ELECTRODE CURRENT COLLECTOR AND SECONDARY BATTERY

Abstract

The present disclosure can improve activation stability of the current cut-off function of the electrode current collector. The electrode current collector 10 disclosed herein includes a sheet-like resin base material 12, and a metal thin film 14 provided on a surface 12a, 121 of the resin base material 12. in the electrode current collector 10 disclosed herein, the surface 12a. 12b of the resin base material 12 in contact with the metal thin films 14 has a surface rough ness Rz of 2 μm or more. This can largely improve the adhesion between the resin base material 12 and the metal thin film 14. Thus, when abnormal heat generation occurs, the resin base material 12 is melted and deformed so as to pull the metal thin film 14, thereby breaking the metal thin films 14. As a result, the current cut-off function can be stably activated, and the progression of abnormal heat generation can be substantially prevented, as appropriate.

Claims

1. An electrode current collector for a secondary battery, the electrode current collector comprising: a sheet-like resin base material; and a metal thin film provided on a surface of the resin base material, wherein the surface of the resin base material in contact with the metal thin film has a surface roughness Rz of 2 μm or more.

2. The electrode current collector according to claim 1, wherein the resin base material is made of a resin material having a melting start temperature of 95° C. to 300° C.

3. The electrode current collector according to claim 2, wherein the resin material includes at least one selected from the group consisting of low-density polyethylene, high-density polyethylene, polypropylene, polyolefin, and polyethylene terephthalate.

4. The electrode current collector according to claim 1, wherein the resin base material has a surface roughness Rz of 15 μm or less.

5. The electrode current collector according to claim 1, wherein the resin base material has a thickness t1 of 10 μm or more to 40 μm or less.

6. The electrode current collector according to claim 1, wherein the metal thin film has a film thickness t2 of 2 μm or more.

7. The electrode current collector according to claim 1, wherein the surface roughness Rz of the resin base material and the film thickness t2 of the metal thin film satisfy the following equation (1):
Rz−t2≥−3   (1).

8. A secondary battery comprising: a pair of electrodes consisting of a positive electrode and a negative electrode, wherein at least one of the pair of electrodes comprises: an electrode current collector, and an electrode active material layer provided on a surface of the electrode current collector, and the electrode current collector is the electrode current collector according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] FIG. 1 is a schematic cross-sectional view of an electrode current collector according to an embodiment.

[0017] FIG. 2 is a schematic cross-sectional view of a secondary battery according to an embodiment.

[0018] FIG. 3 is a schematic cross-sectional view of a configuration of a wound electrode body of a secondary battery according to an embodiment.

DETAILED DESCRIPTION

[0019] The following describes an embodiment of the present disclosure with reference to the drawings. The matters necessary for executing the present disclosure (e.g., materials and structures of members except for the electrode current collector), except for matters specifically herein referred to can be grasped as design matters of those skilled in the art based on the related art in the preset field. The present disclosure can be executed based on the contents disclosed herein and the technical knowledge in the present field. In the following drawings which are referred to in the following description, the same members/portions which exhibit the same action are denoted by the same reference numeral. The dimensional relation (such as length, width, or thickness) in each drawing does not reflect the actual dimensional relation.

[0020] 1. Electrode Current Collector

[0021] An embodiment of the electrode current collector disclosed herein will be described below with reference to FIG. 1. FIG. 1 is a schematic cross-sectional view of the electrode current collector according to this embodiment.

[0022] The electrode current collector 10 illustrated in FIG. 1 is used in an electrode for a secondary battery. As will be described in detail later, electrode active material layers are provided on the respective surfaces of the electrode current collector 10, thereby producing an electrode for a secondary battery. Although the present disclosure is not limited thereto, the total thickness T of the electrode current collector 10 is preferably 5 μm or more, more preferably 6 μm or more, particularly preferably 10 μm or more, in light of the mechanical strength of the electrode current collector 10. On the other hand, when the total thickness T of the electrode current collector 10 is small, the voltage of the electrode active material layer can be increased relative to the capacity of the secondary battery, which can contribute to a higher energy density. In light of this fact, the total thickness T of the electrode current collector 10 is preferably 20 μm or less, more preferably 18 μm or less, particularly preferably 15 μm or less. Further, the plane shape of the electrode current collector 10 is not particularly limited, and can he changed, as appropriate, according to the shape of the electrode to be produced. For example, various shapes such as stripe, rectangular, circular, and elliptical shapes can be employed as a plane shape of the electrode current collector 10 without particular limitations.

