Secondary battery, battery module, and vehicle

Abstract

To provide a secondary battery having excellent lifetime characteristics and low resistance.SOLUTION: A secondary battery is provided according to an embodiment. The secondary battery includes: a wound electrode group including a positive electrode, a negative electrode containing a negative electrode active material, and a separator; and an exterior member accommodating the wound electrode group. The negative electrode active material contains a niobium-titanium composite oxide. A proportion (Rblack) determined by the following method is within the range of more than 2.0% and 20.0% or less. The proportion (Rblack) is determined by a method including the steps of: obtaining, by X-ray CT, 800 cross-sectional images orthogonal to a winding axis of the wound electrode group; binarizing each of the cross-sectional images; determining, as a percentage, a proportion of an area (Sb) of a black portion to an area (St) of the wound electrode group defined by an outer periphery of the wound electrode group in each of the binarized cross-sectional images; and simply averaging a plurality of the proportions obtained in each of the cross-sectional images.SELECTED DRAWING: Figure 6

Description

[Technical field]

[0001] The present invention relates to a secondary battery, a battery module, and a vehicle. [Background technology]

[0002] In recent years, research and development of secondary batteries such as non-aqueous electrolyte secondary batteries, such as lithium-ion secondary batteries, as high energy density batteries, has been actively promoted. Secondary batteries such as non-aqueous electrolyte secondary batteries are expected to be used as power sources for vehicles such as hybrid electric vehicles and electric vehicles, and for uninterruptible power sources for mobile phone base stations. In addition, since the demand for power sources for mobile services such as autonomous industrial robots and drones is rapidly increasing, secondary batteries are required to have not only high energy density but also other excellent performances such as rapid charge and discharge performance and long-term reliability.

[0003] Materials containing Ti and Nb are being investigated as electrode materials for secondary batteries. Such niobium titanium composite oxide materials are expected to have high charge / discharge capacity. However, niobium titanium composite oxide materials expand and contract in volume during rapid charging and charge / discharge cycles. This is because the crystal structure skeleton changes significantly as lithium ions are inserted and removed from the crystal structure. This expansion and contraction causes slight deformation of the electrodes and changes in battery performance. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] JP 2009-266661 A [Non-patent literature]

[0005] [Non-Patent Document 1] Dr. Michael et al., Image Processing with ImageJ, Reprinted from the July 2004 issue of Biophotonics International copyrighted by Laurin Publishing Co. INC. Summary of the Invention [Problem to be solved by the invention]

[0006] An object of the present invention is to provide a secondary battery having excellent life characteristics and low resistance, a battery module including this secondary battery, and a vehicle on which this battery module is mounted. [Means for solving the problem]

[0007] According to an embodiment, a secondary battery is provided. The secondary battery includes a wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator, and an exterior member that houses the wound electrode group. A void portion exists inside the wound electrode group. The void portion is formed by wrinkles. , scattered on a cross section perpendicular to the winding axis of the wound electrode group void is The negative electrode active material contains a niobium titanium composite oxide. The ratio (R black ) is in the range of more than 2.0% and not more than 20.0%. black ) is determined by a method including the steps of: obtaining 800 cross-sectional images perpendicular to the winding axis of the wound electrode group by X-ray computed tomography (hereinafter referred to as X-ray CT); converting each of the 800 cross-sectional images into 256 monochrome gradations, and then binarizing them by setting a threshold value so that the areas corresponding to the positive electrode, negative electrode, and separator become white areas and the void areas become black areas; determining, in each of the 800 binarized cross-sectional images, the ratio of the area (Sb) of the black areas to the area (St) of the wound electrode group defined by the outer periphery of the wound electrode group, as a percentage; and simply averaging the multiple ratios obtained in each of the 800 cross-sectional images.

[0008] According to another embodiment, a battery module including a secondary battery according to the embodiment is provided.

[0009] According to another embodiment, a vehicle including a battery module according to the embodiment is provided. [Brief description of the drawings]

[0010] [Figure 1] FIG. 2 is an exploded perspective view illustrating an example of a secondary battery according to the embodiment. [Diagram 2] 2 is a partially exploded perspective view of the secondary battery shown in FIG. 1, as viewed from below. [Diagram 3] FIG. 2 is a partially exploded perspective view of an electrode group used in the secondary battery shown in FIG. [Figure 4] 2 is a partially exploded perspective view of the secondary battery shown in FIG. 1 as viewed from above. [Diagram 5] 4 is a cross-sectional image obtained by X-ray CT of the secondary battery according to the embodiment. [Figure 6] 6 is an image obtained by binarizing the cross-sectional image shown in FIG. 5 . [Figure 7] 9 is an image obtained by binarizing the cross-sectional image shown in FIG. 8. [Figure 8] 11 is another cross-sectional image obtained by X-ray CT of the secondary battery according to the embodiment. [Figure 9] FIG. 4 is a front view showing a schematic view of a secondary battery being restrained according to the embodiment. [Figure 10] FIG. 4 is a side view illustrating a state in which the secondary battery according to the embodiment is restrained. [Figure 11] FIG. 2 is a perspective view of the secondary battery shown in FIG. [Figure 12] FIG. 2 is an exploded perspective view illustrating an example of a battery module according to the embodiment. [Figure 13] 13 is a cross-sectional view that illustrates the battery module illustrated in FIG. 12. [Figure 14] 1 is a cross-sectional view illustrating an example of a vehicle according to an embodiment. [Figure 15] 13 is an X-ray CT image of a cross section perpendicular to the winding axis of a wound electrode group for an example secondary battery according to a comparative example. [Figure 16] 16 is an image obtained by binarizing the cross-sectional image shown in FIG. 15 . [Figure 17] 13 is an X-ray CT image of a cross section parallel to the winding axis of a wound electrode group for an example secondary battery according to a comparative example. [Figure 18] 18 is an image obtained by binarizing the cross-sectional image shown in FIG. 17. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0011] Hereinafter, the embodiments will be described with reference to the drawings. Note that the same reference numerals are used to designate common components throughout the embodiments, and duplicated descriptions will be omitted. Each figure is a schematic diagram for explaining the embodiments and for facilitating understanding thereof, and the shapes, dimensions, ratios, etc. may differ from those of the actual device, but these can be appropriately modified in design by taking into consideration the following explanation and known techniques.

[0012] (First embodiment) According to a first embodiment, a secondary battery is provided. The secondary battery includes a wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator, and an exterior member that houses the wound electrode group. The negative electrode active material includes a niobium titanium composite oxide. The ratio (R black ) is in the range of more than 2.0% and not more than 20.0%. black ) is determined by a method including the steps of: obtaining 800 cross-sectional images perpendicular to the winding axis of the wound electrode group by X-ray CT; converting each of the 800 cross-sectional images into 256 monochrome gradations, and then binarizing them by setting a threshold value so that the parts corresponding to the positive electrode, negative electrode, and separator become white parts and void parts that may exist inside the wound electrode group become black parts; determining, in each of the 800 binarized cross-sectional images, the ratio of the area (Sb) of the black parts to the area (St) of the wound electrode group defined by the outer periphery of the wound electrode group, as a percentage; and simply averaging the multiple ratios obtained in each of the 800 cross-sectional images.

[0013] The lattice volume of the niobium titanium composite oxide changes as lithium ions are absorbed and released during charging and discharging of the secondary battery. Therefore, when a negative electrode containing the niobium titanium composite oxide is repeatedly charged and discharged, the active material-containing layer expands and contracts. In particular, the volume change of the niobium titanium composite oxide is the largest during the initial charging of the secondary battery. Immediately after the secondary battery is manufactured (before the initial charging), the electrode material such as the active material particles constituting the active material-containing layer is distributed at a relatively uniform density within the layer. However, when this secondary battery is initially charged, the volume expansion of the niobium titanium composite oxide may cause a large difference between the density of the electrode material in a certain part of the layer and the density of the electrode material in another part of the layer.

[0014] On the other hand, when manufacturing a wound electrode group in which a belt-like and sheet-like negative electrode, a separator, and a positive electrode are wound, these sheets are generally wound so that no gaps are generated between them. Then, the wound electrode group is housed in an exterior member having a predetermined volume. From the viewpoint of increasing the battery capacity, there is no or almost no gap between the side wall of the exterior member and the wound electrode group.

[0015] Therefore, when a wound electrode group that does not include extra gaps is subjected to an initial charge, wrinkles may be formed in at least a part of the wound electrode group due to uneven expansion of the negative electrode active material-containing layer or because there is no escape route for the stress caused by the expansion of the negative electrode active material-containing layer. The present inventors have focused on the degree of wrinkle formation and found that a secondary battery with excellent life characteristics and low resistance can be obtained by controlling the degree of wrinkle formation.

[0016] The degree of wrinkle formation in the wound electrode group is evaluated based on tomography by X-ray CT. When tomography is performed multiple times by X-ray CT along the winding axis direction of the wound electrode group, multiple black and white images (grayscale images) showing the cross section of the wound electrode group are obtained. In other words, multiple cross-sectional images perpendicular to the winding axis of the wound electrode group are obtained. In each of these cross-sectional images, the parts corresponding to the negative electrode, positive electrode, and separator that constitute the wound electrode group are mainly shown in white, and the parts corresponding to the gaps formed by the wrinkles are mainly shown in black. The cross-sectional images are binarized under predetermined conditions, and the ratio of the area of ​​the black parts corresponding to the wrinkles to the cross-sectional area of ​​the wound electrode group is calculated, so that the degree of wrinkle formation can be quantitatively evaluated. A specific evaluation method will be described later, but when performing X-ray CT, in order to evaluate the degree of wrinkle formation over the entire wound electrode group, multiple cross-sectional images at different positions along the winding axis direction are prepared by tomography. Specifically, 800 cross-sectional images are prepared. The degree of wrinkle formation is evaluated by calculating the above-mentioned ratio for each image and averaging these ratios. In the present specification and claims, this average is referred to as the "ratio (R black )"

[0017] In the secondary battery according to the embodiment, the ratio of the area of ​​the black portion to the cross-sectional area of ​​the wound electrode group (R black ) is in the range of more than 2.0% and not more than 20.0%. When the ratio is in this range, moderate wrinkles are formed in the wound electrode group. In this case, for example, it is possible to suppress the formation of an excessive coating on the positive electrode surface or the negative electrode surface. In addition, in this case, the formed wrinkles can become a diffusion path for gas. In other words, not only are wrinkles formed during the initial charge, but gas is likely to flow out of the wound electrode group through these wrinkles. This makes it possible to suppress the distance between the positive and negative electrodes from becoming too large. Therefore, the secondary battery can achieve excellent life characteristics and low battery resistance.

