JP2015057788A - Method for manufacturing nonaqueous electrolyte battery - Google Patents

Abstract

PROBLEM TO BE SOLVED: To achieve excellent battery characteristics by preventing a battery element from moving in covering material, and preventing breakage of a joint part between a lead and the battery element.SOLUTION: A high-capacity nonaqueous electrolyte battery in which a battery element is covered with a laminated film, comprises a porous polymer layer comprising vinylidene fluoride as a component between the laminated film and the battery element. The porous polymer layer comprising the vinylidene fluoride as a component is made of at least one kind of copolymer comprising polyvinylidene fluoride and the vinylidene fluoride as a component, and the thickness of the porous polymer layer is preferably in a range of 1.0 μm or more to 5.0 μm or less. It is more preferable that the porous polymer layer contains inorganic particles such as metal oxide.

Description

  The present invention relates to a non-aqueous electrolyte battery, and more particularly to a large-capacity non-aqueous electrolyte battery manufactured using a laminate film as an exterior material.

  In recent years, many portable electronic devices such as a camera-integrated VTR (videotape recorder), a mobile phone, or a portable computer have appeared, and their size and weight have been reduced. Accordingly, the development of batteries, particularly secondary batteries, has been actively promoted as portable power sources for electronic devices. Among these, lithium ion secondary batteries are attracting attention as being capable of realizing a high energy density.

  In recent years, the battery has been further reduced in size, weight, and thickness by using a laminated film or the like instead of a battery can made of aluminum or iron, which is a battery exterior material.

  However, when a material having low rigidity such as a laminate film is used for the exterior material, the force for pressing the battery element is weak, and the battery element easily moves inside when an impact such as vibration or dropping is applied. For this reason, there is a problem that the connecting portion between the lead taken out of the battery and the battery element is damaged and the internal resistance increases. In particular, large-sized and high-power laminate-coated batteries for in-vehicle use have a large problem because of their large weight and size.

  Here, in Patent Document 1 below, a separator protrudes from one end of the electrode group and is fused and fixed to the inner surface of the exterior member, thereby reducing the voltage and increasing the internal resistance after receiving a vibration shock. It is disclosed that there is an inhibitory effect.

  Patent Document 2 below discloses that there is an effect of suppressing damage even when subjected to impact or deformation pressure by fixing resin by inserting resin between the power generation element and the bag-like container. Has been.

Japanese Patent Laid-Open No. 2007-87652 JP 2003-109667 A

  However, in the method shown in Patent Document 1, the strength of the separator is small and it is not sufficient to suppress the movement of the battery element. Further, the method disclosed in Patent Document 2 has a problem in that it is difficult to control the shape and thickness of the resin, so that the size of the battery is increased, and as a result, the energy density cannot be increased.

  In view of the above problems, the present invention provides a non-aqueous electrolyte battery that realizes high battery characteristics by suppressing the movement of the battery element inside the exterior material and suppressing the breakage of the connection portion between the lead and the battery element. Objective.

In order to solve the problem, the non-aqueous electrolyte battery of the present invention includes a battery element in which a positive electrode and a negative electrode face each other with a separator interposed therebetween,
A non-aqueous electrolyte, a metal layer, an outer resin layer formed on the outer surface of the metal layer, and an inner resin layer formed on the inner surface of the metal layer are laminated, and the battery element and the non-aqueous electrolyte are bonded by thermal fusion. Laminating film that covers and accommodates inside,
A positive electrode lead electrically connected to the positive electrode and led out from the heat-sealed seam of the laminate film;
A negative electrode lead that is electrically connected to the negative electrode and is led out from the heat-sealed joint of the laminate film;
And a porous polymer layer containing vinylidene fluoride as a component formed between the laminate film and the battery element.

  In the above non-aqueous electrolyte battery, the porous polymer layer containing vinylidene fluoride as a component is composed of at least one of polyvinylidene fluoride and a copolymer containing vinylidene fluoride as a component, and the porous polymer layer The thickness is preferably 1.0 μm or more and 5.0 μm or less. It is also preferred that the porous polymer layer further contains inorganic particles such as alumina.

  In this invention, the movement of the battery element in the laminate film can be suppressed by the porous polymer layer containing vinylidene fluoride as a component provided between the battery element and the laminate film.

  According to this invention, it can suppress that the connection part of an electrode lead and a battery element is damaged, and a battery characteristic falls.

It is a basic diagram which shows an example of the battery element which comprises the battery to which this invention is applied. It is a perspective view which shows one structural example of the positive electrode and negative electrode which are used for the battery to which this invention is applied. It is a perspective view which shows one structural example of the battery element of the battery to which this invention is applied. It is sectional drawing which shows the structure of the exterior material which coat | covers the battery element of this invention. It is process drawing which shows the U-shaped bending process of the electrode tab of the battery element of this invention. It is process drawing which shows the U-shaped bending process of the electrode tab of the battery element of this invention. It is process drawing which shows the connection process of the electrode tab and electrode lead of the battery element of this invention. It is process drawing which shows the bending process of the electrode lead connected with the battery element of this invention. It is the perspective view and sectional drawing which show the structure of the battery element in 2nd Embodiment of this invention. It is a perspective view which shows the structure of the battery unit using the nonaqueous electrolyte battery of this invention. It is a disassembled perspective view which shows the structure of the battery unit using the nonaqueous electrolyte battery of this invention. It is a perspective view which shows the structure of the battery module using the nonaqueous electrolyte battery of this invention. It is a perspective view which shows the structure of the battery module using the nonaqueous electrolyte battery of this invention. It is a perspective view which shows the structure of the battery module using the nonaqueous electrolyte battery of this invention. It is a perspective view which shows the structure of the battery module using the nonaqueous electrolyte battery of this invention. It is the perspective view and sectional drawing which show the structure of the other battery element used for the nonaqueous electrolyte battery of this invention. It is the perspective view and sectional drawing which show the structure of the other battery element used for the nonaqueous electrolyte battery of this invention.

Embodiments of the present invention will be described below with reference to the drawings. The description will be made in the following order.
1. 1st Embodiment (example which shows the structure of the nonaqueous electrolyte battery of this invention)
2. Second embodiment (an example in which battery elements having other configurations are used)
3. Third Embodiment (Example in which porous polymer layer is formed without being integrated with gel electrolyte)
4). Fourth Embodiment (Example of Battery Unit and Battery Module Using Nonaqueous Electrolyte Battery of the Invention)
5. Other embodiment (modification)

1. First Embodiment (1-1) Configuration of Nonaqueous Electrolyte Battery FIG. 1A is a perspective view showing an appearance of a nonaqueous electrolyte battery 1 according to an embodiment of the present invention, and FIG. 1 is an exploded perspective view showing a configuration of an electrolyte battery 1. FIG. 1C is a perspective view showing a configuration of the lower surface of the nonaqueous electrolyte battery 1 shown in FIG. 1A, and FIG. 1D is a cross sectional view showing an aa ′ cross section of the nonaqueous electrolyte battery 1 in FIG. 1A. . In the following description, in the nonaqueous electrolyte battery 1, the portion from which the positive electrode lead 3 is led out is the top portion, the portion facing the top portion, the portion from which the negative electrode lead 4 is led out is the bottom portion, and the top portion and the bottom portion. Both sides sandwiched between the two are defined as side portions. Moreover, about an electrode, an electrode lead, etc., a side part-side part direction is demonstrated as width.

  The nonaqueous electrolyte battery 1 of the present invention has a battery element 10 covered with a laminate film 2, and a positive lead 3 connected to the battery element 10 and a portion where the laminate films 2 are sealed together. A negative electrode lead 4 is led out of the battery. The positive electrode lead 3 and the negative electrode lead 4 are led out from opposite sides.

  The thickness of the battery element 10 is preferably 5 mm or more and 20 mm or less. If it is less than 5 mm, it is thin, so there is little influence of heat storage, and heat tends to escape even if there are no irregularities on the cell surface. On the other hand, if it exceeds 20 mm, the distance from the battery surface to the center of the battery becomes too large, and only a heat release from the battery surface will cause a temperature difference in the battery, which tends to affect the life performance.

  Moreover, it is preferable that the discharge capacity of the battery element 10 is 3 Ah or more and 50 Ah or less. If it is less than 3 Ah, since the battery capacity is small, there is a tendency that heat generation can be suppressed by other methods such as reducing the battery capacity by decreasing the battery capacity, such as increasing the thickness of the current collector foil. If it exceeds 50 Ah, the heat capacity of the battery becomes large, it becomes difficult to dissipate heat, and the temperature variation in the battery tends to increase. Here, the discharge capacity of the battery element 10 described above is the nominal capacity of the non-aqueous electrolyte battery 1, and the nominal capacity is constant voltage constant current charging and discharging with an upper limit voltage of 3.6 V and a charging current of 0.2 C. It is calculated from the discharge capacity when the conditions are a constant current discharge with a discharge end voltage of 2.0 V and a discharge current of 0.2 C.

  The battery element 10 accommodated in the nonaqueous electrolyte battery 1 is formed by laminating a rectangular positive electrode 11 shown in FIG. 2A or 2B and a rectangular negative electrode 12 shown in FIG. 2C or FIG. It is a configuration. Specifically, for example, as shown in FIG. 3A and FIG. 3B, the positive electrode 11 and the negative electrode 12 are alternately stacked via separators 13 bent in a zigzag manner.

[Battery element]
The battery element 10 has a stacked electrode structure in which rectangular positive electrodes 11 and rectangular negative electrodes 12 are alternately stacked via separators 13. In the first embodiment, battery elements are sequentially stacked as separator 13, negative electrode 12, separator 13, positive electrode 11,... Negative electrode 12, separator 13 so that the outermost layer of the battery element is separator 13. Is used. In the present invention, a porous polymer layer 14 containing vinylidene fluoride as a component is provided between the battery element 10 and the laminate film 2. That is, the above-described porous polymer layer 14 is formed on the surface of the separator 13 that is the outermost layer of the battery element 10.

  From the battery element 10, a positive electrode tab 11 </ b> C that extends from each of the plurality of positive electrodes 11 and a negative electrode tab 12 </ b> C that extends from each of the plurality of negative electrodes 12 are led out. The plurality of stacked positive electrode tabs 11 </ b> C are configured to be bent so as to have a substantially U-shaped cross section with an appropriate slack at the bent portion. A positive electrode lead 3 is connected to the tip of the stacked positive electrode tabs 11C by a method such as ultrasonic welding or resistance welding.

  Similarly to the positive electrode 11, the negative electrode tabs 12 </ b> C are configured such that a plurality of the negative electrode tabs 12 </ b> C are folded and bent so as to have a substantially U-shaped cross section with an appropriate slack at the bent portion. The negative electrode lead 4 is connected to the tip of the stacked negative electrode tabs 12C by a method such as ultrasonic welding or resistance welding.

  Hereinafter, each part which comprises the battery element 10 is demonstrated.

[Positive lead]
As the positive electrode lead 3 connected to the positive electrode tab 11C, a metal lead body made of, for example, aluminum (Al) can be used. In the large-capacity nonaqueous electrolyte battery 1 of the present invention, in order to extract a large current, the width of the positive electrode lead 3 is set thicker than that of the conventional case, and the thickness is set thicker.

  Although the width of the positive electrode lead 3 can be arbitrarily set, the width wa of the positive electrode lead 3 is preferably 50% or more and 100% or less with respect to the width Wa of the positive electrode 11 in that a large current can be taken out. Further, when the positive electrode lead 3 and the negative electrode lead 4 are led out from the same side, the width wa of the positive electrode lead 3 needs to be less than 50% of the width Wa of the positive electrode 11. This is because the positive electrode lead 3 needs to be provided at a position where it does not contact the negative electrode lead 4. In this case, the width wa of the positive electrode lead 3 is preferably 15% or more and 40% or less of the width Wa of the positive electrode 11 in order to achieve both the sealing property of the laminate film 2 and high current charge / discharge. More preferably, it is 40% or less.

  The thickness of the positive electrode lead 3 is preferably 150 μm or more and 250 μm or less. When the thickness of the positive electrode lead 3 is less than 150 μm, the amount of current that can be taken out becomes small. When the thickness of the positive electrode lead 3 exceeds 250 μm, since the positive electrode lead 3 is too thick, the sealing property of the laminate film 2 on the lead lead-out side is lowered, and moisture intrusion becomes easy.

