JP6066464B2 - Electrolytic solution for non-aqueous electrolyte secondary battery and non-aqueous electrolyte secondary battery using the same - Google Patents

Description

  The present invention relates to an electrolytic solution for a non-aqueous electrolyte secondary battery and a non-aqueous electrolyte secondary battery using the same.

Non-aqueous electrolyte secondary batteries are attracting attention as a power source for electronic devices because of their high energy density and light weight. In particular, button-type non-aqueous electrolyte secondary batteries are small in size and are therefore portable electronic devices such as mobile phones. Widely used.
A non-aqueous electrolyte secondary battery mounted on an electronic device may be heated to 50 ° C. or higher by heat generated from the electronic device. A non-aqueous electrolyte secondary battery tends to have a low discharge capacity when heated for a long period of time.
In addition, with the miniaturization of electronic devices, non-aqueous electrolyte secondary batteries are being surface-mounted on the board, and the mounting method is reflow soldering (reflow processing). It has become mainstream. In the reflow process, the nonaqueous electrolyte secondary battery is heated at about 250 to 260 ° C., so that a large amount of heat is applied to the nonaqueous electrolyte secondary battery. For this reason, a non-aqueous electrolyte secondary battery may have a remarkably low discharge capacity due to reflow treatment.
Conventionally, in order to cope with such reflow soldering at a high temperature, an electrolytic solution for a lithium secondary battery using an organic ether compound as a solvent has been proposed (for example, Patent Document 1).

JP 2004-327282 A

However, as in Patent Document 1, the one using only an organic ether compound as a solvent has a problem that the storage characteristics are not sufficient.
Therefore, the present invention provides an electrolyte for a non-aqueous electrolyte secondary battery that can improve storage characteristics, and a non-aqueous electrolyte secondary battery including the same.

The electrolyte solution for a non-aqueous electrolyte secondary battery of the present invention contains a non-aqueous solvent and a supporting salt. Examples of the non-aqueous solvent include vinylene carbonate and a cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher. The ratio of the vinylene carbonate is 20 to 40% by volume, and the ratio of the cyclic carbonate is 60 to 80% by volume.
The electrolyte solution for a non-aqueous electrolyte secondary battery of the present invention contains a non-aqueous solvent and a supporting salt. Examples of the non-aqueous solvent include vinylene carbonate and a glycol ether having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher. The ratio of the vinylene carbonate is 5 to 50% by volume, and the ratio of the glycol ether is 50 to 95% by volume.
The electrolyte solution for a non-aqueous electrolyte secondary battery of the present invention contains vinylene carbonate, a cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher, a sulfone, and a supporting salt, and the proportion of the vinylene carbonate is It is 20 to 40% by volume, the ratio of the cyclic carbonate is 30 to 40% by volume, and the ratio of the sulfone is 30 to 50% by volume.

  The nonaqueous electrolyte secondary battery of the present invention is characterized by including the electrolytic solution of the present invention.

  ADVANTAGE OF THE INVENTION According to this invention, the electrolyte solution for nonaqueous electrolyte secondary batteries by which the storage characteristic was improved can be provided, and a nonaqueous electrolyte secondary battery provided with the same.

It is sectional drawing of the nonaqueous electrolyte secondary battery concerning one Embodiment of this invention.

The nonaqueous electrolyte secondary battery 1 of the present invention will be described below with reference to FIG.
The nonaqueous electrolyte secondary battery 1 has a so-called coin-type structure.
In FIG. 1, reference numeral 2 denotes a bottomed cylindrical main body (positive electrode can) 12, a covered cylindrical lid (negative electrode can) 22 that closes the opening of the positive electrode can 12, and the inner peripheral surface of the positive electrode can 12. And a gasket 40 provided along the inner periphery of the positive electrode can 12 and sealed by caulking the periphery of the opening of the positive electrode can 12 inside. In the nonaqueous electrolyte secondary battery 1, a positive electrode 10 and a negative electrode 20 are disposed opposite to each other with a separator 30 in a storage container 2 and filled with an electrolytic solution 50. The positive electrode 10, the negative electrode 20, and the separator 30 are impregnated with the electrolytic solution 50 filled in the storage container 2.

    The positive electrode 10 is bonded to the inner bottom surface of the positive electrode can 12 by a positive electrode current collector 14 made of a conductive resin adhesive containing carbon as a conductive filler, and the negative electrode 20 is a negative electrode current collector similar to the positive electrode current collector 14. The body 24 is adhered to the inner top surface of the negative electrode can 22.