[0018] If this ratio is 2.0% or less, there is a possibility that gas diffusion is insufficient due to insufficient wrinkles. In addition, if the adhesion between the positive electrode, the separator, and the negative electrode is too high, the formation of a coating film may be promoted, and the resistance may increase. On the other hand, if this ratio exceeds 20.0%, there are places in the wound electrode group where the distance between the positive and negative electrodes is too far due to the formation of excessive wrinkles. The resistance tends to increase due to such places. In addition, in this case, the distortion of the active material-containing layer may cause damage such as cracks in the active material-containing layer itself. If such damage occurs, there is a possibility that the electron conduction path between the active material particles and / or between the active material-containing layer and the current collector may be lost at the corresponding places.

[0019] Ratio (R black ) is preferably in the range of 2.5% to 15.0%, and more preferably in the range of 2.5% to 10.0%.

[0020] Hereinafter, the secondary battery according to the embodiment will be described in detail.

[0021] An example of a secondary battery will be described with reference to the drawings, but the embodiment of the secondary battery is not limited thereto. Fig. 1 is an exploded perspective view of a secondary battery according to an embodiment. Fig. 2 is a partially exploded perspective view of the secondary battery shown in Fig. 1 as viewed from below. Fig. 3 is a partially exploded perspective view of an electrode group used in the secondary battery shown in Fig. 1. Fig. 4 is a partially exploded perspective view of the secondary battery shown in Fig. 1 as viewed from above. The secondary battery may be, for example, a lithium secondary battery or a nonaqueous electrolyte secondary battery containing a nonaqueous electrolyte.

[0022] The secondary battery 100 includes an exterior member 1, a wound electrode group 2 housed in the exterior member 1, and a nonaqueous electrolyte (not shown) impregnated in the wound electrode group 2. The exterior member 1 has a bottomed rectangular tubular container 3 and a sealing plate 4 fixed to the opening of the container 3, for example, by welding. The shape of the exterior member is not particularly limited as long as it can house the wound electrode group, but the exterior member has, for example, a rectangular parallelepiped or cubic shape. The secondary battery 100 can be, for example, a sealed rectangular nonaqueous electrolyte secondary battery.

[0023] As shown in Fig. 3, the wound electrode group 2 includes a positive electrode 5 and a negative electrode 6 wound in a flat shape around a virtual winding axis 2p with a separator 7 between them. The positive electrode 5 includes a strip-shaped positive electrode collector made of, for example, a metal foil, a positive electrode current collector tab 5a having one end parallel to the long side of the positive electrode current collector, and a positive electrode active material layer 5b formed on the positive electrode current collector except for at least the portion of the positive electrode current collector tab 5a. On the other hand, the negative electrode 6 includes a strip-shaped negative electrode collector made of, for example, a metal foil, a negative electrode current collector tab 6a having one end parallel to the long side of the negative electrode current collector, and a negative electrode active material layer 6b formed on the negative electrode current collector except for at least the portion of the negative electrode current collector tab 6a.

[0024] Such positive electrode 5, separator 7, and negative electrode 6 are wound with the positions of the positive electrode 5 and the negative electrode 6 shifted so that the positive electrode current collector tab 5a protrudes from the separator 7 in the direction of the winding axis 2p of the electrode group, and the negative electrode current collector tab 6a protrudes in the opposite direction from the separator 7. By such winding, the electrode group 2 has the spirally wound positive electrode current collector tab 5a protruding from one end face, and the spirally wound negative electrode current collector tab 6a protruding from the other end face, as shown in FIG.

[0025] The wound electrode group 2 includes two flat portions 2a formed by flatly stacking the positive electrode 5, the separator 7, and the negative electrode 6, and two curved portions 2b formed by stacking the positive electrode 5, the separator 7, and the negative electrode 6 in a curved state. The two flat portions 2a face each other with the winding axis 2p as a boundary. The two curved portions 2b face each other via the two flat portions 2a.

[0026] As shown in FIG. 1 and FIG. 2, the positive electrode lead 8 has a connection plate 8a for electrically connecting to the positive electrode terminal 9, a through hole 8b opened in the connection plate 8a, and a strip-shaped current collecting portion 8c that branches into two from the connection plate 8a and extends downward. The current collecting portion 8c of the positive electrode lead 8 sandwiches the positive electrode current collecting tab 5a of the electrode group 2 between them and is electrically connected to the positive electrode current collecting tab 5a by welding. On the other hand, the negative electrode lead 10 has a connection plate 10a for electrically connecting to the negative electrode terminal 11, a through hole 10b opened in the connection plate 10a, and a strip-shaped current collecting portion 10c that branches into two from the connection plate 10a and extends downward. The current collecting portion 10c of the negative electrode lead 10 sandwiches the negative electrode current collecting tab 6a of the electrode group 2 between them and is electrically connected to the negative electrode current collecting tab 6a by welding. The method for electrically connecting the positive and negative electrode leads 8, 10 to the positive and negative electrode current collecting tabs 5a, 6a is not particularly limited, but examples thereof include welding such as ultrasonic welding or laser welding.

[0027] The electrode guard 12 has a side wall 12a covering the end faces of the positive and negative electrode current collecting tabs 5a and 6a, and a side wall 12b curved in a U-shape so as to cover the outermost periphery of the positive and negative electrode current collecting tabs 5a and 6a. The upper end of the electrode guard 12 is open so that the electrode group 2 can be stored therein. The positive electrode current collecting tab 5a of the electrode group 2 is covered by the electrode guard 12 with the current collecting portion 8c of the positive electrode lead 8 welded thereto. The connection plate 8a of the positive electrode lead 8 is located above the electrode guard 12. On the other hand, the negative electrode current collecting tab 6a of the electrode group 2 is covered by the electrode guard 12 with the current collecting portion 10c of the negative electrode lead 10 welded thereto. The connection plate 10a of the negative electrode lead 10 is located above the electrode guard 12. The two electrode guards 12 are fixed to the electrode group 2 by insulating tape 13.

[0028] 1, 2, and 4, the sealing plate 4 has a rectangular plate shape. The sealing plate 4 has through holes 4a and 4b for attaching positive and negative electrode terminals 9 and 11. The sealing plate 4 also has a liquid injection hole 20.

[0029] The liquid filling hole 20 is also used to release gas generated inside the battery after the electrolyte is filled therethrough. The liquid filling hole 20 is sealed by a sealing lid 14. The sealing lid 14 is fixed to the surface of the sealing plate 4 by, for example, welding. The sealing lid 14 has a disk shape here, but the shape is not particularly limited as long as it can seal the liquid filling hole 20. The sealing lid 14 is formed from a metal such as aluminum or an aluminum alloy.

[0030] 2, an insulating plate 16 is disposed on the back surface of the sealing plate 4. The insulating plate 16 has a recess 16a at one end for accommodating the connection plate 8a of the positive electrode lead 8, and a recess 16b at the other end for accommodating the connection plate 10a of the negative electrode lead 10. An opening is provided between the recess 16a and the recess 16b, exposing the back surface of the sealing plate 4. The recess 16a and the recess 16b of the insulating plate 16 have through holes communicating with the through holes 4a and 4b of the sealing plate 4, respectively.

[0031] The positive and negative electrode terminals 9, 11 each have a rectangular plate-shaped head 9a, 11a and a shaft 9b, 11b extending from the head 9a, 11a. The insulating gasket 17 has a through hole 17a into which the shaft 9b, 11b of the positive and negative electrode terminals 9, 11 are inserted. The shaft 9b of the positive electrode terminal 9 is inserted into the through hole 17a of the insulating gasket 17, the through hole 4a of the sealing plate 4, the through hole of the insulating plate 16, and the through hole 8b of the connection plate 8a of the positive electrode lead 8, and is fixed by crimping to these members. As a result, the positive electrode terminal 9 is electrically connected to the positive electrode current collecting tab 5a via the positive electrode lead 8. On the other hand, the shaft portion 11b of the negative electrode terminal 11 is inserted into the through hole 17a of the insulating gasket 17, the through hole 4b of the sealing plate 4, the through hole of the insulating plate 16, and the through hole 10b of the connection plate 10a of the negative electrode lead 10, and is fixed by crimping to these members. As a result, the negative electrode terminal 11 is electrically connected to the negative electrode current collecting tab 6a via the negative electrode lead 10.

[0032] The container 3 will be described in more detail with reference to Fig. 4. The container 3 includes a bottom wall (container bottom wall) 30 and side walls (container side walls) 31a, 31b, 32a, and 32b. In the container 3, the bottom wall 30 and the side walls 31a, 31b, 32a, and 32b form a storage space in which the electrode group 2 is stored. The storage space opens to one side (upper side) in the Z direction of the container 3. The opening of the storage space is closed by a sealing plate 4.

[0033] In the container 3, each of the side walls 31a, 31b, 32a, and 32b extends from the bottom wall 30 to the sealing plate 4 along the Z direction. The bottom wall 30 has a rectangular plate shape having a pair of long sides facing each other and a pair of short sides facing each other. The long side walls 31a and 31b are arranged apart from each other along the Y direction with the storage space in between. The short side walls 32a and 32b are arranged apart from each other along the X direction with the storage space in between. Each of the long side walls 31a and 31b extends from the short side wall 32a to the short side wall 32b along the X direction. Each of the short side walls 32a and 32b extends from the long side wall 31a to the long side wall 31b along the Y direction.

[0034] In the container 3, the dimension from the outer surface of the long side wall 31a to the outer surface of the long side wall 31b is the same or approximately the same as the dimension in the Y direction of the container 3. In addition, in the container 3, the dimension from the outer surface of the short side wall 32a to the outer surface of the short side wall 32b is the same or approximately the same as the dimension in the X direction of the container 3. If the thickness of the side walls is constant, the binding force on the wound electrode group 2 changes by changing the dimension in the Y direction of the container 3 or the dimension in the X direction of the container 3. The dimension in the Y direction of the container 3 and the dimension in the X direction of the container 3 can be controlled by changing the dimension of the bottom wall 30. The means for binding the wound electrode group 2 will be described in detail later.

[0035] As shown in FIG. 4 and FIGS. 1 and 2, the wound electrode group 2 is accommodated in the exterior member 1 such that, for example, its winding axis 2p is parallel or substantially parallel to the bottom wall 30 of the exterior member 1. The wound electrode group 2 may be accommodated in the exterior member 1 such that its winding axis 2p is orthogonal or substantially orthogonal to the bottom wall 30.

[0036] The winding axis 2p of the wound electrode group 2 is preferably parallel to the bottom wall 30 of the container 3 and also parallel to both of the two long-side side walls 31a and 31b. In other words, among the flat-type electrode groups 2, it is preferable that the two flat portions 2a provided with the winding axis 2p interposed therebetween face the two long-side side walls 31a and 31b, respectively. In this case, the flat portions of the wound electrode group 2 having a large area are easily constrained by the long-side side walls 31a and 31b having a large area. Therefore, in this case, there is an advantage that it is easy to control the amount of wrinkles in the wound electrode group 2. The method for adjusting the amount of wrinkles will be described in detail later.

