JP6571349B2 - Flexible lithium ion storage battery - Google Patents

Description

One embodiment of the present invention relates to a flexible lithium ion storage battery and an electronic device.

Note that one embodiment of the present invention is not limited to the above technical field. The technical field of one embodiment of the invention disclosed in this specification and the like relates to an object, a method, or a manufacturing method. Alternatively, one embodiment of the present invention relates to a process, a machine, a manufacture, or a composition (composition of matter). Therefore, the technical field of one embodiment of the present invention disclosed in this specification more specifically includes a semiconductor device, a display device, a liquid crystal display device, a light-emitting device, a lighting device, a storage battery, a memory device, a driving method thereof, or As an example, their production methods can be mentioned.

In recent years, various types of storage batteries such as storage batteries such as lithium ion storage batteries, lithium ion capacitors, air batteries, and fuel cells have been actively developed. Lithium-ion batteries that have a particularly high output and high energy density are portable information terminals such as mobile phones, smartphones and notebook personal computers, portable music players, electronic devices such as digital cameras, medical devices, hybrid vehicles (HEV), The demand for electric vehicles (EV), next-generation clean energy vehicles such as plug-in hybrid vehicles (PHEV), stationary storage batteries, etc. is rapidly expanding with the development of the semiconductor industry and the growing demand for energy savings. It has become indispensable to. In recent years, expectations for flexible devices or wearable devices have increased, and there is an urgent need to develop a flexible lithium ion storage battery that can be deformed following the deformation of the device, that is, a flexible storage battery. Some have been started (Patent Document 1).

The lithium ion storage battery includes a positive electrode, a negative electrode, a separator, an electrolytic solution, and an outer package that covers these. Generally, in a lithium ion storage battery, a positive electrode in which a positive electrode mixture containing a positive electrode active material that absorbs and releases lithium ions is applied to both surfaces of a positive electrode current collector made of a metal such as aluminum, and a negative electrode current collector made of copper or the like. The negative electrode which apply | coated the negative mix containing the negative electrode active material which occludes / releases lithium ion on both surfaces of the body is used. Further, the separator is sandwiched between the positive electrode and the negative electrode to be insulated, and the positive electrode and the negative electrode are electrically connected to the positive electrode terminal and the negative electrode terminal provided on the exterior body. The exterior body has a certain shape such as a cylindrical shape or a polygonal shape.

JP 2004-241250 A

When the flexible lithium ion storage battery is a stacked lithium ion storage battery, the stress applied to the storage battery due to the deformation is different in each part of the stacked structure. For example, when a stacked lithium ion storage battery is deformed so as to wind a certain shaft, the stacked structure inside the storage battery is subjected to compressive stress in the portion close to the shaft and tensile stress in the portion far from the shaft. Join.

If the internal structure of the storage battery is integrated in this way, there is no room to relieve stress generated in each part due to the deformation of the storage battery, and fatigue (damage) will eventually occur in the internal laminated structure when the deformation of the storage battery is repeated. It can accumulate and lead to destruction.

Further, as the number of deformations of the storage battery increases as well as the internal laminated structure, fatigue (damage) is accumulated in the battery members and the exterior body that holds the electrolytic solution. Further, since the state of deformation of the internal structure is different from the state of deformation of the exterior body, for example, the internal structure may be subjected to deformation stress exceeding the degree of deformation of the internal structure that the exterior body can tolerate. In this case, the internal structure applies stress directly to the exterior body, and fatigue (damage) is accumulated in the exterior body. As the accumulation of fatigue (damage) proceeds, the exterior body or the sealing structure may eventually be destroyed, and air may enter the storage battery.

When a lithium ion storage battery is damaged and air enters the inside, the internal member of the storage battery may become moisture in the air or may generate heat and ignite, and may lead to a serious accident such as an explosion.

In view of the above, an object of one embodiment of the present invention is to provide a storage battery in which damage to an exterior body due to deformation is suppressed in a flexible storage battery. Another object is to provide a storage battery in which damage to internal structures due to deformation is suppressed. Another object is to provide a storage battery including an exterior body that can allow deformation of an internal structure. Another object is to achieve safety in a flexible storage battery.

Another object of one embodiment of the present invention is to provide a highly safe lithium ion storage battery or electronic device having flexibility. Another object of one embodiment of the present invention is to provide a novel lithium ion storage battery, a novel electronic device, or the like.

Note that the description of these problems does not disturb the existence of other problems. Note that one embodiment of the present invention does not have to solve all of these problems. Issues other than these will be apparent from the description of the specification, drawings, claims, etc., and other issues can be extracted from the descriptions of the specification, drawings, claims, etc. It is.

One embodiment of the present invention includes an internal structure and an exterior body, and the internal structure includes at least a first stacked body and a second stacked body, and the first stacked body includes The first current collector, the second stacked body has the second current collector, and the surface of the first current collector is a first region where no electrode active material is formed. The surface of the second current collector has a second region in which no electrode active material is formed, the exterior body wraps the internal structure, and at least a part of the first region is A flexible lithium ion storage battery in contact with at least a part of the second region.

Another embodiment of the present invention includes an internal structure and an exterior body, and the internal structure includes at least a first stacked body and a second stacked body. The laminated body has a first current collector, the second laminated body has a second current collector, and no electrode active material is formed on the surface of the first current collector. The first current region has a second region on which the surface of the second current collector is not formed with an electrode active material, the outer package encloses the internal structure and the void, At least a part of the region is in contact with at least a part of the second region, and the first laminate and the second laminate can slide with each other. Is a flexible lithium ion storage battery that can occupy at least part of the void.

Another embodiment of the present invention includes an internal structure and an exterior body, and the internal structure includes at least a first stacked body and a second stacked body, and includes the first stacked body. The body has a first current collector, the second stacked body has a second current collector, and the surface of the first current collector has no electrode active material formed thereon. The surface of the second current collector has a second region in which no electrode active material is formed, and the exterior body wraps the internal structure and the void, and the first region At least a portion of which is in contact with at least a portion of the second region, and by sliding, the internal structure can occupy at least a portion of the space, and the internal structure has the first axis. The gap is a flexible lithium ion in which the length A of the outer edge of the cross-sectional shape in a plane perpendicular to the first axis satisfies the formula (1). It is a storage battery.

However, in formula (1), L represents the length of the cross-sectional shape of said surface of the internals, T is, represents the thickness of the cross-sectional shape of said surface of the internals, r ₂ is the internal structure It represents the distance from the surface farthest from the first axis of the object to the first axis.

Note that in one embodiment of the present invention, a flexible lithium ion storage battery including an electrolytic solution may be used. Further, in one embodiment of the present invention, a flexible lithium ion storage battery that has an electrolytic solution and can be occupied by the electrolytic solution may be used. In one embodiment of the present invention, the first current collector may be a positive electrode current collector, and the second current collector may be a positive electrode current collector, and may be a flexible lithium ion storage battery. In one embodiment of the present invention, the first current collector may be a negative electrode current collector, and the second current collector may be a negative electrode current collector, and may be a flexible lithium ion storage battery.

Further, the electronic device may include a flexible lithium ion storage battery according to one embodiment of the present invention, a display, and an operation button.

One embodiment of the present invention can provide a storage battery in which damage to an exterior body due to deformation is suppressed in a flexible storage battery. Or the storage battery by which the damage of the internal structure accompanying a deformation | transformation was suppressed can be provided. Or the storage battery which has an exterior body which can accept | permit a deformation | transformation of an internal structure can be provided. Alternatively, it is possible to ensure safety in a flexible storage battery.

One embodiment of the present invention can provide a highly safe lithium ion storage battery or an electronic device having flexibility. Alternatively, according to one embodiment of the present invention, a novel lithium ion storage battery, a novel electronic device, or the like can be provided.

Note that the description of these problems does not disturb the existence of other problems. Note that one embodiment of the present invention does not have to solve all of these problems. Issues other than these will be apparent from the description of the specification, drawings, claims, etc., and other issues can be extracted from the descriptions of the specification, drawings, claims, etc. It is.

The figure explaining a lithium ion storage battery. The figure explaining the cross-section of a lithium ion storage battery. The figure explaining the cross-section of the internal structure of a lithium ion storage battery. The figure explaining a lithium ion storage battery and its cross-section. The figure explaining the cross-section of a lithium ion storage battery, and the cross-section in a deformation | transformation state. The figure explaining the cross-sectional shape of an internal structure. The figure explaining a curvature radius. The figure explaining a curvature radius. The figure explaining a coin-type storage battery. The figure explaining a cylindrical storage battery. The figure explaining a laminate-type storage battery. The figure which shows the external appearance of a storage battery. The figure which shows the external appearance of a storage battery. The figure for demonstrating the preparation methods of a storage battery. The figure explaining the laminate-type storage battery which has flexibility. The figure for demonstrating the example of a storage battery. The figure for demonstrating the example of a storage battery. The figure for demonstrating the example of a storage battery. The figure for demonstrating the example of a storage battery. The figure for demonstrating the example of a storage battery. The figure which shows the application form of a storage battery. FIG. 10 is a block diagram illustrating one embodiment of the present invention. 1 is a conceptual diagram illustrating one embodiment of the present invention. FIG. 10 is a circuit diagram illustrating one embodiment of the present invention. FIG. 10 is a circuit diagram illustrating one embodiment of the present invention. 1 is a conceptual diagram illustrating one embodiment of the present invention. FIG. 10 is a block diagram illustrating one embodiment of the present invention. 6 is a flowchart illustrating one embodiment of the present invention. The perspective view explaining the example of a structure of a storage battery, a top view, and sectional drawing. The figure explaining the example of the preparation methods of a storage battery. The perspective view explaining the example of a structure of a storage battery, a top view, and sectional drawing. The figure explaining the example of the preparation methods of a storage battery.

Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. However, the present invention is not limited to the following description, and it will be easily understood by those skilled in the art that modes and details can be variously changed. In addition, the present invention is not construed as being limited to the description of the embodiments below.

Note that in each drawing described in this specification, the size of each component such as the size and thickness of the positive electrode, the negative electrode, the active material layer, the separator, and the outer package is exaggerated for clarity of description. May have been. Therefore, each component is not necessarily limited to the size, and is not limited to the relative size between the components.

In this specification and the like, the ordinal numbers attached as the first, second, third, etc. are used for the sake of convenience and do not indicate the order of steps or the positional relationship between the upper and lower sides. Therefore, for example, the description can be made by appropriately replacing “first” with “second” or “third”. In addition, the ordinal numbers described in this specification and the like may not match the ordinal numbers used to specify one embodiment of the present invention.

In the structures of the present invention described in this specification and the like, the same portions or portions having similar functions are denoted by the same reference numerals in different drawings, and description thereof is not repeated. In addition, when referring to a portion having a similar function, the hatch pattern may be the same, and there may be no particular reference.

In this specification, the term “flexibility” refers to the property that an object is soft and can be bent. The property is that the object can be deformed according to the external force applied to the object, and it does not matter whether there is elasticity or the ability to restore the shape before deformation. A flexible storage battery can be deformed according to an external force. The storage battery having flexibility can be used by being fixed in a deformed state, can be used after being repeatedly deformed, or can be used in an undeformed state. In this specification and the like, the inside of the outer package refers to a region surrounded by the outer package in the lithium ion storage battery, and there are structures such as a positive electrode, a negative electrode, an active material layer, and a separator, and an electrolytic solution. It is an area to do.

In addition, the contents described in the embodiments for carrying out the present invention can be used in appropriate combination.

(Embodiment 1)
In this embodiment, a lithium ion storage battery 110 according to one embodiment of the present invention and a manufacturing method thereof will be described.

FIG. 1 illustrates a lithium ion storage battery 110 according to one embodiment of the present invention. The lithium ion storage battery 110 has an internal structure 117 wrapped in an exterior body 116. The internal structure 117 includes an electrode and a separator, and the electrode is electrically connected to the lead electrode 115.

2 is a cross-sectional view of the lithium ion storage battery 110 according to one embodiment of the present invention cut along A1-A2 in FIG. 1 and an enlarged view thereof. As shown in FIG. 2, the lithium ion storage battery 110 described in the present embodiment includes a first stacked body 100 a, a second stacked body 100 b, and a third stacked body 100 c as the electrolytic solution 107 and the internal structure 117. , A fourth stacked body 100d. In addition, although the number of the laminated bodies which the lithium ion storage battery 110 demonstrated in this Embodiment has is mainly 4, it is not limited to this. Each stacked body includes a negative electrode current collector 101, a negative electrode active material layer 102, a separator 103, a positive electrode active material layer 104, and a positive electrode current collector 105.

Further, in the lithium ion storage battery 110 described in this embodiment, the first stacked body 100a to the fourth stacked body 100d have the same stacked structure as shown in the enlarged view of FIG. In the body, the stacking order of the constituent layers is alternately reversed. However, each laminated body is not limited to having the same laminated structure.

In the lithium ion storage battery 110 described in the present embodiment, the surface of the first stacked body 100a where the active material of the positive electrode current collector is not formed and the active material of the positive electrode current collector of the second stacked body 100b. The surface on which the negative electrode current collector of the second stacked body 100b is not formed and the active material of the negative electrode current collector of the third stacked body 100c are formed. The surface where the active material of the negative electrode current collector of the third stacked body 100c is not formed and the active material of the negative electrode current collector of the fourth stacked body 100d are formed. There is no contact with the surface. However, in the lithium ion storage battery 110 according to one embodiment of the present invention, all the stacked bodies are not limited to being in contact with each other's current collectors.

Since each current collector is a thin-film member made of a metal material as will be described later, the surface is extremely flat and the friction coefficient is small. However, on the surface where the active material layer is formed on the surface, generally, the surface of the current collector on which the active material is not formed has a shape with larger irregularities, the friction coefficient is increased, and the active material is further increased. Depending on the composition of the material forming the layer, adhesion to the structure in contact with the surface may be exhibited.

That is, since the current collector and the separator are laminated through the active material layer inside each laminated body, the friction between each layer is large, and all the structural bodies constituting the laminated body are handled as one body. The layers are not separated from each other unless a certain amount of force is applied from the outside. On the other hand, the current collector surfaces of each laminate are in contact with each other, and the surface of each current collector has a small coefficient of friction, so that each laminate can easily slide on each other in response to external force. .

In the flexible stacked lithium ion storage battery 110 according to one embodiment of the present invention, when the lithium ion storage battery 110 is deformed, the exterior body and the internal structure are also deformed, and stress due to the deformation is applied. Here, the state before and after the deformation of the internal structure of the stacked lithium ion storage battery will be described with reference to FIG.

FIG. 3A shows a cross-sectional view of the internal structure of the stacked lithium ion storage battery 110 before deformation. FIGS. 3B and 3C are cross-sectional views of the internal structure of the stacked lithium ion storage battery 110 in a deformed state. 3D is an enlarged view of part of FIG. 3B, and FIG. 3E is an enlarged view of part of FIG. 3C. In addition, in FIG. 3, 100a thru | or 100d has shown each laminated body. In FIG. 3, the number of stacked bodies is 4, but the number of stacked bodies is not limited to this.

First, FIG. 3B is a diagram showing a case where the friction between the stacked bodies is large, and even if the lithium ion storage battery 110 is deformed, the stacked bodies are not slid and deformed as a whole. FIG. 3D is an enlarged view of part of FIG. The friction between each laminated body is large, and the case where the sliding between each laminated body by a deformation | transformation does not arise is represented. Due to the deformation, tensile stress is generated in some laminates, while compressive stress is generated in other laminates, and each laminate is subjected to different stresses. It cannot be resolved.

When the magnitude of deformation exceeds the limit, the difference in stress applied to each laminate becomes too large, and irreversible peeling occurs between the laminates. Or since the stress concerning each layer which comprises each laminated body also becomes large too much, damages (damage), such as a crack and a fracture | rupture, are produced in each layer. Even when the size of the deformation does not exceed the limit, if the deformation is repeated many times, such a problem occurs due to accumulation of damage due to stress. In any case, it becomes a serious problem for the function of the lithium ion storage battery 110, and it will be unable to endure further use.

