JP5476612B2 - Method for producing transfer film and method for producing electrode plate for electrochemical device - Google Patents

Description

  The present invention relates to a transfer film, and a negative electrode for a secondary battery and a lithium secondary battery formed using the same, and in particular, a transfer film for transferring a lithium layer, a negative electrode for an electrochemical device to which the lithium layer is transferred, and The present invention relates to a lithium secondary battery and an electric double layer capacitor.

  In recent years, negative electrode materials such as Si (silicon) and Sn (tin) have attracted attention in order to increase the capacity of nonaqueous electrolyte secondary batteries. For example, the theoretical discharge capacity of Si is about 4199 mAh / g, which is about 11 times the theoretical discharge capacity of graphite. However, these negative electrode materials are known to have problems with cycle characteristics. Therefore, in place of these negative electrode materials, attempts have been made to improve cycle characteristics by using oxides, nitrides or oxynitrides of Si or Sn.

  However, Si, Sn, or their oxides and nitrides have a problem of large irreversible capacity. That is, since the proportion of some of the lithium ions released from the positive electrode during the initial charge remains occluded in the negative electrode is large, the battery capacity becomes smaller than the theoretical capacity of the negative electrode material. In order to avoid this irreversible capacity, a technique is disclosed in which lithium corresponding to the irreversible capacity is inserted in the negative electrode in advance, and then a battery is assembled and charging / discharging is started (see, for example, Patent Documents 1 to 4). By using these methods, lithium ions released from the positive electrode during the first charge can be recovered from the negative electrode at a high rate, and the battery capacity is increased.

  Patent Document 1 includes a negative electrode mixture layer containing a negative electrode active material containing at least one selected from the group consisting of Si, Sn, and Si—Ti alloys, and covers the surface of the negative electrode mixture layer. Discloses forming a metal lithium layer by vapor deposition or sputtering.

  Patent Document 2 discloses a method in which a lithium oxide layer is formed on a silicon oxide thin film formed on a current collector, a metal lithium layer is further formed, and lithium is supplemented with silicon oxide. Yes.

  Patent Document 3 discloses the production of a negative electrode including a step of forming a negative electrode mixture layer capable of inserting and extracting light metals, and a step of forming a light metal layer on the negative electrode mixture layer by a dry film formation method. The law is disclosed.

  The methods described in Patent Documents 1 to 3 are effective as a method of supplementing lithium into the active material layer, but as a simpler method, a transfer method of lithium foil as shown in Patent Document 4 can be mentioned. .

Also in the electric double layer capacitor, lithium is used in advance for charging / discharging by preliminarily applying lithium to the activated carbon forming the negative electrode (pre-doping).
Japanese Patent Laying-Open No. 2005-063805 Japanese Patent Laid-Open No. 2003-162997 JP 2005-038720 A JP-A-10-289708

Japanese Patent Laying-Open No. 2005-063805 Japanese Patent Laid-Open No. 2003-162997 JP 2005-038720 A JP-A-10-239708

  However, a method of applying a lithium foil corresponding to an irreversible capacity by pasting on a negative electrode active material is expensive because a thin lithium foil is difficult to manufacture. As described in Patent Document 4, the transfer method is a method of simply supplementing lithium. However, when lithium is formed on the support and then applied to the active material by transfer, the transfer from the support to the lithium is performed. There was a problem that it was difficult to peel off.

  The present invention solves the above-described conventional problems, and provides a transfer film for easily imparting lithium corresponding to an irreversible capacity to an active material, and draws out the characteristics of a high-performance active material. And a lithium secondary battery and an electric double layer capacitor using the same.

  In order to solve the conventional problems, the transfer film of the present invention includes a substrate, a release layer, an auxiliary layer, and a lithium layer sequentially formed on the substrate.

  With this configuration, the lithium layer can be easily peeled and transferred from the transfer film.

