Patent Application
20140045021
The present invention relates to a nonaqueous electrolyte secondary battery that allows a nonaqueous electrolyte having a high viscosity to easily penetrate the inside of an electrode assembly.
Alkaline secondary batteries typified by nickel-hydrogen batteries and nonaqueous electrolyte secondary batteries typified by lithium ion batteries have been widely used as a power supply for driving portable electronic equipment, such as cell phones including smartphones, portable personal computers, PDAs, and portable music players. In addition, alkaline secondary batteries and nonaqueous electrolyte secondary batteries have been widely used as a power supply for driving electric vehicles (EVs) and hybrid electric vehicles (HEVs and PHEVs), and in stationary storage battery systems for suppressing output fluctuation of solar power generation and wind power generation, for example, and for a peak shift of system power that utilizes the power during the daytime while saving the power during the nighttime.
The use of EVs, HEVs, and PHEVs or the stationary storage battery system especially requires high capacity and high output characteristics. The size of each battery is therefore increased, and a plurality of batteries are connected in series or in parallel for use. Therefore, nonaqueous electrolyte secondary batteries have been generally used for these purposes in view of space efficiency. When physical strength is needed, a metal prismatic outer can with one side open, and a metal sealing plate for sealing this opening are generally adopted as an outer can of a battery.
Increasing longevity is essential in nonaqueous electrolyte secondary batteries used for the above-mentioned purposes. Therefore, various additives are added to a nonaqueous electrolyte in order to prevent degradation. For example, JP-A-2009-129541 discloses that, in a nonaqueous electrolyte secondary battery, a cyclic phosphazene compound and various salts having an oxalate complex as an anion are added to a nonaqueous electrolyte. JP-T-2010-531856 and JP-A-2010-108624 describe the addition of lithium bis(oxalato)borate (Li[B(C2O4)2], hereinafter referred to as “LiBOB”), which is a lithium salt having an oxalate complex as an anion, as represented by the following structural formula (I).
For example, Japanese Patent No. 3439085 discloses the invention of a nonaqueous electrolyte secondary battery in which lithium difluorophosphate (LiPF2O2) is added to a nonaqueous electrolyte in order to prevent self-discharge at charge storage and improve storage characteristics after charging.
When a cyclic phosphazene compound and various salts having an oxalate complex as an anion disclosed in JP-A-2009-129541 are added to the nonaqueous electrolyte, fire resistance of the nonaqueous electrolyte is improved, which can provide a nonaqueous electrolyte secondary battery having excellent battery characteristics and high safety. When LiBOB disclosed in JP-T-2010-531856 and JP-A-2010-108624 is added to a nonaqueous electrolyte, a protective layer including a lithium ion conductive layer that is thin and extremely stable is formed on the surface of a carbon negative electrode active material of the nonaqueous electrolyte secondary battery. This protective layer is stable even in a high temperature, consequently preventing the carbon negative electrode active material from decomposing the nonaqueous electrolyte. This leads to an advantage of providing excellent cycling characteristics and improving the safety of a battery.
In the nonaqueous electrolyte secondary battery disclosed in Japanese Patent No. 3439085, LiPF2O2 and lithium are reacted to form a high-quality protective covering onto an interface of a positive electrode active material and a negative electrode active material. This protective covering prevents direct contact between an active material in a state of charge and an organic solvent, thereby preventing decomposition of the nonaqueous electrolyte due to contact between the active material and the nonaqueous electrolyte. Consequently, an advantageous function effect of improving charge storage characteristics can be attained.
In a nonaqueous electrolyte secondary battery using a nonaqueous electrolyte that contains a lithium salt having an oxalate complex as an anion or LiPF2O2 added in a nonaqueous solvent, the viscosity of the nonaqueous electrolyte is high and the wettability of an outer can and the nonaqueous electrolyte is also high. Therefore, a problem arises in that the nonaqueous electrolyte remains at the point where it contacts the outer can and is less likely to penetrate the inside of the electrode assembly.
An advantage of some aspects of the invention is to provide a nonaqueous electrolyte secondary battery which allows a nonaqueous electrolyte to easily penetrate the inside of an electrode assembly and the time to pore the nonaqueous electrolyte to be shorten even if the nonaqueous electrolyte that contains a lithium salt having an oxalate complex as an anion or LiPF2O2 added in the nonaqueous solvent is used as the nonaqueous electrolyte of the nonaqueous electrolyte secondary battery.
