Method and system for manufacturing doped electrode

Abstract

Provided is a method for manufacturing a doped electrode comprising an active material layer doped with an alkali metal. A belt-like electrode comprising an active material layer is carried along a path passing through a doping tank which accommodates: a doping solution containing ions of the alkali metal and an aprotic organic solvent; a counter electrode unit; and a guide mechanism. In the doping tank, the distance between the electrode and the counter electrode unit is maintained in a fixed range by the guide mechanism which is installed between the electrode and the counter electrode unit. In the doping tank, the electrode and the counter electrode unit are electrically connected via the doping solution.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This international application claims priority based on Japanese Patent Application No. 2021-106788 filed with the Japan Patent Office on June 28, 2021, and the entire contents of Japanese Patent Application No. 2021-106788 are incorporated by reference into this international application. [Technical field]

[0002] The present disclosure relates to a method and system for manufacturing a doped electrode. [Background technology]

[0003] In recent years, electronic devices have become increasingly smaller and lighter, and this has led to an increased demand for smaller and lighter batteries used as the power source for these electronic devices.

[0004] In order to satisfy such demands for miniaturization and weight reduction, non-aqueous electrolyte secondary batteries, such as lithium ion secondary batteries, have been developed. In addition, lithium ion capacitors are known as power storage devices that can be used in applications that require high energy density and high output. Furthermore, sodium ion batteries and capacitors are also known that use sodium, which is less expensive and more abundant than lithium.

[0005] In such batteries and capacitors, a process of doping an electrode with an alkali metal in advance (generally called pre-doping) is adopted for various purposes. As a method of pre-doping an electrode with an alkali metal, for example, there is a continuous method. In the continuous method, pre-doping is performed while a strip-shaped electrode is transported in a doping solution. In the doping solution, the electrode faces an alkali metal electrode. The continuous method is disclosed in Patent Documents 1 to 4. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] Japanese Patent Application Publication No. 10-308212 [Patent Document 2] JP 2008-77963 A [Patent Document 3] JP 2012-49543 A [Patent Document 4] JP 2012-49544 A Summary of the Invention [Problem to be solved by the invention]

[0007] The strip-shaped electrode may have distortion, uneven thickness, wrinkles, etc. If the strip-shaped electrode has distortion, uneven thickness, wrinkles, etc., when performing continuous pre-doping, there will be places where the gap between the electrode and the alkali metal electrode is small. In the places where the gap between the electrode and the alkali metal electrode is small, the alkali metal is likely to precipitate. In addition, there will be a state where the degree of progress of pre-doping differs between the places where the gap between the electrode and the alkali metal electrode is small and other places (hereinafter referred to as doping unevenness).

[0008] In one aspect of the present disclosure, it is preferable to provide a method and system for producing a doped electrode that can suppress alkali metal precipitation and uneven doping. [Means for solving the problem]

[0009] One aspect of the present disclosure is a method for producing a doped electrode including an active material layer doped with an alkali metal. In the method for producing a doped electrode, a strip-shaped electrode including an active material layer is transported along a path passing through a doping tank that contains a doping solution including an alkali metal ion and an aprotic organic solvent, a counter electrode unit, and a guide mechanism, and in the doping tank, the guide mechanism installed between the strip-shaped electrode including the active material layer and the counter electrode unit keeps the distance between the strip-shaped electrode including the active material layer and the counter electrode unit within a certain range, and in the doping tank, the strip-shaped electrode including the active material layer and the counter electrode unit are electrically connected via the doping solution.

[0010] According to a method for producing a doped electrode that is one aspect of the present disclosure, precipitation of alkali metal and uneven doping can be suppressed.

[0011] Another aspect of the present disclosure is a system for manufacturing a doped electrode including an active material layer doped with an alkali metal, the system for manufacturing a doped electrode including a doped electrode including an active material layer doped with an alkali metal, the system for manufacturing a doped electrode including a doping tank configured to accommodate a doping solution including an alkali metal ion and an aprotic organic solvent, a counter electrode unit accommodated in the doping tank, a guide mechanism accommodated in the doping tank, a conveying unit configured to convey a strip-shaped electrode including the active material layer along a path passing through the doping tank, and a connection unit configured to electrically connect a conveying roller of the conveying unit to the counter electrode unit.

[0012] The guide mechanism is disposed between the strip-shaped electrode including the active material layer and the counter electrode unit, and is configured to maintain a distance between the strip-shaped electrode including the active material layer and the counter electrode unit within a certain range in the doping tank.

[0013] According to a system for manufacturing a doped electrode that is another aspect of the present disclosure, precipitation of alkali metal and uneven doping can be suppressed. [Brief description of the drawings]

[0014] [Figure 1] FIG. 2 is a plan view showing the configuration of an electrode. [Diagram 2] 2 is a cross-sectional view showing a cross section taken along line II-II in FIG. [Diagram 3] FIG. 1 is an explanatory diagram illustrating a configuration of an electrode manufacturing system. [Figure 4] 4A to 4C are explanatory diagrams illustrating the configuration and arrangement of a guide mechanism. [Diagram 5] 5 is a plan view of the X plane in FIG. 4 as viewed from the Y direction. [Figure 6] 3 is a cross-sectional view showing the configuration of a guide bar and a guide roll, taken along a cross section perpendicular to the axial direction. FIG. [Figure 7]FIG. 2 is a perspective view showing the configuration and arrangement of a guide mechanism including a guide roll. [Figure 8] FIG. 4 is an explanatory diagram showing the position of a negative electrode in an active material layer forming section. [Figure 9] FIG. 11 is an explanatory diagram showing a method of joining the ends together. [Figure 10] FIG. 11 is an explanatory diagram showing a method of joining the ends together. [Explanation of symbols]

[0015] 1...electrode, 1A...doped electrode, 3...current collector, 5...active material layer, 6...active material layer forming section, 7...active material layer unformed section, 11...electrode manufacturing system, 15...electrolyte treatment tank, 17, 19...doped tank, 23...cleaning tank, 25, 27, 29, 31, 33, 35, 37, 39, 40, 47, 49, 51, 52, 59, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93...conveyor roller, 101...supply roll, 103...winding roll, 105...support stand, 107...circulation filtration unit, 109, 111...power source, 117...tub cleaner, 119... Recovery unit, 121... end sensor, 123, 135... partition plate, 125, 127, 145, 147... support rod, 137, 139, 141, 143... counter electrode unit, 144... mask, 149, 151... space, 153... conductive base material, 155... alkali metal-containing plate, 161... filter, 163... pump, 165... piping, 201... guide mechanism, 203... guide bar, 205... main body, 207... surface portion, 209... guide roll, 211... base, 301, 303, 305... negative electrode, 401... end, 403... end, 405... connecting member, 407... hole DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0016] Exemplary embodiments of the present disclosure will now be described with reference to the drawings. First Embodiment 1. Electrode 1 Configuration The structure of the electrode 1 will be described with reference to Figures 1 and 2. The electrode 1 has a strip-like shape. The electrode 1 includes a current collector 3 and an active material layer 5. The current collector 3 has a strip-like shape. The active material layers 5 are formed on both sides of the current collector 3.

[0017] The surface of the electrode 1 includes an active material layer formed portion 6 and an active material layer unformed portion 7. The active material layer formed portion 6 is a portion where an active material layer 5 is formed. The active material layer unformed portion 7 is a portion where an active material layer 5 is not formed. In the active material layer unformed portion 7, the current collector 3 is exposed.

