JP4652984B2 - Electronic equipment with built-in non-aqueous secondary battery - Google Patents

Description

  The present invention relates to an electronic device incorporating a non-aqueous secondary battery excellent in safety.

  Non-aqueous secondary batteries typified by lithium ion secondary batteries have a large capacity, high voltage, high energy density, and high output, and therefore there is an increasing demand. And further increase in capacity and increase in charge voltage of non-aqueous secondary batteries are also being studied, and further increase in discharge capacity is expected by increasing the amount of charge of the battery.

By the way, when increasing the capacity of a non-aqueous secondary battery, the amount of heat generated by the battery increases during overcharging, the battery tends to run out of heat, and a reduction in battery safety becomes a problem. As means for solving this problem, as disclosed in Patent Document 1, Patent Document 2, Patent Document 3, Patent Document 4, and the like, it is effective to contain an aromatic compound in the electrolytic solution.
JP-A-5-36439 JP-A-7-302614 Japanese Patent Laid-Open No. 9-50822 JP-A-10-275632

  However, when an aromatic compound is contained in the electrolytic solution, a film that suppresses reaction with the electrolytic solution is formed on the surface of the active material of the positive electrode or the negative electrode. There has been a problem that the battery characteristics such as the discharge capacity are deteriorated in a discharge with a large current as compared with a battery using an electrolytic solution not containing an aromatic compound. In particular, when the aromatic compound is contained in an amount of 2% by mass or more with respect to the total mass of the electrolyte in order to improve the safety during overcharge to a certain level or more, the above-described deterioration in battery characteristics may be noticeable. It was.

Electronic devices of the present invention comprises a positive electrode, a negative electrode, comprising a separator, and a non-aqueous electrolyte solution, an electronic device with a built-in non-aqueous secondary battery formed in rectangular shapes or laminate shape, the non The water secondary battery is pressed in the thickness direction, and the positive electrode and the negative electrode are stacked via the separator to form an electrode laminate, and the non-aqueous electrolyte is based on the total mass of the electrolyte. The separator has an MD direction and a TD direction, the thermal shrinkage rate at 150 ° C. in the TD direction is 30% or less, and the thickness of the separator 5 to 20 μm, air permeability is 500 seconds / 100 ml or less, charged to 4.25 V at 0.2 C, and then charged at 4.25 V for 7 hours, followed by explosion-proof thermostat The temperature is increased from 20 ° C to 150 ° C at a rate of 5 ° C / min. Warmed, and wherein the maximum temperature of the surface temperature of the battery during the test to hold for 60 minutes battery 0.99 ° C. is 165 ° C. or less.

  In order to solve the above-mentioned problems, the present inventors have conducted various studies on the configuration of a non-aqueous secondary battery containing an aromatic compound in an electrolytic solution. As a result, the separator has a thickness of 5 to 20 μm. Thus, it has been found that the use of a battery having an air permeability of 500 seconds / 100 ml or less can achieve both the safety and load characteristics of the battery when overcharged.

  Furthermore, by using various separators that satisfy the above-described configuration, a non-aqueous secondary battery including an electrode laminate in which a positive electrode and a negative electrode are laminated via a separator and a non-aqueous electrolyte is manufactured, and storage characteristics at high temperatures are obtained. investigated. As a result, it has been clarified that some batteries generate an internal short circuit when they are held in a high temperature environment. That is, when the battery is left in a temperature environment of about 150 ° C., the positive electrode and the negative electrode are in direct contact with each other at the end of the electrode due to the shrinkage of the separator, causing a short circuit, and the temperature of the battery is greatly increased. It was found that this could result in This is because when the thickness of the separator is reduced to 20 μm or less, thermal contraction of the separator is likely to occur even if it is sandwiched between the positive electrode and the negative electrode. It turned out to be more strictly limited. In particular, in a situation where the battery is built in an electronic device and used, heat generated inside the battery during charging is hardly released to the outside, and the temperature of the battery unexpectedly increases. The inventors have found that the stability of the battery under a temperature environment of about 150 ° C. is important, and have reached the present invention.

  In addition to the additive for the electrolytic solution, the present inventors have also examined a more effective mounting form of the battery in an electronic device using a non-aqueous secondary battery.