The electrolytic solution 50 is obtained by dissolving a supporting salt in a non-aqueous solvent. The non-aqueous solvent is vinylene carbonate (hereinafter also referred to as a solvent A) and has a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher. And a cyclic carbonate and at least one selected from glycol ethers having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher (hereinafter sometimes referred to as solvent B).
The electrolytic solution 50 exhibits high storage characteristics when the solvent A and the solvent B are used in combination.
The melting point is a value measured according to JIS K0064, and is a value measured according to JIS K3331 in the case of room temperature or lower.

Further, the viscosity (20 ° C.) of the electrolytic solution 50 is preferably 5 mPa · s or less, and more preferably 3 mPa · s or less. By setting it as such a viscosity, the fall of the discharge capacity in normal temperature environment can be prevented. The viscosity of the solvent can be adjusted by the types of the solvent A and the solvent B and the blending ratio.
The viscosity is a value measured according to JIS K7117-1 using a B-type viscometer.

  The solvent A is vinylene carbonate (boiling point: 162 ° C., melting point: 17 ° C.) that is liquid at room temperature represented by the following general formula (1).

  The solvent A has an effect of forming a film suitable for the electrode surface during storage, charging / discharging, and reflow, and suppressing deterioration of battery characteristics.

The ratio of the solvent A in the non-aqueous solvent is not particularly limited, but is preferably 5 to 40% by volume, more preferably 10 to 30% by volume, and particularly preferably 10 to 20% by volume.
If it is more than the said lower limit, a favorable film | membrane can be formed on the electrode surface and a battery characteristic fall can be prevented favorable. If it is below the upper limit, reflow resistance can be improved.

The solvent B is at least one selected from a cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher, and a glycol ether having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher.
By containing the solvent B, the film formation on the electrode by the solvent A can be made better.

Examples of the cyclic carbonate include propylene carbonate (melting point: −49 ° C., boiling point 242 ° C.) and butylene carbonate (melting point: −53 ° C., boiling point 240 ° C.). Examples of the glycol ether include methyl tetraglyme (melting point). -30 [deg.] C., boiling point 275 [deg.] C.) and the like, among which methyl tetraglyme, butylene carbonate, and propylene carbonate are preferable, butylene carbonate and propylene carbonate are more preferable, and propylene carbonate is particularly preferable. Solvent B can be used singly or in appropriate combination of two or more.

Although the ratio of the solvent B in a solvent is not specifically limited, 10-90 volume% is preferable, 15-85 volume% is more preferable, and 20-80 volume% is especially preferable.
If it is in the said range, a preservation | save characteristic will improve more and the improvement of reflow tolerance can be aimed at.

The volume ratio represented by the solvent A / solvent B is preferably 4/3 to 1/10, more preferably 1/2 to 1/10, and still more preferably 1/4 to 1/10.
If it is in the said range, a preservation | save characteristic will improve more and the improvement of reflow tolerance can be aimed at.

  The total of the solvent A and the solvent B in the non-aqueous solvent is preferably 20% by volume or more, more preferably 50% by volume or more, further preferably 60% by volume or more, and may be 100% by volume.

The electrolytic solution 50 may contain sulfone (solvent C) in addition to the solvent A and the solvent B. When the electrolytic solution 50 contains the solvent C, the reflow resistance can be further improved.
In the sulfone here, two alkyl groups bonded to the sulfur atom of the sulfonyl group (—SO ₂ —) are bonded to each other, and these alkyl group and the S atom form a ring structure. Also good.

  Examples of the solvent C include sulfolane (boiling point: 285 ° C., melting point: 28 ° C.) represented by the following general formula (2), and 3-methylsulfolane (boiling point: 274 ° C., melting point 6) represented by the following general formula (3). And dimethyl sulfone (boiling point: 238 ° C., melting point 107 ° C.) represented by the following general formula (4), and ethyl methyl sulfone represented by the following general formula (5) (boiling point: 239 ° C., melting point: 34 ° C) and chain sulfones such as isopropylmethylsulfone (boiling point: 225 ° C, melting point: -8 ° C) represented by the following general formula (6), among which sulfolane having a boiling point of 240 ° C or higher, 3 -Methylsulfolane is preferred, and sulfolane that improves storage properties is particularly preferred.

