Patent Application
20140045043
The present invention relates to a nonaqueous electrolyte secondary battery.
In recent years, there have been various endeavors to use nonaqueous electrolyte secondary batteries in, for example, electric vehicles, hybrid cars, and the like. As set forth in, for example, JP-A-2012-048959, high output characteristics are required of such nonaqueous electrolyte secondary batteries.
The inventors of the present invention have discovered, as a result of diligent researches, that the problem that the output characteristics decline at low temperatures occurs in a nonaqueous electrolyte secondary battery including a negative electrode provided on the outer periphery side and having a high capacity of not less than 21 Ah.
An advantage of some aspects of the invention is to provide a nonaqueous electrolyte secondary battery that has improved low-temperature output characteristics.
A nonaqueous electrolyte secondary battery of the invention includes an electrode assembly and a nonaqueous electrolyte. The electrode assembly includes a positive electrode, a negative electrode, and a separator. The negative electrode is opposed to the positive electrode. The separator is disposed between the positive electrode and the negative electrode. The capacity of the battery is not less than 21 Ah. The negative electrode is provided on the outer periphery side of the electrode assembly. The nonaqueous electrolyte contains lithium difluorophosphate.
The invention enables provision of a nonaqueous electrolyte secondary battery that has improved low-temperature output characteristics.
The invention will be described with reference to the accompanying drawings, wherein like numbers reference like elements.
A preferred embodiment that implements the invention will now be described with reference to the accompanying drawings. However, the following embodiment is merely an illustrative example and does not limit the invention in any way.
In the accompanying drawings, to which reference will be made in describing the embodiment and other matters, members that have substantially the same functions are assigned the same reference numerals throughout. In addition, the accompanying drawings, to which reference will be made in describing the embodiment and other matters, are schematic representations, and the proportions of the dimensions of the objects depicted in the drawings may differ from the proportions of the dimensions of the actual objects. The proportions of the dimensions of the objects may differ among the drawings. The concrete proportions of the dimensions of the objects should be determined in view of the following description.
A nonaqueous electrolyte secondary battery 1 shown in
The “battery capacity” in this case means the capacity of the battery when the battery has been charged at a constant current of 1 It to a voltage of 4.1 V, then charged for 1.5 hours at a constant voltage of 4.1V, and then discharged at a constant current of 1 It to a voltage of 2.5 V.
The nonaqueous electrolyte secondary battery 1 includes a container 10 shown in
The container 10 has a container body 11 and a sealing plate 12. The container body 11 is provided in the form of a rectangular tube of which one end is closed. In other words, the container body 11 is provided in the form of a bottomed square tube. The container body 11 has an opening. This opening is sealed up by the sealing plate 12. Thereby, the interior space approximately parallelepiped is formed into a compartment. The electrode assembly 20 and the nonaqueous electrolyte are housed in this interior space.
A positive electrode terminal 13 and a negative electrode terminal 14 are connected to the sealing plate 12. The positive electrode terminal 13 and the negative electrode terminal 14 are each electrically insulated from the sealing plate 12 by insulating material not shown in the drawings.
As shown in
The ratio of the height dimension H of the container 10 viewed from the front to its length dimension L (height dimension H/length dimension L) will preferably be not more than 0.8; more preferably it will be not less than 0.5 and not more than 0.8, and still more preferably not less than 0.6 and not more than 0.7.
The length dimension L of the container 10 will preferably be 90 to 180 mm, and more preferably will be 110 to 160 mm. The height dimension H of the container 10 will preferably be 70 to 120 mm, and more preferably will 80 to 100 mm. The thickness dimension T of the container 10 will preferably be 10 to 30 mm, and more preferably will be 12 to 28 mm.
As shown in
The positive electrode 21 includes the positive electrode substrate 21a and a positive electrode active material layer 21b. The positive electrode substrate 21a can be formed of aluminum, an aluminum alloy, or other materials. The positive electrode active material layer 21b is provided on at least one surface of the positive electrode substrate 21a. The positive electrode active material layer 21b will preferably contain particles of a lithium transition metal compound as positive electrode active material.