[0023] The electrode current collector 10 according to the present embodiment has a lamination structure where the surfaces of the resin base material 12 are covered with the metal thin films 14. As mentioned above, the electrode current collector 10 having this type of lamination structure has a current cut-off function of melting and deforming the resin base material 12 and thus breaking the metal thin film 14 at the time when abnormal heat generation occurs due to internal short-circuit. The electrode current collector 10 according to the present embodiment is configured to stably activate the current cut-off function, and appropriately prevent the progression of abnormal heat generation. The following describes each layer constituting the electrode current collector 10 in detail.

[0024] (1) Resin Base Material

[0025] The resin base material 12 is a sheet-like resin member. The resin material constituting the resin base material 12 can be selected from known resin materials, as appropriate, in consideration of the temperature environment of the secondary battery to be used during normal use and during abnormal heat generation. For example, for a lithium ion secondary battery, the temperature environment during normal use may be −10° C. to 70° C., and the temperature environment during abnormal heat generation may be 100° C. or more. The resin material of the resin base material 12 preferably holds its shape during normal use, and is melted and deformed during abnormal heat generation, in consideration of such temperature environments. In light of more appropriately preventing melting and deforming during normal use, the melting start temperature of the resin material of the resin base material 12 is preferably 90° C. or more, more preferably 95° C. or more, particularly preferably 100° C. or more. In light of more appropriately melting and deforming during abnormal heat generation, the melting start temperature of the resin material of the resin base material 12 is preferably 300° C. or less, more preferably 275° C. or less, particularly preferably 250° C. or less. Examples of the resin material satisfying the melting start temperature include low density polyethylene (the melting start temperature: 95° C. to 130° C.), high density polyethylene (the melting start temperature: 120° C. to 140° C.), polypropylene (the melting start temperature: 168° C.), polyolefin (the melting start temperature: 120° C. to 140° C.), and polyethylene terephthalate (the melting start temperature: 265° C.).

[0026] In the electrode current collector 10 according to the present embodiment, the surface roughness Rz of each of the surfaces 12a, 12b of the resin base material 12 in contact with the metal thin films 14 is set to 2 μm or more. This allows the metal thin films 14 to be broken when abnormal heat generation occurs, thereby stably activating the current cut-off function of the electrode current collector 10. Specifically, in the electrode current collector 10 according to the present embodiment, the surface roughness Rz of each of the surfaces 12a, 12b of the resin base material 12 is set to 2 μm or more, thereby largely improving the adhesion between the resin base material 12 and the metal thin films 14. This makes it possible to melt and deform the resin base material 12 so as to pull the metal thin films 14 when abnormal heat generation occurs. Accordingly, the metal thin films 14 are broken to stably activate the current cut-off function.

[0027] The larger the surface roughness Rz of the resin base material 12, the higher the adhesion between the resin base material 12 and the metal thin films 14, which tends to improve activation stability of the current cut-off function. In light of this fact, the surface roughness Rz of each of the surfaces 12a, 12b of the resin base material 12 is preferably 2.5 μm or more, more preferably 3 μm or more, particularly preferably 3.5 μm or more. In light of improvement in activation stability of the current cut-off function, the upper limit of the surface roughness Rz of the resin base material 12 is not particularly limited. However, if the surface roughness Rz of each of the surfaces 12a, 12b of the resin base material 12 is reduced, it becomes easier to form metal thin films 14 on the surfaces 12a, 12b of the resin base material 12. in light of this fact, the surface roughness Rz of each of the surfaces 12a, 12b of the resin base material 12 is preferably 15 μm or less, more preferably 10 μm or less, particularly preferably 5 μm or less.

