Patent Application
20170358792
The invention relates to a method of manufacturing a nonaqueous electrolyte secondary battery and a nonaqueous electrolyte secondary battery.
Japanese Patent Application Publication No. 2007-250424 (JP 2007-250424 A) discloses a nonaqueous electrolyte secondary battery in which an electrolyte contains a sugar alcohol fatty acid ester compound in an amount of 1 wt % to a saturated solubility.
In JP 2007-250424 A, the sugar alcohol fatty acid ester compound is added to a liquid electrolyte, that is, an electrolytic solution. According to this configuration, when a battery is overcharged, lithium (Li) metal deposited on a negative electrode reacts with the sugar alcohol fatty acid ester compound, and thus lithium metal can be inactivated. As a result, the improvement of safety during overcharge can be expected. However, according to this configuration, battery resistance increases.
According to the invention, an increase in battery resistance can be suppressed while improving safety during overcharge.
According to a first aspect of the invention, there is provided a method of manufacturing a nonaqueous electrolyte secondary battery, the method including: a kneading step of kneading a carbon-based negative electrode active material, a binder, and a sugar alcohol with each other to form a negative electrode mixture paste; and an application step of applying the negative electrode mixture paste to a negative electrode current collector to form a negative electrode mixture layer.
When a sugar alcohol fatty acid ester compound is added to an electrolytic solution as in the case of the related art, an increase in battery resistance is expected due to the following reasons. The electrolytic solution permeates not only into a negative electrode mixture layer but also into a positive electrode mixture layer. Accordingly, the sugar alcohol fatty acid ester compound also permeates into the positive electrode mixture layer. The sugar alcohol fatty acid ester compound cannot withstand a positive electrode potential and is decomposed to form a resistance film. As a result, the battery resistance increases. In addition, the amount of a sugar alcohol supplied to the negative electrode mixture layer also decreases.
The permeation of the electrolytic solution into the negative electrode mixture layer is not likely to be uniform. That is, the distribution of the sugar alcohol fatty acid ester compound in the negative electrode mixture layer is not likely to be uniform. Therefore, it is presumed that, in a portion of the negative electrode mixture layer where the abundance of the sugar alcohol in the negative electrode mixture layer is small, the inactivation of lithium metal is insufficient. In particular, during high-rate (high-current) overcharge, the amount of lithium metal deposited increases, the effect thereof is a concern.
On the other hand, in the above-described method, due to the following reasons, an increase in battery resistance can be suppressed while improving safety during overcharge. In the above-described method, the sugar alcohol itself is used instead of the sugar alcohol fatty acid ester compound. The sugar alcohol is kneaded with the carbon-based negative electrode active material to form the negative electrode mixture paste. Using the negative electrode mixture paste, the negative electrode mixture layer containing the sugar alcohol is formed. As a result, in the negative electrode mixture layer, the sugar alcohol can be uniformly distributed. Moreover, the sugar alcohol has high affinity to the carbon-based negative electrode active material. Therefore, the elution of the sugar alcohol from the negative electrode mixture layer is suppressed. Furthermore, in order for the sugar alcohol to permeate into the positive electrode mixture layer, it is necessary that the sugar alcohol move to the positive electrode mixture layer side after being dissolved in the electrolytic solution. Therefore, an increase in resistance caused by the permeation of the sugar alcohol into the positive electrode mixture layer can be suppressed.
The sugar alcohol may be at least one selected from the group consisting of mannitol, xylitol, sorbitol, and maltitol. The reason for this is that the improvement of safety during overcharge can be expected from the above sugar alcohols.
A mixing amount of the sugar alcohol is 0.1 parts by mass to 7.0 parts by mass with respect to 100 parts by mass of the carbon-based negative electrode active material. The reason for this is that, with the above-described range, the improvement of safety during overcharge can be expected.
The kneading step may include: a first kneading step of kneading the binder, the sugar alcohol, a thickener, and a solvent with each other to obtain a first mixture; a second kneading step of kneading the first mixture and the carbon-based negative electrode active material with each other to obtain a second mixture; and a dilution-dispersion step of adding the solvent to the second mixture and kneading the solvent and the second mixture with each other to obtain the negative electrode mixture paste. With the above-described configuration, the uniformity of the sugar alcohol distribution in the negative electrode mixture layer may be improved.