[0018] The portion 7 without the active material layer formed has a band-like shape extending in the longitudinal direction L of the electrode 1. The portion 7 without the active material layer formed is located at an end of the electrode 1 in the width direction W of the electrode 1.

[0019] The current collector 3 is preferably a metal foil such as copper, nickel, or stainless steel. The current collector 3 may be a metal foil on which a conductive layer mainly made of a carbon material is formed. The thickness of the current collector 3 is, for example, 5 to 50 μm.

[0020] The active material layer 5 can be produced, for example, by applying a slurry containing an active material, a binder, and the like onto the current collector 3 and drying it.

[0021] Examples of binders include rubber-based binders such as styrene-butadiene rubber (SBR) and NBR; fluorine-based resins such as polytetrafluoroethylene and polyvinylidene fluoride; polypropylene, polyethylene, and fluorine-modified (meth)acrylic binders as disclosed in JP-A-2009-246137.

[0022] The slurry may contain other components in addition to the active material and the binder. Examples of the other components include a conductive agent and a thickener. Examples of the conductive agent include carbon black, graphite, vapor-grown carbon fiber, and metal powder. Examples of the thickener include carboxymethylcellulose, its Na salt or ammonium salt, methylcellulose, hydroxymethylcellulose, ethylcellulose, hydroxypropylcellulose, polyvinyl alcohol, oxidized starch, phosphorylated starch, and casein.

[0023] The thickness of the active material layer 5 is not particularly limited. The thickness of the active material layer 5 is, for example, 5 to 500 μm, preferably 10 to 200 μm, and particularly preferably 10 to 100 μm. The active material contained in the active material layer 5 is not particularly limited as long as it is an electrode active material applicable to a battery or capacitor that utilizes the insertion and desorption of alkali metal ions. The active material may be either a negative electrode active material or a positive electrode active material.

[0024] The negative electrode active material is not particularly limited. Examples of the negative electrode active material include carbon materials such as composite carbon materials, metals or semimetals such as Si and Sn that can be alloyed with lithium, or materials containing oxides thereof. Examples of the composite carbon material include graphite, easily graphitized carbon, difficultly graphitized carbon, and composite carbon materials in which graphite particles are coated with pitch or resin carbide. Specific examples of the carbon material include the carbon materials described in JP-A-2013-258392. Specific examples of the material containing metals or semimetals that can be alloyed with lithium, or oxides thereof, include materials described in JP-A-2005-123175 and JP-A-2006-107795.

[0025] Examples of the positive electrode active material include transition metal oxides, sulfur-based active materials, activated carbon, etc. Examples of the transition metal oxides include cobalt oxide, nickel oxide, manganese oxide, vanadium oxide, etc. Examples of the sulfur-based active material include simple sulfur, metal sulfides, etc. Both the positive electrode active material and the negative electrode active material may be made of a single material or may be made of a mixture of two or more materials.

[0026] The active material contained in the active material layer 5 is pre-doped with an alkali metal using an electrode production system 11 described later. The alkali metal pre-doped into the active material is preferably lithium or sodium, and particularly preferably lithium. When the electrode 1 is used for producing an electrode for a lithium ion secondary battery, the density of the active material layer 5 is preferably 1.30 to 2.00 g / cc, and particularly preferably 1.40 to 1.90 g / cc.

[0027] 2. Configuration of electrode manufacturing system 11 The configuration of the electrode manufacturing system 11 will be described with reference to Fig. 3 to Fig. 7. As shown in Fig. 3, the electrode manufacturing system 11 includes an electrolyte treatment tank 15, dope tanks 17, 19, a cleaning tank 23, transport rollers 25, 27, 29, 31, 33, 35, 37, 39, 40, 47, 49, 51, 52, 59, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93 (hereinafter, these may be collectively referred to as a transport roller group), a supply roll 101, a take-up roll 103, a support stand 105, a circulation filtration unit 107, two power sources 109, 111, a tub cleaner 117, a recovery unit 119, an end sensor 121, counter electrode units 137, 139, 141, 143, a mask 144, and a guide mechanism 201. The group of transport rollers corresponds to a transport unit.

[0028] The electrolyte treatment tank 15 is a rectangular tank that is open at the top. The bottom surface of the electrolyte treatment tank 15 has a substantially U-shaped cross section. The electrolyte treatment tank 15 includes a partition plate 123. The partition plate 123 is supported by a support rod 125 that penetrates its upper end. The support rod 125 is fixed to a wall or the like (not shown). The partition plate 123 extends in the vertical direction, and divides the inside of the electrolyte treatment tank 15 into two spaces.

[0029] The transport roller 33 is attached to the lower end of the partition plate 123. The partition plate 123 and the transport roller 33 are supported by a support rod 127 that penetrates them. The vicinity of the lower end of the partition plate 123 is cut out so as not to come into contact with the transport roller 33. A space exists between the transport roller 33 and the bottom surface of the electrolyte treatment tank 15.

[0030] The doping tank 17 is a rectangular tank with an open top. The bottom surface of the doping tank 17 has a substantially U-shaped cross section. The doping tank 17 is provided with a partition plate 135.

[0031] The partition plate 135 is supported by a support rod 145 that passes through its upper end. The support rod 145 is fixed to a wall (not shown) or the like. The partition plate 135 extends in the vertical direction and divides the inside of the dope tank 17 into two spaces. The transport roller 40 is attached to the lower end of the partition plate 135. The partition plate 135 and the transport roller 40 are supported by a support rod 147 that passes through them. The partition plate 135 is cut out near its lower end so as not to come into contact with the transport roller 40. A space exists between the transport roller 40 and the bottom surface of the dope tank 17.

[0032] The four counter electrode units 137 , 139 , 141 , and 143 , the four masks 144 , and the four guide mechanisms 201 are housed in the doping tank 17 .

[0033] The counter electrode unit 137 is disposed on the upstream side of the doping tank 17. The counter electrode units 139 and 141 are disposed to sandwich the partition plate 135 from both sides. The counter electrode unit 143 is disposed on the downstream side of the doping tank 17.

[0034] A space 149 exists between the counter electrode unit 137 and the counter electrode unit 139. A space 151 exists between the counter electrode unit 141 and the counter electrode unit 143. The counter electrode units 137, 139, 141, and 143 are connected to one pole of the power source 109.

[0035] The counter electrode units 137, 139, 141, and 143 may be connected to separate power sources. In this case, the counter electrode units 137, 139, 141, and 143 can be controlled individually. In addition, it becomes easier to electrically adjust the counter electrode units 137, 139, 141, and 143 according to the degree of doping of the electrode 1 in the doping process. As a result, it becomes easier to manufacture a desired doped electrode 1A. The doped electrode 1A is an electrode 1 including an active material layer 5 doped with an alkali metal.

[0036] 4, the counter electrode unit 137 has a configuration in which a conductive base material 153 and an alkali metal-containing plate 155 are laminated together. The counter electrode unit 137 is disposed such that the alkali metal-containing plate 155 and the electrode 1 to be transported face each other.

[0037] Examples of the material of the conductive base material 153 include copper, stainless steel, and nickel. The form of the alkali metal-containing plate 155 is not particularly limited, and examples thereof include an alkali metal plate and an alkali metal alloy plate. The thickness of the alkali metal-containing plate 155 is, for example, 0.03 to 6 mm. The counter electrode units 139, 141, and 143 have the same configuration as the counter electrode unit 137. The counter electrode units 139, 141, and 143 are also arranged such that the alkali metal-containing plate 155 and the electrode 1 to be transported face each other.

