Patent Application
20110039140
The present invention particularly relates to a positive electrode for a nonaqueous battery, an electrode group including the positive electrode and a method for producing the same, and a rectangular nonaqueous secondary battery including the electrode group and a method for producing the same.
In recent years, lithium secondary batteries have widely been used as driving power supplies for mobile electronic devices and communication devices. In such a lithium secondary battery, in general, a carbon material capable of inserting and extracting lithium is used as a negative electrode, and a composite oxide of transition metal and lithium such as LiCoO2 etc., is used as a positive electrode to provide the secondary battery with high potential and high discharge capacity. With increase of functions of the electronic devices and communication devices, batteries with higher capacity have been in demand.
To realize a high capacity lithium secondary battery, for example, the battery capacity can be increased by increasing a volume of the positive and negative electrodes contained in a battery case, and reducing empty space except for space occupied by the electrodes in the battery case. Further, the battery capacity can be increased by applying a mixture paste made of a material of the positive or negative electrode to a current collector core, drying the paste to form an active material layer, and pressing the active material layer at high pressure to be compressed to a predetermined thickness, thereby increasing a filling density of the active material.
When the filling density of the active material in the electrode increases, it would be difficult to penetrate a nonaqueous electrolyte, which is injected in a battery case and has a relatively high viscosity, into small gaps in an electrode group formed by winding or stacking the positive and negative electrodes at high density with a separator interposed therebetween. Accordingly, it requires a long time to impregnate the electrode group with a predetermined amount of the nonaqueous electrolyte. Further, with an increased filling density of the active material of the electrode, porosity of the electrode is reduced, thereby making penetration of the electrolyte into the electrode group difficult. Therefore, impregnation of the electrode group with the nonaqueous electrolyte is greatly impaired, thereby varying the distribution of the nonaqueous electrolyte in the electrode group.
To overcome this disadvantage, grooves for guiding the nonaqueous electrolyte are formed in a surface of a negative electrode active material layer along a penetrating direction of the nonaqueous electrolyte to allow the nonaqueous electrolyte to penetrate into the whole part of the negative electrode. When the width or depth of the grooves is increased, the impregnation can be done in a short time. However, this reduces the amount of the active material, and therefore, charge/discharge capacity may decrease, or a reaction between the electrodes may become nonuniform, thereby deteriorating battery characteristics. Taking these into consideration, a method for setting the width and depth of the grooves to predetermined values has been proposed (see, e.g., Patent Document 1).
However, the grooves formed in the surface of the negative electrode active material layer may cause break of the electrode when the electrode is wound to form the electrode group. Therefore, a method for preventing the break of the electrode while improving the impregnation has been proposed. In this method, the grooves are formed in the surface of the electrode to form an inclination angle with a longitudinal direction of the electrode in order to distribute tensile force applied in the longitudinal direction of the electrode when the electrode is wound to form an electrode group. This can prevent the break of the electrode (see, e.g., Patent Document 2).
Another method has also been proposed, although it is not intended to improve the impregnation with the electrolyte. In this method, a porous film having convex portions partially formed on a surface facing the positive or negative electrode is provided for the purpose of alleviating overheat caused by overcharge. Accordingly, a larger amount of the nonaqueous electrolyte is held in gaps between the convex portions of the porous film and the electrode than in the other parts, thereby inducing an overcharge reaction in the gaps in a concentrated manner. This can alleviate the overcharge of a battery, and can alleviate the overheat due to the overcharge (see, e.g., Patent Document 3).
In a lithium secondary battery which has achieved high capacity in the above-described manner, for example, the separator may be damaged by a foreign matter that enters the battery for some reason, and an internal short circuit between the positive and negative electrodes may occur. In this case, a current intensively flows through the short circuited portion, thereby causing abrupt heat generation. This may cause decomposition of the positive and negative electrode materials, or boiling or decomposition of the electrolyte, thereby generating gas etc. A solution to these disadvantages derived from the internal short circuit has been proposed, in which a porous protective film is formed to cover the surface of the negative or positive electrode active material layer to reduce the internal short circuit (see, e.g., Patent Documents 4 and 5).
Patent Document 1: Japanese Patent Publication No. H09-298057
Patent Document 2: Japanese Patent Publication No. H11-154508
Patent Document 3: Japanese Patent Publication No. 2006-12788
Patent Document 4: Japanese Patent Publication No. H07-220759
Patent Document 5: Pamphlet of International Patent Publication No. 2005/029614
According to the conventional method of Patent Document 2, the electrolyte can penetrate into the electrodes in a shorter time as compared with the case where the electrodes are not provided with grooves. However, the time required for the penetration cannot be greatly reduced because the grooves are formed in only one of the surfaces of the electrode. Thus, the penetration takes quite a long time, an amount of the electrolyte evaporated cannot easily be reduced as much as possible, and the loss of the electrolyte cannot easily be reduced. Further, the grooves formed in only one of the surfaces of the electrode cause stress on the electrode. Therefore, the electrode tends to be curled on the side where the grooves are not formed.
According to the conventional method of Patent Document 3, the electrode group formed by winding the positive and negative electrodes with the separator interposed therebetween includes a useless, non-reactive portion which does not contribute to a battery reaction. Thus, space inside the battery case cannot effectively be used, thereby making the increase of the battery capacity difficult.
According to a method for forming the grooves in the surfaces of the active material layers formed on each surface of an electrode, a pair of rollers having a plurality of protrusions on their surfaces are arranged above and below the electrode, and the rollers are rotated and moved on the surfaces of the electrode while applying pressure thereto. In this method (hereafter referred to as “roll pressing”), a plurality of grooves can simultaneously be formed in each of the surfaces of the electrode. Therefore, this method is suitable for mass-production.
In view of the conventional technologies described in Patent Documents 4 and 5, the inventors of the present application have found the following problems as a result of examination of various types of electrodes including the grooves formed in the surfaces of the active material layers by roll pressing for the purpose of improving impregnation with the electrolyte.
a) to 7(d) are perspective views illustrating steps for producing an electrode 103. First, as shown in
Then, as shown in
A possible cause of this phenomenon is as follows. The roll pressing is performed by continuously passing the electrode hoop material 111 through a gap between the rollers. Therefore, the grooves 110 are formed in the surface of the porous protective film 128 to extend in the surface of the active material layer 113 on each of the surfaces of the double-coated part 114, and are formed also in the surface of the porous protective film 128 to extend in the active material layer 113 of the single-coated part 117. Specifically, when forming the grooves 110, the negative electrode active material layer 113 stretches. In the double-coated part 114, the active material layers 113 formed on the surfaces of the electrode stretch to the same extent. In the single-coated part 17, in contrast, the active material layer 113 stretches only on one of the surfaces thereof. Thus, due to tensile stress of the active material layer 113, the single-coated part 117 is greatly deformed to curve on the side on which the active material layer 113 is not formed.