According to a second aspect of the invention, there is provided a nonaqueous electrolyte secondary battery including: a negative electrode current collector; and a negative electrode mixture layer that is formed on the negative electrode current collector. The negative electrode mixture layer contains a carbon-based negative electrode active material, a binder, and a sugar alcohol. When a section of the negative electrode mixture layer in a thickness direction is divided into six measurement regions by trisecting the negative electrode mixture layer in a width direction and further bisecting the negative electrode mixture layer in the thickness direction, all the measurement regions satisfy the following expression (I).
0.8<Mi/Mave<1.2 (I)
In the expression (I), i represents an integer of 1 to 6, Mi represents an NMR signal intensity of the sugar alcohol in each of the measurement regions, and Mave represents an average value of M1, M2, M3, M4, M5, and M6.
As described above, by controlling the distribution of the sugar alcohol in the negative electrode mixture layer, the safety during overcharge can be improved.
The average value (Mave) may be 10 to 700. As a result, the improvement of safety during overcharge can be expected.
According to the above-described aspects, an increase in battery resistance can be suppressed while improving safety during overcharge.
Features, advantages, and technical and industrial significance of exemplary embodiments of the invention will be described below with reference to the accompanying drawings, in which like numerals denote like elements, and wherein:
Hereinafter, an embodiment of the invention (hereinafter, referred to as “the embodiment”) will be described in detail. However, the embodiment is not limited to the following description.
[Method of Manufacturing Nonaqueous Electrolyte Secondary Battery]
[Negative Electrode Preparation Step (S100)]
The negative electrode preparation step includes: a kneading step of kneading a carbon-based negative electrode active material (hereinafter, also referred to simply as “negative electrode active material”), a binder, and a sugar alcohol with each other to form a negative electrode mixture paste; and an application step of applying the negative electrode mixture paste to a negative electrode current collector to form a negative electrode mixture layer.
[Preparation Step (S101)]
In the preparation step (S101), the respective materials including the sugar alcohol, the negative electrode active material, the thickener, and the binder are prepared.
[Sugar Alcohol]
The sugar alcohol is a polyol which is produced by an aldehyde group of sugar being reduced. The sugar alcohol is in the form of a powder or a solution. The sugar alcohol may be, for example, mannitol, xylitol, sorbitol, maltitol, lactitol, or oligosaccharide alcohol. In particular, when mannitol, xylitol, sorbitol, or maltitol is used, the improvement of safety during overcharge can be expected. Among these, one kind may be used alone, or two or more kinds may be used in combination as the sugar alcohol. That is, the sugar alcohol may be at least one selected from the group consisting of mannitol, xylitol, sorbitol, and maltitol.
The sugar alcohol may have a chain structure or a ring structure. In consideration of reactivity with lithium metal, it is preferable that the sugar alcohol has a chain structure. Due to the same reason, it is preferable that the valence of the sugar alcohol is 5 to 6. The valence refers to the number of alcoholic hydroxy groups present in the molecular structure of the sugar alcohol. In consideration the above-described conditions, it is preferable that the sugar alcohol is at least one selected from the group consisting of mannitol, xylitol, and sorbitol.
The sugar alcohol is highly hydrophilic due to the alcoholic hydroxy group. Therefore, water is preferable as a solvent during the preparation of the paste because the dispersibility of the sugar alcohol is improved. The mixing amount of the sugar alcohol in the negative electrode mixture may be 0.1 parts by mass to 7.0 parts by mass with respect to 100 parts by mass of the carbon-based negative electrode active material. Within the above-described range, the improvement of safety during overcharge can be expected. The lower limit of the mixing amount may be 0.3 parts by mass or 1.0 part by mass. The upper limit of the mixing amount may be 5.0 parts by mass or 4.0 parts by mass. Within the above-described ranges, the safety during overcharge can be significantly improved.