[0028] The “surface roughness Rz” herein is “10-point average height” defined in JIS B601. The 10-point average height represents a difference value between the mean value of the heights of the five tallest peaks and the mean of the depths of the five deepest valleys, measured from a line parallel to the average line of the reference length cut from the cross-sectional curve and not crossing the cross-sectional curve, in the direction perpendicular to the average fine.

[0029] A means for adjusting the surface roughness Rz of the resin base material 12 to be in the above-mentioned range is not particularly limited, and various known surface processing means may be employed. For example, a file or the like is used to make fine scratches on the surfaces 12a and 12b of the resin base material 12, whereby the resin base material 12 having a desired surface roughness Rz can be obtained. The roughing process on the surfaces 12a and 12b of the resin base material 12 is not limited to tiling described above, but may also be performed by chemical action using chemicals or the like.

[0030] The film thickness t1 of the resin base material 12 is preferably adjusted, as appropriate, inconsideration of the activation stability of the current cut-off function. Specifically, the larger the film thickness t1 of the resin base material 12, the larger the amount of deformation of the resin base material 12 at the time when the abnormal heat generation occurs, which makes is easier to break the metal thin films 14. In light of this fact, the film thickness t1 of the resin base material 12 is preferably 1 μm or more, more preferably 5 μm or more, particularly preferably 10 μm or more. The resin base material 12 does not influence directly on the battery performance (e.g., the battery resistance, the energy density) of the secondary battery. Thus, if a certain level or more of the activation stability is ensured, the film thickness t1 of the resin base material 12 is preferably made low. For example, the film thickness t1 of the resin base material 12 is preferably 50 μm or less, more preferably 45 μm or less, particularly preferably 40 μm or less. This allows the volumes of the metal thin films 14 and the electrode active material layer to be ensured sufficiently. This can contribute to the improvement in the function of the secondary battery.

[0031] (2) Metal Thin Film

[0032] The metal thin films 14 are thin films provided on the surfaces of the resin base material 12. The metal thin films 14 each contain a metal material having predetermined electroconductivity as a main component. Examples of an electroconductive metal contained in each metal thin film 14 include aluminum, copper, nickel, and titanium. The metal thin film 14 may contain an element other than the electroconductive metal. For example, the metal thin film 14 may be made of an alloy material (such as SUS) containing the above-mentioned electroconductive metal. The metal thin film 14 may contain inevitable impurities generated in the manufacturing processes. Further, the electroconductive metal which is a main component of the metal thin film 14 is preferably changed, as appropriate, according to the electrode to be produced. For example, for a current collector (positive electrode current collector) used in a positive electrode of a lithium ion secondary battery, the metal thin film 14 preferably contains aluminum as a main component. For example, for a current collector (negative electrode current collector) used in a negative electrode of a lithium ion secondary battery, the metal thin film 14 preferably contains copper as a main component.

[0033] A means for forming the metal thin films 14 on the respective surfaces of the resin base material 12 is not particularly limited, and known means can be employed without particular limitations. For example, the metal thin films 14 may be formed by vapor deposition of the metal material on the respective surfaces of the resin base material 12 using physical vapor deposition such as a vacuum vapor deposition. Alternatively, the metal thin films 14 may be formed on the respective surfaces of the resin base material 12 also by pressure bonding of metal foil, which has been formed separately, to the respective surfaces of the resin base material 12.

[0034] Similarly to the film thickness ti of the resin base material 12, the film thickness t2 of each of the metal thin films 14 is also preferably adjusted, as appropriate, in consideration of activation stability of the current cut-off function. Specifically, the smaller the film thickness t2 of the metal thin film 14, the easier the metal thin film 14 is broken at the time when the abnormal heat generation occurs, which tends to improve activation stability of the current cut-off function. In light of this fact, the film thickness t2 of each metal thin film 14 is preferably 10 urn or less, more preferably 7.5 μm or less, particularly preferably 5 μm or less. In contrast, in the electrode current collector 10 according to the present embodiment, the resin base material 12 having rough surface is melted and deformed so as to pull the metal thin films 14. Accordingly, the current cut-off function can be sufficiently activated even when the film thickness t2 of each of the metal thin films 14 is made larger than before. Thus, according to the present embodiment, the metal thin films 14 each having a film thickness t2 of 2 μm or more, which is higher than before, can also be termed to decrease the battery resistance. In the electrode current collector 10 according to the present embodiment, the battery resistance can be reduced by increasing the film thickness t2 of each of the metal thin films 14 to 2.5 μm or more (more suitably, 3 μm or more).

