JP6766359B2 - Non-aqueous electrolyte Non-aqueous electrolyte for secondary batteries and non-aqueous electrolyte secondary batteries - Google Patents

Description

The present invention relates to a non-aqueous electrolyte secondary battery for a non-aqueous electrolyte secondary battery and a non-aqueous electrolyte secondary battery, particularly a non-aqueous electrolyte secondary battery characterized by a non-aqueous electrolyte solution.

Non-aqueous electrolyte secondary batteries typified by lithium secondary batteries have been used as power sources for mobile devices such as laptop computers and mobile phones, but in recent years, electric vehicles (EVs), hybrid electric vehicles (HEVs), and plugs have been used. It is also used as a power source for automobiles such as in-hybrid vehicles (PHEV).

A non-aqueous electrolyte secondary battery generally includes a positive electrode containing a positive electrode active material, a negative electrode containing a negative electrode active material, a separator, and a non-aqueous electrolytic solution containing a non-aqueous solvent and a lithium salt.
The positive electrode active material constituting the non-aqueous electrolyte secondary battery is a lithium-containing transition metal oxide, the negative electrode active material is a carbon material typified by graphite, and the non-aqueous electrolyte solution is a cyclic carbonate such as ethylene carbonate. It is widely known that an electrolyte such as lithium hexafluorophosphate (LiPF ₆ ) is dissolved in a non-aqueous solvent containing a chain carbonate such as diethyl carbonate as a main component.

Further, there are also known inventions in which a halogenated carbonate is contained in a non-aqueous electrolyte solution as described above for various purposes (see Patent Documents 1 to 4).

Patent Document 1 states, "A non-aqueous electrolyte secondary that is safe and has excellent characteristics, which makes the non-aqueous electrolyte flame-retardant and self-extinguishing, and does not impair the battery characteristics by using this electrolyte. As "the purpose of providing a battery" (paragraph [0006]), "a negative electrode using a material capable of electrochemically storing and releasing lithium, and a positive electrode using a material capable of electrochemically storing and releasing lithium". In a non-aqueous electrolyte secondary battery composed of a non-aqueous electrolyte solution in which a lithium salt is dissolved as an electrolyte in a non-aqueous solvent, the non-aqueous solvent is a mixture containing one or more cyclic esters and one or more chain esters. A non-aqueous electrolyte secondary battery comprising a solvent, in which the mixed solvents are compatible with each other, and at least one of the chain esters is a halogenated chain carbonate represented by the general formula (1). The invention of "." (Claim 1) is described.

Further, in Patent Document 1, "Charge current 280 mA, charge voltage 4.2 V constant current constant voltage charge, discharge current 280 mA, discharge termination voltage 2.5 V constant current discharge is performed three times to measure the capacity. The third discharge capacity was taken as the capacity of the battery. ”(Paragraph [0023]).
In the examples, EC (ethylene carbonate) is used as the cyclic ester, and TFEMC (2,2,2-trifluoroethylmethyl carbonate) + DMC (dimethyl carbonate) is used as the chain ester, and the mixing ratio is used. A non-aqueous electrolyte solution having a (volume ratio) of 1: 1: 1 (see Example 2 in Table 1 of paragraph [0018]) and the like are shown.

Patent Document 2 states, "By optimizing the electrolyte composition of a non-aqueous electrolyte secondary battery having a lithium-nickel-manganese composite oxide on the positive electrode, the charge / discharge cycle performance of a high-voltage non-aqueous electrolyte secondary battery can be improved. For the purpose of "improving" (paragraph [0013]), "the positive electrode active material is a general formula Li _x N _y Mn _2-y O _4-δ (provided that 0 <x <1.1, 0.45 <y <. In a non-aqueous electrolyte secondary battery which is a lithium-nickel-manganese composite oxide represented by 0.55, 0 ≦ δ <0.4), the non-aqueous electrolyte contains a cyclic carbonate and a chain carbonate, and the cyclic carbonate is contained. The invention of "a non-aqueous electrolyte battery, characterized in that at least one of carbonate or chain carbonate contains a fluorine element" (claim 1) is described.