[Negative Electrode Active Material]
In the embodiment, the carbon-based negative electrode active material is used. The carbon-based negative electrode active material is a carbon material capable of storing and releasing Li ions. For example, natural graphite, artificial graphite, or coke can be used as the carbon-based negative electrode active material. The carbon-based negative electrode active material has high affinity to the sugar alcohol. Accordingly, by adopting the carbon-based negative electrode active material, the elution of the sugar alcohol from the negative electrode mixture layer can be suppressed.
[Thickener]
The thickener imparts adhesiveness to the negative electrode mixture paste. As a result, the state where the negative electrode active material is dispersed in the negative electrode mixture paste can be stabilized. The dried thickener has a function of bonding particles of the negative electrode active material to each other or bonding the negative electrode active material to the negative electrode current collector. When water is used as the solvent, for example, carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), polyethylene oxide (PEO), or polyacrylic acid (PAA) can be used as the thickener. The mixing amount of the thickener in the negative electrode mixture may be, for example, about 0.5 parts by mass to 2.0 parts by mass with respect to 100 parts by mass of the negative electrode active material.
[Binder]
The binder is not particularly limited as long as it can bond particles of the negative electrode active material to each other or can bond the negative electrode active material to the negative electrode current collector. It is preferable that the binder has superior dispersibility in water. The binder may be, for example, styrene-butadiene rubber (SBR), acrylic rubber (AR), or urethane rubber (UR). The mixing amount of the binder in the negative electrode mixture may be, for example, about 0.5 parts by mass to 2.0 parts by mass with respect to 100 parts by mass of the negative electrode active material.
[First Kneading Step (S102)]
In the first kneading step, the binder, the sugar alcohol, the thickener, and the solvent are kneaded with each other to obtain a first mixture. A kneading machine is not particularly limited. The kneading machine may be, for example, a planetary mixer. Kneading conditions may be appropriately adjusted based on, for example, the batch amount, the powder properties, and the composition. For example, the binder, the sugar alcohol, the thickener, and the solvent may be put into a planetary mixer and may be kneaded with each other for a predetermined amount of time. As a result, the first mixture is obtained. By dispersing or dissolving the sugar alcohol in the solvent in advance as described above, the sugar alcohol is likely to be attached to the carbon-based negative electrode active material.
[Second Kneading Step (S103)]
In the second kneading step, the first mixture and the carbon-based negative electrode active material are kneaded with each other to obtain a second mixture. Specifically, the carbon-based negative electrode active material may be additionally put into the planetary mixer, and the components may be kneaded with each other for a predetermined amount of time. As a result, the second mixture is obtained. The solid content proportion of the second mixture may be about 60 mass % to 80 mass %. By kneading the respective materials into a so-called thick paste, the dispersibility of the respective materials can be improved. Here, the solid content proportion refers to the mass proportion of components of the mixture excluding liquid (solvent).
[Dilution-Dispersion Step (S104)]
In the dilution-dispersion step, the solvent is added to the second mixture, and the solvent and the second mixture are kneaded with each other to obtain the negative electrode mixture paste. Specifically, water may be additionally put into the planetary mixer, and the components may be kneaded with each other for a predetermined amount of time. As a result, the negative electrode mixture paste is obtained. At this time, the solid content proportion of the negative electrode mixture paste may be about 45 mass % to 55 mass %. Next, the negative electrode mixture paste may undergo a treatment such as degassing or mesh passing.
[Application Step (S105)]
In the application step (S105), the negative electrode mixture paste is applied to a predetermined position on the negative electrode current collector. As a result, the negative electrode mixture layer is formed. An application method is not particularly limited. The application method may be, for example, gravure printing or die coating. The coating mass may be appropriately adjusted based on the battery specification. The paste coating film can be dried using, for example, a hot air drying furnace. The negative electrode mixture layer may be formed on both main surfaces (front and back surfaces) of the negative electrode current collector. The negative electrode current collector is, for example, a copper (Cu) foil.
Next, the thickness of the negative electrode mixture layer is adjusted using a rolling mill or the like. Using a slitter or the like, the negative electrode mixture layer and the negative electrode current collector are processed to have a predetermined dimension. In this way, a negative electrode 20 shown in
[Positive Electrode Preparation Step (S200)]
In the positive electrode preparation step, a positive electrode 10 shown in
The positive electrode 10 can be prepared, for example, as follows. The positive electrode active material, a conductive material, and a binder are kneaded with each other in a solvent to obtain a positive electrode mixture paste. The positive electrode mixture paste is applied to a predetermined position on the positive electrode current collector 11. By drying the paste coating film, the positive electrode mixture layer 12 is formed. The positive electrode mixture layer 12 is rolled to adjust the thickness. The positive electrode mixture layer 12 and the positive electrode current collector 11 are processed to have a predetermined dimension.