On the other hand, FIG. 3C is a diagram showing a case where the friction between the stacked bodies is small, for example, because the stacked bodies are in contact with each other on the surface where the active material of the current collector is not formed. It is. FIG. 3E is an enlarged view of part of FIG. When the friction between the stacked bodies is small, the stress applied to the stacked bodies according to the deformation of the lithium ion storage battery 110 is alleviated by sliding between the stacked bodies.

Therefore, even if the lithium ion storage battery 110 is largely deformed, the generated stress is relieved by sliding, so that separation between the stacked bodies is difficult to occur. Alternatively, since stress applied to each layer constituting each laminate is also reduced, damage (damage) given to each layer is reduced, and cracks and breaks are less likely to occur. Further, even when many deformations are repeated, the structure is such that the stress is easily relaxed, and therefore, the accumulation of damage is small.

The lithium ion storage battery according to one embodiment of the present invention has a low friction between the stacked bodies, and the stacked bodies can slide with each other according to the deformation of the storage battery. Become. Or it becomes the storage battery by which the damage of the internal structure accompanying a deformation | transformation was suppressed. Therefore, it is possible to secure safety in the flexible storage battery.

By the way, in the lithium ion storage battery which concerns on 1 aspect of this invention, although each laminated body can mutually be slid and the damage by deformation | transformation is suppressed, it cannot necessarily be deform | transformed large indefinitely. This is because if the size of deformation of the storage battery is increased, another problem occurs.

This problem will be described with reference to FIGS. 4A illustrates a lithium ion storage battery 110 according to one embodiment of the present invention, and FIG. 4B illustrates a cross-sectional structure taken along dashed line B1-B2 in FIG. In the lithium ion storage battery according to one embodiment of the present invention, the stacked bodies can slide with each other, but the storage battery includes a lead electrode 115 for supplying power to the outside, and the lead electrode 115 includes a plurality of lead electrodes 115. Since the stacked bodies are connected to the current collector, it is desirable that the stacked bodies are fixed to each other at the end portion on the side where the lead electrode 115 exists. If the end portion is not fixed, each of the stacked bodies slides differently when the storage battery is deformed. Therefore, the sliding size of the lead electrode 115 to which the current collector of each stacked body is connected is large. This is because stress due to the difference occurs.

FIG. 5 shows a change in the cross-sectional shape accompanying deformation of the lithium ion storage battery 110 in which the stacked bodies are fixed to each other at one end. First, FIG. 5A is a diagram showing a cross-sectional structure of a lithium ion storage battery before deformation. In this figure, the number of stacked bodies is 4, but in the lithium ion storage battery according to one embodiment of the present invention, the number of stacked bodies is not limited to 4. In addition, as shown to FIG. 5 (A), an exterior body can be made larger than the magnitude | size sufficient to wrap all the laminated bodies inside. By providing the gap 118 (in reality, the region occupied by the electrolytic solution) inside the storage battery in this way, there is room for the exterior body and the laminate to slide with each other. It is possible to prevent damage from occurring.

FIG. 5B shows a cross-sectional structure of the deformed lithium ion storage battery 110. While the stacked bodies are fixed to each other on the side having the lead electrode 115, the stacked bodies slide to each other in other portions, so that the cross-sectional structure shown in FIG. 5B is obtained. Here, as understood from FIG. 5B, when the degree of deformation of the lithium ion storage battery increases, the gap (area occupied by the electrolyte) 118 inside the storage battery decreases due to the change in the cross-sectional shape. Further, when the storage battery is to be deformed to a greater extent than shown in FIG. 5B, the gap is used up, causing interference with the exterior body, and eventually the laminate gives stress to the exterior body or Damage to the laminate may occur. For this reason, it is desirable to provide a gap 118 in the storage battery according to the magnitude of deformation assumed in the storage battery.

On the other hand, if the gap 118 is excessively large, a volume increase that is not directly related to the capacity of the storage battery is generated, which causes a problem because the capacity value per volume of the storage battery is decreased.

The gap is provided by setting the length of the exterior body in the cross section shown in FIG. 5 (A) to a length longer than that necessary to cover the internal structure. The size of the gap required to continue to cover the internal structure without interference can be derived from the assumed size of deformation applied to the storage battery, and it is also necessary to provide the gap of that size. The length of the exterior body can be derived.

Accordingly, a flexible lithium ion storage battery that can prevent damage to the exterior body due to deformation of the storage battery and suppresses a decrease in capacity per volume due to an increase in the gap as much as possible will be described below.

<Shape change and gap setting of flexible lithium ion storage battery>
First, the shape change of a flexible lithium ion storage battery will be described. In order to make the explanation clearer, a schematic diagram of the outer ring shape of the internal structure of the storage battery in FIG. 5A (a combination of all the laminated bodies) is shown in FIG. That is, FIG. 6A is a diagram showing the outer ring shape of the internal structure 117 of the lithium ion storage battery before being deformed. Moreover, the schematic of the outer ring | wheel shape of the internal structure 117 of the lithium ion storage battery in FIG.5 (B) is shown in FIG.6 (B). That is, FIG. 6B is a diagram showing the outer ring shape of the internal structure 117 of the deformed lithium ion storage battery 110. In this figure, the end of the internal structure far from the center of curvature 1101 is 1105, the end of the internal structure far from the center of curvature 1101 is 1103 and 1105, and the end close to the center of curvature of the internal structure. The parts are 1102 and 1104, respectively, and the point closer to the center of curvature of the internal structure is 1106.

In FIG. 6A, the length of the laminated body (for example, the length between 1102 and 1104) in the cross section is L, and the thickness of the internal structure (for example, the length between 1102 and 1103) is T. And Next, FIG. 6 (B) is a diagram showing a cross-sectional structure of the internal structure 117 of the lithium ion storage battery to which deformation having a size enough to use the gap is given. In FIG. 6 (B), the starting curvature center 1101 of the deformation, the distance to the end point of the end portion 1103 of the far side of the internal structure 117 from curvature center 1101 (the radius of the arc) and _{r 2.} Furthermore, the distance (arc radius) from the center of curvature 1101 to the end 1102 of the internal structure closer to the center of curvature 1101 is r ₁ .

First, the perimeter of the outer ring shape of the internal structure 117 in the cross section of FIG. 6A is 2L + 2T. Next, the length of the outer ring shape of the internal structure in the cross section of FIG. First, the thickness of the internal structure (the length between 1104 and 1105) at one end where the stacked bodies are fixed to each other is T because it does not change before and after deformation.

Next, the length of the part near the center of curvature of the internal structure (the arc between 1102 and 1104) and the part far from the center of curvature (the arc between 1103 and 1105) are also measured before and after deformation of the storage battery. Since it does not change at L, each becomes L. In the lithium ion storage battery according to one embodiment of the present invention, since the stacked bodies can slide with each other, the stacked bodies slide with each other according to deformation of the storage battery, and the stress is relieved. This is because it does not change.

Therefore, the change in the circumference of the outer ring shape of the internal structure 117 accompanying the deformation of the storage battery is obtained by examining the length of the remaining part (between 1102 and 1103). Here, the point 1106 on the side close to the center of curvature of the internal structure will be described. The point 1106 is an intersection of a straight line connecting the end portion 1103 far from the center of curvature of the internal structure and the center of curvature 1101 and a side near the center of curvature of the outer ring shape of the internal structure. Then, since the center of curvature 1101 is also the center of curvature of the arc (the arc between 1102 and 1104) which is a shape closer to the center of curvature of the internal structure, it is far from the arc and the center of curvature of the internal structure. The straight line connecting the end 1103 on the side and the center of curvature 1101 is orthogonal to the point 1106. Further, since the arc between the end 1102 and the point 1106 has a small central angle, it can be approximated by a straight line. Therefore, when the end 1103, the end 1102 and the point 1106 are connected, a right triangle is formed. Therefore, the length between the end 1102 and the end 1103 is determined by using the lengths of the other two sides of the triangle. It can be obtained by the Pythagorean theorem.

First, the length between the point 1106 and the end portion 1103 is T because it is the thickness of the internal structure 117.

Next, the length between the point 1106 and the end 1102 is obtained by subtracting the length of the arc between the point 1106 and the end 1104 from the length L of the arc connecting the end 1102 and the end 1104. Length. Therefore, consider the arc length L ₁ between the point 1106 and the end 1104.

The length of the arc is a value obtained by multiplying the product of the diameter and the circumference ratio π by the ratio of the central angle occupying 360 °. That, _{L 1} is represented by the following formula (2).

Here, r ₁ represents the radius of an arc that is a shape closer to the center of curvature of the internal structure, and θ represents the central angle of the arc. By the way, although the length of the part far from the center of curvature of the internal structure (the arc between 1103 and 1105) is L, the part is an arc having a central angle of θ and a radius of r _2. The following equation (3) is established.

Here, when Expression (3) is applied to Expression (2), the following Expression (4) is established.

Accordingly, in a right triangle connecting the end portion 1103 and the end 1102 and the point 1106, when the length of the hypotenuse and _{T 1,} the Pythagorean theorem, holds the equation (5) below.

When equation (4) is applied to equation (5), the following equation (6) holds for the length of T ₁ .

Furthermore, the radius of the outer ring-shaped arc of the inner structure far from the center of curvature 1101 is r ₂ , and the radius of the outer ring-shaped arc of the inner structure closer to the center of curvature 1101 is r ₁ , the difference Is the thickness T of the internal structure, r ₁ is a value obtained by subtracting T from r ₂ . Therefore, _{T 1} from the equation (6) is represented by the following formula (7).

In a state before the lithium ion storage battery is deformed, the length between the end 1103 and the end 1102 is the thickness T of the internal structure. Since the length between the end portion 1103 and the end 1102 in the state after deformation is T _1, the increase in length between the end portion 1103 and the end portion 1102 by the deformation of the lithium-ion battery, T ₁ −T, which is a value represented by the following formula (8).

That is, it is desirable that a gap that allows the increase is provided inside the storage battery. In short, in the cross section shown in FIG. 6, the length of the exterior body is the length of the outer edge of the internal structure before deformation. It is desirable that the length is 2L + 2T plus T ₁ −T which is an increase due to deformation. In other words, based on the thickness and length of the internal structure, the size of the gap for preventing damage to the exterior body of the storage battery can be derived from the desired radius of curvature as the deformation size of the storage battery.

In conclusion, when the lithium ion storage battery 110 is deformed by the axis that is the center of curvature, the length of the cross section of the exterior body in the plane perpendicular to the axis is the length of the outer ring shape of the internal structure 117 at the time of deformation. The length may be 2L + T + T ₁ or more. When the length of the exterior body in that case is set to A, A satisfy | fills following formula (1).

The technical idea is only in the lithium ion storage battery according to one aspect of the present invention in which the friction between the stacked bodies is small, and the stacked bodies are slid from each other and released from stress according to the deformation of the storage battery. It also solves existing problems.

Next, a lithium ion storage battery according to one embodiment of the present invention will be described.

≪Positive electrode structure≫
First, the positive electrode will be described. The positive electrode includes a positive electrode active material layer 104 and a positive electrode current collector 105.

As the positive electrode active material used for the positive electrode active material layer 104, a material capable of inserting and removing carrier ions such as lithium ions can be used. For example, an olivine type crystal structure, a layered rock salt type crystal structure, or the like can be used. Or a lithium-containing material having a spinel crystal structure.

Typical examples of olivine type lithium-containing materials (general formula LiMPO ₄ (M is Fe (II), Mn (II), Co (II) or Ni (II))) include LiFePO ₄ , LiNiPO ₄ , LiCoPO ₄ . _{4, LiMnPO 4, LiFe a Ni} b PO 4, LiFe a Co b PO 4, LiFe a Mn b PO 4, LiNi a Co b PO 4, LiNi a Mn b PO 4 (a + b ≦ 1, 0 <a <1 _{, 0 <b <1),} LiFe c Ni d Co e PO 4, LiFe c Ni d Mn e PO 4, LiNi c Co d Mn e PO 4 (c + d + e ≦ 1, 0 <c <1,0 <d < _{1,0 <e <1), LiFe} f Ni g Co h Mn i PO 4 (f + g + h + i is 1 or less, 0 <f <1,0 <g <1,0 <h <1,0 <i 1), and the like.

For example, lithium iron phosphate (LiFePO ₄ ) satisfies the requirements for a positive electrode active material in a well-balanced manner, such as safety, stability, high capacity density, high potential, and the presence of lithium ions extracted during initial oxidation (charging). Therefore, it is preferable.

Examples of the lithium-containing material having a layered rock salt type crystal structure include NiCo-based materials such as lithium cobaltate (LiCoO ₂ ), LiNiO ₂ , LiMnO ₂ , Li ₂ MnO ₃ , and LiNi _0.8 Co _0.2 O ₂ ( The general formula is NiMn series such as LiNi _x Co _1-x O ₂ (0 <x <1)), LiNi _0.5 Mn _0.5 O ₂ (general formula is LiNi _x Mn _1-x O ₂ (0 _{<x <1)),} also referred to as NiMnCo system (NMC such _{LiNi 1/3 Mn 1/3 Co 1/3 O 2} . general _{formula, LiNi x Mn y Co 1-} x-y O 2 (x> 0 , Y> 0, x + y <1)). _{Moreover, Li (Ni 0.8 Co 0.15 Al} 0.05) O 2, Li 2 MnO 3 -LiMO 2 (M is Co, Ni or Mn) may also be mentioned, and the like.

Particularly, LiCoO ₂ has the capacity is large, it is stable in the atmosphere as compared to LiNiO _2, because there are advantages such that it is thermally stable than LiNiO _2, preferred.

Examples of the lithium-containing material having a spinel crystal structure include LiMn ₂ O ₄ , Li _{1 + x} Mn _2−x O ₄ , Li (MnAl) ₂ O ₄ , LiMn _1.5 Ni _0.5 O _{4 and the} like. It is done.

When a small amount of lithium nickelate (LiNiO ₂ or LiNi _1-x MO ₂ (M = Co, Al, etc.)) is mixed with a lithium-containing material having a spinel type crystal structure containing manganese such as LiMn ₂ O ₄ , manganese There are advantages such as suppression of elution and suppression of electrolyte decomposition.

Further, as the positive electrode active material, the general formula Li _(2-j) MSiO ₄ (M is Fe (II), Mn (II), Co (II), or Ni (II)) (j is 0 or more and 2 or less) The complex oxide represented by these can be used. Representative examples of the general formula Li _(2-j) MSiO ₄ include Li _(2-j) FeSiO ₄ , Li _(2-j) NiSiO ₄ , Li _(2-j) CoSiO ₄ , Li _(2-j) MnSiO _{4, Li (2-j)} Fe k Ni l SiO 4, Li (2-j) Fe k Co l SiO 4, Li (2-j) Fe k Mn l SiO 4, Li (2-j) Ni k Co _{l SiO 4, Li (2-} j) Ni k Mn l SiO 4 (k + l is 1 or _{less, 0 <k <1,0 <l} <1), Li (2-j) Fe m Ni n Co q SiO 4, _{Li (2-j) Fe m} Ni n Mn q SiO 4, Li (2-j) Ni m Co n Mn q SiO 4 (m + n + q is 1 or less, 0 <m <1,0 <n <1,0 <q _{<1), Li (2-} j) Fe r Ni s Co t Mn _u SiO ₄ (r + s + t + u is 1 or less, 0 <r <1, 0 <s <1, 0 <t <1, 0 <u <1).