Further, Patent Document 2, "of the present invention, the positive electrode active material is the formula _{Li x Ni y Mn 2-y} O 4-δ ( where, 0 <x <1.1,0.45 <y <0. In a non-aqueous electrolyte secondary battery which is a lithium-nickel-manganese composite oxide represented by 55, 0 ≦ δ <0.4), the non-aqueous electrolyte contains a cyclic carbonate and a chain carbonate, and the cyclic carbonate or In a non-aqueous electrolyte secondary battery in which at least one of the chain carbonates contains a fluorine element, the oxidative decomposition reaction of the non-aqueous solvent under high voltage is suppressed. ”(Paragraph [0015]),“ As a result, The problem of depletion of the electrolyte due to oxidative decomposition of the electrolyte under high voltage at the positive electrode, which is peculiar to 5V class batteries, has been improved, and the charge / discharge cycle performance has been improved. A non-aqueous electrolyte secondary battery can be obtained. Therefore, the industrial value of the present invention is extremely large. ”(Paragraph [0016]).
Then, in the examples, fluorinated ethylene carbonate (FEC) is used as the cyclic carbonate containing the above-mentioned fluorine element, and fluorinated ethyl methyl carbonate (TFEMC) is used as the above-mentioned chain carbonate containing the fluorine element. Non-aqueous electrolytes with = 4: 6 (vol ratio) (see paragraphs [0043], [0044], [0048], [0051] Table 1 Examples 5 and 6) and the like are shown.

Patent Document 3 describes "providing a non-aqueous electrolyte solution for a secondary battery having excellent discharge load characteristics, high temperature storage characteristics, and cycle characteristics" (paragraph [0006]), and "storing ions and storing ions". Non-aqueous electrolyte solution including a negative electrode and a positive electrode that can be released and a non-aqueous electrolyte solution A non-aqueous electrolyte solution used in a secondary battery, wherein the non-aqueous electrolyte solution has an electrolyte and a non-aqueous solvent, and the non-aqueous electrolyte solution. A non-aqueous electrolyte solution in which the solvent contains a carbonate having a halogen atom and also contains a monofluorophosphate and / or a difluorophosphate. ”(Claim 1),“ Halogen atom The carbonates contained are fluoroethylene carbonate, 4,4-difluoroethylene carbonate, 4,5-difluoroethylene carbonate, 4-fluoro-4-methylethylene carbonate, 4-fluoro-5-methylethylene carbonate, 4- (fluoromethyl). The non-aqueous electrolyte solution according to claim 1 or 2, wherein the compound is at least one selected from the group consisting of −ethylene carbonate and 4- (trifluoromethyl) -ethylene carbonate. ”(Claim. Item 3), "The carbonate having a halogen atom is fluoromethylmethyl carbonate, bis (fluoromethyl) carbonate, difluoromethylmethyl carbonate, 2,2-difluoroethylmethyl carbonate, ethyl- (2,2-difluoroethyl) carbonate, Bis (2,2-difluoroethyl) carbonate, 2,2,2-trifluoroethyl methyl carbonate, ethyl- (2,2,2-trifluoroethyl) carbonate, bis (2,2,2-trifluoroethyl) The invention of the non-aqueous electrolyte solution according to claim 1 or 4, which is at least one compound selected from the group consisting of carbonates "(claim 5).

Further, Patent Document 3 describes that "... 4.4V-CCCV (0.05C cut) charging was performed, and then high temperature storage was performed under the conditions of 85 ° C. for 24 hours" (. Paragraph, [0411]).
Then, in the examples, fluoroethylene carbonate + ethyl methyl carbonate + ethyl (2,2-difluoroethyl) carbonate (38.4: 60.6: 1.0), fluoroethylene carbonate + ethyl methyl carbonate + ethyl (2). , 2-Difluoroethyl) carbonate (38.1: 51.6: 10.3), fluoroethylene carbonate + ethylmethyl carbonate + bis (2,2,2-trifluoroethyl) carbonate (37.2: 50.3) 12.5), ethylene carbonate + ethyl methyl carbonate + ethyl- (2,2,2-trifluoroethyl) carbonate (35.4: 63.6: 1.0), ethylene carbonate + ethyl methyl carbonate + ethyl- Non-aqueous solvents (% by mass) such as (2,2,2-trifluoroethyl) carbonate (35.0: 54.0: 11.0) are shown.

Patent Document 4 states that "providing a positive electrode active material for a non-aqueous electrolyte secondary battery that suppresses gas generation during charge storage and metal elution at the positive electrode without impairing the discharge rate characteristics" (paragraph [0005]). The subject is "a non-aqueous electrolyte secondary battery provided with a non-aqueous electrolyte containing a non-aqueous solvent, wherein the non-aqueous solvent is fluoroethylene carbonate, difluorobutylene carbonate, fluorinated chain carbonate and fluorinated. A non-aqueous electrolyte secondary battery containing at least one of the chain carboxylic acid esters, the total content of which is more than 50% by volume based on the total volume of the non-aqueous solvent. "(Claim 1). The invention is described.