If an end part of the electrode 103 (including the core exposed part 118 and the single-coated part 117 continuous with the core exposed part 118) is curved by cutting the electrode hoop material 111, the electrodes 103 may be misaligned when they are wound to form an electrode group. Further, in the case where the electrode group is formed by stacking the electrodes 103, the electrodes may possibly be bent. Furthermore, the end part of the electrode 103 may not reliably be chucked in transferring the electrode 103, resulting in failure in transfer of the electrode 103, or falling of the active material. This may reduce not only productivity, but also reliability of the batteries.
In view of the above-described problems, the present invention has been achieved. An object of the invention is to provide a positive electrode for a nonaqueous battery which allows good impregnation with an electrolyte, and has high productivity and reliability, an electrode group for the nonaqueous battery and a method for producing the same, and a rectangular nonaqueous secondary battery and a method for producing the same.
A positive electrode for a nonaqueous battery of the present invention includes: an active material layer which is formed on a surface of a current collector core, and is covered with a porous protective film. The positive electrode includes: a double-coated part which includes the active material layer and the porous protective film formed on each surface of the current collector core; a core exposed part which is located at an end of the current collector core, and does not include the active material layer and the porous protective film; and a single-coated part which is located between the double-coated part and the core exposed part, and includes the active material layer and the porous protective film formed only on one of the surfaces of the current collector core. A plurality of grooves are formed in each surface of the double-coated part, while the grooves are not formed in the single-coated part. The grooves are formed in a surface of the porous protective film to extend in a surface of the active material layer, and a thickness of the porous protective film is smaller than a depth of the grooves. A positive electrode current collector lead is connected to the core exposed part. The positive electrode is wound in such a manner that the core exposed part constitutes a last wound end, or the positive electrode is accordion-folded in such a manner that the core exposed part constitutes an outermost layer.
The above-described configuration can improve impregnation with an electrolyte, thereby reducing time required for the impregnation. Further, a useless portion which does not contribute to a battery reaction can be eliminated, and tensile force applied by the positive electrode active material layer formed in the single-coated part can be alleviated. This can prevent the core exposed part and the single-coated part continuous with the core exposed part from greatly deforming into a curved shape. When forming the electrode group, deformation of the electrode group due to the thickness of the current collector lead can be prevented. This makes a distance between the negative and positive electrodes of the electrode group uniform, thereby improving cycle characteristics. In addition, the porous protective film can improve an insulation property of the positive electrode, thereby reducing an internal short circuit.
In the positive electrode for the nonaqueous battery of the present invention, the porous protective film is preferably made of a material containing inorganic oxide as a main ingredient. This can further improve the insulation property of the positive electrode. The inorganic oxide which is the main ingredient of the porous protective film may preferably contain alumina and/or silica as a main ingredient. Thus, the positive electrode can be provided with high resistance to heat, high insolubility to the electrolyte, high reliability, and high insulation property.
In the positive electrode for the nonaqueous battery of the present invention, a phase of the grooves formed in one of the surfaces of the double-coated part is preferably symmetric with a phase of the grooves formed in the other surface of the double-coated part. This can reduce damage to the positive electrode caused by forming the grooves in the positive electrode as much as possible, and can prevent break of the positive electrode when the positive electrode is wound to form an electrode group.
In the positive electrode for the nonaqueous battery of the present invention, the depth of the grooves formed in each of the surfaces of the double-coated part is preferably in the range of 4 μm to 20 μm. This can improve penetration of the electrolyte, and can prevent the active material from falling.
In the positive electrode for the nonaqueous battery of the present invention, the grooves formed in each of the surfaces of the double-coated part are preferably arranged at a pitch of 100 μm to 200 μm in the longitudinal direction of the positive electrode. This can reduce damage to the positive electrode caused by forming the grooves in the positive electrode as much as possible. The grooves formed in each of the surfaces of the double-coated part preferably extend from one lateral end to the other lateral end of the positive electrode. This allows easy impregnation of the electrode group with the electrolyte from an end face of the electrode group, thereby reducing time required for the impregnation. Further, the grooves formed in one of the surfaces of the double-coated part, and the grooves formed in the other surface of the double-coated part are preferably inclined at an angle of 45° relative to the longitudinal direction of the positive electrode in different directions, so as to extend in directions crossing each other at right angles. This can avoid the formation of the grooves running in the direction which allows easy break of the positive electrode, thereby preventing concentration of stress. Thus, the break of the positive electrode can be prevented.
In the positive electrode for the nonaqueous battery of the present invention, the positive electrode current collector lead, and the active material layer and the porous protective film of the single-coated part are preferably arranged on the same surface of the current collector core. When forming the electrode group, this can prevent deformation of the electrode group due to the thickness of the current collector lead. Therefore, a distance between the negative and positive electrodes of the electrode group becomes uniform, thereby improving cycle characteristics.
An electrode group for a nonaqueous battery of the present invention includes: a positive electrode and a negative electrode wound with a separator interposed therebetween, wherein the positive electrode is the positive electrode for the nonaqueous battery of the present invention, the negative electrode includes a negative electrode active material layer formed on each surface of a negative electrode current collector core, and the single-coated part of the positive electrode constitutes an outermost turn, or an outermost layer of the electrode group.
In the electrode group for the nonaqueous battery of the present invention, the surface of the current collector core in the single-coated part of the positive electrode on which the active material layer and the porous protective film are not formed preferably constitutes an outermost circumferential surface, or an outermost layer of the electrode group. This can prevent useless provision of the active material layer on a portion of the electrode group which does not contribute to the battery reaction when the battery is working.
A method for producing the electrode group for the nonaqueous battery of the present invention includes: preparing the positive electrode for the nonaqueous battery of the present invention; preparing a negative electrode including a negative electrode active material layer formed on each surface of a negative electrode current collector core; and winding the positive electrode and the negative electrode with a separator interposed therebetween in such a manner that the core exposed part of the positive electrode constitutes a last wound end, or accordion-folding the positive electrode and the negative electrode with the separator interposed therebetween in such a manner that the core exposed part of the positive electrode constitutes an outermost layer.
In a rectangular nonaqueous secondary battery of the present invention, the electrode group for the nonaqueous battery of the present invention is contained in a battery case; a predetermined amount of a nonaqueous electrolyte is injected in the battery case, and an opening of the battery case is hermetically sealed.