Further, as a positive electrode active material, A _x M ₂ (XO ₄ ) ₃ (A is Li, Na, or Mg) (M is Fe, Mn, Ti, V, Nb, or Al) (X is S, P , Mo, W, As, or Si), a NASICON compound represented by the general formula can be used. Examples of NASICON compounds include Fe ₂ (MnO ₄ ) ₃ , Fe ₂ (SO ₄ ) ₃ , and Li ₃ Fe ₂ (PO ₄ ) ₃ . Further, as a positive electrode active material, a compound represented by a general formula of Li ₂ MPO ₄ F, Li ₂ MP ₂ O ₇ , Li ₅ MO ₄ (M is Fe or Mn), a perovskite type fluoride such as NaFeF ₃ , FeF _3, etc. Metal, chalcogenides such as TiS ₂ and MoS ₂ (sulfides, selenides, tellurides), lithium-containing materials having an inverse spinel crystal structure such as LiMVO ₄ , vanadium oxides (V ₂ O ₅ , V ₆ O ₁₃ , LiV ₃ O ₈ or the like), manganese oxide, organic sulfur, or the like can be used.

In addition, when carrier ions are alkali metal ions other than lithium ions or alkaline earth metal ions, as the positive electrode active material, an alkali metal (for example, sodium or potassium) is used instead of lithium in the above compound or oxide. Alkaline earth metals (eg, calcium, strontium, barium, beryllium, magnesium, etc.) may be used. For example, a sodium-containing layered oxide such as NaFeO ₂ or Na _2/3 [Fe _1/2 Mn _1/2 ] O ₂ can be used as the positive electrode active material.

A material obtained by combining a plurality of the above materials may be used as the positive electrode active material. For example, a solid solution obtained by combining a plurality of the above materials can be used as the positive electrode active material. For example, a solid solution of LiCo _1/3 Mn _1/3 Ni _1/3 O ₂ and Li ₂ MnO ₃ can be used as the positive electrode active material.

As the positive electrode active material, a material having an average primary particle diameter of 50 nm or more and 100 μm or less is preferably used.

The positive electrode active material, together with the negative electrode active material, plays a central role in the battery reaction of the storage battery and releases and absorbs carrier ions. In order to increase the life of the storage battery, it is preferable that the material has a small capacity related to the irreversible reaction of the battery reaction, and it is preferable that the material has high charge / discharge efficiency.

Since the active material is in contact with the electrolytic solution, the active material reacts with the electrolytic solution, and when the active material is lost and deteriorated due to the reaction, the capacity of the storage battery is reduced. It is desirable that this reaction does not occur.

As the conductive assistant for the electrode, acetylene black (AB), graphite (graphite) particles, carbon nanotubes, graphene, fullerene, or the like can be used.

The conductive assistant can form an electrically conductive network in the electrode. The conductive auxiliary agent can maintain the electric conduction path between the positive electrode active materials. By adding a conductive additive to the positive electrode active material layer, the positive electrode active material layer 101 having high electrical conductivity can be realized.

In addition to typical polyvinylidene fluoride (PVDF), polyimide, polytetrafluoroethylene, polyvinyl chloride, ethylene propylene diene polymer, fluororubber, polymethyl methacrylate, polyethylene, nitrocellulose, and the like can be used as the binder.

The content of the binder with respect to the total amount of the positive electrode active material layer 104 is preferably 1 wt% or more and 10 wt% or less, more preferably 2 wt% or more and 8 wt% or less, and further preferably 3 wt% or more and 5 wt% or less. In addition, the content of the conductive additive with respect to the total amount of the positive electrode active material layer 101 is preferably 1 wt% or more and 10 wt% or less, and more preferably 1 wt% or more and 5 wt% or less.

When the positive electrode active material layer 104 is formed using a coating method, a positive electrode active material, a binder, a conductive additive, and a dispersion medium are mixed to prepare an electrode slurry, which is applied onto the positive electrode current collector 105 and dried. Just do it.

Note that the positive electrode current collector 105 can be formed using a material that has high conductivity and does not alloy with carrier ions such as lithium, such as metals such as stainless steel, gold, platinum, aluminum, and titanium, and alloys thereof. Alternatively, an aluminum alloy to which an element that improves heat resistance, such as silicon, titanium, neodymium, scandium, or molybdenum, is added can be used. Alternatively, a metal element that forms silicide by reacting with silicon may be used. Examples of metal elements that react with silicon to form silicide include zirconium, titanium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, nickel, and the like. As the positive electrode current collector, a foil shape, a plate shape (sheet shape), a net shape, a punching metal shape, an expanded metal shape, or the like can be used as appropriate.

Note that a structure in which the positive electrode active material layer 104 is provided on one surface of the positive electrode current collector 105 and the positive electrode active material layer is not provided on the other surface can be employed. In that case, in the state where the positive electrode active material layer is not provided, the surface of the positive electrode current collector 105 is flat and has a small friction coefficient. Therefore, when the surface where the positive electrode active material layer of another positive electrode current collector is not provided is in contact with the surface, both current collectors can slide with each other according to the stress.

The positive electrode of the lithium ion storage battery can be manufactured through the above steps.

<Negative electrode configuration>
Next, the negative electrode will be described. The negative electrode includes a negative electrode active material layer 102 and a negative electrode current collector 101. The process for forming the negative electrode will be described below.

Examples of the negative electrode active material used for the negative electrode active material layer 102 include carbon, graphitizable carbon (soft carbon), non-graphitizable carbon (hard carbon), carbon nanotubes, graphene, and carbon black. is there. Examples of graphite include artificial graphite such as mesocarbon microbeads (MCMB), coke-based artificial graphite, and pitch-based artificial graphite, and natural graphite such as spheroidized natural graphite. In addition, the shape of graphite includes a scale-like shape and a spherical shape.

In addition to the carbon-based material, a material capable of performing a charge / discharge reaction by an alloying / dealloying reaction with lithium can be used as the negative electrode active material. For example, a material containing at least one of Ga, Si, Al, Ge, Sn, Pb, Sb, Bi, Ag, Zn, Cd, In, and the like can be used. Such an element has a larger capacity than carbon, and silicon is particularly preferable because its theoretical capacity is as high as 4200 mAh / g. Examples of alloy materials using such elements include Mg ₂ Si, Mg ₂ Ge, Mg ₂ Sn, SnS ₂ , V ₂ Sn ₃ , FeSn ₂ , CoSn ₂ , Ni ₃ Sn ₂ , and Cu ₆ Sn _5. , Ag ₃ Sn, Ag ₃ Sb, Ni ₂ MnSb, CeSb ₃ , LaSn ₃ , La ₃ Co ₂ Sn ₇ , CoSb ₃ , InSb, SbSn, and the like.

Further, as the negative electrode active material, SiO, SnO, SnO _2, titanium dioxide _(TiO 2), lithium titanium oxide _{(Li 4 Ti 5 O 12)} , lithium - graphite intercalation compound _{(Li x C} 6), niobium pentoxide ( An oxide such as Nb ₂ O ₅ ), tungsten oxide (WO ₂ ), or molybdenum oxide (MoO ₂ ) can be used.

Further, as the anode active material, a double nitride of lithium and a transition metal, _{Li 3-x M x} N with Li ₃ N type structure (M is Co, Ni or Cu) can be used. For example, Li _2.6 Co _0.4 N ₃ shows a large charge / discharge capacity (900 mAh / g, 1890 mAh / cm ³ ) and is preferable.

When a lithium and transition metal double nitride is used, since the negative electrode active material contains lithium ions, it can be combined with a material such as V ₂ O ₅ or Cr ₃ O ₈ that does not contain lithium ions as the positive electrode active material. Note that even when a material containing lithium ions is used for the positive electrode active material, lithium and transition metal double nitride can be used as the negative electrode active material by previously desorbing lithium ions contained in the positive electrode active material.

A material that causes a conversion reaction can also be used as the negative electrode active material. For example, a transition metal oxide that does not undergo an alloying reaction with lithium, such as cobalt oxide (CoO), nickel oxide (NiO), or iron oxide (FeO), may be used as the negative electrode active material. As a material causing the conversion reaction, oxides such as Fe ₂ O ₃ , CuO, Cu ₂ O, RuO ₂ and Cr ₂ O ₃ , sulfides such as CoS _0.89 , NiS and CuS, Zn ₃ N _{2 are further included.} This also occurs in nitrides such as Cu ₃ N and Ge ₃ N ₄ , phosphides such as NiP ₂ , FeP ₂ and CoP ₃ , and fluorides such as FeF ₃ and BiF ₃ .

As an example of the negative electrode active material, a material having a particle size of 50 nm to 100 μm may be used.

Note that in both the positive electrode active material layer 104 and the negative electrode active material layer 102, a plurality of active material materials may be used in combination at a specific ratio. By using a plurality of materials for the active material layer, the performance of the active material layer can be selected in more detail.

As the conductive assistant for the electrode, acetylene black (AB), graphite (graphite) particles, carbon nanotubes, graphene, fullerene, or the like can be used.

The conductive assistant can form an electrically conductive network in the electrode. The conductive auxiliary agent can maintain the electric conduction path between the negative electrode active materials. By adding a conductive additive in the negative electrode active material layer, the negative electrode active material layer 102 having high electrical conductivity can be realized.

In addition to typical polyvinylidene fluoride (PVDF), as a binder, polyimide, polyvinyl chloride, ethylene propylene diene polymer, styrene-butadiene rubber, acrylonitrile-butadiene rubber, fluorine rubber, polyvinyl acetate, polymethyl methacrylate, polyethylene, Nitrocellulose or the like can be used.

The content of the binder with respect to the total amount of the negative electrode active material layer 102 is preferably 1 wt% or more and 10 wt% or less, more preferably 2 wt% or more and 8 wt% or less, and further preferably 3 wt% or more and 5 wt% or less. In addition, the content of the conductive additive with respect to the total amount of the negative electrode active material layer 103 is preferably 1 wt% or more and 10 wt% or less, and more preferably 1 wt% or more and 5 wt% or less.

Next, the negative electrode active material layer 102 is formed over the negative electrode current collector 101. When the negative electrode active material layer 102 is formed using a coating method, a negative electrode active material, a binder, a conductive additive, and a dispersion medium are mixed to prepare a slurry, which is applied to the negative electrode current collector 101 and dried. If necessary after drying, press treatment may be performed.

Note that the negative electrode current collector 101 is made of a material that is highly conductive and does not alloy with carrier ions such as lithium, such as metals such as stainless steel, gold, platinum, iron, copper, titanium, and tantalum, and alloys thereof. be able to. Alternatively, a metal element that forms silicide by reacting with silicon may be used. Examples of metal elements that react with silicon to form silicide include zirconium, titanium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, nickel, and the like. The negative electrode current collector 102 can have a foil shape, a plate shape (sheet shape), a net shape, a columnar shape, a coil shape, a punching metal shape, an expanded metal shape, or the like as appropriate. The negative electrode current collector 101 may have a thickness of 5 μm to 30 μm. In addition, an undercoat layer may be provided on a part of the surface of the electrode current collector using graphite or the like.

Note that a structure in which the negative electrode active material layer 102 is provided on one surface of the negative electrode current collector 101 and the negative electrode active material layer is not provided on the other surface can be employed. In that case, in a state where the negative electrode active material layer is not provided, the surface of the negative electrode current collector 101 is flat and has a small friction coefficient. Therefore, when the surface where the negative electrode active material layer of another negative electrode current collector is not provided is in contact with the surface, both current collectors can slide with each other in accordance with the stress.

Through the above steps, the negative electrode of the lithium ion storage battery can be produced.

≪Separator configuration≫
The separator 103 will be described. As a material for the separator 103, paper, nonwoven fabric, glass fiber, or synthetic fiber such as nylon (polyamide), vinylon (polyvinyl alcohol fiber), polyester, acrylic, polyolefin, polyurethane, or the like may be used. However, it is necessary to select a material that does not dissolve in the electrolyte solution described later.

More specifically, as the material of the separator 103, for example, a fluoropolymer, a polyether such as polyethylene oxide or polypropylene oxide, a polyolefin such as polyethylene or polypropylene, polyacrylonitrile, polyvinylidene chloride, polymethyl methacrylate, polymethyl acrylate, Polyvinyl alcohol, polymethacrylonitrile, polyvinyl acetate, polyvinyl pyrrolidone, polyethyleneimine, polybutadiene, polystyrene, polyisoprene, polyurethane polymers and derivatives thereof, cellulose, paper, nonwoven fabric, glass fiber alone, or Two or more types can be used in combination.

The separator 103 must have an insulating performance that prevents contact between both electrodes, a performance that retains an electrolytic solution, and an ionic conductivity. As a method for producing a membrane having a function as a separator, there is a method by stretching the membrane. For example, there is a stretch opening method in which a molten polymer material is developed to dissipate heat, and the obtained film is stretched in a biaxial direction parallel to the film to form holes.

The separator can be incorporated into the lithium ion storage battery through the above steps.

≪Electrolyte composition≫

The electrolyte solution 107 that can be used for the lithium ion storage battery according to one embodiment of the present invention is preferably a non-aqueous solution (solvent) containing an electrolyte (solute).

As a solvent for the electrolytic solution 107, a material capable of moving carrier ions is used. For example, an aprotic organic solvent is preferable, and ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate, chloroethylene carbonate, vinylene carbonate, γ-butyrolactone, γ-valerolactone, dimethyl carbonate (DMC), diethyl carbonate ( DEC), ethyl methyl carbonate (EMC), methyl formate, methyl acetate, methyl butyrate, 1,3-dioxane, 1,4-dioxane, dimethoxyethane (DME), dimethyl sulfoxide, diethyl ether, methyl diglyme, acetonitrile, benzo One kind of nitrile, tetrahydrofuran, sulfolane, sultone, etc., or two or more kinds thereof can be used in any combination and ratio.

In addition, by using a polymer material that is gelled as the solvent of the electrolytic solution 107, safety against liquid leakage and the like is increased. Further, the lithium ion storage battery can be made thinner and lighter. Typical examples of the polymer material to be gelated include silicone gel, acrylic gel, acrylonitrile gel, polyethylene oxide gel, polypropylene oxide gel, and fluorine polymer gel.

In addition, by using one or more ionic liquids (also called room temperature molten salts) that are flame retardant and vaporizable as the solvent of the electrolyte, the internal temperature can be reduced due to internal short circuit or overcharge of the lithium ion storage battery. Even if it rises, it is possible to prevent the explosion or ignition of the lithium ion storage battery. Thereby, the safety | security of a lithium ion storage battery can be improved.

Further, as the electrolytic solution used for the storage battery, it is preferable to use a highly purified electrolytic solution having a small content of elements other than the constituent elements of the granular dust and the electrolytic solution (hereinafter also simply referred to as “impurities”). Specifically, the mass ratio of impurities to the electrolytic solution is preferably 1% or less, preferably 0.1% or less, and more preferably 0.01% or less. Moreover, you may add additives, such as vinylene carbonate, to electrolyte solution.

As the electrolytes dissolved in the above solvent, when using a lithium carrier ion, e.g. _{LiPF 6, LiClO 4, LiAsF 6} , LiBF 4, LiAlCl 4, LiSCN, LiBr, LiI, Li 2 SO 4, Li 2 B ₁₀ Cl ₁₀ , Li ₂ B ₁₂ Cl ₁₂ , LiCF ₃ SO ₃ , LiC ₄ F ₉ SO ₃ , LiC (CF ₃ SO ₂ ) ₃ , LiC (C ₂ F ₅ SO ₂ ) ₃ , LiN (CF ₃ SO ₂ ) ₂ , lithium salt such as LiN (C ₄ F ₉ SO ₂ ) (CF ₃ SO ₂ ), LiN (C ₂ F ₅ SO ₂ ) ₂ , or two or more of these in any combination and ratio Can be used.

In the above-described electrolyte, the case where the carrier ions are lithium ions has been described, but carrier ions other than lithium ions can also be used. As carrier ions other than lithium ions, in the case of alkali metal ions or alkaline earth metal ions, as the electrolyte, in the lithium salt, instead of lithium, an alkali metal (for example, sodium or potassium), an alkaline earth metal ( For example, calcium, strontium, barium, beryllium, magnesium, or the like) may be used.