  A sealant 5, which is an adhesive film for improving the adhesion between the laminate film 2 and the positive electrode lead 3, is provided on a part of the positive electrode lead 3. The sealant 5 is made of a resin material having high adhesion to a metal material. For example, when the positive electrode lead 3 is made of the metal material described above, the sealant 5 is made of a polyolefin resin such as polyethylene, polypropylene, modified polyethylene, or modified polypropylene. It is preferred that

  The thickness of the sealant 5 is preferably 70 μm or more and 130 μm or less. If it is less than 70 μm, the adhesion between the positive electrode lead 3 and the laminate film 2 is poor, and if it exceeds 130 μm, the amount of molten resin flowing at the time of heat-sealing is large, which is not preferable in the production process.

[Negative lead]
For the negative electrode lead 4 connected to the negative electrode tab 12C, a metal lead body made of nickel (Ni) or the like can be used, for example. In the large-capacity non-aqueous electrolyte battery 1 of the present invention, in order to extract a large current, the width of the negative electrode lead 4 is set to be thicker and thicker than in the past. The width of the negative electrode lead 4 is preferably substantially equal to the width of the negative electrode tab 12C described later.

  The width of the negative electrode lead 4 can be arbitrarily set, but the width wb of the negative electrode lead 4 is preferably 50% or more and 100% or less with respect to the width Wb of the negative electrode 12 in that a large current can be taken out. Further, when the positive electrode lead 3 and the negative electrode lead 4 are led out from the same side, the width wb of the negative electrode lead 4 needs to be less than 50% of the width Wb of the negative electrode 12. This is because the negative electrode lead 4 needs to be provided at a position where it does not come into contact with the positive electrode lead 3. In this case, the width wb of the negative electrode lead 4 is preferably 15% or more and 40% or less of the width Wb of the negative electrode 12 in order to achieve both the sealing property of the laminate film 2 and high current charge / discharge. More preferably, it is 40% or less.

  The thickness of the negative electrode lead 4 is preferably 150 μm or more and 250 μm or less as in the positive electrode lead 3. When the thickness of the positive electrode lead 3 is less than 150 μm, the amount of current that can be taken out becomes small. When the thickness of the positive electrode lead 3 exceeds 250 μm, since the positive electrode lead 3 is too thick, the sealing property of the laminate film 2 on the lead lead-out side is lowered, and moisture intrusion becomes easy.

  A part of the negative electrode lead 4 is provided with a sealant 5, which is an adhesion film for improving the adhesion between the laminate film 2 and the negative electrode lead 4, similarly to the positive electrode lead 3.

  The width wa of the positive electrode lead 3 and the width wb of the negative electrode lead 4 are usually the same width w (hereinafter, when the positive electrode lead 3 width wa and the negative electrode lead 4 width wb are equal, the positive electrode lead 3 width wa and the negative electrode lead 3). 4 width wb is appropriately referred to as electrode lead width w without distinction). When the width Wa of the positive electrode 11 and the width Wb of the negative electrode 12 are different, the electrode lead width w is 50% or more with respect to the wider electrode width W of the width Wa of the positive electrode 11 and the width Wb of the negative electrode 12. It is preferable that it is 100% or less. Further, when the positive electrode lead 3 and the negative electrode lead 4 are led out from the same side, the width w of the electrode lead is preferably 15% or more and 40% or less, and 35% or more and 40% or less with respect to the width W of the electrode. It is more preferable that

[Positive electrode]
As shown in FIG. 2A, the positive electrode 11 is formed by forming positive electrode active material layers 11B containing a positive electrode active material on both surfaces of the positive electrode current collector 11A. As the positive electrode current collector 11A, for example, a metal foil such as an aluminum (Al) foil, a nickel (Ni) foil, or a stainless steel (SUS) foil is used.

  Further, a positive electrode tab 11C is integrally extended from the positive electrode current collector 11A. The stacked positive electrode tabs 11 </ b> C are bent so that the cross section is substantially U-shaped, and the tip is connected to the positive electrode lead 3 by a method such as ultrasonic welding or resistance welding.

  The positive electrode active material layer 11B is formed on the rectangular main surface portion of the positive electrode current collector 11A. The extending portion in a state where the positive electrode current collector 11 </ b> A is exposed has a function as a positive electrode tab 11 </ b> C that is a connection tab for connecting the positive electrode lead 3. The width of the positive electrode tab 11C can be arbitrarily set. In particular, when the positive electrode lead 3 and the negative electrode lead 4 are led out from the same side, the width of the positive electrode tab 11 </ b> C needs to be less than 50% of the width of the positive electrode 11. Such a positive electrode 11 can be obtained by forming a positive electrode active material layer 11B on one side of a rectangular positive electrode current collector 11A so as to provide a positive electrode current collector exposed portion and cutting unnecessary portions.

  The positive electrode active material layer 11B includes, for example, a positive electrode active material, a conductive agent, and a binder. The positive electrode active material includes any one or more positive electrode materials capable of inserting and extracting lithium as the positive electrode active material. Other materials may be included.

  As a positive electrode material capable of inserting and extracting lithium, for example, a lithium-containing compound is preferable. This is because a high energy density can be obtained. Examples of the lithium-containing compound include a composite oxide containing lithium and a transition metal element, and a phosphate compound containing lithium and a transition metal element. Especially, what contains at least 1 sort (s) of the group which consists of cobalt, nickel, manganese, and iron as a transition metal element is preferable. This is because a higher voltage can be obtained.

Examples of the composite oxide containing lithium and a transition metal element include lithium cobalt composite oxide (Li _x CoO ₂ ), lithium nickel composite oxide (Li _x NiO ₂ ), and lithium nickel cobalt composite oxide (Li _x Ni). _1-z Co _z O ₂ (z <1)), lithium nickel cobalt manganese composite oxide (Li _x Ni _(1-vw) Co _v Mn _w O ₂ (v + w <1)), or lithium having a spinel structure Examples thereof include manganese composite oxide (LiMn ₂ O ₄ ) and lithium manganese nickel composite oxide (LiMn _2−t N _t O ₄ (t <2)). Among these, a complex oxide containing cobalt is preferable. This is because a high capacity can be obtained and excellent cycle characteristics can be obtained. Examples of the phosphate compound containing lithium and a transition metal element include a lithium iron phosphate compound (LiFePO ₄ ) or a lithium iron manganese phosphate compound (LiFe _1-u Mn _u PO ₄ (u <1)). Is mentioned.

Specific examples of such a lithium composite oxide include lithium cobaltate (LiCoO ₂ ), lithium nickelate (LiNiO ₂ ), and lithium manganate (LiMn ₂ O ₄ ). A solid solution in which a part of the transition metal element is substituted with another element can also be used. Examples thereof include nickel cobalt composite lithium oxide (LiNi _0.5 Co _0.5 O ₂ , LiNi _0.8 Co _0.2 O _2, etc.). These lithium composite oxides can generate a high voltage and have an excellent energy density.

  Furthermore, as a composite particle in which the surface of the core particle made of any of the above lithium-containing compounds is coated with fine particles made of any of the other lithium-containing compounds, from the viewpoint that higher electrode filling properties and cycle characteristics can be obtained. Also good.

In addition, examples of positive electrode materials capable of inserting and extracting lithium include oxides such as vanadium oxide (V ₂ O ₅ ), titanium dioxide (TiO ₂ ), manganese dioxide (MnO ₂ ), and iron disulfide. (FeS ₂ ), disulfides such as titanium disulfide (TiS ₂ ) and molybdenum disulfide (MoS ₂ ), and chalcogenides containing no lithium such as niobium diselenide (NbSe ₂ ) (particularly layered compounds and spinel compounds) ), Lithium-containing compounds containing lithium, and conductive polymers such as sulfur, polyaniline, polythiophene, polyacetylene, or polypyrrole. Of course, the positive electrode material capable of inserting and extracting lithium may be other than the above. Further, two or more kinds of the series of positive electrode materials described above may be mixed in any combination.

  As the conductive agent, for example, a carbon material such as carbon black or graphite is used. As the binder, for example, polyvinylidene fluoride (PVdF), polytetrafluoroethylene (PTFE), a copolymer mainly composed of these, and the like are used.

[Negative electrode]
The negative electrode 12 is formed by forming a negative electrode active material layer containing a negative electrode active material on both surfaces of a negative electrode current collector. The negative electrode current collector is made of a metal foil such as a copper (Cu) foil, a nickel (Ni) foil, or a stainless steel (SUS) foil.

  A negative electrode tab 12C is integrally extended from the negative electrode current collector 12A. The plurality of stacked negative electrode tabs 12C are bent so that the cross section is substantially U-shaped, and the negative electrode lead 4 is connected to the tip by a method such as ultrasonic welding or resistance welding.

The negative electrode active material layer 12B is formed on the rectangular main surface portion of the negative electrode current collector 12A. The extending portion in a state where the negative electrode current collector 12 </ b> A is exposed has a function as a negative electrode tab 12 </ b> C that is a connection tab for connecting the negative electrode lead 4. The width of the negative electrode tab 12C can be arbitrarily set. In particular,
When the positive electrode lead 3 and the negative electrode lead 4 are led out from the same side, the width of the negative electrode tab 12 </ b> C needs to be less than 50% of the width of the negative electrode 12. In such a negative electrode 12, a negative electrode active material layer 12B is formed on one side of a rectangular negative electrode current collector 12A so as to provide a negative electrode current collector exposed portion,
It can be obtained by cutting unnecessary parts.

  The negative electrode active material layer 12B includes any one or more of negative electrode materials capable of inserting and extracting lithium as a negative electrode active material, and a binder, a conductive agent, and the like as necessary. Other materials may be included. At this time, the chargeable capacity of the negative electrode material capable of inserting and extracting lithium is preferably larger than the discharge capacity of the positive electrode. The details regarding the binder and the conductive agent are the same as those of the positive electrode.

  Examples of the negative electrode material capable of inserting and extracting lithium include a carbon material. Examples of the carbon material include graphitizable carbon, non-graphitizable carbon having a (002) plane spacing of 0.37 nm or more, and graphite having a (002) plane spacing of 0.34 nm or less. It is. More specifically, there are pyrolytic carbons, cokes, glassy carbon fibers, organic polymer compound fired bodies, activated carbon or carbon blacks. Among these, the cokes include pitch coke, needle coke, petroleum coke and the like. The organic polymer compound fired body is obtained by firing and carbonizing a phenol resin, a furan resin, or the like at an appropriate temperature. The carbon material is preferable because the change in crystal structure associated with insertion and extraction of lithium is very small, so that a high energy density can be obtained, and excellent cycle characteristics can be obtained. The shape of the carbon material may be any of a fibrous shape, a spherical shape, a granular shape, and a scale shape.

  As the negative electrode material capable of inserting and extracting lithium in addition to the carbon material described above, for example, it can store and release lithium and constitute at least one of a metal element and a metalloid element The material which has as an element is mentioned. This is because a high energy density can be obtained. Such a negative electrode material may be a single element, an alloy or a compound of a metal element or a metalloid element, and may have one or two or more phases thereof at least in part. The “alloy” in the present invention includes an alloy containing one or more metal elements and one or more metalloid elements in addition to an alloy composed of two or more metal elements. Further, the “alloy” may contain a nonmetallic element. This structure includes a solid solution, a eutectic (eutectic mixture), an intermetallic compound, or one in which two or more of them coexist.

  Examples of the metal element or metalloid element described above include a metal element or metalloid element capable of forming an alloy with lithium. Specifically, magnesium (Mg), boron (B), aluminum (Al), gallium (Ga), indium (In), silicon (Si), germanium (Ge), tin (Sn), lead (Pb), Examples thereof include bismuth (Bi), cadmium (Cd), silver (Ag), zinc (Zn), hafnium (Hf), zirconium (Zr), yttrium (Y), palladium (Pd), and platinum (Pt). Among these, at least one of silicon and tin is preferable, and silicon is more preferable. This is because a high energy density can be obtained because the ability to occlude and release lithium is large.

  Examples of the negative electrode material having at least one of silicon and tin include at least a part of a simple substance, an alloy or a compound of silicon, a simple substance, an alloy or a compound of tin, or one or more phases thereof. The material which has in is mentioned.