[0035] As a result of study, the present inventors confirmed that the activation stability of the current cut-off function can be further improved by adjusting the surface roughness Rz of the resin base material 12 and the film thickness t2 of each of the metal thin films 14 so as to satisfy the following equation (1). In light of more suitably improving the activation stability of the current cut-off function, the difference (Rz−t2) between the surface roughness Rz of the resin base material 12 and the film thickness t2 of each of the metal thin films 14 is preferably −2.5 or more, more preferably −2 or more.

Rz−t2≥−3   (1)

[0036] In light of achieving both of the activation stability of the current cut-off function and the electrode current collector 10 at high level, it is preferred that the above-mentioned equation (1) is satisfied, and the film thickness t2 of each of the metal thin films 14 is set to 2 μm or more.

[0037] (3) Other Embodiments

[0038] An embodiment of the electrode current collector disclosed herein was described above. The embodiment is not intended to limit the present disclosure. For example, in the embodiment, the metal thin films 14 are formed on the both surfaces 12a, 12b of the resin base material 12, and the surface roughness Rz of each of the surfaces 12a, 12b is adjusted to 2 μm or more. However, if the electrode active material layer is provided on only one surface of the electrode current collector, the metal thin film may be formed on only one surface of the resin base material. In this case, the surface of the resin base material in contact with the metal thin film may be subjected to rough surface processing to have a surface roughness Rz of 2 μm or more. The electrode current collector disclosed herein may include a layer besides the resin base material and the metal thin film. An example of the layer other than the resin base material and the metal thin film can be, a corrosion-resistant layer containing a carbon material as a main component. The corrosion-resistant layer formed on the surface of the metal thin film can substantially prevent corrosion of the metal thin film in contact with the electrode active material layer.

[0039] 2. Secondary Battery

[0040] Next, a secondary battery including the electrode current collector 10 according to the above-mentioned embodiment will be described. FIG. 2 is a schematic cross-sectional view of the secondary battery according to this embodiment. FIG. 3 is a schematic cross-sectional view of a configuration of a wound electrode body of a secondary battery according to this embodiment. In FIGS. 2 and 3, the reference X indicates the “width direction”, and the reference Z indicates the “height direction.” Such directions are defined for convenience of explanation and are not intended to limit the installation configuration of the secondary battery described below.

[0041] As shown in FIG. 2, the secondary battery 100 according to this embodiment includes a battery case 20 and an electrode body 30. As shown in FIG. 3. the electrode body 30 of the secondary battery 100 includes a pair of electrodes consisting of a positive electrode 40 and a negative electrode 50. In the present embodiment, the electrode current collector 10 according to the embodiment is used in each of current collectors (a positive electrode current collector 42 and a negative electrode current collector 52) of the electrodes. The following describes a specific structure of the secondary battery 100 according to the present embodiment.

[0042] (1) Battery Case

[0043] The battery case 20 is a container housing an electrode body 30. As shown in FIG. 2, the battery case 20 according to the present embodiment includes a flat, rectangular case body 22 having an opening in its upper surface and a lid 24 closing the opening of the case body 22. The case body 22 and the lid 24 are each made of a metal material such as aluminum. Further, to the lid 24, a positive electrode terminal 26 and a negative electrode terminal 28 are attached. An upper end 26a of the positive electrode terminal 26 is exposed to the outside of the battery case 20, and a lower end 26b of the same is connected to the positive electrode 40 of the electrode body 30 inside the battery case 20. Similarly, an upper end 28a of the negative electrode terminal 28 is exposed to the outside of the battery case 20, and a lower end 28b of the same is connected to a negative electrode 50 of the electrode body 30 inside the battery case 20. The lid 24 is provided with a safety valve 29 for discharging gas generated inside the battery case 20. The battery case 20 according to the present embodiment houses a nonaqueous electrolyte 70 in addition to the electrode body 30. Components of the nonaqueous electrolyte 70 can be those which can be used in commonly used secondary batteries can be used without particular limitations, and do not limit the present disclosure. Thus, the detailed description of the nonaqueous electrolyte 70 is omitted.