The electrolytic solution may react with the positive electrode current collector to corrode the positive electrode current collector. In order to prevent such corrosion, it is preferable to add several wt% LiPF ₆ to the electrolytic solution. This is because a nonconductive film is formed on the surface of the positive electrode current collector, and the nonconductive film suppresses the reaction between the electrolytic solution and the positive electrode current collector. However, in order not to dissolve the positive electrode active material layer, the concentration of LiPF ₆ is 10 wt% or less, preferably 5 wt% or less, more preferably 3 wt% or less.

<External body configuration>
Next, the exterior body 116 will be described. The exterior body 116 is provided with a metal thin film having excellent flexibility such as aluminum, stainless steel, copper, nickel on a film made of a material such as polyethylene, polypropylene, polycarbonate, ionomer, polyamide, etc. A film having a three-layer structure in which an insulating synthetic resin film such as a polyamide-based resin or a polyester-based resin is provided on the outer surface of the exterior body can be used. By setting it as such a three-layer structure, while permeating | transmitting electrolyte solution and gas, the insulation is ensured and it has electrolyte solution resistance collectively. The exterior body is folded inward and stacked, or the inner surfaces of the two exterior bodies face each other and are heated to apply heat, so that the material on the inner surface melts and the two exterior bodies can be fused and sealed. A structure can be made.

Assuming that the part where the outer package is fused and the sealing structure is formed is a sealing part, when the outer package is folded inward and overlapped, the sealing part is formed at a place other than the crease. The first region and the second region overlapping the first region are fused together. When two exterior bodies are stacked, a sealing portion is formed on the entire outer periphery by a method such as heat fusion.

Note that in one embodiment of the present invention, the exterior body 116 is desirably a certain length or longer in order to provide a gap inside the lithium ion storage battery 110 as described above.

≪Flexible storage battery≫
When a flexible material is selected from the materials of the members described in this embodiment and used, a flexible lithium ion storage battery can be manufactured. In recent years, research and development of deformable devices has been active. There is a demand for flexible storage batteries as storage batteries used in such devices.

In the case where the storage battery sandwiching the electrodes 1805 such as the electrode / electrolytic solution is curved with the two films as the outer package, the curvature radius 1802 of the film 1801 closer to the curvature center 1800 of the storage battery is the film farther from the curvature center 1800. It is smaller than the radius of curvature 1804 of 1803 (FIG. 7A). When the storage battery is curved so that the cross section has an arc shape, compressive stress is applied to the surface of the film close to the center of curvature 1800, and tensile stress is applied to the surface of the film far from the center of curvature 1800 (FIG. 7B).

When a flexible lithium ion storage battery is deformed, a large stress is applied to the exterior body. However, if a pattern formed by recesses or protrusions is formed on the surface of the exterior body, a compressive stress or a tensile stress is caused by the deformation of the storage battery. Even if it is applied, the influence of strain can be suppressed. Therefore, the storage battery can be deformed in a range where the radius of curvature of the exterior body on the side close to the center of curvature is 50 mm, preferably 30 mm.

The curvature radius of the surface will be described with reference to FIG. In FIG. 8A, in a plane 1701 obtained by cutting the curved surface 1700, a part of a curve 1702 included in the curved surface 1700 is approximated to a circular arc, the radius of the circle is set as a curvature radius 1703, and the center of the circle is set as a curvature. The center is 1704. FIG. 8B shows a top view of the curved surface 1700. FIG. 8C is a cross-sectional view in which a curved surface 1700 is cut along a plane 1701. When cutting a curved surface with a plane, the radius of curvature of the curve appearing in the cross section varies depending on the angle of the plane with respect to the curved surface and the cutting position. In this specification, the smallest radius of curvature is the radius of curvature of the surface. And

In addition, the cross-sectional shape of the storage battery is not limited to a simple arc shape, and a part of the storage battery can have a circular arc shape. For example, the shape shown in FIG. It can also be S-shaped. In the case where the curved surface of the storage battery has a shape having a plurality of centers of curvature, the exterior body closer to the center of curvature of the two exterior bodies on the curved surface having the smallest curvature radius among the curvature radii at each of the plurality of curvature centers The storage battery can be deformed in a range where the radius of curvature is 50 mm, preferably 30 mm.

≪Assembly and aging of storage battery≫
Next, by combining the above-described constituent members and sealing the outer package 207, as shown in FIGS. 1 and 2, the positive electrode current collector 105, the positive electrode active material layer 104, the separator 103, and the negative electrode active material An internal structure including a plurality of stacked bodies in which the layer 102 and the negative electrode current collector 101 are stacked is sealed with the outer body 107 together with the electrolytic solution 107.

Next, an aging process is performed. First, the ambient temperature is kept at, for example, room temperature, and constant current charging is performed at a low rate up to the matching voltage. Next, the gas generated in the region inside the exterior body by charging is released to the outside of the exterior body. Next, charging is performed at a higher rate than the first charging.

Then, store for a long time in a slightly high temperature environment. For example, it is stored for 24 hours or more in an environment of 40 ° C. or higher.

After being stored for a long time in a slightly high temperature environment, the gas generated in the region inside the exterior body is released again. Further, the battery is discharged at a rate of 0.2 C in a room temperature environment, charged at the same rate, discharged at the same rate again, and further charged at the same rate. And an aging process is complete | finished by discharging at the same rate.

As described above, the storage battery according to the present invention can be manufactured.

This embodiment can be implemented in appropriate combination with any of the other embodiments.

Note that in this specification and the like, when at least one specific example is described in a drawing or text described in one embodiment, it is easy for those skilled in the art to derive a superordinate concept of the specific example. To be understood. Therefore, in the case where at least one specific example is described in a drawing or text described in one embodiment, the superordinate concept of the specific example is also disclosed as one aspect of the invention. Aspects can be configured. One embodiment of the invention is clear.

Note that in this specification and the like, at least the contents shown in the drawings (may be part of the drawings) are disclosed as one embodiment of the invention, and can constitute one embodiment of the invention It is. Therefore, if a certain content is described in the figure, even if it is not described using sentences, the content is disclosed as one aspect of the invention and may constitute one aspect of the invention. Is possible. Similarly, a drawing obtained by extracting a part of the drawing is also disclosed as one embodiment of the invention, and can constitute one embodiment of the invention. And it can be said that one aspect of the invention is clear.

Note that one embodiment of the present invention is described in this embodiment. Alternatively, in another embodiment, one embodiment of the present invention will be described. Note that one embodiment of the present invention is not limited thereto. That is, in this embodiment and other embodiments, various aspects of the invention are described; therefore, one embodiment of the present invention is not limited to a particular aspect. For example, as an embodiment of the present invention, an example in which the present invention is applied to a flexible lithium ion secondary battery has been described; however, one embodiment of the present invention is not limited thereto. In some cases or depending on the situation, one embodiment of the present invention includes various secondary batteries, lead storage batteries, lithium ion polymer secondary batteries, nickel / hydrogen storage batteries, nickel / cadmium storage batteries, nickel / iron storage batteries, nickel -You may apply to a zinc storage battery, a silver oxide zinc storage battery, a solid battery, an air battery, a primary battery, a capacitor, or an electric double layer capacitor, an ultra capacitor, a super capacitor, a lithium ion capacitor, etc. Alternatively, for example, depending on circumstances or circumstances, one embodiment of the present invention may not be applied to a lithium ion secondary battery.

(Embodiment 2)
In this embodiment, a structure of a storage battery according to one embodiment of the present invention will be described with reference to FIGS.

≪Coin-type storage battery≫
FIG. 9A is an external view of a coin-type (single-layer flat type) storage battery, and FIG. 9B is a cross-sectional view thereof.

In the coin-type storage battery 300, a positive electrode can 301 also serving as a positive electrode terminal and a negative electrode can 302 also serving as a negative electrode terminal are insulated and sealed with a gasket 303 formed of polypropylene or the like. The positive electrode 304 is formed by a positive electrode current collector 305 and a positive electrode active material layer 306 provided so as to be in contact therewith. In addition to the positive electrode active material, the positive electrode active material layer 306 may include a binder (binder) for increasing the adhesion of the positive electrode active material, a conductive auxiliary agent for increasing the conductivity of the positive electrode active material layer, and the like. Good.

The negative electrode 307 is formed of a negative electrode current collector 308 and a negative electrode active material layer 309 provided so as to be in contact therewith. In addition to the negative electrode active material, the negative electrode active material layer 309 may include a binder (binder) for increasing the adhesion of the negative electrode active material, a conductive auxiliary agent for increasing the conductivity of the negative electrode active material layer, and the like. Good. A separator 310 and an electrolyte (not shown) are provided between the positive electrode active material layer 306 and the negative electrode active material layer 309.

The material shown in Embodiment Mode 1 can be used for each constituent member.

For the positive electrode can 301 and the negative electrode can 302, a metal such as nickel or titanium, or an alloy thereof or an alloy of these with another metal (for example, stainless steel) having corrosion resistance to the electrolytic solution is used. Can do. In order to prevent corrosion by the electrolytic solution, it is preferable to coat nickel or the like. The positive electrode can 301 and the negative electrode can 302 are electrically connected to the positive electrode 304 and the negative electrode 307, respectively.

The negative electrode 307, the positive electrode 304, and the separator 310 are impregnated in an electrolyte, and the positive electrode 304, the separator 310, the negative electrode 307, and the negative electrode can 302 are laminated in this order with the positive electrode can 301 facing down, as shown in FIG. 9B. Then, the positive electrode can 301 and the negative electrode can 302 are pressure-bonded via a gasket 303 to manufacture a coin-shaped storage battery 300.

Here, the flow of current when the storage battery is charged will be described with reference to FIG. When a storage battery using lithium is regarded as a closed circuit, the movement of lithium ions and the flow of current are in the same direction. In addition, in a storage battery using lithium, the anode (anode) and the cathode (cathode) are interchanged by charging and discharging, and the oxidation reaction and the reduction reaction are interchanged. Therefore, the electrode having a high reaction potential is called the positive electrode. An electrode with a low is called a negative electrode. Therefore, in the present specification, the positive electrode is referred to as “positive electrode” or “whether the battery is being charged, discharged, a reverse pulse current is applied, or a charge current is applied. The positive electrode is referred to as a “positive electrode”, and the negative electrode is referred to as a “negative electrode” or a “− electrode (negative electrode)”. If the terms anode (anode) and cathode (cathode) related to the oxidation reaction or reduction reaction are used, the charge and discharge are reversed, which may cause confusion. Therefore, the terms anode (anode) and cathode (cathode) are not used in this specification. If the terms anode (anode) or cathode (cathode) are used, specify whether charging or discharging, and indicate whether it corresponds to the positive electrode (positive electrode) or the negative electrode (negative electrode). To do.

A charger is connected to the two terminals shown in FIG. 9C, and the storage battery 400 is charged. As charging of the storage battery 400 proceeds, the potential difference between the electrodes increases. In FIG. 9C, the battery flows from the external terminal of the storage battery 400 toward the positive electrode 402, flows in the storage battery 400 from the positive electrode 402 toward the negative electrode 404, and flows from the negative electrode toward the external terminal of the storage battery 400. The direction of current is positive. That is, the direction in which the charging current flows is the current direction.

≪Cylindrical storage battery≫
Next, an example of a cylindrical storage battery will be described with reference to FIG. As shown in FIG. 10A, the cylindrical storage battery 600 has a positive electrode cap (battery lid) 601 on the top surface and a battery can (outer can) 602 on the side surface and bottom surface. The positive electrode cap and the battery can (outer can) 602 are insulated by a gasket (insulating packing) 610.

FIG. 10B is a diagram schematically showing a cross section of a cylindrical storage battery. Inside the hollow cylindrical battery can 602, a battery element in which a strip-like positive electrode 604 and a negative electrode 606 are wound with a separator 605 interposed therebetween is provided. Although not shown, the battery element is wound around a center pin. The battery can 602 has one end closed and the other end open. For the battery can 602, a metal such as nickel or titanium that is corrosion resistant to an electrolytic solution, an alloy thereof, or an alloy of these with another metal (for example, stainless steel) can be used. In order to prevent corrosion by the electrolytic solution, it is preferable to coat nickel or the like. Inside the battery can 602, the battery element in which the positive electrode, the negative electrode, and the separator are wound is sandwiched between a pair of opposing insulating plates 608 and 609. Further, a non-aqueous electrolyte (not shown) is injected into the inside of the battery can 602 provided with the battery element. As the non-aqueous electrolyte, the same one as a coin-type storage battery can be used.

The positive electrode 604 and the negative electrode 606 may be manufactured in the same manner as the positive electrode and the negative electrode of the coin-type storage battery described above. However, since the positive electrode and the negative electrode used in the cylindrical storage battery are wound, an active material is applied to both sides of the current collector. It differs in the point to form. A positive electrode terminal (positive electrode current collecting tab) 603 is connected to the positive electrode 604, and a negative electrode terminal (negative electrode current collecting tab) 607 is connected to the negative electrode 606. Both the positive electrode terminal 603 and the negative electrode terminal 607 can use a metal material such as aluminum. The positive terminal 603 is resistance-welded to the safety valve mechanism 612, and the negative terminal 607 is resistance-welded to the bottom of the battery can 602. The safety valve mechanism 612 is electrically connected to the positive electrode cap 601 via a PTC element (Positive Temperature Coefficient) 611. The safety valve mechanism 612 disconnects the electrical connection between the positive electrode cap 601 and the positive electrode 604 when the increase in the internal pressure of the battery exceeds a predetermined threshold value. The PTC element 611 is a heat-sensitive resistance element that increases in resistance when the temperature rises, and prevents abnormal heat generation by limiting the amount of current by increasing the resistance. For the PTC element, barium titanate (BaTiO ₃ ) -based semiconductor ceramics or the like can be used.

≪Laminated storage battery≫
Next, an example of a laminate-type storage battery will be described with reference to FIG. If the laminate-type storage battery has a flexible structure, the storage battery can be bent in accordance with the deformation of the electronic apparatus if it is mounted on an electronic apparatus having at least a part of the flexibility.

A laminate-type storage battery 500 illustrated in FIG. 11A includes a positive electrode 503 having a positive electrode current collector 501 and a positive electrode active material layer 502, a negative electrode 506 having a negative electrode current collector 504 and a negative electrode active material layer 505, and a separator 507. And an electrolytic solution 508 and an exterior body 509. A separator 507 is provided between a positive electrode 503 and a negative electrode 506 provided in the exterior body 509. The exterior body 509 is filled with the electrolytic solution 508. As the electrolytic solution 508, the electrolytic solution described in Embodiment 1 can be used.

In the laminated storage battery 500 illustrated in FIG. 11A, the positive electrode current collector 501 and the negative electrode current collector 504 also serve as terminals for obtaining electrical contact with the outside. Therefore, part of the positive electrode current collector 501 and the negative electrode current collector 504 may be disposed so as to be exposed to the outside from the exterior body 509. Further, the positive electrode current collector 501 and the negative electrode current collector 504 are not exposed to the outside from the exterior body 509, and the tab electrode and the positive electrode current collector 501 or the negative electrode current collector 504 are ultrasonically bonded using a tab electrode. The tab electrode may be exposed to the outside.

In the laminate-type storage battery 500, a metal thin film having excellent flexibility such as aluminum, stainless steel, copper, or nickel is formed on the exterior body 509 on a film made of a material such as polyethylene, polypropylene, polycarbonate, ionomer, or polyamide. Further, a laminate film having a three-layer structure in which an insulating synthetic resin film such as a polyamide resin or a polyester resin is provided on the metal thin film as the outer surface of the outer package can be used.

An example of a cross-sectional structure of a laminate-type storage battery 500 is shown in FIG. In FIG. 11A, for the sake of simplicity, an example in which two current collectors are used is shown, but actually, a plurality of electrode layers are used.