[0037] <X-ray CT Conditions and Binarization Conditions> Hereinafter, the imaging conditions during X-ray CT and the conditions for performing binarization will be described with reference to the images actually taken by X-ray CT. FIG. 5 is an image showing a cross section obtained by performing tomographic imaging on the secondary battery according to Example 1 described later by X-ray CT. FIG. 6 is an image obtained by binarizing the image according to FIG. 5 under predetermined conditions.

[0038] First, a secondary battery to be measured is placed in an X-ray CT device, and the tube voltage is set to 10-300 kV, the tube current to 10-600 μA, and the focal spot size to about 5 μm. For example, a TXS300 Micro manufactured by Tesco Corporation or a device having equivalent functions is used as the X-ray CT device. Under these conditions, tomography is performed using X-ray CT. FIG. 5 is a black-and-white image (grayscale image) of a cross section perpendicular to the winding axis 2p of the wound electrode group 2 taken under these conditions. In the X-ray CT, 800 cross-sectional images are taken at different shooting positions along the winding axis 2p. FIG. 5 is one of the multiple cross-sectional images thus obtained. The shooting positions along the winding axis 2p are taken at 800 or more locations at intervals of at least 0.125% when the length of the wound electrode group 2 along the winding axis 2p is taken as 100%. The intervals between the multiple images taken by the CT scan may be even closer.

[0039] In Fig. 5, a wound electrode group 2 is housed inside an exterior member 1 having a substantially rectangular cross-sectional shape. The wound electrode group 2 is housed in the exterior member 1 such that its winding axis (not shown) is parallel to the bottom wall 30 of the exterior member 1 and also parallel to the two long side walls 31a and 31b. The wound electrode group 2 is the electrode group described with reference to Fig. 3 etc. The wound electrode group 2 may include at least one wrinkle w.

[0040] FIG. 6 shows an image obtained by binarizing FIG. 5. In the binarization process, Image J shown in Non-Patent Document 1 is used as image processing software. The cross-sectional image is converted to 256 monochrome gradations and binarized by setting a threshold value. The threshold value is set so that the parts corresponding to the negative electrode, separator, and positive electrode in the cross section of the wound electrode group are displayed in white, and the parts corresponding to the wrinkles (voids) are displayed in black. Next, the area (St) of the wound electrode group 2 defined by the outer periphery of the wound electrode group 2 is obtained. The area St is the sum of the area (Sw) of the white part and the area (Sb) of the black part corresponding to the wrinkles before binarization. The area Sb of the black part is divided by the area St of the wound electrode group 2 and multiplied by 100 to calculate the ratio X of the area Sb of the black part to the area St of the wound electrode group 2 in the binarized image as a percentage.

[0041] The ratio X is calculated for each of the 800 images obtained by X-ray CT by the above operation. The calculated ratio X values ​​are simply averaged to obtain the average value. This average value is called the "ratio (R black )".

[0042] Furthermore, for the secondary battery according to the embodiment, it is more preferable that cross-sectional image B obtained by X-ray CT and binarization, which is a cross-sectional image parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member, has a horizontally elongated black portion. A method for preparing cross-sectional image B will be described below, and the fact that cross-sectional image B has a horizontally elongated black portion indicates that the wound electrode group has a void portion extending in a direction substantially parallel to the winding axis therein.

[0043] The cross-sectional image B is a binarized image prepared by the following method. First, cross-sectional photography of the secondary battery is performed under the same conditions as the above-mentioned X-ray CT. However, the cross-sectional image to be obtained is a cross-sectional image A that is parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member. The position of the cross section to be photographed is, for example, half the length of the short side of the bottom wall 30 having a rectangular shape.

[0044] Next, the same binarization process as the above-mentioned binarization process is performed on the obtained cross-sectional image A. In this way, a binarized cross-sectional image B can be obtained.

[0045] Fig. 7 is a cross-sectional image B obtained by the above method. Fig. 8 is an X-ray CT image corresponding to the above-mentioned cross-sectional image A. The X-ray CT image shown in Fig. 8 is an image taken using an X-ray CT device under the same conditions as those in Fig. 5 described above. The binary image shown in Fig. 7 is an image obtained by performing the same process as that used to obtain the binary image shown in Fig. 6 described above on the X-ray CT image shown in Fig. 8.

[0046] The horizontally elongated black portion 50 shown in FIG. 7 is preferably a black region that occupies 50% or more of the width of the wound electrode group and has a maximum width along the height direction of the wound electrode group that is 2.0% to 20.0% of the height of the wound electrode group. The maximum width is more preferably 3.0% to 10.0%. Here, the width of the wound electrode group is the width in a direction parallel to the bottom wall of the exterior member at a position half the height 2H of the white portion in the binary image (cross-sectional image B). The width of the wound electrode group can be the width in a direction parallel to the winding axis direction. The direction indicating the height 2H of the white portion in the binary image (cross-sectional image B) (height direction of the wound electrode group 2) is a direction perpendicular to the bottom wall of the exterior member.

[0047] As described above, the horizontally elongated black portion 50 corresponds to the elongated gap portion (thick wrinkle) G that extends approximately parallel to the winding axis in the wound electrode group. Such gap portion G functions as a diffusion path for gas generated during charging and discharging. Therefore, the distance between the positive and negative electrodes is unlikely to increase with charging and discharging, which has the effect of making it difficult for resistance to increase. In other words, when the cross-sectional image B has the horizontally elongated black portion 50, excellent life characteristics and low battery resistance can be achieved.

[0048] <Secondary battery manufacturing method> The secondary battery 100 is produced, for example, by the following method. First, the wound electrode group 2 is produced and housed in the exterior member 1. The wound electrode group 2 can be produced, for example, as follows. A positive electrode 5 and a negative electrode 6 are laminated with a separator 7 interposed therebetween to obtain a laminate of the positive electrode 5, the negative electrode 6, and the separator 7. After this laminate is wound, the obtained wound body is further pressed to produce the wound electrode group 2 having a flat shape.

[0049] When the wound electrode group 2 is housed in the exterior member 1, specifically, after the fabricated wound electrode group 2 is dried, the positive and negative electrode leads 8, 10 are welded to the positive and negative electrode current collector tabs 5a, 6a of the electrode group 2. Next, an electrode guard 12 is attached to the positive and negative electrode current collector tabs 5a, 6a of the electrode group 2, and the electrode guard 12 is fixed to the electrode group 2 with an insulating tape 13. Next, the positive and negative electrode terminals 9, 11, the sealing plate 4, and the positive and negative electrode leads 8, 10 are integrated by crimping, and then the sealing plate 4 is fixed to the opening of the exterior member 1 by welding. In this way, the electrode group 2 is housed in the exterior member 1. In addition, the positive and negative electrode leads 8 and 10, the electrode guard 12, and the insulating tape 13 are also housed in the exterior member 1. Then, an electrolyte is injected into the exterior member 1 through the liquid inlet 20, and the liquid inlet 20 is sealed.

[0050] Next, after restraining the wound electrode group 2, the secondary battery is subjected to an initial charge. When the secondary battery is subjected to an initial charge, lithium ions are inserted into the niobium titanium composite oxide contained in the negative electrode active material, and the negative electrode active material-containing layer expands. This can cause wrinkles to form in at least a part of the wound electrode group. The restraint of the wound electrode group 2 will be described in detail below, but if the secondary battery is subjected to an initial charge with the wound electrode group 2 restrained, the formation of wrinkles can be suppressed. Restraint refers to the application of pressure to the secondary battery or the wound electrode group. The greater the pressure applied to the wound electrode group 2 by restraint, the smaller the amount of wrinkles tends to be. When the amount of wrinkles is reduced, the ratio (R black ) is also reduced.

[0051] One method for restraining the wound electrode group 2 is to restrain the wound electrode group 2 from the outside of the exterior member 1 using one or more restraining jigs 60, as shown in Fig. 9 and Fig. 10. Fig. 9 is a front view showing a schematic view of the secondary battery being restrained. Fig. 10 is a schematic side view showing a partial cross section of the secondary battery being restrained.

[0052] 9 and 10, pressure is applied to the wound electrode group 2 via a pair of side walls (long side walls 31a and 31b) of the exterior member 1. In other words, the exterior member 1 is clamped by one or more restraining jigs 60. Here, the pair of side walls of the exterior member 1 refers to two side walls between which flat portions 2a of the wound electrode group 2 face each other. Therefore, pressure is applied to the wound electrode group 2 mainly to the flat portions 2a. The flat portions 2a of the wound electrode group 2 are shown in FIGS. 3 and 5.

[0053] An example of the restraining jig 60 is a metal plate made of a metal such as aluminum. In the example shown in Fig. 9 and Fig. 10, two restraining jigs 60 (here, aluminum plates) each hold an exterior member 1 via a bakelite plate 61. The two restraining jigs 60 are fixed in a state in which they pressurize the exterior member 1 in the direction in which they approach each other by tightening restraining means 62 such as bolts and nuts. The restraining jigs 60 and the bakelite plate 61 may be provided with through holes (not shown) at predetermined positions into which the restraining means 62 such as bolts and nuts can be inserted.

[0054] For example, a plate in which a resin such as phenol resin is laminated onto a base material such as paper or cloth can be used as the bakelite board 61. The thickness of the bakelite board 61 is, for example, 2 mm to 40 mm.

[0055] By interposing the bakelite plate 61 between the metal plate and the exterior member 1, it is possible to suppress deformation of the metal plate when the exterior member 1 is restrained. Therefore, it is possible to apply uniform pressure to the exterior member 1, and in turn to the flat portion 2a of the electrode group 2 housed in the exterior member 1.

[0056] Another method for restraining the wound electrode group 2 is to reduce the width of the bottom wall 30 of the bottomed rectangular tubular container 3 constituting the exterior member 1. When adjusting the width of the bottom wall 30 in order to change the restraining force on the wound electrode group 2, the width 30w of the bottom wall 30 is adjusted in a direction perpendicular to the winding axis 2p of the wound electrode group 2. In adjusting the width 30w of the bottom wall 30, for example, the width of the short side of the rectangular bottom wall is reduced. In this case, the pressure applied to the wound electrode group 2 can be controlled without using the restraining jig 60. However, the restraining jig 60 may be further used. By reducing the width 30w of the bottom wall 30, the pressure applied to the wound electrode group 2 can be increased. In other words, the exterior member 1 can function as the restraining jig 60.

