LITHIUM ELECTRODE, METHOD FOR MAKING IT AND LITHIUM SECONDARY BATTERY USING IT

Description

Technical Field

[0001] The present invention relates to a method for preparing a lithium electrode having enhanced lifetime properties.Background Art

[0002] Until recently, there has been considerable interest in developing high energy density batteries using lithium as a negative electrode. For example, compared to other electrochemical systems having a lithium-inserted carbon electrode and a nickel or cadmium electrode reducing battery energy density by increasing the weight and volume of a negative electrode with the presence of non-electroactive materials, lithium metal has a low weight and high capacity properties, and therefore, has attracted much attention as a negative electrode active material of an electrochemical battery. A lithium metal negative electrode or a negative electrode including mainly lithium metal provides an opportunity to form batteries that are lighter and have a higher energy density compared to batteries such as lithium-ion, nickel metal hydride or nickel-cadmium batteries. Such characteristics are highly preferred with batteries for portable electronic devices such as mobile phones and laptop computers wherein a premiums is paid for a low weight.

[0003] Existing lithium ion batteries have an energy density of approximately 700 Wh / l using graphite in a negative electrode, and lithium cobalt oxide (LCO) in a positive electrode. However, with recent expansion of fields requiring high energy density, needs to increase energy density of lithium ion batteries have been constantly raised. For example, energy density needs to be increased in order to increase a driving distance of electric vehicles to 500 km or longer on a single charge.

[0004] In order to increase the energy density of a lithium ion battery, use of a lithium electrode has increased. However, lithium metal is a highly reactive metal and is difficult to handle, and has a problem of handling being difficult in a process.

[0005] In order to resolve such a problem, various attempts have been made to prepare electrodes using lithium metal.

[0006] For example, Korean Patent No. 0635684 relates to a method for forming a lithium electrode having a glass protective layer, and discloses a method for preparing a lithium electrode by forming a protective layer on a releasing agent layer-deposited substrate (PET), depositing lithium on the protective layer, and then depositing a current collector on the lithium, however, the lithium surface is exposed during the lithium deposition process increasing a thickness of an oxide layer (native layer), which may adversely affect lifetime properties of a battery.

[0007] In addition, polyvinylidene fluoride hexafluoropropylene (PVdF-HFP) has been used sometimes as a material of a protective layer for a lithium electrode, but has had a problem of lithium metal being damaged by external moisture due to insufficient moisture barrier properties.

[0008] Accordingly, development of technologies on methods for preparing a lithium electrode having a small and uniform thickness by minimizing oxide layer formation through protecting lithium from moisture and open air when preparing a lithium electrode has been continuously required.Prior Art Documents

[0009] Patent Document 1: Korean Patent No. 0635684, "Method for Forming Encapsulated Lithium Electrode Having Glass Protective Layer" Patent Document 2: Korean Patent Application Laid-Open Publication No. 2017-0026098, "Lithium Metal Battery Including Lithium Metal Anode, Method of Preparing the Lithium Metal Anode, and Protective Layer Prepared According to the Method"

[0010] EP 3 428 998 A1 and EP 3 667 774 A2, which are prior art pursuant to Article 54(3) EPC, disclose negative electrodes comprising a lithium metal layer and a protective layer thereon.

[0011] US 2017 / 0324097 A1 discloses a negative electrode comprising a protective layer on a lithium metal or lithium metal alloy layer. The protective includes particles and a crosslinked material of a polymerizable oligomer located between the particles.Disclosure Technical Problem

[0012] As a result of extensive studies in view of the above, the inventors of the present invention have identified that, by forming a protective layer to protect lithium metal that is vulnerable to moisture from moisture or open air and, as a material of the protective layer, introducing an olefin-based ion conducting polymer which is a cyclic olefin copolymer (COC) having ion conductivity and hydrophobicity, properties such as moisture barrier properties for lithium metal and lithium ion conductivity are strengthened compared to PVDF-HFP that has been generally used as a material of a protective layer for lithium metal, and lithium dendrite formation and growth are prevented, and as a result, lifetime properties and energy density of a battery are enhanced.Technical Solution

[0013] According to an aspect of the present invention, there is provided a method for preparing a lithium electrode, comprising (P1) forming a protective layer by coating an olefin-based ion conducting polymer on a substrate; and (P2) transferring the protective layer onto a lithium metal layer; wherein the olefin-based ion conducting polymer is a cyclic olefin copolymer (COC).