In FIG. 11B, the number of electrode layers is 16 as an example. In addition, even if the number of electrode layers is 16, the storage battery 500 has flexibility. FIG. 11B illustrates a structure in which the negative electrode current collector 504 has eight layers and the positive electrode current collector 501 has eight layers in total. FIG. 11B shows a cross section of the negative electrode take-out portion, in which an eight-layer negative electrode current collector 504 is ultrasonically bonded. Of course, the number of electrode layers is not limited to 16, and may be large or small. When there are many electrode layers, it can be set as the storage battery which has more capacity | capacitance. Moreover, when there are few electrode layers, it can be made thin and can be set as the storage battery excellent in flexibility.

Here, an example of an external view of a laminate-type storage battery 500 is shown in FIGS. 12 and 13 include a positive electrode 503, a negative electrode 506, a separator 507, an exterior body 509, a positive electrode tab electrode 510, and a negative electrode tab electrode 511.

FIG. 14A shows an external view of the positive electrode 503 and the negative electrode 506. The positive electrode 503 includes a positive electrode current collector 501, and the positive electrode active material layer 502 is formed on the surface of the positive electrode current collector 501. The positive electrode 503 has a region where the positive electrode current collector 501 is partially exposed (referred to as a tab region). The negative electrode 506 includes a negative electrode current collector 504, and the negative electrode active material layer 505 is formed on the surface of the negative electrode current collector 504. The negative electrode 506 has a region where the negative electrode current collector 504 is partially exposed, that is, a tab region. The area and shape of the tab region included in the positive electrode and the negative electrode are not limited to the example illustrated in FIG.

≪Method for producing laminated storage battery≫
Here, an example of a method for manufacturing a laminated storage battery whose external view is shown in FIG. 12 will be described with reference to FIGS.

First, the negative electrode 506, the separator 507, and the positive electrode 503 are stacked. FIG. 14B illustrates the negative electrode 506, the separator 507, and the positive electrode 503 which are stacked. Here, an example in which five sets of negative electrodes and four sets of positive electrodes are used is shown. Next, the tab regions of the positive electrode 503 are joined to each other and the positive electrode tab electrode 510 is joined to the tab region of the outermost positive electrode. For joining, for example, ultrasonic welding or the like may be used. Similarly, the tab regions of the negative electrode 506 are joined together, and the negative electrode tab electrode 511 is joined to the tab region of the outermost negative electrode.

Next, the negative electrode 506, the separator 507, and the positive electrode 503 are disposed over the exterior body 509.

Next, as shown in FIG. 14C, the exterior body 509 is bent at a portion indicated by a broken line. Then, the outer peripheral part of the exterior body 509 is joined. For example, thermocompression bonding or the like may be used for bonding. At this time, a region (hereinafter referred to as an introduction port) that is not joined to a part (or one side) of the exterior body 509 is provided so that the electrolytic solution 508 can be put later.

Next, the electrolytic solution 508 is introduced into the exterior body 509 from the introduction port provided in the exterior body 509. The introduction of the electrolytic solution 508 is preferably performed in a reduced pressure atmosphere or an inert gas atmosphere. Finally, the inlet is joined. Thus, the storage battery 500 which is a laminate type storage battery can be manufactured.

In the present embodiment, coin-type, laminate-type, and cylindrical-type storage batteries are shown as storage batteries, but various types of storage batteries such as other sealed storage batteries and prismatic storage batteries can be used. Alternatively, a structure in which a plurality of positive electrodes, negative electrodes, and separators are stacked, or a structure in which positive electrodes, negative electrodes, and separators are wound may be employed.

FIG. 10 illustrates an example in which a flexible laminate-type storage battery is mounted on an electronic device. As an electronic device to which a storage battery having a flexible shape is applied, for example, a television device (also referred to as a television or a television receiver), a monitor for a computer, a digital camera, a digital video camera, a digital photo frame, a mobile phone ( Large-sized game machines such as a mobile phone, a mobile phone device), a portable game machine, a portable information terminal, a sound reproduction device, and a pachinko machine.

In addition, a storage battery having a flexible shape can be incorporated along the inner or outer wall of a house or building, or along the curved surface of the interior or exterior of an automobile.

FIG. 15A illustrates an example of a mobile phone. A mobile phone 7400 is provided with a display portion 7402 incorporated in a housing 7401, operation buttons 7403, an external connection port 7404, a speaker 7405, a microphone 7406, and the like. Note that the mobile phone 7400 includes a storage battery 7407.

FIG. 15B illustrates a state where the mobile phone 7400 is bent. When the cellular phone 7400 is deformed by an external force to bend the whole, the storage battery 7407 provided therein is also curved. At that time, the state of the bent storage battery 7407 is shown in FIG. The storage battery 7407 is a laminate type storage battery.

FIG. 15D illustrates an example of a bangle display device. A portable display device 7100 includes a housing 7101, a display portion 7102, operation buttons 7103, and a storage battery 7104. FIG. 15E shows the state of the storage battery 7104 bent.

≪Example of storage battery structure≫
A structural example of the storage battery will be described with reference to FIGS.

FIGS. 16A and 16B are external views of a storage battery. The storage battery includes a circuit board 900 and a storage battery 913. A label 910 is attached to the storage battery 913. Further, as illustrated in FIG. 16B, the storage battery includes a terminal 951, a terminal 952, and an antenna 915.

The circuit board 900 includes a terminal 911 and a circuit 912. The terminal 911 is connected to the terminal 951, the terminal 952, the antenna 914, the antenna 915, and the circuit 912. Note that a plurality of terminals 911 may be provided, and each of the plurality of terminals 911 may be a control signal input terminal, a power supply terminal, or the like.

The circuit 912 may be provided on the back surface of the circuit board 900. The antenna 914 and the antenna 915 are not limited to a coil shape, and may be a linear shape or a plate shape, for example. An antenna such as a planar antenna, an aperture antenna, a traveling wave antenna, an EH antenna, a magnetic field antenna, or a dielectric antenna may be used. Alternatively, the antenna 914 or the antenna 915 may be a flat conductor. The flat conductor can function as one of electric field coupling conductors. That is, the antenna 914 or the antenna 915 may function as one of the two conductors of the capacitor. Thereby, not only an electromagnetic field and a magnetic field but power can also be exchanged by an electric field.

The line width of the antenna 914 is preferably larger than the line width of the antenna 915. Accordingly, the amount of power received by the antenna 914 can be increased.

The storage battery includes a layer 916 between the antenna 914 and the antenna 915 and the storage battery 913. The layer 916 has a function of preventing the influence of the storage battery 913 on the electromagnetic field, for example. As the layer 916, for example, a magnetic material can be used.

In addition, the structure of a storage battery is not limited to FIG.

For example, as shown in FIGS. 17A-1 and 17A-2, an antenna is provided on each of a pair of opposed surfaces of the storage battery 913 shown in FIGS. 16A and 16B. It may be provided. 17A-1 is an external view seen from one side direction of the pair of surfaces, and FIG. 17A-2 is an external view seen from the other side direction of the pair of surfaces. In addition, about the same part as the storage battery shown to FIG. 16 (A) and FIG. 16 (B), description of the storage battery shown to FIG. 16 (A) and FIG. 16 (B) can be used suitably.

As shown in FIG. 17A-1, an antenna 914 is provided on one of a pair of surfaces of the storage battery 913 with a layer 916 sandwiched therebetween, and as shown in FIG. 17A-2, the pair of surfaces of the storage battery 913 An antenna 915 is provided with the layer 917 interposed therebetween. The layer 917 has a function of preventing the influence of the storage battery 913 on the electromagnetic field, for example. As the layer 917, for example, a magnetic material can be used.

With the above structure, the size of both the antenna 914 and the antenna 915 can be increased.

Alternatively, as shown in FIGS. 17 (B-1) and 17 (B-2), each of the pair of opposed surfaces of the storage battery 913 shown in FIGS. 16 (A) and 16 (B) is different. An antenna may be provided. FIG. 17B-1 is an external view seen from one side of the pair of surfaces, and FIG. 17B-2 is an external view seen from the other side of the pair of surfaces. In addition, about the same part as the storage battery shown to FIG. 16 (A) and FIG. 16 (B), description of the storage battery shown to FIG. 17 (A) and FIG. 17 (B) can be used suitably.

As shown in FIG. 17 (B-1), an antenna 914 and an antenna 915 are provided on one of a pair of surfaces of the storage battery 913 with a layer 916 interposed therebetween, and as shown in FIG. An antenna 918 is provided with the layer 917 interposed between the other of the pair of surfaces. The antenna 918 has a function of performing data communication with an external device, for example. For the antenna 918, for example, an antenna having a shape applicable to the antenna 914 and the antenna 915 can be used. As a communication method between the storage battery and other devices via the antenna 918, a response method that can be used between the storage battery and other devices, such as NFC, can be applied.

Alternatively, as illustrated in FIG. 18A, a display device 920 may be provided in the storage battery 913 illustrated in FIGS. 16A and 16B. The display device 920 is electrically connected to the terminal 911 through the terminal 919. Note that the label 910 is not necessarily provided in a portion where the display device 920 is provided. In addition, about the same part as the storage battery shown to FIG. 16 (A) and FIG. 16 (B), description of the storage battery shown to FIG. 16 (A) and FIG. 16 (B) can be used suitably.

The display device 920 may display, for example, an image indicating whether charging is being performed, an image indicating the amount of stored power, or the like. As the display device 920, for example, electronic paper, a liquid crystal display device, an electroluminescence (also referred to as EL) display device, or the like can be used. For example, power consumption of the display device 920 can be reduced by using electronic paper.

Alternatively, as illustrated in FIG. 18B, a sensor 921 may be provided in the storage battery 913 illustrated in FIGS. 16A and 16B. The sensor 921 is electrically connected to the terminal 911 through the terminal 922. In addition, about the same part as the storage battery shown to FIG. 16 (A) and FIG. 16 (B), description of the storage battery shown to FIG. 16 (A) and FIG. 16 (B) can be used suitably.

Examples of the sensor 921 include displacement, position, velocity, acceleration, angular velocity, rotation speed, distance, light, liquid, magnetism, temperature, chemical substance, sound, time, hardness, electric field, current, voltage, power, radiation, and flow rate. It has only to have a function capable of measuring humidity, gradient, vibration, odor, or infrared. By providing the sensor 921, for example, data (temperature, etc.) indicating the environment where the storage battery is placed can be detected and stored in the memory in the circuit 912.

Furthermore, a structural example of the storage battery 913 will be described with reference to FIGS.

A storage battery 913 illustrated in FIG. 19A includes a wound body 950 in which a terminal 951 and a terminal 952 are provided inside a housing 930. The wound body 950 is impregnated with the electrolytic solution inside the housing 930. The terminal 952 is in contact with the housing 930, and the terminal 951 is not in contact with the housing 930 by using an insulating material or the like. Note that in FIG. 19A, the housing 930 is illustrated separately for convenience, but in actuality, the wound body 950 is covered with the housing 930, and the terminals 951 and 952 are included in the housing 930. Extends outside. As the housing 930, a metal material or a resin material can be used.

Note that as illustrated in FIG. 19B, the housing 930 illustrated in FIG. 19A may be formed using a plurality of materials. For example, in a storage battery 913 illustrated in FIG. 19B, a housing 930a and a housing 930b are attached to each other, and a wound body 950 is provided in a region surrounded by the housing 930a and the housing 930b.

As the housing 930a, an insulating material such as an organic resin can be used. In particular, by using a material such as an organic resin on the surface where the antenna is formed, electric field shielding by the storage battery 913 can be suppressed. Note that an antenna such as the antenna 914 or the antenna 915 may be provided inside the housing 930a if the shielding of an electric field by the housing 930a is small. As the housing 930b, for example, a metal material can be used.

Furthermore, the structure of the wound body 950 is shown in FIG. The wound body 950 includes a negative electrode 931, a positive electrode 932, and a separator 933. The wound body 950 is a wound body in which the negative electrode 931 and the positive electrode 932 are stacked with the separator 933 interposed therebetween, and the laminated sheet is wound. Note that a plurality of stacked layers of the negative electrode 931, the positive electrode 932, and the separator 933 may be stacked.

The negative electrode 931 is connected to a terminal 911 illustrated in FIG. 16 through one of a terminal 951 and a terminal 952. The positive electrode 932 is connected to the terminal 911 illustrated in FIG. 16 through the other of the terminal 951 and the terminal 952.

≪Example of electronic equipment: Example of mounting on a vehicle≫
Next, an example in which a storage battery is mounted on a vehicle will be described. When the storage battery is mounted on a vehicle, a next-generation clean energy vehicle such as a hybrid vehicle (HEV), an electric vehicle (EV), or a plug-in hybrid vehicle (PHEV) can be realized.

FIG. 16 illustrates a vehicle using one embodiment of the present invention. A car 8100 illustrated in FIG. 21A is an electric car that uses an electric motor as a power source for traveling. Or it is a hybrid vehicle which can select and use an electric motor and an engine suitably as a motive power source for driving | running | working. By using one embodiment of the present invention, a vehicle that can be repeatedly charged and discharged can be realized. The automobile 8100 has a storage battery. The storage battery not only drives an electric motor, but can supply power to a light-emitting device such as a headlight 8101 or a room light (not shown).

The storage battery can supply power to a display device such as a speedometer or a tachometer included in the automobile 8100. Further, the storage battery can supply power to a semiconductor device such as a navigation gate system included in the automobile 8100.

A vehicle 8100 illustrated in FIG. 21B can charge a storage battery of the vehicle 8100 by receiving power from an external charging facility by a plug-in method, a non-contact power supply method, or the like. FIG. 21B shows a state in which the storage battery mounted on the automobile 8100 is charged via the cable 8022 from the ground installation type charging device 8021. When charging, the charging method, connector standard, and the like may be appropriately performed by a predetermined method. The charging device 8021 may be a charging station provided in a commercial facility, or may be a household power source. For example, the storage battery 8024 mounted on the automobile 8100 can be charged by power supply from the outside by plug-in technology. Charging can be performed by converting AC power into DC power via a converter such as an ACDC converter.

In addition, although not shown, the power receiving device can be mounted on the vehicle, and electric power can be supplied from the ground power transmitting device in a contactless manner and charged. In the case of this non-contact power supply method, charging can be performed not only when the vehicle is stopped but also during traveling by incorporating a power transmission device on a road or an outer wall. In addition, this non-contact power feeding method may be used to transmit and receive power between vehicles. Furthermore, a solar cell may be provided in the exterior part of the vehicle, and the storage battery may be charged when the vehicle stops or travels. An electromagnetic induction method or a magnetic field resonance method can be used for such non-contact power supply.

According to one embodiment of the present invention, the cycle characteristics of a storage battery are improved, and the reliability can be improved. According to one embodiment of the present invention, the characteristics of the storage battery can be improved, and thus the storage battery itself can be reduced in size and weight. If the storage battery itself can be reduced in size and weight, the cruising distance can be improved because it contributes to weight reduction of the vehicle. Moreover, the storage battery mounted in the vehicle can also be used as a power supply source other than the vehicle. In this case, it is possible to avoid using a commercial power source at the peak of power demand.

This embodiment can be implemented in appropriate combination with any of the other embodiments.

(Embodiment 3)
A battery control unit (BMU) that can be used in combination with the storage battery described in Embodiments 1 and 2 as a battery cell, and a transistor suitable for a circuit included in the battery control unit. This will be described with reference to FIGS. In the present embodiment, a battery control unit of a storage battery having battery cells connected in series will be described.

When charging / discharging is repeated for a plurality of battery cells connected in series, the capacity (output voltage) varies depending on variations in characteristics between the battery cells. In battery cells connected in series, the capacity at the time of overall discharge depends on the battery cells having a small capacity. If the capacity varies, the capacity at the time of discharge decreases. In addition, if charging is performed with reference to a battery cell having a small capacity, there is a risk of insufficient charging. Further, if charging is performed based on a battery cell having a large capacity, there is a risk of overcharging.

Therefore, the battery control unit of the storage battery having the battery cells connected in series has a function of aligning the variation in capacity between the battery cells that causes insufficient charging or overcharging. The circuit configuration for aligning the variation in capacity between battery cells includes a resistance method, a capacitor method, or an inductor method, but here is an example of a circuit configuration that can use a transistor with a small off-current to equalize the variation in capacity. Will be described.