A nonaqueous electrolyte secondary battery of an aspect of the invention includes: a flat electrode assembly including a positive electrode, a negative electrode, and a separator interposed therebetween; an outer can storing the flat electrode assembly and a nonaqueous electrolyte; and a sealing plate sealing an opening portion of the outer can. The flat electrode assembly has a portion thereof other than the side facing the sealing plate, covered with an insulating sheet. The nonaqueous electrolyte contains at least one of a lithium salt having an oxalate complex as an anion and lithium difluorophosphate (LiPF2O2) at the time of making the nonaqueous electrolyte secondary battery. The wettability of the insulating sheet to the nonaqueous electrolyte is lower than that of the outer can to the nonaqueous electrolyte.
In the nonaqueous electrolyte secondary battery of the invention, the flat electrode assembly has a portion thereof other than the side facing the sealing plate, covered with the insulating sheet, and the wettability of this insulating sheet to the nonaqueous electrolyte is lower than that of the outer can to the nonaqueous electrolyte. Thus, the nonaqueous electrolyte can penetrate the inside of the electrode assembly more easily than the inside of an electrode assembly with no insulating sheet, even if the nonaqueous electrolyte contains at least one of the lithium salt having the oxalate complex as an anion and LiPF2O2. Therefore, the nonaqueous electrolyte secondary battery of the invention shortens the time to pour the nonaqueous electrolyte and improves manufacturing efficiency of a battery. The insulating sheet may have a box shape formed by bending one insulating sheet or a bag shape formed by folding one insulating sheet and bonding both lateral edges thereof.
A compound capable of reversibly absorbing and desorbing lithium ions may be selected to be used as appropriate as the positive electrode active material that can be used in the nonaqueous electrolyte secondary battery of the invention. Such electrode active materials include lithium transition-metal composite oxides that are represented by LiMO2 (M is at least one of Co, Ni, and Mn) and are capable of reversibly absorbing and desorbing lithium ions, namely, LiCoO2, LiNiO2, LiNiyCo1-yO2 (y=0.01 to 0.99), LiMnO2, LiCoxMnyNizO2 (x+y+z=1), LiMn2O4, or LiFePo4. Such lithium transition-metal composite oxides may be used alone, or two or more of them may be mixed to be used. Furthermore, lithium cobalt composite oxides with different metal element such as zirconium, magnesium, and aluminum added thereto may be used as well.
The following shows examples of a nonaqueous solvent that can be used for the nonaqueous electrolyte in the nonaqueous electrolyte secondary battery of the invention: a cyclic carbonate such as ethylene carbonate (EC), propylene carbonate (PC), and butylene carbonate (BC); a fluorinated cyclic carbonate; a cyclic carboxylic ester such as γ-butyrolactone (γ-BL) and γ-valerolactone (γ-VL); a chain carbonate such as dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), methylpropyl carbonate (MPC), and dibutyl carbonate (DBC); fluorinated chain carbonate; a chain carboxylic ester such as methyl pivalate, ethyl pivalate, methyl isobutyrate, and methyl propionate; an amide compound such as N,N′-dimethylformamide and N-methyl oxazolidinone; and a sulfur compound such as sulfolane. It is desirable that two or more of them be mixed to be used.
In the nonaqueous electrolyte secondary battery of the invention, the lithium salt that is commonly used as an electrolyte salt for an nonaqueous electrolyte secondary battery may be used as the electrolyte salt dissolved in the nonaqueous solvent. Examples of such a lithium salt are as follows: LiPF6, LiBF4, LiCF3SO3, LiN(CF3SO2)2, LiN(C2F5SO2)2, LiN(CF3SO2)(C4F9SO2), LiC(CF3SO2)3, LiC(C2F5SO2)3, LiAsF6, LiClO4, Li2B10Cl10, Li2B12Cl12, and mixtures of these substances. In particular, among them, it is preferable that LiPF6 (lithium hexafluorophosphate) be used. The amount of dissolution of the electrolyte salt with respect to the nonaqueous solvent is preferably from 0.8 to 1.5 mol/L.
