Patent Application
20210313574
The present invention relates to a negative electrode for a lithium ion secondary battery.
Conventionally, a negative electrode for a lithium ion secondary battery that uses a metal porous body having continuous pores as a current collector and having a mixture including a negative electrode active material filled in the continuous ventilation holes of the metal porous body, wherein the negative electrode active material is one selected from the group consisting of carbon, tin, silicon, and lithium titanate has been known (for example, refer to Patent Literature 1).
In the above negative electrode for the lithium ion secondary battery, the above mixture is filled in the continuous ventilation holes and wrapped in the metal skeleton, thus being hardly left off, and therefore the amount of a binder in the mixture can be reduced to relatively increase the content ratio of the negative electrode active material, allowing the high capacity of the lithium ion secondary battery to be achieved.
Patent Literature 1: Japanese Patent Laid-Open No. 2012-256584
However, in the negative electrode for the lithium ion secondary battery described in Patent Literature 1, a part of the above metal porous body may be exposed on the outer surface, and in this case, an internal short circuit of the lithium ion secondary battery easily occurs, leading a disadvantage that cell deterioration accelerates and charge-and-discharge cycle characteristics deteriorate.
In addition, using graphite as a negative electrode active material can increase the capacity, but Li precipitation (dendrite) easily occurs and an internal short circuit easily occurs, leading a disadvantage that the charge-and-discharge cycle characteristics deteriorate.
On the other hand, in order to suppress an internal short circuit, an oxide such as lithium titanate (LTO) is used as a negative electrode active material, leading to a disadvantage of reduction of the capacity.
The object of the present invention is to eliminate such inconvenience and to provide a negative electrode for a lithium ion secondary battery capable of obtaining a lithium ion secondary battery having a high capacity and excellent charge-and-discharge cycle characteristics.
In order to achieve such an object, a negative electrode for a lithium ion secondary battery of the present invention comprises: a current collector composed of a metal porous body having a three-dimensional network structure; and a negative electrode active material held on the current collector, and comprises an overcoat layer covering an outer surface of the current collector, and the overcoat layer comprises hard carbon.
According to the negative electrode for the lithium ion secondary battery of the present invention, the outer surface of the current collector is covered with the overcoat layer, and thereby the metal porous body is not exposed and an internal short circuit of the lithium ion secondary battery can be prevented.
In addition, graphite and the like used for the negative electrode active material has an Li precipitation area that is in a plateau form at a low potential in which Li easily precipitates, and hard carbon included in the overcoat layer has an Li precipitation area that is not in a plateau form at a low potential and thus can significantly suppress Li precipitation. As a result, the overcoat layer suppresses growth of dendrite due to Li precipitation and thus can prevent an internal short circuit of the lithium ion secondary battery.
Therefore, according to the negative electrode for the lithium ion secondary battery of the present invention, the lithium ion secondary battery having a high capacity and excellent charge-and-discharge cycle characteristics can be obtained by preventing an internal short circuit of the lithium ion secondary battery when a high-capacity active material such as graphite is also used as the negative electrode active material.
In the negative electrode for the lithium ion secondary battery of the present invention, the negative electrode active material is preferably at least one selected from the group consisting of artificial graphite, natural graphite, hard carbon, Si, and Si compounds. The negative electrode for the lithium ion secondary battery of the present invention certainly provides a high capacity of the lithium ion secondary battery by using any of the above negative electrode active materials, and can improve the durability of the charge-and-discharge cycle.
In addition, in the negative electrode for the lithium ion secondary battery of the present invention, the negative electrode active material is more preferably artificial graphite or natural graphite. The negative electrode for the lithium ion secondary battery of the present invention further certainly provides a high capacity of the lithium ion secondary battery by using any of artificial graphite or natural graphite as the negative electrode active material, and can further improve the durability of the charge-and-discharge cycle.
Hereinafter, embodiments of the present invention will be described in more detail with reference to the accompanying drawings.
As shown in
As the above metal porous body constituting the above current collector 3, those that can be suitably used are made of a conductive metal such as nickel, copper, stainless steel, or titanium, and have a porosity of 90 to 98%, a number of pores (cells) of 46 to 50/inch, a pore diameter of 0.4 to 0.6 mm, a specific surface area of 4500 to 5500 m2/m3, and a thickness of 0.8 to 1.2 mm. The above metal porous body is preferably made of copper.
The above metal porous body made of copper can be produced by applying carbon paint to a urethane foam with open cells to perform a conductive treatment, forming a predetermined amount of copper layer by electroplating, thermally decomposing and removing the urethane foam and carbon paint, and reducing the oxidized copper layer under hydrogen gas atmosphere. As the metal porous body produced in this manner, “Celmet” (registered trademark) of copper or nickel, manufactured by Sumitomo Electric Industries, Ltd. can be used.