A method for producing the rectangular nonaqueous secondary battery of the present invention includes: preparing the positive electrode for the nonaqueous battery of the present invention; preparing a negative electrode including a negative electrode active material layer formed on each surface of a negative electrode current collector core; winding the positive electrode and the negative electrode with a separator interposed therebetween in such a manner that the core exposed part of the positive electrode constitutes a last wound end, or accordion-folding the positive electrode and the negative electrode with the separator interposed therebetween in such a manner that the core exposed part of the positive electrode constitutes an outermost layer, thereby producing an electrode group; and introducing the electrode group and the nonaqueous electrolyte in the battery case, and sealing the battery case.
According to the present invention, a plurality of grooves are formed in the surface of the porous protective film to extend in the surface of the active material layer on each of the surfaces of the double-coated part, while the grooves are not formed in the single-coated part. This can improve the impregnation with the electrolyte, and can prevent the core exposed part and the single-coated part continuous with the core exposed part of the positive electrode from significantly deforming in the curved shape.
Since the electrodes are wound in such a manner that the core exposed part of the positive electrode current collector core to which the positive electrode current collector lead is connected constitutes a last wound end, or the electrodes are accordion-folded in such a manner that the core exposed part of the positive electrode current collector core to which the positive electrode current collector lead is connected constitutes an outermost layer, a useless portion of the positive electrode active material layer which is located at an outer circumference of the electrode group, and does not contribute to a battery reaction can be eliminated, and space inside the battery case can effectively be used, thereby increasing battery capacity. Further, the positive electrode current collector lead would not form a protrusion at the innermost turn of the electrode group, thereby preventing deformation of the electrode group due to the thickness of the current collector lead. Thus, a distance between the positive and negative electrodes of the electrode group becomes uniform, thereby improving cycle characteristics.
The active material layer formed on the surface of the current collector core is covered with the porous protective film. This can improve the insulation property of the positive electrode, thereby reducing the internal short circuit.
As described above, a positive electrode for a nonaqueous battery which allows good impregnation with an electrolyte, and has high productivity and reliability, an electrode group for the nonaqueous battery, and a rectangular nonaqueous secondary battery can be provided.
a) is a perspective view illustrating a positive electrode hoop material in the step of producing a positive electrode for a battery according to the embodiment of the invention,
a) is a perspective view illustrating a positive electrode hoop material in the step of producing a conventional positive electrode for a battery,
An embodiment of the present invention will be described below in detail with reference to the drawings. In the drawings, components having substantially the same function are indicated by the same reference characters for the sake of easy description. The present invention is not limited to the following embodiment.
The electrode group 1 is placed in a rectangular battery case 7 having a closed end together with an insulator 5. Then, a negative electrode current collector lead 16 extending from an upper portion of the electrode group 1 is connected to a terminal 6 provided with an insulating gasket 8 attached to a peripheral edge thereof. A positive electrode current lead 20 extending from the upper portion of the electrode group 1 is connected to a sealing plate 9. The sealing plate 9 is inserted in an opening of the battery case 7, and the sealing plate 9 and the battery case 7 are welded along an outer rim of the opening of the battery case 7, thereby sealing the opening of the battery case 7. Thereafter, a nonaqueous electrolyte (not shown) constituted of a predetermined amount of a nonaqueous solvent is injected in the battery case 7 through a plug port 45, and then a plug 46 is welded to the sealing plate 9. In this way, the rectangular nonaqueous secondary battery 15 is produced.
a) to 2(d) are perspective views illustrating the steps of producing the positive electrode 2.
The positive electrode mixture paste for forming the positive electrode 2 is prepared by mixing and dispersing a positive electrode active material and a binder in an appropriate dispersion medium using a dispersing machine, such as a planetary mixer, and kneading the mixture to obtain viscosity suitable for application to the current collector core 12 made of aluminum foil etc.
Examples of the positive electrode active material include composite oxides, for example, lithium cobaltate and denatured lithium cobaltate (lithium cobaltate containing aluminum or magnesium in the state of solid solution), lithium nickelate and denatured lithium nickelate (lithium nickelate partially substituted with cobalt), and lithium manganate and denatured lithium manganate.
Examples of a conductive agent include, for example, carbon blacks such as acetylene black, Ketchen black, channel black, furnace black, lamp black, thermal black, etc., and various types of graphites. They may be used alone, or in combination.
Examples of the binder for the positive electrode include, for example, PVdF (polyvinylidene fluoride), denatured polyvinylidene fluoride, PTFE (polytetrafluoroethylene), a rubber particle binder having an acrylate unit, etc. An acrylate monomer or an acrylate oligomer having a reactive functional group may be mixed in the binder.
Then, the above-described positive electrode mixture paste is applied to the current collector core 12 to form a positive electrode active material layer 13 of a predetermined thickness. The layer is dried, and then is pressed to a predetermined thickness over the almost entire surface, thereby forming the positive electrode 2.
In the positive electrode hoop material 11, a double-coated part 14 which includes the positive electrode active material layer 13 formed on each surface of the current collector core 12, a single-coated part 17 which includes the positive electrode active material layer 13 formed only on one of the surfaces of the current collector core 12, and a core exposed part 18 which does not include the positive electrode active material layer 13 on the current collector core 12 are provided, thereby constituting an electrode component part 19. The positive electrode hoop material 11 includes a multiple ones of the electrode component part 19 continuously formed in a longitudinal direction thereof. The electrode component part 19 in which the positive electrode active material layer 13 is partially provided can easily be formed by applying the positive electrode active material layer 13 by a known intermittent application process.
b) illustrates a porous protective film 28 formed by applying a coating prepared by mixing a small amount of a water soluble polymeric binder in an inorganic additive to the surface of the positive electrode active material layer 13, and drying the coating. The porous protective film 28 is not formed on the core exposed part 18 which does not contribute to a battery reaction. Due to the absence of the porous protective film 28 on the core exposed part 18, battery capacity increases. Further, in a step described later (see
The porous protective film 28 has a protective function of reducing an internal short circuit in a battery configured as shown in
c) illustrates the positive electrode hoop material 11 in which grooves 10 are formed only in the surfaces of the positive electrode active material layers 13 formed on the surfaces of each of the double-coated parts 14, while the grooves 10 are not formed in the positive electrode active material layer 13 of each of the single-coated parts 17.
The thickness of the porous protective film 28 is not particularly limited, but the thickness is preferably smaller than the depth of the grooves 10 described later. For example, when the depth of the grooves 10 (the depth of the grooves formed in both of the porous protective film 28 and the negative electrode active material layer 13) is 4 to 10 μm, the thickness of the porous protective film 28 is preferably 2 to 4 μm. When the thickness of the porous protective film is smaller than 2 μm, the protective function of reducing the internal short circuit would disadvantageously be insufficient.