In the nonaqueous electrolyte secondary battery of the invention, the lithium salt having the oxalate complex as an anion is preferably contained in the nonaqueous electrolyte in an amount of 0.01 to 2.0 mol/L, more preferably from 0.05 to 0.2 mol/L at the time of making the nonaqueous electrolyte secondary battery. Furthermore, in the nonaqueous electrolyte secondary battery of the invention, LiPF2O2 is preferably contained in the nonaqueous electrolyte in an amount of 0.01 to 2.0 mol/L, more preferably 0.01 to 0.1 mol/L at the time of making the nonaqueous electrolyte secondary battery. In the nonaqueous electrolyte secondary battery of the invention, the additive amount of the lithium salt having the oxalate complex as an anion or LiPF2O2 in the nonaqueous electrolyte may be added as the electrolyte salt whose principal element is the lithium salt having the oxalate complex as an anion or LiPF2O2. However, a large additive amount of the lithium salt having the oxalate complex as an anion or LiPF2O2 in the nonaqueous electrolyte increases the viscosity of the nonaqueous electrolyte. Therefore, various electrolyte salts as above may be used as principal elements, and the lithium salt having the oxalate complex as an anion or LiPF2O2 may be added as an additive substance in a small amount, for example, about 0.1 mol/L. When the lithium salt having the oxalate complex as an anion or LiPF2O2 is added as the additive substance, depending on the additive amount thereof, all of the lithium salt having the oxalate complex as an anion or LiPF2O2 is consumed for forming the protective covering on the positive electrode or negative electrode at the initial charge. This might lead to a case in which no lithium salt having the oxalate complex as an anion or LiPF2O2 is substantially in the nonaqueous electrolyte. The invention also includes this case. Thus, the invention includes any case in which the nonaqueous electrolyte of the nonaqueous electrolyte secondary battery before the initial charge contains the lithium salt having the oxalate complex as an anion or LiPF2O2.
In the nonaqueous electrolyte secondary battery of the invention, it is preferable that the outer can be made using aluminum or aluminum alloy and the insulating sheet be made using polyolefin.
Polyolefin has smaller wettability to a nonaqueous electrolyte than aluminum or aluminum alloy (has a larger contact angle). If the insulating sheet is formed using polyolefin and the outer can is formed using aluminum or aluminum alloy, the wettability of the insulating sheet to the nonaqueous electrolyte is smaller than that of the outer can to the nonaqueous electrolyte. This allows the above-mentioned effect to be successfully attained. The following may be adopted as the insulating sheet: an insulating sheet made using polypropylene, an insulating sheet made using polyethylene, an insulating sheet made using a mixture of polypropylene and polyethylene, or a multi-layer sheet of polypropylene and polyethylene.
In the nonaqueous electrolyte secondary battery of the invention, the flat electrode assembly preferably has the outermost side thereof covered with a separator.
Such a structure allows the nonaqueous electrolyte to easily penetrate between the separator on the outermost side and the insulating sheet on the further outer side, and further shortens the time to pore the nonaqueous electrolyte.
In the nonaqueous electrolyte secondary battery of the invention, the battery capacity is preferably 5 Ah or more, and can be 20 Ah or more.
When the battery capacity is high, the areas of the positive electrode and the negative electrode are large. The area in which the outer can and the flat electrode assembly facing each other is accordingly large, and the nonaqueous electrolyte is less likely to penetrate the inside of the electrode assembly. Even in such a case, the nonaqueous electrolyte secondary battery of the invention improves the penetration speed of the nonaqueous electrolyte into the electrode assembly, and provides the particularly excellent effect of adding the lithium salt having the oxalate complex as an anion or LiPF2O2 to the nonaqueous electrolyte.
In the nonaqueous electrolyte secondary battery of the invention, it is preferable that the positive electrode, the negative electrode, and the separator be each elongated, that the flat electrode assembly be formed by winding an elongated positive electrode and the elongated negative electrode with the elongated separator interposed therebetween, and that the winding numbers of the positive electrode and the negative electrode be each 20 or more. In such a case, the winding numbers of the positive electrode and the negative electrode may be each 40 or more.
Such a structure enables a prismatic nonaqueous electrolyte secondary battery with high capacity to be manufactured easily.
In the nonaqueous electrolyte secondary battery of the invention, the thickness of the insulating sheet is preferably from 0.1 to 0.5 mm.
The insulating sheet is used not only for improving the penetration properties of the nonaqueous electrolyte into the electrode assembly but also for ensuring the insulating properties between the flat electrode assembly and the outer can. When the thickness of this insulating sheet is from 0.1 to 0.5 mm, the insulating sheet has higher strength and ensures the insulating properties more reliably.
In the nonaqueous electrolyte secondary battery of the invention, it is preferable that the lithium salt having the oxalate complex as an anion be lithium bis(oxalato)borate (Li[B(C2O4)2], hereinafter referred to as “LiBOB”).