[0057] Here, referring to FIG. 11, the dimensions of the secondary battery (exterior member) according to the embodiment are illustrated. FIG. 11 is a perspective view that shows a schematic appearance of the secondary battery shown in FIG. 1, FIG. 2, and FIG. 4. The dimensions of the exterior member are not particularly limited, but the width of the battery parallel to the X direction is, for example, within a range of 1 cm to 30 cm. The thickness of the battery parallel to the Y direction is, for example, within a range of 1 cm to 30 cm. The width of the bottom wall 30 described above may be the thickness of the battery parallel to the Y direction in FIG. 11. The height of the battery parallel to the Z direction is, for example, within a range of 1 cm to 30 cm. In FIG. 11, the X direction and the Y direction are perpendicular to each other, and the Z direction is perpendicular to both the X direction and the Y direction.

[0058] Although not shown, another method for restraining the wound electrode group 2 is to insert a spacer between a side wall (e.g., side wall 31a) of the exterior member 1 and the flat portion 2a of the wound electrode group 2. The spacer may be, for example, an elastic body such as an elastomer.

[0059] The initial charging conditions are not particularly limited, but may be, for example, the following conditions: The secondary battery is charged at 25°C with a current value of 0.5C to 2.0C until the battery voltage reaches 2.0V to 3.0V. The current value during charging is expressed in units of 1C, which is the current value at which the State of Charge (SOC) of the secondary battery becomes 0% in 1 hour when the battery is discharged from a state where the SOC is 100%.

[0060] After the initial charge, aging may be performed as necessary. Aging forms a protective film on the surface of the negative electrode active material-containing layer and the surface of the positive electrode active material-containing layer, for example. In aging, for example, a battery with an SOC of 20% to 150% is kept in a dryer kept at a temperature of, for example, 45°C to 120°C. The aging time is, for example, 10 hours to 100 hours. If the SOC of the battery during aging is increased, the aging temperature is increased, and / or the aging time is extended, a volume change of the active material occurs due to charging, which applies stress to the electrodes, and the amount of wrinkles tends to increase.

[0061] Since an excessive amount of coating increases the battery resistance, it is preferable to perform appropriate aging. However, if the coating is thick, there is an advantage that self-discharge is easily reduced. After aging, the battery can be opened as necessary to release gas generated in the battery. After this gas release, a vacuum may be drawn optionally, and then the battery is resealed.

[0062] When the secondary battery is subjected to aging while the binding force of the wound electrode group 2 is large, a coating is likely to form due to the high adhesion between the negative electrode, separator, and positive electrode. In other words, if the amount of wrinkles is small after the first charge, a coating is likely to form during subsequent aging. On the other hand, when the secondary battery is subjected to aging while the binding force of the wound electrode group 2 is small, there are areas (wrinkles) where the adhesion between the negative electrode, separator, and positive electrode is poor, so a coating is less likely to form compared to when the binding force is large. By controlling the binding force on the wound electrode group 2, the ratio (R black ) can be adjusted to be within the range of more than 2.0% and not more than 20.0%. blackWhen the temperature is within this range, a secondary battery having excellent life characteristics and low resistance can be obtained.

[0063] In addition, the amount of wrinkles, that is, the ratio (R black The constraint on the wound electrode group for adjusting the amount of wrinkles may or may not be released after the initial charge and / or aging. In order to adjust the amount of wrinkles, it is desirable that the wound electrode group is constrained at least during the initial charge and / or aging. The niobium titanium composite oxide also expands and contracts during repeated charge and discharge after the initial charge and / or aging, but the ratio (R black ) is affected by the ratio (R black ) is small compared to its impact on

[0064] Next, each member included in the secondary battery will be described in detail.

[0065] The secondary battery may further include an electrolyte held in the wound electrode group. The wound electrode group and the electrolyte are housed in an exterior member. The secondary battery may further include an electrode guard for preventing electrical connection between the positive and negative electrodes and the exterior member.

[0066] The negative electrode, positive electrode, separator, electrolyte, exterior member, and electrode guard included in the secondary battery will be described.

[0067] (1) Negative electrode The negative electrode may include a negative electrode current collector and a negative electrode active material-containing layer. The negative electrode active material-containing layer may be formed on one or both sides of the negative electrode current collector. The negative electrode active material-containing layer may include a negative electrode active material including a niobium titanium composite oxide, and may optionally include a conductive agent and a binder.

[0068] The niobium titanium composite oxide has, for example, a monoclinic crystal structure. The monoclinic niobium titanium composite oxide is, for example, represented by the general formula Li x Ti 1-y M1 y Nb 2-z M2 z O7+δ and a composite oxide represented by the general formula Li x Ti 1-y M3 y+z Nb 2-z O 7-δ Here, M1 is at least one selected from the group consisting of Zr, Si, and Sn. M2 is at least one selected from the group consisting of V, Ta, and Bi. M3 is at least one selected from Mg, Fe, Ni, Co, W, Ta, and Mo. Each subscript in the composition formula satisfies 0≦x≦5, 0≦y<1, 0≦z<2, and -0.3≦δ≦0.3.

[0069] Specific examples of monoclinic niobium titanium composite oxides include Nb2TiO7, Nb2Ti2O9, and Nb 10 Ti2O 29 , Nb 14 TiO 37 and Nb 24 TiO 62 The monoclinic niobium titanium composite oxide may be a substituted niobium titanium composite oxide in which at least a part of Nb and / or Ti is substituted with a different element. Examples of the substituted element include Na, K, Ca, Co, Ni, Si, P, V, Cr, Mo, Ta, Zr, Mn, Fe, Mg, B, Pb, and Al. The substituted niobium titanium composite oxide may contain one type of substituted element, or may contain two or more types of substituted elements.

[0070] The negative electrode active material may contain other active materials besides the niobium titanium composite oxide. Examples of the other active materials include lithium titanate having a ramsdellite structure (e.g., Li 2+y Ti3O7, 0≦y≦3), lithium titanates with spinel structure (e.g., Li 4+x Ti5O 12 , 0≦x≦3), monoclinic titanium dioxide (TiO2(B)), anatase titanium dioxide, rutile titanium dioxide, hollandite titanium composite oxide, and orthorhombic titanium-containing composite oxide.

[0071] As an example of an orthorhombic titanium-containing composite oxide, Li 2+a M(I) 2-b Ti 6-c M(II) d O 14+σ Here, M(I) is at least one selected from the group consisting of Sr, Ba, Ca, Mg, Na, Cs, Rb, and K. M(II) is at least one selected from the group consisting of Zr, Sn, V, Nb, Ta, Mo, W, Y, Fe, Co, Cr, Mn, Ni, and Al. The subscripts in the composition formula are 0≦a≦6, 0≦b<2, 0≦c<6, 0≦d<6, and -0.5≦σ≦0.5. Specific examples of orthorhombic titanium-containing composite oxides include Li 2+a Na2Ti6O 14 (0≦a≦6).

[0072] The proportion of the niobium titanium composite oxide in the negative electrode active material is, for example, 50 mass % or more, and preferably 80 mass % or more.

[0073] The conductive agent is blended to improve the current collecting performance and to reduce the contact resistance between the active material and the current collector. Examples of the conductive agent include vapor grown carbon fiber (VGCF), carbon black such as acetylene black, graphite, carbon nanofibers, and carbonaceous materials such as carbon nanotubes. One of these may be used as the conductive agent, or two or more may be used in combination as the conductive agent. Alternatively, instead of using a conductive agent, a carbon coating or an electronically conductive inorganic material coating may be applied to the surface of the active material particles.

[0074] The binder is blended to fill the gaps between the dispersed active materials and to bind the active materials and the negative electrode current collector. Examples of the binder include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), fluorine-based rubber, styrene butadiene rubber, polyacrylic acid compounds, imide compounds, carboxymethyl cellulose (CMC), and salts of CMC. One of these may be used as the binder, or two or more may be used in combination as the binder.

[0075] The mixing ratio of the negative electrode active material, the conductive agent, and the binder in the negative electrode active material-containing layer can be appropriately changed depending on the application of the negative electrode. For example, it is preferable to mix the negative electrode active material, the conductive agent, and the binder in a ratio of 70% by mass or more and 96% by mass or less, 2% by mass or more and 28% by mass or less, and 2% by mass or more and 28% by mass or less, respectively. By making the amount of the conductive agent 2% by mass or more, the current collection performance of the negative electrode active material-containing layer can be improved. In addition, by making the amount of the binder 2% by mass or more, the binding property between the negative electrode active material-containing layer and the current collector becomes sufficient, and excellent cycle performance can be expected. On the other hand, it is preferable to make the conductive agent and the binder 28% by mass or less, respectively, in order to increase the capacity.

[0076] The negative electrode current collector is provided with a potential at which lithium (Li) is inserted and extracted from the active material, for example, 1.0 V (vs. Li / Li + ) is used. For example, the current collector is preferably made of copper, nickel, stainless steel, aluminum, or an aluminum alloy containing one or more elements selected from Mg, Ti, Zn, Mn, Fe, Cu, and Si. The thickness of the current collector is preferably 5 μm or more and 20 μm or less. A current collector having such a thickness can balance the strength and weight of the electrode.

[0077] The negative electrode current collector may also include a portion on the surface of which the negative electrode active material-containing layer is not formed, and this portion can function as a negative electrode current collecting tab.

[0078] The density of the negative electrode active material-containing layer (excluding the current collector) is 1.8 g / cm 3 More than 2.8g / cm 3 A negative electrode having a density of the negative electrode active material-containing layer within this range is excellent in energy density and electrolyte retention. The density of the negative electrode active material-containing layer is preferably 2.1 g / cm or less. 3 More than 2.6g / cm 3 It is more preferable that:

[0079] The negative electrode can be produced, for example, by the following method. First, an active material, a conductive agent, and a binder are suspended in a solvent to prepare a slurry. This slurry is applied to one or both sides of a current collector. Next, the applied slurry is dried to obtain a laminate of an active material-containing layer and a current collector. After that, this laminate is pressed. In this manner, the negative electrode is produced.

[0080] Alternatively, the negative electrode may be prepared by the following method: first, the active material, the conductive agent, and the binder are mixed to obtain a mixture, then the mixture is formed into pellets, and then the pellets are placed on a current collector to obtain the negative electrode.

[0081] (2) Positive electrode The positive electrode may include a positive electrode current collector and a positive electrode active material-containing layer. The positive electrode active material-containing layer may be formed on one or both sides of the positive electrode current collector. The positive electrode active material-containing layer may include a positive electrode active material, and optionally a conductive agent and a binder.

[0082] As the positive electrode active material, for example, an oxide or a sulfide can be used. The positive electrode may contain one type of compound alone as the positive electrode active material, or may contain two or more types of compounds in combination. Examples of oxides and sulfides include compounds that can insert and remove Li or Li ions.