Further, Patent Document 4 states that "the end-of-charge voltage is not particularly limited, but is preferably 4.4 V or higher, more preferably 4.5 V, and particularly preferably 4.5 to 5.0 V. The composition of the non-aqueous solvent described below is particularly suitable for high voltage applications where the battery voltage is 4.4 V or higher "(paragraph [0009]).
Then, in the examples, "4-fluoroethylene carbonate (FEC), trans-4,5-difluoro-4,5-dimethyl-1,3-dioxolan-2-one (DFBC), 2,2, 2-Trifluoroethyl methyl carbonate (FEMC) was adjusted to a volume ratio of 10:15:75, and LiPF ₆ was added to this solvent at a volume ratio of 1.0 mol / l to prepare a non-aqueous electrolyte. (Paragraph [0038]) (Example 1), "Same as in Example 1 except that methyl 3,3,3-trifluoropropionate (FMP) was used instead of FEMC" (paragraph [0040]]. ) To prepare a non-aqueous electrolyte (Example 2), "Part of FMP was replaced with ethyl methyl carbonate (EMC), and the volume ratio was changed to FEC: DFSC: FMP: EMC = 10: 15: 45: 30. A non-aqueous electrolyte was prepared in the same manner as in Example 2 (“Example 1” seems to be an erroneous description of “Example 2”) ”(paragraph [0041]) except that the non-aqueous electrolyte was prepared so as to be. Example 3) etc. are shown.

JP-A-11-40195 Japanese Unexamined Patent Publication No. 2005-78820 Japanese Unexamined Patent Publication No. 2008-277000 Japanese Unexamined Patent Publication No. 2015-11549

The invention described in Patent Document 1 is referred to as 2,2,2-trifluoroethylmethyl carbonate (hereinafter referred to as "TFEMC") for the purpose of providing a non-aqueous electrolyte secondary battery that is safe and has excellent characteristics. ) Is used, but it is not intended to improve high rate discharge performance at high voltage, and ethyl methyl carbonate (hereinafter referred to as "EMC") and fluoroethylene carbonate (hereinafter referred to as "EMC") are used. , "FEC") is not specifically described.
The invention described in Patent Document 2 uses a mixed solvent of FEC and TFEMC for the purpose of improving the charge / discharge cycle performance of the high-voltage non-aqueous electrolyte secondary battery, but improves the high-rate discharge performance. It is not intended to contain EMC, and it is not described that it contains EMC.
The invention described in Patent Document 3 has an object of providing a non-aqueous electrolyte solution for a secondary battery having excellent discharge load characteristics, high temperature storage characteristics, and cycle characteristics, and a halogen atom in a non-aqueous solvent of the electrolytic solution. However, there is no example in which TFEMC is contained as a non-aqueous solvent for a non-aqueous electrolyte secondary battery used at a high voltage.
Patent Document 4 describes a mixture of FEC, DFBC, and TFEMC in a solvent for a non-aqueous electrolyte secondary battery, with an object of suppressing gas generation during charge storage and metal elution at the positive electrode without impairing the discharge rate characteristics. Although it has been shown to use a solvent, it has not been shown to use a solvent containing EMC and TFEMC to improve high rate discharge performance at high voltages.
As described above, the charge / discharge cycle performance can be improved by using a mixed solvent of FEC and TFEMC at a high voltage (for example, 4.4 V (vs. Li ^/ Li ⁺ ) or more at the positive electrode potential). However, there is a problem that the high rate discharge performance is lowered.
Therefore, in view of the above problems, it is an object of the present invention to provide a non-aqueous electrolyte secondary battery capable of improving high rate discharge performance at high voltage by improving the non-aqueous solvent of the non-aqueous electrolyte. To do.

In the present invention, the following means are adopted in order to solve the above problems.
(1) Non-aqueous electrolyte solution containing a non-aqueous solvent and an electrolyte salt A non-aqueous electrolyte solution for a secondary battery, wherein the non-aqueous solvent uses EMC and TFEMC as main solvents, and EMC: TFEMC = 80 on a volume basis. : 20-60: a proportion of 40 (however, the following (a), excluding those falling under (b).).
(A) The non-aqueous solvent contains 3% by volume or more of a fluorine-containing cyclic carbonate and contains 0.1 to 40 parts by volume of a fluorine-containing unsaturated hydrocarbon compound with respect to 100 parts by volume of the fluorine-containing cyclic carbonate.
(B) The non-aqueous electrolyte solution contains fluoroethylene carbonate (FEC), ethyl methyl carbonate (EMC), 2,2,2-trifluoroethyl methyl carbonate (TFEMC), flame retardant, and lithium salt (2). ) Non-aqueous electrolytic solution according to (1) The non-aqueous electrolytic solution for a secondary battery, wherein the non-aqueous solvent contains FEC.
(3) A non-aqueous electrolytic solution secondary battery including a positive electrode, a negative electrode, and a non-aqueous electrolytic solution, wherein the non-aqueous electrolytic solution is the non-aqueous electrolytic solution according to (1) or (2).
(4) In the non-aqueous electrolyte secondary battery of the above (3), the positive electrode potential is 4.4 V (vs. Li ^/ Li ⁺ ) or more.