[0014] The lithium metal layer may include rolled lithium.

[0015] A release layer may be formed on at least one surface of the substrate, and the release layer may be one or more types selected from the group consisting of Si, melamine and fluorine.Advantageous Effects

[0016] According to the present invention, by using an ion conducting cyclic olefin copolymer (COC) exhibiting hydrophobicity as a material of a protective layer for protecting lithium metal in a lithium electrode, moisture barrier properties for lithium metal and lithium ion conductivity are more strengthened, and lithium dendrite formation and growth are prevented, and as a result, battery performance may be enhanced.

[0017] In addition, a lithium electrode having a small and uniform thickness can be prepared by the protective layer preventing lithium metal from being exposed to an external environment such as moisture or open air during a manufacturing process, and thereby minimizing oxide layer (native layer) formation on the lithium metal surface.Description of Drawings

[0018] FIG. 1 [Deleted] FIG. 2 is a graph presenting results of measuring a water vapor transmission rate depending on film types. FIG. 3 is a graph presenting discharge capacity and Coulombic efficiency measured by charging and discharging coin cells each manufactured in Example 2 and Comparative Examples 1 and 2. Best Mode

[0019] Hereinafter, the present invention will be described in more detail in order to illuminate the present invention.

[0020] Terms or words used in the present specification and the claims are not to be interpreted limitedly to common or dictionary meanings, and shall be interpreted as meanings and concepts corresponding to technological ideas of the present disclosure based on a principle in which the inventors may suitably define the concepts of terms in order to describe the invention in the best possible way.Lithium Electrode

[0021] Lithium metal is a material having high reactivity with moisture, and a surface of a lithium metal layer included in a lithium electrode may be deteriorated by reacting with moisture. In view of the above, the method of the present invention produces a lithium electrode provided with a protective layer capable of enhancing battery performance while protecting the lithium electrode from moisture.

[0022] In the present invention, the olefin-based ion conducting polymer exhibits hydrophobicity and may protect a lithium metal layer from moisture or open air, and in addition, may be a polymer having excellent conductivity for lithium ions while being swollen in an electrolyte.

[0023] The olefin-based ion conducting polymer may have a solubility index of 15 Mpa to 45 Mpa, preferably 20 Mpa to 40 Mpa and more preferably 20 Mpa to 35 Mpa. The ion conducting polymer having a solubility index in the above-mentioned range has an advantage of conducting lithium ions by the protective layer being swollen by a solvent of an electrolyte liquid.

[0024] The olefin-based ion conducting polymer is a cyclic olefin copolymer (COC), which is advantageous as a protective layer material of a lithium metal layer due to its properties of being stable for an electrolyte liquid and moisture.

[0025] In the present invention, the olefin-based ion conducting polymer exhibits hydrophobic properties with low affinity for water, and may exhibit excellent moisture barrier properties for a lithium metal layer.

[0026] As a result, the olefin-based ion conducting polymer exhibits low a water vapor transmission rate, and exhibits a water vapor transmission rate of, for example, 200 g / m 2< .day or less, preferably 180 g / m 2< .day or less and more preferably 150 g / m 2< .day or less, which is suitable as a material of a protective layer for a lithium electrode.

[0027] In the present invention, the protective layer may have an ion conductivity of 10 -6< S / cm to 10 -1< S / cm, preferably 10 -5< S / cm to 10 -2< S / cm and more preferably 10 -4< S / cm to 10 -3< S / cm. This has an advantage of satisfying rate performance for driving a battery.

[0028] In addition, the protective layer may have a thickness of 0.01 µm to 50 µm, preferably 0.1 µm to 40 µm and more preferably 0.5 µm to 20 µm. When the thickness of the protective layer is less than the above-mentioned range, functions of protecting a lithium metal layer from moisture or open air become inferior, damaging the lithium metal layer, or lithium dendrite growth may not be prevented, and the thickness being greater than the above-mentioned range may be disadvantageous for commercialization due to an increased electrode thickness.

[0029] In the present invention, the lithium metal layer may have a thickness of 5 µm to 50 µm, preferably 15 µm to 30 µm and more preferably 18 µm to 25 µm. When thickness of the lithium metal layer is less than the above-mentioned range, battery capacity and lifetime properties may decline, and the thickness being greater than the above-mentioned range may be disadvantageous for commercialization due to an increased lithium electrode thickness.