[0083] Examples of such compounds include, for example, manganese dioxide (MnO2), iron oxide, copper oxide, nickel oxide, lithium manganese composite oxide (e.g., Li x Mn2O4 or Li x MnO2; 0 < x ≦ 1), lithium nickel composite oxide (e.g., Li x NiO2; 0 < x ≦ 1), lithium cobalt composite oxide (e.g., Li x CoO2; 0 < x ≦ 1), lithium nickel cobalt composite oxide (e.g., Li x Ni 1-y Co y O2; 0 < x ≦ 1, 0 < y < 1), lithium manganese cobalt composite oxide (e.g., Li x Mn y Co 1-y O2; 0 < x ≦ 1, 0 < y < 1), lithium manganese nickel composite oxide having a spinel structure (e.g., Li x Mn 2-y Ni y O4; 0 < x ≦ 1, 0 < y < 2), lithium phosphate having an olivine structure (e.g., Li x FePO4; 0 < x ≦ 1, Li x Fe 1-y Mn y PO4; 0 < x ≦ 1, 0 < y < 1, Li x CoPO4; 0 < x ≦ 1), iron sulfate (Fe2(SO4)3), vanadium oxide (e.g., V2O5), and lithium nickel cobalt manganese composite oxide (Li x Ni 1-y-z Co y Mn z O2; 0 < x ≦ 1, 0 < y < 1, 0 < z < 1, y + z < 1) are included.

[0084] Among the above, examples of more preferred compounds as the positive electrode active material include lithium manganese composite oxide having a spinel structure (e.g., Li x Mn2O4; 0 < x ≦ 1), lithium nickel composite oxide (e.g., Li x NiO2; 0 < x ≦ 1), lithium cobalt composite oxide (e.g., Li xCoO2; 0 < x ≤ 1), lithium nickel cobalt composite oxide (e.g., Li x Ni 1-y Co y O2; 0 < x ≤ 1, 0 < y < 1), lithium manganese nickel composite oxide having a spinel structure (e.g., Li x Mn 2-y Ni y O4; 0 < x ≤ 1, 0 < y < 2), lithium manganese cobalt composite oxide (e.g., Li x Mn y Co 1-y O2; 0 < x ≤ 1, 0 < y < 1), lithium iron phosphate (e.g., Li x FePO4; 0 < x ≤ 1), and lithium nickel cobalt manganese composite oxide (Li x Ni 1-y-z Co y Mn z O2; 0 < x ≤ 1, 0 < y < 1, 0 < z < 1, y + z < 1) are included. When these compounds are used as the positive electrode active material, the positive electrode potential can be increased.

[0085] When a room temperature molten salt is used as the electrolyte of the battery, it is preferable to use a positive electrode active material containing lithium iron phosphate, Li x VPO4F (0 ≤ x ≤ 1), lithium manganese composite oxide, lithium nickel composite oxide, lithium nickel cobalt composite oxide, or a mixture thereof. Since these compounds have low reactivity with the room temperature molten salt, the cycle life can be improved. Details of the room temperature molten salt will be described later.

[0086] The primary particle size of the positive electrode active material is preferably 100 nm or more and 1 μm or less. The positive electrode active material with a primary particle size of 100 nm or more is easy to handle in industrial production. The positive electrode active material with a primary particle size of 1 μm or less enables smooth progress of solid-state diffusion of lithium ions.

[0087] The specific surface area of the positive electrode active material is preferably 0.1 m 2 / g or more and 10 m 2 / g or less. The positive electrode active material with a specific surface area of 0.1 m 2A positive electrode active material having a specific surface area of ​​10m / g or more can secure sufficient sites for absorbing and releasing Li ions. 2 A positive electrode active material having a specific surface area of ​​100 / g or less is easy to handle in industrial production and can ensure good charge-discharge cycle performance.

[0088] The binder is blended to fill the gaps between the dispersed positive electrode active material and to bind the positive electrode active material and the positive electrode current collector. Examples of the binder include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), fluorine-based rubber, polyacrylic acid compounds, imide compounds, carboxy methyl cellulose (CMC), and salts of CMC. One of these may be used as the binder, or two or more may be used in combination as the binder.

[0089] The conductive agent is blended to improve current collection performance and reduce contact resistance between the positive electrode active material and the positive electrode current collector. Examples of the conductive agent include vapor grown carbon fiber (VGCF), carbon black such as acetylene black, graphite, carbon nanofiber, and carbon nanotube, and other carbonaceous materials. One of these may be used as the conductive agent, or two or more may be combined and used as the conductive agent. The conductive agent may also be omitted.

[0090] In the positive electrode active material-containing layer, the positive electrode active material and the binder are preferably mixed in an amount of 80% by mass to 98% by mass and 2% by mass to 20% by mass, respectively.

[0091] By making the amount of binder 2% by mass or more, sufficient electrode strength can be obtained. In addition, the binder can function as an insulator. Therefore, by making the amount of binder 20% by mass or less, the amount of insulator contained in the electrode is reduced, and the internal resistance can be reduced.

[0092] When a conductive agent is added, the positive electrode active material, the binder, and the conductive agent are preferably mixed in proportions of 77% by mass or more and 95% by mass or less, 2% by mass or more and 20% by mass or less, and 3% by mass or more and 15% by mass or less, respectively.

[0093] By making the amount of the conductive agent 3% by mass or more, the above-mentioned effects can be achieved. Also, by making the amount of the conductive agent 15% by mass or less, the ratio of the conductive agent in contact with the electrolyte can be reduced. If this ratio is low, decomposition of the electrolyte during high-temperature storage can be reduced.

[0094] The positive electrode current collector is preferably an aluminum foil or an aluminum alloy foil containing one or more elements selected from Mg, Ti, Zn, Ni, Cr, Mn, Fe, Cu, and Si.

[0095] The thickness of the aluminum foil or aluminum alloy foil is preferably 5 μm or more and 20 μm or less, more preferably 15 μm or less. The purity of the aluminum foil is preferably 99 mass% or more. The content of transition metals such as iron, copper, nickel, and chromium contained in the aluminum foil or aluminum alloy foil is preferably 1 mass% or less.

[0096] The positive electrode current collector may also include a portion on the surface of which the positive electrode active material-containing layer is not formed, and this portion can function as a positive electrode current collecting tab.

[0097] The positive electrode can be produced, for example, by the following method. First, an active material, a conductive agent, and a binder are suspended in a solvent to prepare a slurry. This slurry is applied to one or both sides of a current collector. Next, the applied slurry is dried to obtain a laminate of an active material-containing layer and a current collector. Then, this laminate is pressed. In this manner, a positive electrode is produced.

[0098] Alternatively, the positive electrode may be prepared by the following method: first, the active material, the conductive agent, and the binder are mixed to obtain a mixture, then the mixture is formed into pellets, and then the pellets are placed on a current collector to obtain a positive electrode.

[0099] (3) Separator The separator is formed, for example, from a porous film containing polyethylene (PE), polypropylene (PP), cellulose, or polyvinylidene fluoride (PVdF), or a synthetic resin nonwoven fabric. From the viewpoint of safety, it is preferable to use a porous film formed from polyethylene or polypropylene. This is because these porous films melt at a certain temperature and are capable of cutting off electric current.

[0100] A solid electrolyte layer containing solid electrolyte particles can also be used as the separator. The solid electrolyte layer may contain one type of solid electrolyte particles or may contain multiple types of solid electrolyte particles. The solid electrolyte layer may be a solid electrolyte composite membrane containing solid electrolyte particles. The solid electrolyte composite membrane is, for example, a membrane formed from solid electrolyte particles using a polymer material. The solid electrolyte layer may contain at least one selected from the group consisting of a plasticizer and an electrolyte salt. When the solid electrolyte layer contains an electrolyte salt, for example, the alkali metal ion conductivity of the solid electrolyte layer can be further increased.

[0101] Examples of the polymeric material include polyethers, polyesters, polyamines, polyethylenes, silicones, and polysulfides.

[0102] As the solid electrolyte, it is preferable to use an inorganic solid electrolyte. Examples of the inorganic solid electrolyte include an oxide-based solid electrolyte or a sulfide-based solid electrolyte. As the oxide-based solid electrolyte, it is preferable to use a lithium phosphate solid electrolyte having a NASICON-type structure and represented by the general formula LiM2(PO4)3. M in the above general formula is preferably at least one element selected from the group consisting of titanium (Ti), germanium (Ge), strontium (Sr), zirconium (Zr), tin (Sn), and aluminum (Al). The element M more preferably contains any one of Ge, Zr, and Ti and Al.

[0103] Specific examples of the lithium phosphate solid electrolyte having a NASICON-type structure include LATP (Li 1+x Al x Ti 2-x (PO4)3), Li 1+x Al x Ge 2-x (PO4)3, Li 1+x Al x Zr 2-x (PO4)3. X in the above formula is in the range of 0 < x ≤ 5, and preferably in the range of 0.1 ≤ x ≤ 0.5. As the solid electrolyte, it is preferable to use LATP. LATP has excellent water resistance and is less likely to cause hydrolysis in the secondary battery.

[0104] Also, as the oxide-based solid electrolyte, amorphous LIPON (Li 2.9 PO 3.3 N 0.46 ), or garnet-type LLZ (Li7La3Zr2O 12 ) may be used.

[0105] (4) Electrolyte As the electrolyte, for example, a liquid non-aqueous electrolyte or a gel non-aqueous electrolyte can be used. The liquid non-aqueous electrolyte is prepared by dissolving an electrolyte salt as a solute in an organic solvent. The concentration of the electrolyte salt is preferably 0.5 mol / L or more and 2.5 mol / L or less.

[0106] Examples of the electrolyte salt include lithium salts such as lithium perchlorate (LiClO4), lithium hexafluorophosphate (LiPF6), lithium tetrafluoroborate (LiBF4), lithium hexafluoroarsenate (LiAsF6), lithium trifluoromethanesulfonate (LiCF3SO3), and lithium bistrifluoromethylsulfonylimide (LiN(CF3SO2)2), and mixtures thereof. The electrolyte salt is preferably one that is difficult to oxidize even at high potentials, and LiPF6 is most preferred.

[0107] Examples of organic solvents include cyclic carbonates such as propylene carbonate (PC), ethylene carbonate (EC), and vinylene carbonate (VC); chain carbonates such as diethyl carbonate (DEC), dimethyl carbonate (DMC), and methyl ethyl carbonate (MEC); cyclic ethers such as tetrahydrofuran (THF), 2-methyl tetrahydrofuran (2MeTHF), and dioxolane (DOX); chain ethers such as dimethoxyethane (DME) and diethoxyethane (DEE); γ-butyrolactone (GBL), acetonitrile (AN), and sulfolane (SL). These organic solvents can be used alone or as a mixed solvent.