[0038] As shown in FIG. 3, the mask 144 is attached to each of the counter electrode units 137, 139, 141, and 143. As shown in FIG. 4, the mask 144 is attached to the surface of the counter electrode units 137, 139, 141, and 143 on the side of the alkali metal-containing plate 155. The mask 144 does not cover the portion of the counter electrode units 137, 139, 141, and 143 facing the active material layer forming portion 6, but covers the other portions. The mask 144 facilitates fine adjustment of the doping width. The doping width is the width of the portion of the electrode 1 where pre-doping is performed. The mask 144 can suppress pre-doping to portions other than the active material layer forming portion 6.

[0039] Examples of the material of the mask 144 include polyethylene, polypropylene, polyphenylene sulfide, nylon, polyether ether ketone, and polytetrafluoroethylene. Polypropylene is preferable as the material of the mask 144. The thickness of the mask 144 is preferably, for example, 10 μm or more and 10 mm or less, and more preferably 50 μm or more and 5 mm or less.

[0040] As shown in FIG. 1, guide mechanisms 201 are respectively installed between the electrode 1 and the counter electrode unit 137, between the electrode 1 and the counter electrode unit 139, between the electrode 1 and the counter electrode unit 141, and between the electrode 1 and the counter electrode unit 143.

[0041] In the following, the guide mechanism 201 installed between the electrode 1 and the counter electrode unit 137 is referred to as the guide mechanism 201 on the counter electrode unit 137 side. Moreover, the guide mechanism 201 installed between the electrode 1 and the counter electrode unit 139 is referred to as the guide mechanism 201 on the counter electrode unit 139 side. Moreover, the guide mechanism 201 installed between the electrode 1 and the counter electrode unit 141 is referred to as the guide mechanism 201 on the counter electrode unit 141 side. Moreover, the guide mechanism 201 installed between the electrode 1 and the counter electrode unit 143 is referred to as the guide mechanism 201 on the counter electrode unit 143 side.

[0042] The guide mechanism 201 includes a plurality of guide bars 203, as shown in, for example, Figs. 3 to 5. The guide bars 203 may have various shapes. 203 is preferably a cylindrical member. When the guide bar 203 is a cylindrical member, even when the guide bar 203 comes into contact with the electrode 1, damage to the electrode 1 can be suppressed. The guide bars 203 are arranged along the conveying direction of the electrode 1. The distance between the arranged guide bars 203 (hereinafter referred to as the pitch distance) is preferably set within a range of, for example, 0.05 m to 1.1 m, more preferably within a range of 0.1 m to 1.0 m, and particularly preferably within a range of 0.1 m to 0.6 m. The axial direction of the guide bar 203 is parallel to the width direction W of the electrode 1. The guide bars 203 are not in contact with, for example, the alkali metal-containing plate 155. The guide bar 203 does not rotate, unlike, for example, a guide roll 209 described later. Of the guide bars 203, a surface portion 207 described later may rotate.

[0043] When electrode 1 is moved toward alkali metal-containing plate 155, electrode 1 comes into contact with guide bar 203. Electrode 1 that has come into contact with guide bar 203 cannot move further in the direction of alkali metal-containing plate 155.

[0044] The guide bar 203 includes a main body portion 205 and a surface portion 207, as shown in FIG. 6, for example. The main body portion 205 is a cylindrical member. The surface portion 207 is a layer formed on the surface of the main body portion 205. The surface portion 207 covers the main body portion 205. The surface portion 207 is formed, for example, by applying a coating material to the surface of the main body portion 205. The surface portion 207 is, for example, pressure-bonded to the surface of the main body portion 205. For example, the tubular surface portion 207 covers the main body portion 205. The main body portion 205 is made of a material including one or more selected from the group consisting of a thermoplastic resin, a thermosetting resin, a photocurable resin, a metal, and a metal oxide. The surface portion 207 includes, for example, an organic matter. Examples of organic materials include Teflon (registered trademark), polyethylene, polypropylene, polyphenylene sulfide, perfluoroalkoxy fluororesin (PFA), polyvinylidene fluoride, polyether ether ketone, polyimide, phenol resin, melamine resin, urea resin, polyester resin, epoxy resin, ethylene propylene rubber, butyl rubber, acrylonitrile rubber, fluororubber, chlorosulfonated polyethylene rubber, etc. When the surface portion 207 is made of the above-mentioned organic material, damage to the electrode 1 can be further suppressed.

[0045] Any guide bar 203 included in the guide mechanism 201 on the counter electrode unit 137 side is defined as the first guide bar. Of the guide bars 203 included in the guide mechanism 201 on the counter electrode unit 139 side, the guide bar 203 closest to the first guide bar is defined as the second guide bar. In the transport direction of the electrode 1, the position of the first guide bar and the position of the second guide bar are shifted. The amount of shift between the position of the first guide bar and the position of the second guide bar is defined as the shift amount A. The shift amount A is preferably set to a value within a range of 15 mm to 100 mm, and more preferably set to a value within a range of 30 mm to 50 mm. The shift amount A is, for example, 30 mm.

[0046] Any guide bar 203 included in the guide mechanism 201 on the counter electrode unit 141 side is defined as the third guide bar. Of the guide bars 203 included in the guide mechanism 201 on the counter electrode unit 143 side, the guide bar 203 closest to the third guide bar is defined as the fourth guide bar. In the transport direction of the electrode 1, the position of the third guide bar and the position of the fourth guide bar are shifted. The amount of shift between the position of the third guide bar and the position of the fourth guide bar is defined as the shift amount B. The shift amount B is preferably set to a value within a range of 15 mm or more and 100 mm or less, and more preferably set to a value within a range of 30 mm or more and 50 mm or less. The shift amount B is, for example, 30 mm.

[0047] The electrode 1 passes between the guide mechanism 201 on the counter electrode unit 137 side and the guide mechanism 201 on the counter electrode unit 139 side. The guide mechanism 201 on the counter electrode unit 137 side prevents the distance between the electrode 1 and the counter electrode unit 137 from becoming excessively small. The guide mechanism 201 on the counter electrode unit 139 side prevents the distance between the electrode 1 and the counter electrode unit 139 from becoming excessively small.

[0048] The electrode 1 passes between the guide mechanism 201 on the counter electrode unit 141 side and the guide mechanism 201 on the counter electrode unit 143 side. The guide mechanism 201 on the counter electrode unit 141 side prevents the distance between the electrode 1 and the counter electrode unit 141 from becoming excessively small. The guide mechanism 201 on the counter electrode unit 143 side prevents the distance between the electrode 1 and the counter electrode unit 143 from becoming excessively small.

[0049] Therefore, the four guide mechanisms 201 housed in the doping tank 17 keep the distance between the electrode 1 and the counter electrode units 137, 139, 141, and 143 within a certain range. The certain range is, for example, preferably 3 mm or more and 20 mm or less, more preferably 5 mm or more and 16 mm or less, and particularly preferably 5 mm or more and 8 mm or less. The distance between the electrode 1 and the counter electrode units 137, 139, 141, and 143 is the distance between the surface of the alkali metal-containing plate 155 and the electrode 1 in the thickness direction of the electrode 1.