The positive electrode active material may be a material capable of storing and releasing Li ions. For example, a Li-containing composite oxide can be used as the positive electrode active material. Specifically, for example, LiCoO2, LiNiO2, LiNiaCobO2 (wherein, a+b=1, 0<a<1, and 0<b<1), LiMnO2, LiMn2O4, LiNiaCobMncO2 (wherein, a+b+c=1, 0<a<1, 0<b<1, and 0<c<1), or LiFePO4 can be used as the positive electrode active material.
For example, the conductive material may be amorphous carbon such as acetylene black (AB) or graphite. The mixing amount of the conductive material may be, for example, about 1 parts by mass to 10 parts by mass with respect to 100 parts by mass of the positive electrode active material. The binder may be, for example, polyvinylidene fluoride (PVDF) or polytetrafluoroethylene (PTFE). The mixing amount of the binder may be, for example, about 1 parts by mass to 10 parts by mass with respect to 100 parts by mass of the positive electrode active material.
[Electrode Group Preparation Step (S300)]
In the electrode group preparation step, an electrode group 80 shown in
The electrode group 80 is a wound electrode group. That is, the electrode group 80 is prepared by arranging the positive electrode 10 and the negative electrode 20 to face each other with the separators 40 therebetween and winding the components around a winding axis AW. At this time, the portions Ep where the current collectors are exposed are arranged at end portions in a width direction WD. After being wound, the electrode group 80 is formed into a flat shape.
The separator prevents electrical contact between the positive electrode 10 and the negative electrode 20 while allowing penetration of Li ions. For example, the separator may be a microporous membrane formed of polyethylene (PE), polypropylene (PP), or the like.
The separator may be obtained by laminating plural microporous membranes. A heat resistance layer containing an inorganic filler (for example, alumina particles) may be formed on a surface of the separator. The thickness of the separator may be, for example, 5 μm to 40 μm. The pore size and porosity of the separator may be appropriately adjusted such that the air permeability is a desired value.
[Case Accommodation Step (S400)]
In the case accommodation step, the electrode group is accommodated in an external case. As shown in
[Liquid Injection Step (S500)]
In the liquid injection step, the electrolytic solution is injected into the external case. An electrolytic solution 81 can be injected, for example, through a liquid injection hole provided on the external case 50. After the injection, the liquid injection hole is sealed using predetermined means. The electrolytic solution 81 is impregnated into the electrode group 80. At this time, in the wound electrode group, the electrolytic solution is not likely to permeate into the electrode group, and the permeation may be non-uniform. The residue of the electrolytic solution 81 which is not impregnated into the electrode group 80 remains in the external case 50.
The electrolytic solution is a liquid electrolyte in which a supporting electrolyte is dissolved in a nonaqueous solvent. The nonaqueous solvent may be: a cyclic carbonate such as ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), or γ-butyrolactone (γBL); or may be a chain carbonate such as dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), or diethyl carbonate (DEC). Among these nonaqueous solvents, a combination of two or more kinds may be used. From the viewpoint of electrical conductivity and electrochemical stability, it is preferable that a mixture of a cyclic carbonate and a chain carbonate is used. At this time, a volume ratio of the cyclic carbonate to the chain carbonate may be about 1:9 to 5:5.
The supporting electrolyte may be, for example, Li salts such as LiPF6, LiBF4, LiClO4, LiAsF6, Li(CF3SO2)2N, or LiCF3SO3. Among these supporting electrolytes, a combination of two or more kinds may be used. The concentration of the supporting electrolyte in the electrolytic solution may be about 0.5 mol/L to 2.0 mol/L.