[0108] The gelled non-aqueous electrolyte is prepared by combining a liquid non-aqueous electrolyte with a polymeric material, such as polyvinylidene fluoride (PVdF), polyacrylonitrile (PAN), polyethylene oxide (PEO), or a mixture thereof.

[0109] Alternatively, as the nonaqueous electrolyte, in addition to liquid nonaqueous electrolytes and gel nonaqueous electrolytes, room temperature molten salts containing lithium ions (ionic melts), polymer solid electrolytes, inorganic solid electrolytes, and the like may be used.

[0110] Room temperature molten salts (ionic melts) refer to organic salts consisting of a combination of organic cations and anions that can exist as a liquid at room temperature (15°C or higher and 25°C or lower). Room temperature molten salts include room temperature molten salts that exist as a liquid by themselves, room temperature molten salts that become liquid when mixed with an electrolyte salt, room temperature molten salts that become liquid when dissolved in an organic solvent, and mixtures of these. In general, the melting point of room temperature molten salts used in secondary batteries is 25°C or lower. In addition, organic cations generally have a quaternary ammonium skeleton.

[0111] The polymer solid electrolyte is prepared by dissolving an electrolyte salt in a polymer material and solidifying it.

[0112] The inorganic solid electrolyte is a solid material that has Li-ion conductivity.

[0113] (5) Exterior materials The material of the exterior member including the sealing plate can be, for example, aluminum, aluminum alloy, iron (Fe), nickel (Ni) plated iron, stainless steel (SUS), etc. When the positive and negative electrode terminals 9, 11 are made of aluminum or an aluminum alloy, the positive and negative electrode leads 8, 10 can be made of aluminum or an aluminum alloy.

[0114] (6) Electrode guard The resin used for the electrode guard can be any resin that is not easily damaged by the electrolyte, and examples of the resin that can be used include polyethylene, polypropylene, ethylene vinyl acetate copolymer, ethylene vinyl acetate alcohol copolymer, ethylene-acrylic acid copolymer, ethylene-ethyl acrylate copolymer, ethylene-methyl acrylate copolymer, ethylene methacrylic acrylate copolymer, ethylene-methyl methacrylic acid copolymer, ionomer, polyacrylonitrile, polyvinylidene chloride, polytetrafluoroethylene, polychlorotrifluoroethylene, polyphenylene ether, polyethylene terephthalate, and polytetrafluoroethylene. The above resins may be used alone or in combination. Among them, polypropylene or polyethylene is preferably used.

[0115] According to a first embodiment, a secondary battery is provided. The secondary battery includes a wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator, and an exterior member that houses the wound electrode group. The negative electrode active material includes a niobium titanium composite oxide. The ratio (R black ) is in the range of more than 2.0% and not more than 20.0%. black ) is determined by a method including the steps of: obtaining 800 cross-sectional images perpendicular to the winding axis of the wound electrode group by X-ray CT; converting each of the 800 cross-sectional images into monochrome 256 gradations, and then binarizing the images by setting a threshold value so that the areas corresponding to the positive electrode, negative electrode, and separator become white areas and voids that may exist inside the wound electrode group become black areas; determining, in each of the 800 binarized cross-sectional images, the ratio of the area (Sb) of the black areas to the area (St) of the wound electrode group defined by the outer periphery of the wound electrode group, as a percentage; and simply averaging the multiple ratios obtained in each of the 800 cross-sectional images. black ) in the range of more than 2.0% and not more than 20.0% can achieve excellent life characteristics and low battery resistance.

[0116] Second embodiment According to a second embodiment, a battery module is provided. The battery module according to the second embodiment includes one or more secondary batteries according to the first embodiment. When the battery module includes a plurality of unit cells, the unit cells are electrically connected in series, in parallel, or in a combination of series and parallel.

[0117] The battery module 200 will be specifically described with reference to the exploded perspective view of Fig. 12 and the cross-sectional view of Fig. 13. In the battery module 200 shown in Fig. 12, the secondary battery 100 according to the first embodiment is used as a cell 201. The cross-sectional view of Fig. 13 is a cross section including the positive electrode terminal 203B and the negative electrode terminal 206B in the exploded perspective view of Fig. 12.

[0118] The plurality of single cells 201 have, outside the exterior can of the battery, positive electrode terminals 203 (203A, 203B) provided on a positive electrode gasket 202, a sealing lid 204, and negative electrode terminals 206 (206A, 206B) provided on a negative electrode gasket 205. The single cells 201 shown in FIG. 12 are arranged in a staggered arrangement. The single cells 201 shown in FIG. 12 are connected in series, but may be connected in parallel by changing the arrangement method, or may be connected in a combination of series and parallel.

[0119] The plurality of single cells 201 are housed in a lower case 207 and an upper case 208. The lower case 207 includes a partition wall 216 that separates the storage spaces of the plurality of single cells 201 from one another. The upper case 208 is provided with power input / output terminals 209 and 210 (positive electrode terminal 209, negative electrode terminal 210) for the battery module. The upper case 208 is provided with an opening 211 aligned with the positions of the positive electrode terminal 203 and the negative electrode terminal 206 of the single cell 201, and the positive electrode terminal 203 and the negative electrode terminal 206 are exposed from the opening 211. The exposed positive electrode terminal 203A is connected to the negative electrode terminal 206A of the adjacent single cell 201 by a bus bar 212, and the exposed negative electrode terminal 206A is connected to the positive electrode terminal 203A of the adjacent single cell 201 on the opposite side to the adjacent one by the bus bar 212. Positive electrode terminal 203B not connected by bus bar 212 is connected to positive electrode terminal 214A provided on substrate 213, and positive electrode terminal 214A is connected to positive power input / output terminal 209 via a circuit on substrate 213. Negative electrode terminal 206B not connected by bus bar 212 is connected to negative electrode terminal 214B provided on substrate 213, and negative electrode terminal 214B is connected to negative power input / output terminal 210 via a circuit on substrate 213.

[0120] The power input / output terminals 209 and 210 are connected to a charging power source and / or a load (not shown) to charge and use the battery module 200. The upper case 208 is sealed with a lid 215. The board 213 may be provided with a charge / discharge protection circuit. In addition, additional configurations may be added as appropriate, such as a configuration that allows information on deterioration of the single cell 201 to be output from a terminal (not shown).

[0121] The initial charging and / or aging of the cells 201 may be performed after the battery module 200 is assembled. In this case, by narrowing the distance between the partition walls 216 provided in the lower case 207, a restraining force can be applied to the cells 201. For example, by reducing the width of each storage space in which the cells 201 are stored, a restraining force can be applied to the cells 201. The width of the storage space referred to here refers to the width of the storage space along the direction in which the cells 201 are arranged.

[0122] According to the second embodiment, a battery module is provided. Therefore, according to the present embodiment, a battery module having excellent life characteristics and low resistance can be provided.

[0123] Third embodiment According to a third embodiment, a vehicle is provided. The vehicle is equipped with the battery module according to the second embodiment.

[0124] In the vehicle according to the third embodiment, the battery module, for example, recovers regenerative energy of the vehicle's motive power. The vehicle may include a mechanism for converting the kinetic energy of the vehicle into regenerative energy.

[0125] Examples of the vehicle according to the third embodiment include a two-wheeled to four-wheeled hybrid electric vehicle, a two-wheeled to four-wheeled electric vehicle, an electric-assisted bicycle, and a railroad car.

[0126] The mounting position of the battery module in the vehicle is not particularly limited. For example, when the battery module is mounted in an automobile, the battery module can be mounted in the engine compartment, the rear of the vehicle body, or under the seat of the vehicle.

[0127] The vehicle may be equipped with a plurality of battery modules. In this case, the batteries included in each battery module may be electrically connected in series, electrically connected in parallel, or electrically connected in a combination of series and parallel connections.

[0128] Next, an example of a vehicle according to a third embodiment will be described with reference to the drawings.

[0129] FIG. 14 is a partial see-through view that illustrates an example of a vehicle according to an embodiment.

[0130] A vehicle 400 shown in Fig. 14 includes a vehicle body 40 and a battery module 200 according to the embodiment. In the example shown in Fig. 14, the vehicle 400 is a four-wheeled automobile.

[0131] The vehicle 400 may be equipped with a plurality of battery modules 200. In this case, the batteries (e.g., single cells or assembled batteries) included in the battery module 200 may be connected in series, in parallel, or in a combination of series and parallel connections.

[0132] 14 illustrates an example in which the battery module 200 is mounted in an engine room located in the front of the vehicle body 40. As described above, the battery module 200 may be mounted, for example, in the rear of the vehicle body 40 or under a seat. This battery module 200 can be used as a power source for the vehicle 400. In addition, this battery module 200 can recover regenerative energy for the motive power of the vehicle 400.

[0133] The vehicle according to the third embodiment is equipped with the battery module according to the second embodiment. Therefore, according to this embodiment, it is possible to provide a vehicle equipped with a battery module that has excellent life characteristics and low resistance.

[0134] [Example] Examples will be described below, but the embodiments are not limited to the examples described below.

[0135] Example 1 In Example 1, a secondary battery was produced in the following manner.

[0136] <Preparation of positive electrode> The positive electrode active material is LiNi with an average primary particle size of 2 μm. 0.5 Co 0.2 Mn 0.3 A slurry for forming an active material-containing layer was prepared by mixing 90% by mass of O2 composite oxide, 5% by mass of graphite powder as a conductive agent, and 5% by mass of PVdF as a binder in an N-methyl-2-pyrrolidone (NMP) solvent. The above mixing amounts are the masses relative to the mass of the positive electrode active material-containing layer. The prepared slurry was applied to both sides of an aluminum alloy foil (purity 99.3%) having a thickness of 15 μm and dried to obtain a laminate. The laminate was pressed to prepare a positive electrode having a positive electrode active material-containing layer having a thickness of 40 μm.

[0137] <Preparation of negative electrode> As the active material, the average particle diameter D 50 A monoclinic Nb2TiO7 (NTO) powder with a particle size of 10 μm was prepared. The active material particles, acetylene black powder as a conductive agent, carboxymethylcellulose (CMC) sodium salt powder as a thickener, and styrene butadiene rubber (SBR) as a binder were used as materials for the active material-containing layer. The compounding ratio of these materials was NTO:acetylene black:CMC:SBR=93:5:1:1 by mass ratio. These materials were mixed in the following order while stirring the solvent pure water to prepare a slurry. After dissolving carboxymethylcellulose sodium salt in pure water, SBR was further mixed to obtain a dispersion. Acetylene black was dispersed in this dispersion, and finally NTO powder was dispersed and stirred to obtain a slurry. The obtained slurry was applied to one side of an aluminum alloy foil (purity 99.3%) with a thickness of 15 μm, and the coating was dried to obtain a laminate consisting of a current collector and an active material-containing layer. The laminate was pressed to obtain an active material-containing layer having a thickness of 59 μm and an electrode density of 2.5 g / cm. 3 A negative electrode having the above structure was fabricated.