The ratio of the solvent C in the non-aqueous solvent is not particularly limited, but is preferably 10 to 80% by volume, more preferably 15 to 70% by volume, still more preferably 20 to 60% by volume, and particularly preferably 25 to 50%.
If it is less than the lower limit, the reflow resistance may not be sufficiently increased, and if it exceeds the upper limit, the storage characteristics may be deteriorated.

  The ratio represented by (solvent A + solvent B) / solvent C is preferably 1/4 to 4/1, more preferably 1/3 to 3/1, and particularly preferably 1/2 to 2/1. If it is less than the lower limit, the storage characteristics may be deteriorated, and if it exceeds the upper limit, the reflow resistance may not be sufficiently increased.

  In addition to the solvents A, B, and C, the electrolytic solution 50 may contain 20 to 30% by volume of a chain carbonate that is an arbitrary solvent having a melting point of −20 ° C. or less as long as the effects of the present invention are not impaired.

As the chain carbonate, diethyl carbonate (H ₅ C ₂ OCOOC ₂ H ₅ , melting point: −43 ° C., boiling point: 127 ° C.), ethyl methyl carbonate (H ₅ C ₂ OCOOCH ₃ , melting point: −55 ° C., boiling point: 108 ° C) and the like.

As the supporting salt, a known substance used as a supporting salt in the electrolyte solution of the nonaqueous electrolyte secondary battery can be used. For example, LiCH ₃ SO ₃ , LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiN (C ₂ F ₅ SO ₂ ) ₂ , LiC (CF ₃ SO ₂ ) ₃ , LiN (CF ₃ SO ₃ ) ₂ , Organic acid lithium salts such as LiN (FSO ₂ ) ₂ , lithium salts such as LiPF ₆ , LiBF ₄ , LiB (C ₆ H ₅ ) ₄ , LiCl, LiBr, and other inorganic acid lithium salts can be used. Among these, lithium salts that are compounds having lithium ion conductivity are preferable, LiN (CF ₃ SO ₂ ) _2, LiN (FSO ₂ ) _{2, and} LiBF ₄ are more preferable, heat resistance and reactivity with moisture are low, and storage is performed. From the viewpoint of sufficiently exhibiting the characteristics, LiN (CF ₃ SO ₂ ) ₂ is particularly preferable. These supporting salts can be used singly or in appropriate combination of two or more.

  The content of the supporting salt in the electrolytic solution 50 can be determined in consideration of the type of the supporting salt and the like. For example, when a lithium salt is used, 0.1 to 3.5 mol / L is preferable, and 0.5 to 3. 0 mol / L is more preferable, and 1 to 2.5 mol / L is particularly preferable. If the lithium salt concentration is too high or too low, the electrical conductivity is lowered, which may adversely affect the battery characteristics.

As the material of the positive electrode can 12, conventionally known materials are used, and examples thereof include stainless steel.
The material of the negative electrode can 22 is the same as the material of the positive electrode can 12.

Examples of the positive electrode 10 include those containing a conventionally known positive electrode active material.
Examples of the positive electrode active material include molybdenum oxide, lithium manganese oxide, lithium iron phosphate compound, lithium cobalt oxide, lithium nickel oxide, and vanadium oxide, and molybdenum oxide and lithium manganese oxide are preferable. . When the positive electrode 10 contains these exemplified positive electrode active materials, the heat resistance of the nonaqueous electrolyte secondary battery 1 is increased, and a reduction in discharge capacity due to reflow treatment or heating during use is suppressed.
Examples of the molybdenum oxide include MoO ₃ and MoO _2. Among them, MoO ₃ is preferable.
Examples of the lithium manganese oxide include Li ₄ Mn _5-w M ¹ _w O ₁₂ (0 ≦ w <1, M ¹ is Ni, Co, Ti, Fe, Cr, Al, Mo, V, Cu, Nb, At least one of Zn, Ca and Mg), LiMn _2-y M ² _y O ₄ (0 ≦ y <1, M ² is the same as M ¹ ), Li ₂ Mn _4-z M ³ _z O ₉ (0 ≦ z <1, M ³ is the same as M ¹ ), and the like. Among them, Li ₄ Mn ₅ O ₁₂ in which w = 0 is preferable.
Examples of the lithium iron phosphate compound include LiFe _1-p M ⁴ _p PO ₄ (0 ≦ p ≦ 1, M ⁴ is at least one of Mn, Ni, Co, Ti, Al, Cr, V, and Nb. ), Li ₃ Fe _{2 -q} M ⁵ _q (PO ₄ ) ₃ (0 ≦ q ≦ 1, M ⁵ is the same as M ⁴ ), etc., among which LiFePO ₄ is preferable.
Examples of the lithium cobalt oxide include LiCo _1-r M ⁶ _r O ₂ (0 ≦ r <1, M ⁶ is Mn, Ti, Fe, Cr, Al, Mo, V, Cu, Nb, Zn, Ca, At least one of Mg), and the like. Among these, LiCoO ₂ is preferable.
Examples of the lithium nickel oxide include LiNi _1-s M ⁷ _s O ₂ (0 ≦ s <1, M ⁷ is Mn, Co, Ti, Fe, Cr, Al, Mo, V, Cu, Nb, Zn, And at least one of Ca and Mg). Among these, LiNiO ₂ is preferable.
Examples of the vanadium oxide include V ₂ O ₅ , V ₃ O ₈ , V ₆ O _{13 and the} like, among which V ₂ O ₅ is preferable.
A positive electrode active material may be used individually by 1 type, and may be used in combination of 2 or more type.