[0030] The lithium metal layer may be formed on one surface of a current collector, and in this case, the protective layer may be formed on the whole surface of the lithium metal layer except the surface of the lithium metal layer in contact with a current collector.

[0031] The lithium metal layer may be formed with rolled lithium, and rolled lithium metal may be attached on a current collector

[0032] When the current collector is a porous current collector, the lithium metal layer may be included in a pore of the porous current collector, and herein, the protective layer may be provided on the whole surface of the porous current collector except a terminal connected to the porous current collector and extended to the outside.Lithium Secondary Battery

[0033] The lithium electrode described above can be incorporated into a lithium secondary battery.

[0034] In the lithium secondary battery, the lithium electrode may be included as a negative electrode, and the lithium secondary battery may include an electrolyte provided between the negative electrode and a positive electrode.

[0035] The shape of the lithium secondary battery is not limited, and examples thereof may include a coin-type, a flat plate-type, a cylinder-type, a horn-type, a button-type, a sheet-type or a laminate-type. In addition, the lithium secondary battery may be manufactured as a flow battery by further including tanks each storing a positive electrode electrolyte liquid and a negative electrode electrolyte liquid, and pumps moving each of the electrolyte liquids to an electrode cell.

[0036] The electrolyte may be an electrolyte liquid into which the negative electrode and the positive electrode are impregnated.

[0037] The lithium secondary battery may further include a separator provided between the negative electrode and the positive electrode. As the separator placed between the negative electrode and the positive electrode, any may be used as long as it separates and insulates a negative electrode and a positive electrode, and allows ion transport between the negative electrode and the positive electrode. For example, the separator may be a non-conductive porous membrane or an insulating porous membrane. More specifically, polymer non-woven fabrics such as non-woven fabrics made of polypropylene materials or non-woven fabrics made of polyphenylene sulfide materials; or porous films of olefin-based resins such as polyethylene or polypropylene may be included as an example, and these may be combined in two or more types.

[0038] The lithium secondary battery may further include a positive electrode electrolyte liquid on a positive electrode side and a negative electrode electrolyte liquid on a negative electrode side separated by a separator. The positive electrode electrolyte liquid and the negative electrode electrolyte liquid may each include a solvent and an electrolyte salt. The positive electrode electrolyte liquid and the negative electrode electrolyte liquid may be the same as or different from each other.

[0039] The electrolyte liquid may be an aqueous electrolyte liquid or a non-aqueous electrolyte liquid. The aqueous electrolyte liquid may include water as a solvent, and the non-aqueous electrolyte liquid may include a non-aqueous solvent as a solvent.

[0040] The non-aqueous solvent is not particularly limited, and those generally used in the art may be selected, and the non-aqueous solvent may be selected form the group consisting of, for example, carbonate-based, ester-based, ether-based, ketone-based, organosulfur-based, organophosphorus-based, aprotic solvents and combinations thereof.

[0041] The electrolyte salt refers to those dissociated into cations and anions in water or a non-aqueous organic solvent, is not particularly limited as long as it is capable of transferring lithium ions in a lithium secondary battery, and those generally used in the art may be selected.

[0042] In the electrolyte liquid, a concentration of the electrolyte salt may be greater than or equal to 0.1 M and less than or equal to 3 M. In this case, charge and discharge properties of a lithium secondary battery may be effectively obtained.

[0043] The electrolyte may be a solid electrolyte membrane or a polymer electrolyte membrane.

[0044] Materials of the solid electrolyte membrane and the polymer electrolyte membrane are not particularly limited, and those generally used in the art may be employed. For example, the solid electrolyte membrane may include a composite metal oxide, and the polymer electrolyte membrane may be a membrane having a conducting polymer provided inside a porous substrate.

[0045] In a lithium secondary battery, the positive electrode means an electrode in which lithium-containing ions are reduced by receiving electrons when discharging the battery. On the contrary, a role of a negative electrode (oxidation electrode) is performed when charging the battery, and electrons are released by oxidizing a positive electrode active material and lithium-containing ions are lost.

[0046] The positive electrode may include a positive electrode current collector and a positive electrode active material layer formed on the positive electrode current collector.