[0050] The guide mechanism 201 may include a plurality of guide rolls 209 as shown in FIG. 7, for example. The guide roll 209 faces the electrode 1 being transported. The guide roll 209 is a cylindrical member. The plurality of guide rolls 209 are lined up along the transport direction of the electrode 1. The distance between the lined up guide rolls 209 is also referred to as the pitch distance below. The pitch distance of the guide rolls 209 is an interval set within a range of, for example, 0.1 m or more and 1.0 m or less. The axial direction of the guide roll 209 is parallel to the width direction W of the electrode 1. The guide roll 209 is attached to a base 211 so as to be rotatable about its central axis.

[0051] The guide roll 209 includes a main body 205 and a surface portion 207, as shown in FIG. 6, for example. The main body 205 is a cylindrical member. The surface portion 207 is a layer formed on the surface of the main body 205. The surface portion 207 covers the main body 205. The surface portion 207 is formed, for example, by applying a coating material to the surface of the main body 205. The surface portion 207 is, for example, pressure-bonded to the surface of the main body 205. For example, the tubular surface portion 207 covers the main body 205. The main body 205 is made of a material including one or more selected from the group consisting of a thermoplastic resin, a thermosetting resin, a photocurable resin, a metal, and a metal oxide. The surface portion 207 includes, for example, an organic substance. Examples of organic materials include Teflon, polyethylene, polypropylene, polyphenylene sulfide, PFA, polyvinylidene fluoride, polyether ether ketone, polyimide, phenol resin, melamine resin, urea resin, polyester resin, epoxy resin, ethylene propylene rubber, butyl rubber, acrylonitrile rubber, fluororubber, chlorosulfonated polyethylene rubber, etc. When the surface portion 207 is made of the above-mentioned organic material, damage to the electrode 1 can be further suppressed.

[0052] In the guide mechanism 201 including the guide roll 209, the deviation amounts A and B can be set to, for example, 30 mm, similarly to the guide mechanism 201 including the guide bar 203. In the case of the guide mechanism 201 including the guide roll 209, the deviation amounts A and B are deviation amounts of the position of the guide roll 209.

[0053] The doping tank 19 basically has the same configuration as the doping tank 17. In the doping tank 19, the counter electrode units 137, 139, 141, 143, the mask 144, and the guide mechanism 201 are arranged in the same manner as in the doping tank 17.

[0054] However, inside the dope tank 19, there is a transport roller 52 instead of the transport roller 40. Also, the counter electrode units 137, 139, 141, and 143 housed in the dope tank 19 are connected to one pole of the power source 111.

[0055] The cleaning tank 23 basically has the same configuration as the electrolytic solution treatment tank 15. However, inside the cleaning tank 23, a transport roller 75 is present instead of the transport roller 33.

[0056] The dope solution carried out from the dope tank 19 adheres to the electrode 1 that has passed through the dope tank 19. In the cleaning tank 23, the dope solution adhering to the electrode 1 is efficiently removed. This makes it easier to handle the electrode 1 in the next process.

[0057] The cleaning tank 23 contains, for example, the following cleaning liquid. The cleaning liquid is preferably an organic solvent, and preferably contains an aprotic solvent having a boiling point of 150° C. or less at 1 atmospheric pressure. Examples of the aprotic solvent having a boiling point of 150° C. or less at 1 atmospheric pressure include at least one solvent selected from carbonate-based solvents, ester-based solvents, ether-based solvents, hydrocarbon-based solvents, ketone-based solvents, and nitrile-based solvents.

[0058] Among these, carbonate-based solvents are preferred. As the carbonate-based solvent, at least one selected from dimethyl carbonate, diethyl carbonate, methyl propyl carbonate, and ethyl methyl carbonate is particularly preferred. By using such a cleaning solution, it becomes easy to remove the cleaning solution from the electrode 1 after cleaning.

[0059] In addition, since the dope solution carried out from the dope tank 19 accumulates in the cleaning tank 23, it is preferable to maintain the cleaning solution at a constant quality by adding or replacing the cleaning solution. The quality of the cleaning solution can be grasped by installing sensors such as an insulation resistance meter or a conductivity meter in the cleaning tank 23 and periodically checking the values ​​measured by these sensors.

[0060] Among the group of conveying rollers, the conveying rollers 37, 39, 49, and 51 are made of a conductive material. The conveying rollers 37, 39, 49, and 51 are conductive power supply rollers. Examples of the conductive material include stainless steel, gold, copper, and rhodium. Copper is particularly preferable as the conductive material. The conductive material may be a mixture of two or more materials. The presence of the conductive material, particularly on the surface of the power supply roller, makes it easier to suppress the reaction between the doped electrode 1A and the power supply roller. As a result, it is possible to mass-produce high-quality doped electrodes 1A.

[0061] Among the group of conveying rollers, the conveying rollers that are not conductive power supply rollers are made of elastomer, except for the bearing parts. The group of conveying rollers conveys the electrode 1 along a certain path. The path is a path from the supply roll 101 through the electrolyte treatment tank 15, the dope tank 17, the dope tank 19, the cleaning tank 23, and the tub cleaner 117, and then to the take-up roll 103.

[0062] The portion of the path along which the electrode 1 is transported by the transport roller group that passes through the electrolyte treatment tank 15 is a path in which the electrode 1 first moves downward via transport rollers 29 and 31, and then the direction of movement is changed to upward by transport roller 33.

[0063] The portion of the path along which the electrode 1 is transported by the transport roller group that passes through the dope tank 17 is as follows. First, the transport roller 37 changes the direction of movement downward, so that the electrode 1 moves downward through the space 149 of the dope tank 17. Next, the transport roller 40 changes the direction of movement upward, so that the electrode 1 moves upward through the space 151 of the dope tank 17. Finally, the transport roller 47 changes the direction of movement horizontally, so that the electrode 1 moves toward the dope tank 19.

[0064] The portion of the path along which the transport roller group transports the electrode 1 that passes through the dope tank 19 is as follows. First, the transport roller 49 changes the direction of movement downward, causing the electrode 1 to move downward through the space 149 of the dope tank 19. Next, the transport roller 52 changes the direction of movement upward, causing the electrode 1 to move upward through the space 151 of the dope tank 19. Finally, the transport roller 59 changes the direction of movement horizontally, causing the electrode 1 to move toward the cleaning tank 23.

[0065] In addition, in the portion of the path along which the group of transport rollers transports electrode 1 that passes through cleaning tank 23, first, the direction of movement is changed downward by transport roller 73, causing electrode 1 to move downward, and then, the direction of movement is changed upward by transport roller 75.

[0066] The electrode 1 is wound around the supply roll 101. That is, the supply roll 101 holds the electrode 1 in a wound state. The active material in the electrode 1 held by the supply roll 101 has not yet been doped with an alkali metal.

[0067] The group of transport rollers pulls out and transports the electrode 1 held by the supply roll 101. The winding roll 103 winds up and stores the electrode 1 transported by the group of transport rollers. When the electrode 1 is transported along a path passing through the doping tanks 17 and 19, the active material layer 5 is doped with an alkali metal. The method of doping the alkali metal is a method of electrically doping the active material with the alkali metal using counter electrode units 137, 139, 141, and 143 provided opposite the electrode 1 in the doping tanks 17 and 19. By doping the active material layer 5 with the alkali metal, the electrode 1 becomes a doped electrode 1A including an active material layer 5 doped with the alkali metal. The electrode 1 stored on the winding roll 103 is a doped electrode 1A.