 When using a granular positive electrode active material, the average particle diameter is not specifically limited, For example, 0.1-100 micrometers is preferable and 1-50 micrometers is more preferable. If it is less than the above lower limit value, the reactivity in the reflow treatment becomes too high to be handled, and if it exceeds the above upper limit value, the discharge rate may be lowered. The average particle diameter is a mass average particle diameter measured using a laser diffraction method.

 The content of the positive electrode active material in the positive electrode 10 is determined in consideration of the discharge capacity and the like required for the nonaqueous electrolyte secondary battery 1, and is preferably 50 to 95% by mass, and more preferably 70 to 88% by mass, for example. If it is less than the above lower limit value, it is difficult to obtain a sufficient discharge capacity, and if it exceeds the above upper limit value, it tends to be difficult to form the positive electrode 10.

The positive electrode 10 may contain a conductive additive (the conductive additive used for the positive electrode 10 may be referred to as a positive conductive additive). Examples of the positive electrode conductive assistant include carbon materials such as furnace black, ketjen black, acetylene black, and graphite. These positive electrode conductive aids may be used alone or in combination of two or more.
4-40 mass% is preferable, for example, and, as for content of the positive electrode conductive support agent in the positive electrode 10, 10-20 mass% is more preferable. If it is less than the said lower limit, it will be difficult to obtain sufficient electroconductivity, and when forming the positive electrode 10 in a pellet form, it will be difficult to shape | mold, and if it exceeds the said upper limit, there exists a possibility that the discharge capacity of the positive electrode 10 may become insufficient.

The positive electrode 10 may contain a binder (the binder used for the positive electrode 10 may be referred to as a positive electrode binder). As the positive electrode binder, conventionally known materials can be used. For example, polymers such as polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), styrene butadiene rubber (SBR), polyacrylic acid (PA), carboxy, etc. Examples thereof include methyl cellulose (CMC) and polyvinyl alcohol (PVA). Among them, polyacrylic acid is preferable, and cross-linked polyacrylic acid is more preferable. These positive electrode binders may be used alone or in combination of two or more. In addition, when using polyacrylic acid, it is preferable to adjust polyacrylic acid to pH 3-10 previously. For adjusting the pH, an alkali metal hydroxide such as lithium hydroxide or an alkaline earth metal hydroxide such as magnesium hydroxide can be used.
The content of the positive electrode binder in the positive electrode 10 is, for example, 1 to 20% by mass.

The size of the positive electrode 10 is determined according to the size of the nonaqueous electrolyte secondary battery 1.
The thickness of the positive electrode 10 is determined according to the size of the non-aqueous electrolyte secondary battery 1, and if the non-aqueous electrolyte secondary battery 1 is a button-type non-aqueous electrolyte secondary battery for backup, 300 to 1000 μm.

The positive electrode 10 is obtained by a conventionally known manufacturing method. The method for producing the positive electrode 10 includes, for example, mixing the component (A), the component (B), and, if necessary, a positive electrode conductive additive and / or a positive electrode binder to form a positive electrode mixture. And a method of pressure molding.
The pressure at the time of pressure molding is determined in consideration of the type of the positive electrode conductive additive, and is, for example, 0.2 to 5 ton / cm ² .