The negative electrode for an electrochemical device of the present invention includes a current collector, an active material layer formed on the current collector, a lithium layer formed on the active material layer, and an auxiliary formed on the lithium layer. A negative electrode for a secondary battery having a layer,
The lithium layer and the auxiliary layer are formed by being transferred from the transfer film.

  Since the negative electrode for electrochemical devices of this configuration can easily transfer the lithium layer onto the active material layer, it is excellent in productivity and can easily compensate for the irreversible capacity of the active material layer.

  According to the transfer film of the present invention, the lithium layer can be easily peeled and transferred from the transfer film. The auxiliary layer transferred together with the lithium layer protects the lithium layer from moisture and oxygen contained in the handling atmosphere after the transfer, and prevents the lithium from reacting with moisture and oxygen and losing its activity. Furthermore, by forming a pattern of the auxiliary layer, it is possible to pattern transfer the auxiliary layer and the lithium layer without forming a pattern of lithium, which is difficult to handle compared to general metals.

  The negative electrode for an electrochemical element of the present invention can be formed using the transfer film of the present invention, and can be a high energy density negative electrode excellent in suppression of irreversible capacity.

  Since the lithium secondary battery of the present invention has the negative electrode of the present invention, it can be a high capacity and highly reliable battery in which irreversible capacity is avoided.

  Since the electric double layer capacitor of the present invention has the negative electrode of the present invention, it can be a high-capacity and highly reliable capacitor in which irreversible capacitance is avoided and pre-doping is performed.

Schematic sectional view showing an example of a transfer film in Embodiment 1 of the present invention Schematic diagram showing a transfer process in Embodiment 1 of the present invention. Schematic sectional view showing an example of a transfer film in Embodiment 2 of the present invention Schematic diagram showing a transfer process in Embodiment 2 of the present invention Schematic sectional view showing the sectional structure of the negative electrode in the first and second embodiments of the present invention Schematic which shows an example of the manufacturing apparatus of the film for transfer in Embodiment 1 and 2 of this invention Schematic showing an example of a transfer film and negative electrode manufacturing apparatus in Embodiments 1 and 2 of the present invention

  Hereinafter, preferred embodiments for carrying out the present invention will be described with reference to the drawings.

  Embodiment 1 FIG. 1 is a schematic sectional view showing an example of a transfer film of the present invention. In FIG. 1, the transfer film 49 includes a substrate 45, a release layer 46, an auxiliary layer 47, and a lithium layer 48 that are sequentially formed on the substrate 45. The substrate 45 should be made of a polymer film such as polyethylene terephthalate, polyethylene naphthalate, polyethylene sulfide, polyamide, polyimide, metal foil such as aluminum, copper, nickel, stainless steel, or other sheet-like material. I can do it. A substrate provided with a base layer on the surface of the substrate 45 can also be used. When the releasability of the release layer 46 is adjusted by appropriately selecting the type and thickness of the release agent, the transfer film 49 is integrated with the lithium layer 48 and the auxiliary layer 47 from the release layer 46. Release and transfer. For example, BL6, BL7, and BL8 (all trade names) of Reiko Co., Ltd. are examples of those obtained by forming a release layer on a polymer substrate, and can be used for the purposes of the present invention. The thickness of the board | substrate 45 can be selected suitably, for example, is 25 micrometers.

  As the material of the auxiliary layer 47, various metals such as copper, aluminum, and nickel can be used, and metal oxides and nitrides can also be used. When a metal oxide or nitride is used as the auxiliary layer 47, the auxiliary layer 47 and lithium in the lithium layer 48 may react. If the auxiliary layer 47 is sufficiently thin, lithium affected by the reaction Since there are few, it is possible to use a metal oxide or nitride. The material of the auxiliary layer 47 is selected according to the influence of the auxiliary layer 47 remaining after transfer. In view of the original purpose of transferring the lithium layer 48, the auxiliary layer 47 is preferably thin. However, the thickness of the auxiliary layer 47 is 5 nm or more from the viewpoint of protecting the surface of the lithium layer 48 and protecting the surface of the release layer 46. Film thickness is preferred.