An example of the lithium transition metal compound that will preferably be used is a lithium oxide, for example, that contains at least one of the transition metals cobalt, nickel, and manganese. The following can be cited as specific examples of lithium oxides that contain at least one of the transition metals cobalt, nickel, and manganese: LiCoO2, LiNiO2, LiNiyCo1-yO2 (y=0.01 to 0.99), LiMnO2, LiMn2O4, and LiNixCoyMnzO2 (x+y+z=1). Of these, LiNixCoyMnzO2 (x+y+z=1) will preferably be used as the positive electrode active material. The positive electrode active material layer 21b may contain other components such as conductive material and binder as appropriate in addition to the positive electrode active material.
The negative electrode 22 includes the negative electrode substrate 22a and a negative electrode active material layer 22b. The negative electrode substrate 22a can be formed of copper, a copper alloy, or other materials. The negative electrode active material layer 22b is provided on at least one surface of the negative electrode substrate 22a. The negative electrode substrate 22a contains negative electrode active material. There is no particular limitation on the negative electrode active material, provided that it is able to reversibly absorb and desorb lithium. Examples of the negative electrode active material that will preferably be used are: carbon material, material that alloys with lithium, and metal oxide such as tin oxide. The following specific examples of carbon material can be cited: natural graphite, artificial graphite, mesophase pitch-based carbon fiber (MCF), mesocarbon microbeads (MCMB), coke, hard carbon, fullerene, and carbon nanotubes. Examples of material that can alloy with lithium are: one or more metals selected from the group consisting of silicon, germanium, tin, and aluminum, or an alloy containing one or more metals selected from the group consisting of silicon, germanium, tin, and aluminum. Of these, natural graphite will preferably be used as the negative electrode active material. The negative electrode active material layer 22b may contain other components such as conductive material and binder as appropriate in addition to the negative electrode active material.
The separator can be formed of a porous sheet of plastic such as polyethylene and polypropylene.
The electrode assembly 20 is housed inside the container 10. The nonaqueous electrolyte is also housed inside the container 10. The nonaqueous electrolyte contains lithium difluorophosphate (LiPO2F2) as solute.
In addition to lithium difluorophosphate, the nonaqueous electrolyte may contain as solute a substance such as: LiXFy (where X is P, As, Sb, B, Bi, Al, Ga, or In, and y is 6 when X is P, As, or Sb, and y is 4 when X is B, Bi, Al, Ga, or In); lithium perfluoroalkyl sulfonic acid imide LiN(CmF2m+1SO2)(CnF2n+1SO2) (where m and n are independently integers from 1 to 4); lithium perfluoroalkyl sulfonic acid methide LiC(CpF2p+1SO2)(CqF2q+1SO2)(CrF2r+1SO2) (where p, q, and r are independently integers from 1 to 4); LiCF3SO3; LiClO4; Li2B10Cl10; and Li2B12Cl12. Of these, the nonaqueous electrolyte may contain, as solute, at least one of LiPF6, LiBF4, LiN(CF3SO2)2, LiN(C2F5SO2)2, LiN(CF3SO2)(C4F9SO2), LiC(CF3SO2)3, LiC(C2F5SO2)3, and lithium bis(oxalato)borate (LiBOB), for example.
The nonaqueous electrolyte may contain as solvent, for example, cyclic carbonate, chain carbonate, or a mixture of cyclic carbonate and chain carbonate. Specific examples of cyclic carbonate are ethylene carbonate, propylene carbonate, butylene carbonate, and vinylene carbonate. Specific examples of chain carbonate are dimethyl carbonate, methylethyl carbonate, and diethyl carbonate.
Nonaqueous electrolyte secondary batteries that are used for electric vehicles, hybrid vehicles, and the like are required to have high output characteristics at low temperatures since they are used in cold regions as well as other regions.
However, as mentioned above, the inventors have discovered by diligent research that, for example, the low-temperature output characteristics decline in a nonaqueous electrolyte secondary battery including a negative electrode provided on the outer periphery side and having a high battery capacity of not less than 21 Ah when charge-discharge cycling is carried out repeatedly in low-temperature environments.
As a result of further diligent research, the inventors have discovered that in a nonaqueous electrolyte secondary battery including a negative electrode provided on the outer periphery side and having a high battery capacity of not less than 21 Ah, the low-temperature output characteristics are improved by configuring the nonaqueous electrolyte to contain lithium difluorophosphate.
