JP2018090751A - Adhesive sheet for batteries, method for producing adhesive sheet for batteries, and lithium ion battery - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an adhesive sheet for batteries that exhibits excellent adhesion to an adherend even when the adhesive sheet for batteries contacts an electrolyte, and ensures close contact between a base material and an adhesive layer, and a lithium ion battery, and a method for producing the adhesive sheet for batteries.SOLUTION: An adhesive sheet for batteries 1 has a base material 11, a hard coat layer 12 provided on one surface side of the base material 11, and an adhesive layer 13 provided on one surface side of the hard coat layer 12 when the other surface side of it has the base material 11 provided thereon. The hard coat layer 12 is formed from a hard coat layer composition containing a heat crosslinker.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a battery pressure-sensitive adhesive sheet, a method for producing a battery pressure-sensitive adhesive sheet, and a lithium ion battery produced using the same.

  In some batteries, a strip-shaped laminate formed by laminating a positive electrode, a negative electrode, and a separator located between them is housed in a wound state. Electrode extraction tabs made of a conductor are connected to the positive electrode and the negative electrode, respectively. Via these electrode extraction tabs, the positive electrode and the negative electrode are electrically connected to the positive electrode terminal and the negative electrode terminal of the battery, respectively. .

  An adhesive tape is used for winding the laminate and fixing the electrode take-out tab to the electrode. Patent Document 1 discloses such an adhesive tape. These pressure-sensitive adhesive tapes are composed of a base material and a pressure-sensitive adhesive layer provided on one surface of the base material.

JP 2011-138632 A

  The adhesive tape used inside the battery may come into contact with the electrolyte filled in the battery, or may be exposed to heat generated during charging and discharging. In particular, in recent years, development of small and high-performance batteries has been promoted, and the adhesive tape used in the battery is exposed to more severe conditions.

  In order to exhibit the performance as a battery, the adhesive tape is required to exhibit a good adhesive force to the adherend even when exposed to the severe conditions as described above. Also, the adhesive tape itself is required to maintain high adhesion between the base material and the adhesive layer. However, the conventional adhesive tape sometimes fails to satisfy such a requirement.

  The present invention has been made in view of such a situation, and even when the battery pressure-sensitive adhesive sheet is in contact with the electrolyte, it exhibits a good adhesive force to the adherend, and the substrate. It aims at providing the manufacturing method of the adhesive sheet for batteries and the lithium ion battery which were excellent in the adhesiveness between an adhesive layer, and this adhesive sheet for batteries.

  In order to achieve the above object, first, the present invention provides a base material, a hard coat layer provided on one surface side of the base material, and a surface side of the hard coat layer opposite to the base material. A battery pressure-sensitive adhesive sheet is provided, wherein the hard coat layer is formed from a composition for a hard coat layer containing a thermal crosslinking agent (Invention). 1). In the present specification, the concept of a tape is included in the sheet. Further, the hard coat layer in the present specification means a layer made of a material harder than the base material, and does not mean a layer existing in the outermost layer of the film.

  According to the said invention (invention 1), even if it is a case where an adhesive sheet contacts electrolyte solution by providing a hard-coat layer between a base material and an adhesive layer, a hard-coat layer is electrolyte solution. The permeation is blocked and the electrolytic solution is less likely to enter the adhesive layer. Thereby, an adhesive layer exhibits favorable adhesive force with respect to a to-be-adhered body. Moreover, according to the said invention (invention 1), when a hard-coat layer is formed from the composition for hard-coat layers containing a thermal crosslinking agent, by the effect | action of the component derived from the said thermal-crosslinking agent or a thermal-crosslinking agent, Adhesion between the hard coat layer and the pressure-sensitive adhesive layer and adhesion between the hard coat layer and the base material are improved, so that the adhesion between the base material and the pressure-sensitive adhesive layer is excellent.

  In the said invention (invention 1), it is preferable that the said thermal crosslinking agent is an isocyanate type crosslinking agent (invention 2).

  In the said invention (invention 1 and 2), it is preferable that the said composition for hard-coat layers contains the said thermal crosslinking agent, an active energy ray hardening component, and an inorganic filler (invention 3).

  In the said invention (invention 1-3), it is preferable that the said base material is a film which consists of a polymer which has a nitrogen-containing ring structure in a principal chain (invention 4).

  In the said invention (invention 1-4), it is preferable that the said adhesive layer is formed from the adhesive composition containing a (meth) acrylic acid ester polymer (invention 5).

  Secondly, the present invention comprises a base material, a hard coat layer provided on one surface side of the base material, and an adhesive layer provided on a surface of the hard coat layer opposite to the base material. A method for producing a pressure-sensitive adhesive sheet for a battery, comprising: an active energy applied to a coating film of a composition for a hard coat layer containing at least an active energy ray-curable component and a thermal cross-linking agent, which is applied to one side of a substrate. A battery is characterized by forming a pressure-sensitive adhesive layer in close contact with the hard coat layer by laminating a hard coat layer formed by irradiating a wire and a coating film of the pressure-sensitive adhesive composition, and then curing. A method for producing an adhesive sheet is provided (Invention 6).

  3rdly, this invention is fixed in the state in which two or more conductors contacted inside the battery using the said adhesive sheet for batteries (invention 1-5). An ion battery is provided (Invention 7).

  According to the battery pressure-sensitive adhesive sheet and the lithium ion battery according to the present invention, even when the battery pressure-sensitive adhesive sheet is in contact with the electrolytic solution, it exhibits a good adhesive force to the adherend, Excellent adhesion to the pressure-sensitive adhesive layer. In addition, according to the method for manufacturing a battery pressure-sensitive adhesive sheet according to the present invention, the substrate and the pressure-sensitive adhesive layer exhibit good adhesion to the adherend even when they are in contact with the electrolytic solution. The adhesive sheet for batteries which is excellent in the adhesiveness in between can be manufactured.

It is sectional drawing of the adhesive sheet for batteries which concerns on one Embodiment of this invention. It is a partial section exploded perspective view of a lithium ion battery concerning one embodiment of the present invention. It is an expansion | deployment perspective view of the electrode body of the lithium ion battery which concerns on one Embodiment of this invention.

Hereinafter, embodiments of the present invention will be described.
[Battery adhesive sheet]
As shown in FIG. 1, a battery pressure-sensitive adhesive sheet 1 according to an embodiment of the present invention includes a base material 11, a hard coat layer 12 provided on one surface side of the base material 11, and a hard coat layer 12. It is comprised from the adhesive layer 13 provided in the opposite side to the base material 11, and the peeling sheet 14 provided in the opposite side to the hard-coat layer 12 in the adhesive layer 13. FIG.

  Here, “battery pressure-sensitive adhesive sheet” in the present specification is a pressure-sensitive adhesive sheet used at a place where there is a possibility of contact with the electrolyte in the production of a battery, preferably a pressure-sensitive adhesive sheet used inside the battery. It may be an adhesive sheet for battery interior. The battery is preferably a non-aqueous battery. Accordingly, the battery electrolyte is preferably a non-aqueous electrolyte. The pressure-sensitive adhesive sheet for a battery in the present specification is preferably a pressure-sensitive adhesive sheet that is affixed to a part that may be immersed in the electrolyte solution inside the non-aqueous battery or a part that may contact the electrolyte solution. As the non-aqueous battery, a lithium ion battery is particularly preferable.

  According to the battery pressure-sensitive adhesive sheet 1 according to the present embodiment, the electrolyte solution that has entered the substrate 11 is blocked by the hard coat layer 12, and thus passes through the hard coat layer 12 and reaches the pressure-sensitive adhesive layer 13. Is estimated to be suppressed. Thereby, it is estimated that the quantity of the electrolyte solution which penetrates into the pressure-sensitive adhesive layer 13 is reduced.

  Note that even if the hard coat layer 12 is laminated not on the surface of the base material 11 and the pressure-sensitive adhesive layer 13 but on the surface of the base material 11 opposite to the pressure-sensitive adhesive layer 13, the electrolytic solution infiltrates. Can be expected to some extent. However, even with such a configuration, it is estimated that the electrolyte that has entered from the end of the base material 11 reaches the pressure-sensitive adhesive layer 13 that contacts the base material 11 through the inside of the base material 11. The Some of the materials of the base material 11 that are generally used have a very high permeability of the electrolytic solution, and when such a material is used, a predetermined amount of the electrolytic solution is obtained from only the end portion. 11 and then enters the pressure-sensitive adhesive layer 13.

  On the other hand, in the battery pressure-sensitive adhesive sheet 1 according to the present embodiment, by providing the hard coat layer 12 between the base material 11 and the pressure-sensitive adhesive layer 13, only the electrolyte solution that enters the base material 11 from the main surface can be used. In addition, the electrolyte solution that enters the substrate 11 from the end is also blocked by the hard coat layer 12, so that it is estimated that the electrolyte solution reaches the pressure-sensitive adhesive layer 13.

  As described above, in the battery pressure-sensitive adhesive sheet 1 according to the present embodiment, the amount of the electrolyte solution entering the pressure-sensitive adhesive layer 13 is reduced, so that the adhesive strength is maintained well, and the pressure-sensitive adhesive sheet 1 is removed from the adherend. While being prevented from being peeled off, the amount of the component of the pressure-sensitive adhesive layer 13 eluted into the electrolytic solution is reduced.