Using LiBOB as the lithium salt having the oxalate complex as an anion provides the nonaqueous electrolyte secondary battery capable of attaining further preferable cycling characteristics. LiBOB is preferably contained in an amount of 0.01 to 2.0 mol/L, more preferably 0.05 to 0.2 mol/L, at the time of making the nonaqueous electrolyte secondary battery.
In the prismatic nonaqueous electrolyte secondary battery of the invention, 90% or more of the inner surfaces of the outer can and the sealing plate preferably faces the insulating sheet.
When 90% or more of the inner surfaces of the outer can and the sealing plate faces the insulating sheet, the nonaqueous electrolyte is less likely to remain at the point where it contacts the inner surfaces of the outer can and the sealing plate, and is more likely to penetrate the inside of the electrode assembly.
In the nonaqueous electrolyte secondary battery of the invention, it is preferable that the flat electrode assembly include a wound positive electrode substrate exposed portion formed on one end thereof, that the flat electrode assembly include a wound negative electrode substrate exposed portion formed on the other end thereof, that the positive electrode substrate exposed portion and the negative electrode substrate exposed portion be each divided into two segments, that the two segments of the positive electrode substrate exposed portion be disposed so that a conductive member held in a resin member is arranged therebetween, and that the two segments of the negative electrode substrate exposed portion be disposed so that a conductive member held in a resin member is arranged therebetween.
Such a structure enables the two segments of the substrate exposed portion, the conductive member, and a collector to be connected at a time by the series resistance welding method. Moreover, it is preferable that the resistance welding be performed so as to form a weld mark passing through each stacked portion of the two segments of the substrate exposed portion. Therefore, less current is needed for the resistance welding, compared to the case where the resistance welding is performed so as to form a weld mark passing through the whole stacked portion of the non-divided positive electrode substrate exposed portion or negative electrode substrate exposed portion. In addition, a plurality of conductive members are held in a resin member. This allows the conductive members to be stably positioned and disposed between the two segments of the substrate exposed portion, and improves the quality of the resistance welded portion to achieve low resistance.
The invention will be described with reference to the accompanying drawings, wherein like numbers reference like elements.
An embodiment of the invention will be described below in detail with reference to the accompanying drawings. However, the embodiment described below is merely an illustrative example for understanding the technical spirit of the invention and is not intended to limit the invention to the embodiment. The invention may be equally applied to various modifications without departing from the technical spirit described in the claims A flat electrode assembly to be used in the invention may be applied to a flat electrode assembly that has a plurality of layers of a positive electrode substrate exposed portion formed on one end and a plurality of layers of a negative electrode substrate exposed portion formed on the other end by stacking or winding a positive electrode and a negative electrode with a separator interposed therebetween. The following will describe an example of a flat winding electrode assembly.
First, a prismatic nonaqueous electrolyte secondary battery in accordance with an embodiment will be described with reference to
As illustrated in
The width and length of a negative electrode active material mixture layer 12a of the negative electrode 12 are larger than those of a positive electrode active material mixture layer 11a. It is preferable that the positive electrode substrate be formed using foil of aluminum or aluminum alloy having a thickness of about from 10 to 20 μm, while the negative electrode substrate be formed using foil of copper or copper alloy having a thickness of about from 5 to 15 μm. A specific composition of the positive electrode active material mixture layer 11a and the negative electrode active material mixture layer 12a will be described later.
As shown in
The stacked layers of the positive electrode substrate exposed portion 15 are electrically connected to a positive electrode terminal 18 of aluminum material with a positive electrode collector 17 of aluminum material interposed therebetween. Likewise, the stacked layers of the negative electrode substrate exposed portion 16 are electrically connected to a negative electrode terminal 20 of copper material with a negative electrode collector 19 of copper material interposed therebetween. As shown in
As described above, the flat winding electrode assembly 14 is formed by attaching the positive electrode collector 17 and the negative electrode collector 19 to the positive electrode terminal 18 and the negative electrode terminal 20 that are provided to the sealing plate 23, respectively. As shown in
A current interruption mechanism 27 operated by a gas pressure generated inside the battery is provided between the positive electrode collector 17 and the positive electrode terminal 18. A gas exhaust valve 28 that is open when a gas pressure higher than the working pressure of the current interruption mechanism 27 is applied is also provided on the sealing plate 23. Therefore, the inside of the nonaqueous electrolyte secondary battery 10 is sealed. The nonaqueous electrolyte secondary battery 10 alone may be used, or a plurality of nonaqueous electrolyte secondary batteries 10 connected in series or in parallel may be used for various purposes. When a plurality of nonaqueous electrolyte secondary batteries 10 connected in series or in parallel are used, the external positive electrode terminal and the external negative electrode terminal may be provided separately to connect the respective batteries with a bus bar.