[0044] The battery case is not particularly limited as long as it can house the electrode body, and may not be a rectangular case made of metal as shown in FIG. 2. The shape of the battery case may be, for example, a circular shape (a cylindrical shape, a coin shape, and a button shape). Further, the material of the battery case may not be a metal material. For example, the secondary battery disclosed herein may he a laminated battery where an electrode body and a nonaqueous electrolyte are encapsulated inside a bag-shaped laminate film.

[0045] (2) Electrode Body

[0046] As shown in FIG. 3, the electrode body 30 includes a long sheet-shaped positive electrode 40, a long sheet-shaped negative electrode 50, and a separator 60. Specifically, the electrode body 30 in the present embodiment is a wound electrode body obtained by winding a laminate obtained by stacking two separators 60 via the positive electrode 40 and the negative electrode 50, in the longitudinal direction.

[0047] The positive electrode 40 includes a positive electrode current collector 42, and a positive electrode active material layer 44 provided on each of the surfaces (both surfaces) of the positive electrode current collector 42. As mentioned above, in the present embodiment, the electrode current collector 10 having the above-described configuration (see FIG. 1) is used in the positive electrode current collector 42. The positive electrode active material layer 44 is a layer containing a positive electrode active material as a main component, and is provided on the surface of each of the metal thin films 14 (see FIG. 1) of the electrode current collector 10. The positive electrode active material layer 44 may further contains additives such as a binder and an electroconductive material in addition to the positive electrode active material. Materials contained in the positive electrode active material layer 44 can be those which can be used in commonly used secondary batteries without particular limitations, and do not limit the present disclosure. Thus, the detailed description is omitted. One side edge of the positive electrode 40 in the width direction (the left side edge in FIG. 3) is not provided with the positive electrode active material layer 44, and on the side edge, a positive electrode exposed portion 46 to which the positive electrode current collector 42 is exposing is formed. As shown in FIG. 2, a positive electrode terminal 26 is connected to a positive electrode connection portion 30a which is a wound positive electrode exposed portion 46. Accordingly, an electroconductive path to which the positive electrode terminal 26 and the positive electrode active material layer 44 are electrically connected via the metal thin film of the positive electrode current collector 42 is constructed.

[0048] As shown in FIG. 3, the negative electrode 50 includes a negative electrode current collector 52 and a negative electrode active material layer 54 provided on each of the surfaces (both surfaces) of the negative electrode current collector 52. In the present embodiment, the electrode current collector 10 having a configuration shown in FIG. 1 is used also in the negative electrode current collector 52. The negative electrode active material layer 54 is a layer containing a negative electrode active material as a main component, and is provided on the surface of each of the metal thin films 14 (see FIG. 1) of the electrode current collector 10. The negative electrode active material layer 54 may further contain additives such as a binder and a thickener besides the negative electrode active material. Materials contained in the negative electrode active material layer 54 can be those which can be used in commonly used secondary batteries without particular limitations, and do not limit the present disclosure. Thus, the detailed description is omitted. One side edge of the negative electrode 50 in the width direction (the right side edge in FIG. 3) is not provided with a negative electrode active material layer 54, and on the side edge, a negative electrode exposed portion 56 to which the negative electrode current collector 52 is exposing is formed. As shown in FIG. 2, a negative electrode terminal 28 is connected to a negative electrode connection portion 30b which is a wound. negative electrode exposed portion 56. Accordingly, an electroconductive path to which the negative electrode terminal 28 and the negative electrode active material layer 54 are electrically connected via the metal thin film of the negative electrode current collector 52 is constructed.