  In addition, the hard coat layer 12 of the battery pressure-sensitive adhesive sheet 1 according to the present embodiment is formed from a composition for a hard coat layer containing a thermal crosslinking agent, and contains a thermal crosslinking agent or a component derived from a thermal crosslinking agent. contains. The adhesiveness between the hard coat layer 12 and the pressure-sensitive adhesive layer 13 and the adhesiveness between the hard coat layer 12 and the substrate 11 are improved by the action of the thermal crosslinking agent or the component derived from the thermal crosslinking agent. In particular, the thermal crosslinking agent in the hard coat layer 12 easily reacts with the reactive functional group of the adhesive main agent in the pressure-sensitive adhesive layer 13, so that the adhesion is easily improved between those layers. Even when the battery pressure-sensitive adhesive sheet 1 is in contact with the electrolytic solution, high adhesion is maintained between the hard coat layer 12 and the pressure-sensitive adhesive layer 13 and between the hard coat layer 12 and the substrate 11. As a result, the adhesion between the substrate 11 and the pressure-sensitive adhesive layer 13 is excellent. Thereby, in the battery manufactured using the adhesive sheet 1 for batteries, it is suppressed that peeling arises between the base material 11 and the adhesive layer 13. FIG.

  Further, the battery pressure-sensitive adhesive sheet 1 according to the present embodiment includes the hard coat layer 12, so that insulation can be ensured even when the base material 11 and the pressure-sensitive adhesive layer 13 are carbonized. Safety can be improved.

  In the battery using the battery pressure-sensitive adhesive sheet 1 according to the present embodiment having the above-described effects, the performance degradation due to the pressure-sensitive adhesive sheet is suppressed, battery malfunction, thermal runaway and short circuit are suppressed, and the battery Reliability is improved.

1. Each component 1-1. Base Material In the battery pressure-sensitive adhesive sheet 1 according to this embodiment, the base material 11 preferably has flame retardancy that satisfies the flame retardancy level V-0 of the UL94 standard. Since the base material 11 has such flame retardancy, even when the base material 11 generates heat due to use of a normal battery, the base material 11 is prevented from being modified or deformed. In addition, even when a problem occurs in the battery and heat is excessively generated, ignition and combustion of the base material 11 are suppressed, and a serious accident is prevented.

  The material of the base material 11 can be appropriately selected from the viewpoints of adhesion to the hard coat layer 12, flame retardancy, heat resistance, insulation, reactivity with the electrolytic solution, permeability of the electrolytic solution, and the like. In particular, it is preferable to use a resin film as the substrate 11. Examples of the resin film include a polyester film such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate, a polyolefin film such as a polyethylene film and a polypropylene film, a polyamide film, a polyimide film, a polyamideimide film, etc. Film made of coalescence, cellophane, diacetyl cellulose film, triacetyl cellulose film, acetyl cellulose butyrate film, polyvinyl chloride film, polyvinylidene chloride film, polyvinyl alcohol film, ethylene-vinyl acetate copolymer film, polystyrene film, polycarbonate film , Polymethylpentene film, polysulfone film, polyether ether Ketone film, polyethersulfone film, polyetherimide film, fluororesin film, acrylic resin film, polyurethane resin film, norbornene polymer film, cyclic olefin polymer film, cyclic conjugated diene polymer film, vinyl alicyclic Examples thereof include resin films such as hydrocarbon polymer films or laminated films thereof. Among them, a film made of a polymer containing nitrogen in the main chain is preferable, a film made of a polymer having a nitrogen-containing ring structure in the main chain is particularly preferable, and further, a nitrogen-containing ring structure and an aromatic ring structure in the main chain. A film made of a polymer having the above is preferred. Specifically, a polyimide film and a polyamideimide film are preferable, and a polyimide film is particularly preferable. In a film made of a polymer having a nitrogen-containing ring structure in the main chain, a reaction involving cleavage of the nitrogen-containing ring and addition of a thermal cross-linking agent (particularly an isocyanate cross-linking agent) in the hard coat layer 12 is likely to occur. The adhesiveness with the coat layer 12 becomes higher. Among these, the polyimide film is particularly excellent in adhesion with the hard coat layer 12 and also excellent in flame retardancy.

  The thickness of the substrate 11 is preferably 5 to 200 μm, particularly preferably 10 to 100 μm, and further preferably 15 to 40 μm. When the thickness of the base material 11 is 5 μm or more, moderate rigidity is imparted to the base material 11, and curling is caused even when curing shrinkage occurs when the hard coat layer 12 is formed on the base material 11. Generation is effectively suppressed. Moreover, when the thickness of the base material 11 is 200 μm or less, the battery pressure-sensitive adhesive sheet 1 has appropriate flexibility, and on the surface where there is a step as in the case where the electrode and the electrode take-out tab are fixed. Even when the battery pressure-sensitive adhesive sheet 1 is affixed, the step can be satisfactorily followed.

1-2. Hard Coat Layer (1) Composition of Hard Coat Layer The hard coat layer 12 of the battery pressure-sensitive adhesive sheet 1 according to this embodiment is formed from a hard coat layer composition containing a thermal crosslinking agent. In other words, the hard coat layer 12 of the battery pressure-sensitive adhesive sheet 1 according to the present embodiment contains a thermal crosslinking agent or a component derived from a thermal crosslinking agent. As described above, the hard coat layer 12 is between the pressure-sensitive adhesive layer 13 and the battery pressure-sensitive adhesive sheet 1 even when the battery pressure-sensitive adhesive sheet 1 comes into contact with the electrolytic solution due to the action of the thermal crosslinking agent or the component derived from the thermal crosslinking agent. And high adhesiveness can be exhibited between the base material 11 and the substrate 11.

  The hard coat layer 12 is preferably cured by irradiation with active energy rays. Therefore, the hard coat layer composition for forming the hard coat layer 12 preferably contains an active energy ray-curable component and a thermal crosslinking agent, and in particular, the active energy ray-curable component and the thermal crosslinker. It is preferable to contain an agent and an inorganic filler.

(1-1) Active energy ray-curable component The active energy ray-curable component is not particularly limited as long as it is cured by irradiation with active energy rays and exhibits a desired hardness.

  Specific active energy ray-curable components include polyfunctional (meth) acrylate monomers, (meth) acrylate prepolymers, etc., among which polyfunctional (meth) acrylate monomers and / or (meta ) An acrylate-based prepolymer is preferred. The polyfunctional (meth) acrylate monomer and the (meth) acrylate prepolymer may be used alone or in combination. In the present specification, (meth) acrylate means both acrylate and methacrylate. The same applies to other similar terms.

  Examples of the multifunctional (meth) acrylate monomer include 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, and polyethylene glycol diene. (Meth) acrylate, hydroxypivalate neopentyl glycol di (meth) acrylate, dicyclopentanyl di (meth) acrylate, caprolactone modified dicyclopentenyl di (meth) acrylate, ethylene oxide modified di (meth) acrylate phosphoric acid, allylation Cyclohexyl di (meth) acrylate, isocyanurate di (meth) acrylate, trimethylolpropane tri (meth) acrylate, dipentaerythritol tri (meth) acrylate, propionic acid modified dipentae Thritol tri (meth) acrylate, pentaerythritol tri (meth) acrylate, propylene oxide modified trimethylolpropane tri (meth) acrylate, tris (acryloxyethyl) isocyanurate, propionic acid modified dipentaerythritol penta (meth) acrylate, dipentaerythritol Examples include polyfunctional (meth) acrylates such as hexa (meth) acrylate and caprolactone-modified dipentaerythritol hexa (meth) acrylate. These may be used individually by 1 type and may be used in combination of 2 or more type. The polyfunctional (meth) acrylate monomer is not particularly limited, but it is more preferable that the molecular weight is less than 1000 from the viewpoint of preventing the inorganic filler from coming out of the hard coat layer 12 under immersion in the electrolyte.

  On the other hand, examples of the (meth) acrylate-based prepolymer include polyester acrylate-based, epoxy acrylate-based, urethane acrylate-based, polyol acrylate-based prepolymers, and the like. A prepolymer may be used individually by 1 type and may be used in combination of 2 or more type.

  The active energy ray-curable component constituting the hard coat layer 12 of the present embodiment preferably has a glass transition point after curing of 130 ° C. or higher, more preferably 150 ° C. or higher, and a glass transition point is observed. It is particularly preferred that it is not. When the glass transition point of the active energy ray-curable component is as described above, the heat resistance of the hard coat layer 12 is excellent, and the battery pressure-sensitive adhesive sheet 1 provided with such a hard coat layer 12 is included. The battery performance and safety are also excellent.

  In addition, when using 2 or more types of active energy ray hardening components in the hard-coat layer 12 of this embodiment, it is preferable that those active energy ray hardening components are mutually excellent in compatibility.

(1-2) Thermal crosslinking agent Examples of the thermal crosslinking agent include isocyanate crosslinking agents, epoxy crosslinking agents, amine crosslinking agents, melamine crosslinking agents, aziridine crosslinking agents, hydrazine crosslinking agents, and aldehyde crosslinking agents. Oxazoline-based crosslinking agents, metal alkoxide-based crosslinking agents, metal chelate-based crosslinking agents, metal salt-based crosslinking agents, ammonium salt-based crosslinking agents, and the like. Among these, it is preferable to use an isocyanate type crosslinking agent from a viewpoint which is excellent in adhesiveness with the adhesive layer 13 and the base material 11. In addition, a thermal crosslinking agent can be used individually by 1 type or in combination of 2 or more types.