[0068] The support stand 105 supports the electrolytic solution treatment tank 15, the dope tanks 17 and 19, and the cleaning tank 23 from below. The height of the support stand 105 can be changed. The circulation filtration units 107 are provided in the dope tanks 17 and 19, respectively. The circulation filtration units 107 include a filter 161, a pump 163, and a pipe 165.

[0069] In the circulation filtration unit 107 provided in the dope tank 17, a pipe 165 is a circulation pipe that goes out from the dope tank 17, passes through a pump 163 and a filter 161, and returns to the dope tank 17. The dope solution in the dope tank 17 circulates through the pipe 165 and the filter 161 by the driving force of the pump 163, and returns to the dope tank 17 again.

[0070] At this time, foreign matter in the dope solution is filtered by the filter 161. Examples of the foreign matter include foreign matter precipitated from the dope solution and foreign matter generated from the electrode 1. The material of the filter 161 is, for example, a resin such as polypropylene or polytetrafluoroethylene. The pore size of the filter 161 can be appropriately set. The pore size of the filter 161 is, for example, 0.2 μm or more and 50 μm or less.

[0071] The circulation filtration unit 107 provided in the dope tank 19 has a similar configuration and provides the same effects as those of the dope tank 19. For convenience, the dope solution is not shown in FIG.

[0072] One terminal of the power source 109 is connected to the transport rollers 37 and 39. The other terminal of the power source 109 is connected to the counter electrode units 137, 139, 141, and 143 provided in the dope tank 17. The electrode 1 contacts the transport rollers 37 and 39. The electrode 1 and the counter electrode units 137, 139, 141, and 143 are in a dope solution, which is an electrolyte. Therefore, in the dope tank 17, the electrode 1 and the counter electrode units 137, 139, 141, and 143 are electrically connected via the electrolyte. The path of the electrical connection between the electrode 1 and the counter electrode units 137, 139, 141, and 143 corresponds to the connection unit.

[0073] One terminal of the power source 111 is connected to the transport rollers 49 and 51. The other terminal of the power source 111 is connected to the counter electrode units 137, 139, 141, and 143 provided in the dope tank 19. The electrode 1 contacts the transport rollers 49 and 51. The electrode 1 and the counter electrode units 137, 139, 141, and 143 are in a dope solution, which is an electrolyte. Therefore, in the dope tank 19, the electrode 1 and the counter electrode units 137, 139, 141, and 143 are electrically connected via the electrolyte. The path of the electrical connection between the electrode 1 and the counter electrode units 137, 139, 141, and 143 corresponds to the connection unit.

[0074] The tub cleaner 117 cleans the portion 7 of the doped electrode 1A where the active material layer is not formed. If residual organic components derived from the doping solution or the like remain in the portion 7 of the doped electrode 1A where the active material layer is not formed, welding defects are likely to occur when the portion 7 of the doped electrode 1A where the active material layer is not formed is welded.

[0075] The recovery units 119 are disposed in each of the electrolyte treatment tank 15, the dope tanks 17 and 19, and the cleaning tank 23. The recovery units 119 recover the liquid that the electrode 1 takes out of the tanks and return it to the tank.

[0076] The end sensor 121 detects the position of the end of the electrode 1 in the width direction W. An end position adjustment unit (not shown) adjusts the positions of the supply roll 101 and the take-up roll 103 in the width direction W based on the detection result of the end sensor 121.

[0077] 3. Composition of the dope solution When the electrode manufacturing system 11 is used, a dope solution is contained in the electrolyte treatment tank 15 and the dope tanks 17 and 19. The dope solution contains alkali metal ions and a solvent. The dope solution is an electrolyte.

[0078] Examples of the solvent include organic solvents. Examples of the organic solvent include aprotic organic solvents. Examples of the aprotic organic solvent include dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, vinylene carbonate, vinyl ethylene carbonate, ethylene carbonate, fluoroethylene carbonate, propylene carbonate, butylene carbonate, dipropyl carbonate, γ-butyrolactone, sulfolane, diethylene glycol dimethyl ether (diglyme), diethylene glycol methyl ethyl ether, triethylene glycol dimethyl ether (triglyme), triethylene glycol butyl methyl ether, and tetraethylene glycol dimethyl ether (tetraglyme).

[0079] When the solvent is the above-mentioned aprotic organic solvent, it is possible to efficiently dope the electrode 1. In addition, by using the doped electrode 1A that has been doped with the above-mentioned aprotic organic solvent, a secondary battery with high battery stability can be obtained.

[0080] As the aprotic organic solvent, an organic solvent belonging to a specific group is preferable. As the organic solvent belonging to the specific group, for example, dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, vinylene carbonate, vinyl ethylene carbonate, ethylene carbonate, fluoroethylene carbonate, and propylene carbonate are preferable.

[0081] When the solvent is an organic solvent belonging to a specific group, it is possible to particularly efficiently dope the electrode 1. Furthermore, by using a doped electrode 1A that has been doped with an organic solvent belonging to a specific group, a secondary battery with particularly high battery stability can be obtained.

[0082] In addition, as the aprotic organic solvent, for example, an ionic liquid such as a quaternary imidazolium salt, a quaternary pyridinium salt, a quaternary pyrrolidinium salt, a quaternary piperidinium salt, etc. The aprotic organic solvent may be composed of a single component, or may be a mixed solvent of two or more components.

[0083] The alkali metal ions contained in the dope solution are ions constituting an alkali metal salt. The alkali metal salt is preferably a lithium salt or a sodium salt. The anion moiety constituting the alkali metal salt is, for example, PF6 - , PF3(C2F5)3 - , PF3(CF3)3 - Phosphorus anion with fluoro group such as BF4 - , BF2(CF)2 - , BF3(CF3) - , B(CN)4 - Boron anions with fluoro or cyano groups such as N(FSO2)2 - , N(CF3SO2)2 - , N(C2F5SO2)2 - Sulfonylimide anions with fluoro groups such as CF3SO3 - and the like.

[0084] The concentration of the alkali metal salt in the doping solution is preferably 0.1 mol / L or more, and more preferably in the range of 0.5 to 1.5 mol / L. When the concentration of the alkali metal salt is within this range, pre-doping of the alkali metal proceeds efficiently.

[0085] The dope solution may further contain additives such as vinylene carbonate, vinyl ethylene carbonate, 1-fluoroethylene carbonate, 1-(trifluoromethyl)ethylene carbonate, succinic anhydride, maleic anhydride, propane sultone, and diethyl sulfone.

[0086] The doping solution may further contain a flame retardant such as a phosphazene compound. The amount of the flame retardant added is preferably 1 part by mass or more, more preferably 3 parts by mass or more, and even more preferably 5 parts by mass or more, per 100 parts by mass of the doping solution, from the viewpoint of effectively controlling the thermal runaway reaction when doping with an alkali metal. Also, the amount of the flame retardant added is preferably 20 parts by mass or less, more preferably 15 parts by mass or less, and even more preferably 10 parts by mass or less, per 100 parts by mass of the doping solution, from the viewpoint of obtaining a high-quality doped electrode 1A.

[0087] 4. Method for manufacturing doped electrode 1A using electrode manufacturing system 11 The manufacturing method of the doped electrode 1A is as follows. The electrode 1 before pre-doping is wound around the supply roll 101. Next, the electrode 1 before pre-doping is pulled out from the supply roll 101 and sent to the take-up roll 103 along the above-mentioned path. Next, the electrolyte treatment tank 15, the doping tanks 17 and 19, and the cleaning tank 23 are raised and set in the fixed positions shown in FIG.