 A conventionally well-known thing is used as the positive electrode electrical power collector 14, For example, the conductive resin adhesive etc. which use carbon as a conductive filler are mentioned.

The negative electrode 20 is appropriately determined according to the voltage value of the nonaqueous electrolyte secondary battery 1 and the like. When the voltage value of the non-aqueous electrolyte secondary battery 1 is 2 to 3 V, examples of the negative electrode 20 include SiO, Si (hereinafter sometimes referred to as SiO _x (0 ≦ x <2) in general), SnO _v ( Examples include 0 ≦ v <1), C (graphite, hard carbon, etc.), Li ₄ Ti ₅ O ₁₂ , LiAl, etc. as an active material (the active material used for the negative electrode may be referred to as a negative electrode active material). Among these, those containing SiO _x (0 ≦ x <2) and C are preferred, and those containing SiO _x (x = 1) are more preferred. Note that SiO _x (0 ≦ x <2) may be used in an amorphous state that shows broad in an X-ray diffraction pattern, but was previously disproportionated by subjecting SiO _x (0 ≦ x <2) to heat treatment. It may be used in a state.
Although content of the negative electrode active material in the negative electrode 20 is not specifically limited, For example, it is 40-85 mass%. The content is mainly determined by the conductivity of the negative electrode active material, and even if it is a negative electrode active material with low conductivity, the content can be increased if the conductivity is improved by coating the surface with carbon or the like. .

The negative electrode 20 can contain a conductive additive (the conductive aid used for the negative electrode 20 may be referred to as a negative conductive agent). The negative electrode conductive auxiliary is the same as the positive electrode conductive auxiliary.
The negative electrode 20 can contain a binder (the binder used for the negative electrode 20 may be called a negative electrode binder). As the negative electrode binder, a conventionally known material can be used. For example, polyvinylidene fluoride (PVDF), styrene butadiene rubber (SBR), polyacrylic acid (PA), carboxymethyl cellulose (CMC), polyimide (PI), polyamideimide (PAI) and the like can be mentioned, among which polyacrylic acid is preferable, and cross-linked polyacrylic acid is more preferable. These negative electrode binders may be used individually by 1 type, and may be used in combination of 2 or more type. In addition, when using polyacrylic acid, it is preferable to adjust polyacrylic acid to pH 3-10 previously. For adjusting the pH, an alkali metal hydroxide such as lithium hydroxide or an alkaline earth metal hydroxide such as magnesium hydroxide can be used.
The content of the negative electrode binder in the negative electrode 20 is, for example, 1 to 20% by mass.

  The size of the negative electrode 20 is appropriately determined according to the size of the positive electrode 10.

 The separator 30 can apply what was conventionally used for the separator of a nonaqueous electrolyte secondary battery, for example, glass, such as alkali glass, borosilicate glass, quartz glass, lead glass, polyphenylene sulfide, polyethylene terephthalate, polyamide, polyimide, etc. Nonwoven fabric made of the above resin. Among these, a glass nonwoven fabric is preferable, and a borosilicate glass nonwoven fabric is more preferable. Since the glass nonwoven fabric has excellent mechanical strength and high ion permeability, the internal resistance can be reduced and the discharge capacity can be improved.

 The thickness of the separator 30 is determined in consideration of the size of the nonaqueous electrolyte secondary battery 1, the material of the separator 30, and the like, and is, for example, 5 to 300 μm.

  The material of the gasket 40 is preferably a resin having a heat distortion temperature of 230 ° C. or higher. If the heat distortion temperature is 230 ° C. or higher, for example, reflow treatment can prevent the gasket 40 from being significantly deformed and the electrolyte solution 50 from leaking out. Examples of the material of the gasket 40 include polyphenyl sulfide (PPS), polyethylene terephthalate (PET), polyamide (PA), liquid crystal polymer (LCP), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer resin (PFA), and polyether. Ether ketone resin (PEEK), polyether nitrile resin (PEN), polyether ketone resin (PEK), polyarylate resin, polybutylene terephthalate resin (PBT), polycyclohexanedimethylene terephthalate resin, polyether sulfone resin (PES), Examples thereof include polyamino bismaleimide resin, polyetherimide resin, and fluororesin. Moreover, what added glass fiber, my cowsker, ceramic fine powder, etc. to these materials with the addition amount of 30 mass% or less can be used conveniently. By using such a material, deformation of the gasket 40 can be prevented in reflow soldering, and volatilization and leakage of the electrolytic solution 50 can be prevented.