[0138] <Preparation of electrolyte> A mixed solvent of propylene carbonate and diethyl carbonate in a volume ratio of 1:2 was prepared. LiPF6 was then dissolved in this mixed solvent at a concentration of 1.2 M to prepare a liquid nonaqueous electrolyte.

[0139] <Preparation of secondary battery> The positive electrode obtained above, a separator made of a nonwoven fabric having a thickness of 20 μm, and a negative electrode were laminated with the separator interposed between them so that the positive electrode active material-containing layer and the negative electrode active material-containing layer faced each other to obtain a laminate. Next, this laminate was spirally wound so that the negative electrode was located at the outermost periphery to prepare an electrode group. When winding, the sheets were wound while applying a certain tension to each sheet so that no unnecessary gaps were generated between the sheets. The wound electrode group was hot-pressed at 90° C. to prepare a flat electrode group.

[0140] The obtained electrode group was housed in a bottomed rectangular metal can made of stainless steel with a wall thickness of 0.25 mm. The bottom wall of the metal can was rectangular. The direction of the winding axis of the electrode group housed in the exterior member was parallel to the bottom wall and parallel to the long side wall. The length of the short side of the bottom wall of the metal can was 21.5 mm. Since the thickness of each wall of the pair of long side walls provided in the exterior member was 0.25 mm as described above, the distance from the outer surface of one long side wall to the outer surface of the other long side wall was 22.0 mm. The metal can was provided with a valve that leaks gas when the internal pressure reaches 2 atmospheres or more. The electrolyte was introduced into the metal can and impregnated into the electrode group to prepare a secondary battery that had not yet been charged.

[0141] <Attaching the restraining jig> A restraining jig was attached to the fabricated secondary battery that had not yet been charged for the first time, by the method described with reference to Figs. 9 and 10. Specifically, a pair of long side walls of the exterior member were restrained from both sides by a bakelite plate and a metal plate as restraining jigs. At this time, the restraining width from one bakelite plate to the other bakelite plate was 22.0 mm. In this way, a restraining force was applied to the secondary battery.

[0142] <Initial charging and aging process> The secondary battery in a restrained state, which had not been initially charged, was charged at 1C at an environmental temperature of 25° C. Under these conditions, the secondary battery was charged to 2.5 V, and the SOC was set to 100%. After that, an aging treatment was performed for 60 hours in a temperature environment of 60° C. In this manner, the secondary battery according to Example 1 was produced.

[0143] Example 2 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 100 hours.

[0144] Example 3 A secondary battery was produced in the same manner as in Example 1, except that the SOC during aging was changed to 120%.

[0145] Example 4 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 100 hours and the SOC during aging was changed to 120%.

[0146] Example 5 A secondary battery was produced in the same manner as in Example 1, except that the conditions were changed so that no binding force was applied from the outside of the exterior member during aging.

[0147] Example 6 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours, the aging temperature was changed to 80° C., and the SOC during aging was changed to 120%.

[0148] Example 7 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours, the aging temperature was changed to 80° C., and the SOC during aging was changed to 150%.

[0149] Example 8 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours and the aging temperature was changed to 80°C.

[0150] Example 9 A secondary battery was produced in the same manner as in Example 1, except that the aging temperature was changed to 80°C.

[0151] Example 10 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours and the aging temperature was changed to 95°C.

[0152] Example 11 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours, the aging temperature was changed to 95°C, and the conditions were changed so that no external restraining force was applied to the exterior member during aging.

[0153] Example 12 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 24 hours, the aging temperature was changed to 95° C., and the SOC during aging was changed to 60%.

[0154] (Example 13) A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 90 hours and the aging temperature was changed to 45°C.

[0155] Example 14 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 90 hours, the aging temperature was changed to 45° C., and the SOC during aging was changed to 120%.

[0156] Example 15 A secondary battery was produced in the same manner as in Example 1, except that the aging time was changed to 90 hours, the aging temperature was changed to 45° C., and the SOC during aging was changed to 150%.

[0157] Example 16 A secondary battery was fabricated in the same manner as in Example 1, except that the direction of the winding axis in the electrode group housed in the exterior member was changed to a direction perpendicular to the bottom wall.

[0158] (Example 17) A secondary battery was fabricated in the same manner as in Example 16, except that the condition was changed such that no external restraining force was applied to the exterior member during aging.

[0159] (Comparative Example 1) A secondary battery was fabricated in the same manner as in Example 8, except that the restraint width was narrowed to 21.5 mm.

[0160] (Comparative Example 2) A secondary battery was fabricated in the same manner as in Example 1, except that the aging temperature was changed to 95°C and the condition was changed such that no external restraining force was applied to the exterior member during aging.

[0161] (Comparative Example 3) As the active material, instead of Nb2TiO7, Li4Ti5O with an average particle diameter D 50 of 0.8 μm was used, and a secondary battery was fabricated in the same manner as in Example 1. 12

[0162] (Comparative Example 4) A secondary battery was fabricated in the same manner as in Example 1, except that the first charge and aging treatment were not performed.

[0163] (Obtaining and Binarizing X-ray CT Images) X-ray CT imaging was performed on the secondary battery according to each example in accordance with the method described in the first embodiment. Thereafter, binarization processing was performed in accordance with the method described in the first embodiment, and the "ratio (R black )" was calculated. In Table 1 below, the "ratio (R black )" is shown in the column of "black area ratio (R black )(%)".

[0164] ​The X-ray CT image and the binarized image of the cross section perpendicular to the winding axis of the wound electrode group, obtained for Example 1, are shown in Figs. 5 and 6, respectively. As another example, the X-ray CT image and the binarized image of the cross section perpendicular to the winding axis of the wound electrode group, obtained for Comparative Example 1, are shown in Figs. 15 and 16, respectively. Comparative Example 1 has a ratio (R black ) is smaller than that of Example 1. When Fig. 5 and Fig. 6 relating to Example 1 are visually compared with Fig. 15 and Fig. 16 relating to Comparative Example 1, it can be seen that relatively large wrinkles w (black portions) are scattered in the images shown in Fig. 5 and Fig. 6.

[0165] For each secondary battery example, a cross-sectional image A parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member was captured by X-ray CT according to the method described in the first embodiment. The obtained cross-sectional image A was binarized according to the method described in the first embodiment to obtain a cross-sectional image B (binarized image). The "maximum width (%) of the horizontally elongated black portion along the height direction of the wound electrode group" was calculated from the cross-sectional image B.

[0166] The X-ray CT image and the binary image of the cross section parallel to the winding axis of the wound electrode group and parallel to the long side wall, obtained for Example 1, are shown in Fig. 8 and Fig. 7, respectively. As another example, the X-ray CT image and the binary image of the cross section parallel to the winding axis of the wound electrode group and parallel to the long side wall, obtained for Comparative Example 1, are shown in Fig. 17 and Fig. 18, respectively. When Fig. 8 and Fig. 7 of Example 1 are visually compared with Fig. 17 and Fig. 18 of Comparative Example 1, it can be seen that there are many relatively thick wrinkles (black regions) extending in the lateral direction (direction parallel to the winding axis) in the images shown in Fig. 8 and Fig. 7.

[0167] <Evaluation of gas generation amount> The secondary battery after the aging treatment in each example was sealed in a container with the inside in a vacuum state, and then the exterior member was opened and the amount of gas that escaped was measured. The amount of gas generated is an index for evaluating the life characteristics.

[0168] <Capacity retention rate measurement> Charge and discharge were performed under the conditions of a potential range of 1.5V to 3.0V, a charge and discharge current value of 20A, and an environmental temperature of 45°C. In the charge and discharge, the battery was first charged to 3.0V and then discharged to 1.5V. This constitutes one charge and discharge cycle, and the initial discharge capacity was measured. This charge and discharge cycle was repeated 300 times, and the discharge capacity after the 300th cycle was measured. The discharge capacity after the 300th cycle was divided by the initial discharge capacity and multiplied by 100 to evaluate the capacity retention rate after 300 cycles as a percentage. The capacity retention rate after 300 cycles is an index for evaluating the life characteristics.

[0169] <0.2 seconds DC resistance measurement> First, the SOC of the secondary battery prepared in each example was adjusted to 50%. Next, a current was passed three times for 0.2 seconds at the specified current values ​​shown below. The first current value was 20A, the second current value was 100A, and the third current value was 200A. For each pass, the DC resistance was estimated from the voltage difference before and after the current was passed, and the average value was defined as the "0.2 second DC resistance."

[0170] The above results are summarized in Table 1. In Table 1, "maximum width (%) of horizontally elongated black portion along the height direction of the wound electrode group" is the maximum width of the horizontally elongated black portion 50 described with reference to FIG. 7. This ratio is the ratio of the maximum width along the height direction of the wound electrode group among the black regions having a length of 50% or more of the width of the wound electrode group to the height of the wound electrode group (height 2H of the white portion). In other words, this ratio can be calculated by dividing [the height direction width of the black region having the maximum width along the height direction of the wound electrode group among the black regions having a length of 50% or more of the width of the wound electrode group] by [the height of the wound electrode group] and multiplying by 100. The width of the wound electrode group is the width in the direction parallel to the winding axis direction.

[0171] [Table 1]

[0172] From Table 1, we can see the following: When comparing Examples 1 to 17, which used Nb2TiO7 as the negative electrode active material, with Comparative Examples 1 to 4, the ratio of the area of ​​the black part to the cross-sectional area of ​​the wound electrode group (R black It can be seen that in Examples 1 to 17 in which the ratio of the capacity retention rate to the gas generation rate is in the range of more than 2.0% and not more than 20.0%, the capacity retention rate is high, the amount of gas generated is small, and the resistance value tends to be low.

[0173] Black area ratio (R black In Comparative Example 1, where the wrinkle amount was 2.0% or less, the gas diffusion was poor due to an insufficient wrinkle amount, and gas accumulation occurred between the electrodes, which led to non-uniformity in the reaction, and thus the capacity retention rate was poor.

[0174] In Comparative Example 2, the black area ratio (R black ) exceeded 20.0%. In cases where the amount of wrinkles was excessive like this, excessive load was placed on the electrodes, which may have damaged the electrode layers and caused a lack of electronic conductive paths in the positive and negative electrodes. It is also believed that the resistance tended to increase due to the excessive distance between the positive and negative electrodes.