  As an alloy of silicon, for example, as a second constituent element other than silicon, tin (Sn), nickel (Ni), copper (Cu), iron (Fe), cobalt (Co), manganese (Mn), zinc ( One containing at least one of the group consisting of Zn), indium (In), silver (Ag), titanium (Ti), germanium (Ge), bismuth (Bi), antimony (Sb) and chromium (Cr) Can be mentioned. Examples of tin alloys include silicon (Si), nickel (Ni), copper (Cu), iron (Fe), cobalt (Co), and manganese (Mn) as second constituent elements other than tin (Sn). , Zinc (Zn), indium (In), silver (Ag), titanium (Ti), germanium (Ge), bismuth (Bi), antimony (Sb) and chromium (Cr). Including.

  Examples of the tin compound or the silicon compound include those containing oxygen (O) or carbon (C), and include the second constituent element described above in addition to tin (Sn) or silicon (Si). You may go out.

  In particular, as a negative electrode material containing at least one of silicon (Si) and tin (Sn), for example, tin (Sn) is used as the first constituent element, and in addition to the tin (Sn), the second configuration What contains an element and a 3rd structural element is preferable. Of course, this negative electrode material may be used together with the negative electrode material described above. The second constituent element is cobalt (Co), iron (Fe), magnesium (Mg), titanium (Ti), vanadium (V), chromium (Cr), manganese (Mn), nickel (Ni), copper (Cu ), Zinc (Zn), gallium (Ga), zirconium (Zr), niobium (Nb), molybdenum (Mo), silver (Ag), indium (In), cerium (Ce), hafnium (Hf), tantalum (Ta) ), Tungsten (W), bismuth (Bi), and silicon (Si). The third constituent element is at least one selected from the group consisting of boron (B), carbon (C), aluminum (Al), and phosphorus (P). This is because the cycle characteristics are improved by including the second element and the third element.

  Among them, tin (Sn), cobalt (Co) and carbon (C) are included as constituent elements, and the content of carbon (C) is in the range of 9.9 mass% to 29.7 mass%, tin (Sn) In addition, a CoSnC-containing material in which the ratio of cobalt (Co) to the total of cobalt (Co) (Co / (Sn + Co)) is in the range of 30% by mass to 70% by mass is preferable. This is because in such a composition range, a high energy density is obtained and an excellent cycle characteristic is obtained.

  This SnCoC-containing material may further contain other constituent elements as necessary. Examples of other constituent elements include silicon (Si), iron (Fe), nickel (Ni), chromium (Cr), indium (In), niobium (Nb), germanium (Ge), titanium (Ti), and molybdenum. (Mo), aluminum (Al), phosphorus (P), gallium (Ga), bismuth (Bi), and the like are preferable, and two or more of them may be included. This is because the capacity characteristic or cycle characteristic is further improved.

  The SnCoC-containing material has a phase containing tin (Sn), cobalt (Co), and carbon (C), and this phase has a low crystallinity or an amorphous structure. preferable. In the SnCoC-containing material, it is preferable that at least a part of carbon as a constituent element is bonded to a metal element or a metalloid element as another constituent element. The decrease in cycle characteristics is thought to be due to aggregation or crystallization of tin (Sn) or the like, but such aggregation or crystallization is suppressed when carbon is combined with other elements. It is.

  Further, examples of the negative electrode material capable of inserting and extracting lithium include metal oxides or polymer compounds capable of inserting and extracting lithium. Examples of the metal oxide include iron oxide, ruthenium oxide, and molybdenum oxide. Examples of the polymer compound include polyacetylene, polyaniline, and polypyrrole.

  The negative electrode material capable of inserting and extracting lithium may be other than the above. Moreover, 2 or more types of said negative electrode materials may be mixed by arbitrary combinations.

  The negative electrode active material layer 12B may be formed by any of, for example, a gas phase method, a liquid phase method, a thermal spray method, a baking method, or a coating method, or a combination of two or more thereof. When the negative electrode active material layer 12B is formed using a vapor phase method, a liquid phase method, a thermal spraying method or a firing method, or two or more of these methods, the negative electrode active material layer 12B and the negative electrode current collector 12A include It is preferable to alloy at least a part of the interface. Specifically, the constituent elements of the negative electrode current collector 12A diffuse into the negative electrode active material layer 12B at the interface, the constituent elements of the negative electrode active material layer 12B diffuse into the negative electrode current collector 12A, or the constituent elements thereof It is preferable that they diffuse to each other. This is because breakage due to expansion and contraction of the negative electrode active material layer 12B due to charge / discharge can be suppressed, and electronic conductivity between the negative electrode active material layer 12B and the negative electrode current collector 12A can be improved. .

  As the vapor phase method, for example, physical deposition method or chemical deposition method, specifically, vacuum deposition method, sputtering method, ion plating method, laser ablation method, thermal chemical vapor deposition (CVD; Chemical Vapor Deposition) Or plasma chemical vapor deposition. As the liquid phase method, a known method such as electroplating or electroless plating can be used. The firing method is, for example, a method in which a particulate negative electrode active material is mixed with a binder and dispersed in a solvent and then heat treated at a temperature higher than the melting point of the binder. A known method can also be used for the firing method, for example, an atmospheric firing method, a reactive firing method, or a hot press firing method.

  As the binder, for example, polyvinylidene fluoride (PVdF), styrene butadiene rubber (SBR) or the like is used.

[Separator]
The separator is made of an insulating thin film having a high ion permeability and a predetermined mechanical strength. Specifically, for example, it is composed of a porous film made of a polyolefin-based material such as polypropylene (PP) or polyethylene (PE), or a porous film made of an inorganic material such as a ceramic nonwoven fabric. A structure in which the above porous films are laminated may be employed. Among them, those including a polyolefin-based porous film such as polyethylene and polypropylene are preferable because they have excellent separability between the positive electrode 11 and the negative electrode 12 and can further reduce internal short circuit and open circuit voltage drop.

  In the first embodiment, a polymer material containing vinylidene fluoride is attached to both surfaces of the separator 13 in advance. As a result, the polymer material containing vinylidene fluoride and the non-aqueous electrolyte later react to form a porous polymer layer 14 that retains the non-aqueous electrolyte and becomes a gel. The polymer material containing vinylidene fluoride is attached to both end portions of the separator 13 which is the outermost layer of the battery element 10 with a width slightly wider than the positive electrode 11 and the negative electrode 12. In addition, a polymer material containing vinylidene fluoride is attached to both ends of the separator 13, and a matrix polymer, which is another polymer material for gelling the nonaqueous electrolyte, is attached to the other part of the separator 13. You may do it. In addition, the polymer material may not be attached to the ends other than the both ends of the separator 13, and the separator 13 sandwiched between the positive electrode 11 and the negative electrode 12 may be impregnated with a non-aqueous electrolyte. Thereby, when the battery element 10 is manufactured later, the porous polymer layer 14 containing vinylidene fluoride is formed on the separator 13 located on the outermost layer of the battery element 10.

  In the large-capacity nonaqueous electrolyte battery of the present invention, the thickness of the separator can be suitably used in the range of 5 μm to 25 μm, and more preferably 7 μm to 20 μm. If the separator is too thick, the amount of the active material filled decreases, the battery capacity decreases, and the ionic conductivity decreases and the current characteristics deteriorate. On the other hand, if the film is too thin, the mechanical strength of the film decreases.

[Configuration of non-aqueous electrolyte battery]
The nonaqueous electrolyte battery 1 includes a battery element 10 as described above enclosed in a laminate film 2 together with a nonaqueous electrolyte, and a porous material containing vinylidene fluoride between the battery element 10 and the laminate film 2. A polymer layer 14 is formed. The thickness of the porous polymer layer 14 containing vinylidene fluoride is preferably 1.0 μm or more and 5.0 μm or less. When the thickness of the porous polymer layer 14 is 1.0 μm or less, damage to the joint between the battery element 10 and the electrode lead due to vibration cannot be suppressed, and the internal resistance of the battery is increased. . When the thickness of the porous polymer layer 14 exceeds 5.0 μm, the volume of the porous polymer layer 14 that is not a power generation element increases, and the volume efficiency of the battery decreases.

[Nonaqueous electrolyte]
The nonaqueous electrolyte is obtained by dissolving an electrolyte salt in a nonaqueous solvent, and is enclosed in the laminate film 2 together with the battery element 10. As the nonaqueous electrolyte, a nonaqueous electrolytic solution in which an electrolyte salt is dissolved in a nonaqueous solvent, or a gel electrolyte formed by incorporating the nonaqueous electrolytic solution into a matrix polymer can be used. The porous polymer layer 14 containing vinylidene fluoride in the first embodiment is a gel formed on both surfaces of the separator 13 by attaching a polymer containing vinylidene fluoride to both surfaces of the separator 13. Part of non-aqueous electrolyte.

The electrolyte salt contains, for example, one or more light metal salts such as a lithium salt. Examples of the lithium salt include lithium hexafluorophosphate (LiPF ₆ ), lithium tetrafluoroborate (LiBF ₄ ), lithium perchlorate (LiClO ₄ ), lithium hexafluoroarsenate (LiAsF ₆ ), lithium tetraphenylborate _{(LiB (C 6 H 5)} 4), methanesulfonic acid lithium (LiCH ₃ SO _3), lithium trifluoromethanesulfonate (LiCF ₃ SO _3), tetrachloroaluminate lithium (LiAlCl _4), six Examples thereof include dilithium fluorosilicate (Li ₂ SiF ₆ ), lithium chloride (LiCl), and lithium bromide (LiBr). Among them, at least one selected from the group consisting of lithium hexafluorophosphate (LiPF ₆ ), lithium tetrafluoroborate (LiBF ₄ ), lithium perchlorate (LiClO ₄ ), and lithium hexafluoroarsenate (LiAsF ₆ ). One is preferable, and lithium hexafluorophosphate (LiPF ₆ ) is more preferable. This is because the resistance of the non-aqueous electrolyte is lowered. In particular, it is preferable to use lithium tetrafluoroborate (LiBF ₄ ) together with lithium hexafluorophosphate (LiPF ₆ ). This is because a high effect can be obtained.

  Examples of the non-aqueous solvent include ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), and methyl propyl carbonate (MPC). ), Γ-butyrolactone, γ-valerolactone, 1,2-dimethoxyethane, tetrahydrofuran, 2-methyltetrahydrofuran, tetrahydropyran, 1,3-dioxolane, 4-methyl-1,3-dioxolane, 1,3-dioxane, 1,4-dioxane, methyl acetate, ethyl acetate, methyl propionate, ethyl propionate, methyl butyrate, methyl isobutyrate, methyl trimethyl acetate, ethyl trimethyl acetate, acetonitrile, glutaronitrile, adiponitrile, methoxyacetonitrile, 3-methoxypro Pionitri N, N-dimethylformamide, N-methylpyrrolidinone, N-methyloxazolidinone, N, N'-dimethylimidazolidinone, nitromethane, nitroethane, sulfolane, trimethyl phosphate or dimethyl sulfoxide can be used. This is because, in an electrochemical device such as a battery provided with a nonaqueous electrolyte, excellent capacity, cycle characteristics and storage characteristics can be obtained. These may be used alone or in combination of two or more.

  Especially, as a solvent, what contains at least 1 sort (s) of the group which consists of ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and ethyl methyl carbonate (EMC) is used. It is preferable. This is because a sufficient effect can be obtained. In this case, in particular, ethylene carbonate or propylene carbonate having a high viscosity (high dielectric constant) solvent (for example, relative dielectric constant ε ≧ 30) and dimethyl carbonate having a low viscosity solvent (for example, viscosity ≦ 1 mPa · s). It is preferable to use a mixture containing diethyl carbonate or ethyl methyl carbonate. This is because the dissociation property of the electrolyte salt and the ion mobility are improved, so that a higher effect can be obtained.

  When the gel electrolyte layer is formed, a polymer material having a property compatible with a non-aqueous solvent is generally used as the matrix polymer. As such a matrix polymer, silicon gel, acrylic gel, acrylonitrile gel, polyphosphazene modified polymer, polyethylene oxide, polypropylene oxide, and their composite polymers, cross-linked polymers, modified polymers, and the like are used. In addition, as a fluorine-based polymer, polyvinylidene fluoride (PVdF), vinylidene fluoride (VdF), hexafluoropropylene (HFP), trifluoroethylene (TFE) and at least one kind of chlorotrifluoroethylene (CTFE) are used as a repeating unit. Examples thereof include a polymer such as a copolymer. Such a polymer may be used individually by 1 type, and may mix and use 2 or more types.