[0088] Next, the dope solution is placed in the electrolytic solution processing tank 15 and the dope tanks 17 and 19. The dope solution is the one described above in "3. Composition of the dope solution." The cleaning tank 23 is placed with a cleaning solution.

[0089] Next, the electrode 1 is transported along the above-mentioned path from the supply roll 101 to the take-up roll 103 by a group of transport rollers. The path along which the electrode 1 is transported includes a path passing through the doping tanks 17 and 19. When the electrode 1 passes through the doping tanks 17 and 19, the active material contained in the active material layer 5 is pre-doped with an alkali metal.

[0090] The electrode 1 wound around the supply roll 101 is taken as a wound body. As the electrode 1 continues to be transported, the wound body gradually becomes smaller. In order to continuously manufacture the doped electrode 1A, it is necessary to replace the wound body midway. When replacing the wound body, it is desirable to join an end portion in the longitudinal direction L of the electrode 1 contained in the wound body before replacement to an end portion in the longitudinal direction L of the electrode 1 contained in the wound body after replacement (hereinafter, this will be referred to as joining the ends together). When the ends are joined together, the time loss caused by the replacement of the wound body can be reduced, and the productivity of the doped electrode 1A can be increased.

[0091] As a method for joining the ends, for example, as shown in Fig. 9, there is a method in which an end 401 in the longitudinal direction L of the electrode 1 included in the wound body before replacement and an end 403 in the longitudinal direction L of the electrode 1 included in the wound body after replacement are joined by a connecting member 405. The connecting member 405 is, for example, a tape, a fusion film, or the like. The connecting member 405 straddles the end portions 401, 403. The connecting member 405 is joined to the end portions 401, 403.

[0092] As a method for joining the ends, for example, there is a method shown in FIG. 10. A hole 407 is formed in each of the ends 401 and 403. The hole 407 penetrates the electrode 1. The connecting member 405 spans the ends 401 and 403. For example, one connecting member 405 is folded in half and sandwiches the ends 401 and 403 from both sides. Also, two connecting members 405 may sandwich the ends 401 and 403 from both sides. The connecting member 405 covers the hole 407 on both sides of the ends 401 and 403. The connecting member 405 is a heat-sealing film. The connecting member 405 is fused to the ends 401 and 403 on both sides of the ends 401 and 403. Also, the connecting member 405 on one side of the electrode 1 and the connecting member 405 on the opposite side of the electrode 1 are in contact with each other through the hole 407 and fused to each other.

[0093] In the method shown in FIG. 10, even when the connecting member 405 is immersed in a dope solution or when high tension is applied to the connecting member 405, the ends 401 and 403 are unlikely to separate.

[0094] In the doping tanks 17 and 19, the distance between the electrode 1 and the counter electrode units 137, 139, 141, and 143 is kept within a certain range by a guide mechanism 201 installed between the electrode 1 and the counter electrode units 137, 139, 141, and 143. The certain range is, for example, 5 mm to 16 mm.

[0095] Furthermore, the group of transport rollers transports the electrode 1 to the cleaning tank 23. The electrode 1 is cleaned in the cleaning tank 23 while being transported by the group of transport rollers.

[0096] Furthermore, the group of transport rollers continuously transports the electrode 1 to a tub cleaner 117. The portion of the electrode 1 transported to the tub cleaner 117 has already been subjected to pre-doping processing and has become a doped electrode 1A. The tub cleaner 117 cleans a portion 7 of the doped electrode 1A where an active material layer is not formed.

[0097] The doped electrode 1A may be a positive electrode or a negative electrode. When manufacturing a positive electrode, the electrode manufacturing system 11 dopes a positive electrode active material with an alkali metal. When manufacturing a negative electrode, the electrode manufacturing system 11 dopes a negative electrode active material with an alkali metal.

[0098] When lithium is absorbed in the negative electrode active material of a lithium ion capacitor, the doping amount of the alkali metal is preferably 70 to 95% of the theoretical capacity of the negative electrode active material.When lithium is absorbed in the negative electrode active material of a lithium ion secondary battery, the doping amount of the alkali metal is preferably 10 to 30% of the theoretical capacity of the negative electrode active material.

[0099] 5. Manufacturing method of secondary battery An example of the secondary battery is a lithium ion secondary battery. The secondary battery includes an electrode cell. The electrode cell has a configuration in which a negative electrode and a positive electrode are stacked. In the secondary battery, for example, the negative electrode is manufactured by the above-mentioned "4. Manufacturing method of doped electrode 1A using electrode manufacturing system 11". Next, the negative electrode and the positive electrode are stacked to form an electrode cell.

[0100] 6. Effects of the electrode manufacturing system 11 and the method for manufacturing the doped electrode 1A (6-1) The guide mechanism 201 keeps the distance between the electrode 1 and the counter electrode units 137, 139, 141, and 143 within a certain range in the doping tanks 17 and 19. This makes it possible to suppress uneven doping and deposition of alkali metals.

[0101] (6-2) The certain range is from 5 mm to 16 mm, which can further suppress uneven doping and precipitation of alkali metals.

[0102] (6-3) The guide mechanism 201 includes a guide bar 203 or a guide roll 209. This can further suppress uneven doping and precipitation of alkali metals.

[0103] 6, the electrode 1 comes into contact with the surface portion 207 containing an organic substance. Therefore, damage to the electrode 1 by the guide bar 203 or the guide roll 209 can be suppressed.

[0104] (6-5) In the doping tanks 17 and 19, the pitch distance is 0.1 m or more and 1.0 m or less. Therefore, uneven doping and deposition of alkali metals can be further suppressed.

[0105] 7. Working Example Example 1 (i) Fabrication of Electrode 1 A long strip-shaped current collector 3 was prepared. The current collector 3 was a negative electrode current collector. The size of the current collector 3 was 130 mm wide, 100 mm long, and 8 μm thick. The surface roughness Ra of the current collector 3 was 0.1 μm. The current collector 3 was made of copper foil. An active material layer 5 was formed on each of both sides of the current collector 3. The active material layer 5 was a negative electrode active material layer.

[0106] The coating amount of the active material layer 5 is 100 g / m 2As shown in FIG. 1, the active material layer 5 was formed along the longitudinal direction of the current collector 3. The active material layer 5 was formed over a width of 120 mm from one end of the current collector 3 in the width direction W. The width of the portion 7 where the active material layer was not formed at the other end of the current collector 3 in the width direction W was 10 mm. The portion 7 where the active material layer was not formed is a portion where the active material layer 5 was not formed. Thereafter, the electrode 1 was obtained by drying and pressing.

[0107] The active material layer 5 contained a negative electrode active material, carboxymethyl cellulose, acetylene black, a binder, and a dispersant in a mass ratio of 88:3:5:3:1. The negative electrode active material was a mixture of a Si-based active material and a graphite-based active material. The negative electrode active material contained a Si-based active material and a graphite-based active material in a mass ratio of 2:8. The acetylene black corresponds to a conductive agent.

[0108] (ii) Fabrication of counter electrode units 137, 139, 141, and 143 A polypropylene (PP) resin film was attached onto the copper plate. The copper plate had a length of 1000 mm, a width of 220 mm, and a thickness of 3 mm. The resin film had a length of 800 mm, a width of 120 mm, and a thickness of 470 μm. The resin film had a mesh shape with multiple openings. The opening ratio of the resin film was 50%.