In the positive electrode hoop material 11 provided with the grooves 10, the positive electrode current collector lead 20 is welded to the current collector core 12 of the core exposed part 18, and the positive electrode current collector lead 20 is coated with an insulation tape 21. Then, the positive electrode hoop material 11 is cut by a cutter at the core exposed parts 18 adjacent to the double-coated parts 14 to be divided into the electrode component parts 19 as shown in
The positive electrode 2 produced in this manner includes, as shown in
When forming the grooves 10 in the positive electrode active material layer 13 and the porous protective film 28 of the double-coated part 14 of the positive electrode 2, a large force is applied to the relatively hard positive electrode active material layer 13 on each surface of the double-coated part 14. In this case, the grooves 10 are not formed in the single-coated part 17, thereby effectively alleviating deformation of the electrode into a curved shape.
The positive electrode 2 configured in the above-described manner offers the following advantages.
Specifically, when the positive electrode 2 and the negative electrode 3 are wound into spiral form, or accordion-folded, with the separator 4 interposed therebetween to constitute the electrode group 1, the core exposed part 18 to which the positive electrode current collector lead 20 is attached constitutes a last wound end, and a surface of the single-coated part 17 of the positive electrode 2 on which the positive electrode active material layer 13 is not formed constitutes an outermost circumferential surface of the electrode group 1 as shown in
Further, the grooves 10 are not formed in the positive electrode active material layer 13 and the porous protective film 28 of the single-coated part 17. Therefore, when cutting the positive electrode hoop material 11 into the electrodes as shown in
Further, the positive electrode current collector lead 20 is connected to the surface of the core exposed part 18 of the positive electrode 2 same as the surface of the single-coated part 17 on which the positive electrode active material layer 13 is formed, and constitutes a last wound end. Thus, the positive electrode current collector lead 20 would not form a protrusion at the innermost turn of the electrode group, thereby preventing deformation of the wound electrodes. This allows easy placement of the electrode group 1 in the battery case 7, and a distance between the negative electrode 3 and the positive electrode 2 becomes uniform, thereby improving cycle characteristics.
When cutting the positive electrode current collector lead 20, burrs may be formed. When the positive electrode current collector lead 20 is connected to the inner surface of the outermost circumferential portion of the electrode group 1, the burrs are located radially outside the electrode group 1. This can prevent the burrs from penetrating the positive electrode current collector 20, and from contacting the positive electrode active material layer 13 located radially inside the electrode group 1.
As described later in Example 1, the negative electrode 3 includes a negative electrode active material layer containing a material capable of holding lithium formed on each surface of a negative electrode current collector core.
The grooves 10 will be described in detail with reference to
When the pitch P of the grooves 10 is small, a large number of grooves 10 can be formed to increase the total cross-sectional area of the grooves 10, thereby improving the penetration of the electrolyte. To examine this relationship, three types of positive electrodes 2 were formed, in which the depth D of the grooves 10 was fixed to 8 μm, while the pitch P was changed to 80 μm, 170 μm, and 260 μm. Then, three types of electrode groups 1 using the positive electrodes 2, respectively, were placed in the battery cases 7 to compare time required for the penetration of the electrolyte. As a result, the penetration time was about 20 minutes when the pitch P was 80 μm, about 23 minutes when the pitch P was 170 μm, and about 30 minutes when the pitch P was 260 μm. This indicates that the smaller pitch P of the grooves 10 allows faster penetration of the electrolyte into the electrode group 1.
When the pitch P of the grooves 10 is set smaller than 100 μm, the penetration of the electrolyte improves. However, the porous protective film 28 and the positive electrode active material layer 13 are compressed at many portions thereof due to the increased number of grooves 10, thereby increasing the filling density of the active material too much. Further, a planar area in the surface of the positive electrode active material layer 13 free from the grooves 10 is reduced too much, and a portion of the surface between two adjacent grooves 10 is protruded, which is easily crushed. When the protruded portion is crushed by chucking the electrode in a transfer process, the thickness of the positive electrode active material layer 13 may disadvantageously vary.
On the other hand, when the pitch P of the grooves 10 exceeds 200 μm, the current collector core 12 stretches, and the porous protective film 28 and the positive electrode active material layer 13 are greatly stressed. Further, peel resistance of the active material on the current collector core 12 decreases, and the active material may easily fall from the current collector core 12.
The decrease in peel resistance due to the increase in pitch P of the grooves 10 will be described in detail below.
When the positive electrode hoop material 11 passes between groove forming rollers 22, 23 which are the same rollers, groove forming protrusions 22a, 23a of the groove forming rollers 22, 23 bite into the porous protective film 28 and the positive electrode active material layer 13 on each surface of the double-coated part 14, thereby simultaneously forming the grooves 10 in the porous protective film 28 and the positive electrode active material layer 13. In this case, loads of the groove forming protrusions 22a, 23a are simultaneously applied to, and are canceled at portions of the double-coated part 14 where the groove forming protrusions 22a, 23a overlap with each other with the double-coated part 14 interposed therebetween. That is, the loads are canceled only at the portions of the double-coated part 14 where the grooves 10 formed on the surfaces of the double-coated part 14 overlap with each other with the double-coated part 14 interposed therebetween. Except for these portions, the loads of the groove forming protrusions 22a, 23a are received only by the current collector core 12.
Thus, when the grooves 10 are formed in the surfaces of the double-coated part 14 at a large pitch P to extend in the directions crossing each other at right angles, portions to which the loads of the groove forming protrusions 22a, 23a are applied increase in length, thereby applying a large load to the current collector core 12. This stretches the current collector core 12, and the active material may flake from the porous protective film 28 and the positive electrode active material layer 13, or the active material may peel from the current collector core 12, thereby decreasing peel resistance of the porous protective film 28 and the positive electrode active material layer 13 on the current collector core 12.
In order to verify that the peel resistance decreases with the increase of the pitch P of the grooves 10, four types of positive electrodes 2 were formed, in which the depth D of the grooves 10 were fixed to 8 μm, and the pitch P of the grooves 10 was changed to 460 μm, 260 μm, 170 μm, and 80 μm. As a result of a peeling test of these positive electrodes 2, the peel resistance was about 4 N/m, about 4.5 N/m, about 5 N/m, and about 6 N/m in the descending order of the pitch P. This verifies that the peel resistance decreases with the increase of the pitch P of the grooves 10, and the active material easily falls.