[Nonaqueous Electrolyte Secondary Battery]
Using the above-described method, a battery 100 shown in
First, a section of the negative electrode mixture layer 22 shown in
For the identification and quantitative analysis of the sugar alcohol, a nuclear magnetic resonance (NMR) method is used. The measurement procedure is as follows. First, the negative electrode mixture is obtained from each of the measurement regions R1 to R6. The negative electrode mixture may be obtained at a position near the center of each of the measurement regions. Next, the negative electrode mixture is dissolved in a deuterated solvent. Examples of the deuterated solvent include deuterated chloroform (CDCl3) and deuterated dimethyl sulfoxide (CD3)2SO). The negative electrode mixture dissolved in the deuterated solvent is analyzed by 1H-NMR spectroscopy. A reference material is, for example, tetramethylsilane (TMS). By checking the obtained NMR spectrum against the known NMR spectrum database, the sugar alcohol can be identified. A quantitative signal is selected based on the NMR spectrum of the sugar alcohol, and the area of the quantitative signal is obtained as an NMR signal intensity of the sugar alcohol.
In the above-described measurement, for example, an NMR signal intensity obtained from the measurement region R1 is set as M1. The average value (Mave) of M1 to M6 is calculated. At this time, the absolute quantity may be determined using a calibration curve method. By dividing M1 to M6 by Mave, M1/Mave to M6/Mave, that is, Mi/Mave (i represents an integer of 1 to 6) is calculated. At this time, the negative electrode mixture layer 22 according to the embodiment satisfies the above expression (I). On the other hand, for example, when the sugar alcohol is dissolved in the electrolytic solution to permeate into the negative electrode mixture layer, the distribution of the sugar alcohol becomes non-uniform, and the expression (I) is not satisfied. That is, since the electrolytic solution and the sugar alcohol are not likely to permeate into up to the measurement region R5, M5/Mave is 0.8 or less. On the other hand, in the measurement regions R1 and R3, the electrolytic solution and the sugar alcohol are likely to remain, and M1/Mave and M3/Mave are 1.2 or more.
As the thickness and width of the negative electrode mixture layer increase, the above-described tendency becomes more severe. Accordingly, it can be said that the embodiment is efficient on a negative electrode mixture layer having a large thickness and a large width. The thickness of the negative electrode mixture layer may be 50 μm to 200 μm. The lower limit of the thickness may be 75 μm or 100 μm. The upper limit of the thickness may be 150 μm or 125 μm. The width of the negative electrode mixture layer may be 50 mm to 200 mm. The lower limit of the width may be 75 mm. The upper limit of the width may be 150 mm, 125 mm, or 100 mm.
In the expression (I), the lower limit of Mi/Mave may be 0.81, 0.83, or 0.89. The upper limit of Mi/Mave may be 1.17, 1.16, or 1.12. As a result, the improvement of safety during overcharge can be expected.
The average value (Mave) may be 10 to 700. At this time, the mixing amount of the sugar alcohol in the negative electrode mixture layer is, for example, 0.1 parts by mass to 7.0 parts by mass with respect to 100 parts by mass of the negative electrode active material. The average value (Mave) may be 30 to 500. At this time, the mixing amount of the sugar alcohol in the negative electrode mixture layer is, for example, 0.3 parts by mass to 5.0 parts by mass with respect to 100 parts by mass of the negative electrode active material.
Hereinabove, the embodiment has been described using the square battery as an example. However, the embodiment is not limited to the square battery. The embodiment may be applied to a cylindrical battery or a laminate battery. The electrode group is not limited to the wound electrode group. The electrode group may be a laminated electrode group.
Hereinafter, the embodiment will be described in more detail using Examples. However, the embodiment is not limited to the following Examples.
[Preparation of Nonaqueous Electrolyte Secondary Battery]
Nonaqueous electrolyte secondary batteries (rated capacity: 25 Ah) according to Samples A1 to A8 and Samples B1 to B4 were prepared as follows. Samples A1 to A8 correspond to Examples, and Samples B1 to B4 correspond to Comparative Examples.
[Sample A1]
1. Negative Electrode Preparation Step
1-1. Preparation Step
The following materials were prepared.
Carbon-based negative electrode active material: natural graphite
Thickener: CMC
Binder: SBR
Solvent: water
Sugar alcohol: mannitol
Negative electrode current collector: Cu foil (thickness: 10 μm, width: 80.9 mm).