  The isocyanate-based crosslinking agent contains at least a polyisocyanate compound. Examples of the polyisocyanate compound include aromatic polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate and xylylene diisocyanate, aliphatic polyisocyanates such as hexamethylene diisocyanate, alicyclic polyisocyanates such as isophorone diisocyanate and hydrogenated diphenylmethane diisocyanate, etc. , And their biuret bodies, isocyanurate bodies, and adduct bodies that are a reaction product with low molecular active hydrogen-containing compounds such as ethylene glycol, propylene glycol, neopentyl glycol, trimethylolpropane, and castor oil. Among these, from the viewpoint of adhesion between the pressure-sensitive adhesive layer 13 and the substrate 11, trimethylolpropane-modified aliphatic polyisocyanate is preferable, and trimethylolpropane-modified hexamethylene diisocyanate is particularly preferable.

  The content of the thermal crosslinking agent in the hard coat layer composition is preferably 1 part by mass or more, more preferably 5 parts by mass or more, with respect to 100 parts by mass of the active energy ray-curable component. In particular, it is preferably 10 parts by mass or more, more preferably 20 parts by mass or more. In addition, the content is preferably 90 parts by mass or less, particularly preferably 50 parts by mass or less, and further preferably 30 parts by mass or less. Adhesiveness with the adhesive layer 13 and the base material 11 becomes more excellent because content of a thermal crosslinking agent exists in said range.

(1-3) Inorganic filler It is preferable that the composition for hard-coat layers which comprises the hard-coat layer 12 of this embodiment contains an inorganic filler. By including an inorganic filler, rigidity is imparted to the hard coat layer 12 of the present embodiment, and the battery adhesive sheet 1 is torn or punctured due to impact or the like under high temperature or electrolyte immersion. Can be prevented.

  Preferred inorganic fillers include powders such as silica, alumina, boehmite, talc, calcium carbonate, titanium oxide, iron oxide, silicon carbide, boron nitride, zirconium oxide, beads spheroidized from these, single crystal fibers, glass fibers, and the like. These may be used alone or in combination of two or more. Among these, silica, alumina, boehmite, titanium oxide, zirconium oxide, and the like are preferable, and silica, alumina, and zirconium oxide are particularly preferable from the viewpoint of dispersibility in the active energy ray-curable component. These inorganic fillers can also be used in the form of sols dispersed in a dispersion medium.

  The inorganic filler is also preferably surface-modified. An example of such an inorganic filler is reactive silica.

  In this specification, “reactive silica” refers to silica fine particles whose surface is modified with an organic compound having an active energy ray-curable unsaturated group. Silica fine particles (reactive silica) surface-modified with an organic compound having an active energy ray-curable unsaturated group are usually, for example, silanol groups on the surface of silica fine particles having an average particle diameter of 1 to 200 nm and the silanol groups. It can be obtained by reacting an active energy ray-curable unsaturated group-containing organic compound having a functional group capable of reacting (for example, an isocyanate group, an epoxy group, a carboxy group, etc.). In addition, as said active energy ray hardening unsaturated group, a (meth) acryloyl group and a vinyl group can be mentioned preferably.

  As an organic-inorganic hybrid material (organosilica sol) containing such reactive silica and the above-mentioned polyfunctional (meth) acrylate monomer and / or (meth) acrylate prepolymer, for example, trade name “OPSTAR Z7530” "OPSTAR Z7524", "OPSTAR TU4086", "OPSTAR Z7537" (manufactured by JSR Corporation), etc. can be used.

  Other examples of preferred inorganic fillers include alumina ceramic nanoparticles, silica sol in which silica fine particles with exposed silanol groups on the silica surface are suspended in a colloidal state in the dispersion medium, and silanol groups on the silica surface with silane coupling. And organosilica sol surface-treated with an agent.

  The inorganic filler used in the present embodiment preferably has an average particle size of 1 to 1000 nm, particularly preferably 10 to 500 nm, and further preferably 15 to 200 nm. When the average particle size of the inorganic filler is 1 nm or more, the hard coat layer 12 obtained by curing the hard coat layer composition has higher surface hardness. Moreover, when the average particle diameter of the inorganic filler is 1000 nm or less, the dispersibility of the inorganic filler in the hard coat layer composition becomes excellent, and when the hard coat layer 12 is formed on the substrate 11, Generation of irregularities on the surface of the hard coat layer 12 opposite to the substrate 11 can be effectively prevented. Furthermore, by forming the pressure-sensitive adhesive layer 13 on the surface, very high smoothness can be obtained on the surface of the pressure-sensitive adhesive layer 13 opposite to the hard coat layer 12. Thereby, the adhesive layer 13 can exhibit the outstanding adhesiveness with respect to a to-be-adhered body. In addition, the average particle diameter of an inorganic filler shall be measured with the laser diffraction scattering type particle size distribution measuring apparatus.

  It is preferable that content of the inorganic filler in the hard-coat layer 12 of this embodiment is 0-90 mass% (90 mass% or less) with respect to the hard-coat layer 12, and it is more preferable that it is 30-85 mass%. Preferably, it is 40-80 mass%, It is especially preferable that it is 45-70 mass%. When it contains an inorganic filler, the rigidity provided to the hard-coat layer 12 becomes higher because the content is 30% by mass or more. On the other hand, layer formation using the composition for hard-coat layers becomes easy because content of an inorganic filler is 90 mass% or less.

(1-4) Other components The composition for forming the hard-coat layer 12 of this embodiment may contain various additives other than the component mentioned above. Examples of various additives include photopolymerization initiators, antioxidants, antistatic agents, silane coupling agents, antioxidants, thermal polymerization inhibitors, colorants, surfactants, storage stabilizers, plasticizers, and lubricants. , Antifoaming agents, organic fillers and the like.

  When the hard coat layer 12 is formed using ultraviolet rays as active energy rays, it is preferable to use a photopolymerization initiator. The photopolymerization initiator is not particularly limited as long as it functions as a photopolymerization initiator of the active energy ray-curable component to be used. For example, acylphosphine oxide compounds, benzoin compounds, acetophenone compounds, titanocene compounds, thioxanthones Compounds, peroxide compounds and the like. Specifically, 1-hydroxycyclohexyl phenyl ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 2,2-dimethoxy-1,2-diphenylethane-1-one, benzoin, benzoin Examples include methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzyl diphenyl sulfide, tetramethyl thiuram monosulfide, azobisisobutyronitrile, dibenzyl, diacetyl, and β-chloranthraquinone. These may be used individually by 1 type and may be used in combination of 2 or more type.

  In general, the content of the photopolymerization initiator in the hard coat layer composition is preferably 0.1 to 20 parts by mass with respect to 100 parts by mass of the active energy ray-curable component. It is preferably 15 parts by mass.

(2) Thickness of the hard coat layer The thickness of the hard coat layer 12 is preferably 0.1 to 10 μm, particularly preferably 0.5 to 7 μm, and more preferably 1 to 4 μm. preferable. When the thickness of the hard coat layer 12 is 0.1 μm or more, the penetration of the hard coat layer 12 by the electrolytic solution is effectively blocked. Further, since the thickness of the hard coat layer 12 is 10 μm or less, the battery pressure-sensitive adhesive sheet 1 has appropriate flexibility, and has a step as in the case where the electrode and the electrode take-out tab are fixed. Even when the battery adhesive sheet 1 is attached to the battery, the battery adhesive sheet 1 can follow the steps well.

(3) Physical Properties of Hard Coat Layer In the battery pressure-sensitive adhesive sheet 1 according to this embodiment, the hard coat layer 12 in the state provided on the substrate 11 is a load of 250 g / cm ² using # 0000 steel wool. It is preferable that the hard coat layer 12 is rubbed back and forth for 10 cm, 10 times, so that no scratch is generated. With such steel wool resistance evaluation, the permeation of the hard coat layer 12 of the electrolytic solution is effectively blocked, and the pressure-sensitive adhesive layer 13 even when the battery pressure-sensitive adhesive sheet 1 comes into contact with the electrolytic solution. However, the adhesive strength is maintained well, and peeling of the battery pressure-sensitive adhesive sheet 1 from the adherend is effectively suppressed.

1-3. Pressure-sensitive adhesive layer The pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 13 is not particularly limited as long as it exerts a desired adhesive force on the adherend and can secure adhesion to the hard coat layer 12. Examples of such adhesives include acrylic adhesives, silicone adhesives, rubber adhesives, and urethane adhesives. Especially, the acrylic adhesive which is excellent in adhesiveness with the hard-coat layer 12 formed from the composition for hard-coat layers containing a thermal crosslinking agent is preferable. The acrylic pressure-sensitive adhesive easily reacts with the thermal crosslinking agent or the component derived from the thermal crosslinking agent in the hard coat layer 12, thereby improving the adhesion with the hard coat layer 12 and contacting the electrolytic solution. Even if it exists, the adhesiveness is maintained effectively.

  The acrylic pressure-sensitive adhesive is preferably obtained from a pressure-sensitive adhesive composition containing the (meth) acrylic acid ester polymer (A) (hereinafter sometimes referred to as “pressure-sensitive adhesive composition P”). In addition to the (meth) acrylic acid ester polymer (A), the pressure-sensitive adhesive composition P preferably contains a crosslinking agent (B), and more preferably contains a silane coupling agent (C). In the present specification, the term “polymer” includes the concept of “copolymer”.