As described above, according to the present invention, the electrolyte for the non-aqueous electrolyte secondary battery is at least one selected from vinylene carbonate, cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher, and glycol ether. Storage characteristics can be improved by containing seeds.
This is because the solvent can form a film on the electrode that suppresses excessive reaction with the electrolytic solution on the electrode surface, and the solvent (B) adjusts the electrolytic solution to a viscosity suitable for the battery reaction. It is considered that the film formation by the solvent A can be made better, and deterioration due to storage can be suppressed.

 In the above-described embodiment, a coin-type nonaqueous electrolyte secondary battery including a storage container in which a stainless steel positive electrode can and a stainless steel negative electrode can are crimped has been described as an example. It is not limited. For example, the nonaqueous electrolyte secondary battery has a structure in which the opening of the ceramic container body is sealed with a ceramic lid by a heat treatment such as seam welding using a metal sealing member. Good.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited by these examples.

EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited by these examples.
In addition, the solvent in a table | surface is shown with the following abbreviations.
VC: vinylene carbonate, EC: ethylene carbonate, PC: propylene carbonate, BC: butylene carbonate, MTG: methyltetraglyme, SL: sulfolane, MSL: 3-methylsulfolane, GBL: γ-butyrolactone

(Evaluation method)
<Storage characteristics>
About six obtained nonaqueous electrolyte secondary batteries, it heated for 10 minutes at the preheating temperature of 180 degreeC, and performed the reflow test by heating for 20 seconds at the heating temperature of 240 degreeC 3 times. After this treatment, the battery was discharged in a 24 ° C. environment at a constant current of 5 μA (discharge current) until the voltage reached 2.0V. And it applied for 48 hours by the voltage of 3.3V in a 24 degreeC environment. Thereafter, the capacity when discharged at a constant current of 5 μA (discharge current) to a voltage of 2.0 V in an environment of 24 ° C. was measured, and this value was defined as V1 ′, and the period during which V1 ′ decreased to 50% was measured. . The period during which V1 ′ in Comparative Example 1 decreases to 50% is defined as 100, and the relative period in which V1 ′ in Tables 1 to 4 and Comparative Examples 1 to 19 similarly decrease to 50% is obtained. Was used as an index of storage characteristics.

<Capacity maintenance rate>
About the obtained 6 nonaqueous electrolyte secondary batteries, it applied for 48 hours by the voltage of 3.6V in 24 degreeC environment. Then, the capacity | capacitance at the time of discharging until it became voltage 2.0V by constant current 5 microampere (discharge current) in a 24 degreeC environment was measured, and this value was set to V1. Next, the six nonaqueous electrolyte secondary batteries subjected to the above-described treatment were subjected to reflow soldering twice in an environment of 260 ° C., and a voltage of 2. μA (discharge current) at a constant current of 5 μA in an environment of 24 ° C. The capacity at the time of discharging until reaching 0 V was measured, this value was taken as V2, and the capacity retention rate (%) was calculated by the following equation (a). The calculated value was defined as the capacity maintenance rate. The larger the capacity retention rate, the better the reflow resistance.

   Capacity maintenance ratio (%) = V2 ÷ V1 × 100 (a)

(Examples 1 to 22, Comparative Examples 1 to 19) [ Example 4 (Reference Example 1) ]
A non-aqueous electrolyte secondary battery similar to the non-aqueous electrolyte secondary battery 1 shown in FIG. 1 was produced as follows.
According to Tables 1 to 4, 70 parts by mass of a positive electrode active material, 28 parts by mass of carbon as a positive electrode conductive auxiliary agent, and 2 parts by mass of cross-linked polyacrylic acid as a binder were mixed to obtain a positive electrode mixture. 7 mg of this positive electrode mixture was pressure-molded at ² ton / cm ² to obtain a disk-type positive electrode having a diameter of 2 mm and a thickness of 600 μm.
The negative electrode active materials listed in Tables 1 to 4 were pulverized, and 45 parts by mass of the pulverized product, 40 parts by mass of carbon, and 15 parts by mass of cross-linked polyacrylic acid were mixed to obtain a negative electrode mixture. 1.0 mg of this negative electrode mixture was pressure-molded at ² ton / cm ² to obtain a disk-shaped pellet-shaped negative electrode having a diameter of 2.0 mm and a thickness of 200 μm.
According to Tables 1-4, each solvent was mixed to make a non-aqueous solvent, and a supporting salt was dissolved in the obtained non-aqueous solvent to obtain an electrolyte solution.