The flat winding electrode assembly 14 used in the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment is used when high capacity of 20 Ah or more and high output characteristics are required. For example, the winding number of the positive electrode 11 is 43, in other words, the total number of stacked layers of the positive electrode substrate exposed portion 15 is 86. When the winding number is 30 or more, in other words, the total number of stacked layers is 60 or more, the capacity of the battery can be 20 Ah or more without increasing the size of the battery beyond necessity.
When the total number of stacked layers of the positive electrode substrate exposed portion 15 or the negative electrode substrate exposed portion 16 is large, a large amount of welding current is needed to form a weld mark 15a or 16a passing through the whole stacked layer portions of the stacked positive electrode substrate exposed portion 15 or the negative electrode substrate exposed portion 16 in resistance-welding the positive electrode collector 17 and the negative electrode collector 19 to the positive electrode substrate exposed portion 15 and the negative electrode substrate exposed portion 16, respectively.
As shown in
When the positive electrode substrate exposed portion 15 or the negative electrode substrate exposed portion 16 is divided into two segments, welding current needed to form a weld mark 15a or 16a passing through the whole stacked layer portion of the stacked positive electrode substrate exposed portion 15 or the negative electrode substrate exposed portion 16 is small compared to a case in which there is no division. This prevents sputters during resistance welding, thereby preventing a trouble such as an internal short in the winding electrode assembly 14 due to the sputters. Thus, the resistance welding is performed between the positive electrode collector 17 and the positive electrode substrate exposed portion 15 and between the positive electrode substrate exposed portion 15 and the positive electrode conductive members 29. Resistance welding is also performed between the negative electrode collector 19 and the negative electrode substrate exposed portion 16 and between the negative electrode substrate exposed portion 16 and the negative electrode conductive members 31.
The resistance-welding methods with the positive electrode intermediate member 30 including the positive electrode substrate exposed portion 15, the positive electrode collector 17, and the positive electrode conductive members 29, and with the negative electrode intermediate member 32 including the negative electrode substrate exposed portion 16, the negative electrode collector 19, and the negative electrode conductive members 31 in the flat winding electrode assembly 14 of the embodiment will be described in detail below. In the embodiment, the shapes of the positive electrode conductive members 29 and the negative electrode conductive members 31 may be substantially the same, and the shapes of the positive electrode intermediate member 30 and the negative electrode intermediate member 32 may be substantially the same. The resistance-welding methods are substantially the same as well. Therefore, the positive electrode 11 will be described below as an example.
The positive electrode substrate exposed portion 15 of the flat winding electrode assembly 14 produced as above is divided into two segments from the winding central part to both sides and is collected centering on a quarter of the thickness of the electrode assembly. Subsequently, the positive electrode collector 17 is provided on both surfaces on the outermost periphery side of the positive electrode substrate exposed portion 15. On the inner periphery side of the positive electrode substrate exposed portion 15, the positive electrode intermediate member 30 including the positive electrode conductive members 29 is inserted between the two segments of the positive electrode substrate exposed portion 15 so that respective projections on both sides of the positive electrode conductive members 29 are brought into contact with the positive electrode substrate exposed portion 15. For example, the positive electrode collector 17 is made of an aluminum plate that has a thickness of 0.8 mm.
The positive electrode conductive members 29 held by the positive electrode intermediate member 30 of the embodiment have projections that have, for example, a shape of a circular truncated cone and are formed on two surfaces facing each other on the cylindrical main body. As long as the positive electrode conductive members 29 are made of metal and blockish, any shape such as a cylinder, a prism, and an elliptic cylinder may be adopted. Materials made of copper, copper alloy, aluminum, aluminum alloy, tungsten, molybdenum, etc., may be used as a formation material of the positive electrode conductive members 29. Among the materials made of these metals, the following configurations may be adopted: the projection on which nickel plate is applied; and the projection and its base area formed of metal material that facilitates heat generation such as tungsten and molybdenum and, for example, brazed to the main body of the cylindrical positive electrode conductive members 29 made of copper, copper alloy, aluminum or aluminum alloy.