[0047] In the present specification, a material of a positive electrode active material of the positive electrode active material layer is not particularly limited as long as it reduces lithium-containing ions when discharged and oxidizes them when charged while being used in a lithium secondary battery with the negative electrode. For example, a transition metal oxide or a sulfur (S)-based composite may be included, and specifically, at least one of LiCoO 2 , LiNiO 2 , LiFePO 4 , LiMn 2 O 4 , LiNi x Co y MnzO 2 (herein, x+y+z=1), Li 2 FeSiO 4 , Li 2 FePO 4 F and Li 2 MnO 3 may be included.

[0048] In addition, when the positive electrode is a sulfur (S)-based composite, the lithium secondary battery may be a lithium sulfur battery. The sulfur (S)-based composite is not particularly limited, and positive electrode materials generally used in the art may be selected and used.

[0049] A battery module can be produced which includes the lithium secondary battery as a unit cell.

[0050] The battery module may be formed by stacking with a bipolar plate provided between two or more of the lithium secondary batteries.

[0051] When the lithium secondary battery is a lithium air battery, the bipolar plate may be porous so as to provide air supplied from the outside to a positive electrode included in each of the lithium air electrodes. For example, porous stainless steel or porous ceramics may be included.

[0052] The battery module may be specifically used as a power supply of electric vehicles, hybrid electric vehicles, plug-in hybrid electric vehicles or systems for power storage.Method for Preparing Lithium Electrode

[0053] Hereinafter, the method for preparing a lithium electrode according to the present invention will be described in more detail by each step.Step (P1)

[0054] In step (P1), a protective layer for protecting lithium metal is formed by coating an olefin-based ion conducting polymer (COC) on a substrate.

[0055] In the present invention, the protective layer protects lithium metal from an external environment such as moisture or open air in a series of processes preparing a lithium electrode, and may minimize formation of a surface oxide layer (native layer).

[0056] Accordingly, materials forming the protective layer need to have a high moisture-blocking ability, have stability for an electrolyte liquid, have a high electrolyte liquid moisture content, and have excellent oxidation-reduction stability.

[0057] The olefin-based ion conducting polymer has excellent ion conductivity and is stable to moisture and an electrolyte liquid.

[0058] The olefin-based ion conducting polymer for metal protection may be dissolved in an organic solvent to prepare an olefin-based ion conducting polymer solution having a solid concentration of 0.1% to 10%, and the solution is coated to form a protective layer.

[0059] A coating solution for forming the protective layer may be prepared by dissolving the olefin-based ion conducting polymer as described above in a solvent, and herein, the solid concentration may be from 0.1% to 10%, preferably from 1% to 10% and more preferably from 2% to 5%. When the concentration of the coating solution is less than the above-mentioned range, viscosity is very low making the coating process difficult to proceed, and when the concentration is greater than the above-mentioned range, viscosity is high making it difficult to form the coating layer to a target coating thickness. Herein, the solvent for forming the coating solution may be one or more types selected from the group consisting of toluene, cyclohexane, N-methyl-2-pyrrolidone (NMP), dimethylformamide (DMF), dimethylacetamide (DMAc), tetramethyl urea, dimethyl sulfoxide (DMSO) and triethyl phosphate. Particularly, when using NMP, solubility of the polymer for forming the protective layer as described above is high, and forming the protective layer using a coating process may be advantageous.

[0060] In addition, a coating method for forming the protective layer may be selected from the group consisting of dip coating, spray coating, spin coating, die coating, roll coating, slot-die coating, bar coating, gravure coating, comma coating, curtain coating and micro-gravure coating, but is not limited thereto, and coating methods that may be used for forming a coating layer in the art may be diversely used.

[0061] The substrate may include one or more types selected from the group consisting of polyethylene terephthalate (PET), polyimide (PI), poly(methyl methacrylate) (PMMA), cellulose tri-acetate (TAC), polypropylene, polyethylene and polycarbonate.

[0062] In addition, the substrate may have a release layer formed on at least one surface, and preferably may have a release layer formed on both surfaces.

[0063] The release layer may include one or more types selected from the group consisting of Si, melamine and fluorine.

[0064] The release layer may be formed using a coating method, and although the coating method may be selected from the group consisting of, for example, dip coating, spray coating, spin coating, die coating and roll coating, the coating method is not limited thereto, and coating methods that may be used for forming a coating layer in the art may be diversely used.

[0065] In addition, the substrate may include an oligomer block coating on at least one surface. Herein, the oligomer block coating means a barrier for preventing oligomer migration caused by oligomers remaining in the substrate without being polymerized escaping outside the substrate and contaminating lithium.