(1) Each component (1-1) (meth) acrylic acid ester polymer (A)
The (meth) acrylic acid ester polymer (A) contains a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group as a monomer unit constituting the polymer. Can be expressed. Examples of the (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, and (meth) acrylic acid n-. Butyl, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isooctyl (meth) acrylate, n-decyl (meth) acrylate, (meth) acrylic acid Examples include n-dodecyl, myristyl (meth) acrylate, palmityl (meth) acrylate, stearyl (meth) acrylate, and the like. Especially, it is preferable that the C1-C8 (meth) acrylic acid ester of an alkyl group is contained from a viewpoint of improving adhesiveness more. These may be used alone or in combination of two or more.

  The (meth) acrylic acid ester polymer (A) preferably contains 50% by mass or more of a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms as the monomer unit constituting the polymer. In particular, the content is preferably 60% by mass or more, and more preferably 70% by mass or more. When the (meth) acrylic acid alkyl ester is contained in an amount of 50% by mass or more, the (meth) acrylic acid ester polymer (A) can exhibit suitable tackiness. Moreover, (meth) acrylic acid ester polymer (A) contains 97 mass% or less of (meth) acrylic acid alkyl ester whose carbon number of an alkyl group is 1-20 as a monomer unit which comprises the said polymer. In particular, it is preferably contained in an amount of 90% by mass or less, more preferably 85% by mass or less. By setting the (meth) acrylic acid alkyl ester to 97% by mass or less, a suitable amount of other monomer components can be introduced into the (meth) acrylic acid ester polymer (A).

  The (meth) acrylic acid ester polymer (A) has a glass transition as a homopolymer as a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms as the monomer unit constituting the polymer. It is also preferable to use a monomer (hard monomer) having a temperature (Tg) exceeding 0 ° C. and a monomer (soft monomer) having a glass transition temperature (Tg) as a homopolymer of 0 ° C. or less. Thereby, the elution resistance with respect to electrolyte solution can be made more excellent. In this case, the mass ratio of the hard monomer to the soft monomer is preferably 5:95 to 40:60, and particularly preferably 20:80 to 30:70.

  Examples of the hard monomer include methyl acrylate (Tg 10 ° C.), methyl methacrylate (Tg 105 ° C.), isobornyl acrylate (Tg 94 ° C.), isobornyl methacrylate (Tg 180 ° C.), adamantyl acrylate (Tg 115 ° C.), and methacrylic acid. And adamantyl (Tg 141 ° C.). These may be used alone or in combination of two or more.

  Among the above hard monomers, methyl acrylate, methyl methacrylate and isobornyl acrylate are preferred from the viewpoint of further exerting the performance of the hard monomer while preventing adverse effects on properties such as adhesiveness, and particularly methyl acrylate and methacrylic acid. Methyl is preferred.

  Preferable examples of the soft monomer include acrylic acid alkyl esters having a linear or branched alkyl group having 2 to 12 carbon atoms. For example, 2-ethylhexyl acrylate (Tg-70 ° C.), n-butyl acrylate (Tg-54 ° C.) and the like are preferable, and n-butyl acrylate is particularly preferable. These may be used alone or in combination of two or more.

  The (meth) acrylic acid ester polymer (A) may contain other monomers as monomer units constituting the polymer, if desired. The other monomer may be a monomer containing a reactive functional group (reactive functional group-containing monomer) or a monomer not containing a reactive functional group. By containing the reactive functional group-containing monomer, the crosslinking agent (B) described later reacts with the reactive functional group of the reactive functional group-containing monomer to form a crosslinked structure and improve the cohesive strength of the pressure-sensitive adhesive. To do. In addition, the thermal crosslinking agent in the hard coat layer 12 can react with the reactive functional group of the reactive functional group-containing monomer and chemically bond. Thereby, the adhesiveness of the adhesive layer 13 and the hard-coat layer 12 improves more.

  The reactive functional group-containing monomer includes a monomer having a carboxy group in the molecule (carboxy group-containing monomer), a monomer having a hydroxyl group in the molecule (hydroxyl group-containing monomer), and a monomer having an amino group in the molecule (amino group-containing monomer). ) And the like. Among these, it is preferable that the (meth) acrylic acid ester polymer (A) includes a carboxy group-containing monomer as a monomer unit constituting the polymer. When a metal chelate crosslinking agent is used as the crosslinking agent (B) described later, the carboxy group derived from the carboxy group-containing monomer reacts with the metal chelate crosslinking agent during the crosslinking of the (meth) acrylate polymer (A). As a result, a crosslinked structure which is a three-dimensional network structure is formed. The pressure-sensitive adhesive having a cross-linked structure resulting from the reaction between the carboxy group and the metal chelate-based cross-linking agent has high resistance to an electrolytic solution, particularly a non-aqueous electrolytic solution, and is difficult to elute even when contacted with the electrolytic solution.

  Examples of the carboxy group-containing monomer include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, and citraconic acid. Among these, acrylic acid is preferable. According to acrylic acid, the above effect is more excellent. The carboxy group-containing monomers may be used alone or in combination of two or more.

  The (meth) acrylic acid ester polymer (A) preferably contains a carboxy group-containing monomer as a lower limit of 0.5% by mass or more, particularly 1% by mass or more, as a monomer unit constituting the polymer. It is preferable to contain 3% by mass or more. In addition, the (meth) acrylic acid ester polymer (A) preferably contains a carboxy group-containing monomer as an upper limit value of 30% by mass or less, and 25% by mass or less as a monomer unit constituting the polymer. More preferably, the content is preferably 20% by mass or less, and more preferably 10% by mass or less. When the (meth) acrylic acid ester polymer (A) contains a carboxy group-containing monomer in the above amount as a monomer unit, the above-described effect is more excellent in the obtained pressure-sensitive adhesive.

  Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, (meth And (meth) acrylic acid hydroxyalkyl esters such as 3-hydroxybutyl acrylate and 4-hydroxybutyl (meth) acrylate. These may be used alone or in combination of two or more.

  Examples of the amino group-containing monomer include aminoethyl (meth) acrylate, n-butylaminoethyl (meth) acrylate, and the like. These may be used alone or in combination of two or more.

  The reactive functional group-containing monomer is preferably only the above-mentioned carboxy group-containing monomer in order not to inhibit the effect obtained by the cross-linked structure by the reaction between the carboxy group and the metal chelate cross-linking agent.

  On the other hand, examples of monomers that do not contain reactive functional groups include, for example, (meth) acrylic acid alkoxyalkyl esters such as methoxyethyl (meth) acrylate and ethoxyethyl (meth) acrylate, (meth) acrylic acid N, N-dimethylaminoethyl, (meth) acrylic acid N, N-dimethylaminopropyl, (meth) acrylic acid ester having a non-crosslinking tertiary amino group such as (meth) acryloylmorpholine, (meth) acrylamide, dimethylacrylamide , Vinyl acetate, styrene and the like. These may be used alone or in combination of two or more.

  The polymerization mode of the (meth) acrylic acid ester polymer (A) may be a random copolymer or a block copolymer.

  The weight average molecular weight of the (meth) acrylic acid ester polymer (A) is preferably 50,000 or more as a lower limit, particularly preferably 100,000 or more, and more preferably 200,000 or more. When the lower limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is not less than the above, the resulting adhesive is more excellent in elution resistance to the electrolytic solution.

  The weight average molecular weight of the (meth) acrylic acid ester polymer (A) is preferably 2.5 million or less as an upper limit, more preferably 2 million or less, and particularly preferably 1.5 million or less. Furthermore, it is preferable that it is 1.3 million or less. When the upper limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is not more than the above, the pressure-sensitive adhesive of the resulting pressure-sensitive adhesive is more excellent. In addition, the weight average molecular weight in this specification is the value of standard polystyrene conversion measured by the gel permeation chromatography (GPC) method.

  In the adhesive composition P, the (meth) acrylic acid ester polymer (A) may be used singly or in combination of two or more.

(1-2) Crosslinking agent (B)
As the crosslinking agent (B), the same thermal crosslinking agent that can be used in the hard coat layer 12 can be used, and among them, it is preferable to use a metal chelate crosslinking agent. In this case, the (meth) acrylic acid ester polymer (A) preferably contains a carboxy group-containing monomer as a monomer unit constituting the polymer. With this combination, as described above, the obtained pressure-sensitive adhesive has high resistance to an electrolytic solution, particularly a non-aqueous electrolytic solution, and is difficult to elute even when in contact with the electrolytic solution. Therefore, the adhesive does not adversely affect the battery performance, thereby suppressing battery malfunction, thermal runaway and short circuit due to the adhesive sheet.

  As the metal chelate-based crosslinking agent, a metal chelate compound whose metal atom is aluminum, zirconium, titanium, zinc, iron, tin or the like can be used. Of these, an aluminum chelate compound is particularly preferred. The aluminum chelate compound exhibits the above-mentioned elution resistance to the electrolytic solution particularly effectively.

  Examples of the aluminum chelate compound include diisopropoxy aluminum monooleyl acetoacetate, monoisopropoxy aluminum bis oleyl acetoacetate, monoisopropoxy aluminum monooleate monoethyl acetoacetate, diisopropoxy aluminum monolauryl acetoacetate, diisopropoxy Aluminum monostearyl acetoacetate, diisopropoxy aluminum monoisostearyl acetoacetate, monoisopropoxy aluminum mono-N-lauroyl-β-alanate monolauryl acetoacetate, aluminum tris (acetylacetonate), monoacetylacetonate aluminum bis ( Isobutyl acetoacetate) chelate, monoacetylacetonate aluminum Umubisu (2-ethylhexyl acetoacetate) chelate, monoacetylacetonate aluminum bis (dodecyl acetoacetate) chelate, monoacetylacetonate aluminum bis (oleyl acetoacetate) chelate, and the like. Among these, aluminum tris (acetylacetonate) is preferable from the viewpoint of the above effects. These may be used alone or in combination of two or more.