  FIG. 2 is a schematic diagram showing a transfer process using the transfer film 47 according to the first embodiment of the present invention. In FIG. 2, the same components as those in FIG. 2, the transfer film 49 and the transfer target 50 shown in FIG. 1 are joined to bond the transfer target 50 and the lithium layer 48, and then the transfer target 50 is separated when the substrate 45 is separated. The lithium layer 48 and the auxiliary layer 47 are transferred and transferred thereon. Depending on the material design, most of the release layer 46 can remain on the substrate 45 without being transferred, or can be partially transferred together with the auxiliary layer 47. When the transfer target 50 is a battery electrode plate, it is generally desirable that the release layer 46 remain on the substrate 45 for reasons such as preventing side reactions. In order to join the transfer body 50 and the transfer film 49, both pieces of the transfer body 50 and the transfer film 49 may be pressed substantially in parallel to each other, but they are formed in a long roll shape. A method in which the transferred transfer film 49 and the transfer target 50 formed in a separate long roll are sequentially wound and pressure-bonded is preferable from the viewpoint of high production efficiency.

(Embodiment 2)
FIG. 3 is a schematic cross-sectional view showing another example of the transfer film of the present invention. In FIG. 3, the same components as those in FIG. The transfer film 49 shown in FIG. 3 differs from the configuration of the transfer film 49 shown in FIG. 1 in that the auxiliary layer 47 is patterned. The pattern of the auxiliary layer 47 means that the auxiliary layer 47 does not uniformly cover the entire surface of the release layer 46, for example, rectangular auxiliary layers are arranged in a grid pattern, and the mesh-like gaps and A state where lithium is arranged on the surface of the auxiliary layer. When the release property of the release layer 46 is adjusted by appropriately selecting the type and thickness of the release agent, the transfer film 49 has the lithium layer 48 and the auxiliary layer 47 integrated according to the pattern of the auxiliary layer 47. The release layer 46 is released and transferred. The thickness of the lithium layer 48 can be arbitrarily set, and is 2 μm to 20 μm, for example, when used for eliminating the irreversible capacity of the negative electrode.

  FIG. 4 is a schematic diagram showing a transfer process using the transfer film 47 according to the second embodiment of the present invention. 4, the same components as those in FIG. 2 are denoted by the same reference numerals, and the description thereof is omitted. In FIG. 4, the transfer film 49 and the transferred object 50 shown in FIG. 3 are bonded to bond the transferred object 50 and the lithium layer 48, and then the transferred object 50 is separated when the substrate 45 is separated. The lithium layer 48 and the auxiliary layer 47 are transferred and transferred thereon. At that time, as shown in FIG. 4, the lithium layer 48 and the auxiliary layer 47 are transferred according to the pattern of the auxiliary layer 47, and the lithium in which the auxiliary layer 47 is not patterned remains on the release layer 46. The toner is not transferred to the transfer target 50.

  The reason why such a transfer can be performed is that the part where the lithium layer is directly formed on the release agent is formed by the heat at the time of forming the lithium layer 48 or the chemical reaction of the release layer 46 with the release agent. This is because the moldability is lowered, and as a result, only the portion where the auxiliary layer 47 is formed can maintain the mold release property.

  Further, as in the first embodiment, most of the release layer 46 can remain on the substrate 45 without being transferred, or can be partially transferred together with the auxiliary layer 47 by material design. When the transfer target 50 is a battery electrode plate, it is generally desirable that the release layer 46 remain on the substrate 45 for reasons such as preventing side reactions. In order to join the transfer body 50 and the transfer film 49, both pieces of the transfer body 50 and the transfer film 49 may be pressed substantially in parallel to each other, but they are formed in a long roll shape. A method in which the transferred transfer film 49 and the transfer target 50 formed in a separate long roll are sequentially wound and pressure-bonded is preferable from the viewpoint of high production efficiency.