[0066] For example, unpolymerized oligomers may be present in a PET film, and these oligomers may migrate outside the PET film and contaminate lithium, and therefore, the oligomer block coating may be formed on at least one surface of the PET film in order to prevent this phenomenon.

[0067] In addition, having a lower oligomer content in the substrate may be advantageous since the problem of the oligomer escaping from the substrate may be prevented.Step (P2)

[0068] In Step (P2), the protective layer formed in Step (P1) is transferred onto a lithium metal layer.

[0069] Herein, the lithium metal layer may be formed with rolled lithium, and the rolled lithium may be formed on at least one surface of a current collector.

[0070] The current collector may be one type selected from the group consisting of copper, aluminum, nickel, titanium, baked carbon and stainless steel.

[0071] According to the present invention, a lithium electrode in which a current collector, a lithium metal layer and a protective layer are consecutively laminated may be prepared using a method of forming a lithium metal protective layer and then transferring the lithium metal protective layer on a lithium metal layer to prepare a lithium electrode.

[0072] In addition, a lithium electrode having a small and uniform thickness may be prepared by the protective layer preventing lithium metal from being exposed to an external environment such as moisture or open air during a manufacturing process, and thereby minimizing oxide layer (native layer) formation on the lithium metal surface.

[0073] In addition, the lithium electrode prepared as above has excellent thickness uniformity while having a small thickness when rolled lithium is used as the lithium metal layer, and as a result, may greatly enhance energy density when used in a battery.Examples

[0074] Hereinafter, preferred examples are provided in order to illustrate the present invention.Preliminary Experimental Example: Experiment on Moisture Barrier Properties of COC

[0075] In order to judge suitability of COC as a material of a protective layer for a lithium electrode, a COC water vapor transmission rate (WVTR) was measured, and moisture barrier properties were identified. Herein, the water vapor transmission rate (g / m 2< .day) means an amount [g] of water passing through a film with an area of 1 m 2< for a day, and a lower water vapor transmission rate means favorable moisture barrier properties.

[0076] Water was put in each of three cups, and the three cups were covered with each of a triacetyl cellulose film (TAC), a film coating PVdF-HFP on TAC (TAC / PVdF-HFP) and a film coating COC on TAC (TAC / COC). Herein, as the TAC, UZ60 Grade of Fuji Corporation.

[0077] After a day had passed, a water vapor transmission rate for each of the films was measured using a water vapor transmission rate measuring device (TSY-T3, Labthink International).

[0078] FIG. 2 is a graph presenting results of measuring a water vapor transmission rate depending on film types.

[0079] When referring to FIG. 2, water vapor transmission rates of the TAC, the TAC / PVdF-HFP and the TAC / COC were measured as 327 g, 319 g and 146 g, respectively, and it was identified that, with a water vapor transmission rate of the TAC / COC being the lowest leading to excellent moisture barrier properties, COC has suitable properties as a material of a protective layer for a lithium electrode.Example 1 (reference example): Preparation of Lithium Electrode and Lithium Secondary Battery (1) Preparation of Lithium Electrode

[0080] As a substrate, a release PET film (manufactured by SKC hi-tech & marketing (former SKC Haas) RX12G 50 µm) having a release layer formed on both surfaces was prepared.

[0081] On one surface of the substrate, a cyclic olefin copolymer (COC) coating solution was prepared as a coating solution for forming a protective layer for protecting lithium metal. The COC coating solution was prepared as a solution having a 5% solid concentration by dissolving COC (manufactured by Topas, 6013 Grade) in a cyclohexane solvent.

[0082] The COC coating solution was coated on one surface of the release PET film to a thickness of 0.2 µm using a micro-gravure coater to form a COC protective layer.

[0083] A lithium metal layer having a thickness of 20 µm was formed by depositing lithium metal on the protective layer using a vacuum deposition method (evaporation deposition) at a temperature of 600°C, and a structure in which the release PET film, the COC protective layer and the lithium metal layer are consecutively laminated was wound at a rate of 1 m / min.