  Examples of other metal chelate compounds include titanium tetrapropionate, titanium tetra-n-butyrate, titanium tetra-2-ethylhexanoate, zirconium sec-butyrate, zirconium diethoxy-tert-butyrate, and triethanol. Examples thereof include amine titanium dipropionate, ammonium lactate ammonium salt, and tetraoctylene glycol titanate. These may be used alone or in combination of two or more.

  Said metal chelate type crosslinking agent may be used individually by 1 type, and may be used in combination of 2 or more type.

  Content of the metal chelate type crosslinking agent in the pressure-sensitive adhesive composition P according to the present embodiment is 0.1 parts by mass or more as a lower limit with respect to 100 parts by mass of the (meth) acrylic acid ester polymer (A). Preferably, it is preferably 0.2 part by mass or more, and more preferably 0.3 part by mass or more. The content of the metal chelate crosslinking agent is preferably 5 parts by mass or less, particularly preferably 4 parts by mass or less, and more preferably 3 parts by mass or less as an upper limit. When the content of the metal chelate crosslinking agent is in the above range, the above-described effect becomes more excellent.

(1-3) Silane coupling agent (C)
The pressure-sensitive adhesive composition P preferably contains a silane coupling agent (C). When the silane coupling agent (C) is contained, even when the pressure-sensitive adhesive layer 13 is in contact with the electrolytic solution, excellent adhesive force is exerted on the adherend (particularly with respect to the metal member). Moreover, the obtained pressure-sensitive adhesive layer 13 has higher adhesion to the hard coat layer 12. Therefore, it is possible to prevent peeling and the like at the interface between the hard coat layer 12 and the pressure-sensitive adhesive layer 13 by immersing the battery pressure-sensitive adhesive sheet in the electrolytic solution solvent, and to increase the adhesive strength after immersion in the electrolytic solution solvent. Can do. Further, when the release sheet 14 is peeled from the pressure-sensitive adhesive layer 13, it can be effectively suppressed that the pressure-sensitive adhesive layer 13 is transferred to the release sheet 14 and peeled off from the hard coat layer 12.

  The silane coupling agent (C) is preferably an organosilicon compound having at least one alkoxysilyl group in the molecule and having good compatibility with the (meth) acrylic acid ester polymer (A).

  Examples of the silane coupling agent (C) include polymerizable unsaturated group-containing silicon compounds such as vinyltrimethoxysilane, vinyltriethoxysilane, and methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, Mercapto groups such as silicon compounds having an epoxy structure such as 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropyldimethoxymethylsilane Contains amino groups such as silicon compounds, 3-aminopropyltrimethoxysilane, N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane Silicon compound, 3-chloropropyltrimethoxysilane, 3-isocyanatopropyltriethoxysilane, or at least one of them, and alkyl groups such as methyltriethoxysilane, ethyltriethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane Examples include condensates with silicon compounds. Among these, from the viewpoint of the above effects, a silicon compound having an epoxy structure is preferable, and 3-glycidoxypropyltrimethoxysilane is particularly preferable. These may be used individually by 1 type and may be used in combination of 2 or more type.

  The content of the silane coupling agent (C) in the adhesive composition P is preferably 0.01 parts by mass or more with respect to 100 parts by mass of the (meth) acrylic acid ester polymer (A). It is more preferably 0.05 parts by mass or more, particularly preferably 0.1 parts by mass or more, and further preferably 0.3 parts by mass or more. Further, the content is preferably 5 parts by mass or less, particularly preferably 4 parts by mass or less, and further preferably 3 parts by mass or less. When the content of the silane coupling agent (C) is within the above range, the adhesive strength after immersion in the electrolytic solution becomes more excellent.

(1-4) Various Additives Various additives that are usually used for acrylic pressure-sensitive adhesives, such as tackifiers, antioxidants, softeners, fillers, and the like are added to the pressure-sensitive adhesive composition P as required. can do. In addition, the below-mentioned polymerization solvent and dilution solvent shall not be contained in the additive which comprises the adhesive composition P.

(2) Manufacture of adhesive composition The adhesive composition P manufactured the (meth) acrylic acid ester polymer (A), and the obtained (meth) acrylic acid ester polymer (A), if desired, It can manufacture by adding a crosslinking agent (B), a silane coupling agent (C), an additive, etc.

  The (meth) acrylic acid ester polymer (A) can be produced by polymerizing a mixture of monomers constituting the polymer by an ordinary radical polymerization method. The polymerization of the (meth) acrylic acid ester polymer (A) can be performed by a solution polymerization method or the like using a polymerization initiator as desired. Examples of the polymerization solvent include ethyl acetate, n-butyl acetate, isobutyl acetate, toluene, acetone, hexane, methyl ethyl ketone, and the like. Two or more kinds may be used in combination.

  Examples of the polymerization initiator include azo compounds and organic peroxides, and two or more kinds may be used in combination. Examples of the azo compound include 2,2′-azobisisobutyronitrile, 2,2′-azobis (2-methylbutyronitrile), 1,1′-azobis (cyclohexane 1-carbonitrile), 2 , 2′-azobis (2,4-dimethylvaleronitrile), 2,2′-azobis (2,4-dimethyl-4-methoxyvaleronitrile), dimethyl 2,2′-azobis (2-methylpropionate) 4,4′-azobis (4-cyanovaleric acid), 2,2′-azobis (2-hydroxymethylpropionitrile), 2,2′-azobis [2- (2-imidazolin-2-yl) Propane] and the like.

  Examples of organic peroxides include benzoyl peroxide, t-butyl perbenzoate, cumene hydroperoxide, diisopropyl peroxydicarbonate, di-n-propyl peroxydicarbonate, and di (2-ethoxyethyl) peroxy. Examples include dicarbonate, t-butyl peroxyneodecanoate, t-butyl peroxybivalate, (3,5,5-trimethylhexanoyl) peroxide, dipropionyl peroxide, diacetyl peroxide and the like.

  In addition, in the said superposition | polymerization process, the weight average molecular weight of the polymer obtained can be adjusted by mix | blending chain transfer agents, such as 2-mercaptoethanol.

  Once the (meth) acrylic acid ester polymer (A) is obtained, the solution of the (meth) acrylic acid ester polymer (A) is optionally mixed with a crosslinking agent (B), a silane coupling agent (C), and an additive. Etc. are added and mixed thoroughly to obtain an adhesive composition P.

  In addition, in order to adjust the adhesive composition P to a viscosity suitable for coating or to adjust the pressure-sensitive adhesive layer to a desired film thickness, in addition to the above-described polymerization solvent, it is diluted with a diluent solvent or the like, It is good also as a coating liquid mentioned later. Examples of the dilution solvent include ethyl acetate, n-butyl acetate, isobutyl acetate, toluene, acetone, hexane, methyl ethyl ketone, and the like, and two or more kinds may be used in combination.

(3) Physical properties of pressure-sensitive adhesive / pressure-sensitive adhesive layer In the battery pressure-sensitive adhesive sheet 1 according to this embodiment, the pressure-sensitive adhesive after immersing the pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 13 in a solvent of a nonaqueous electrolytic solution at 80 ° C. for 72 hours. The gel fraction of the agent is preferably 60% or more as a lower limit, particularly preferably 70% or more, and more preferably 80% or more. When the lower limit value of the gel fraction is as described above, the amount of pressure-sensitive adhesive eluted when the pressure-sensitive adhesive layer 13 is in contact with the electrolytic solution can be kept low. Thereby, malfunction, thermal runaway and short circuit of the battery using the battery adhesive sheet 1 are effectively suppressed.

  On the other hand, the upper limit of the gel fraction is preferably 100% or less, particularly preferably 99% or less, and more preferably 98% or less. When the upper limit of the gel fraction is 98% or less, the battery pressure-sensitive adhesive sheet 1 has appropriate flexibility, and is used for a battery on a surface where a step exists as in the case where the electrode and the electrode take-out tab are fixed. Even when the pressure-sensitive adhesive sheet 1 is pasted, the steps can be satisfactorily followed.

  In addition, the solvent of a non-aqueous electrolyte solution here is a preparation liquid in which ethylene carbonate and diethyl carbonate are mixed at a volume ratio of 1: 1, and the test method of the gel fraction is as shown in the test examples described later. .

(4) Thickness of the pressure-sensitive adhesive layer The thickness of the pressure-sensitive adhesive layer 13 (value measured according to JIS K7130) is preferably 1 to 50 μm, particularly preferably 3 to 15 μm, and further 4 It is preferably ˜9 μm. When the thickness of the pressure-sensitive adhesive layer 13 is 1 μm or more, the battery pressure-sensitive adhesive sheet 1 can exhibit good adhesive force. Moreover, when the thickness of the pressure-sensitive adhesive layer 13 is 50 μm or less, it is possible to effectively reduce the amount of the electrolyte that enters from the end of the pressure-sensitive adhesive layer 13.

1-4. Release sheet The release sheet 14 protects the adhesive layer until the battery pressure-sensitive adhesive sheet 1 is used, and is peeled off when the battery pressure-sensitive adhesive sheet 1 is used. In the battery pressure-sensitive adhesive sheet 1 according to this embodiment, the release sheet 14 is not necessarily required.