  FIG. 5 is a schematic cross-sectional view showing a cross-sectional structure of a negative electrode for an electrochemical element (hereinafter also referred to as a negative electrode) formed using the transfer film 49 in the first and second embodiments of the present invention. In FIG. 5, the same components as those in FIG.

  In FIG. 5, the negative electrode 20 has an active material layer 21 formed on a sheet-like current collector 22. The surface of the active material layer 21 has a transferred lithium layer 48. Further, the auxiliary layer 47 is transferred together with the lithium layer 48 on the surface of the lithium layer 48. The surface of the lithium layer 48 formed on the active material layer 21 is covered with the auxiliary layer 47, thereby suppressing a chemical reaction caused by moisture, oxygen, etc. in the handling atmosphere on the lithium surface. I can do it. Further, when lithium adheres to the conveyance system in the product production process, it is possible to prevent running failure and blocking during winding.

  In FIG. 5, the active material layer 21 is formed only on one surface of the current collector 22, but the active material layer 21 is formed on both surfaces of the current collector 22, and a lithium layer 48 and an auxiliary layer 47 are formed on each surface. May be transferred.

  The active material contained in the active material layer 21 is not particularly limited as long as it is electrochemically reactive with lithium. However, a silicon simple substance or a silicon alloy that has a relatively high reactivity with lithium and can be expected to have a high capacity. A compound containing silicon and oxygen, a compound containing silicon and nitrogen, a simple substance of tin, a tin alloy, a compound containing tin and oxygen, and a compound containing tin and nitrogen, or carbon represented by graphite and activated carbon It is preferable to include at least one selected from the group consisting of compounds containing carbon. It is because the improvement degree by this invention becomes remarkable.

  The transfer film in Embodiment 1 and Embodiment 2 can be produced by, for example, the following method.

  FIG. 6 is a schematic view showing an example of a manufacturing apparatus for constituting the transfer film 49 in the first and second embodiments. In FIG. 6, the same components as those in FIG.

  In FIG. 6, the inside of the vacuum chamber 2 is exhausted by the exhaust pump 1. The long substrate 45 unwound from the unwinding roll 8 in the vacuum chamber 2 travels along the peripheral surfaces of the transport roller 5 and the cylindrical first can 6 and the second can 7, and the winding roll 3. Rolled up. A release agent is applied to the substrate 45 in advance, and a release layer 46 (not shown) is formed. In the first can 6, the substrate 45 travels so that the release layer 46 is on the outside. In the auxiliary layer application source 13, the material of the auxiliary layer 47 is put in an evaporation container such as a crucible. The auxiliary layer application source 13 is heated by a heating device (not shown) such as an electron beam, and the material of the auxiliary layer 47 evaporates.

  The lithium supply source 46 contains lithium in an evaporation container made of SUS304 or the like. The lithium application source 46 is heated by a heating device (not shown) such as a heater, and lithium evaporates.

  The substrate 45 is exposed to the material of the auxiliary layer 47 coming from the auxiliary layer application source 13 via the opening of the shielding plate 10 in a state along the first can 6, and thus on the release layer 46 of the substrate 45. An auxiliary layer 47 (not shown) is formed. Next, the lithium layer 48 (not shown) is formed on the auxiliary layer 47 by being exposed to the lithium flying from the lithium application source 46 through the opening of the shielding plate 10 along the second can 7. Laminated.

  The auxiliary layer 47 can be formed by methods other than electron beam evaporation, and dry processes such as sputtering can be widely applied. Although the auxiliary layer 47 can be formed by a wet printing process, for example, screen printing, the reaction between the auxiliary layer 47 and the lithium layer 48 during the formation of the lithium layer 48 is likely to be significant. It is preferable to form by a process. As shown in FIG. 3, when the auxiliary layer 47 is formed by patterning, for example, the auxiliary layer 47 can be formed by installing a mask that moves in synchronization with the first can 6 in front of the first can 6. is there.