1-2. First Kneading Step
CMC, SBR, mannitol, and water were put into a planetary mixer and were kneaded with each other. As a result, a first mixture was obtained. At this time, the mixing amounts of solid components in the first mixture were adjusted as follows: CMC (1 part by mass), SBR (1 part by pass), and mannitol (1 part by mass) with respect to 100 parts by mass of the negative electrode active material.
1-3. Second Kneading Step
Natural graphite (100 parts by mass) was put into the planetary mixer, and the first mixture and the natural graphite were kneaded with each other to obtain a second mixture.
1-4. Dilution-Dispersion Step
Water was additionally added to the planetary mixer, and the components were kneaded with each other. As a result, a negative electrode mixture paste was obtained. The addition amount of water was adjusted such that the solid content proportion of the negative electrode mixture paste was 50 mass %.
1-5. Application Step
Using a die coater, the negative electrode mixture paste was applied to one main surface of the Cu foil. Next, the paste coating film was dried in a hot air drying furnace. As a result, a negative electrode mixture layer was formed.
Using the same method as described above, a negative electrode mixture layer was formed on the other main surface of the Cu foil. Using a rolling mill, the negative electrode mixture layer was rolled. The negative electrode mixture layer and the Cu foil were processed to have a predetermined dimension. As a result, the negative electrode 20 shown in
Width W22 of negative electrode mixture layer 22: 60.9 mm
Width W21 of portion Ep where current collector was exposed: 20.0 mm
Thickness of negative electrode mixture layer 22: 100 μm
2. Positive Electrode Preparation Step
2-1. Preparation Step
The following materials were prepared.
Positive electrode active material: LiNi1/3Co1/3Mn1/3O2
Conductive material: acetylene black
Binder: PVDF
Solvent: NMP
Positive electrode current collector: Al foil (thickness: 20 μm, width: 78.0 mm).
2-2. Kneading Step
LiNi1/3Co1/3Mn1/3O2, acetylene black, PVDF, and NMP were put into the planetary mixer and were kneaded with each other. As a result, a positive electrode mixture paste was obtained.
2-3. Application Step
The positive electrode mixture paste was applied to both main surfaces of the Al foil. Next, the paste coating film was dried in a hot air drying furnace. As a result, a positive electrode mixture layer was formed. Using a rolling mill, the positive electrode mixture layer was rolled. The positive electrode mixture layer and the Al foil were processed to have a predetermined dimension. As a result, the positive electrode 10 shown in
Width W12 of positive electrode mixture layer 12: 58.0 mm
Width W11 of portion Ep where current collector was exposed: 20.0 mm
3. Electrode Group Preparation Step
A microporous membrane separator (width: 63.0 mm) formed of PE was prepared. As shown in
4. Case Accommodation Step
The square external case 50 was prepared. The external dimension of the external case 50 was length 75 mm×width 120 mm×depth 15 mm. The thickness of a side wall of the external case 50 was 1 mm. The positive electrode terminal 70 and the negative electrode terminal 72 provided on the sealing plate 54 were connected to the electrode group 80. As shown in
5. Liquid Injection Step
LiPF6 was dissolved in a nonaqueous solvent (EC:EMC:DEC=3:5:2 (volume ratio)) to prepare an electrolytic solution. The concentration of LiPF6 was 1.0 mol/L. The electrolytic solution was injected through the liquid injection hole provided on the external case 50.
6. Initial Charging and Discharging
First, the battery was charged at a current value of 1 C until the voltage reached 4.1 V. Next, the battery was discharged at a current value of ⅓ C until the voltage reached 3.0 V. Here, the unit “C” for the current value refers to the current value at which the rated capacity of a battery is completely discharged in 1 hour.