  Examples of the release sheet 14 include polyethylene film, polypropylene film, polybutene film, polybutadiene film, polymethylpentene film, polyvinyl chloride film, vinyl chloride copolymer film, polyethylene terephthalate film, polyethylene naphthalate film, and polybutylene terephthalate film. , Polyurethane film, ethylene vinyl acetate film, ionomer resin film, ethylene / (meth) acrylic acid copolymer film, ethylene / (meth) acrylic acid ester copolymer film, polystyrene film, polycarbonate film, polyimide film, fluororesin film A liquid crystal polymer film or the like is used. These crosslinked films are also used. Furthermore, these laminated films may be sufficient.

  The release surface of the release sheet 14 (the surface in contact with the pressure-sensitive adhesive layer 13) is preferably subjected to a release treatment. Examples of the release agent used for the release treatment include alkyd, silicone, fluorine, unsaturated polyester, polyolefin, and wax release agents.

  Although there is no restriction | limiting in particular about the thickness of the peeling sheet 14, Usually, it is about 20-150 micrometers.

2. Physical properties of battery adhesive sheet, etc. The adhesive strength of the battery adhesive sheet 1 according to the present embodiment to the aluminum plate (adhesive strength before immersion in the electrolyte solvent) is preferably 0.5 N / 25 mm or more as a lower limit value. In particular, it is preferably 0.75 N / 25 mm or more, and more preferably 1.0 N / 25 mm or more. Since the lower limit value of the adhesive strength of the battery pressure-sensitive adhesive sheet 1 before immersing the electrolytic solution in the solvent is as described above, the battery pressure-sensitive adhesive sheet 1 is attached to the adherend (particularly metal) before the battery pressure-sensitive adhesive sheet 1 contacts the electrolytic solution. The problem of peeling off from the member is less likely to occur. The upper limit value of the adhesive strength before immersion in the electrolyte solvent is not particularly limited, but is usually preferably 50 N / 25 mm or less, particularly preferably 30 N / 25 mm or less, and more preferably 10 N / 25 mm or less. Is preferred. In addition, the adhesive force in this specification means the adhesive force measured by 180 degree peeling method based on JISZ0237: 2009 fundamentally, and the detailed measuring method is as showing in the test example mentioned later.

  Moreover, the adhesive force (electrolysis) with respect to the aluminum plate of the said adhesive sheet 1 after sticking the adhesive sheet 1 for batteries which concerns on this embodiment to an aluminum plate, and immersing in the solvent of a non-aqueous electrolyte solution at 80 degreeC for 72 hours. The lower limit of the adhesive strength after immersion in the liquid solvent is preferably 0.5 N / 25 mm or more, more preferably 0.75 N / 25 mm or more, and particularly preferably 1.0 N / 25 mm or more. Further, it is preferably 2.0 N / 25 mm or more. Since the lower limit value of the adhesive strength of the battery pressure-sensitive adhesive sheet 1 after immersion in the electrolytic solution solvent is as described above, even if the battery pressure-sensitive adhesive sheet 1 is in contact (immersion) with the electrolytic solution, the battery pressure-sensitive adhesive sheet 1 is The problem of peeling off from the adherend (particularly metal member) hardly occurs. The upper limit value of the adhesive strength after immersion in the electrolyte solution is not particularly limited, but it is usually preferably 40 N / 25 mm or less, particularly preferably 20 N / 25 mm or less, and more preferably 10 N / 25 mm or less. Is preferred. The battery pressure-sensitive adhesive sheet 1 according to this embodiment includes a hard coat layer 12 between the base material 11 and the pressure-sensitive adhesive layer 13, and further contains a silane coupling agent (C). By having the pressure-sensitive adhesive layer 13 formed using the above, it is possible to achieve an excellent adhesive force in the above range. In addition, the solvent of the non-aqueous electrolyte solution here is a preparation solution in which ethylene carbonate and diethyl carbonate are mixed at a volume ratio of 1: 1.

  The adhesive strength after immersion in the electrolyte solvent is preferably 50% or more, more preferably 60% or more, and particularly preferably 70% or more with respect to the adhesive strength before the electrolyte solvent immersion. Further, it is preferably 90% or more.

  The thickness of the battery pressure-sensitive adhesive sheet 1 (excluding the thickness of the release sheet 14) is preferably 10 to 250 μm, particularly preferably 15 to 110 μm, and more preferably 20 to 45 μm. When the thickness of the battery pressure-sensitive adhesive sheet 1 is in the above range, the battery pressure-sensitive adhesive sheet 1 becomes more suitable with both adhesive force and heat resistance.

3. Method for Producing Battery Adhesive Sheet In order to produce battery adhesive sheet 1 according to this embodiment, the coating film of the composition for hard coat layer applied to one surface side of substrate 11 is irradiated with active energy rays. After forming the hard coat layer 12 (hard coat layer 12 before curing) and the coating film of the adhesive composition P, the adhesive layer 13 adhered to the hard coat layer 12 is formed by curing. It is preferable to do. Thereby, the heat-crosslinking agent in the hard coat layer 12 reacts with the (meth) acrylic acid ester polymer (A) in the pressure-sensitive adhesive composition P, and chemically bonds to the hard coat layer 12 and the adhesive. Adhesiveness with the agent layer 13 is remarkably improved. Even when the battery pressure-sensitive adhesive sheet 1 is in contact with the electrolytic solution, the adhesion between the hard coat layer 12 and the pressure-sensitive adhesive layer 13 is very excellent, and between the hard coat layer 12 and the pressure-sensitive adhesive layer 13. Peeling is effectively suppressed.

  Specifically, the battery pressure-sensitive adhesive sheet 1 according to the present embodiment produces a laminate of the base material 11 and the hard coat layer 12 and a laminate of the adhesive composition P coating film and the release sheet 14 respectively. Then, after laminating these laminates so that the hard coat layer 12 and the coating film of the adhesive composition P are in contact with each other, curing is performed to form the adhesive layer 13 from the coating film of the adhesive composition P. Can be manufactured. In addition, from the viewpoint of further improving the adhesion between the hard coat layer 12 and the pressure-sensitive adhesive layer 13, the corona treatment or the plasma treatment is performed on the surface to which one of these layers is bonded or the surface to which both layers are bonded. It is also preferable to bond both layers after performing a surface treatment such as.

  The laminated body of the base material 11 and the hard coat layer 12 can be produced as follows, for example. First, a coating liquid containing the hard coat layer composition and, if desired, a solvent is applied to one main surface of the substrate 11 and dried. The coating solution may be applied by a conventional method, for example, a bar coating method, a knife coating method, a Mayer bar method, a roll coating method, a blade coating method, a die coating method, or a gravure coating method. Drying can be performed, for example, by heating at 80 to 150 ° C. for about 30 seconds to 5 minutes.

Thereafter, the layer formed by drying the coating solution is irradiated with active energy rays to cure the layer and form the hard coat layer 12. As the active energy rays, for example, electromagnetic waves or charged particle beams having energy quanta can be used, and specifically, ultraviolet rays, electron beams, or the like can be used. In particular, ultraviolet rays that are easy to handle are preferred. Irradiation with ultraviolet rays can be performed by a high-pressure mercury lamp, a xenon lamp, or the like, and the irradiation amount of ultraviolet rays is preferably about 50 to 1000 mW / cm ^{2 in} illuminance. Further, the light quantity is preferably 50~10000mJ / cm ^2, more preferably 80~5000mJ / cm ^2, and particularly preferably 200~2000mJ / cm ^2. On the other hand, the electron beam irradiation can be performed by an electron beam accelerator or the like, and the electron beam irradiation amount is preferably about 10 to 1000 krad.

  The laminated body of the coating film of the adhesive composition P and the peeling sheet 14 can be produced as follows, for example.

  The above-mentioned adhesive composition P and a coating solution containing a solvent as required are applied to the release surface of the release sheet 14 and subjected to heat treatment to form a coating film of the adhesive composition P.

  The heat treatment can also serve as a drying treatment for volatilizing the diluted solvent of the coating solution. When performing heat processing, it is preferable that heating temperature is 50-150 degreeC, and it is especially preferable that it is 70-120 degreeC. The heating time is preferably 30 seconds to 10 minutes, particularly preferably 50 seconds to 2 minutes.

  After the hard coat layer 12 on the substrate 11 and the coating film of the adhesive composition P on the release sheet 14 are bonded, curing is performed. This curing is usually performed at room temperature (for example, 23 ° C., 50% RH) for about 1 to 2 weeks. Thereby, the coating film of the adhesive composition P becomes the adhesive layer 13, and the adhesive layer 13 adhered to the hard coat layer 12 is formed.

  As another manufacturing method of the battery pressure-sensitive adhesive sheet 1 according to the present embodiment, a hard coat layer 12 (before curing) is formed on a substrate 11, and the adhesive composition is directly applied to the hard coat layer 12 (before curing). After forming the coating film of the thing P, you may form the adhesive layer 13 closely_contact | adhered to the hard-coat layer 12 by curing.

[Lithium ion battery]
The lithium ion battery which concerns on one Embodiment of this invention is fixed in the state in which two or more conductors contacted inside the battery using the adhesive sheet for batteries mentioned above. It is preferable that at least one of the two or more conductors has a sheet shape, and at least one has a linear shape or a tape shape. Hereinafter, a lithium ion battery according to a preferred embodiment will be described.