[0109] Furthermore, a lithium (Li) foil was attached onto the resin film. The length and width of the Li foil were the same as the length and width of the resin film. The thickness of the Li foil was 2 mm. The resin film and the Li foil were pressed onto a copper plate using a roll press device to obtain counter electrode units 137, 139, 141, and 143. The linear pressure during pressing was 5 kgf / cm. The copper plate corresponds to the conductive substrate 153. The Li foil corresponds to the alkali metal-containing plate 155.

[0110] (iii) Fabrication of doped electrode 1A 3 was prepared, and the electrode 1 was passed through the electrode manufacturing system 11. Furthermore, counter electrode units 137, 139, 141, and 143, a mask 144, and a guide mechanism 201 were installed in the doping tanks 17 and 19, respectively.

[0111] The material of the guide bar 203 was SUS. The shape of the guide bar 203 was a cylinder with a diameter of 2 mm. The position of the guide bar 203 was such that the distance between the alkali metal-containing plate 155 and the electrode 1 was maintained at 5 mm. The pitch distance was 500 mm. The values ​​of the deviation amounts A and B were each 30 mm. The conditions of the guide mechanism 201 are shown in Table 1. In Table 1, "distance between the electrode and the counter electrode unit" means the distance between the alkali metal-containing plate 155 and the electrode 1 in the thickness direction of the electrode 1.

[0112] [Table 1] Next, a dope solution was supplied into the dope tanks 17 and 19. The dope solution was a solution containing 1.2 M LiPF6. The solvent of the dope solution was a mixed solution containing EC (ethylene carbonate) and DMC (dimethyl carbonate) in a volume ratio of 3:7.

[0113] Next, the electrode 1 and the counter electrode units 137, 139, 141, and 143 fed through the electrode manufacturing system 11 were connected to a DC power supply equipped with a current and voltage monitor. While the electrode 1 was transported at a speed of 2.1 m / min, a current of 269 A was applied to the entire electrode manufacturing system 11 to perform pre-doping. At this time, the pre-doping current density per unit area of ​​the electrode 1 was 35 mA / cm. 2 In addition, at this time, the center in the width direction W of active material layer 5 included in electrode 1 and the center in the width direction W of the Li foil included in counter electrode units 137, 139, 141, and 143 coincided.

[0114] (iv) Evaluation of voltage in stable voltage state In the manufacture of the doped electrode 1A, after the start of pre-doping, the voltage change was soon within ±0.05V (hereinafter referred to as a stable voltage state). Once the stable voltage state was reached, no continued increase in voltage was observed even with continued pre-doping. A lower voltage in the stable voltage state is preferable. The voltage in the stable voltage state was evaluated according to the following criteria. The evaluation results are shown in Table 1. In Example 1, the voltage in the stable voltage state was 3.6V.

[0115] A: The voltage in the stable voltage state is less than 3.5V.

[0116] B: The voltage in the stable voltage state is 3.5V or more and less than 5.0V.

[0117] C: The voltage in the stable voltage state is 5.0 V or more.

[0118] (v) Evaluation of Li precipitation The doped electrode 1A thus obtained was evaluated for Li precipitation by the following method. It was visually confirmed whether or not white precipitates were observed on the doped electrode 1A. If precipitates were observed, a small amount of the precipitate was taken out and immersed in ethanol. It was confirmed whether or not a reaction between the precipitate and ethanol was observed. If a reaction between the precipitate and ethanol was observed, it was determined that Li precipitation had occurred. If precipitates were observed, they were classified into "micro precipitates" and "precipitation" according to the following criteria. "Micro precipitates" refers to a case where the area of ​​the part where Li precipitation was observed is less than 10% of the area of ​​the part where pre-doping was performed. "Presence of precipitation" refers to a case where the area of ​​the part where Li precipitation was observed is 10% or more of the area of ​​the part where pre-doping was performed. The evaluation results are shown in Table 1.

[0119] (vi) Evaluation of charge / discharge efficiency distribution The charge / discharge efficiency distribution of the doped electrode 1A was evaluated by the following method. In a dry room with a dew point of -60°C, a part of the doped electrode 1A was punched out using a Thomson blade manufactured by Takahashi Katasei Co., Ltd. The punched out part was used as the negative electrode. The shape of the negative electrode was a rectangle with a length of 2.6 cm and a width of 4.0 cm. The negative electrode had a terminal weld protruding from one side of the rectangle to the outer periphery.

[0120] Next, a first evaluation half-cell was fabricated using the negative electrode by the following method.

[0121] A separator, a counter electrode, and a separator were laminated in this order on one side of the negative electrode. A separator, a counter electrode, and a separator were laminated in this order on the opposite side of the negative electrode. As a result, a laminate was obtained. The separator was made of a 35 μm thick polyethylene nonwoven fabric. The counter electrode was made of copper lath foil with metallic lithium attached. The basic shape of the copper lath foil was a rectangle with a length of 2.6 cm and a width of 3.9 cm. The copper lath foil had a terminal weld protruding from one side of the rectangle toward the outer periphery.

[0122] Next, the four sides of the laminate were taped. Next, the negative electrode terminal weld and the counter electrode terminal weld were ultrasonically welded to a copper terminal. The terminal size was 5 mm wide, 50 mm long, and 0.2 mm thick.

[0123] Next, the laminate was sandwiched between two laminate films. The shape of the laminate film was rectangular. The size of the laminate film was 6.5 cm long and 8.0 cm wide. Three of the four sides of the two laminate films were fused together. As a result, the two laminate films became a bag with only one side open. The laminate was contained in the bag.

[0124] Next, the laminate in the bag was vacuum-impregnated with an electrolyte. The electrolyte was a solution containing 1.2 M LiPF6. The solvent for the electrolyte was a mixture of EC (ethylene carbonate) and DMC (dimethyl carbonate) in a volume ratio of 3:7.

[0125] Next, one of the four sides of the bag that had not yet been fused was fused. The first evaluation half-cell was completed through the above steps. The second and third evaluation half-cells were also produced using a method similar to that used to produce the first evaluation half-cell.

[0126] The negative electrodes used in the first to third evaluation half-cells are punched out from different positions of one doped electrode 1A. As shown in FIG. 8, the negative electrode 301 used in the first evaluation half-cell is punched out from a position of the active material layer-formed portion 6 on the side of the active material layer-unformed portion 7 in the width direction W. The negative electrode 303 used in the second evaluation half-cell is punched out from a position of the active material layer-formed portion 6 in the center in the width direction W. The negative electrode 305 used in the third evaluation half-cell is punched out from a position of the active material layer-formed portion 6 on the opposite side to the active material layer-unformed portion 7 in the width direction W.

[0127] The first to third evaluation half-cells correspond to secondary batteries, and the manufacturing method of the first to third evaluation half-cells corresponds to the manufacturing method of the secondary batteries.

[0128] The first to third evaluation half-cells were placed in a thermostatic chamber at 25° C. Next, the initial charge-discharge efficiency E, represented by the following formula (1), was calculated for each of the first to third evaluation half-cells. The unit of the initial charge-discharge efficiency E is %. (Formula 1) E=(C1 / C2)×100 C1 is the initial discharge capacity. C2 is the initial charge capacity. The units of C1 and C2 are mAh / cm 2 The initial discharge capacity C1 is the capacity when the cell is charged at a constant current of 10 mA until the cell voltage becomes 0.01 V, and then the charging is continued until the current value drops to 1 mA while applying a constant voltage of 0.01 V. The initial charge capacity C2 is the capacity when the cell is discharged at a constant current of 10 mA until the cell voltage becomes 2.0 V after measuring the initial discharge capacity C1.