In this way, a nonaqueous electrolyte secondary battery according to Sample A1 was obtained. Preparation conditions of Sample A1 are shown in the table of
[Samples A2 to A4]
Samples A2 to A4 were obtained using the same method as in Sample A1, except that xylitol, sorbitol, and maltitol were used as shown in
[Samples A5 to A8]
Samples A5 to A8 were obtained using the same method as in Sample A1, except that the mixing amount of mannitol was changed as shown in
[Sample B1]
In Sample B1, a negative electrode mixture paste was prepared as follows. Natural graphite (100 parts by mass), CMC (1 part by mass), SBR (1 part by mass), and water were put into a planetary mixer and were kneaded with each other. Next, water was additionally put into the planetary mixer, and the components were kneaded with each other to obtain a negative electrode mixture paste. The solid content proportion of the negative electrode mixture paste was 50 mass %.
In Sample B1, mannitol was further added to the electrolytic solution prepared above in “5. Liquid Injection”. The addition amount of mannitol in the battery was set as 1 part by mass with respect to 100 parts by mass of the negative electrode active material. Sample B1 was obtained using the same method as in Sample A1, except for the above-described configurations.
[Samples B2 to B4]
Samples B2 to B4 were obtained using the same method as in Sample B1, except that xylitol, sorbitol, and maltitol were used as shown in
[Evaluation]
Each of the samples was evaluated as follows.
1. Distribution of Sugar Alcohol in Negative Electrode Mixture Layer
After initial charging and discharging, the battery having a voltage of 3.0 V was disassembled to extract the electrode group. A rectangular measurement sample was cut out from a region R0 shown in
2. Battery Resistance
The state of charge (SOC) of the battery was adjusted to 60% at 25° C. Pulse discharging was performed under conditions of 250 A (10 C)×10 seconds to measure a voltage drop amount. The IV resistance was calculated based on a relationship between the voltage drop amount and the current value. This measurement was performed on 10 batteries for each of the samples, and the average value was calculated. The results are shown in
3. 1 C Overcharge Test
The battery was charged to 4.5 V at a constant current value of 25 A (1 C). At this time, the maximum peak temperature was measured using a thermocouple attached to a side surface of the battery. The results are shown in
4. 10 C Overcharge Test
The maximum peak temperature was measured using the same method as in “1 C overcharge test”, except that the current value was changed to 250 A (10 C). The results are shown in
[Results and Discussion]
1. Samples B1 to B4
As shown in
In Sample B1 to B4, the safety during the 1 C overcharge test was high. However, during the 10 C overcharge test, an increase in temperature was observed. It can be understood that the reason for this is the distribution of the sugar alcohol in the negative electrode mixture layer. As shown in
2. Samples A1 to A7
In Samples A1 to A7, an increase in battery resistance was able to be suppressed. The reason for this is presumed to be that, in these samples, the sugar alcohol was added during the preparation of the negative electrode mixture paste, and thus substantially no sugar alcohol was present in the positive electrode mixture layer.
In Samples A1 to A7, even during the 10 C overcharge test, an increase in temperature was small. As shown in
3. Kind of Sugar Alcohol
As shown in
As a result of comparing Samples A1 to A4 to each other, it was found that, when mannitol, xylitol, or sorbitol was used, the effect was high. Therefore, it is preferable that the sugar alcohol is at least one selected from the group consisting of mannitol, xylitol, and sorbitol.
4. Mixing Amount of Sugar Alcohol
As shown in
The above-described method of manufacturing a nonaqueous electrolyte secondary battery includes: a kneading step of kneading a carbon-based negative electrode active material, a binder, and a sugar alcohol with each other to form a negative electrode mixture paste; and an application step of applying the negative electrode mixture paste to a negative electrode current collector to form a negative electrode mixture layer. It can be verified from the above description that, with the above-described method, an increase in battery resistance can be suppressed while improving safety during overcharge.
In the nonaqueous electrolyte secondary battery, when a section of the negative electrode mixture layer in a thickness direction is divided into six measurement regions by trisecting the negative electrode mixture layer in a width direction and further bisecting the negative electrode mixture layer in the thickness direction, all the measurement regions satisfy the expression (I). It can be verified from the above description that, in the above-described nonaqueous electrolyte secondary battery, the safety during overcharge is high.
Hereinabove, the embodiment and the examples of the invention have been described. It is primarily intended that the configurations of the embodiment and the examples can be appropriately combined.
The embodiment and Examples disclosed herein are merely exemplary in all respects and are not particularly limited.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-257567 | Dec 2014 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2015/002377 | 12/18/2015 | WO | 00 |