[0049] The separator 60 is an insulation sheet placed between the positive electrode 40 and the negative electrode 50. The separator 60 has a porous structure having multiple fine pores. In this secondary battery 100, charge carriers (e.g., lithium ions) move between the positive electrode 40 and the negative electrode 50 via the fine pores of the separator 60, thereby performing charging and discharging. Materials of the separator 60 can be those which can be used in commonly used secondary batteries without particular limitations, and do not limit the present disclosure. Thus, the detailed description is omitted.

[0050] In the secondary battery 100 according to the present embodiment, the electrode current collector 10 having the configuration shown in FIG. 1 is used in each of the positive electrode current collector 42 and the negative electrode current collector 52. As mentioned above, the electrode current collector 10 having the configuration shown in FIG. 1 allows appropriate breakage of the metal thin films 14 when abnormal heat generation occurs due to internal short-circuit. This blocks the electroconductive path from the positive electrode active material layer 44 formed via the metal thin film of the positive electrode current collector 42 to the positive electrode terminal 26 (or the electroconductive path from the negative electrode active material layer 54 formed via the metal thin film of the negative electrode current collector 52 to the negative electrode terminal 28), thereby substantially preventing progression of the abnormal heat generation. Thus, according to the present embodiment, the current cut-off mechanism which has many components and may cause an increase in the manufacturing cost is not necessary to be provided in the positive electrode terminal 26 and the negative electrode terminal 28, thereby constructing a highly safe secondary battery at low cost.

[0051] The electrode current collector disclosed herein is not limited to be applied to the secondary battery having the above-mentioned structure, and can be applied to secondary batteries having various known structures without particular limitations. For example, the above-mentioned secondary battery 100 is a rectangular battery constructed by housing the wound electrode body 30 in a metal, rectangular battery case 20. However, the electrode current collector disclosed herein may also be applied to a laminated battery. For the laminated battery, a multi-layered electrode body obtained by stacking a plurality (typically, about 80 to 100) of sheet-like positive electrodes and sheet-like negative electrodes via separators is housed inside a laminate film together with a nonaqueous electrolyte, When the electrode current collector disclosed herein is used as the electrode current collector used in the positive electrodes and the negative electrodes of the laminated battery, the progression of the abnormal heat generation can be substantially prevented suitably.

TEST EXAMPLES

[0052] Test Examples of the present disclosure will be described below. Test Examples are not intended to limit the present disclosure.

[0053] [First Test]

[0054] In this test, three kinds of resin base materials each having a different surface roughness Rz were provided, and metal thin films (copper thin films) were formed on the respective surfaces of each of the resin base materials, thereby producing negative electrode current collectors. Then, secondary batteries using the respective negative electrode current collectors were constructed, and the activation stability of the current cut-off function at the time when heat generates was evaluated.

[0055] 1. Preparation of Samples

(1) Sample 1

[0056] In Sample 1, a sheet-like positive electrode was produced by the following procedures. First, a positive electrode active material (lithium-nickel-cobalt-manganese composite oxide: LiNi.sub.0.33Co.sub.0.33Mn.sub.0.33O.sub.2), an electroconductive material (acetylene black: AB), a binder (polyvinylidene fluoride: PVdF), and a solvent (n-methylpyrrolidone: NMP) were mixed to prepare a positive electrode slurry. The mixing ratio (weight ratio) among the positive electrode active material, the electroconductive material, and the binder was set to 85:10:5. Then, the positive electrode slurry was applied to the surfaces of a positive electrode current collector by the doctor blade method. As the positive electrode current collector in this test, an aluminum foil having a thickness of 15 μm was used. The positive electrode slurry on the surfaces of the positive electrode current collector was then heated to about 80° C. in the air, then held for 10 hours in a vacuum environment at 120° C. to perform a drying process, thereby removing the solvent from the positive electrode slurry. Thus, a positive electrode active material layer was formed on the surface of the positive electrode current collector. Thereafter, the resultant was subjected to press processing to pressure-bond the positive electrode active material layer and the positive electrode current collector. Thus, a positive electrode for test (the electrode area: 22 cm.sup.2) was produced.