After the grooves 10 are formed, cross-sections of the positive electrodes 2 were checked. In the positive electrode 2 provided with the grooves 10 at a large pitch P of 260 μm, the current collector core 12 was curved, and part of the active material was slightly peeled and separated from the current collector core 12.
Thus, the pitch P of the grooves 10 is preferably set in the range of 100 μm to 200 μm, both inclusive.
The grooves 10 formed in one of the surfaces of the double-coated part 14, and the grooves 10 formed in the other surface of the double-coated part 14 extend in the directions crossing each other. Therefore, when the groove forming protrusions 22a, 23a bite into the porous protective film 28 and the positive electrode active material layer 13 on each surface of the double-coated part 14, warp in the porous protective film 28 and the positive electrode active material layer 13 on one surface, and warp in the porous protective film 28 and the positive electrode active material layer 13 on the other surface are advantageously canceled each other. Further, when the grooves 10 are formed in the corresponding surfaces at the same pitch, a distance between portions of the double-coated part 14 where the grooves 10 overlap with each other is the minimum, thereby reducing the load applied to the current collector core 12. This increases peel resistance of the active material on the current collector core 12, thereby effectively preventing the active material from falling. Further, since the grooves 10 formed in one of the surfaces of the positive electrode 2, and the grooves 10 formed in the other surface of the positive electrode 2 extend in the directions crossing each other, the electrolyte is allowed to penetrate through the grooves 10. This can improve impregnation of the electrode group 1 with the electrolyte.
The grooves 10 formed in one of the surfaces of the double-coated part 14 are arranged in a pattern having a phase symmetric with a phase of a pattern of the grooves 10 formed in the other surface of the double-coated part 14. Accordingly, the porous protective film 28 and the positive electrode active material layer 13 formed on each surface of the double-coated part 14 stretch in the same manner when the grooves 10 are formed, and the porous protective film 28 and the positive electrode active material layer 13 would not be warped even after the formation of the grooves 10.
With the provision of the grooves 10 in each of the surfaces of the double-coated part 14, a larger amount of the electrolyte can uniformly be held as compared with the case where the grooves 10 are formed only in one of the surfaces of the double-coated part 14. This can ensure long cycle life.
The depth D of the grooves 10 will be described with reference to
The penetration of the electrolyte improves as the depth D of the grooves 10 increases. However, the active material is severely compressed at portions where the grooves 10 are formed. Thus, lithium ions cannot move freely, and the lithium ions are less received. As a result, lithium metal may easily be deposited. Further, the positive electrode 2 is thickened as the depth D of the grooves 10 increases, and the stretch of the positive electrode 2 increases, thereby causing easy peeling of the porous protective film 28 and the positive electrode active material layer 13 from the current collector core 12. Further, the thickened positive electrode 2 may cause troubles in manufacture. For example, the porous protective film 28 and the positive electrode active material layer 13 may peel from the current collector core 12 in winding the electrodes to form the electrode group 1, or the electrode group 1 whose diameter is increased due to the increase in thickness of the positive electrode 2 may rub an end of an opening of the battery case 7 when the electrode group 1 is placed in the battery case 7, thereby making the placement of the electrode group 1 difficult. In addition, when the porous protective film 28 and the positive electrode active material layer 13 tend to easily peel from the current collector core 12, conductivity deteriorates, thereby affecting the battery characteristics.
The peel resistance of the porous protective film 28 and the positive electrode active material layer 13 on the current collector core 12 presumably decreases as the depth D of the grooves 10 increases. Specifically, the positive electrode active material layer 13 is thickened as the depth D of the grooves 10 increases. The increase in thickness results in decrease in peel resistance because a large force is applied in a direction of peeling the active material from the current collector core 12.
In order to verify this relationship, four types of positive electrodes 2 were formed, in which the pitch P of the grooves 10 was fixed to 170 μm, and the depth D of the grooves 10 was changed to 25 μm, 12 μm, 8 μm, and 3 μm. As a result of a peeling test of these positive electrodes 2, the peel resistance was about 4 N/m, about 5 N/m, about 6 N/m, and about 7 N/m in the descending order of the depth D. This verifies that the peel resistance decreases as the depth D of the grooves 10 increases.
From the foregoing, the followings have been found with respect to the depth D of the grooves 10. Specifically, when the depth D of the grooves 10 is set smaller than 4 μm, the penetration or impregnation of the electrolyte is insufficient. On the other hand, when the depth D of the grooves 10 exceeds 20 μm, the peel resistance of the active material on the current collector core 12 decreases. As a result, the battery capacity may decrease, or the fallen active material may penetrate the separator 4 to contact with the negative electrode 3, thereby causing an internal short circuit. Thus, when the depth D of the grooves 10 is reduced as much as possible, and the number of the grooves 10 is increased, the disadvantageous phenomena can be prevented from occurring, and good penetration of the electrolyte can be obtained. For these purposes, the depth D of the grooves 10 should be set in the range of 4 μm to 20 μm, both inclusive, preferably 5 to 15 μm, more preferably 6 to 10 μm.
In an example of the present embodiment, the pitch P of the grooves 10 is set to 170 μm, and the depth D of the grooves 10 is set to 8 μm. However, the pitch P may be set in the range of 100 μm to 200 μm, both inclusive. The depth D of the grooves 10 may be set in the range of 4 μm to 20 μm, both inclusive, preferably 5 to 15 μm, more preferably 6 to 10 μm.
In order to verify the preferred ranges, three types of positive electrodes 2 were formed, i.e., a first positive electrode 2 including the grooves 10 having the depth D of 8 μm formed in each of the surfaces of the double-coated part 14 at the pitch P of 170 μm, a second positive electrode 2 including the grooves of the same depth D arranged at the same pitch P in only one of the surfaces of the double-coated part 14, and a third positive electrode 2 including no grooves 10 in the surfaces thereof. A plurality sets of batteries were produced by placing three types of electrode groups 1 constituted of these positive electrodes 2 in the battery cases 7. A predetermined amount of the electrolyte was injected in each of the battery cases, and the battery cases were evacuated to impregnate the electrode group with the electrolyte. Then, the batteries were disassembled to check the degree of impregnation of the positive electrode 2 with the electrolyte.
Immediately after the injection of the electrolyte, the positive electrode 2 including no grooves 10 in the surfaces thereof was impregnated with the electrolyte only by 60% of an area thereof In the positive electrode 2 including the grooves 10 in only one of the surfaces thereof, 100% of an area of the surface provided with the grooves 10 was impregnated with the electrolyte, while about 80% of an area of the surface provided with no grooves 10 was impregnated with the electrolyte. Contrary to this, in the positive electrode 2 provided with the grooves 10 in each of the surfaces thereof, 100% of an area of each of the surfaces was impregnated with the electrolyte.