[Porous polymer layer containing vinylidene fluoride as a component]
The porous polymer layer 14 provided in the nonaqueous electrolyte battery 1 according to the first embodiment has a separator 13 attached with a polymer material having a function as the matrix polymer described above, and holds a nonaqueous electrolyte. It is comprised by. That is, the gel electrolyte layer and the porous polymer layer 14 are integrally formed. For the surface of the separator 13 in this embodiment, a polymer material containing vinylidene fluoride as a component as a matrix polymer is used. Specifically, polyvinylidene fluoride (PVdF), a copolymer containing vinylidene fluoride (VdF) and hexafluoropropylene (HFP) as repeating units, vinylidene fluoride (VdF), hexafluoropropylene (HFP) and chloro A copolymer containing trifluoroethylene (CTFE) as a repeating unit is preferably used.

  In the case where polyvinylidene fluoride (PVdF) is used as the polymer material constituting the porous polymer layer 14, it is preferable to use polyvinylidene fluoride having a weight average molecular weight of 500,000 to 1,500,000. This is because the effect of suppressing the movement of the battery element 10 is high.

  In addition, inorganic particles may be mixed in the porous polymer layer 14. While the strength of the porous polymer layer 14 is improved, irregularities are generated in the porous polymer layer 14, and the deviation between the battery element 10 and the laminate film 2 can be further suppressed. For this reason, an increase in internal resistance can be further suppressed.

Examples of the inorganic particles include metal oxides, metal nitrides, metal carbides and the like having electrical insulation. As the metal oxide, alumina (Al ₂ O ₃ ), magnesia (MgO), titania (TiO ₂ ), zirconia (ZrO ₂ ), silica (SiO ₂ ) and the like can be suitably used. As the metal nitride, silicon nitride (Si ₃ N ₄ ), aluminum nitride (AlN), boron nitride (BN), titanium nitride (TiN), or the like can be preferably used. As the metal carbide, silicon carbide (SiC), boron carbide (B ₄ C), or the like can be suitably used. These heat-resistant particles may be used alone or in admixture of two or more. Moreover, since inorganic particles are excellent in heat resistance and oxidation resistance, they are preferable because they do not impair the effect of suppressing the movement of the battery element 10 even when the battery temperature rises.

  For example, a polymer material containing vinylidene fluoride as a component may be attached only to one surface portion of the separator 13 that is the outermost layer of the battery element 10.

[Laminate film]
The laminate film 2 that is an exterior material for packaging the battery element 10 has a configuration in which resin layers are provided on both surfaces of a metal layer 2a made of metal foil. The general configuration of the laminate film can be represented by a laminated structure of the outer resin layer 2b / metal layer 2a / inner resin layer 2c, and the inner resin layer 2c is formed so as to face the battery element 10. An adhesive layer having a thickness of about 2 μm or more and 7 μm or less may be provided between the outer resin layer 2b and the inner resin layer 2c and the metal layer 2a. Each of the outer resin layer 2b and the inner resin layer 2c may be composed of a plurality of layers.

  The metal material constituting the metal layer 2a may have a function as a moisture-permeable barrier film, such as an aluminum (Al) foil, a stainless steel (SUS) foil, a nickel (Ni) foil, and plated iron. (Fe) foil or the like can be used. Especially, it is preferable to use the aluminum foil which is thin and lightweight and excellent in workability. In particular, from the viewpoint of workability, for example, annealed aluminum (JIS A8021P-O), (JIS A8079P-O), or (JIS A1N30-O) is preferably used.

  The thickness of the metal layer 2a is preferably 30 μm or more and 150 μm or less. When the thickness is less than 30 μm, the material strength is poor. Moreover, when it exceeds 150 micrometers, while processing becomes remarkably difficult, the thickness of the laminate film 2 will increase and it will lead to the fall of the volume efficiency of a nonaqueous electrolyte battery.

  The inner resin layer 2c is a portion that is melted by heat and fused to each other. Polyethylene (PE), non-axially oriented polypropylene (CPP), polyethylene terephthalate (PET), low density polyethylene (LDPE), high density polyethylene (HDPE) Further, linear low density polyethylene (LLDPE) or the like can be used, and a plurality of types can be selected and used.

  The thickness of the inner resin layer 2c is preferably 20 μm or more and 50 μm or less. If it is less than 20 μm, the adhesiveness is lowered and the pressure buffering action becomes insufficient, and a short circuit is likely to occur. On the other hand, when the thickness exceeds 50 μm, moisture cannot easily enter through the inner resin layer 2c, and there is a possibility that gas is generated inside the battery, the battery is swollen, and battery characteristics are deteriorated. The thickness of the inner resin layer 2c is the thickness before the battery element 10 is packaged. Since the two inner resin layers 2c are fused together after the laminate film 2 is packaged and sealed with respect to the battery element 10, the thickness of the inner resin layer 2c may be out of the above range.

  The inner resin layer 2c may be provided with irregularities on the surface by, for example, embossing. Thereby, the slidability between the porous polymer layer 14 and the laminate film 2 is deteriorated, and the movement suppressing effect of the battery element 10 can be further enhanced.

  As the outer resin layer 2b, polyolefin resin, polyamide resin, polyimide resin, polyester, or the like is used because of its beautiful appearance, toughness, and flexibility. Specifically, nylon (Ny), polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), and polybutylene naphthalate (PBN) are used. Is also possible.

  Note that the outer resin layer 2b preferably has a higher melting point than the inner resin layer 2c in order to melt the inner resin layers 2c by thermal fusion and adhere the laminate film 2. This is because only the inner resin layer 21c is melted at the time of heat sealing. For this reason, the outer resin layer 2b can select a material that can be used depending on the resin material selected as the inner resin layer 2c.

  The thickness of the outer resin layer 2b is preferably 25 μm or more and 35 μm or less. If the thickness is less than 25 μm, the function as a protective layer is inferior.

  The battery element 10 as described above is packaged with the laminate film 2 described above. At this time, the positive electrode lead 3 connected to the positive electrode tab 11C and the negative electrode lead 4 connected to the negative electrode tab 12C are led out of the battery from the sealing portion of the laminate film 2. As shown in FIG. 1B, the laminate film 2 is provided with a battery element storage portion 7 formed in advance by deep drawing. The battery element 10 is stored in the battery element storage portion 7.

  In this invention, the peripheral part of the battery element 10 is heated by the heater head, and the laminate films 2 covering the battery element 10 from both sides are heat-sealed and sealed. In particular, at the lead lead-out side, it is preferable to heat-seal the laminate film 2 with a heater head provided with a notch in a shape that avoids the positive electrode lead 3 and the negative electrode lead 4. This is because the load applied to the positive electrode lead 3 and the negative electrode lead 4 can be reduced to produce a battery. This method can prevent a short circuit during battery fabrication.

  The nonaqueous electrolyte battery 1 of the present invention has high safety and battery characteristics by controlling the thickness of the lead lead-out portion after sealing the laminate film 2 by heat sealing.

(1-2) Method for Producing Nonaqueous Electrolyte Battery The nonaqueous electrolyte battery as described above can be produced by the following steps.

[Production of positive electrode]
A positive electrode active material, a conductive agent, and a binder are mixed to prepare a positive electrode mixture, and the positive electrode mixture is dispersed in a solvent such as N-methyl-2-pyrrolidone to obtain a positive electrode mixture slurry. Subsequently, the positive electrode mixture slurry is applied to both surfaces of the belt-like positive electrode current collector 11A, and the solvent is dried. Then, the positive electrode active material layer 11B is formed by compression molding with a roll press or the like to obtain a positive electrode sheet. . The positive electrode sheet is cut into a predetermined size to produce the positive electrode 11. At this time, the positive electrode active material layer 11B is formed so that a part of the positive electrode current collector 11A is exposed. This exposed portion of the positive electrode current collector 11A is defined as a positive electrode tab 11C. Moreover, you may cut | disconnect the unnecessary part of the positive electrode collector exposed part as needed, and may form the positive electrode tab 11C. Thereby, the positive electrode 11 in which the positive electrode tab 11C is integrally formed is obtained.

[Production of negative electrode]
A negative electrode active material and a binder are mixed to prepare a negative electrode mixture, and this negative electrode mixture is mixed with N-methyl-2.
-Disperse in a solvent such as pyrrolidone to make a negative electrode mixture slurry. Subsequently, the negative electrode mixture slurry is applied to the negative electrode current collector 12A, and the solvent is dried. Then, the negative electrode active material layer 12B is formed by compression molding using a roll press or the like to obtain a negative electrode sheet. The negative electrode sheet is cut into a predetermined size to produce the negative electrode 12. At this time, the negative electrode active material layer 12B is formed so that a part of the negative electrode current collector 12A is exposed. The exposed portion of the negative electrode current collector 12A is defined as a negative electrode tab 12C. Moreover, you may cut | disconnect the unnecessary part of a negative electrode collector exposed part, and may form the negative electrode tab 12C as needed. Thereby, the negative electrode 12 in which the negative electrode tab 12C is integrally formed is obtained.

[Preparation of separator]
As the separator 13, a microporous resin film having a polymer material containing vinylidene fluoride attached to the surface is used. In such a separator, a polymer solution in which a polymer material containing vinylidene fluoride is dissolved in a solvent such as N-methyl-2-pyrrolidone is applied to the surface of the microporous resin film and dried to remove the solvent. Can be obtained.

[Lamination process]
Next, as shown in FIGS. 3A and 3B, the positive electrode 11 and the negative electrode 12 are alternately inserted between the zigzag separators 13, for example, the separator 13, the negative electrode 12, the separator 13, the positive electrode 11, the separator 13, and the negative electrode 12... A predetermined number of positive electrodes 11 and negative electrodes 12 are stacked so as to be the separator 13, the negative electrode 12, and the separator 13. Then, it fixes in the state pressed so that the positive electrode 11, the negative electrode 12, and the separator 13 might closely_contact | adhere, and the battery element 10 is produced. In order to fix the battery element 10 more firmly, for example, a fixing member 6 such as an adhesive tape can be used. In the case of fixing using the fixing member 6, for example, the fixing member 6 is provided on both side portions of the battery element 10.

  Next, the plurality of positive electrode tabs 11C and the plurality of negative electrode tabs 12C are bent so as to have a U-shaped cross section. The electrode tab is bent as follows, for example.

[First tab U-bending step]
The plurality of positive electrode tabs 11C drawn from the laminated positive electrode 11 and the plurality of negative electrode tabs 12C drawn from the laminated negative electrode 12 are bent so as to have a substantially U-shaped cross section. The first U-shaped bending step is a step for providing the positive electrode tab 11C and the negative electrode tab 12C with an optimal U-shaped bending shape in advance. By providing an optimal U-shaped bent shape in advance, the positive electrode tab 11C and the negative electrode tab are formed when the positive electrode tab 3C and the negative electrode tab 12C connected to the positive electrode lead 3 and the negative electrode lead 4 are bent later to form a U-shaped bent portion. It is possible to prevent stress such as tensile stress from being applied to 12C.

  FIG. 5 is a side view for explaining the first U-bending step of the negative electrode tab 12C. In FIG. 5, each process performed about the negative electrode tab 12C is demonstrated. Note that the first U-bending step is similarly performed on the positive electrode current collector 11A.

First, as shown in FIG. 5A, the battery element is disposed on the upper part of the work set base 30 a having the U-shaped bending thin plate 31. The U-shaped bending thin plate 31 is slightly smaller than the thickness of the battery element 10, specifically, at least the total thickness of the plurality of negative electrode tabs 12 </ b> C ₁ to 12 </ b> C ₄ from the work set base 30 a. It is installed to protrude. With such a configuration, it bend outer peripheral side of the negative electrode tab 12C ₄ is to prevent to a position within the range of the thickness of the battery element 10, the non-aqueous increase and appearance of the electrolyte cell 1 having a thickness failure occurs it can.

  Subsequently, as shown in FIG. 5B, the battery element 10 is lowered or the work set base 30a is raised. At this time, since the space efficiency of the nonaqueous electrolyte battery 1 is improved as the gap between the battery element 10 and the U-shaped bending thin plate 31 is smaller, for example, the gap between the battery element 10 and the U-shaped bending thin plate 31 is gradually smaller. To be.

  As shown in FIG. 5C, after the battery element 10 is placed on the work set base 30a and a bent portion is formed on the negative electrode tab 12C, the roller 32 is lowered as shown in FIGS. 5D and 5E to lower the negative electrode tab 12C. Is bent into a U shape.