As the transistor with low off-state current, a transistor including an oxide semiconductor (OS transistor) in a channel formation region is preferable. By using an OS transistor with a small off-state current in the circuit configuration of the battery control unit of the storage battery, the amount of charge leaking from the battery can be reduced, and a decrease in capacity over time can be suppressed.

As the oxide semiconductor used for the channel formation region, an In-M-Zn oxide (M is Ga, Sn, Y, Zr, La, Ce, or Nd) is used. In the target used for forming the oxide semiconductor film, when the atomic ratio of metal elements is In: M: Zn = x ₁ : y ₁ : z _{1 ,} x ₁ / y ₁ is 1/3 or more 6 Hereinafter, it is further 1 or more and 6 or less, and z ₁ / y ₁ is preferably 1/3 or more and 6 or less, and more preferably 1 or more and 6 or less. Note that when z ₁ / y ₁ is greater than or equal to 1 and less than or equal to 6, a CAAC-OS film can be easily formed as the oxide semiconductor film.

Here, the CAAC-OS film is described.

The CAAC-OS film is one of oxide semiconductor films having a plurality of c-axis aligned crystal parts.

Confirming a plurality of crystal parts by observing a bright field image of a CAAC-OS film and a combined analysis image (also referred to as a high-resolution TEM image) of a CAAC-OS film with a transmission electron microscope (TEM: Transmission Electron Microscope). Can do. On the other hand, a clear boundary between crystal parts, that is, a crystal grain boundary (also referred to as a grain boundary) cannot be confirmed even by a high-resolution TEM image. Therefore, it can be said that the CAAC-OS film is unlikely to decrease in electron mobility due to crystal grain boundaries.

When a high-resolution TEM image of a cross section of the CAAC-OS film is observed from a direction substantially parallel to the sample surface, it can be confirmed that metal atoms are arranged in layers in the crystal part. Each layer of metal atoms has a shape reflecting unevenness of a surface (also referred to as a formation surface) or an upper surface on which the CAAC-OS film is formed, and is arranged in parallel with the formation surface or the upper surface of the CAAC-OS film. .

On the other hand, when a high-resolution TEM image of a plane of the CAAC-OS film is observed from a direction substantially perpendicular to the sample surface, it can be confirmed that metal atoms are arranged in a triangular shape or a hexagonal shape in a crystal part. However, there is no regularity in the arrangement of metal atoms between different crystal parts.

When structural analysis is performed on a CAAC-OS film using an X-ray diffraction (XRD) apparatus, for example, in the analysis of a CAAC-OS film having an InGaZnO ₄ crystal by an out-of-plane method, A peak may appear when the diffraction angle (2θ) is around 31 °. Since this peak is attributed to the (009) plane of the InGaZnO ₄ crystal, the crystal of the CAAC-OS film has c-axis orientation, and the c-axis is oriented in a direction substantially perpendicular to the formation surface or the top surface. Can be confirmed.

Note that when the CAAC-OS film including an InGaZnO ₄ crystal is analyzed by an out-of-plane method, a peak may also appear when 2θ is around 36 ° in addition to the peak where 2θ is around 31 °. A peak at 2θ of around 36 ° indicates that a crystal having no c-axis alignment is included in part of the CAAC-OS film. The CAAC-OS film preferably has a peak at 2θ of around 31 ° and no peak at 2θ of around 36 °.

The CAAC-OS film is an oxide semiconductor film with a low impurity concentration. The impurity is an element other than the main component of the oxide semiconductor film, such as hydrogen, carbon, silicon, or a transition metal element. In particular, an element such as silicon, which has a stronger bonding force with oxygen than the metal element included in the oxide semiconductor film, disturbs the atomic arrangement of the oxide semiconductor film by depriving the oxide semiconductor film of oxygen, and has crystallinity. It becomes a factor to reduce. In addition, heavy metals such as iron and nickel, argon, carbon dioxide, and the like have large atomic radii (or molecular radii). Therefore, if they are contained inside an oxide semiconductor film, the atomic arrangement of the oxide semiconductor film is disturbed, resulting in crystallinity. It becomes a factor to reduce. Note that the impurity contained in the oxide semiconductor film might serve as a carrier trap or a carrier generation source.

The CAAC-OS film is an oxide semiconductor film with a low density of defect states. For example, oxygen vacancies in the oxide semiconductor film can serve as carrier traps or can generate carriers by capturing hydrogen.

A low impurity concentration and a low density of defect states (small number of oxygen vacancies) is called high purity intrinsic or substantially high purity intrinsic. A highly purified intrinsic or substantially highly purified intrinsic oxide semiconductor film has few carrier generation sources, and thus can have a low carrier density. Therefore, a transistor including the oxide semiconductor film is unlikely to have electrical characteristics (also referred to as normally-on) in which the threshold voltage is negative. A highly purified intrinsic or substantially highly purified intrinsic oxide semiconductor film has few carrier traps. Therefore, a transistor including the oxide semiconductor film has a small change in electrical characteristics and has high reliability. Note that the charge trapped in the carrier trap of the oxide semiconductor film takes a long time to be released, and may behave as if it were a fixed charge. Therefore, a transistor including an oxide semiconductor film with a high impurity concentration and a high density of defect states may have unstable electrical characteristics.

In addition, a transistor including a CAAC-OS film has little variation in electrical characteristics due to irradiation with visible light or ultraviolet light.

Note that an OS transistor has a larger band gap than a transistor having silicon in a channel formation region (Si transistor), and thus dielectric breakdown is less likely to occur when a high voltage is applied. When battery cells are connected in series, a voltage of several hundred volts is generated. For the circuit configuration of a battery control unit of a storage battery applied to such a battery cell, it is suitable to use the OS transistor described above. ing.

FIG. 22 shows an example of a block diagram of a storage battery. A storage battery BT00 shown in FIG. 22 is connected in series with a terminal pair BT01, a terminal pair BT02, a switching control circuit BT03, a switching circuit BT04, a switching circuit BT05, a transformation control circuit BT06, and a transformation circuit BT07. A battery unit BT08 including a plurality of battery cells BT09.

Further, in the storage battery BT00 of FIG. 22, a portion constituted by a terminal pair BT01, a terminal pair BT02, a switching control circuit BT03, a switching circuit BT04, a switching circuit BT05, a transformation control circuit BT06, and a transformation circuit BT07. Can be referred to as a battery control unit.

The switching control circuit BT03 controls operations of the switching circuit BT04 and the switching circuit BT05. Specifically, the switching control circuit BT03 determines the battery cell (discharge battery cell group) to be discharged and the battery cell (charge battery cell group) to be charged based on the voltage measured for each battery cell BT09.

Further, the switching control circuit BT03 outputs a control signal S1 and a control signal S2 based on the determined discharge battery cell group and charge battery cell group. The control signal S1 is output to the switching circuit BT04. This control signal S1 is a signal for controlling the switching circuit BT04 so as to connect the terminal pair BT01 and the discharge battery cell group. The control signal S2 is output to the switching circuit BT05. This control signal S2 is a signal for controlling the switching circuit BT05 so as to connect the terminal pair BT02 and the rechargeable battery cell group.

In addition, the switching control circuit BT03 is based on the configuration of the switching circuit BT04, the switching circuit BT05, and the transformer circuit BT07 so that terminals of the same polarity are connected between the terminal pair BT02 and the rechargeable battery cell group. A control signal S1 and a control signal S2 are generated.

Details of the operation of the switching control circuit BT03 will be described.

First, the switching control circuit BT03 measures the voltage for each of the plurality of battery cells BT09. Then, the switching control circuit BT03, for example, sets the battery cell BT09 having a voltage equal to or higher than a predetermined threshold as a high voltage battery cell (high voltage cell) and the battery cell BT09 having a voltage lower than the predetermined threshold as a low voltage battery cell (constant Voltage cell).

Various methods can be used for determining the high voltage cell and the low voltage cell. For example, the switching control circuit BT03 determines whether each battery cell BT09 is a high voltage cell or a low voltage cell with reference to the voltage of the battery cell BT09 having the highest voltage or the lowest voltage among the plurality of battery cells BT09. You may judge. In this case, the switching control circuit BT03 determines whether each battery cell BT09 is a high voltage cell or a low voltage cell by determining whether the voltage of each battery cell BT09 is equal to or higher than a predetermined ratio with respect to the reference voltage. Can be judged. Then, the switching control circuit BT03 determines the discharge battery cell group and the charge battery cell group based on the determination result.

In the plurality of battery cells BT09, a high voltage cell and a low voltage cell can be mixed in various states. For example, in the switching control circuit BT03, among the high voltage cells and the low voltage cells, the portion where the highest number of high voltage cells are connected in series is the discharge battery cell group. In addition, the switching control circuit BT03 sets a portion where the most low voltage cells are continuously connected in series as a rechargeable battery cell group. Further, the switching control circuit BT03 may preferentially select the battery cell BT09 close to overcharge or overdischarge as the discharge battery cell group or the charge battery cell group.

Here, an operation example of the switching control circuit BT03 in the present embodiment will be described with reference to FIG. FIG. 23 is a diagram for explaining an operation example of the switching control circuit BT03. For convenience of explanation, FIG. 23 illustrates an example in which four battery cells BT09 are connected in series.

First, in the example of FIG. 23A, when the voltages of the battery cells a to d are the voltages Va to Vd, a case where Va = Vb = Vc> Vd is shown. That is, three continuous high voltage cells a to c and one low voltage cell d are connected in series. In this case, the switching control circuit BT03 determines three consecutive high voltage cells a to c as a discharge battery cell group. Further, the switching control circuit BT03 determines the low voltage cell D as a rechargeable battery cell group.

Next, the example of FIG. 23B shows a case where Vc >> Vb = Vc >> Vd. That is, two continuous low voltage cells a and b, one high voltage cell c, and one low voltage cell d near overdischarge are connected in series. In this case, the switching control circuit BT03 determines the high voltage cell c as a discharge battery cell group. In addition, since the low voltage cell d is close to overdischarge, the switching control circuit BT03 preferentially determines the low voltage cell d as a charging battery cell group instead of the two consecutive low voltage cells a and b.

Finally, the example of FIG. 23C shows a case where Va> Vb = Vc = Vd. That is, one high voltage cell a and three consecutive low voltage cells b to d are connected in series. In this case, the switching control circuit BT03 determines the high voltage cell a as a discharge battery cell group. In addition, the switching control circuit BT03 determines three consecutive low voltage cells b to d as a rechargeable battery cell group.

The switching control circuit BT03 is a control signal in which information indicating the discharge battery cell group to which the switching circuit BT04 is connected is set based on the results determined as in the examples of FIGS. 23 (A) to (C). The control signal S2 in which information indicating S1 and the rechargeable battery cell group to which the switching circuit BT05 is connected is set is output to the switching circuit BT04 and the switching circuit BT05.

The above has described the details of the operation of the switching control circuit BT03.

The switching circuit BT04 sets the connection destination of the terminal pair BT01 to the discharge battery cell group determined by the switching control circuit BT03 according to the control signal S1 output from the switching control circuit BT03.

The terminal pair BT01 is composed of a pair of terminals A1 and A2. The switching circuit BT04 connects either one of the terminals A1 and A2 to the positive terminal of the battery cell BT09 located on the most upstream side (high potential side) in the discharge battery cell group, and the other to the discharge battery cell group. The connection destination of the terminal pair BT01 is set by connecting to the negative electrode terminal of the battery cell BT09 located most downstream (low potential side). Note that the switching circuit BT04 can recognize the position of the discharge battery cell group using the information set in the control signal S1.

The switching circuit BT05 sets the connection destination of the terminal pair BT02 to the rechargeable battery cell group determined by the switching control circuit BT03 according to the control signal S2 output from the switching control circuit BT03.

The terminal pair BT02 is configured by a pair of terminals B1 and B2. The switching circuit BT05 connects either one of the terminals B1 and B2 to the positive terminal of the battery cell BT09 located on the most upstream side (high potential side) in the charging battery cell group, and the other to the charging battery cell group. The connection destination of the terminal pair BT02 is set by connecting to the negative electrode terminal of the battery cell BT09 located most downstream (low potential side). Note that the switching circuit BT05 can recognize the position of the rechargeable battery cell group using the information set in the control signal S2.

24 and 25 are circuit diagrams showing configuration examples of the switching circuit BT04 and the switching circuit BT05.

In FIG. 24, the switching circuit BT04 includes a plurality of transistors BT10 and buses BT11 and BT12. The bus BT11 is connected to the terminal A1. The bus BT12 is connected to the terminal A2. One of the sources or drains of the plurality of transistors BT10 is connected to the buses BT11 and BT12 alternately every other one. The other of the sources or drains of the plurality of transistors BT10 is connected between two adjacent battery cells BT09.

Note that, among the plurality of transistors BT10, the other of the source and the drain of the transistor BT10 located at the uppermost stream is connected to the positive terminal of the battery cell BT09 located at the uppermost stream of the battery unit BT08. In addition, among the plurality of transistors BT10, the other of the source and the drain of the transistor BT10 located on the most downstream side is connected to the negative electrode terminal of the battery cell BT09 located on the most downstream side of the battery unit BT08.

The switching circuit BT04 is one of the plurality of transistors BT10 connected to the bus BT11 and one of the plurality of transistors BT10 connected to the bus BT12 according to the control signal S1 applied to the gates of the plurality of transistors BT10. The discharge battery cell group and the terminal pair BT01 are connected to each other by bringing them into a conductive state. Thereby, the positive electrode terminal of battery cell BT09 located in the most upstream in the discharge battery cell group is connected with either one of terminal A1 or A2 of a terminal pair. Moreover, the negative electrode terminal of battery cell BT09 located in the most downstream in the discharge battery cell group is connected to either the terminal A1 or A2 of the terminal pair, that is, the terminal not connected to the positive electrode terminal.

An OS transistor is preferably used as the transistor BT10. Since the OS transistor has a small off-state current, it is possible to reduce the amount of charge leaked from a battery cell that does not belong to the discharge battery cell group, and to suppress a decrease in capacity over time. In addition, the OS transistor is unlikely to break down when a high voltage is applied. Therefore, even if the output voltage of the discharge battery cell group is large, the battery cell BT09 connected to the transistor BT10 to be turned off and the terminal pair BT01 can be insulated.

In FIG. 24, the switching circuit BT05 includes a plurality of transistors BT13, a current control switch BT14, a bus BT15, and a bus BT16. The buses BT15 and BT16 are disposed between the plurality of transistors BT13 and the current control switch BT14. One of the sources or drains of the plurality of transistors BT13 is alternately connected to the buses BT15 and BT16 alternately. The other of the sources or drains of the plurality of transistors BT13 is connected between two adjacent battery cells BT09.

Note that, among the plurality of transistors BT13, the other of the source and the drain of the transistor BT13 located at the uppermost stream is connected to the positive terminal of the battery cell BT09 located at the uppermost stream of the battery unit BT08. In addition, among the plurality of transistors BT13, the other of the source and the drain of the transistor BT13 located on the most downstream side is connected to the negative terminal of the battery cell BT09 located on the most downstream side of the battery unit BT08.

As the transistor BT13, an OS transistor is preferably used similarly to the transistor BT10. Since the OS transistor has a small off-state current, it is possible to reduce the amount of charge leaked from a battery cell that does not belong to the rechargeable battery cell group, and to suppress a decrease in capacity over time. In addition, the OS transistor is unlikely to break down when a high voltage is applied. Therefore, even if the voltage for charging the charged battery cell group is large, the battery cell BT09 to which the transistor BT13 to be turned off and the terminal pair BT02 can be insulated.

The current control switch BT14 has a switch pair BT17 and a switch pair BT18. One end of the switch pair BT17 is connected to the terminal B1. The other end of the switch pair BT17 is branched by two switches. One switch is connected to the bus BT15 and the other switch is connected to the bus BT16. One end of the switch pair BT18 is connected to the terminal B2. The other end of the switch pair BT18 is branched by two switches. One switch is connected to the bus BT15 and the other switch is connected to the bus BT16.