[0084] After that, the lithium metal layer was transferred onto a Cu current collector using a roll press machine (calendering machine CLP-1015, manufactured by CIS) to prepare a lithium electrode in which the Cu current collector, the lithium metal layer and the COC protective layer are consecutively laminated.(2) Manufacture of Lithium Secondary Battery

[0085] A coin cell-type lithium secondary battery was manufactured in a composition of the electrode prepared using the above-mentioned method, a positive electrode of LCO (manufactured by LandF Corporation, LFX20N), and an electrolyte liquid of mixing ethylene carbonate (EC), diethyl carbonate (DEC) and dimethyl carbonate (DMC) in a ratio of 1:2:1 and adding 1 mol of LiPF 6 and 2 wt% of vinylene carbonate (VC) thereto.Example 2: Preparation of Lithium Electrode and Lithium Secondary Battery (1) Preparation of Lithium Electrode

[0086] As a substrate, a release PET film (manufactured by SKC hi-tech & marketing (former SKC Haas) RX12G 50 µm) having a release layer formed on both surfaces was prepared.

[0087] On one surface of the substrate, a cyclic olefin copolymer (COC) coating solution was prepared as a coating solution for forming a protective layer for protecting lithium metal. The COC coating solution was prepared as a solution having a 5% solid concentration by dissolving COC (manufactured by Topas, 6013 Grade) in a cyclohexane solvent.

[0088] The COC coating solution was coated on one surface of the release PET film to a thickness of 0.2 µm using a micro-gravure coater to form a COC protective layer.

[0089] In addition, rolled lithium (Honjo Metal Co., Ltd., Japan) was prepared as a lithium metal layer, and Cu foil was adhered on one surface of the rolled lithium.

[0090] After that, the COC protective layer was transferred onto the rolled lithium metal layer using a roll press machine (calendering machine CLP-1015, manufactured by CIS) to prepare a lithium electrode in which the Cu current collector, the rolled lithium metal layer and the COC protective layer are consecutively laminated (Li / COC).(2) Manufacture of Lithium Secondary Battery

[0091] A coin cell-type lithium secondary battery was manufactured in a composition of the electrode prepared using the above-mentioned method, a positive electrode of LCO (manufactured by LandF Corporation, LFX20N), and an electrolyte liquid of mixing ethylene carbonate (EC), diethyl carbonate (DEC) and dimethyl carbonate (DMC) in a ratio of 1:2:1 and adding 1 mol of LiPF 6 and 2 wt% of vinylene carbonate (VC) thereto.Comparative Example 1: Preparation of Lithium Electrode and Lithium Secondary Battery

[0092] Preparation was performed in the same manner as in Example 1 except that bare Li was used as the lithium electrode, and a lithium secondary battery was manufactured using the same (bare Li).Comparative Example 2: Preparation of Lithium Electrode and Lithium Secondary Battery

[0093] A lithium electrode and a lithium secondary battery were prepared in the same manner as in Example 1, except that, instead of the COC coating solution, a PVDF-HFP coating solution prepared as a 5% solution by dissolving PVDF-HFP (manufactured by Arkema, LBG Grade) in an NMP solvent was used as the coating solution for forming a protective layer to form a PVDF-HFP protective layer (Li / PVdF).Experimental Example 1: Measurement on Discharge Capacity and Coulombic Efficiency of Lithium Electrode

[0094] For the coin cells manufactured in each of Example 2 and Comparative Examples 1 and 2, charge and discharge Crates were set at 0.2 C and 0.5 C, respectively, in a charger and discharger, and then a cycle progressed.

[0095] FIG. 3 is a graph presenting discharge capacity and Coulombic efficiency measured by charging and discharging the coin cells each manufactured in Example 2 and Comparative Examples 1 and 2.

[0096] When referring to FIG. 3, it was seen that, whereas charge and discharge progressed close to 25 cycles in the coin cell of Example 2 (Li / COC), cycle fading started before 15 cycles in the coin cell of Comparative Example 2 (Li / PVdF), and a cycle life of Example 2 also increased compared to Comparative Example 1 (bare Li). From such results, it was seen that lifetime properties were able to be enhanced when using COC in a protective layer of a lithium electrode.

Claims

1. A method for preparing a lithium electrode, comprising (P1) forming a protective layer by coating an olefin-based ion conducting polymer on a substrate, and (P2) transferring the protective layer onto a lithium metal layer, wherein the olefin-based ion conducting polymer is a cyclic olefin copolymer (COC).

2. The method of Claim 1, wherein the lithium metal layer comprises rolled lithium.

3. The method of Claim 1 or 2, wherein a release layer is formed on at least one surface of the substrate.

4. The method of Claim 3, wherein the release layer comprises one or more of Si, melamine and fluorine.