The thickness of the U-bending thin plate 31 is preferably 1 mm or less, for example, about 0.5 mm. The U-shaped bending thin plate 31 may be made of a material having a strength necessary for forming a bent shape in the plurality of positive electrode tabs 11C or the negative electrode tabs 12C even in such a thin shape. The strength required for the U-shaped bending thin plate 31 varies depending on the number of stacked positive electrodes 11 and negative electrodes 12, the hardness of materials used for the positive electrode tab 11C and the negative electrode tab 12C, and the like. As U-bending thin plate 31 is thin, the bending can be reduced curvature of the negative electrode tab 12C ₁ of the innermost, preferably it is possible to reduce the space required for bending the negative electrode tab 12C. As the U-shaped bending thin plate 31, for example, stainless steel (SUS), a reinforced plastic material, a plated steel material, or the like can be used.

[Current collector exposed portion cutting step]
Next, the tip of the negative electrode tab 12 </ b> C having the U-shaped bent portion is trimmed. In the current collector exposed portion cutting step, a U-shaped bent portion having an optimal shape is formed in advance, and excess portions of the positive electrode tab 11C and the negative electrode tab 12C are cut in accordance with the U-shaped bent shape. FIG. 6 is a side view for explaining a cutting step of the negative electrode tab 12C. The current collector exposed portion cutting step is performed in the same manner for the positive electrode tab 11C.

  As shown in FIG. 6A, the upper surface and the bottom surface of the battery element 10 on which the U-shaped bent portion is formed in the first U-shaped bending step are reversed, and the work set table 30b having the current collector slack relief portion 33 is placed on the work set base 30b. The battery element 10 is fixed.

Next, as shown in FIG. 6B, the leading end portion of the negative electrode tab 12C ₁ to the negative electrode tab 12C _{4 with} the U-shaped bent portion extending from the U-shaped bent portion to the distal end is substantially L-shaped along the work set base 30b. The tip is deformed so that At this time, by maintaining the shape necessary for forming the U-shaped bent portion again, a larger sag occurs as the negative electrode tab 12C ₄ on the bent outer peripheral side. When such slack enters the current collector slack escape portion 33 of the work set base 30b, the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ can be deformed without stress. The negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ may be deformed in a state where the tip portions of the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are fixed.

Subsequently, as shown in FIG. 6C, after the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are pressed against the work set base 30b by the current collector holder 34, for example, as shown in FIG. 6D and FIG. The tips of the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are cut and aligned with a cutting blade 35 provided along the presser 34. Cut portion of the negative electrode tab 12C ₁ ~ negative electrode tab 12C _4, as the tip of the negative electrode tabs 12C ₁ ~ negative electrode tab 12C ₄ when again subjected to U-bending after is positioned within a range of thickness of the battery element 10, At least the surplus portions at the tips of the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are cut.

[Electrode lead connection process]
Subsequently, the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are connected to the negative electrode lead 4. In the tab connection process, the positive electrode tab 11C and the negative electrode tab 12C, and the positive electrode lead 3 and the negative electrode lead 4 are fixed while maintaining the optimum U-shaped bent shape formed in the first U-shaped bending process. Thereby, the positive electrode tab 11C and the positive electrode lead 3, and the negative electrode tab 12C and the negative electrode lead 4 are electrically connected. FIG. 7 is a side view for explaining a connection process between the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4. Although not shown, it is assumed that a sealant 5 is provided in advance on the negative electrode lead 4. The connection process is performed in the same manner for the positive electrode tab 11 </ b> C and the positive electrode lead 3.

As shown in FIG. 7A, reversing the top and bottom surfaces of the negative electrode tab 12C ₁ ~ cell element 10 obtained by cutting the tip excess of the negative electrode tab 12C ₄ in the electrode terminal cutting process again. Next, as shown in FIG. 7B, the battery element 10 is fixed on the work set base 30 c having the current collector formation maintaining plate 36. The bending inner circumferential side of the negative electrode tab 12C ₁ is positioned the tip of the current collector forming sustaining plate 36, while maintaining the bent shape of the negative electrode tab 12C ₁ ~ negative electrode tab 12C _4, for example, generated from the anchoring device Prevent the influence of external factors such as ultrasonic vibration.

Subsequently, as shown in FIG. 7C, the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 are fixed by, for example, ultrasonic welding. The ultrasonic welding, for example, an anvil 37a provided in the lower portion of the negative electrode tab 12C ₁ ~ negative electrode tab 12C _4, horn 37b provided in the upper portion of the negative electrode tab 12C ₁ ~ negative electrode tab 12C ₄ is used. The negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are set in advance on the anvil 37a, the horn 37b is lowered, and the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 are held between the anvil 37a and the horn 37b. Then, ultrasonic vibration is applied to the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 by the anvil 37a and the horn 37b. Accordingly, the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 are fixed to each other.

  In the tab connection step, the negative electrode lead 4 may be connected to the negative electrode tab 12C so that the inner peripheral side bending margin Ri described above with reference to FIG. 7C is formed. The inner peripheral side bending margin Ri is equal to or greater than the thicknesses of the positive electrode lead 3 and the negative electrode lead 4.

Next, the negative electrode lead 4 fixed to the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ is bent into a predetermined shape. 8A to 8C are side views for explaining the tab bending process of the negative electrode lead 4. Similarly, the tab bending step and the electrode lead connecting step are performed for the positive electrode tab 11C and the positive electrode lead 3 as well.

As shown in FIG. 8A, the upper surface and the bottom surface of the battery element 10 to which the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 are fixed in the connecting step are reversed again, so The battery element 10 is fixed on the work set base 30d. The connection portion between the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ and the negative electrode lead 4 is placed on the tab folding table 38a.

Subsequently, as shown in FIG. 8B, pressing the connecting portion between the negative electrode tab 12C ₁ ~ negative electrode tab 12C ₄ and negative electrode lead 4 at block 38b, by lowering the roller 39 as shown in FIG. 8C, the tab folding The negative electrode lead 4 protruding from the base 38a and the block 38b is bent.

[Second tab U-bending process]
Subsequently, as shown in FIG. 8D, the U-shaped bending thin plate 31 is disposed so as to be interposed between the battery element 10 and the block 38b that holds the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ . Subsequently, as shown in FIG. 8E, the negative electrode tab 12C ₁ to the negative electrode tab 12C ₄ are bent by 90 ° along the U-shaped bent shape formed in the first U-shaped bending step shown in FIG. To do. At this time, as described above, the negative electrode lead 4 and the negative electrode tab 12C are connected so that the inner periphery side bend Ri is formed as shown in FIG. 7C. Thus, in the second tab U-bending step, the negative electrode tab 12C can be bent in a direction substantially perpendicular to the electrode surface without coming into contact with the positive electrode 11 and the negative electrode 12 on which the negative electrode lead 4 is laminated.

  At this time, it is preferable that the negative electrode lead 4 be bent together with the sealant 5 which has been heat-welded in advance. The bent portion of the negative electrode lead 4 is covered with the sealant 5, and the negative electrode lead 4 and the laminate film 2 can be structured not to directly contact each other. This structure greatly reduces the risk of rubbing between the resin layer inside the laminate film 2 and the negative electrode lead 4 due to long-term vibration, impact, etc., damage to the laminate film 2, and short-circuiting with the metal layer of the laminate film 2. be able to. In this way, the battery element 10 is produced.

[Exterior process]
Thereafter, the produced battery element 10 is covered with the laminate film 2, and one of the side portions, the top portion, and the bottom portion are heated and heat-sealed by a heater head. The top part and the bottom part from which the positive electrode lead 3 and the negative electrode lead 4 are led out are heated and heat-sealed by, for example, a heater head having a notch.

  Subsequently, a nonaqueous electrolytic solution is injected from the opening of the other side portion that is not heat-sealed. Finally, the laminating film 2 on the side where the liquid is poured is heat-sealed, and the battery element 10 is sealed in the laminating film 2. Thereafter, the battery element 10 is pressurized and heated from the outside of the laminate film 2 to hold the non-aqueous electrolyte in a polymer material containing vinylidene fluoride. Thereby, a gel electrolyte layer is formed between the positive electrode 11 and the negative electrode 12. Further, by forming a gel electrolyte layer on the surface of the separator 13 on the outermost surface of the battery element 10, a porous polymer layer 14 containing vinylidene fluoride as a component is simultaneously formed between the battery element 10 and the laminate film 2. Is done.

2. Second Embodiment In the second embodiment, the battery element 10 having a configuration different from that of the first embodiment and the method of forming the porous polymer layer 14 different from that of the first embodiment are used. Will be described. Hereinafter, only the configuration relating to the configuration of the battery element 10 slightly different from the first embodiment and the formation of the porous polymer layer 14 containing vinylidene fluoride as a component will be described.

(2-1) Configuration of non-aqueous electrolyte battery [battery element]

  As in the first embodiment, the battery element 10 housed in the nonaqueous electrolyte battery 1 includes a rectangular positive electrode 11 shown in FIG. 2A or 2B and a rectangular negative electrode 12 shown in FIG. 2C or 2D. Is a configuration in which the separators 13 are stacked. Specifically, for example, as shown in FIGS. 9A and 9B, the positive electrode 11 and the negative electrode 12 are alternately stacked via rectangular separators 13.

  The battery element 10 has a stacked electrode structure in which positive electrodes 11 and negative electrodes 12 are alternately stacked via rectangular separators 13. In the second embodiment, battery elements are sequentially stacked such as a negative electrode 12, a separator 13, a positive electrode 11, a separator 13... Separator 13, and a negative electrode 12 so that the outermost layer of the battery element is, for example, the negative electrode 12. Is used. The nonaqueous electrolyte battery 1 in the second embodiment is provided with a porous polymer layer 14 containing vinylidene fluoride as a component between the battery element 10 and the laminate film 2. That is, the porous polymer layer 14 containing vinylidene fluoride as a component is formed on the surface of the negative electrode 12 that is the outermost layer of the battery element 10. In the battery element 10 of the second embodiment, gel electrolyte layers (not shown) are formed in advance on both surfaces of the positive electrode 11 and the negative electrode 12. The gel electrolyte layer provided on the outermost layer of the battery element 10 also has the function of the porous polymer layer 14 of the present invention. For this reason, the gel electrolyte layer is composed of the same components as the porous polymer layer 14.

  From the battery element 10, a positive electrode tab 11 </ b> C that extends from each of the plurality of positive electrodes 11 and a negative electrode tab 12 </ b> C that extends from each of the plurality of negative electrodes 12 are led out. The plurality of stacked positive electrode tabs 11 </ b> C are configured to be bent so as to have a substantially U-shaped cross section with an appropriate slack at the bent portion. A positive electrode lead 3 is connected to the tip of the stacked positive electrode tabs 11C by a method such as ultrasonic welding or resistance welding.

  Similarly to the positive electrode 11, the negative electrode tabs 12 </ b> C are configured such that a plurality of the negative electrode tabs 12 </ b> C are folded and bent so as to have a substantially U-shaped cross section with an appropriate slack at the bent portion. The negative electrode lead 4 is connected to the tip of the stacked negative electrode tabs 12C by a method such as ultrasonic welding or resistance welding.

(2-2) Method for Producing Nonaqueous Electrolyte Battery The nonaqueous electrolyte battery as described above can be produced by the following steps.

[Preparation of positive and negative electrodes]
The positive electrode 11 and the negative electrode 12 can be produced by the same method as in the first embodiment. In the second embodiment, gel electrolyte layers are previously formed on both surfaces of the positive electrode 11 and the negative electrode 12. As described above, in the second embodiment, the gel electrolyte layer provided on the outermost layer of the battery element 10 also has the function of the porous polymer layer 14 of the present invention. For this reason, the gel electrolyte is obtained by mixing a precursor solution obtained by mixing a non-aqueous electrolyte similar to the first embodiment and a polymer material containing vinylidene fluoride that also functions as a matrix polymer on both surfaces of the positive electrode 11 and the negative electrode 12. And formed by volatilizing an unnecessary solvent.

[Preparation of separator]
Unlike the first embodiment, the separator 13 in the second embodiment does not attach a polymer material containing vinylidene fluoride to the surface of the microporous resin film. This is because a gel electrolyte layer having a function as the porous polymer layer 14 is formed on both surfaces of the positive electrode 11 and the negative electrode 12 in advance.