A plurality of, for example, here two pieces of positive electrode conductive members 29 are integrally held by the positive electrode intermediate member 30 formed using a resin material. In such a case, the respective electrode conductive members 29 are held so as to be in parallel with each other. The positive electrode intermediate member 30 may have any shape such as a prism and cylinder. However, a landscape prism is desirable in order that the positive electrode intermediate member 30 is stably positioned and fixed between the two segments of the positive electrode substrate exposed portion 15. It is preferable that the corners of the positive electrode intermediate member 30 be chamfered in order not to hurt or deform the soft positive electrode substrate exposed portion 15 even if contacting the positive electrode substrate exposed portion 15. At least a part to be inserted between the two segments of the positive electrode substrate exposed portion 15 may be chamfered.
The length of the prismatic positive electrode intermediate member 30 varies depending on the size of the prismatic nonaqueous electrolyte secondary battery 10, but it may be from 20 mm to tens of mm. The width of the prismatic positive electrode intermediate member 30 may be as much as the height of the positive electrode conductive members 29, but at least both ends of the positive electrode conductive members 29 as welded portions may be exposed. It is preferable that both ends of the positive electrode conductive members 29 protrude from the surface of the positive electrode intermediate member 30, but the positive electrode conductive members 29 do not necessarily protrude. Such a structure enables the positive electrode conductive members 29 to be held in the positive electrode intermediate member 30, and the positive electrode intermediate member 30 to be stably positioned and disposed between the two segments of the positive electrode substrate exposed portion 15.
Subsequently, the flat winding electrode assembly 14, which includes the positive electrode collector 17 and the positive electrode intermediate member 30 holding the positive electrode conductive members 29 disposed therein, is arranged between a pair of resistance welding electrodes (not shown in the drawings). The pair of resistance welding electrodes are each brought into contact with the positive electrode collector 17 disposed on both surfaces of the outermost periphery side of the positive electrode substrate exposed portion 15. An appropriate pressure is then applied between the pair of resistance welding electrodes, thereby performing the resistance welding under predetermined certain conditions. In this resistance welding, the positive electrode intermediate member 30 is stably positioned and disposed between the two segments of the positive electrode substrate exposed portion 15, which improves the dimensional accuracy between the positive electrode conductive members 29 and the pair of resistance welding electrodes, enables the resistance welding to be performed in an accurate and stable state, and curbs variation in the welding strength.
Next, the detailed structure of the positive electrode collector 17 and the negative electrode collector 19 of the embodiment will be described with reference to
The positive electrode collector 17 is produced, for example, by punching out an aluminum plate in a particular shape and bending it. This positive electrode collector 17 has a rib 17a formed on a main body part where resistance welding is performed to a bundle of the positive electrode substrate exposed portion 15. The negative electrode collector 19 is produced, for example, by punching out a copper plate in a particular shape and bending it. This negative electrode collector 19 also has a rib 19a formed on the main body part where the resistance welding is performed to a bundle of the negative electrode substrate exposed portion 16.
The rib 17a of the positive electrode collector 17 and the rib 19a of the negative electrode collector 19 serve as a shield in order to prevent sputters generated during the resistance welding from entering the inside of the flat winding electrode assembly 14, and as a radiation fin in order to prevent a portion other than the resistance welded portion of the positive electrode collector 17 and the negative electrode collector 19 from being melted by heat generated during the resistance welding. The ribs 17a and 19a are provided at a right angle from the main body of the positive electrode collector 17 and the negative electrode collector 19, respectively, but the angle need not necessarily be vertical. Even a tilt of about ±10° from the right angle brings the same function effect.
In the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment, the example shows that two ribs are provided corresponding to the resistance welding position along the longitudinal direction as the rib 17a of the positive electrode collector 17 and the rib 19a of the negative electrode collector 19. However, the configuration is not limited to this case. One rib may be provided, or ribs may be formed on both sides in the width direction. When ribs are formed on both sides in the width direction, their heights may be either the same or different. If their heights are different, it is preferable that the rib around the flat winding electrode assembly 14 be provided at a higher position than the other.