[0057] Next, a sheet-like negative electrode was produced by the following procedures. First, a negative electrode active material (graphite) and a binder (PVdF) were mixed to prepare a negative electrode slurry. The mixing ratio (weight ratio) between the negative electrode active material and the binder was set to 95:5. Then, the negative electrode slurry was applied to the surfaces of a negative electrode current collector by the doctor blade method. In this test, as the negative electrode current collector, an electrode current collector where a metal thin film (copper thin film) was formed on each of both surfaces of a resin base material (polyethylene terephthalate) was used. In the production of the negative electrode current collector, the surfaces of the resin base material were filed to adjust its surface roughness Rz to 2 μm. Then, copper was vapor-deposited on the surfaces of the resin base material, Thus, the metal thin film (copper thin film) having a film thickness of 4 μm was formed. Subsequently, the negative electrode slurry applied on the surfaces of the negative electrode current collector was then heated to about 80° C. in the air, held for 10 hours in a vacuum environment at 120° C. to perform a drying process, thereby forming a negative electrode active material layer. Thereafter, the resultant was subjected to press processing to pressure-bond the negative electrode active material layer and the negative electrode current collector. Thus, a negative electrode for test (the electrode area: 24 m.sup.2) was produced.

[0058] Then, the positive electrode and the negative electrode were stacked via two separators and a positive electrode collector foil. Thus, a laminate electrode body was produced. Then, the positive electrode terminal and the negative electrode terminal were connected to the laminate electrode body, and a nonaqueous electrolyte was permeated into the laminate electrode body. Thereafter, the laminate electrode body was encapsulated inside the laminate film. Thus, a laminated battery for test was produced. In the present test, as the nonaqueous electrolyte, used was one obtained by mixing ethylene carbonate (EC) and ethyl methyl carbonate (EMC) at a ratio (volume ratio) of 3:7, and dissolving a supporting electrolyte (lithium hexafluorophosphate: LiPF.sub.6) at a concentration of 1 mol/dm.sup.3 in the mixed solvent.

[0059] (2) Sample 2

[0060] In Sample 2, a laminated battery for test was produced in the same procedures as in Sample 1 except that the surface roughness Rz of the resin base material of the negative electrode current collector was changed to 0.3 μm.

[0061] (3) Sample 3

[0062] In Sample 3, a laminated battery for test was produced in the same procedures as in Sample 1 except that the surfaces of the resin base material of the negative electrode current collector were not subjected to a surface roughening process.

[0063] 2. Evaluation Test

[0064] In this test, abnormal heat generation was caused on the laminated battery of each sample by internal short-circuit, and the activation stability of the current cut-off function of the electrode current collector (negative electrode current collector) was evaluated. Specifically, the battery of each sample was charged with constant current (CC charging) at a rate of 20 C up to SOC 100%, then paused for 30 minutes. Then, a needle with a diameter of 0.5 mm was inserted into the center of the battery with the voltage maintained at 4.1 V by performing constant voltage charging (CV charging), causing abnormal heat generation due to an internal short-circuit. Then, a high current resolution logger was used to measure the current flowing at 100 us after the needle was inserted, to check whether or not the current cut-off function of the negative electrode current collector was activated. Table 1 shows the results.

TABLE-US-00001 TABLE 1 Configuration of Negative Electrode Current Collector Current (mA) Maximum Surface Film Thickness Flowing at 100 us Roughness Rz (μm) of t2 (μm) of After Needle was Resin Base Material Copper Thin Film Inserted Sample 1 2 4 62 Sample 2 0.3 4 756 Sample 3 — 8 832

[0065] As shown in Table 1, only in Sample 1, the current was cut off immediately after abnormal heat generation occurs due to internal short-circuit, and the flowing current dropped significantly. This demonstrates that if the surface roughness Rz of the resin base material is 2 μm or more, the current cut-off function can be activated more easily when abnormal heat generation occurs. It is assumed that such an effect is obtained because the increase in the surface roughness Rz of the resin base material to improve adhesion between the resin base material and the metal thin films results in melting and deforming of the resin base material to pull the metal thin films, and appropriate breakage of the metal thin films.