To check time required for impregnating the whole part of the positive electrode 2 with the electrolyte after the injection, the batteries were disassembled and checked every hour. As a result, in the positive electrode 2 provided with the grooves 10 in each of the surfaces thereof, 100% of each of the surfaces was impregnated with the electrolyte immediately after the injection. In the positive electrode 2 provided with the grooves 10 in only one of the surfaces thereof, 100% of the surface provided with no grooves 10 was impregnated with the electrolyte after a lapse of two hours. In the positive electrode 2 provided with no grooves 10 in the surfaces thereof, 100% of each of the surfaces was impregnated with the electrolyte after a lapse of five hours. However, in a portion of the positive electrode 2 impregnated immediately after the injection, the amount of the electrolyte was small, thereby varying the distribution of the electrolyte. The results indicate that the positive electrode 2 with the grooves 10 formed in each of the surfaces thereof can be impregnated with the electrolyte in about half the time required to completely impregnate the positive electrode 2 including the grooves 10 of the same depth D formed in only one of the surfaces thereof, and can increase the cycle life of the battery.
During the cycle test, the batteries were disassembled to examine the distribution of the electrolyte in the electrode provided with the grooves 10 in only one of the surfaces thereof for the purpose of examining the cycle life by checking the amount of EC (ethylene carbonate), which is a main ingredient of the nonaqueous electrolyte, extracted per unit area of the electrode. As a result, irrespective of a portion of the electrode where the extraction was performed, the surface provided with the grooves 10 contained EC in an amount larger by about 0.1 to 0.15 mg than the surface which was not provided with the grooves 10. Specifically, when the grooves 10 are formed in each of the surfaces, the EC amount in the surfaces of the electrode was the largest, and the surfaces were uniformly impregnated with the electrolyte without uneven distribution of the electrolyte. In the surface provided with no grooves 10, however, the amount of the electrolyte was small, thereby increasing internal resistance, and reducing the cycle life.
The grooves 10 are formed to extend from one lateral end to the other lateral end of the porous protective film 28 and the positive electrode active material layer 13. This can significantly improve the penetration of the electrolyte into the electrode group 1, thereby greatly reducing the penetration time. In addition, since the impregnation of the electrode group 1 with the electrolyte is significantly improved, depletion of the electrolyte for charge/discharge of the battery can effectively be prevented, and uneven distribution of the electrolyte in the electrode group 1 can be prevented. Further, with the grooves 10 inclined relative to the longitudinal direction of the positive electrode 2, the impregnation of the electrode group 1 with the electrolyte improves, and stress caused on the electrodes in the winding step for forming the electrode group 1 can be prevented, thereby effectively preventing break of the positive electrode 2.
A process of forming the grooves 10 in the surfaces of the double-coated part 14 will be described with reference to
As shown in
The groove forming rollers 22, 23 are the same rollers, and each of which includes a plurality of groove forming protrusions 22a, 23a extending at a helix angle of 45° with respect to an axial center thereof. Each of the groove forming protrusions 22a, 23a is easily and precisely formed by coating the entire surface of an iron roller body with chromium oxide by thermal spraying to form a ceramic layer, and partially melting the ceramic layer by laser application to form a predetermined pattern. The groove forming rollers 22, 23 are almost the same rollers as a laser-engraved ceramic roller generally used in the field of printing. The groove forming rollers 22, 23 made of chromium oxide have hardness of HV1150 or higher, i.e., they are considerably hard. Therefore, the rollers are resistant to sliding movement and wear, and are capable of ensuring life ten or more times longer than that of iron rollers.
Thus, when the positive electrode hoop material 11 passes through the gap between the groove forming rollers 22, 23, each of which is provided with a number of groove forming protrusions 22a, 23a, the grooves 10 extending in the directions crossing each other at right angles can be formed in the porous protective film 28 and the positive electrode active material layer 13 on each of the surfaces of the double-coated part 14 of the positive electrode hoop material 11 as shown in
Each of the groove forming protrusions 22a, 23a has a cross-sectional shape which allows formation of the grooves 10 having the cross-sectional shape shown in
For rotating the groove forming rollers 22, 23, rotary force applied by a servomotor etc. is transferred to the groove forming roller 23, and the rotation of the groove forming roller 23 is transferred to the groove forming roller 22 through a pair of gears 24, 27 which are attached to roller shafts of the groove forming rollers 22, 23, respectively, and engage with each other. Thus, the groove forming rollers 22, 23 rotate at the same rotational speed.
As a process for forming the grooves 10 by biting the groove forming protrusions 22a, 23a of the groove forming roller 22, 23 into the porous protective film 28 and the positive electrode active material layer 13, there are two types of processes. One is a constant dimension process of setting the depth D of the grooves 10 by controlling the gap between the groove forming rollers 22, 23. The other is a constant pressure process in which the groove forming roller 23 to which the rotary force is transferred is fixed, and pressure applied to the groove forming roller 22 capable of moving up and down is adjusted in view of correlation between pressure applied to the groove forming protrusions 22a, 23a and the depth D of the grooves 10, thereby setting the depth D of the grooves 10. In the present invention, the grooves 10 are preferably formed by the constant pressure process.
A reason why the constant pressure process is preferable is as follows. In the constant dimension process, it is difficult to precisely set the gap between the groove forming rollers 22, 23 for setting the depth D of the grooves 10 in the order of μm. In addition, deflections of the roller shafts of the groove forming rollers 22, 23 directly affect the depth D of the grooves 10. In the constant pressure process, pressure for pressing the groove forming roller 22 (e.g., air pressure of an air cylinder) can automatically be adjusted to be constant even if the thickness of the double-coated part 14 varies, although it is slightly affected by the filling density of the active material in the positive electrode active material layer 13. Thus, the grooves 10 of the predetermined depth D can be formed with high productivity.
In forming the grooves 10 by the constant pressure process, the positive electrode hoop material 11 has to pass through the gap between the groove forming rollers 22, 23 without forming the grooves 10 in the porous protective film 28 and the positive electrode active material layer 13 of the single-coated part 17 of the positive electrode hoop material 11. In this case, a stopper can be provided between the groove forming rollers 22, 23 to keep the groove forming roller 22 in a non-pressing state with respect to the single-coated part 17. The “non-pressing state” indicates a state where the groove forming roller 22 abuts the single-coated part 17, but does not form the grooves 10 (a non-contact state is also included).