  Formation of the lithium layer 48 is not limited to resistance heating vapor deposition, and various dry processes such as electron beam vapor deposition and sputtering can be used.

  FIG. 7 is a schematic diagram showing an example of a manufacturing apparatus for forming the negative film 20 while forming the transfer film 49 in the first and second embodiments. 7, the same components as those in FIGS. 1 and 6 are denoted by the same reference numerals, and the description thereof is omitted.

  The left portion of FIG. 7 has a transfer film production function similar to that of FIG. That is, in FIG. 7, the inside of the vacuum chamber 2 is exhausted by the exhaust pump 1. The long substrate 45 unwound from the unwinding roll 8 in the vacuum chamber 2 travels along the peripheral surfaces of the transport roller 5 and the cylindrical first can 6 and the second can 7, and moves the transfer roller 4A. Via, it is wound up on the winding roll 3A. The transfer roller 4A will be described later.

  A release agent is applied to the substrate 45 in advance, and a release layer 46 (not shown) is formed. In the first can 6, the substrate 45 travels so that the release layer 46 is on the outside. In the auxiliary layer application source 13, the material of the auxiliary layer 47 is put in an evaporation container such as a crucible. The auxiliary layer application source 13 is heated by a heating device (not shown) such as an electron beam, and the material of the auxiliary layer 47 evaporates.

  The lithium supply source 46 contains lithium in an evaporation container made of SUS304 or the like. The lithium application source 46 is heated by a heating device (not shown) such as a heater, and lithium evaporates.

  The substrate 45 is exposed to the material of the auxiliary layer 47 coming from the auxiliary layer application source 13 via the opening of the shielding plate 10 in a state along the first can 6, and thus on the release layer 46 of the substrate 45. An auxiliary layer 47 (not shown) is formed. Subsequently, the substrate 45 is exposed to lithium flying from the lithium application source 46 through the opening of the shielding plate 10 in a state along the first can 6, so that the lithium layer 48 is formed on the auxiliary layer 47. (Not shown) are stacked.

  In FIG. 7, the auxiliary layer 47 and the lithium layer 48 are provided in a state where the substrate 45 is along the first can 6, but may be provided separately in two cans as shown in FIG. 6. .

  In addition, the right portion of FIG. 7 has an active material layer manufacturing function and a transfer function. That is, the long current collector 22 unwound from the unwinding roll 8B in the vacuum chamber 2 travels along the peripheral surfaces of the transport roller 5 and the cylindrical third can 14, and passes through the transfer roller 4B. Then, it is wound around the winding roll 3B. The current collector 22 used here is a sheet-like foil made of copper, nickel or the like. In the active material application source 9, silicon or tin is put in a crucible or the like. The active material application source 9 is heated by a heating device (not shown) such as an electron beam, and silicon or tin evaporates.

  When the current collector 22 is exposed to silicon, tin, or the like flying from the active material applying source 9 through the opening of the shielding plate 10 in a state along the third can 14, silicon or tin is deposited on the current collector 22. An active material layer 21 (not shown) made of tin is formed.

  When forming the active material layer 21 of a compound containing silicon and oxygen, a compound containing silicon and nitrogen, a compound containing tin and oxygen, or a compound containing tin and nitrogen, oxygen gas or nitrogen gas is used. The active material layer 21 is obtained by introducing from the gas introduction pipe 11 and evaporating silicon or tin from the active material application source 9 under these atmospheres. The manufacturing method of the active material layer 21 is not particularly limited as long as the structure of the electrode plate of the present invention can be obtained, but it is preferable to use a dry process such as a vapor deposition method, a sputtering method, or a CVD method.