Suitable examples of the above negative electrode active material 4 include a high-capacity negative electrode active material consisting of at least one selected from the group consisting of, for example, artificial graphite, natural graphite, hard carbon, Si, and Si compounds, and any of artificial graphite or natural graphite is particularly suitable.
The overcoat layer 5 comprises hard carbon and preferably has a thickness in the range of 3 to 70 μm per side, for example. When the thickness of the overcoat layer 5 is less than 3 μm, the content of hard carbon is low, and the effect may not be obtained. In addition, when the thickness of the overcoat layer 5 is more than 70 μm, the content of hard carbon becomes excessive, and the energy density of the lithium ion secondary battery decreases.
A method for producing the negative electrode for the lithium ion secondary battery of the present embodiment will be described.
When the negative electrode for the lithium ion secondary battery 1 of the present embodiment is produced, a slurry for the negative electrode active material is prepared by mixing the above negative electrode active material 4, at least one selected from the group consisting of carboxymethyl cellulose, styrene-butadiene rubber, sodium polyacrylate, and polyvinylidene fluoride as a binder, and carbon black as a conductive aid in a mass ratio of negative electrode active material:binder:conductive aid=80 to 99.5:0.5 to 20:0 to 10 so as to obtain a total amount of 100, and then by diluting with an organic solvent such as N-methylpyrrolidone or pure water.
The slurry for the overcoat layer is prepared by mixing hard carbon, at least one selected from the group consisting of carboxymethyl cellulose, styrene-butadiene rubber, sodium polyacrylate, and polyvinylidene fluoride as a binder, and carbon black as a conductive aid in a mass ratio of hard carbon:binder:conductive aid=80 to 99:05 to 19.5:0 to 0.5 so as to obtain a total amount of 100, and then by diluting with organic solvent such as N-methylpyrrolidone or pure water.
Subsequently, the above slurry for the negative electrode active material is applied to one side of the current collector 3 composed of the above metal porous body by, for example, extruding from a nozzle at a predetermined pressure. The solvent of the above slurry for the negative electrode active material is dried and removed, and then the above slurry for the negative electrode active material is similarly applied to the other side of the current collector 3 composed of the above metal porous body, and the solvent of the slurry for the negative electrode active material is dried and removed again.
The above slurry for the overcoat layer is applied to both sides of the above current collector 3 to which the above slurry for the negative electrode active material has been applied, in the same manner as the slurry for the above negative active material
The above current collector having the above slurry for the negative electrode active material and the above slurry for the overcoat layer applied thereto is dried in the atmosphere at a temperature in the range of 110 to 130° C. for 11 to 13 hours, and is roll-pressed so as to obtain a predetermined density of each stuffy. The negative electrode for the lithium ion secondary battery 1 of the present embodiment is obtained by drying in a vacuum at a temperature in the range of 110 to 130° C. for 11 to 13 hours.
A lithium ion secondary battery can be configured by sandwiching a separator between the negative electrode for the lithium ion secondary battery 1 of the present embodiment and a positive electrode in a container, impregnating with an electrolytic solution, and sealing the container.
The above positive electrode that can be used is, for example, one holding a positive electrode active material in the current collector composed of the metal porous body having the above three-dimensional network structure. In this case, the above metal porous body is preferably made of aluminum. The above metal porous body can be produced by applying carbon paint to an urethane foam with open cells to perform a conductive treatment, using a plating bath including 1-ethyl-3-methylimidazolium chloride and aluminum chloride (AlCl3) in a molar ratio of 33:67 and further including a small amount of phenanthroline to perform electroplating in an inert atmosphere to form a predetermined amount of aluminum layer, and thermally decomposing and removing the urethane foam and carbon paint under the condition where excessive oxidation of the aluminum surface is suppressed in an oxygen-containing atmosphere at a temperature in the range of 500 to 660° C. As the metal porous body produced in this manner, “Aluminum Celmet” (registered trademark), manufactured by Sumitomo Electric Industries, Ltd. can be used.
In addition, examples of the above positive electrode active material that can be used include at least one selected from the group consisting of, for example, Li(Ni1/3Co1/3Mn1/3)O2, Li(Ni1/6Co4/6Mn1/6)O2, Li(Ni5/10Co2/10Mn3/10)O2, Li(Ni6/10Co2/10Mn2/10)O2, Li(Ni8/10Co1/10Mn1/10)O2, and Li(Ni0.8Co0.15Al0.05)O2.