Preparation of Positive Electrode
The following describes a specific composition of the positive electrode active material mixture layer 11a and the negative electrode active material mixture layer 12a and a specific composition of the nonaqueous electrolyte used in the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment. Lithium nickel cobalt manganese composite oxide represented by LiNi0.35Co0.35Mn0.30O2 was used as the positive electrode active material. This lithium nickel cobalt manganese composite oxide, carbon powder as a conductive agent, and polyvinylidene fluoride (PVdF) as a binding agent were weighed so that the mass ratio would be 88:9:3, and were mixed with N-methyl-2-pyrrolidone (NMP) as dispersion media to produce a positive electrode active material mixture slurry. This positive electrode active material mixture slurry was applied with a die coater onto both sides of the positive electrode substrate of aluminum foil whose thickness was, for example, 15 μm to form the positive electrode active material mixture layer onto both sides of the positive electrode substrate. Next, the resultant object was dried to remove NMP as an organic solvent, and was pressed with a roll press to have a particular thickness. The electrode thus obtained was slit in a particular width on one end of the electrode in the width direction along the whole longitudinal direction to form the positive electrode substrate exposed portion 15 that had no positive electrode active material mixture layer formed onto both sides, and whereby the positive electrode 11 of the structure shown in
Preparation of Negative Electrode
The negative electrode was produced as follows: 98 parts by mass of graphite powder, 1 part by mass of carboxymethylcellulose (CMC) as a thickening agent, and 1 part by mass of styrene-butadiene-rubber (SBR) as a binding agent were dispersed in water to produce a negative electrode active material mixture slurry. This negative electrode active material mixture slurry was applied with a die coater onto both sides of the negative electrode collector of copper foil whose thickness was 10 μm, and was dried to form the negative electrode active material mixture layer onto both sides of the negative electrode collector. Next, the resultant object was pressed with a press roller to have a particular thickness. The electrode thus obtained was slit in a particular width on one end of the electrode in the width direction along the whole longitudinal direction to form the negative electrode substrate exposed portion 16 that had no negative electrode active material mixture layer formed onto both sides, and whereby the negative electrode 12 of the structure shown in
Preparation of Nonaqueous Electrolyte
The nonaqueous electrolyte was produced as follows: as a solvent, ethylene carbonate (EC) and methyl ethyl carbonate (MEC) were mixed with a volume ratio (25° C. and 1 atmosphere) of 3:7; LiPF6 as an electrolyte salt was added to the mixed solvent so that the concentration would be 1 mol/L; and then LiBOB as a lithium salt having an oxalate complex as an anion and LiPF2O2 were further added so that the concentrations would be 0.1 mol/L and 0.05 mol/L, respectively. The added LiBOB is reacted on the surface of the negative electrode at the initial charge to form a protective covering. Therefore, in the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment, all LiBOB added to the nonaqueous electrolyte is not necessarily present in the form of LiBOB. Similarly, LiPF2O2 causes a protective covering to be formed on the surface of the positive electrode and the negative electrode at the initial charge and discharge. Therefore, in the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment, all LiPF2O2 added to the nonaqueous electrolyte is not necessarily present in the form of LiPF2O2.
Production of Prismatic Nonaqueous Electrolyte Secondary Battery
The negative electrode 12 and the positive electrode 11 produced as above were wound while being insulated from each other with the separator 13 interposed therebetween so as to dispose the negative electrode 12 onto the outermost periphery side. Subsequently, the resultant object was formed to be flat, and whereby the flat winding electrode assembly 14 was produced. The negative electrode 12 on the outermost side has the surface thereof covered with the separator 13. In the flat winding electrode assembly 14, the winding numbers of the positive electrode 11 and the negative electrode 12 were 43 and 44, respectively, in other words, the numbers of stacked layers of the positive electrode 11 and the negative electrode 12 were 86 and 88, respectively, and the design capacity was 20 Ah. Furthermore, the total numbers of stacked layers of the positive electrode substrate exposed portion 15 and the negative electrode substrate exposed portion 16 were 86 and 88, respectively. As shown in
As described above, the flat winding electrode assembly 14 was formed by attaching the positive electrode collector 17 and the negative electrode collector 19 to the positive electrode terminal 18 and the negative electrode terminal 20 that were provided to the sealing plate 23, respectively. As shown in
In the prismatic nonaqueous electrolyte secondary battery of the embodiment, the insulating sheet 24 is disposed on the inner surface of the outer can 25, which will improve the penetration speed of the nonaqueous electrolyte into the flat winding electrode assembly. Specifically, using an insulating sheet whose wettability is lower than the wettability between the outer can 25 and the nonaqueous electrolyte as the insulating sheet 24 will be effective in improving the penetration speed of the nonaqueous electrolyte into the electrode assembly.