[0175] Comparative Example 3 is an example that does not contain niobium titanium composite oxide. In Comparative Example 3, Li4Ti5O 12 This is an example using Li4Ti5O 12 When using a 100% Cr-Al-Si alloy, wrinkles are less likely to occur inside the wound electrode group, and the life characteristics and battery resistance are improved by the amount of wrinkles (ratio (R black )) is not easily affected by the control.

[0176] In the case of Comparative Example 4 where the aging treatment is not performed, the black area ratio (R black ) was 2.0% or less. In this case, although the battery resistance was low, the life characteristics (capacity retention rate) were poor.

[0177] Ratio (R black ) is within the range of 2.5% to 15.0%, it is possible to achieve high levels of long life characteristics and low resistance.

[0178] When the maximum width of the horizontally elongated black portion along the height direction of the wound electrode group is 2.0% or more and 20.0% or less of the height of the wound electrode group, an appropriate gas diffusion path in the direction parallel to the winding axis can be secured, thereby efficiently removing the gas generated between the electrodes.

[0179] According to at least one of the above-described embodiments and examples, a secondary battery is provided. The secondary battery includes a wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator, and an exterior member that houses the wound electrode group. The negative electrode active material includes a niobium titanium composite oxide. The ratio (R black ) is in the range of more than 2.0% and not more than 20.0%. black ) is determined by a method including the steps of obtaining 800 cross-sectional images perpendicular to the winding axis of the wound electrode group by X-ray CT, converting each of the 800 cross-sectional images into 256 monochrome gradations, and then binarizing the images by setting a threshold value so that the parts corresponding to the positive electrode, negative electrode, and separator become white parts and void parts that may exist inside the wound electrode group become black parts, determining the ratio of the area (Sb) of the black parts to the area (St) of the wound electrode group defined by the outer periphery of the wound electrode group in each of the binarized 800 cross-sectional images as a percentage, and simply averaging the multiple ratios obtained in each of the 800 cross-sectional images. This secondary battery can achieve excellent life characteristics and low battery resistance.

[0180] Although some embodiments of the present invention have been described, these embodiments are presented as examples and are not intended to limit the scope of the invention. These embodiments can be implemented in various other forms, and various omissions, substitutions, and modifications can be made without departing from the spirit of the invention. These embodiments and their modifications are included in the scope and spirit of the invention, and are also included in the scope of the invention and its equivalents described in the claims. The invention as set forth in the claims of the present application as originally filed is set forth below. [1] A wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator; and an exterior member that houses the wound electrode group, The negative electrode active material contains a niobium titanium composite oxide, Ratio (R black ) is in the range of more than 2.0% and not more than 20.0%, The ratio (R black )teeth, obtaining 800 cross-sectional images perpendicular to the winding axis of the wound electrode group by X-ray computed tomography (hereinafter referred to as X-ray CT); a step of converting each of the 800 cross-sectional images into monochrome images with 256 gradations, and then binarizing the images by setting a threshold value so that the portions corresponding to the positive electrode, the negative electrode, and the separator are shown as white portions and void portions that may be present inside the wound electrode group are shown as black portions; determining, in each of the 800 binarized cross-sectional images, a ratio of an area (Sb) of the black portion to an area (St) of the wound electrode group defined by an outer periphery of the wound electrode group, in percentage; and calculating a simple average of a plurality of the ratios obtained in each of the 800 cross-sectional images. [2] The ratio (R black ) is within a range of 2.5% to 15.0%. [3] The exterior member includes a container having a bottomed rectangular tubular shape and a sealing plate, The container includes a bottom wall and a plurality of side walls extending from a peripheral portion of the bottom wall in a direction perpendicular to the bottom wall, The secondary battery according to [1] or [2], wherein the winding axis of the wound electrode group extends parallel to the bottom wall. [4] The bottom wall has a rectangular shape; The side walls include two long side walls corresponding to the long sides of the bottom wall and two short side walls corresponding to the short sides of the bottom wall, The secondary battery according to [3], wherein the winding axis of the wound electrode group extends parallel to the two long side walls. [5] A cross-sectional image B obtained by X-ray CT and binarization, the cross-sectional image B being parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member, has a horizontally elongated black portion, The cross-sectional image B is obtaining a cross-sectional image A by X-ray CT at a position half the length of the short side of the bottom wall, the cross-sectional image A being parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member; and converting the cross-sectional image A into a monochrome image with 256 gradations, and then binarizing the image by setting a threshold value so that the portions corresponding to the positive electrode, the negative electrode, and the separator are white portions and voids that may exist inside the wound electrode group are black portions. The horizontally elongated black portion is The secondary battery according to [4], wherein in the cross-sectional image B, a black region occupies 50% or more of the width of the wound electrode group and has a maximum width along the height direction of the wound electrode group of 2.0% or more and 20.0% or less. [6] The niobium titanium composite oxide has the general formula Li x Ti 1-y M1 y Nb 2-z M2 z O 7+δ and a composite oxide represented by the general formula Li x Ti 1-y M3 y+z Nb 2-z O 7-δ At least one selected from the group consisting of composite oxides represented by The M1 is at least one selected from the group consisting of Zr, Si, and Sn, the M2 is at least one selected from the group consisting of V, Ta, and Bi, and the M3 is at least one selected from the group consisting of Mg, Fe, Ni, Co, W, Ta, and Mo, The secondary battery according to any one of [1] to [5], wherein x satisfies 0≦x≦5, y satisfies 0≦y<1, z satisfies 0≦z<2, and δ satisfies −0.3≦δ≦0.3. [7] A battery module comprising the secondary battery according to any one of [1] to [6]. [8] The battery module according to [7], comprising a plurality of the secondary batteries, the secondary batteries being electrically connected in series, in parallel, or in a combination of series and parallel. [9] A vehicle equipped with a battery module described in [7] or [8].

[10] A vehicle as described in [9], including a mechanism for converting kinetic energy of the vehicle into regenerative energy. [Explanation of symbols]

[0181] 1... exterior member, 2... electrode group, 3... container, 4... sealing plate, 5... positive electrode, 6... negative electrode, 7... separator, 8... positive electrode lead, 9, 203... positive electrode terminal, 10... negative electrode lead, 11, 206... negative electrode terminal, 12... electrode guard, 13... insulating tape, 14, 204... sealing cover, 16... insulating plate, 17... insulating gasket, 20... filling port, 27A... positive electrode side backup lead, 27B... negative electrode side backup lead, 30... bottom wall, 31, 32... side wall, 40... wheel Both main bodies, 50...horizontal black portion, 60...restraint jig, 61...bakelite plate, 62...restraint means, 100...secondary battery, 200...battery module, 201...single cell, 202...positive electrode gasket, 205...negative electrode gasket, 207...lower case, 208...upper case, 209, 210...power input / output terminals, 211...opening, 212...bus bar, 213...substrate, 214A...positive electrode terminal, 214B...negative electrode terminal, 215...lid, 216...partition wall, 400...vehicle.

Claims

1. A wound electrode group including a positive electrode, a negative electrode including a negative electrode active material, and a separator; and an exterior member that houses the wound electrode group, A gap portion is present inside the wound electrode group, the void portions are formed by wrinkles and are voids scattered in a cross section perpendicular to a winding axis of the wound electrode group, The negative electrode active material contains a niobium titanium composite oxide, Ratio (R black ) is in the range of more than 2.0% and not more than 20.0%, The ratio (R black )teeth, X-ray Computed Tomography (hereinafter referred to as X-ray CT) obtaining 800 cross-sectional images of the wound electrode group perpendicular to the winding axis; a step of converting each of the 800 cross-sectional images into monochrome 256 gradations, and then binarizing the images by setting a threshold value so that the portions corresponding to the positive electrode, the negative electrode, and the separator are white portions and the void portions are black portions; determining, in each of the 800 binarized cross-sectional images, a ratio of an area (Sb) of the black portion to an area (St) of the wound electrode group defined by an outer periphery of the wound electrode group, expressed as a percentage; and calculating a simple average of a plurality of the ratios obtained in each of the 800 cross-sectional images.

2. The ratio (R black ) is in the range of 2.5% to 15.0% according to claim 1 . Secondary battery.

3. The exterior member includes a container having a bottomed rectangular cylindrical shape and a sealing plate, The container includes a bottom wall and a plurality of side walls extending from a peripheral portion of the bottom wall in a direction perpendicular to the bottom wall, The secondary battery according to claim 1 , wherein the winding axis of the wound electrode group extends parallel to the bottom wall.

4. The bottom wall has a rectangular shape, The side walls include two long side walls corresponding to the long sides of the bottom wall and two short side walls corresponding to the short sides of the bottom wall, The secondary battery according to claim 3 , wherein the winding axis of the wound electrode group extends parallel to the two long side walls.

5. a cross-sectional image B obtained by X-ray CT and binarization, the cross-sectional image B being parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member, has a horizontally elongated black portion; The cross-sectional image B is obtaining a cross-sectional image A by X-ray CT at a position half the length of the short side of the bottom wall, the cross-sectional image A being parallel to the winding axis of the wound electrode group and perpendicular to the bottom wall of the exterior member; and converting the cross-sectional image A into a monochrome 256-level image and then binarizing the image by setting a threshold value so that the areas corresponding to the positive electrode, the negative electrode, and the separator are white areas and the void areas are black areas. The horizontally elongated black portion is The secondary battery according to claim 4 , wherein in the cross-sectional image B, the black region occupies 50% or more of the lateral width of the wound electrode group and has a maximum width along the height direction of the wound electrode group of 2.0% or more and 20.0% or less.

6. The niobium titanium composite oxide has the general formula Li x Ti 1-y M1 y Nb 2-z M2 z O 7+δ Represented by and a composite oxide having the general formula Li x Ti 1-y M3 y+z Nb 2-z O 7-δ A composite oxide represented by At least one selected from the group consisting of: The M1 is at least one selected from the group consisting of Zr, Si, and Sn, the M2 is at least one selected from the group consisting of V, Ta, and Bi, and the M3 is at least one selected from the group consisting of Mg, Fe, Ni, Co, W, Ta, and Mo, The x satisfies 0≦x≦5, the y satisfies 0≦y<1, the z satisfies 0≦z<2, and the δ satisfies −0.3≦δ≦0.

3. The secondary battery according to any one of claims 1 to 5.

7. A battery module comprising the secondary battery according to any one of claims 1 to 6.

8. The battery module according to claim 7 , comprising a plurality of the secondary batteries, the secondary batteries being electrically connected in series, in parallel, or in a combination of series and parallel.

9. A vehicle equipped with the battery module according to claim 7 or 8.

10. The vehicle according to claim 9, further comprising a mechanism for converting kinetic energy of the vehicle into regenerative energy.

Images