When the positive electrode 2 is thin, the double-coated part 14 is as thin as about 200 μm. In order to form the grooves 10 having a depth D of 8 μm in the thin double-coated part 14, the grooves 10 have to be formed with higher precision. For this purpose, each of the roller shafts of the groove forming rollers 22, 23 is fitted in bearings without leaving a gap therebetween, except for a gap which allows the bearings to rotate, and the bearings and bearing holders for holding the bearings are also fitted with each other without leaving a gap therebetween. Thus, the positive electrode hoop material 11 is allowed to pass through the gap between the groove forming rollers 22, 23 without wobbling. In this way, the positive electrode hoop material 11 is allowed to smoothly pass through the gap between the groove forming rollers 22, 23 in such a manner that the grooves 10 are precisely formed in the porous protective film 28 and the positive electrode active material layer 13 on each of the surfaces of the double-coated part 14, while the grooves 10 are not formed in the porous protective film 28 and the positive electrode active material layer 13 on the surface of the single-coated part 17.
The present invention has been described by way of the preferred embodiment. However, the embodiment described above is not intended to limit the invention, and can be modified in various ways. For example, the electrode group 1 of the present embodiment is constituted of the positive and negative electrodes 2 and 3 wound with the separator 4 interposed therebetween. However, the similar advantages can be obtained using an electrode group 1 constituted of the positive and negative electrodes 2 and 3 accordion-folded with the separator 4 interposed therebetween in such a manner that the core exposed part 18 of the positive electrode 2 constitutes an uppermost or lowermost layer.
The positive electrode for the battery according to the embodiment of the invention, and a method and an apparatus for producing a rectangular nonaqueous secondary battery using the positive electrode will be described in detail with reference to the drawings. The invention is not limited to the example.
As a positive electrode active material, lithium nickel composite oxide represented by the composition formula of LiNi0.8Co0.15Al0.05O2 was used. To a NiSO4 aqueous solution, cobalt sulfate and aluminum sulfate of the predetermined ratio were added to prepare a saturated aqueous solution. While stirring the saturated aqueous solution, an alkaline solution dissolving sodium hydroxide was slowly dropped therein for neutralization, thereby precipitating ternary system nickel hydroxide Ni0.8Co0.15Al0.05(OH)2. The precipitate was filtered, washed with water, and dried at 80° C. Nickel hydroxide obtained in this manner had an average particle diameter of about 10 μm.
Lithium hydroxide hydrate was added in such a manner the ratio between the sum of numbers of atoms of Ni, Co, and Al and the number of atoms of Li was 1:1.03, and the obtained product was thermally treated in an oxygen atmosphere for 10 hours at 800° C. to obtain LiNi0.8Co0.15Al0.05O2. As a result of powder X-ray diffractometry, the obtained lithium nickel composite oxide had a single phase, hexagonal crystalline structure, in which Co and Al were in the state of solid solution. The obtained product was pulverized, and classified to obtain positive electrode active material powder.
To 100 parts by mass of the active material, 5 parts by mass of acetylene black was added as a conductive agent, and a solution prepared by dissolving PVdF (polyvinylidene fluoride) as a binder in a NMP (N-methyl pyrrolidone) solvent was kneaded with the mixture to prepare paste. The amount of PVdF added was adjusted to 5 parts by mass relative to 100 parts by mass of the active material. The paste was applied to each surface of a current collector core made of 15 μm thick aluminum foil, and the paste was dried and rolled to obtain a positive electrode active material layer. Then, a mixture prepared by kneading a small amount of a binder with alumina having a particle diameter of about 1.2 μm was applied to the surface of the positive electrode active material layer 13 using a roller device for intermittent application to a thickness of about 5 μm, and the mixture was dried to form a porous protective film 28. Thus, a positive electrode hoop material 11 having a thickness of about 200 μm, and a width of about 60 mm was obtained.
Then, as groove forming rollers 22, 23, rollers of 100 mm in outer diameter were used, each of which was provided with groove forming protrusions 22a, 23a on a ceramic outer circumferential surface thereof. The groove forming protrusions 22a, 23a had an angle of 120° at a tip end thereof, and a height of 25 μm, and were arranged at a pitch of 170 μm, while forming a helix angle of 45° with the circumferential direction of the roller. The positive electrode hoop material 11 was allowed to pass between the groove forming rollers 22, 23, thereby forming grooves 10 in each of the surfaces of the double-coated part 14 of the positive electrode hoop material 11. Gears 24, 27 fixed to roller shafts of the groove forming rollers 22, 23 are allowed to engage with each other to drive the groove forming roller 22 to rotate by a servomotor, thereby rotating the groove forming rollers 22, 23 at the same rotational speed.
The groove forming roller 22 was pressed by an air cylinder. The depth D of the grooves 10 were adjusted by adjusting air pressure of the air cylinder. In this case, stoppers prevented the groove forming roller 22 from approaching the groove forming roller 23, and reducing a gap of 100 μm therebetween, which was set as a minimum gap between the groove forming rollers 22, 23, thereby preventing the formation of the grooves 10 in the single-coated part 17. The stoppers were adjusted to keep the gap of 100 μm between the groove forming rollers 22, 23.
For setting the depth D of the grooves 10 to 8 μm, air pressure of the air cylinder for applying pressure to the groove forming roller 22 was adjusted to impose a load of 30 kgf per 1 cm of the width of the positive electrode hoop material 11. The positive electrode hoop material 11 was transferred through the gap between the groove forming rollers 22, 23 at a speed of 5 m/min. With this configuration, the grooves 10 were formed in each of the surfaces of the double-coated part 14 of the positive electrode hoop material 11. The depth D of the grooves 10 in the positive electrode active material layer 13 was measured by a profile measuring instrument. An average depth D of the grooves 10 formed in each of the surfaces of the double-coated part 14 was about 8.5 μm, and the grooves 10 were not formed in the positive electrode active material layer 13 of the single-coated part 17. Whether crack was formed in the positive electrode active material layer 13 or not was checked by a laser microscope, but the crack was not found at all. The positive electrode 2 increased in thickness by about 0.5 μm, and stretched in the longitudinal direction by about 0.1% per cell.
A negative electrode mixture paste was prepared by mixing, in a kneader, 100 parts by weight of artificial graphite as a negative electrode active material, 2.5 parts by weight of styrene-butadiene copolymer rubber particle dispersion (40 wt % of solid content) as a binder relative to 100 parts by weight of the active material (1 part by weight on a basis of solid content of the binder), 1 part by weight of carboxymethyl cellulose as a thickener relative to 100 parts by weight of the active material, and a proper amount of water. The negative electrode mixture paste was applied to a current collector core 12 made of 10 μm thick copper foil, and the paste was dried and pressed by rolling to a total thickness of about 200 μm. Then, the obtained product was cut by a slitter into strips of about 60 mm in width, which is the width of a negative electrode 3 of a rectangular lithium secondary battery having a nominal capacity of 2550 mAh, a diameter of 18 mm, and a height of 65 mm. Thus, a negative electrode hoop material 11 was formed.