When the above positive electrode is produced, a slurry for the positive electrode active material is prepared by mixing the above positive electrode active material, polyvinylidene fluoride (PVDF) as a binder, and carbon black as a conductive aid in the mass ratio of positive electrode active material:binder:conductive aid=80 to 99:05 to 19.5:05 to 19.5 so as to obtain the total amount of 100, and then diluting with an organic solvent such as N-methylpyrrolidone.
The positive electrode is obtained in exactly the same manner as in the case of producing the above negative electrode, except that the above slurry for the positive electrode active material is used instead of the above slurry for the negative electrode active material and the above slurry for the overcoat layer is not used at all.
As the above separator, for example, a microporous polyethylene or polypropylene film can be used.
In addition, examples of the above electrolytic solution that can be used include those obtained by dissolving supporting salts such as LiPF6, LiBF4, LiClO4 at a concentration in the range of 0.1 to 3 mol/L, preferably in the range of 0.6 to 1.5 mol/L in a solvent such as ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, or ethyl methyl carbonate.
Example and Comparative Example of the present invention will be shown as follows.
In the present Example, a negative electrode was prepared as follows by using those made of copper and having a porosity of 95%, a number of pores (cells) of 46 to 50/inch, a pore diameter of 0.5 mm, a specific surface area of 5000 m2/m3, a thickness of 1.0 mm, a length of 150 mm, and a width of 200 mm (Celmet (registered trademark) manufactured by Sumitomo Electric Industries, Ltd.) as a current collector composed of a metal porous body having a three-dimensional network structure in which columnar skeletons are three-dimensionally connected (hereinafter abbreviated as “three-dimensional skeleton current collector”).
A slurry for the negative electrode active material was prepared by mixing natural graphite as a negative electrode active material, a mixture of carboxymethyl cellulose and styrene-butadiene rubber as a binder, and carbon black as a conductive aid in the mass ratio of negative electrode active material:binder:conductive aid=96.5:2.5:1, and then diluting with pure water.
The above slurry for the negative electrode active material was applied to an area of 80 mm in length and 150 mm in width at the center of one side of the above three-dimensional skeleton current collector, and dried in the atmosphere at a temperature of 100° C. for 30 minutes. The above slurry for the negative electrode active material was applied to an area corresponding to the area to which the above slurry for the negative electrode active material was applied on the other side of the above three-dimensional skeleton current collector, and further dried in the atmosphere at a temperature of 100° C. for 30 minutes.
Hard carbon and polyvinylidene fluoride as a binder was mixed in the mass ratio of hard carbon:binder=98:2, and then diluted with N-methylpyrrolidone to prepare a slurry for the overcoat layer.
The above slurry for the overcoat layer was applied to areas to which the above slurry for the negative electrode active material was applied in both sides of the above three-dimensional skeleton current collector having the above slurry for the negative electrode active material applied thereto.
The above three-dimensional skeleton current collector having the above slurry for the negative electrode active material and the above slurry for the overcoat layer applied thereto was dried in the atmosphere at a temperature of 120° C. for 12 hours, roll-pressed, and further dried in vacuum at a temperature of 120° C. for 12 hours.
The negative electrode was obtained by punching into a shape having: a coating area of 34 mm in length and 44 mm in width having the above slurry for the negative electrode active material and the above slurry for the overcoat layer applied thereto; and a tab of 15 mm in length and 30 mm in width not having the above slurry for the negative electrode active material and the above slurry for the overcoat layer applied thereto, in contact with the coating area. The above negative electrode comprises a 230 μm-thick negative electrode active material layer held on the above three-dimensional skeleton current collector, and each of 30 μm-thick overcoat layers formed on both sides thereof.
The positive electrode was prepared as follows by using those made of aluminum and having a porosity of 95%, a number of pores (cells) of 46 to 50/inch, a pore diameter of 0.5 mm, a specific surface area of 5000 m2/m3, a thickness of 1.0 mm, a length of 150 mm, and a width of 200 mm (Aluminum Celmet (registered trademark) manufactured by Sumitomo Electric Industries, Ltd.) as the above three-dimensional skeleton current collector.
The slurry for the positive electrode active material was prepared by mixing Li(Ni5/10Co2/10Mn3/10)O2 as a positive electrode active material, polyvinylidene fluoride as a binder, and carbon black as a conductive aid in the mass ratio of positive electrode active material:binder:conductive aid=94:2:4, and then by diluting with N-methylpyrrolidone.
The above slurry for the positive electrode active material was applied to an area of 80 mm in length and 150 mm in width at the center of one side of the above three-dimensional skeleton current collector, and dried in the atmosphere at a temperature of 100° C. for 30 minutes. The above slurry for the positive electrode active material was applied to an area corresponding to the area to which the above slurry for the positive electrode active material was applied on the other side of the above three-dimensional skeleton current collector, and further dried in the atmosphere at a temperature of 100° C. for 30 minutes.