[Lamination process]
As shown in FIG. 9A and FIG. 9B, the positive electrode 11 and the negative electrode 12 each having a gel electrolyte layer formed on both sides are laminated via a rectangular separator 13. For example, a predetermined number of positive electrodes 11 and negative electrodes 12 are stacked so as to be a negative electrode 12, a separator 13, a positive electrode 11, a separator 13. Then, it fixes in the state pressed so that the positive electrode 11, the negative electrode 12, and the separator 13 might closely_contact | adhere, and the battery element 10 is produced. For fixing, a fixing member 6 such as an adhesive tape is used. The fixing member 6 is provided, for example, on both side portions of the battery element 10 as in the case of the first embodiment shown in FIG. 1B. Thereby, the battery element 10 is formed.

  The U-bending of the positive electrode tab 11C and the negative electrode tab 12C, the connection of the positive electrode lead 3 and the negative electrode lead 4, and the exterior of the laminate film 2 can be performed in the same manner as in the first embodiment.

  In the second embodiment, since the porous polymer layer 14 containing the gel electrolyte layer and vinylidene fluoride as components in advance is formed, heating from the outside of the laminate film 2 containing the battery element 10 is not performed. unnecessary. In addition, you may perform the pressurization for adhere | attaching a gel electrolyte layer, the positive electrode 11, and the negative electrode 12 as needed.

3. Third Embodiment In the third embodiment, the porous polymer layer 14 containing vinylidene fluoride as a component is formed alone on the surface of the battery element 10, that is, the porous polymer layer 14 is formed as a gel electrolyte. A method of forming without being integrated with the layer will be described. The porous polymer layer forming method in the third embodiment can be applied to any battery element 10 in the first embodiment and the second embodiment. A method for forming the battery element 10 according to the embodiment will be described. In addition, since the method for forming the battery element 10 is substantially the same as that of the second embodiment, only the portion related to the formation of the porous polymer layer 14 containing vinylidene fluoride as a component will be described.

(3-1) Method for Manufacturing Nonaqueous Electrolyte Battery The nonaqueous electrolyte battery as described above can be manufactured by the following steps.

[Preparation of positive and negative electrodes]
The positive electrode 11 and the negative electrode 12 can be manufactured by the same method as in the second embodiment. In the third embodiment, a gel electrolyte layer may not be formed on both surfaces of the positive electrode 11 and the negative electrode 12 in advance, and the separator 13 may be impregnated with a nonaqueous electrolytic solution. In addition, the positive electrode 11 and the negative electrode 12 may be used. A gel electrolyte layer may be formed in advance on both sides. Further, a matrix polymer is attached to both surfaces of the separator facing the positive electrode 11 and the negative electrode 12, and after sealing the laminate film 2, a non-aqueous electrolyte and a polymer material containing vinylidene fluoride are reacted to form a gel electrolyte layer. May be.

[Lamination process]
The positive electrode 11 and the negative electrode 12 produced as described above are overlapped with each other through a rectangular separator 13 so as to become, for example, a negative electrode 12, a separator 13, a positive electrode 11 separator 13,. A number of positive electrodes 11 and negative electrodes 12 are stacked. Then, it fixes in the state pressed so that the positive electrode 11, the negative electrode 12, and the separator 13 might closely_contact | adhere, and the battery element 10 is produced.

  The battery element 10 thus manufactured is subjected to U-bending of the positive electrode tab 11C and the negative electrode tab 12C by the same method as in the second embodiment.

  Here, in the laminate film 2 according to the third embodiment, a polymer layer containing vinylidene fluoride is formed in advance at a position facing the battery element 10 on the surface of the inner resin layer 2c. For the polymer layer containing vinylidene fluoride, a coating solution obtained by dissolving a polymer material containing vinylidene fluoride in a highly polar solvent is applied to a predetermined region of the laminate film 2, and the solvent is volatilized and dried. It is formed by. As such a solvent, for example, N-methyl-2-pyrrolidone (NMP), N, N-dimethylacetamide (DMAc), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), acetonitrile or the like is used. Can do.

  The battery element 10 is packaged by a laminate film 2 in which a polymer layer containing vinylidene fluoride is formed in a predetermined region of the inner resin layer 2c. At this time, the battery element 10 and the polymer layer containing vinylidene fluoride formed on the laminate film 2 face each other. Prior to sealing the laminate film 2, a non-aqueous electrolyte is injected into the battery. As a result, the separator 13 is impregnated with the nonaqueous electrolytic solution, or the matrix polymer attached to the surface of the separator 13 by heating and pressurizing from the outside of the battery later reacts with the nonaqueous electrolytic solution, thereby separating the separator 13. A gel electrolyte layer is formed on the surface.

  In the third embodiment, a nonaqueous electrolytic solution or a gel electrolyte layer containing a nonaqueous electrolytic solution is present inside the battery. Therefore, the polymer layer containing vinylidene fluoride is a porous polymer layer 14 containing vinylidene fluoride that has absorbed the nonaqueous solvent and the electrolyte salt inside the battery. As a result, similarly to the first and second embodiments, the movement of the battery element 10 in the laminate film 2 is suppressed, and this is caused by breakage of the connection portion between the positive electrode lead 3 and the negative electrode lead 4 and the battery element 10. A decrease in battery characteristics can be suppressed.

4). Fourth Embodiment In the fourth embodiment, a battery unit using the above-described nonaqueous electrolyte battery 1 and a battery module in which the battery units are combined will be described. In the fourth embodiment, a case will be described in which the nonaqueous electrolyte battery 1 in which the positive electrode lead 3 and the negative electrode lead 4 of the first embodiment are derived from different sides is used.

[Battery unit]
FIG. 10 is a perspective view showing a configuration example of a battery unit to which the present invention is applied. 10A and 10B show the battery unit 100 viewed from different sides. The side mainly shown in FIG. 10A is the front side of the battery unit 100, and is mainly shown in FIG. 10B. Let the side which is present be the back side of the battery unit 100. As shown in FIG. 10, the battery unit 100 includes non-aqueous electrolyte batteries 1-1 and 1-2, a bracket 110, and bus bars 120-1 and 120-2. The nonaqueous electrolyte batteries 1-1 and 1-2 are nonaqueous electrolyte batteries that employ any of the configurations of the first to third embodiments described above.

  The bracket 110 is a support for ensuring the strength of the nonaqueous electrolyte batteries 1-1 and 1-2. The nonaqueous electrolyte battery 1-1 is attached to the front side of the bracket 110, and the rear side of the bracket 110 is attached. A nonaqueous electrolyte battery 1-2 is attached. The bracket 110 has substantially the same shape when viewed from either the front side or the back side, but a chamfered portion 111 is formed at one lower corner, and the chamfered portion 111 is located at the lower right. The side that can be seen is the front side, and the side where the chamfered portion 111 is seen in the lower left is the back side.

  The bus bars 120-1 and 120-2 are substantially L-shaped metal members, and the connection portions connected to the tabs of the nonaqueous electrolyte batteries 1-1 and 1-2 are arranged on the side surface side of the bracket 110. The terminals connected to the outside of the battery unit 100 are mounted on both side surfaces of the bracket 110 so that the terminals are arranged on the upper surface of the bracket 110.

  FIG. 11 is a perspective view showing a state in which the battery unit 100 is disassembled. The upper side of FIG. 11 is the front side of the battery unit 100, and the lower side of FIG. 11 is the back side of the battery unit 100. Hereinafter, the convex portion in which the battery element 10 is housed in the nonaqueous electrolyte battery 1-1 is referred to as a battery body 1-1A. Similarly, the convex part in which the battery element is accommodated in the nonaqueous electrolyte battery 1-2 is referred to as a battery body 1-2A.

  The nonaqueous electrolyte batteries 1-1 and 1-2 are attached to the bracket 110 with the battery body 1-1A and 1-2A side having convex shapes facing each other. That is, in the nonaqueous electrolyte battery 1-1, the surface on which the positive electrode lead 3-1 and the negative electrode lead 4-1 are provided faces the front side, and the nonaqueous electrolyte battery 1-2 has the positive electrode lead 3-2 and the negative electrode lead 4-2. Is attached to the bracket 110 so that the surface on which the slab is provided faces the back side.

  The bracket 110 has an outer peripheral wall 112 and a rib portion 113. The outer peripheral wall 112 is slightly wider than the outer peripheries of the battery bodies 1-1A and 1-2A of the nonaqueous electrolyte batteries 1-1 and 1-2, that is, the nonaqueous electrolyte batteries 1-1 and 1-2 are mounted. It is formed so as to surround the battery main bodies 1-1A and 1-2A. The rib portion 113 is formed on the inner side surface of the outer peripheral wall 112 so as to extend inward from the central portion in the thickness direction of the outer peripheral wall 112.

  In the configuration example of FIG. 11, the nonaqueous electrolyte batteries 1-1 and 1-2 are inserted into the outer peripheral wall 112 from the front side and the back side of the bracket 110, and double-sided tapes 130-1 and 130 having adhesiveness on both sides. -2 is attached to both surfaces of the rib portion 113 of the bracket 110. The double-sided tapes 130-1 and 130-2 have a substantially rectangular shape with a predetermined width along the outer peripheral ends of the non-aqueous electrolyte batteries 1-1 and 1-2. It suffices that the tapes 130-1 and 130-2 are provided only in an area to be attached.

  As described above, the rib portion 113 is formed to extend inward from the inner side surface of the outer peripheral wall 112 by a predetermined width along the outer peripheral ends of the nonaqueous electrolyte batteries 1-1 and 1-2. The inside of the rib 113 is an opening. Accordingly, the nonaqueous electrolyte battery 1-1 is attached to the rib portion 113 by the double-sided tape 130-1 from the front side of the bracket 110, and is attached to the rib portion 113 by the double-sided tape 130-2 from the back side of the bracket 110. A gap is formed between the nonaqueous electrolyte battery 1-2 and the non-aqueous electrolyte battery 1-2.

  That is, since the opening is formed in the central portion of the bracket 110, the nonaqueous electrolyte batteries 1-1 and 1-2 have the thickness of the rib portion 113 and the thickness of the double-sided tapes 130-1 and 130-2. The bracket 110 is attached with a gap having a total size. For example, the nonaqueous electrolyte batteries 1-1 and 1-2 may be slightly swollen due to charging / discharging, gas generation, or the like, but the gap provided by the opening is formed by the nonaqueous electrolyte battery 1-1. And it becomes the space which escapes the swelling of 1-2. Therefore, it is possible to eliminate an influence such as an increase in the thickness of the entire battery unit 100 due to a portion where the nonaqueous electrolyte batteries 1-1 and 1-2 swell.

  Further, when the nonaqueous electrolyte batteries 1-1 and 1-2 are bonded to the rib portion 113, considerable pressure is required when the bonding area is large, but the bonding surface of the rib portion 113 is limited to the outer peripheral end. By doing so, pressure can be applied efficiently and bonding can be easily performed. Thereby, the stress concerning the nonaqueous electrolyte batteries 1-1 and 1-2 at the time of manufacture can be reduced.

  As shown in FIG. 11, by attaching two nonaqueous electrolyte batteries 1-1 and 1-2 to one bracket 110, for example, the bracket 110 is more than a case where one nonaqueous electrolyte battery is attached to one bracket. Thickness and space can be reduced. Thereby, energy density can be improved.

  Moreover, since the rigidity in the thickness direction of the battery unit 100 is obtained by a synergistic effect of bonding the two nonaqueous electrolyte batteries 1-1 and 1-2, the rib portion 113 of the bracket 110 can be thinned. That is, for example, even if the thickness of the rib portion 113 is 1 mm or less (about the limit thickness of resin molding), the battery unit can be obtained by bonding the nonaqueous electrolyte batteries 1-1 and 1-2 from both sides of the rib portion 113. As a whole, sufficient rigidity can be obtained. And by reducing the thickness of the rib part 113, the thickness of the battery unit 100 is reduced and the volume is reduced. As a result, the energy density of the battery unit 100 can be improved.

  Further, in the battery unit 100, the outer peripheral surfaces (both side surfaces and upper and lower surfaces) of the nonaqueous electrolyte batteries 1-1 and 1-2 are the inner peripheral surfaces of the outer peripheral wall 112 of the bracket 110 in order to increase resistance to external stress. The non-aqueous electrolyte batteries 1-1 and 1-2 have a structure that is bonded to the rib portion 113 on a wide surface.

  With such a configuration, the battery unit 100 having a high energy density and strong against external stress can be realized.

[Battery module]
Next, a configuration example of the battery module 200 in which the battery unit 100 is combined will be described with reference to FIGS. The battery module 200 includes a module case 210, a rubber sheet part 220, a battery part 230, a battery cover 240, a fixed sheet part 250, an electric part part 260, and a box cover 270.