[0129] The initial charge-discharge efficiencies E of the first to third evaluation half-cells were designated E1 to E3, respectively. The maximum value of E1 to E3 was designated Emax. The minimum value of E1 to E3 was designated Emin. The value obtained by subtracting Emin from Emax was designated ΔE. In Example 1, E1 was 99%, E2 was 100%, and E3 was 99%.

[0130] The charge / discharge efficiency distribution was evaluated based on the ΔE value according to the following criteria. The evaluation results are shown in Table 1.

[0131] A: ΔE is less than 5%.

[0132] B: ΔE is 5% or more and less than 15%.

[0133] C: ΔE is 15% or more.

[0134] Here, ΔE is an index representing doping unevenness. The smaller ΔE is, the smaller the doping unevenness is. Example 2 A doped electrode 1A was produced and evaluated basically in the same manner as in Example 1. However, the guide bar 203 had a main body portion 205 made of SUS and a surface portion 207 made of PFA. The evaluation results are shown in Table 1.

[0135] In Example 2, the evaluation result of the voltage in a stable voltage state was A. There was no Li deposition. The evaluation result of the charge / discharge efficiency distribution was A. Example 3 Basically, a doped electrode 1A was manufactured and evaluated in the same manner as in Example 2. However, the guide mechanism 201 was equipped with a guide roll 209 as shown in FIG. 7 instead of a guide bar 203. The guide roll 209 had a main body portion 205 made of SUS and a surface portion 207 made of PFA. The evaluation results are shown in Table 1.

[0136] In Example 3, the evaluation result of the voltage in a stable voltage state was A. There was no Li deposition. The evaluation result of the charge / discharge efficiency distribution was A. Example 4 A doped electrode 1A was produced and evaluated basically in the same manner as in Example 2. However, the guide mechanism 201 maintained the distance of 10 mm between the alkali metal-containing plate 155 and the electrode 1. The evaluation results are shown in Table 1.

[0137] In Example 4, the evaluation result of the voltage in a stable voltage state was B. There was no Li deposition. The evaluation result of the charge / discharge efficiency distribution was A. Example 5 A doped electrode 1A was produced and evaluated basically in the same manner as in Example 2. However, the guide mechanism 201 maintained the distance of 3 mm between the alkali metal-containing plate 155 and the electrode 1. The evaluation results are shown in Table 1.

[0138] In Example 5, the evaluation result of the voltage in a stable voltage state was A. The evaluation result of Li precipitation was "microprecipitation present." The evaluation result of the charge / discharge efficiency distribution was B. Example 6 A doped electrode 1A was produced and evaluated basically in the same manner as in Example 2. However, the guide mechanism 201 maintained the distance of 16 mm between the alkali metal-containing plate 155 and the electrode 1. The evaluation results are shown in Table 1.

[0139] In Example 6, the evaluation result of the voltage in a stable voltage state was B. There was no Li deposition. The evaluation result of the charge / discharge efficiency distribution was B. Example 7 A doped electrode 1A was produced and evaluated in a manner basically similar to that of Example 2, except that the pitch distance was set to 100 mm. The evaluation results are shown in Table 1.

[0140] In Example 7, the evaluation result of the voltage in a stable voltage state was A. There was no Li deposition. The evaluation result of the charge / discharge efficiency distribution was A. Example 8 A doped electrode 1A was produced and evaluated in a manner basically similar to that of Example 2, except that the pitch distance was set to 800 mm. The evaluation results are shown in Table 1.

[0141] In Example 8, the evaluation result of the voltage in a stable voltage state was A. No Li deposition was observed. The evaluation result of the charge / discharge efficiency distribution was B. Example 9 A doped electrode 1A was produced and evaluated in a manner basically similar to that of Example 2, except that the pitch distance was set to 1000 mm. The evaluation results are shown in Table 1.

[0142] In Example 9, the evaluation result of the voltage in a stable voltage state was B. The evaluation result of Li precipitation was “microprecipitation present.” The evaluation result of the charge / discharge efficiency distribution was B. Comparative Example 1 A doped electrode 1A was produced and evaluated basically in the same manner as in Example 1, except that the guide mechanism 201 was not installed in the doping tanks 17 and 19. The evaluation results are shown in Table 1.

[0143] In Comparative Example 1, the evaluation result of the voltage in a stable voltage state was C. The evaluation result of Li precipitation was “present.” The evaluation result of the charge / discharge efficiency distribution was C. <Other embodiments> Although the embodiments of the present disclosure have been described above, the present disclosure is not limited to the above-described embodiments and can be implemented in various modified forms.

[0144] (1) The function of one component in each of the above embodiments may be shared by multiple components, or the functions of multiple components may be performed by one component. Also, part of the configuration of each of the above embodiments may be omitted. Also, at least part of the configuration of each of the above embodiments may be added to or substituted for the configuration of another of the above embodiments.

[0145] (2) In addition to the above-described doped electrode manufacturing method and doped electrode manufacturing system, the present disclosure can also be realized in various forms, such as a doped electrode, a secondary battery, and a method for manufacturing a secondary battery.

Claims

1. A method for producing a doped electrode including an active material layer doped with an alkali metal, comprising: A strip-shaped electrode including an active material layer is transported along a path passing through a doping tank that contains a doping solution including an alkali metal ion and an aprotic organic solvent, a counter electrode unit, and a guide mechanism; In the doping tank, the guide mechanism is disposed between the strip-shaped electrode including the active material layer and the counter electrode unit, and the distance between the strip-shaped electrode including the active material layer and the counter electrode unit is kept within a certain range; In the doping tank, the strip-shaped electrode including the active material layer and the counter electrode unit are electrically connected via the doping solution. Method for producing doped electrodes.

2. 2. A method for producing a doped electrode according to claim 1, comprising the steps of: The certain range is a range of 5 mm or more and 16 mm or less. Method for producing doped electrodes.

3. A method for producing a doped electrode according to claim 1 or 2, comprising the steps of: The guide mechanism includes a guide bar or a guide roll. Method for producing doped electrodes.

4. A method for producing a doped electrode according to claim 3, comprising the steps of: The guide bar or the guide roll includes a main body portion made of a material containing one or more selected from the group consisting of a thermoplastic resin, a thermosetting resin, a photocurable resin, a metal, and an oxide of the metal, and a surface portion formed on the surface of the main body portion and made of a material containing an organic substance. Method for producing doped electrodes.

5. A method for producing a doped electrode according to claim 3 or 4, comprising the steps of: In the dope tank, a plurality of the guide bars or the guide rolls are installed at intervals of 0.1 m or more and 1.0 m or less. Method for producing doped electrodes.

6. A system for producing a doped electrode including an active material layer doped with an alkali metal, comprising: a doping tank configured to contain a doping solution including ions of an alkali metal and an aprotic organic solvent; A counter electrode unit accommodated in the doping tank; a guide mechanism accommodated in the dope tank; a conveying unit configured to convey a strip-shaped electrode including the active material layer along a path passing through the doping tank; a connection unit configured to electrically connect a transport roller included in the transport unit and the counter electrode unit; Equipped with the guide mechanism is disposed between the strip-shaped electrode including the active material layer and the counter electrode unit, The guide mechanism is configured to keep a distance between the strip-shaped electrode including the active material layer and the counter electrode unit within a certain range in the doping tank. A system for manufacturing doped electrodes.

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