The above three-dimensional skeleton current collector having the above slurry for the positive electrode active material applied thereto was dried in the atmosphere at a temperature of 120° C. for 12 hours, roll-pressed, and further dried in vacuum at a temperature of 120° C. for 12 hours.
The positive electrode was obtained by punching into a shape having: a coating area of 30 mm in length and 40 mm in width having the above slurry for the positive electrode active material applied thereto; and a tab of 15 mm in length and 30 mm in width not having the above slurry for the negative electrode active material and the above slurry for the overcoat layer applied thereto, in contact with the coating area. The above positive electrode comprises a 380-μm-thick positive electrode active material layer held on the above three-dimensional skeleton current collector.
In the pouch of aluminum laminate, the above positive electrode and the above negative electrode were provided such that the separator was sandwiched therebetween and the tab was exposed outside the pouch. A lithium ion secondary battery was produced by impregnating with an electrolytic solution and then vacuum-sealing.
As the above separator, a microporous polyethylene film having a thickness of 15 μm was used. In addition, as the above electrolytic solution, used were those obtained by dissolving LiPF6 as a supporting salt at a concentration of 1.2 mol/L in a mixed solvent that had been mixed with ethylene carbonate, dimethyl carbonate, and diethyl carbonate in a volume ratio of 40:30:30.
For the lithium ion secondary battery produced in the present Example, the temporary capacity of the positive electrode at a temperature of 25° C. was calculated from the amounts of the active materials of the positive electrode active material. Based on the above temporary capacity, a current value capable of discharging in 5 hours (0.2 C) was determined.
The lithium ion secondary battery produced in the present Example was subjected to constant current charging at 0.2 C to 4.2 V, constant voltage charging at 4.2 V for 1 hour, and then constant current discharging to 2.4 V at 0.2 C. While the capacity at the above constant current discharge was regarded as the rated capacity (mAh/g), an average voltage (V) was defined as a voltage when the capacity was ½ of the rated capacity in the charge-and-discharge curve during the constant current discharge, and the energy density (Wh/g) was calculated from the following equation (1).
Energy density (Wh/g)=Rated capacity (mAh/g)×Average voltage (V) (1)
The results are shown in
In order to obtain a capacity having a charging rate (SOC) of 50% with respect to the above rated current at a temperature of 25° C., charging was performed at 0.2 C for 2.5 hours, and the open circuit voltage (OCV) at this time was defined as E0.
Discharging was performed at a predetermined current value for 10 seconds while measuring the voltage, and then the discharge capacity was charged at 0.2 C, and such operation was repeated with changing the predetermined current value from 0.5 C to 3.0 C by 0.5 C. The current value was plotted on the horizontal axis and the voltage for each current value was plotted on the vertical axis, and the slope of the straight line obtained was the resistance R.
The cutoff voltage Ecutoff was set to 2.4 V, and the above resistance R and the above open circuit voltage E0 were used to calculate the output density (W) from the following equation (2).
W=(|Ecutoff−E0|/R)×Ecutoff (2)
The results are shown in
For the lithium ion secondary battery 1 produced in the present Example, the operation of constant current charging at 0.5 C to 4.2 V and constant current discharging to 2.4 V at 0.5 C at a temperature of −10° C. was regarded as one cycle, and the operation was repeated for 200 cycles.
In the discharge curve of the 200th cycle in the above operation, the differential value of the capacity with respect to the voltage, dQ/dV, was calculated, and the change of dQ/dV with respect to the voltage was determined. The results are shown in
In the present Comparative Example, a negative electrode for a lithium ion secondary battery was prepared in exactly the same manner as in the above Example except that the overcoat layer was not formed at all. In addition, the lithium ion secondary battery was prepared in exactly the same manner as in the above Example except that the negative electrode for the lithium ion secondary battery obtained in the present Comparative Example was used.
The energy density (Wh/g) and the output density (W) were calculated in exactly the same manner as in the above Example except that the lithium ion secondary battery obtained in the present Comparative Example was used, and the change in the capacity retention rate with respect to the number of cycles and the change in dQ/dV with respect to the voltage were determined.
The energy density (Wh/g) is shown in
According to the lithium ion secondary battery of the above Example, it is clear that the energy density (Wh/g) is improved from
In addition, according to the lithium ion secondary battery of the above Example, it is clear that the durability is improved from
In addition,
None
| Number | Date | Country | Kind |
|---|---|---|---|
| 2018-102180 | May 2018 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2019/018564 | 5/9/2019 | WO | 00 |