After the negative and positive electrode hoop materials were dried to remove extra moisture, the electrode hoop materials were wound with a separator 4, which is a porous insulator made of an about 30 μm thick microporous polyethylene film, interposed therebetween in a dry air room to form an electrode group 1. The positive electrode hoop material 11 is cut at the core exposed part 18 located between the double-coated part 14 and the single-coated part 17. Since the groove forming rollers 30, 31 are configured not to form the grooves 10 in the positive electrode active material layer 13 of the single-coated part 17, the core exposed part 18 and the single-coated part 17 were not deformed after the cutting, and operation of a winding machine was not affected. A positive electrode current collector lead 20 was attached to the positive electrode hoop material 11 before the winding using a welder attached to the winding machine.
As a comparative example, the groove forming roller 23 was replaced with a flat roller not including the groove forming protrusions. Then, the gap between the groove forming rollers 22, 23 was set to 100 μm, a load applied to the positive electrode 2 per 1 cm of the width was adjusted to 31 kg, and the grooves 10 having a depth D of about 8 μm were formed only in one of the positive electrode active material layers 13 of the double-coated part 14 to form a positive electrode (Comparative Example 1). Another positive electrode (Comparative Example 2) was formed without forming the grooves 10 in each of the positive electrode active material layers 13 of the double-coated part 14.
Each of the electrode group 1 prepared in this manner were placed in a battery case 7, and an electrolyte was injected in the battery case to examine penetration of the electrolyte.
For evaluation of the penetration of the electrolyte, about 5 g of the electrolyte was fed into the battery case 7, and the battery case 7 was evacuated to allow impregnation with the electrolyte. The electrolyte may be fed into the battery case in several times.
After the predetermined amount of the electrolyte was injected, the battery case 7 was placed in a vacuum booth for evacuation, thereby discharging air in the electrode group. Then, atmospheric air was introduced in the vacuum booth to forcibly allow the electrolyte to penetrate into the electrode group 1 due to differential pressure between the pressure in the battery case 7 and the pressure of the atmospheric air. The evacuation was performed by vacuum suction to a degree of vacuum of −85 kpa. Time required for the penetration was measured as data for comparison of the penetration.
In an actual battery production process, the electrolyte is simultaneously fed to a plurality of battery cases 7, and the battery cases 7 are simultaneously deaerated by evacuation to a degree of vacuum of −85 kpa, and then the atmospheric air is introduced to forcibly allow the electrolyte to penetrate into the electrode group. Thus, the penetration of the electrolyte is finished. A determination of completion of the penetration is made when the electrolyte is no longer found when the inside of the battery case 7 is visually checked from immediately above the battery case 7. To obtain average penetration time which could be used for actual production, the electrolyte is simultaneously allowed to penetrate into multiple cells. Table 1 shows the results.
As apparent from the results shown in Table 1, in the electrode group 1 including the positive electrode 2 in which the grooves 10 having a depth of about 8 μm were formed in the surface of the porous protective film 28 to extend in the surface of the positive electrode active material layer 13, the penetration time was 22 minutes and 17 seconds. In the electrode group 1 including the positive electrode 2 in which only the porous protective film 28 was formed, and the grooves 10 were not formed, the penetration time was 69 minutes and 13 seconds. The results indicate that the provision of the grooves 10 can significantly improve the penetration of the electrolyte, and can greatly reduce the penetration time.
Thus, with use of the positive electrode (Example 1) in which the grooves 10 were formed in the positive electrode active material layer 13 on each surface of the double-coated part 14, the penetration of the electrolyte was significantly improved as compared with the positive electrode (Comparative Example 2) in which the grooves 10 were not formed in any of the positive electrode active material layers 13.
With use of the positive electrode (Comparative Example 1) in which the grooves 10 were formed in one of the positive electrode active material layers 13 of the double-coated part 14, and in the positive electrode active material layer 13 of the single-coated part 17, the electrodes were misaligned in the winding, and the active material fell from the positive electrode active material layer 13 of the single-coated part 17. Therefore, the check of the penetration was stopped. As a possible cause of these disadvantages, when the positive electrode hoop material 11 was cut at the core exposed part 18 adjacent to the double-coated part 14, the single-coated part 17 was warped as shown in
For producing test batteries, the predetermined amount of the electrolyte was injected, evacuation was performed, and the atmospheric air was introduced for the penetration of the electrolyte into the electrode group. The battery of Example 1 showed reduction of the penetration time. Therefore, the electrolyte was less evaporated during the penetration, thereby improving the penetration, and significantly reducing the penetration time. As a result, the opening of the battery case can hermetically be sealed while reducing the amount of the electrolyte evaporated as much as possible. This indicates that the improvement in penetration or impregnation of the electrolyte was able to greatly reduce the loss of the electrolyte.
An electrode group 1 including the positive electrode 2 in which the grooves 10 were formed in the surface of the porous protective film 28 was placed in the battery case 7. Then, about 5 g of an electrolyte prepared by dissolving 1 M LiPF6, and 3 parts by weight of VC (vinylene carbonate) in a solution mixture of EC (ethylene carbonate), DMC (dimethyl carbonate), and MEC (methyl ethyl carbonate) was introduced in the battery case 7, and the battery case 7 was sealed, thereby producing a rectangular lithium battery having a nominal capacity of 2550 mAh, a nominal voltage of 3.7 V, a diameter of 18 mm, and a height of 65 mm.
As a result of a crush test, a nail penetration test, and an external short circuit test performed on the produced battery, the battery did not cause heat generation, and expansion. In an overcharge test, the battery did not cause leakage of the electrolyte, heat generation, and gas generation. Further, in a thermal test at 150° C., the battery did not cause expansion, heat generation, and gas generation. The results indicate that the porous protective film 28 made of alumina effectively functioned to prevent thermal runaway, although the grooves 10 are formed in the porous protective film 28.
A positive electrode for a battery of the present invention allows good impregnation with an electrolyte, has high productivity and reliability, and is able to reduce an internal short circuit. A rectangular nonaqueous secondary battery including an electrode group using the positive electrode is useful for, e.g., driving power supplies for mobile electronic devices and communication devices.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-005484 | Jan 2009 | JP | national |
| 2009-259088 | Nov 2009 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2009/006123 | 11/16/2009 | WO | 00 | 9/14/2010 |