  As shown in FIG. 2, the lithium ion battery 2 according to this embodiment includes a bottomed cylindrical exterior body 21 whose bottom portion forms a negative electrode terminal 23, and a positive electrode terminal 22 provided in an opening of the exterior body 21. And an electrode body 24 provided inside the exterior body 21. In addition, an electrolytic solution is sealed inside the lithium ion battery 2.

  The electrode body 24 has a sheet-like (band-like) positive electrode current collector 241 in which a positive electrode active material layer 241a is laminated, a negative electrode current collector 242 in which a negative electrode active material layer 242a layer is laminated, and a gap between them. And an intervening separator 243. Note that the stacked body of the positive electrode current collector 241 and the positive electrode active material layer 241a may be referred to as a positive electrode, and the stacked body of the negative electrode current collector 242 and the negative electrode active material layer 242a may be referred to as a negative electrode. Sometimes referred to as an electrode. The positive electrode, the negative electrode, and the separator 243 are each wound and inserted into the exterior body 21.

  Further, as shown in FIG. 3, a linear or tape-shaped electrode take-out tab 244 is attached to the positive electrode current collector 241 by the battery adhesive sheet 1 described above, whereby the electrode take-out tab 244 is The positive electrode current collector 241 is electrically connected. The electrode extraction tab 244 is also electrically connected to the positive terminal 22. The negative electrode current collector 242 is electrically connected to the negative electrode terminal 23 via an electrode extraction tab (not shown).

  In general, the positive electrode current collector 241 and the negative electrode current collector 242 are made of a metal such as aluminum, and the electrode extraction tab 244 is made of a metal such as aluminum or copper.

The electrolytic solution used in the lithium ion battery 2 is usually a non-aqueous electrolytic solution. As this non-aqueous electrolytic solution, for example, a lithium salt as an electrolyte is preferably dissolved in a mixed solvent of a cyclic carbonate and a lower chain carbonate. Examples of the lithium salt include fluorine-based complex salts such as lithium hexafluorophosphate (LiPF ₆ ) and lithium borofluoride (LiBF ₄ ), LiN (SO ₂ Rf) ₂ .LiC (SO ₂ Rf) ₃ (where Rf = CF ₃ , C ₂ F ₅ ) or the like is used. Further, as the cyclic carbonate, ethylene carbonate, propylene carbonate and the like are used, and as the lower chain carbonate, dimethyl carbonate, ethyl methyl carbonate, diethyl carbonate and the like are preferably mentioned.

  The lithium ion battery 2 according to the present embodiment can be manufactured by a normal method except that the battery adhesive sheet 1 described above is used for fixing the electrode extraction tab 244.

  In the lithium ion battery 2 according to the present embodiment, the electrode extraction tab 244 is attached to the positive electrode 241 with the battery pressure-sensitive adhesive sheet 1. In this battery pressure-sensitive adhesive sheet 1, by providing the hard coat layer 12 between the base material 11 and the pressure-sensitive adhesive layer 13, the amount of the electrolyte solution entering the pressure-sensitive adhesive layer 13 is reduced. The battery pressure-sensitive adhesive sheet 1 is kept from being peeled off from the adherend. Moreover, the quantity of the component of the adhesive layer 13 which elutes in an electrolyte solution reduces because the quantity of the electrolyte solution which penetrates into the adhesive layer 13 reduces. Thereby, the malfunction of the battery using the adhesive sheet 1, thermal runaway, and a short circuit are suppressed.

  Furthermore, even if the said adhesive sheet 1 for batteries is the state immersed in nonaqueous electrolyte solution, the adhesiveness of the hard-coat layer 12 and the adhesive layer 13, and the adhesiveness of the hard-coat layer 12 and the base material 11 It is excellent in property and it is suppressed that peeling occurs between those layers.

  Furthermore, since the said adhesive sheet 1 for batteries is equipped with the hard-coat layer 12, even if it is a case where the base material 11 and the adhesive layer 13 are carbonized, insulation can be ensured.

  From the above, the lithium ion battery 2 according to the present embodiment is highly reliable as a battery with reduced performance, malfunction, thermal runaway, and short circuit due to the pressure-sensitive adhesive sheet. It is expected to be excellent in temperature stability and safety even under current conditions.

  The embodiment described above is described for facilitating understanding of the present invention, and is not described for limiting the present invention. Therefore, each element disclosed in the above embodiment is intended to include all design changes and equivalents belonging to the technical scope of the present invention.

  For example, in the battery pressure-sensitive adhesive sheet 1, the release sheet 14 may be omitted. In the battery pressure-sensitive adhesive sheet 1, another layer may be provided between the base material 11 and the hard coat layer 12 or between the hard coat layer 12 and the pressure-sensitive adhesive layer 13.

  EXAMPLES Hereinafter, although an Example etc. demonstrate this invention further more concretely, the scope of the present invention is not limited to these Examples etc.

[Example 1]
1. Formation of hard coat layer on substrate 40 parts by mass of dipentaerythritol hexaacrylate (a material in which a glass transition point is not observed after curing) as an active energy ray-curable component, and 5 mass of hydroxycyclohexyl phenyl ketone as a photopolymerization initiator Parts, organosilica sol (manufactured by Nissan Chemical Co., Ltd., trade name “MEK-ST”; average particle size 30 nm) 60 parts by mass (solid content conversion value; the same applies hereinafter), and trimethylolpropane as a thermal crosslinking agent A coating solution for a hard coat layer was prepared by mixing 10 parts by mass of modified hexamethylene diisocyanate (manufactured by Nippon Polyurethane Industry Co., Ltd., trade name “Coronate HL”) and diluting with methyl ethyl ketone.

After applying the above coating solution with a knife coater on one surface of a polyimide film (trade name “Kapton 100H”, thickness 25 μm, flame resistance level V-0 of UL94 standard, manufactured by Toray DuPont, Inc.) as a base material, Dry at 70 ° C. for 1 minute. Next, the said coating film was hardened by irradiating the ultraviolet-ray (illuminance 230mW / cm < ² >, light quantity 510mJ / cm < ² >) with respect to the coating film. This obtained the 1st laminated body in which the hard-coat layer of thickness 2 micrometers was formed in the one surface of a base material.

2. Formation of coating film of adhesive composition on release sheet 76.8 parts by mass of butyl acrylate, 19.2 parts by mass of methyl acrylate and 4 parts by mass of acrylic acid were copolymerized by a solution polymerization method to obtain (meth) acrylic. An acid ester polymer was prepared. When the molecular weight of this polymer was measured using gel permeation chromatography (GPC) described later, the weight average molecular weight (Mw) was 1,000,000.

  Next, 100 parts by mass of the obtained (meth) acrylic acid ester polymer and aluminum tris (acetylacetonate) as a metal chelate-based crosslinking agent (manufactured by Soken Chemical Co., Ltd., trade name “M-5A”) 0.93 By mixing 0.5 parts by mass of 3-glycidoxypropylmethyldimethoxysilane (trade name “KBM-403”, manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent and diluting with methyl ethyl ketone, A coating liquid for the composition was prepared.

  The obtained coating solution was applied to a release treatment surface of a release sheet (trade name “PET251130”, manufactured by Lintec Corporation) on one side of a polyethylene terephthalate film with a silicone release agent, and then applied at 120 ° C. Heat-treated for minutes. Thereby, the 2nd laminated body by which the coating film of the adhesive composition was laminated | stacked on the peeling process surface of the peeling sheet was obtained.

3. Preparation of battery pressure-sensitive adhesive sheet The hard coat layer side surface of the first laminate produced as described above and the coating layer side surface of the second laminate produced as described above were bonded together. Then, it was cured at 23 ° C. and 50% RH for 7 days. Thereby, the adhesive sheet for batteries in which the coating film of the adhesive composition became an adhesive layer was obtained. The pressure-sensitive adhesive layer had a thickness of 7 μm. The thickness of the pressure-sensitive adhesive layer was calculated by obtaining the total thickness of the battery pressure-sensitive adhesive sheet and subtracting the thickness of the first laminate and the release sheet from the total thickness.

[Example 2]
40 parts by mass of dipentaerythritol hexaacrylate (a material in which a glass transition point is not observed after curing) as an active energy ray-curable component, 5 parts by mass of hydroxycyclohexyl phenyl ketone as a photopolymerization initiator, and an organosilica sol as an inorganic filler (Nissan Chemical Co., Ltd., trade name “MEK-ST”; average particle size 30 nm) 60 parts by mass and trimethylolpropane-modified hexamethylene diisocyanate as a thermal crosslinking agent (manufactured by Nippon Polyurethane Industry Co., Ltd., trade name “Coronate HL”) A hard coat layer coating solution was prepared by mixing 5 parts by mass and diluting with methyl ethyl ketone. A battery pressure-sensitive adhesive sheet was produced in the same manner as in Example 1 except that the obtained hard coat layer coating solution was used as the hard coat layer coating solution.

[Comparative Example 1]
40 parts by mass of dipentaerythritol hexaacrylate (a material in which a glass transition point is not observed after curing) as an active energy ray-curable component, 5 parts by mass of hydroxycyclohexyl phenyl ketone as a photopolymerization initiator, and an organosilica sol as an inorganic filler 60 parts by mass (manufactured by Nissan Chemical Co., Ltd., trade name “MEK-ST”; average particle size 30 nm) was mixed and diluted with methyl ethyl ketone to prepare a hard coat layer coating solution. A battery pressure-sensitive adhesive sheet was produced in the same manner as in Example 1 except that the obtained hard coat layer coating solution was used as the hard coat layer coating solution.