In the prismatic nonaqueous electrolyte secondary battery 10 of the embodiment above, an example of adding LiBOB to the nonaqueous electrolyte as an additive is shown. However, in the present invention, as the lithium salt having an oxalate complex as an anion, lithium difluoro(oxalato)borate, lithium tris(oxalato)phosphate, lithium difluoro(bisoxalato)phosphate, and lithium terafluoro(oxalato)phosphate, for example, may be used.
The nonaqueous electrolyte secondary battery 10 of the embodiment shows an example in which the stacked layers of the positive electrode substrate exposed portion 15 and the stacked layers of the negative electrode substrate exposed portion 16 are divided into two segments to interpose therebetween the positive electrode intermediate member 30 including the positive electrode conductive member 29 and the negative electrode intermediate member 32 including the negative electrode conductive member 31, respectively. However, in the invention, it is not necessary to divide the stacked layers of the positive electrode substrate exposed portion 15 or the stacked layers of the negative electrode substrate exposed portion 16 into two segments.
A prismatic nonaqueous electrolyte secondary battery 10A in accordance with a modification will be described with reference to
In the flat winding electrode assembly 14 used in the prismatic nonaqueous electrolyte secondary battery 10A of the modification, the amounts per unit area of a positive electrode active material mixture layer 11a of the positive electrode 11 and a negative electrode active material mixture layer 12a of the negative electrode 12 are larger than those in the embodiment. The winding number of the positive electrode 11 and the negative electrode 12 are 35 and 36, respectively. In other words, the total numbers of stacking layers of the positive electrode 11 and the negative electrode 12 are 70 and 72, respectively. The design capacity is 25 Ah. Furthermore, the total numbers of stacking layers of the positive electrode substrate exposed portion 15 and the negative electrode substrate exposed portion 16 are 70 and 72, respectively. On the positive electrode 11 side, the positive electrode collector 17 is disposed on the surfaces of both sides of the outermost side of the stacked layers of the positive electrode substrate exposed portion 15. On the negative electrode 12 side, the negative electrode collector 19 is disposed on the surfaces of both sides of the outermost side of the stacked layers of the negative electrode substrate exposed portion 16. The resistance welding is performed at two points so that weld marks (not shown in the drawings) are formed so as to pass through the whole bundled layer portions of the stacked positive electrode substrate exposed portion 15 or the stacked negative electrode substrate exposed portion 16.
In the flat winding electrode assembly 14 used in the prismatic nonaqueous electrolyte secondary battery 10A of the modification, the rib 17a formed onto the positive electrode collector 17 and the rib 19a formed onto the negative electrode collector 19 are formed across the two resistance welding points.
In the prismatic nonaqueous electrolyte secondary batteries 10 and 10A of the embodiment and the modification, a lithium salt having an oxalate complex as an anion, such as LiBOB, and LiPF2O2 are added to the nonaqueous electrolyte. An advantageous function effect of the invention can be attained with applications involving a nonaqueous electrolyte having a high viscosity. Only the lithium salt having the oxalate complex as an anion or only LiPF2O2 included increases the viscosity of the nonaqueous electrolyte. Thus, the invention is applicable to these cases as well.
The function effect of increasing the penetration speed of the nonaqueous electrolyte with high viscosity into the electrode assembly by using the insulating sheet of the invention will be successfully attained when it is applied to the case where the nonaqueous electrolyte is less likely to penetrate the inside of electrode assembly. Thus, the function effect of the invention will be successfully attained in the prismatic nonaqueous electrolyte secondary battery in which the positive electrode and the negative electrode on the outermost side each have a large area, in other words, in the prismatic nonaqueous electrolyte secondary battery with high capacity. Therefore, it is preferable that the winding numbers of the positive electrode and the negative electrode be each at least 20 or more, and the battery capacity be 5 Ah or more. More preferably, the winding numbers of the positive electrode and the negative electrode are each 40 or more, and the battery capacity is 20 Ah or more. In this case, the difference in the penetration effect of the nonaqueous electrolyte with high viscosity can be clearly observed between in the case of having the insulating sheet and in the case of not having the insulating sheet.
The prismatic nonaqueous electrolyte secondary batteries of the embodiment and the modification show an example of connecting between the positive electrode substrate exposed portion 15 and the positive electrode collector 17 and between the negative electrode substrate exposed portion 16 and the negative electrode collector 19 by resistance-welding, but the connection can be made by ultrasonic welding or irradiation of high-energy rays such as a laser. Furthermore, different connections may be made on the positive electrode side and the negative electrode side.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012-177279 | Aug 2012 | JP | national |