  The module case 210 is a case for housing the battery unit 100 and mounting it on a device to be used. In the configuration example of FIG. 12, the module case 210 is sized to accommodate 24 battery units 100.

  The rubber sheet portion 220 is a sheet that is laid on the bottom surface of the battery unit 100 to mitigate an impact or the like. In the rubber sheet portion 220, one rubber sheet is provided for every three battery units 100, and eight rubber sheets are prepared to correspond to the 24 battery units 100.

  In the configuration example of FIG. 12, the battery unit 230 is configured by combining 24 battery units 100. In the battery unit 230, three battery units 100 are connected in parallel to form a parallel block 231 and eight parallel blocks 231 are connected in series.

  The battery cover 240 is a cover for fixing the battery unit 230, and has an opening corresponding to the bus bar 120 of the nonaqueous electrolyte battery 1.

  The fixed sheet portion 250 is a sheet that is disposed on the upper surface of the battery cover 240 and is in close contact with the battery cover 240 and the box cover 270 when the box cover 270 is fixed to the module case 210.

  The electrical part 260 includes electrical components such as a charge / discharge control circuit that controls charging / discharging of the battery unit 100. The charge / discharge control circuit is disposed, for example, in a space between the bus bars 120 forming two rows in the battery unit 230.

  The box cover 270 is a cover for closing the module case 210 after each part is accommodated in the module case 210.

  Here, in the battery module 200, the parallel block 231 in which the three battery units 100 are connected in parallel is connected in series to form the battery unit 230. This series connection is included in the electrical part unit 260. It is done with a metal plate. Therefore, in the battery unit 230, the parallel blocks 231 are arranged so that the terminal orientations are alternated for each parallel block 231, that is, the positive terminals and the negative terminals are arranged between the adjacent parallel blocks 231. Is done. Therefore, the battery module 200 needs to be devised so as to avoid terminals having the same polarity arranged in adjacent parallel blocks 231.

  For example, as shown in FIG. 13, in the parallel block 231-1 configured by the battery units 100-1 to 100-3 and the parallel block 231-2 configured by the battery units 100-4 to 100-6, The module case 210 is housed in such an arrangement that the positive terminal and the negative terminal are adjacent to each other. In order to regulate such an arrangement, a chamfered portion 111 formed at one corner of the lower side of the bracket 110 of the battery unit 100 is used.

  For example, as shown in FIGS. 14 and 15, in the parallel block 231, the battery units 100-1 to 100-3 are combined so that the chamfered portions 111-1 to 111-3 are in the same direction. A chamfered region 280 is formed. In the module case 210, inclined portions 290 corresponding to the inclination of the chamfered region 280 are formed. The inclined portions 290 have lengths corresponding to the thicknesses of the three nonaqueous electrolyte batteries 1 and are alternately arranged. Has been placed.

  As described above, when the parallel block 231 is stored in the module case 210 in the wrong direction due to the chamfered region 280 of the parallel block 231 and the inclined portion 290 of the module case 210, The corner portion comes into contact with the inclined portion 290 of the module case 210. In this case, since the parallel block 231 is lifted from the bottom surface of the module case 210, the parallel block 231 is not completely stored in the module case 210. Thereby, in the battery module 200, it is avoided that the terminals of the same polarity are adjacently arranged in the adjacent parallel blocks 231.

  Thus, the battery unit and the battery module using the nonaqueous electrolyte battery according to the present invention are configured. The present invention is not limited to the above-described embodiment, and various modifications based on the technical idea of the present invention are possible.

5. Other Embodiments The structure of the battery element and the method for forming the porous polymer layer containing vinylidene fluoride as a component described in the first to third embodiments are examples, and the present invention is not limited to these. It is not something.

  For example, in the first embodiment, the outermost layer is the separator 13 and in the second embodiment, the outermost layer is the negative electrode 12, but in the first embodiment, the outermost layer is either the positive electrode 11 or the negative electrode 12. These electrodes may be used, and the outermost layer may be the separator 13 in the second embodiment. In the case of using the outermost layer as a separator, in any case where the outermost layer is used as an electrode, a polymer material containing vinylidene fluoride is attached to the outermost layer in advance, and then reacted with a non-aqueous electrolyte to be porous. A method of forming a porous polymer layer, or a method of laminating after forming a porous polymer layer by coating in advance, and after laminating electrodes and separators, a porous polymer layer is formed on the surface of the battery element 10 by coating or the like Any method can be used as long as a porous polymer layer containing vinylidene fluoride as a component is formed on the surface of the battery element 10 such as a forming method.

  A porous polymer layer containing vinylidene fluoride as a component is formed on the surface of the battery element 10 by coating as in the second embodiment, and the separator 13 sandwiched between the positive electrode 11 and the negative electrode 12 is Alternatively, it may be impregnated with a non-aqueous electrolyte.

  The structure of the battery element 10 may be configured as shown in FIG. 16B in which the folding direction of the separator 13 is changed in addition to the structure of the first embodiment shown in FIG. 16A, for example. Alternatively, the positive electrode tab 11C and the negative electrode tab 12C may have a width less than half of the electrode, and the positive electrode tab 11C and the negative electrode tab 12C may extend in the same direction. Further, the battery element structure 10 may be a wound electrode body structure in which a belt-like positive electrode and a negative electrode laminated via a separator are wound.

  The nonaqueous electrolyte battery 1 and the battery module 200 combining the nonaqueous electrolyte battery 1 of the present invention are used for an electric power tool, an electric vehicle, a hybrid electric vehicle, an electric assist bicycle, a power storage system used in a house or a building, and the like. be able to.

  Hereinafter, the present invention will be specifically described by way of examples. In addition, this invention is not limited only to these Examples.

[Example 1]
In Example 1, a non-aqueous electrolyte secondary battery was manufactured by changing the thickness after heat fusion in the lead-out portion of the positive electrode lead and the negative electrode lead, and the battery characteristics were confirmed.

<Example 1-1>
[Production of positive electrode]
97 parts by weight of a lithium phosphate compound (LiFePO ₄ ) having an olivine structure coated with carbon and 3 parts by weight of carbon black are mixed to form a second mixed material, and a dry process for the second mixed material is performed using a ball mill. Mixing was performed for 10 hours.

Next, the second mixed material mixed by the ball mill was fired in a nitrogen (N 2) atmosphere at 550 ° C. As a result, a lithium phosphate compound (LiFePO ₄ ) having an olivine structure coated with carbon was obtained as a positive electrode active material.

  Subsequently, 95 parts by mass of the obtained positive electrode active material, 1 part by mass of graphite as a conductive agent, and 4 parts by mass of polyvinylidene fluoride as a binder were mixed to prepare a positive electrode mixture. The mixture was dispersed in N-methyl-2-pyrrolidone as a dispersion medium to obtain a positive electrode mixture slurry. Subsequently, this positive electrode mixture slurry is uniformly applied to both surfaces of a positive electrode current collector made of an aluminum (Al) foil having a thickness of 15 μm, dried, and then compression molded with a roll press to form a positive electrode active material layer. Then, a positive electrode sheet was produced. At this time, a part of the positive electrode current collector was exposed to prepare a positive electrode active material. Finally, the positive electrode sheet was cut into a predetermined size to produce a positive electrode in which a positive electrode current collector exposed portion was formed on one side of a rectangle.

[Production of negative electrode]
The pulverized graphite powder was prepared as a negative electrode active material. 92 parts by mass of this graphite powder and 8 parts by mass of polyvinylidene fluoride as a binder were mixed to prepare a negative electrode mixture, which was further dispersed in N-methyl-2-pyrrolidone as a dispersion medium. An agent slurry was obtained. Next, the negative electrode mixture slurry is uniformly applied to both surfaces of a negative electrode current collector made of a copper (Cu) foil having a thickness of 12 μm, dried, and then compression molded by a roll press to form a negative electrode active material layer. And the negative electrode sheet was produced. At this time, a part of the negative electrode current collector was exposed to prepare a negative electrode active material. Finally, the negative electrode sheet was cut into a predetermined size to produce a negative electrode in which a negative electrode current collector exposed portion was formed on one side of a rectangle.

[Production of separator with polymer formed on its surface]
A polymer solution was prepared by dissolving a polyvinylidene fluoride (PVdF) polymer having a weight average molecular weight of 1,000,000 in an N-methyl-2-pyrrolidone solution so as to be 8% by mass, and the polymer solution was microporous with a thickness of 16 μm. The film was applied to both sides of a separator made of a conductive polyethylene film using a coating apparatus. Next, the polyethylene film coated with the polymer solution was immersed in deionized water, and then dried to prepare a polymer layer made of porous polyvinylidene fluoride having a thickness of 3 μm on both sides of the polyethylene film.

[Assembly of non-aqueous electrolyte battery]
The positive electrode and the negative electrode produced as described above were laminated via a separator formed with a polymer layer made of porous polyvinylidene fluoride to produce a battery element. At this time, the separator was bent in a zigzag manner, and the positive electrode and the negative electrode were inserted between the separators in order, so that the positive electrode and the negative electrode were stacked via the separator. At this time, the positive electrode and the negative electrode were inserted so that the outermost layer was a porous polymer layer formed on the separator. Then, it fixed with the protective tape so that a positive electrode, a negative electrode, and a separator might not slip | deviate, and it was set as the battery element.

  Furthermore, the produced battery element was pinched | interposed with the exterior material, and 3 sides which left one side part were heat-seal | fused. As the exterior material, a moisture-proof aluminum laminate film in which a nylon film having a thickness of 25 μm, an aluminum foil having a thickness of 40 μm, and a polypropylene film having a thickness of 30 μm were laminated in order from the outermost layer was used. Subsequently, a non-aqueous electrolyte was injected from the side opening that was not thermally fused, and the remaining one side was thermally fused and sealed under reduced pressure. Finally, the battery element covered with the laminate film was sandwiched between iron plates and heated at 90 ° C. for 3 minutes, whereby the separator was bonded to the positive electrode and the negative electrode through the porous polymer layer. Thus, a nonaqueous electrolyte battery having a capacity of 10 Ah and a thickness of 8.0 mm was produced.

<Example 1-2>
As Example 1-1, except that a copolymer obtained by copolymerizing 90 parts by mass of vinylidene fluoride and 10 parts by mass of hexafluoropropylene was used as the polymer dissolved in the N-methyl-2-pyrrolidone solution. Thus, a non-aqueous electrolyte battery was produced.

<Example 1-3>
As a polymer dissolved in the N-methyl-2-pyrrolidone solution, a copolymer obtained by copolymerizing 97 parts by mass of vinylidene fluoride, 4 parts by mass of hexafluoropropylene, and 3 parts by mass of chlorotrifluoroethylene was used. A nonaqueous electrolyte battery was produced in the same manner as Example 1-1 except for the above.

<Example 1-4>
Examples Except for using a copolymer obtained by copolymerizing 99.5 parts by mass of vinylidene fluoride and 0.5 parts by mass of monomethylmaleic acid ester as a polymer dissolved in an N-methyl-2-pyrrolidone solution. A nonaqueous electrolyte battery was produced in the same manner as in 1-1.

<Example 1-5>
Similar to Example 1-1, except that a porous polymer layer was formed only at the end of the separator, and a separator having no porous polymer layer other than the outermost layer sandwiched between the negative electrode and the laminate film was used. Thus, a non-aqueous electrolyte battery was produced.

<Comparative Example 1-1>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1, except that a separator not formed with a porous polymer layer was used.

<Comparative Example 1-2>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that methyl methacrylate was used as the polymer dissolved in the N-methyl-2-pyrrolidone solution.

<Comparative Example 1-3>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that polyvinyl alcohol was used as the polymer dissolved in the N-methyl-2-pyrrolidone solution.

[Evaluation of non-aqueous electrolyte battery]
(A) Measurement of discharge capacity For the non-aqueous electrolyte batteries of the above-described Examples and Comparative Examples, 2 A constant current charging was performed up to an upper limit of 3.6 V under an environment of 23 ° C. Voltage charging was performed until the total charging time was 7 hours. Next, 2A constant current discharge was performed to the final voltage of 2.0 V, and the initial discharge capacity was determined. For each example and comparative example, 20 non-aqueous electrolyte batteries were tested, and the average values are shown in Table 1.

(B) Vibration test About the nonaqueous electrolyte battery of each Example and the comparative example, the nonaqueous electrolyte battery after calculating | requiring an initial discharge capacity was charged to 3.6V. Thereafter, in each of the three axis directions (x axis, y axis, z axis), a vibration test was performed for 90 minutes under conditions of an amplitude of 0.8 mm, a frequency of 10 to 55 Hz, and a sweep speed of 1 Hz / min. 1 kHz). For each example and comparative example, 20 non-aqueous electrolyte batteries were tested, and the average values are shown in Table 1.