To further improve the low-temperature output characteristics of the nonaqueous electrolyte secondary battery 1, the content of the lithium difluorophosphate in the nonaqueous electrolyte will preferably be not less than 0.01 mol/L, and more preferably will be not less than 0.02 mol/L. The content of the lithium difluorophosphate in the nonaqueous electrolyte is usually not more than 0.05 mol/L.
To further improve the low-temperature output characteristics of the nonaqueous electrolyte secondary battery 1, the nonaqueous electrolyte will preferably contain lithium bis(oxalato)borate (LiBOB).
The content of LiBOB will preferably be not less than 0.05 mol/L and not more than 2 mol/L, and will more preferably be not less than 0.08 mol/L and not more than 1 mol/L.
It will suffice for LiBOB to be present in the electrolyte immediately after the nonaqueous electrolyte secondary battery has been assembled. For example, after charge-discharge has been performed following assembly, the LiBOB may in some cases be present in the form of LiBOB alterations. In other cases, at least a part of the LiBOB or the LiBOB alterations may be present on the negative electrode active material layer. Such cases are included in the technical scope of this invention.
The invention will now be described in further detail on the basis of concrete examples. However, the invention is by no means limited to the following examples, and can be implemented in numerous appropriately varied forms without departing from the spirit and scope of the claims.
Positive electrode active material with the composition formula LiNi0.35Co0.35Mn0.30O2 was prepared using the following procedure.
An aqueous solution was prepared by mixing and dissolving particular amounts of nickel sulphate, cobalt sulphate, and manganese sulphate in water. Next, aqueous sodium hydroxide was added while stirring to obtain precipitates of nickel, cobalt, and manganese. The precipitates thus obtained were rinsed and filtered, then subjected to thermal treatment. After that, they were mixed with a particular amount of lithium carbonate, and then baked at 900° C. for 20 hours in an air atmosphere. The resultant substance was crushed and graded to fabricate the positive electrode active material.
The positive electrode active material obtained in the foregoing manner was mixed and kneaded with carbon black serving as conductive agent, and a solution of polyvinylidene fluoride serving as binding agent dispersed in N-methyl pyrrolidone (NMP) so that the solid content mass ratio of the positive electrode active material, carbon black, and polyfluoride vinylidene was 91:6:3, thereby preparing a positive electrode active material slurry.
This positive electrode active material slurry was applied to both surfaces of aluminum alloy foil (thickness 15 μm) serving as the positive electrode substrate, and then dried to remove the NMP used as solvent during the slurry preparation, thereby forming a positive electrode active material layer on the positive electrode substrate. However, no slurry was applied at one end along the longitudinal direction of the positive electrode substrate (same-direction end on both surfaces), and thus the substrate there was left exposed, thereby forming a positive electrode substrate exposed portion. The resultant substance was rolled and then cut into particular dimensions to fabricate the positive electrode.
Negative electrode active material containing graphite were mixed with binding agent containing styrene butadiene rubber and thickening agent containing carboxymethyl cellulose in the mass ratio of 98:1:1, then further mixed with water to prepare a negative electrode active material slurry.
This negative electrode slurry was applied to both surfaces of copper foil (thickness 10 μm) serving as the negative electrode substrate, and then dried to remove the water used as solvent during the slurry preparation, thereby forming a negative electrode active material layer on the negative electrode substrate. However, no slurry was applied at one end along the longitudinal direction of the negative electrode substrate (same-direction end on both surfaces), and thus the substrate there was left exposed, thereby forming a negative electrode substrate exposed portion. The resultant substance was rolled and then cut into particular dimensions to fabricate the negative electrode.
The foregoing positive electrode and negative electrode, and a separator formed of microporous polyethylene membrane were positioned so that a plurality of layers of the substrate exposed portion of the same polarity were overlapped with each other, the substrate exposed portions of the positive electrode and of the negative electrode protruded in opposite directions relative to the winding direction, and moreover the separator was interposed between the positive electrode active material layer and the negative electrode active material layer. Following that, the three members were stacked over each other and wound. An insulative winding fastening tape was then provided, after which the resultant item was pressed to form a flat wound electrode assembly.
Next, an aluminum positive electrode collector and a copper negative electrode collector were connected by laser welding to the positive electrode substrate gathering area where the layers of the positive electrode substrate exposed portion were stacked over each other and to the negative electrode substrate gathering area where the layers of the negative electrode substrate exposed portion were stacked over each other, respectively. Furthermore, the electrode assembly was wound so that the negative electrode was provided on the outermost periphery side.