  The substrate 45 in which the auxiliary layer 47 and the lithium layer 48 are stacked on the release layer 46 in the state along the first can 6 and the current collector 22 on which the active material layer 21 is formed include the transfer roller 4A. And the transfer roller 4B, and the lithium layer 48 and the auxiliary layer 47 are integrally transferred to the active material layer 21. The laminated body in which the lithium layer 48 and the auxiliary layer 47 are integrally transferred is wound around the winding roll 3B as the negative electrode 20 as shown in FIG. When the auxiliary layer 47 is patterned as shown in FIG. 3, the lithium layer 48 and the auxiliary layer 47 formed on the pattern of the auxiliary layer 47 as shown in FIG. The lithium layer formed without the auxiliary layer 47 and directly formed on the release layer 46 on the substrate 45 is wound around the winding roll 3A together with the substrate 45 without being peeled off or transferred. According to this transfer method, it is particularly preferable that transfer can be performed on the active material layer 21 while the surface of lithium is active.

  The negative electrode 20 obtained by such a method includes a positive electrode plate containing a commonly used positive electrode active material such as LiCoO2, LiNiO2, LiMn2O4, a separator made of a microporous film, lithium hexafluorophosphate, and the like. A lithium secondary battery can be produced by using together with an electrolytic solution having lithium ion conductivity of a generally known composition dissolved in cyclic carbonates such as ethylene carbonate and propylene carbonate.

  In addition, the negative electrode 20 is a positive electrode plate generally used for an electric double layer capacitor such as activated carbon, a separator made of a microporous film, and lithium hexafluorophosphate is a cyclic carbonate such as ethylene carbonate or propylene carbonate. An electric double layer capacitor can be manufactured by using together with an electrolytic solution having a lithium ion conductivity of a generally known composition dissolved in a kind.

  It is also possible to use a carbon-based material for the negative electrode used in the electric double layer capacitor. A compound containing silicon and oxygen, a compound containing silicon and nitrogen, a compound containing tin and oxygen, or tin and nitrogen are used. It is also possible to use compounds containing. When a carbon-based material is used, a general coating method using a binder can be applied, but a dry process such as an evaporation method, a sputtering method, or a CVD method can also be used.

  The negative electrode of the present invention can be applied to lithium secondary batteries having various shapes such as a cylindrical shape, a flat shape, a coin shape, and a square shape, and the shape and sealing form of the battery are not particularly limited.

  Further, the negative electrode of the present invention can be applied to electric double layer capacitors having various shapes such as a cylindrical shape, a flat shape, a coin shape, and a square shape, and the shape and sealing form of the capacitor are not particularly limited.

  Hereinafter, the present invention will be described based on examples.

Example 1
An aluminum layer as an auxiliary layer was formed on a release film BL7 manufactured by Reiko Co., Ltd. (trade name: film thickness 16 μm, with a release layer formed on a resin film). The aluminum layer was patterned by an electron beam vacuum deposition method using a metal mask at a film formation rate of 3 nm / second to form a layer having a thickness of 1 μm. The release film was 100 mm in both length and width, and the aluminum layer was both 30 mm in length and width, and was provided at two locations with an interval of 10 mm.

  Further, lithium having a thickness of 3 μm was formed at a deposition rate of 20 nm / s by resistance heating evaporation so as to cover two aluminum layers, and a transfer film as shown in FIG. 3 was produced. When the created transfer film was pressed against a silicon oxide thin film (silicon oxide composition: SiO 0.5, thickness 20 μm) separately produced on a copper foil at about 2 × 10 5 Pa (about 2 kgf / cm 2), FIG. As shown, the lithium layer and the aluminum layer were transferred onto the silicon oxide thin film along the pattern formation of the aluminum layer. This electrode plate can be configured as a secondary battery.