  The above evaluation results are shown in Table 1.

  As can be seen from Table 1, each of Examples 1-1 to 1-5 in which a polymer layer containing porous polyvinylidene fluoride as a component is formed between the battery element and the exterior material has an internal resistance value of 10 mΩ. The initial discharge capacity did not decrease. Even in Example 1-5 in which a polymer layer containing porous polyvinylidene fluoride as a component was formed only between the battery element surface and the separator, an increase in internal resistance was hardly observed.

  On the other hand, Comparative Example 1-1 using a separator in which no polymer layer is formed, and Comparative Example 1-2 using a separator in which a polymer layer not containing polyvinylidene fluoride as a component is used. In Example 1-3, it was confirmed that the internal resistance significantly improved from 14.6 to 16.1 mΩ.

  That is, it is found that if a polymer layer containing porous polyvinylidene fluoride as a component is formed between the outer surface of the battery element and the exterior material, an increase in internal resistance when vibration is applied can be suppressed. It was.

[Example 2]
In Example 2, the battery characteristics were confirmed by changing the thickness of the polymer layer containing porous polyvinylidene fluoride as a component formed on the separator surface.

<Example 2-1>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the thickness of the porous polyvinylidene fluoride polymer layer was changed to 5 μm.

<Example 2-2>
A nonaqueous electrolyte battery was fabricated in the same manner as in Example 1-1, with the thickness of the porous polyvinylidene fluoride polymer layer being 3 μm.

<Example 2-3>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the thickness of the porous polyvinylidene fluoride polymer layer was 1 μm.

<Example 2-4>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the thickness of the porous polyvinylidene fluoride polymer layer was changed to 0.5 μm.

<Comparative Example 2-1>
A non-aqueous electrolyte battery was produced in the same manner as in Example 1-1 except that a separator not formed with a porous polyvinylidene fluoride polymer layer was used.

[Evaluation of non-aqueous electrolyte battery]
(A) Measurement of discharge capacity (b) Vibration test For each non-aqueous electrolyte battery of each example and comparative example, a discharge capacity measurement and a vibration test were performed in the same manner as in Example 1.

  The above evaluation results are shown in Table 2.

  As can be seen from Table 2, Example 2-1 to Example 2-4 in which a porous polyvinylidene fluoride polymer layer was formed between the outer surface of the battery element and the exterior material were porous polyvinylidene fluoride polymers. The initial discharge capacity was high and the internal resistance was small as compared with Comparative Example 2-1 using a separator that did not form a layer. In particular, Example 2-1 to Example 2-3 in which the thickness of the porous polyvinylidene fluoride polymer layer is 1 μm or more are the same as Example 2-4 in which the thickness of the porous polyvinylidene fluoride polymer layer is 0.5 μm. It was found that the internal resistance was further reduced. Further, it was found that when the thickness of the porous polyvinylidene fluoride polymer layer was 1 μm or more, the internal resistance was not significantly reduced.

[Example 3]
In Example 3, the battery characteristics were confirmed by changing the weight average molecular weight of the polyvinylidene fluoride used for forming the porous polyvinylidene fluoride polymer layer.

<Example 3-1>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the weight average molecular weight of polyvinylidene fluoride was changed to 400,000.

<Example 3-2>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the weight average molecular weight of polyvinylidene fluoride was changed to 500,000.

<Example 3-3>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the weight average molecular weight of polyvinylidene fluoride was changed to 800,000.

<Example 3-4>
Similarly to Example 1-1, a non-aqueous electrolyte battery was fabricated with a weight average molecular weight of polyvinylidene fluoride of 1,000,000.

<Example 3-5>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the weight average molecular weight of polyvinylidene fluoride was changed to 1,500,000.

<Example 3-6>
A nonaqueous electrolyte battery was produced in the same manner as in Example 1-1 except that the weight average molecular weight of polyvinylidene fluoride was changed to 1,800,000.

<Comparative Example 3-1>
A non-aqueous electrolyte battery was produced in the same manner as in Example 1-1 except that a separator not formed with a porous polyvinylidene fluoride polymer layer was used.

[Evaluation of non-aqueous electrolyte battery]
(A) Measurement of discharge capacity (b) Vibration test For each non-aqueous electrolyte battery of each example and comparative example, a discharge capacity measurement and a vibration test were performed in the same manner as in Example 1.

  The above evaluation results are shown in Table 3.

  As can be seen from Table 3, Example 3-1 in which the weight average molecular weight of polyvinylidene fluoride used for forming the porous polyvinylidene fluoride polymer layer formed on the separator is 400,000 and the weight average molecular weight of polyvinylidene fluoride is 1.8 million. In Example 3-6, the internal resistance was 11.1-11.7 mΩ. On the other hand, in Example 3-2 to Example 3-5 in which the weight average molecular weight of polyvinylidene fluoride was 500 to 1,500,000, the internal resistance value was remarkably improved to 10 mΩ or less.

  That is, when the weight average molecular weight of the polyvinylidene fluoride used for forming the porous polyvinylidene fluoride polymer layer provided between the outer surface of the battery element and the exterior material is 500 to 1,500,000, vibration is applied. It was found that the effect of suppressing the increase in internal resistance was great.

[Example 4]
In Example 4, a battery property was confirmed by forming a porous polyvinylidene fluoride polymer layer mixed with inorganic oxide particles.

<Example 4-1>
A nonaqueous electrolyte battery was produced in the same manner as Example 1-1.

<Example 4-2>
Alumina (Al ₂ O ₃ ) having an average particle diameter of 0.5 μm was used as the inorganic oxide particles. The porous polyvinylidene fluoride polymer layer containing inorganic oxide particles was formed as follows.

  A polymer solution was prepared by dissolving a polyvinylidene fluoride (PVdF) polymer having a weight average molecular weight of 1 million in an N-methyl-2-pyrrolidone solution so as to be 8% by mass. The above-mentioned alumina fine powder was added to this polymer solution so as to be twice the amount of polyvinylidene fluoride added, and sufficiently stirred.

  The polymer solution to which alumina was added was applied to both sides of a separator made of a microporous polyethylene film having a thickness of 16 μm using a coating apparatus. Next, the polyethylene film coated with the polymer solution was immersed in deionized water, and then dried to prepare a polymer layer made of porous polyvinylidene fluoride having a thickness of 3 μm on both sides of the polyethylene film.

<Example 4-3>
A nonaqueous electrolyte battery was produced in the same manner as in Example 4-2, except that silica (SiO ₂ ) having an average particle diameter of 0.5 μm was used as the inorganic oxide particles.

<Example 4-4>
A nonaqueous electrolyte battery was produced in the same manner as in Example 4-2, except that titania (TiO ₂ ) having an average particle size of 0.5 μm was used as the inorganic oxide particles.

[Evaluation of non-aqueous electrolyte battery]
(A) Measurement of discharge capacity (b) Vibration test For each non-aqueous electrolyte battery of each example and comparative example, a discharge capacity measurement and a vibration test were performed in the same manner as in Example 1.

  The above evaluation results are shown in Table 4.

  As can be seen from Table 4, in Examples 4-2 to 4-4, in which inorganic oxide particles were mixed with a porous polyvinylidene fluoride polymer between the outer surface of the battery element and the exterior material, inorganic oxide particles It was found that the increase in internal resistance was even smaller than in Example 4-1, which did not mix. Therefore, it is more preferable to mix inorganic oxide particles with the porous polyvinylidene fluoride polymer between the outer surface of the battery element and the exterior material.

  Although one embodiment of the present invention has been specifically described above, the present invention is not limited to the above-described embodiment, and various modifications based on the technical idea of the present invention are possible.

  For example, in the above-described embodiment, a case where a laminated electrode body in which a positive electrode and a negative electrode are laminated as a battery is used, or a case where a so-called zigzag folded electrode body that is not wound is used. However, the present invention is not limited to this, and an electrode winding body in which a strip-like positive electrode and a strip-like negative electrode are laminated via a separator and wound in the longitudinal direction is used. The case is also applicable.

DESCRIPTION OF SYMBOLS 1 ... Nonaqueous electrolyte battery 2 ... Laminate film 3 ... Positive electrode lead 4 ... Negative electrode lead 5 ... Sealant 6 ... Fixing member 7 ... Battery element accommodating part 10 ... Battery Element 11 ... Positive electrode 11A ... Positive electrode current collector 11B ... Positive electrode active material layer 11C ... Positive electrode tab 12 ... Negative electrode 12A ... Negative electrode current collector 12B ... Negative electrode active material layer 12C ... Negative electrode tab 13 ... Separator 14 ... Porous polymer layer 100 ... Battery unit 200 ... Battery module

The present invention relates to a method for manufacturing a non-aqueous electrolyte battery, and more particularly to a method for manufacturing a large-capacity non-aqueous electrolyte battery manufactured using a laminate film as an exterior material.

In view of the above problems, the present invention provides a method for manufacturing a non-aqueous electrolyte battery that realizes high battery characteristics by suppressing the movement of the battery element inside the exterior material and suppressing the breakage of the connection portion between the lead and the battery element. The purpose is to do.

In order to solve the problem, a method for producing a nonaqueous electrolyte battery according to the present invention includes a battery element having a positive electrode and a negative electrode facing each other with a separator interposed therebetween, a nonaqueous electrolyte, a metal layer, and an outer surface of the metal layer. The laminated outer resin layer and the inner resin layer formed on the inner surface of the metal layer are laminated, and a laminate film that encloses the battery element and the nonaqueous electrolyte by thermal fusion and accommodates them inside, a positive electrode, and an electric and connected to Ru positive electrode lead, a process for the preparation of the nonaqueous electrolyte battery comprising a negative electrode and electrically connected to Ru negative electrode lead, a plurality drawn from the positive electrode plurality of drawn from the positive electrode tab and the negative electrode Each of the negative electrode tabs is stacked, the positive electrode lead and a plurality of positive electrode tabs, the negative electrode lead and the plurality of negative electrode tabs are fixedly connected, and the plurality of positive electrode tabs connected to the positive electrode lead and the plurality of negative electrodes connected to the negative electrode lead are connected. Each of the tabs is bent, and each of the positive electrode lead and the negative electrode lead is led out from the heat-sealed seam of the laminate film, and a porous film containing vinylidene fluoride as a component is provided between the laminate film and the battery element. Forming a conductive polymer layer .

Claims (9)

A battery element in which a positive electrode and a negative electrode face each other with a separator interposed therebetween;
A non-aqueous electrolyte, a metal layer, an outer resin layer formed on the outer surface of the metal layer, and an inner resin layer formed on the inner surface of the metal layer are laminated. A laminate film that encases and accommodates a non-aqueous electrolyte;
A positive electrode lead that is electrically connected to the positive electrode and is led out from the heat-sealed joint of the laminate film;
A negative electrode lead electrically connected to the negative electrode and led out from the heat-sealed joint of the laminate film;
A non-aqueous electrolyte battery comprising a porous polymer layer containing vinylidene fluoride as a component formed between the laminate film and the battery element. The nonaqueous electrolyte battery according to claim 1, wherein the porous polymer layer containing vinylidene fluoride as a component is made of at least one of polyvinylidene fluoride and a copolymer containing vinylidene fluoride as a component. The nonaqueous electrolyte battery according to claim 2, wherein the thickness of the porous polymer layer is 1.0 μm or more and 5.0 μm or less. The nonaqueous electrolyte battery according to claim 2, wherein the porous polymer layer containing vinylidene fluoride as a component contains polyvinylidene fluoride having a weight average molecular weight of 500,000 to 1,500,000. The nonaqueous electrolyte battery according to claim 2, wherein the porous polymer layer contains inorganic particles. The nonaqueous electrolyte battery according to claim 2, wherein the inner resin layer of the laminate film is roughened. The non-aqueous electrolyte battery according to claim 1, wherein in the battery element, the positive electrode and the negative electrode are alternately stacked via the separator so that the separator is an outermost layer. The nonaqueous electrolyte battery according to claim 7, wherein the porous polymer layer is formed on both surfaces of the separator. The nonaqueous electrolyte battery according to any one of claims 1 to 8, wherein a discharge capacity is 3 Ah or more and 50 Ah or less and a thickness is 5 mm or more and 20 mm or less.

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