In the present invention, by using a non-aqueous electrolytic solution containing a non-aqueous solvent in which EMC and TFEMC are mixed at a specific ratio, the non-aqueous electrolytic solution secondary battery is subjected to a high voltage (for example, a positive electrode potential of 4.4 V (vs)). It is possible to improve the high rate discharge performance when charging to a voltage (Li / Li ⁺ ) or higher).

External perspective view showing an embodiment of a non-aqueous electrolyte secondary battery according to the present invention. Schematic diagram showing a power storage device including a plurality of non-aqueous electrolyte secondary batteries according to the present invention.

FIG. 1 shows an external perspective view of a rectangular non-aqueous electrolyte secondary battery 1 which is an embodiment of the non-aqueous electrolyte secondary battery according to the present invention. The figure is a perspective view of the inside of the container. In the non-aqueous electrolyte secondary battery 1 shown in FIG. 1, the electrode group 2 is housed in the battery container 3. The electrode group 2 is formed by winding a positive electrode having a positive electrode active material and a negative electrode having a negative electrode active material through a separator. The positive electrode is electrically connected to the positive electrode terminal 4 via the positive electrode lead 4', and the negative electrode is electrically connected to the negative electrode terminal 5 via the negative electrode lead 5'.

Here, the non-aqueous electrolyte solution held in the separator contains a non-aqueous solvent and an electrolyte salt dissolved in the non-aqueous solvent. In the present invention, the non-aqueous solvent contains EMC and TFEMC as main solvents. It is characterized in that it is contained in a ratio of EMC: TFEMC = 80:20 to 60:40 on a volume basis.

In the present invention, the non-aqueous solvent contains EMC and TFEMC as main solvents, and contains EMC in an amount of 60 to 80% by volume and TFEMC in a proportion of 20 to 40% by volume.
When the content of EMC in the mixed solvent of EMC and TFEMC is less than 60% by volume or more than 80% by volume, or when the content of TFEMC is less than 20% by volume or more than 40% by volume. Deteriorates high rate discharge performance at high voltage. By setting the EMC content to 60 to 80% by volume and the TFEMC content to 20 to 40% by volume, high rate discharge performance at a high voltage of 4.4 V (vs. Li ^/ Li ⁺ ) or more at the positive electrode potential. The decrease is suppressed.

The FEC is preferably contained in a non-aqueous solvent at high voltage in order to improve the charge / discharge cycle characteristics at 45 ° C. However, if the amount is too large, the thickness of the battery increases significantly due to gas generation, so it is preferably 20% by mass or less of the total non-aqueous solvent. More preferably, it is 5 to 10% by mass of the total non-aqueous solvent.

In the present invention, since the non-aqueous solvent contains EMC and TFEMC as main solvents, the content of both is preferably 80% by mass or more, preferably 90% by mass or more in the total solvent. Is more preferable. A small amount of non-aqueous solvent other than EMC, TFEMC, and FEC may be contained as long as the effects of the present invention are not impaired. As the other non-aqueous solvent, a non-aqueous solvent generally used for the non-aqueous electrolyte solution of the non-aqueous electrolyte secondary battery can be used. For example, cyclic carbonates such as propylene carbonate, ethylene carbonate, butylene carbonate, chloroethylene carbonate, styrene carbonate, catechol carbonate, 1-phenylvinylene carbonate, 1,2-diphenylvinylene carbonate, vinylene carbonate, vinylethylene carbonate, trifluoropropylene carbonate and the like. , Cyclic carboxylic acid esters such as γ-butyrolactone, γ-valerolactone, propiolactone, chain carbonates such as dimethyl carbonate, diethyl carbonate, diphenyl carbonate, chain carboxylic acid esters such as methyl acetate and methyl butyrate, tetrahydrofuran or its like. Derivatives, ethers such as 1,3-dioxane, dimethoxyethane, diethoxyethane, methoxyethoxyethane, methyl diglyme, nitriles such as acetonitrile and benzonitrile, dioxalane or a derivative thereof, etc. alone or a mixture of two or more thereof. Etc. can be mentioned.