Here, the above-mentioned weight average molecular weight (Mw) is a weight average molecular weight in terms of standard polystyrene measured (GPC measurement) using gel permeation chromatography (GPC) under the following conditions.
<Measurement conditions>
GPC measurement device: manufactured by Tosoh Corporation, HLC-8020
GPC column (passed in the following order): TSK guard column HXL-H manufactured by Tosoh Corporation
TSK gel GMHXL (× 2)
TSK gel G2000HXL
・ Measurement solvent: Tetrahydrofuran ・ Measurement temperature: 40 ° C.

[Test Example 1] (Steel Wool Resistance Test)
About the surface of the hard-coat layer in the 1st laminated body obtained in the case of manufacture of the adhesive sheet for batteries of an Example and a comparative example, it is 10 cm with a load of 250 g / cm < ² > using # 0000 steel wool. The surface of the hard coat layer was evaluated according to the following criteria. The results are shown in Table 1.
◯: No linear scratch was observed.
X: A linear wound was seen.

[Test Example 2] (Measurement of gel fraction by immersion in electrolyte solution)
The surface on the coating film side of the adhesive composition of the second laminate obtained in the production of the pressure-sensitive adhesive sheets for batteries of Examples and Comparative Examples and one surface of the polyethylene terephthalate film were peeled with a silicone release agent. The release sheet (trade name “PET251130”, manufactured by Lintec Corporation) was attached to the release-treated surface. Then, it cured for 7 days at 23 degreeC and 50% RH, and obtained the sheet | seat for a measurement which consists of an adhesive layer single side by which both surfaces were protected by the peeling sheet.

  The obtained measurement sheet is cut into a size of 80 mm × 80 mm, the release sheet protecting both sides of the pressure-sensitive adhesive layer is peeled off, wrapped in a polyester mesh (mesh size 200), and its mass is weighed with a precision balance. By subtracting the mass of the mesh alone, the mass of the pressure-sensitive adhesive alone was calculated. The mass at this time is M1. Next, the pressure-sensitive adhesive wrapped in the polyester mesh was immersed in a preparation solution in which ethylene carbonate and diethyl carbonate as an electrolyte solvent were mixed at a volume ratio of 1: 1 at 80 ° C. for 72 hours. Thereafter, the pressure-sensitive adhesive layer is taken out and once immersed in ethanol, the attached electrolyte solvent is dissolved and removed, and then air-dried in an environment of a temperature of 23 ° C. and a relative humidity of 50% for 24 hours. The inside was dried for 12 hours. After drying, the mass was weighed with a precision balance, and the mass of the pressure sensitive adhesive alone was calculated by subtracting the mass of the mesh alone. The mass at this time is M2. The gel fraction (%) was calculated from the formula (M2 / M1) × 100. The results are shown in Table 1.

[Test Example 3] (Measurement of adhesive strength before immersion in electrolyte solution)
The adhesive strength of the adhesive sheet for batteries according to this test example was measured according to JIS Z0237: 2009 except for the operations described below.

  The battery pressure-sensitive adhesive sheets obtained in Examples and Comparative Examples were cut into a width of 25 mm and a length of 250 mm, and then the release sheet was peeled to obtain a test piece. The exposed adhesive layer of the test piece was attached to an aluminum plate as an adherend using a 2 kg rubber roller in an environment of 23 ° C. and 50% RH. Immediately thereafter, the test piece is peeled off from the aluminum plate at a peeling angle of 180 ° and a peeling speed of 300 mm / min using a universal type tensile tester (made by Orientec, trade name “Tensilon UTM-4-100”). Was used to measure the adhesive strength (N / 25 mm). This measured value was taken as the adhesive strength before immersion in the electrolyte solvent. The results are shown in Table 1.

[Test Example 4] (Measurement of adhesive strength after immersion in electrolyte solution)
The adhesive strength of the adhesive sheet for batteries according to this test example was measured according to JIS Z0237: 2009 except for the operations described below.

  The battery pressure-sensitive adhesive sheets obtained in Examples and Comparative Examples were cut into a width of 25 mm and a length of 250 mm, and then the release sheet was peeled to obtain a test piece. The exposed adhesive layer of the test piece was attached to an aluminum plate as an adherend using a 2 kg rubber roller in an environment of 23 ° C. and 50% RH, and left in the same environment for 20 minutes. Then, with the test piece stuck to the aluminum plate, it was immersed for 72 hours at 80 ° C. in a preparation solution in which ethylene carbonate and diethyl carbonate as an electrolyte solvent were mixed at a volume ratio of 1: 1. And immediately after taking out from a preparation liquid, adhesive force (N / 25mm) was measured like the above. This measured value was taken as the adhesive strength after immersion in the electrolyte solution. The results are shown in Table 1.

  In the above test, in the battery pressure-sensitive adhesive sheet of the example, peeling did not occur between the pressure-sensitive adhesive layer and the base material (hard coat layer). Peeling occurred with the material (hard coat layer). From this result, it was found that the battery pressure-sensitive adhesive sheet of the example was excellent in adhesion between the pressure-sensitive adhesive layer and the hard coat layer (base material) even after being immersed in the electrolyte solution solvent.

[Test Example 5] (Evaluation of adhesive layer adhesion)
The release sheet was peeled from the battery pressure-sensitive adhesive sheets obtained in Examples and Comparative Examples, and parallel cuts were made at intervals of 2 mm into the exposed pressure-sensitive adhesive layer, which was used as a test piece. The pressure-sensitive adhesive layer of the test piece is rubbed with a finger at a force of 1.96 N from the vertical direction with respect to the pressure-sensitive adhesive layer, and the presence or absence of peeling of the pressure-sensitive adhesive layer is observed. (Before electrolytic solution solvent immersion) was evaluated. The results are shown in Table 1.
A: There was no peeling of the adhesive layer.
○: The adhesive layer was slightly peeled only around the notch.
X: The entire surface of the pressure-sensitive adhesive layer was peeled off.

  Moreover, said test piece was immersed for 72 hours at 80 degreeC in the preparation liquid which mixed ethylene carbonate and diethyl carbonate by the volume ratio of 1: 1 as electrolyte solution solvent. And after taking out from a preparation liquid, the adhesive layer surface of a test piece is lightly wiped with a paper waste (Nippon Paper Crecia Co., Ltd., brand name "Kimwipe S-200"), and the adhesiveness ( After immersion in the electrolyte solvent). The results are shown in Table 1.

  As is clear from Table 1, the battery pressure-sensitive adhesive sheets of the examples showed high adhesive strength (50% or more with respect to the adhesive strength before immersion in the electrolyte solution solvent) even after being immersed in the electrolyte solution solvent. In addition, the pressure-sensitive adhesive layer of the battery pressure-sensitive adhesive sheet of the example exhibited high adhesion with the base material (hard coat layer) even after being immersed in the electrolyte solvent.

  The pressure-sensitive adhesive composition and battery pressure-sensitive adhesive sheet according to the present invention are suitable for attaching an electrode take-out tab to an electrode (current collector) inside a lithium ion battery.

DESCRIPTION OF SYMBOLS 1 ... Battery adhesive sheet 11 ... Base material 12 ... Hard coat layer 13 ... Adhesive layer 14 ... Release sheet 2 ... Lithium ion battery 21 ... Exterior body 22 ... Positive electrode terminal 23 ... Negative electrode terminal 24 ... Electrode body 241 ... Positive electrode current collection Body 241a ... Positive electrode active material layer 242 ... Negative electrode current collector 242a ... Negative electrode active material layer 243 ... Separator 244 ... Electrode extraction tab

Claims (7)

A substrate;
A hard coat layer provided on one surface side of the substrate;
A pressure-sensitive adhesive layer provided on the surface of the hard coat layer opposite to the base material;
The battery pressure-sensitive adhesive sheet, wherein the hard coat layer is formed from a composition for a hard coat layer containing a thermal crosslinking agent.   The battery pressure-sensitive adhesive sheet according to claim 1, wherein the thermal crosslinking agent is an isocyanate-based crosslinking agent.   The battery pressure-sensitive adhesive sheet according to claim 1, wherein the hard coat layer composition contains the thermal crosslinking agent, an active energy ray-curable component, and an inorganic filler.   The said base material is a film which consists of a polymer which has a nitrogen-containing ring structure in a principal chain, The adhesive sheet for batteries as described in any one of Claims 1-3 characterized by the above-mentioned.   The said adhesive layer is formed from the adhesive composition containing a (meth) acrylic ester polymer, The adhesive sheet for batteries as described in any one of Claims 1-4 characterized by the above-mentioned. . A battery pressure-sensitive adhesive sheet comprising: a base material; a hard coat layer provided on one surface side of the base material; and a pressure-sensitive adhesive layer provided on a surface of the hard coat layer opposite to the base material. A manufacturing method comprising:
A hard coat layer formed by irradiating an active energy ray to a coating film of a composition for a hard coat layer containing at least an active energy ray-curable component and a thermal cross-linking agent, which is applied to one surface side of a substrate; A method for producing a pressure-sensitive adhesive sheet for a battery, comprising forming a pressure-sensitive adhesive layer in close contact with the hard coat layer by laminating a coating film of an adhesive composition and then curing.   Lithium ion, wherein two or more conductors are fixed in contact with each other using the battery adhesive sheet according to any one of claims 1 to 5 inside the battery. battery.

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