The nonaqueous electrolyte was prepared by mixing ethylene carbonate and methylene carbonate in a volume ratio of 3:7, then adding LiPF6 to form a concentration of 1 mol/L, vinylene carbonate to form 0.3% by volume, LiPO2F2 to form 0.05 mol/L, and LiBOB to form 0.1 mol/L.
(5) Assembly of the Battery
The foregoing electrode assembly was inserted into a prismatic outer can, after which the positive and negative electrode collectors were connected to respective electrode external terminals provided on the sealing plate. The foregoing nonaqueous electrolyte was then poured in, and the mouth portion of the outer can was sealed, thereby completing the fabrication of the nonaqueous electrolyte secondary battery of Example 1.
Evaluation of Low-Temperature Output Characteristics
For evaluation of the output characteristics during low-temperature output, the battery was left for three hours in a room temperature of −30° C.; the battery was then charged with a charge current of 5 A to a state of charge 50%; in this state, discharge was performed for 10 seconds with each current of 8 A, 16 A, 24 A, 32 A, and 40 A; the battery voltage in each case was measured; each of the current levels and battery voltages were plotted in a graph; and the output characteristics were then determined by calculation from the I-V characteristics at the time of discharge. Any charge level that had deviated due to discharging was returned to the original charge level by charging with a constant current of 25 A.
In the fabrication of the positive electrode, an evaluation was made of how many positive electrodes could be fabricated relative to an identical number (m) of positive electrode substrates. The start-up adjustment and yield rate were assumed to be equivalent in both continuous coating and intermittent coating. Taking the number of batteries fabricatable with continuous coating as 100%, the number of batteries fabricatable with intermittent coating will be 92% because the positive electrode plate will be longer. In addition, with intermittent coating, there are in actuality many changing points during production, and therefore it is difficult to obtain a yield rate on a par with continuous coating. With intermittent coating, it is also difficult to raise the production speed.
In Example 1 and Comparative Example 2, the negative electrode constitutes the outermost periphery of the electrode assembly, and so continuous coating is possible, without the need to provide a blank for the positive electrode substrate in the positive electrode. In addition, in Comparative Examples 1 and 3, the positive electrode constitutes the outermost periphery of the electrode assembly, and so it is necessary to perform intermittent coating to form the positive electrode.
The nonaqueous electrolyte secondary battery obtained in Example 1 was evaluated on the low-temperature output characteristics and production efficiency.
In Example 1, the negative electrode constituted the outermost periphery of the electrode assembly, and so the positive electrode active material was prepared using continuous coating, without the need to provide a blank when the positive electrode active material layer was applied to the positive electrode substrate. The results thereof are set forth in Table 1.
A nonaqueous electrolyte secondary battery was fabricated in the same manner as for Example 1 except that the electrode assembly was fabricated by winding so that the positive electrode is provided on the outer periphery side and that LiPO2F2 was not added, and its low-temperature output characteristics and production efficiency were evaluated. In Comparative Example 1, the positive electrode constituted the outermost periphery of the electrode assembly, and so it was necessary to perform intermittent coating of the positive electrode active material onto the positive electrode substrate. The results of this evaluation are set forth in Table 1.
A nonaqueous electrolyte secondary battery was fabricated in the same manner as for Example 1 except that LiPO2F2 was not added, and its low-temperature output characteristics and production efficiency were evaluated. The results are set forth in Table 1. In Comparative Example 2, the negative electrode constituted the outermost periphery of the electrode assembly, and so the positive electrode active material was fabricated using continuous coating, without the need to provide a blank during coating of the positive electrode active material layer onto the positive electrode substrate. The results of this evaluation are set forth in Table 1.
A nonaqueous electrolyte secondary battery was fabricated in the same manner as for Example 1 except that the electrode assembly was fabricated by winding so that the positive electrode was provided on the outer periphery side, and its low-temperature output characteristics and production efficiency were evaluated. In Comparative Example 3, the positive electrode constituted the outermost periphery of the electrode assembly, and so it was necessary to perform intermittent coating of the positive electrode active material onto the positive electrode substrate. The results of this evaluation are set forth in Table 1.
The values for low-temperature output are values relative to the low-temperature output characteristic value for Comparative Example 1, which is taken as 100.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012-176786 | Aug 2012 | JP | national |