[0066] [Second Test]

[0067] In this test, the surface roughness Rz of the resin base material was fixed at 2 μm, and five types of negative electrode current collectors with different film thicknesses of the metal thin film were prepared. Then, batteries using the respective negative electrode current collectors were produced, and the battery resistance and the activation stability of the current cut-off function at the time when the abnormal heat generation occurs during normal use of each battery were evaluated.

[0068] 1. Preparation of Samples

[0069] In this test example, four types of laminated batteries (Samples 4 to 7) were prepared under the same conditions as in Sample 1 except that the film thickness of the metal thin film (copper thin film) of the negative electrode current collector was different. In this test, the laminated battery of Sample 1 was also subjected to an evaluation test, Table 2 shows “the surface roughness Rz (μm) of the resin base material,” “The film thickness t2 of the metal thin film,” and “the difference (Rz−t2) between the surface roughness Rz of the resin base material and the film thickness t2 of the metal thin film” of Samples 1 and 4 to 7.

[0070] 2. Evaluation Test

(1) Current Cut-Off Evaluation

[0071] Abnormal heart generation was caused on the batteries of the respective samples in accordance with the same procedures as in the first test and each current flowing at 100 us after the needle was inserted was measured, to check whether or not the current cut-off function of each negative electrode current collector was activated. Table 2 shows the results.

[0072] (2) Evaluation of Battery Resistance

[0073] In this test, the battery resistance of the laminated battery of each of samples was measured. As a device for measuring the battery resistance, a battery charge/discharge system (manufactured by HOKUTO DENKO CORPORATION, HJ-1001 SM8A) was used. For the measurement conditions, the current value of the first cycle was set to 0.2 mA/cm.sup.−2, the upper limit of the voltage (counter electrode graphite) was set to 4.1 V, and the temperature was set to 25° C. Then, after calculating the 1 C rate from the measured battery capacity, a conditioning process was conducted in which three cycles of charging and discharging at the 1 C rate were performed in the range of 2.5 V to 4.1 V (vsLi), and the discharge capacity after the three cycles was used as the initial capacity. Then, each battery was charged up to SOC 60%, then paused for 30 minutes, and discharged at 25° C. at three rates including the IC rate, the 3 C rate, and the SC rate, and the battery resistance was calculated based on the overvoltage after 10 seconds from the start of the discharging. Table 2 shows the results.

TABLE-US-00002 TABLE 2 Configuration of Negative Electrode Current Collector Maximum Film Current (mA) Surface Thickness Flowing at Battery Roughness Rz t2 (μm) of Rz − 100 us Resis- (μm) of Resin Copper t2 After Needle tance Based Material Thin Film (μm) was Inserted (Ω) Sample 1 2 4 −2 62 12.3 Sample 4 2 2 0 56 16.7 Sample 5 2 0.3 1.7 25 251.0 Sample 6 2 5 −3 98 12.0 Sample 7 2 6 −4 368 11.6

[0074] As can be seen from Table 2, in any of Samples 1 and 4 to 7, the flowing current after the occurrence of the abnormal heat generation was lower than that in Samples 2 and 3 in the first test. Among them, in Samples 1 and 4 to 6, the flowing current after the occurrence of the abnormal heat generation decreases particularly largely. This demonstrates that when Rz−t2=3 μm or more, the activation stability of the current cut-off function of the electrode current collector is further improved. Further, in the evaluation of the battery resistance, it was confirmed that the battery resistance of each of Samples 1, 4, 6, and 7 was significantly reduced. This demonstrated that when the metal thin films (copper thin films) each have a film thickness of 2 μm or more, the battery resistance was improved.

[0075] Although the present disclosure was described in detail above, the embodiment is a mere example, and the present disclosure encompasses various modifications and changes of the specific examples.