molten metal element is deposited on the first deprotonated side 7 of the body 11. In other words, the metal element is deposited in a molten form on the first side 7. In this state, the metal element adheres to the body 11 and infiltrates the hollows or cracks in the deprotonated layer 13 that has become porous. Since it is porous, the molten metal element is easily inserted into the deprotonated layer 13 from the first side 7.

[0102] This infiltration of the porous layer 13 by the metal element in particular allows the span of the contact face between the metal element and the body 11 to be maximised, and prevents the formation of unwanted dendrites.

[0103] The method comprises a fifth step 5 of assembling a cathode 15 on the body 11 on the second side 9 opposite the anode 14, which is not protonated following the polishing that took place in the second step 2.

[0104] For this purpose, an adhesive 16 made of a polymer material is used to assemble them together, referred to as a catholyte, the adhesive 16 being an ion conductor allowing the ions to pass.

[0105] For example, a polymer adhesive 16 containing polyethylene oxide of the PEO type, a lithium salt of the LiTFSi (lithium bis-(trifluoromethanesulphonyl)-imide) type, and THF (Tetrahydrofuran) is used. The polymer adhesive 16 is dissolved in the THF (tetrahydrofuran) and then deposited on the second side 9, for example by means of a drop casting method. The cathode 15 is then deposited on the polymer adhesive 16 after the THF has dried, such that the cathode 15 permanently adheres to the second side 9.

[0106] The cathode 15 contains, for example, an active material to be selected from: [0107] a lithium-nickel-manganese-cobalt oxide of the NMC type, such as LiNi.sub.xMn.sub.yCo.sub.zO.sub.2 or Li.sub.2-x-y-zNi.sub.xMn.sub.yCo.sub.zO.sub.2 where x+y+z≤1, [0108] a lithium-nickel-manganese oxide of the LNMO type, such as LiNi.sub.0.5Mn.sub.1.5O.sub.4, [0109] a lithium iron phosphate oxide of the LFP type, such as LiFePO.sub.4, [0110] a lithium manganese oxide of the LMO type, such as LiMn.sub.2O.sub.4, and [0111] a lithium-nickel-cobalt-aluminium oxide of the NCA type, such as LiNiCoAlO.sub.2.

[0112] The cathode 15 is preferably mostly made of this material, together with the polymer adhesive and carbon to improve the ionic and electronic conductivity thereof.

[0113] FIG. 2a) shows a body 11 made entirely of a LLZO-type ceramic material. After the first protonation step, the body 11 comprises a protonated layer 12, 13 around the body 11, as shown in FIG. 2b). A first layer 13 is arranged on a first side 7 of the body 11, and a second layer 12 is arranged on a second side 9 of the body 11.

[0114] The body 11 is then polished on the second side 9 of the body 11, so as to expose an unprotonated part on this side. The body 11 in FIG. 2c) thus has an unprotonated part on the second side 9 and a protonated layer 13 on a first side 7 of the body 11.

[0115] After the third deprotonation step, a porous, deprotonated layer 13 is obtained beneath the unprotonated part, as shown in FIG. 2d). Mini-cavities 18 appear in the deprotonated layer 13 during the deprotonation process.

[0116] According to the fourth step, an anode 14 is formed on the first deprotonated side 7 of the body 11, by depositing a molten metal element, preferably made of lithium, as shown in FIG. 2e).

[0117] The molten metal element infiltrates the porous, deprotonated layer 13, in particular within the mini-cavities 18, such that the contact area between the anode and the electrolyte 8 is increased.

[0118] A cathode 15 is bonded to the second, unprotonated side 9 of the body 11, using polymer adhesive 16, as shown in FIG. 2f).

[0119] This results in a battery 20 with an anode 14 and a cathode 15 on either side of the electrolyte 8, the body 11 having a deprotonated ceramic layer 13 and an unprotonated part superimposed on one another.

[0120] Such a battery 20 can be used in any electronic system, such as a watch, a drone, a mobile phone, a laptop computer, or even an electronic motor vehicle. In the case of a motor vehicle, the battery is of course larger in size.

[0121] It goes without saying that the invention is not limited to the embodiments described with reference to the figures and alternatives can be considered without leaving the scope of the invention.