As the switches included in the switch pair BT17 and the switch pair BT18, OS transistors are preferably used as in the transistors BT10 and BT13.

The switching circuit BT05 connects the charging battery cell group and the terminal pair BT02 by controlling the combination of the on / off state of the transistor BT13 and the current control switch BT14 according to the control signal S2.

As an example, the switching circuit BT05 connects the rechargeable battery cell group and the terminal pair BT02 as follows.

The switching circuit BT05 brings the transistor BT13 connected to the positive terminal of the battery cell BT09 located most upstream in the charging battery cell group into a conductive state in response to the control signal S2 applied to the gates of the plurality of transistors BT10. . Further, the switching circuit BT05 conducts the transistor BT13 connected to the negative terminal of the battery cell BT09 located most downstream in the charging battery cell group in response to the control signal S2 applied to the gates of the plurality of transistors BT10. To.

The polarity of the voltage applied to the terminal pair BT02 can vary depending on the configuration of the discharge battery cell group connected to the terminal pair BT01 and the transformer circuit BT07. Moreover, in order to flow an electric current in the direction which charges a rechargeable battery cell group, it is necessary to connect terminals of the same polarity between the terminal pair BT02 and the rechargeable battery cell group. Therefore, the current control switch BT14 is controlled to switch the connection destination of the switch pair BT17 and the switch pair BT18 according to the polarity of the voltage applied to the terminal pair BT02 by the control signal S2.

As an example, a description will be given of a state where a voltage is applied to the terminal pair BT02 so that the terminal B1 is a positive electrode and the terminal B2 is a negative electrode. At this time, when the battery cell BT09 on the most downstream side of the battery unit BT08 is a charged battery cell group, the switch pair BT17 is controlled to be connected to the positive terminal of the battery cell BT09 by the control signal S2. That is, the switch connected to the bus BT16 of the switch pair BT17 is turned on, and the switch connected to the bus BT15 of the switch pair BT17 is turned off. On the other hand, the switch pair BT18 is controlled to be connected to the negative terminal of the battery cell BT09 by the control signal S2. That is, the switch connected to the bus BT15 of the switch pair BT18 is turned on, and the switch connected to the bus BT16 of the switch pair BT18 is turned off. In this way, terminals having the same polarity are connected between the terminal pair BT02 and the rechargeable battery cell group. And the direction of the electric current which flows from terminal pair BT02 is controlled so that it may become a direction which charges a charging battery cell group.

Further, the current control switch BT14 may be included in the switching circuit BT04 instead of the switching circuit BT05. In this case, the polarity of the voltage applied to the terminal pair BT02 is controlled by controlling the polarity of the voltage applied to the terminal pair BT01 in accordance with the current control switch BT14 and the control signal S1. The current control switch BT14 controls the direction of current flowing from the terminal pair BT02 to the rechargeable battery cell group.

FIG. 25 is a circuit diagram showing a configuration example of the switching circuit BT04 and the switching circuit BT05, which is different from FIG.

In FIG. 25, the switching circuit BT04 includes a plurality of transistor pairs BT21, a bus BT24, and a bus BT25. The bus BT24 is connected to the terminal A1. The bus BT25 is connected to the terminal A2. One ends of the plurality of transistor pairs BT21 are branched by a transistor BT22 and a transistor BT23, respectively. One of the source and the drain of the transistor BT22 is connected to the bus BT24. One of the source and the drain of the transistor BT23 is connected to the bus BT25. The other ends of the plurality of transistor pairs are connected between two adjacent battery cells BT09. Of the plurality of transistor pairs BT21, the other end of the transistor pair BT21 located at the most upstream is connected to the positive terminal of the battery cell BT09 located at the most upstream of the battery unit BT08. Moreover, the other end of the transistor pair BT21 located on the most downstream side of the plurality of transistor pairs BT21 is connected to the negative electrode terminal of the battery cell BT09 located on the most downstream side of the battery unit BT08.

The switching circuit BT04 switches the connection destination of the transistor pair BT21 to either the terminal A1 or the terminal A2 by switching the conduction / non-conduction state of the transistor BT22 and the transistor BT23 according to the control signal S1. Specifically, when the transistor BT22 is in a conductive state, the transistor BT23 is in a nonconductive state, and the connection destination is the terminal A1. On the other hand, when the transistor BT23 is in a conductive state, the transistor BT22 is in a nonconductive state, and the connection destination is the terminal A2. Which of the transistors BT22 and BT23 is turned on is determined by the control signal S1.

Two transistor pairs BT21 are used to connect the terminal pair BT01 and the discharge battery cell group. Specifically, the connection destination of the two transistor pairs BT21 is determined based on the control signal S1, whereby the discharge battery cell group and the terminal pair BT01 are connected. The connection destinations of the two transistor pairs BT21 are controlled by the control signal S1 so that one is the terminal A1 and the other is the terminal A2.

The switching circuit BT05 includes a plurality of transistor pairs BT31, a bus BT34, and a bus BT35. The bus BT34 is connected to the terminal B1. The bus BT35 is connected to the terminal B2. One ends of the plurality of transistor pairs BT31 are branched by a transistor BT32 and a transistor BT33, respectively. One end branched by the transistor BT32 is connected to the bus BT34. One end branched by the transistor BT33 is connected to the bus BT35. The other ends of the plurality of transistor pairs BT31 are connected between two adjacent battery cells BT09. Note that, among the plurality of transistor pairs BT31, the other end of the uppermost transistor pair BT31 is connected to the positive terminal of the battery cell BT09 located at the uppermost stream of the battery unit BT08. Moreover, the other end of the transistor pair BT31 located on the most downstream side of the plurality of transistor pairs BT31 is connected to the negative electrode terminal of the battery cell BT09 located on the most downstream side of the battery unit BT08.

The switching circuit BT05 switches the connection destination of the transistor pair BT31 to either the terminal B1 or the terminal B2 by switching the conduction / non-conduction state of the transistor BT32 and the transistor BT33 according to the control signal S2. Specifically, when the transistor BT32 is in a conductive state, the transistor BT33 is in a nonconductive state, and the connection destination is the terminal B1. On the other hand, when the transistor BT33 is in a conductive state, the transistor BT32 is in a nonconductive state, and the connection destination is the terminal B2. Which of the transistor BT32 and the transistor BT33 becomes conductive is determined by the control signal S2.

Two transistor pairs BT31 are used to connect the terminal pair BT02 and the rechargeable battery cell group. Specifically, the connection destination of the two transistor pairs BT31 is determined based on the control signal S2, whereby the rechargeable battery cell group and the terminal pair BT02 are connected. The connection destinations of the two transistor pairs BT31 are controlled by the control signal S2 so that one is the terminal B1 and the other is the terminal B2.

The connection destination of each of the two transistor pairs BT31 is determined by the polarity of the voltage applied to the terminal pair BT02. Specifically, when a voltage is applied to the terminal pair BT02 such that the terminal B1 is a positive electrode and the terminal B2 is a negative electrode, the upstream transistor pair BT31 is in a conductive state and the transistor BT33 is in a nonconductive state. It is controlled by the control signal S2 so as to be in a state. On the other hand, the downstream transistor pair BT31 is controlled by the control signal S2 so that the transistor BT33 is conductive and the transistor BT32 is nonconductive. Further, when a voltage is applied to the terminal pair BT02 so that the terminal B1 is a negative electrode and the terminal B2 is a positive electrode, the upstream transistor pair BT31 has the transistor BT33 in a conductive state and the transistor BT32 in a nonconductive state. It is controlled by the control signal S2. On the other hand, the transistor pair BT31 on the downstream side is controlled by the control signal S2 so that the transistor BT32 is conductive and the transistor BT33 is nonconductive. In this way, terminals having the same polarity are connected between the terminal pair BT02 and the rechargeable battery cell group. And the direction of the electric current which flows from terminal pair BT02 is controlled so that it may become a direction which charges a charging battery cell group.

The transformation control circuit BT06 controls the operation of the transformation circuit BT07. The transformation control circuit BT06 generates a transformation signal S3 for controlling the operation of the transformation circuit BT07 based on the number of battery cells BT09 included in the discharge battery cell group and the number of battery cells BT09 included in the charge battery cell group. And output to the transformer circuit BT07.

When the number of battery cells BT09 included in the discharge battery cell group is greater than the number of battery cells BT09 included in the charge battery cell group, an excessively large charge voltage is applied to the charge battery cell group. Need to prevent. Therefore, the transformation control circuit BT06 outputs a transformation signal S3 that controls the transformation circuit BT07 so as to step down the discharge voltage (Vdis) within a range in which the rechargeable battery cell group can be charged.

Further, when the number of battery cells BT09 included in the discharge battery cell group is equal to or less than the number of battery cells BT09 included in the charge battery cell group, a charging voltage necessary for charging the charge battery cell group is ensured. There is a need. Therefore, the transformation control circuit BT06 outputs a transformation signal S3 that controls the transformation circuit BT07 so as to boost the discharge voltage (Vdis) in a range where an excessive charging voltage is not applied to the charging battery cell group.

In addition, the voltage value used as the excessive charging voltage can be determined in view of the product specifications of the battery cell BT09 used in the battery unit BT08. The voltage stepped up and stepped down by the transformer circuit BT07 is applied to the terminal pair BT02 as a charging voltage (Vcha).

Here, an operation example of the transformation control circuit BT06 in the present embodiment will be described with reference to FIGS. FIGS. 26A to 26C are conceptual diagrams for explaining an operation example of the transformation control circuit BT06 corresponding to the discharge battery cell group and the charge battery cell group described in FIGS. 23A to 23C. FIG. 26A to 26C illustrate the battery control unit BT41. As described above, the battery control unit BT41 includes the terminal pair BT01, the terminal pair BT02, the switching control circuit BT03, the switching circuit BT04, the switching circuit BT05, the transformation control circuit BT06, and the transformation circuit BT07. The

In the example shown in FIG. 26A, as described in FIG. 23A, three continuous high voltage cells a to c and one low voltage cell d are connected in series. In this case, as described with reference to FIG. 23A, the switching control circuit BT03 determines the high voltage cells a to c as the discharge battery cell group and the low voltage cell d as the charge battery cell group. Then, the transformation control circuit BT06 determines the discharge voltage (Vdis) based on the ratio of the number of the battery cells BT09 included in the charge electric cell group when the number of the battery cells BT09 included in the discharge battery cell group is used as a reference. The step-up / step-down ratio N is calculated.

When the number of battery cells BT09 included in the discharge battery cell group is greater than the number of battery cells BT09 included in the charge battery cell group, the discharge battery is applied as it is to the terminal pair BT02 without being transformed. An excessive voltage may be applied to the battery cell BT09 included in the cell group via the terminal pair BT02. Therefore, in the case as shown in FIG. 26A, it is necessary to lower the charging voltage (Vcha) applied to the terminal pair BT02 below the discharging voltage. Furthermore, in order to charge the charging battery cell group, the charging voltage needs to be larger than the total voltage of the battery cells BT09 included in the charging battery cell group. Therefore, the transformation control circuit BT06 has a step-up / step-down ratio N larger than the ratio of the number of battery cells BT09 included in the charging electric cell group when the number of battery cells BT09 included in the discharge battery cell group is used as a reference. Set.

The transformation control circuit BT06 sets the step-up / step-down ratio N to 1 to the ratio of the number of battery cells BT09 included in the charging electric cell group when the number of battery cells BT09 included in the discharge battery cell group is used as a reference. It is preferable to increase it by about 10%. At this time, the charging voltage is larger than the voltage of the charging battery cell group, but the charging voltage is actually equal to the voltage of the charging battery cell group. However, in order to make the voltage of the charging battery cell group equal to the charging voltage in accordance with the step-up / down ratio N, the transformation control circuit BT06 passes a current for charging the charging battery cell group. This current is a value set in the transformation control circuit BT06.

In the example shown in FIG. 26A, the number of battery cells BT09 included in the discharge battery cell group is three, and the number of battery cells BT09 included in the charge battery cell group is one. BT06 calculates a value slightly larger than 1/3 as the step-up / step-down ratio N. Then, the transformation control circuit BT06 steps down the discharge voltage according to the step-up / step-down ratio N, and outputs a transformation signal S3 that converts it to a charging voltage to the transformation circuit BT07. Then, the transformer circuit BT07 applies the charging voltage transformed according to the transformation signal S3 to the terminal pair BT02. Then, the battery cell BT09 included in the charging battery cell group is charged by the charging voltage applied to the terminal pair BT02.

Also, in the example shown in FIG. 26B and FIG. 26B, the step-up / step-down ratio N is calculated as in FIG. In the examples shown in FIGS. 26B and 26C, the number of battery cells BT09 included in the discharge battery cell group is equal to or less than the number of battery cells BT09 included in the charge battery cell group. N is 1 or more. Therefore, in this case, the transformation control circuit BT06 outputs a transformation signal S3 that boosts the discharge voltage and converts it to a received voltage.

Transformer circuit BT07 converts the discharge voltage applied to terminal pair BT01 into a charge voltage based on transform signal S3. Then, the transformer circuit BT07 applies the converted charging voltage to the terminal pair BT02. Here, the transformer circuit BT07 electrically insulates between the terminal pair BT01 and the terminal pair BT02. Thereby, the transformer circuit BT07 has the absolute voltage of the negative terminal of the battery cell BT09 located most downstream in the discharge battery cell group and the negative terminal of the battery cell BT09 located most downstream in the charge battery cell group. Prevents short circuit due to difference from absolute voltage. Furthermore, as described above, the transformer circuit BT07 converts the discharge voltage, which is the total voltage of the discharge battery cell group, into a charge voltage based on the transform signal S3.

In addition, the transformer circuit BT07 may be an insulation type DC (Direct Current) -DC converter, for example. In this case, the transformation control circuit BT06 controls the charging voltage converted by the transformation circuit BT07 by outputting a signal for controlling the on / off ratio (duty ratio) of the isolated DC-DC converter as the transformation signal S3. .

Insulated DC-DC converters include flyback method, forward method, RCC (Ringing Choke Converter) method, push-pull method, half-bridge method, and full-bridge method. An appropriate method is selected according to the size.

FIG. 27 shows the configuration of a transformer circuit BT07 using an insulated DC-DC converter. Insulated DC-DC converter BT51 has switch part BT52 and transformer part BT53. The switch unit BT52 is a switch that switches on / off the operation of the isolated DC-DC converter, and is realized by using, for example, a MOSFET (Metal-Oxide-Semiconductor Field-Effect Transistor), a bipolar transistor, or the like. Further, the switch unit BT52 periodically switches between the on state and the off state of the isolated DC-DC converter BT51 based on the transform signal S3 that is output from the transform control circuit BT06 and controls the on / off ratio. Note that the switch unit BT52 can take various configurations depending on the method of the insulation type DC-DC converter used. The transformer unit BT53 converts the discharge voltage applied from the terminal pair BT01 into a charge voltage. Specifically, the transformer unit BT53 operates in conjunction with the on / off state of the switch unit BT52, and converts the discharge voltage into a charge voltage according to the on / off ratio. This charging voltage increases as the time in which the switch is turned on in the switching period of the switch unit BT52 is longer. On the other hand, the charging voltage becomes smaller as the time in which the switch is turned on is shorter in the switching cycle of the switch unit BT52. In the case of using an insulated DC-DC converter, the terminal pair BT01 and the terminal pair BT02 can be insulated from each other inside the transformer unit BT53.

A processing flow of the storage battery BT00 in the present embodiment will be described with reference to FIG. FIG. 28 is a flowchart showing a process flow of the storage battery BT00.