  Embodiments of the present invention will be described below. One form of the non-aqueous secondary battery used in the present invention is a non-aqueous secondary battery including a positive electrode, a negative electrode, a separator, and a non-aqueous electrolyte, and the positive electrode and the negative electrode are stacked via a separator. The non-aqueous electrolyte contains 2 to 15% by mass of an aromatic compound with respect to the total mass of the electrolyte, and the separator has an MD direction and a TD direction, The thermal shrinkage rate at 150 ° C. in the TD direction is 30% or less, the thickness is 5 to 20 μm, and the air permeability is 500 seconds / 100 ml or less.

  With this configuration, it is possible to provide a non-aqueous secondary battery that is excellent in safety and load characteristics and excellent in high-temperature storage.

As the aromatic compound contained in the non-aqueous electrolyte, a compound capable of forming a film on the surface of the active material of the positive electrode or the negative electrode in the battery can be used. Specifically, for example, cyclohexylbenzene, isopropylbenzene , T-butylbenzene, octylbenzene, toluene, xylene, etc., compounds having an alkyl group bonded to an aromatic ring, or halogen groups bonded to an aromatic ring, such as fluorobenzene, difluorobenzene, trifluorobenzene, chlorobenzene, etc. In addition to compounds or compounds in which an alkoxy group is bonded to an aromatic ring such as anisole, fluoroanisole, dimethoxybenzene, diethoxybenzene, etc., phthalates such as dibutyl phthalate and di-2-ethylhexyl phthalate, and benzoates Aromatic carboxylic acid ester, methyl phenyl carbonate, butyl phenyl carbonate, carbonate ester having a phenyl group such as diphenyl carbonate or phenyl propionic acid, and biphenyl. Further, the aromatic compound preferably those that dissolve in the electrolyte, have poor stability at ionic compounds, such as _{LiB (C 6 H 5) 4} , it is preferable that the non-ionic. Among them, a compound in which an alkyl group is bonded to an aromatic ring is preferable, and cyclohexylbenzene is particularly preferably used.

  Furthermore, the aromatic compound may be used alone, but an excellent effect is exhibited by using a mixture of two or more, and in particular, a compound in which an alkyl group is bonded to an aromatic ring, By using in combination with a compound in which a halogen group is bonded to an aromatic ring, particularly preferable results in improving safety can be obtained.

  A method for adding an aromatic compound to the nonaqueous electrolytic solution is not particularly limited, but a method of adding an aromatic compound to the electrolytic solution in advance before assembling the battery is common. When the content of the aromatic compound in the non-aqueous electrolyte is increased, the safety of the battery is improved, but the addition amount exceeds 15% by mass with respect to the total mass of the non-aqueous electrolyte containing the aromatic compound. However, even when a separator having a thickness of 20 μm or less and an air permeability of 500 seconds / 100 ml or less is used, the load characteristics are greatly deteriorated. In addition, when the content of the aromatic compound is less than 2% by mass, a decrease in load characteristics hardly causes a problem, and thus the characteristics of the separator are not particularly limited. Therefore, it is effective to use a separator having a thickness of 20 μm or less and an air permeability of 500 seconds / 100 ml or less for a battery containing an aromatic compound in the range of 2 to 15% by mass in the non-aqueous electrolyte. It is.

  Here, the more preferable range of the content of the aromatic compound is 4% by mass or more from the viewpoint of safety and 10% by mass or less from the viewpoint of load characteristics. When a mixture of two or more aromatic compounds is used, the total amount may be within the above range. Particularly, a compound in which an alkyl group is bonded to an aromatic ring and a compound in which a halogen group is bonded to an aromatic ring are used in combination. In this case, the compound in which an alkyl group is bonded to the aromatic ring is preferably 0.5% by mass or more, more preferably 2% by mass or more, and preferably 8% by mass or less. % Or less is more desirable. On the other hand, the compound having a halogen group bonded to the aromatic ring is preferably 1% by mass or more, more preferably 2% by mass or more, and preferably 12% by mass or less, and 4% by mass or less. Is more desirable.

  Examples of the organic solvent used in the non-aqueous electrolyte include chain esters such as dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, and methyl propionate, chain phosphate triesters such as trimethyl phosphate, and 1,2-dimethoxyethane. 1,3-dioxolane, tetrahydrofuran, 2-methyl-tetrahydrofuran, diethyl ether and the like. In addition, amine organic solvents, sulfur organic solvents such as sulfolane, and the like can also be used. Of these, it is desirable to use a chain carbonate such as dimethyl carbonate, diethyl carbonate, or methyl ethyl carbonate. The amount of these organic solvents is preferably less than 90% by volume and more preferably 80% by volume or less with respect to the total volume of the electrolytic solution. Further, from the viewpoint of load characteristics, 40% by volume or more is desirable, 50% by volume or more is more desirable, and 60% by volume or more is most desirable.