The electrolyte salt contained in the non-aqueous electrolyte solution of the present invention is not limited, and an electrolyte salt generally used for a non-aqueous electrolyte secondary battery can be used. For example, lithium (Li) such as LiClO ₄ , LiBF ₄ , LiAsF ₆ , LiPF ₆ , LiSCN, LiBr, LiI, Li ₂ SO ₄ , Li ₂ B ₁₀ Cl ₁₀ , NaClO ₄ , NaI, NaSCN, NaBr, KClO ₄ , KSCN and the like. ), Inorganic ionic salt containing one of sodium (Na) or potassium (K), LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiN (C ₂ F ₅ SO ₂ ) ₂ , LiN (CF ₃ SO) ₂ ) (C ₄ F ₉ SO ₂ ), LiC (CF ₃ SO ₂ ) ₃ , LiC (C ₂ F ₅ SO ₂ ) ₃ , (CH ₃ ) ₄ NBF ₄ , (CH ₃ ) ₄ NBr, (C ₂ H) ₅ ) ₄ NClo ₄ , (C ₂ H ₅ ) ₄ NI, (C ₃ H ₇ ) ₄ NBr, (n-C ₄ H ₉ ) ₄ NC Lo ₄ , (n-C ₄ H ₉ ) ₄ NI, (C ₂₎ H ₅ ) ₄ N-malate, (C ₂ H ₅ ) ₄ N-benzoate, (C ₂ H ₅ ) ₄ N-phthate, lithium stearyl sulfonate, lithium octyl sulfonate, lithium dodecylbenzene sulfonate and other organic ionic salts Etc., and these ionic compounds can be used alone or in combination of two or more.

The concentration of the electrolyte salt in the non-aqueous electrolyte solution is preferably 0.1 mol / l to 5.0 mol / l in order to surely obtain a non-aqueous electrolyte secondary battery having excellent high rate discharge performance. More preferably, it is 0 mol / l to 2.0 mol / l.

The positive electrode active material used for the positive electrode constituting the non-aqueous electrolyte secondary battery of the present invention is electrochemically capable of inserting and removing lithium ions, and has a positive electrode potential of 4.4 V (vs. Li ^/ Li ^+). ) The above is preferable, and lithium transition metal composite oxides, polyanionic compounds, etc., which are generally used as positive electrode active materials for non-aqueous electrolyte secondary batteries, can be used. Examples of the lithium transition metal composite oxide include a lithium nickel manganese composite oxide and a lithium nickel cobalt manganese composite oxide. The lithium-nickel-manganese composite oxide, for _example, LiNi _{0.5 Mn} 1.5 _Li x of _{O 4} or the like _{Ni y Mn 2-y O 4} -δ (0 <x <1.1,0.45 <y < 0.55, 0 ≦ δ <0.4), LiMeO ₂ (Me is a transition metal containing Ni and Mn) such as LiNi _1/2 Mn _1/2 O ₂ , or Li _1.11 Ni _0.29 Mn. Li _{1 + α} Me _1-α O ₂ (0 <α, Me is a transition metal containing Ni and Mn) such as _0.60 O ₂ (Li / Me = 1.25), as a lithium nickel cobalt manganese composite oxide For example, LiMeO ₂ (Me is a transition metal containing Ni, Co and Mn) such as LiNi _1/3 Co _1/3 Mn _1/3 O ₂ , or Li _1.09 Co _0.11 Ni _0.18 Mn _{0. 62} O ₂ (Li / Me = 1.2), Li _1.11 Co _0.11 Ni _0.18 Mn _0.60 O ₂ (Li / Me = 1.25), etc. Li _{1 + α} Me _1-α O ₂ (0 <α, Me is a transition metal containing Ni, Co and Mn) can be used. As the polyanion compound, for example, LiNiPO ₄ , LiCoPO ₄ , Li ₂ CoPO ₄ F, Li ₂ MnSiO _{4 and the} like can be used.

The negative electrode active material used for the negative electrode constituting the non-aqueous electrolyte secondary battery of the present invention is one capable of electrochemically inserting and removing lithium ions, and has a positive electrode potential of 4.4 V (vs. Li /). It is preferable that it can be used at a high voltage in combination with a positive electrode having Li ⁺ ) or higher, and a carbonaceous material generally used as a negative electrode active material of a non-aqueous electrolyte secondary battery, a metal oxide such as tin oxide or silicon oxide, A metal composite oxide, a lithium alloy such as lithium alone or a lithium aluminum alloy, a metal capable of forming an alloy with lithium such as Sn or Si, or the like can be used. Examples of the carbonaceous material include natural graphite, artificial graphite, cokes, non-graphitizable carbon, low-temperature calcinable graphitizable carbon, fullerene, carbon nanotubes, carbon black, activated carbon and the like. These may be used alone or in any combination and ratio of two or more. Of these, carbonaceous materials are preferable from the viewpoint of safety.

It is desirable that the powder of the positive electrode active material and the negative electrode active material has an average particle size of 100 μm or less. In particular, the powder of the positive electrode active material is preferably 10 μm or less for the purpose of improving the high output characteristics of the non-aqueous electrolyte battery. A crusher or a classifier is used to obtain the powder in a predetermined shape. For example, a mortar, a ball mill, a sand mill, a vibrating ball mill, a planetary ball mill, a jet mill, a counter jet mill, a swirling airflow type jet mill, a sieve, or the like is used. At the time of pulverization, wet pulverization in which water or an organic solvent such as hexane coexists can also be used. The classification method is not particularly limited, and a sieve, a wind power classifier, or the like is used as needed for both dry and wet types.