(Example 2)
An aluminum layer as an auxiliary layer was formed on a release film BL7 manufactured by Reiko Co., Ltd. (trade name: film thickness 16 μm, with a release layer formed on a resin film). The aluminum layer was patterned by an electron beam vacuum deposition method using a metal mask at a film formation rate of 3 nm / second to form a layer having a thickness of 1 μm. The release film was 100 mm in both length and width, and the aluminum layer was both 30 mm in length and width, and was provided at two locations with an interval of 10 mm.

Further, lithium having a thickness of 1 μm was formed at a deposition rate of 20 nm / s by resistance heating evaporation so as to cover two aluminum layers, and a transfer film as shown in FIG. 3 was produced. When the produced transfer film was pressed at about 2 × 10 5 Pa (about 2 kgf / cm 2) against a silicon oxide thin film (silicon oxide composition: SiO 0.5, thickness 5 μm) separately produced on a copper foil, FIG. As shown, the lithium layer and the aluminum layer were transferred onto the silicon oxide thin film along the pattern formation of the aluminum layer. Using this electrode plate, an electric double layer capacitor can be constructed and charged and discharged.

(Example 3)
A copper layer as an auxiliary layer was formed on a release film BL7 (trade name: film thickness: 16 μm, having a release layer formed on a resin film) manufactured by Reiko Co., Ltd. The copper layer was patterned by an electron beam vacuum deposition method using a metal mask at a film formation rate of 5 nm / second to form a layer having a thickness of 50 nm. The release film was 100 mm in length and width, and the copper layer was 30 mm in length and width. The release film was provided at two locations with an interval of 10 mm.

  Further, lithium having a thickness of 2 μm was formed at a deposition rate of 40 nm / s by resistance heating evaporation so as to cover two copper layers, and a transfer film as shown in FIG. 3 was produced. When the created transfer film was pressed at about 400 kPa (about 4 kgf / cm 2) onto a carbon thin film (thickness 100 μm) separately produced on a copper foil, as shown in FIG. 4, along the pattern formation of the copper layer, A lithium layer and a copper layer were transferred onto the carbon thin film. When an electric double layer capacitor was configured using this electrode plate, it was confirmed that charging / discharging was possible.

  The transfer film according to the present invention, and the negative electrode for a secondary battery for an electrochemical device, the lithium secondary battery, and the electric double layer capacitor formed using the transfer film can easily impart lithium corresponding to an irreversible capacity to an active material. Since the characteristics of the high-performance active material can be extracted, it is useful as a negative electrode for a secondary battery and a lithium secondary battery using the same.

DESCRIPTION OF SYMBOLS 1 Exhaust pump 2 Vacuum tank 3, 3A, 3B Winding roll 4A, 4B Transfer roller 5 Conveying roller 6 1st can 7 2nd can 8, 8B Unwinding roll 9 Active material provision source 10 Shielding plate 11 Gas introduction pipe 13 Auxiliary Layer application source 14 Third can 20 Negative electrode 21 Active material layer 22 Current collector 45 Substrate 46 Release layer 47 Auxiliary layer 48 Lithium layer 46 Lithium application source 49 Transfer film 50 Transfer object

Claims (3)

Preparing a substrate having a release layer formed on the surface;
Forming an auxiliary layer on the release layer, which is less reactive to the release layer than lithium;
And a step of depositing lithium on the auxiliary layer.   The method for producing a transfer film according to claim 1, wherein the auxiliary layer is a metal, metal oxide, or metal nitride containing at least one of copper, aluminum, and nickel. Preparing a substrate having a release layer formed on the surface;
Forming an auxiliary layer on the release layer, which is less reactive to the release layer than lithium;
Depositing lithium on the auxiliary layer to produce a transfer film;
A step of preparing a negative electrode in which an active material is formed on a current collector;
A method for producing an electrode plate for an electrochemical device, comprising: joining the transfer film and the negative electrode, and transferring the auxiliary layer and the lithium layer.

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