First, the storage battery BT00 acquires a voltage measured for each of the plurality of battery cells BT09 (step S001). Then, the storage battery BT00 determines whether or not the start condition of the operation for aligning the voltages of the plurality of battery cells BT09 is satisfied (step S002). The start condition can be, for example, whether or not the difference between the maximum value and the minimum value of the voltage measured for each of the plurality of battery cells BT09 is equal to or greater than a predetermined threshold. When this start condition is not satisfied (step S002: NO), since the voltage of each battery cell BT09 is balanced, the storage battery BT00 does not execute the subsequent processing. On the other hand, when the start condition is satisfied (step S002: YES), the storage battery BT00 executes a process of aligning the voltages of the battery cells BT09. In this process, the storage battery BT00 determines whether each battery cell BT09 is a high voltage cell or a low voltage cell based on the measured voltage for each cell (step S003). Then, the storage battery BT00 determines a discharge battery cell group and a charge battery cell group based on the determination result (step S004). Further, the storage battery BT00 generates a control signal S1 for setting the determined discharge battery cell group as a connection destination of the terminal pair BT01, and a control signal S2 for setting the determined charge battery cell group as a connection destination of the terminal pair BT02. (Step S005). The storage battery BT00 outputs the generated control signal S1 and control signal S2 to the switching circuit BT04 and the switching circuit BT05, respectively. Then, the switching circuit BT04 connects the terminal pair BT01 and the discharge battery cell group, and the switching circuit BT05 connects the terminal pair BT02 and the discharge battery cell group (step S006). Further, the storage battery BT00 generates a transformation signal S3 based on the number of battery cells BT09 included in the discharge battery cell group and the number of battery cells BT09 included in the charge battery cell group (step S007). Then, the storage battery BT00 converts the discharge voltage applied to the terminal pair BT01 into a charging voltage based on the transformation signal S3, and applies it to the terminal pair BT02 (step S008). Thereby, the electric charge of the discharge battery cell group is moved to the charge battery cell group.

Also, in the flowchart of FIG. 28, a plurality of steps are described in order, but the execution order of each step is not limited to the description order.

As described above, according to the present embodiment, when the charge is transferred from the discharge battery cell group to the charge battery cell group, the charge is temporarily accumulated from the discharge battery cell group and then released to the charge battery cell group as in the capacitor system. No configuration is required. Thereby, the charge transfer efficiency per unit time can be improved. In addition, the discharge battery cell group and the charge battery cell group are individually switched by the switching circuit BT04 and the switching circuit BT05.

Further, the transformer circuit BT07 converts the discharge voltage applied to the terminal pair BT01 based on the number of battery cells BT09 included in the discharge battery cell group and the number of battery cells BT09 group included in the charge battery cell group. And applied to the terminal pair BT02. Thereby, no matter how the discharge-side and charge-side battery cells BT09 are selected, the movement of charges can be realized without any problem.

Furthermore, by using OS transistors for the transistors BT10 and BT13, the amount of charge leaked from the battery cell BT09 that does not belong to the charge battery cell group and the discharge battery cell group can be reduced. Thereby, the fall of the capacity | capacitance of the battery cell BT09 which does not contribute to charge and discharge can be suppressed. In addition, the OS transistor has less variation in characteristics with respect to heat than the Si transistor. Thereby, even if the temperature of battery cell BT09 rises, normal operation | movement, such as switching of the conduction | electrical_connection state and non-conduction state according to control signal S1, S2, can be performed.

Note that this embodiment can be implemented in combination with any of the other embodiments as appropriate.

(Embodiment 4)
≪Other structural examples of storage battery≫

FIG. 29 illustrates a storage battery 2100 according to one embodiment of the present invention. The storage battery is sealed on three sides of the outer package 2107. Further, a positive electrode lead 2121 and a negative electrode lead 2125, a positive electrode 2111, a negative electrode 2115, and a separator 2103 are provided. Note that each electrode is shown as a single layer because the figure is complicated, but at least some of the electrodes have two or more current collectors, and the current collectors are surfaces on which no active material is formed. It touches with.

Here, part of a method for manufacturing the storage battery 2100 illustrated in FIG. 29 will be described with reference to FIGS.

First, the negative electrode 2115 is placed over the separator 2103 (FIG. 30A). At this time, the negative electrode active material layer included in the negative electrode 2115 is disposed so as to overlap with the separator 2103.

Next, the separator 2103 is bent, and the separator 2103 is overlaid on the negative electrode 2113. Next, the positive electrode 2111 is stacked over the separator 2103 (FIG. 30B). At this time, the positive electrode active material layer 2102 included in the positive electrode 2111 is disposed so as to overlap with the separator 2103 and the negative electrode active material layer 2106. Note that in the case of using an electrode in which an active material layer is formed on one side of the current collector, the positive electrode active material layer 102 of the positive electrode 2111 and the negative electrode active material layer 2106 of the negative electrode 2115 are opposed to each other with the separator 2103 interposed therebetween. Deploy.

When a material capable of heat welding such as polypropylene is used for the separator 2103, the electrode is displaced during the manufacturing process by heat-welding a region where the separators 2103 overlap each other and then stacking the next electrode. Can be suppressed. Specifically, it is preferable to thermally weld a region where the separators 2103 overlap with each other, for example, a region 2103a in FIG. 30B, which does not overlap with the negative electrode 2115 or the positive electrode 2111.

By repeating this step, the positive electrode 2111 and the negative electrode 2115 can be stacked with the separator 2103 interposed therebetween as shown in FIG.

Note that a plurality of negative electrodes 2115 and a plurality of positive electrodes 2111 may be alternately sandwiched between separators 2103 that are repeatedly bent in advance.

Next, as illustrated in FIG. 30C, the plurality of positive electrodes 2111 and the plurality of negative electrodes 2115 are covered with a separator 2103.

Furthermore, as shown in FIG. 30D, a plurality of positive electrodes 2111 and a plurality of negative electrodes 2115 are bonded by thermally welding a region where separators 2103 overlap each other, for example, a region 2103b shown in FIG. Cover and bind with a separator 2103.

Note that the plurality of positive electrodes 2111, the plurality of negative electrodes 2115, and the separator 2103 may be bound using a binding material.

In order to stack the positive electrode 2111 and the negative electrode 2115 in such a process, the separator 2103 includes a region between a plurality of positive electrodes 2111 and a plurality of negative electrodes 2115 in a single separator 2103, and a plurality of positive electrodes 2111 and a plurality of negative electrodes. And a region arranged to cover the negative electrode 2115.

In other words, the separator 2103 included in the storage battery 2100 in FIG. 29 is a single separator that is partially folded. A plurality of positive electrodes 2111 and a plurality of negative electrodes 2115 are sandwiched between the folded regions of the separator 2103.

For the structure of the storage battery 2100 other than the bonding region of the outer package 2107, the shapes of the positive electrode 2111, the negative electrode 2115, the separator 2103, and the outer package 2107, and the position shapes of the positive electrode lead 2121 and the negative electrode lead 2125, refer to the description in Embodiment 1. can do. For the manufacturing method of the storage battery 2100d other than the step of stacking the positive electrode 2111 and the negative electrode 2115, the manufacturing method described in Embodiment 1 can be referred to.

FIG. 31 shows a storage battery 100e different from FIG. FIG. 31A is a perspective view of the storage battery 2200, and FIG. 31B is a top view of the storage battery 2200. FIG. 31C1 is a cross-sectional view of the first electrode assembly 2130 and FIG. 31C2 is a cross-sectional view of the second electrode assembly 2131. FIG. 31D is a cross-sectional view taken along dashed-dotted line H1-H2 in FIG. Note that in FIG. 31D, the first electrode assembly 2130, the electrode assembly 2131, and the separator 2103 are extracted and shown for clarity. In addition, since the drawing is complicated, each electrode is shown as a single layer, but at least some of the electrodes have two or more current collectors, and the current collectors are surfaces on which no active material is formed. It touches with.

A storage battery 2200 shown in FIG. 31 is different from the storage battery 2100 of FIG. 29 in the arrangement of the positive electrode 2111 and the negative electrode 2115 and the arrangement of the separator 2103.

As illustrated in FIG. 31D, the storage battery 2200 includes a plurality of first electrode assemblies 2130 and a plurality of electrode assemblies 2131.

As shown in FIG. 31C1, in the first electrode assembly 2130, the positive electrode 2111a having the positive electrode active material layer 2102 on both surfaces of the positive electrode current collector 2101, the separator 2103, and the negative electrode current collector 2105 on both surfaces. A negative electrode 2115a having a material layer 2106, a separator 2103, and a positive electrode current collector 2101 are stacked on a positive electrode 2111a having a positive electrode active material layer 2102 in this order. 31C2, in the second electrode assembly 2131, a negative electrode 2115a having a negative electrode active material layer 2106 on both surfaces of the negative electrode current collector 2105, a separator 2103, and a positive electrode on both surfaces of the positive electrode current collector 2101 A negative electrode 2115a having a negative electrode active material layer 2106 is stacked in this order on both surfaces of a positive electrode 2111a having an active material layer 2102, a separator 2103, and a negative electrode current collector 2105.

Further, as shown in FIG. 31D, the plurality of first electrode assemblies 2130 and the plurality of second electrode assemblies 2131 are covered with a wound separator 2103.

Here, a part of a method for manufacturing the storage battery 2200 illustrated in FIG. 31 will be described with reference to FIGS.

First, the first electrode assembly 2130 is placed over the separator 2103 (FIG. 32A).

Next, the separator 2103 is bent, and the separator 2103 is overlaid on the first electrode assembly 2130. Next, two sets of second electrode assemblies 2131 are stacked above and below the first electrode assembly 2130 with the separator 2103 interposed therebetween (FIG. 32B).

Next, the separator 2103 is wound so as to cover the two sets of second electrode assemblies 2131. Further, two sets of first electrode assemblies 2130 are stacked above and below the two sets of second electrode assemblies 2131 with the separator 2103 interposed therebetween (FIG. 32C).

Next, the separator 2103 is wound so as to cover the two sets of first electrode assemblies 2130 (FIG. 32D).

In order to stack the plurality of first electrode assemblies 2130 and the plurality of electrode assemblies 2131 in such a process, these electrode assemblies are disposed between the separators 2103 wound in a spiral shape.

Note that the positive electrode 2111a of the electrode assembly 2130 disposed on the outermost side is preferably not provided with the positive electrode active material layer 2102 on the outer side.

FIGS. 32C1 and 32C2 illustrate a structure in which the electrode assembly includes three electrodes and two separators, but one embodiment of the present invention is not limited thereto. It is good also as a structure which has 4 or more electrodes and 3 or more separators. By increasing the number of electrodes, the capacity of the storage battery 2200 can be further improved. Alternatively, the structure may include two electrodes and one separator. When there are few electrodes, it can be set as the storage battery 2200 strong against a curve. FIG. 32D illustrates a structure in which the storage battery 2200 includes three sets of the first electrode assembly 2130 and two sets of the second electrode assembly 2131; however, one embodiment of the present invention is not limited thereto. Furthermore, it is good also as a structure which has many electrode assemblies. By increasing the number of electrode assemblies, the capacity of the storage battery 2200 can be further improved. Moreover, it is good also as a structure which has fewer electrode assemblies. When there are few electrode assemblies, it can be set as the storage battery 2200 strong against a curve.

In addition to the arrangement of the positive electrode 2111 and the negative electrode 2115 and the arrangement of the separator 2103 in the storage battery 2200, the description of FIG. 29 can be referred to.

This embodiment can be implemented in appropriate combination with any of the other embodiments.

100a Laminated body 100b Laminated body 100c Laminated body 100d Laminated body 101 Negative electrode current collector 102 Negative electrode active material layer 103 Separator 104 Positive electrode active material layer 105 Positive electrode current collector 107 Electrolytic solution 110 Lithium ion storage battery 115 Lead electrode 116 Exterior body 117 Internal structure Object 118 void 300 storage battery 301 positive electrode can 302 negative electrode can 303 gasket 304 positive electrode 305 positive electrode current collector 306 positive electrode active material layer 307 negative electrode 308 negative electrode current collector 309 negative electrode active material layer 310 separator 400 storage battery 402 positive electrode 404 negative electrode 500 storage battery 501 positive electrode collection Electrode 502 Positive electrode active material layer 503 Positive electrode 504 Negative electrode current collector 505 Negative electrode active material layer 506 Negative electrode 507 Separator 508 Electrolytic solution 509 Exterior body 510 Positive electrode tab electrode 511 Negative electrode tab electrode 515 Tab electrode 516 Tab electrode 600 Storage battery 01 Positive electrode cap 602 Battery can 603 Positive electrode terminal 604 Positive electrode 605 Separator 606 Negative electrode 607 Negative electrode 608 Insulating plate 609 Insulating plate 610 Gasket 611 PTC element 612 Safety valve mechanism 900 Circuit board 910 Label 911 Terminal 912 Circuit 913 Storage battery 914 Antenna 915 Antenna 916 Layer 917 Layer 918 Antenna 919 Terminal 920 Display device 921 Sensor 922 Terminal 930 Case 930a Case 930b Case 931 Negative electrode 932 Positive electrode 933 Separator 951 Terminal 952 Terminal 1101 Center of curvature 1102 End 1103 on the side close to the center of curvature of the internal structure Internal structure End 1104 on the side far from the center of curvature of the object 1104 End 1 on the side near the center of curvature of the internal structure End 1106 on the side far from the center of curvature of the internal structure 1106 Near the center of curvature of the internal structure Point 1700 curved surface 1701 plane 1702 curve 1703 curvature radius 1704 curvature center 1800 curvature center 1801 film 1802 curvature radius 1803 film 1804 curvature radius 1805 electrode / electrolytic solution 2100 storage battery 2101 positive electrode current collector 2102 positive electrode active material layer 2103 separator 2103a region 2103b Region 2105 Negative electrode current collector 2106 Negative electrode active material layer 2107 Exterior body 2111 Positive electrode 2111a Positive electrode 2115 Negative electrode 2115a Negative electrode 2121 Positive electrode lead 2125 Negative electrode lead 2130 First electrode assembly 2131 Second electrode assembly 2200 Storage battery 7100 Portable display device 7101 Case Body 7102 Display portion 7103 Operation button 7104 Storage battery 7400 Mobile phone 7401 Case 7402 Display portion 7403 Operation button 7404 External connection port 7 405 Speaker 7406 Microphone 7407 Storage battery 8021 Charging device 8022 Cable 8024 Storage battery 8100 Car 8101 Headlight S1 Control signal S2 Control signal S3 Transform signal BT00 Storage battery BT01 Terminal pair BT02 Terminal pair BT03 Switch control circuit BT04 Switch circuit BT05 Switch circuit BT06 Switch circuit BT07 Transformer circuit BT08 Battery part BT09 Battery cell BT10 Transistor BT11 Bus BT12 Bus BT13 Transistor BT14 Current control switch BT15 Bus BT16 Bus BT17 Switch pair BT18 Switch pair BT21 Transistor pair BT22 Transistor BT23 Transistor BT24 Bus BT25 Bus BT31 Transistor TBT Transistor T33 Transistor T33 Transistor T33 B 35 bus BT41 battery control unit BT51 isolated DC-DC converter BT52 switch unit BT53 transformer section S001 step S002 step S003 step S004 step S005 step S006 step S007 step S008 step

Claims (1)

A structure having a first laminate and a second laminate that overlaps the first laminate;
An exterior body that wraps the structure,
Between the exterior body and the structure, a space occupied by the electrolyte is provided,
The first laminate is
A first negative electrode active material layer provided on one surface of the first negative electrode current collector;
A first positive electrode active material layer provided on one surface of the first positive electrode current collector;
A first separator provided between the first negative electrode active material layer and the first positive electrode active material layer,
The second laminate is
A second negative electrode active material layer provided on one surface of the second negative electrode current collector;
A second positive electrode active material layer provided on one surface of the second positive electrode current collector;
A second separator provided between the second negative electrode active material layer and the second positive electrode active material layer ,
The other surface of the first positive electrode current collector not provided with the first positive electrode active material layer, and the other surface of the second positive electrode current collector not provided with the second positive electrode active material layer. lithium-ion battery that has a flexible and of the surface is that Sessu.