A positive electrode unit was obtained by adhering the positive electrode to the inner surface of a stainless steel positive electrode can using a positive electrode current collector made of a conductive resin adhesive containing carbon as a conductive filler. The positive electrode unit was dried in the air at 200 ° C. for 10 hours.
Subsequently, the sealing agent was apply | coated to the inner surface of the opening part of the positive electrode can of a positive electrode unit.
A negative electrode is bonded to the inner surface of a stainless steel negative electrode can using a negative electrode current collector made of a conductive resin adhesive containing carbon as a conductive filler, and a lithium foil (diameter: 2 mm, thickness: 200 μm) is formed on the negative electrode. ) Was placed.
Next, the nonwoven fabric made from borosilicate glass fiber was dried, and then punched into a disk shape having a diameter of 3 mm and a thickness of 200 μm to obtain a separator. This separator was placed on the negative electrode, and a gasket was provided in the opening of the negative electrode can to obtain a negative electrode unit.
A total of 5 μL of electrolyte solution was filled in the positive electrode can and the negative electrode can.
The negative electrode unit was fitted into the positive electrode unit so that the lithium foil contacted the separator. Next, the positive electrode can and the negative electrode can were sealed by caulking the opening of the positive electrode can, and then allowed to stand at 25 ° C. for 7 days to obtain the nonaqueous electrolyte secondary battery of each example.
About the obtained nonaqueous electrolyte secondary battery, the storage characteristic mentioned above was evaluated and the result is shown to Tables 1-4. Since Comparative Examples 4 to 8 in Table 2 did not discharge, measurement could not be performed.

  As shown in Tables 1 to 4, Examples 1 to 22 to which the present invention was applied had storage characteristics of 102 or more, while Comparative Examples 4 to 7 using only the solvent A or the solvent B were batteries. The expression of the characteristic was not recognized.

  In Tables 3 and 4, it was confirmed that the storage characteristics were improved by applying the present invention regardless of the type of the positive electrode active material.

(Examples 23 to 28, Comparative Example 20 )
According to Table 5, a nonaqueous electrolyte secondary battery was produced in the same manner as in Example 1.
About the obtained nonaqueous electrolyte secondary battery, the capacity | capacitance maintenance factor mentioned above was evaluated and the result was shown in the table | surface.

表５に示すように、本発明を適用した実施例２３〜２８は、溶媒Ｂのみを用いた比較例２０に比べて、容量維持率が向上していることを確認できた。

As shown in Table 5, in Examples 23 to 28 to which the present invention was applied, it was confirmed that the capacity retention rate was improved as compared with Comparative Example 20 using only the solvent B.

1 Nonaqueous electrolyte secondary battery 2 Storage container 10 Positive electrode 12 Positive electrode can 14 Positive electrode current collector 20 Negative electrode 22 Negative electrode can 24 Negative electrode current collector 30 Separator 40 Gasket 50 Electrolyte

Claims (4)

Containing a non-aqueous solvent and a supporting salt,
The non-aqueous solvent is composed of vinylene carbonate and a cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher. The vinylene carbonate ratio is 20 to 40% by volume, and the cyclic carbonate ratio is 60 to 80%. An electrolytic solution for a non-aqueous electrolyte secondary battery, characterized by being in volume%. Containing a non-aqueous solvent and a supporting salt,
The non-aqueous solvent is composed of vinylene carbonate and a glycol ether having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher. The proportion of the vinylene carbonate is 5 to 50% by volume, and the proportion of the glycol ether is 50 to 95. An electrolytic solution for a non-aqueous electrolyte secondary battery, characterized by being in volume%.   It contains vinylene carbonate, a cyclic carbonate having a melting point of −20 ° C. or lower and a boiling point of 205 ° C. or higher, a sulfone, and a supporting salt, the vinylene carbonate ratio is 20 to 40% by volume, and the cyclic carbonate ratio is 30. An electrolyte solution for a non-aqueous electrolyte secondary battery, which is ˜40 volume%, and the ratio of the sulfone is 30 to 50 volume%.   A non-aqueous electrolyte secondary battery comprising the electrolytic solution according to claim 1.

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