The positive electrode active material and the negative electrode active material, which are the main constituents of the positive electrode and the negative electrode, have been described in detail above. A filler or the like may be contained as another constituent component.

The conductive agent is not limited as long as it is an electronically conductive material that does not adversely affect the battery performance, but is usually natural graphite (scaly graphite, scaly graphite, earthy graphite, etc.), artificial graphite, carbon black, acetylene black, etc. Conductive materials such as Ketjen black, carbon whisker, carbon fiber, metal (copper, nickel, aluminum, silver, gold, etc.) powder, metal fiber, conductive ceramic material, etc. can be included as one kind or a mixture thereof. ..

Among these, acetylene black is preferable as the conductive agent from the viewpoint of electron conductivity and coatability. The amount of the conductive agent added is preferably 0.1% by weight to 50% by weight, particularly preferably 0.5% by weight to 30% by weight, based on the total weight of the positive electrode or the negative electrode. In particular, it is desirable to use acetylene black pulverized into ultrafine particles of 0.1 to 0.5 μm because the required carbon amount can be reduced. These mixing methods are physical mixing, and the ideal is uniform mixing. Therefore, powder mixers such as V-type mixers, S-type mixers, scouring machines, ball mills, and planetary ball mills can be mixed dry or wet.

Examples of the binder include thermoplastic resins such as polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), polyethylene and polypropylene, ethylene-propylene-dienter polymer (EPDM), sulfonated EPDM and styrene butadiene. A polymer having rubber elasticity such as rubber (SBR) and fluororubber can be used as one kind or a mixture of two or more kinds. The amount of the binder added is preferably 1 to 50% by weight, particularly preferably 2 to 30% by weight, based on the total weight of the positive electrode or the negative electrode.

As the filler, a material that does not adversely affect the battery performance can be used. Usually, olefin polymers such as polypropylene and polyethylene, amorphous silica, alumina, zeolite, glass, carbon and the like are used. The amount of the filler added is preferably 30% by weight or less with respect to the total weight of the positive electrode or the negative electrode.

For the positive electrode and the negative electrode, the main components (positive electrode active material for the positive electrode, negative electrode active material for the negative electrode) and other materials are kneaded to form a mixture, which is mixed with an organic solvent such as N-methylpyrrolidone or toluene or water. After that, the obtained mixed solution is coated on a current collector described in detail below, or crimped and heat-treated at a temperature of about 50 ° C. to 250 ° C. for about 2 hours to be suitably produced. To. Regarding the coating method, for example, it is preferable to apply to any thickness and any shape by using means such as roller coating such as an applicator roll, screen coating, doctor blade method, spin coating, and bar coater. It is not limited.

The materials of the positive electrode current collector and the negative electrode current collector are not particularly limited, and known materials can be used.
Examples of the positive electrode current collector include metal materials such as aluminum, stainless steel, nickel plating, titanium and tantalum, and carbonaceous materials such as carbon cloth and carbon paper. Of these, metal materials, especially aluminum, are preferable.
Examples of the negative electrode current collector include metal materials such as copper, nickel, stainless steel, and nickel-plated steel. Of these, copper is preferable in terms of ease of processing and cost.

As the separator, it is preferable to use a microporous membrane, a non-woven fabric, or the like alone or in combination. Examples of the material constituting the separator include polyolefin resins typified by polyethylene and polypropylene, polyester resins typified by polyethylene terephthalate and polybutylene terephthalate, polyvinylidene fluoride, and vinylidene fluoride-hexafluoropropylene copolymers. , Vinylidene Fluoride-Perfluorovinyl Ether Copolymer, Vinylidene Fluoride-Tetrafluoroethylene Copolymer, Vinylidene Fluoride-Trifluoroethylene Copolymer, Vinylidene Fluoride-Fluoroethylene Copolymer, Vinylidene Fluoride-Hexafluoro Alpine copolymer, vinylidene fluoride-ethylene copolymer, vinylidene fluoride-propylene copolymer, vinylidene fluoride-trifluoropropylene copolymer, vinylidene fluoride-tetrafluoroethylene-hexafluoropropylene copolymer, foot Examples thereof include vinylidene compound-ethylene-tetrafluoroethylene copolymer and the like. Above all, a microporous film containing a polyolefin resin typified by polyethylene, polypropylene or the like as a main component is preferable.

Other components of the battery include terminals, an insulating plate, a battery case, and the like, but those that have been conventionally used may be used as they are.

The shape of the non-aqueous electrolyte secondary battery according to the present invention is not particularly limited, and examples thereof include a cylindrical battery, a square battery (rectangular battery), and a flat battery. The present invention can also be realized as a power storage device including a plurality of the above-mentioned non-aqueous electrolyte secondary batteries. An embodiment of the power storage device is shown in FIG. In FIG. 2, the power storage device 30 includes a plurality of power storage units 20. Each power storage unit 20 includes a plurality of non-aqueous electrolyte secondary batteries 1. The power storage device 30 can be mounted as a power source for automobiles such as electric vehicles (EV), hybrid electric vehicles (HEV), and plug-in hybrid vehicles (PHEV).

Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples as long as the gist of the present invention is not exceeded.

(Non-aqueous electrolyte solutions 1 and 2 of the present invention)
In a mixed solvent containing EMC and TFEMC of EMC: TFEMC = 80:20 and 60:40, respectively, in volume ratio, LiPF ₆ as an electrolyte salt was dissolved at a concentration of 1.2 mol / l, and FEC was dissolved therein. The non-aqueous electrolyte solution to which 5.5% by mass is added is referred to as the non-aqueous electrolyte solution 1 and 2 of the present invention.

(Comparative non-aqueous electrolytes 1 to 4)
LiPF ₆ as an electrolyte salt was dissolved at a concentration of 1.2 mol / l in a mixed solvent containing EMC and TFEMC at EMC: TFEMC = 40: 60 and 20:80, respectively, in terms of volume ratio, and FEC was dissolved therein. The non-aqueous electrolyte solution to which 5.5% by mass is added is referred to as the non-aqueous electrolyte solution 1 and 2 of the present invention.
A non-aqueous electrolyte solution prepared by dissolving LiPF ₆ as an electrolyte salt in TFEMC at a concentration of 1.2 mol / l and adding 7.5% by mass of FEC to the solution is used as a comparative non-aqueous electrolyte solution 3.
A non-aqueous electrolyte solution in which LiPF ₆ as an electrolyte salt is dissolved in EMC at a concentration of 1.2 mol / l and 7.5% by mass of FEC is added thereto is used as a comparative non-aqueous electrolyte solution 4.

(Making a positive electrode plate)
As the positive electrode active material, a lithium transition metal composite oxide represented by LiNi _1/3 Co _1/3 Mn _1/3 O ₂ was used. Positive electrode by mass ratio Positive electrode containing active material: polyvinylidene fluoride (PVdF): acetylene black (AB) = 93: 4: 3 (solid matter equivalent) and using N-methylpyrrolidone (NMP) as a solvent. A paste was prepared, and the positive electrode paste was applied to both sides of a strip-shaped aluminum foil current collector having a thickness of 15 μm so that the positive electrode active material was contained at 17 mg / cm ² per unit electrode area. This was pressed by a roller press to form a positive electrode active material layer, and then dried under reduced pressure at 100 ° C. for 14 hours to remove water in the electrode plate. The positive electrode plate was produced in this way.

(Manufacturing of negative electrode plate)
Graphite was used as the negative electrode active material. A negative electrode paste containing graphite: styrene-butadiene rubber (SBR): carboxymethyl cellulose (CMC) = 97: 2: 1 (in terms of solid content) in terms of mass ratio and using water as a solvent was prepared, and the thickness was 10 μm. It was applied to both sides of the strip-shaped copper foil current collector. This was pressed by a roller press to form a negative electrode active material layer, and then dried under reduced pressure at 100 ° C. for 12 hours to remove water in the electrode plate. The negative electrode plate was produced in this way.

(Manufacturing of non-aqueous electrolyte secondary battery)
<Assembly process>
The positive electrode plate and the negative electrode plate are laminated via a separator made of a polyethylene microporous membrane and wound into a flat shape to prepare an electrode group 2 as shown in FIG. 1 and stored in an aluminum battery container 3. Then, the positive and negative electrodes 4 and 5 were attached. The non-aqueous electrolytes 1 and 2 of the present invention and the comparative electrolytes 1 to 4 were injected into the battery container 3 and then sealed. In this way, the non-aqueous electrolyte secondary battery was assembled.

<Initial charge / discharge process>
The non-aqueous electrolyte secondary battery assembled as described above was subjected to a two-cycle initial charge / discharge step at a temperature of 25 ° C. All voltage controls were performed with respect to the voltage between the positive and negative terminals. The charging in the first cycle was a constant current constant voltage charge with a current of 0.2 CmA and a voltage of 4.35 V for 8 hours, and the discharge was a constant current discharge with a current of 0.2 CmA and a final voltage of 2.75 V. The charging in the second cycle was a constant current constant voltage charge with a current of 1.0 CmA and a voltage of 4.35 V for 3 hours, and the discharge was a constant current discharge with a current of 1.0 CmA and a final voltage of 2.75 V. A 10 minute rest period was set after charging and discharging in all cycles. In this way, a non-aqueous electrolyte secondary battery was produced. The non-aqueous electrolyte secondary batteries using the non-aqueous electrolytes 1 and 2 and the comparative electrolytes 1 to 4 of the present invention have initial discharge capacities of 159, 161 and 161, 162, 159 and 160 mAh / g, respectively. It was.

(Each rate discharge test)
A non-aqueous electrolyte secondary battery provided with the non-aqueous electrolytes 1 and 2 of the present invention and comparative non-aqueous electrolytes 1 to 4 produced as described above was subjected to a discharge test at each rate at a temperature of 25 ° C. , The transition of the discharge capacity was investigated. All voltage controls were performed with respect to the voltage between the positive and negative terminals. Charging is a constant current constant voltage charge with a current of 1 CmA and a voltage of 4.35 V for 3 hours, and discharge is a final voltage of 2 at a rate of 5 steps with current values of 0.2 CmA, 0.5 CmA, 1 CmA, 2 CmA, and 5 CmA. A constant current discharge of .75 V was used. Then, the ratio of the discharge capacity at each rate to the discharge capacity at 1 CmA was defined as the discharge capacity retention rate. Here, it is known that when graphite is used for the negative electrode, the value of the positive electrode potential (vs. Li ^/ Li ⁺ ) is about 0.1 V larger than the value of the voltage between terminals. The results of the discharge test at each of the above rates are shown in Table 1.

From Table 1, the following can be seen.
The battery using the comparative non-aqueous electrolyte solution 3 in which the main solvent is only TFEMC has a high discharge capacity when discharging up to a current value of 1 CmA, but the discharge capacity retention rate starts to decrease sharply when the current value reaches 2 CmA, and 5 CmA. Then, it was less than 20% in the case of 1 CmA. The non-aqueous electrolyte battery using the comparative non-aqueous electrolytes 1 and 2 having a volume ratio EMC: TFEMC of the main solvent of 40:60 and 20:80 has a slightly lower discharge capacity retention rate at 2 CmA and at 5 CmA. It dropped sharply. The battery using the comparative non-aqueous electrolyte solution 4 in which the main solvent was only EMC had a discharge capacity retention rate of about the same as that of the battery using the non-aqueous electrolyte solution of the present invention up to 2 CmA, but decreased at 5 CmA. ..
On the other hand, the volume ratio EMC: TFEMC of the main solvent is 80:20 and 60:40, and the battery using the non-aqueous electrolytes 1 and 2 of the present invention containing FEC has a positive electrode potential of 4.4 V (vs). Even with a high voltage of .Li / Li ⁺ ) or higher and a high rate of current value of 5 CmA, a good discharge capacity retention rate of about 70% was shown at 1 CmA.
5 CmA corresponds to a high current value that flows when the accelerator is depressed in an electric vehicle battery or the like, and the non-aqueous electrolyte secondary battery using the non-aqueous electrolyte of the present invention has such a high rate. It can be said that the high rate discharge performance is excellent.

(Explanation of sign)
1 Non-aqueous electrolyte secondary battery 2 Electrode group 3 Battery container 4 Positive terminal 4'Positive lead 5 Negative terminal 5'Negative lead 20 Power storage unit 30 Power storage device

Since the non-aqueous electrolyte secondary battery according to the present invention is excellent in high rate discharge performance, it is useful as a power source for automobiles such as electric vehicles, hybrid vehicles, and plug-in hybrid vehicles.

Claims (4)

Non-aqueous electrolyte solution containing a non-aqueous solvent and an electrolyte salt A non-aqueous electrolyte solution for a secondary battery, wherein the non-aqueous solvent is ethyl methyl carbonate (EMC) and 2,2,2-trifluoroethyl methyl carbonate (TFEMC). ) As the main solvent and containing EMC: TFEMC = 80: 20 to 60:40 on a volume basis. Non-aqueous electrolyte Non-aqueous electrolyte for secondary batteries (However, in the following (a) and (b) Except for applicable items . )
(A) The non-aqueous solvent contains 3% by volume or more of a fluorine-containing cyclic carbonate and contains 0.1 to 40 parts by volume of a fluorine-containing unsaturated hydrocarbon compound with respect to 100 parts by volume of the fluorine-containing cyclic carbonate.
(B) The non-aqueous electrolyte solution contains fluoroethylene carbonate (FEC), ethyl methyl carbonate (EMC), 2,2,2-trifluoroethyl methyl carbonate (TFEMC), flame retardant, and lithium salt. The non-aqueous electrolyte solution for a secondary battery according to claim 1, wherein the non-aqueous solvent contains fluoroethylene carbonate (FEC). A non-aqueous electrolyte secondary battery including a positive electrode, a negative electrode, and a non-aqueous electrolyte, wherein the non-aqueous electrolyte is the non-aqueous electrolyte according to claim 1 or 2. Next battery. The non-aqueous electrolyte secondary battery according to claim 3, wherein the positive electrode potential is 4.4 V (vs. Li ^/ Li ⁺ ) or more.

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