  Furthermore, it is desirable to use an ester having a high dielectric constant (dielectric constant of 30 or more) as a component of other electrolyte solution. Examples of the ester having a high dielectric constant include sulfur esters such as ethylene glycol sulfite together with ethylene carbonate, propylene carbonate, butylene carbonate, γ-butyrolactone, and the like. The ester having a high dielectric constant preferably has a cyclic structure, and a cyclic carbonate such as ethylene carbonate is particularly preferable. The high dielectric constant ester is desirably less than 80% by volume, more desirably 50% by volume or less, and most desirably 35% by volume or less based on the total volume of the electrolytic solution. Further, from the viewpoint of load characteristics, 1% by volume or more is desirable, 10% by volume or more is more desirable, and 25% by volume or more is most desirable.

In order to further enhance the effects of the present invention, it is preferable to dissolve a solvent having a —SO ₂ — bond, particularly a solvent having a —O—SO ₂ — bond, in the electrolytic solution. Examples of the solvent having such —O—SO ₂ — bond include 1,3-propane sultone, methyl ethyl sulfonate, diethyl sulfate and the like. The content is preferably 0.5% by mass or more, more preferably 1% by mass or more, and preferably 10% by mass or less, more preferably 5% by mass or less, based on the total mass of the electrolytic solution.

  The nonaqueous electrolytic solution may contain a polymer component such as polyethylene oxide or polymethyl methacrylate, and may be used as a gel electrolyte.

As the electrolyte of the electrolytic solution, for _{example, LiClO 4, LiPF 6, LiBF} 4, LiAsF 6, LiSbF 6, LiCF 3 SO 3, LiC 4 F 9 SO 3, LiCF 3 CO 2, Li 2 C 2 F 4 (SO 3 ) ₂ , LiN (RfSO ₂ ) (Rf′SO ₂ ), LiN (RfOSO ₂ ) (Rf′OSO ₂ ), LiC (RfSO ₂ ) ₃ , LiC _n F _{2n + 1} SO ₃ (n ≧ 2), LiN ( RfOSO ₂ ) ₂ [wherein Rf and Rf ′ are the same or different fluoroalkyl groups], polymer imide lithium salt and the like are used alone or in admixture of two or more. When these are incorporated into the film on the electrode surface, good ion conductivity can be imparted to the film, and the effect is particularly high when LiPF ₆ is used. The concentration of the electrolyte in the electrolytic solution is not particularly limited, but is preferably 1 mol / l or more because safety is improved, and more preferably 1.2 mol / l or more. Further, if it is less than 1.7 mol / l, the load characteristics are improved, and it is more desirable if it is less than 1.5 mol / l.

  The separator has an MD direction and a TD direction, the thermal shrinkage rate at 150 ° C. in the TD direction is 30% or less, the thickness is 5 to 20 μm, and the air permeability is 500 seconds. / 100ml or less of separator is used. In a non-aqueous secondary battery using a non-aqueous electrolyte containing an aromatic compound in the range of 2 to 15% by mass, in order to obtain good load characteristics, the separator has a thickness of 20 μm or less and its air permeability The degree is required to be 500 seconds / 100 ml or less. Moreover, in order to prevent an internal short circuit in the high temperature state of the battery, the separator needs to have an MD direction and a TD direction, and the thermal shrinkage rate at 150 ° C. in the TD direction is 30% or less. Here, the MD direction refers to a film resin take-off direction at the time of manufacturing the separator, as disclosed in JP 2000-172420 A, and the TD direction refers to a direction orthogonal to the MD direction. . In the present invention, a separator having such directionality is used. The thermal contraction rate in the TD direction was maintained at 150 ° C. by sandwiching a separator of 45 mm length and 60 mm width between two glass plates having a smooth surface of 5 mm thickness, 50 mm length and 80 mm width (mass: 47 g). After standing still in a thermostat bath and holding for 2 hours, the temperature was returned to room temperature (20 ° C.), and the length of shrinkage in the TD direction was compared with the length of the separator before shrinkage.

  The thickness of the separator needs to be 20 μm or less for load characteristics and high capacity, and is preferably as thin as possible. However, in order to maintain good insulation and reduce thermal shrinkage, the thickness of the separator is 5 μm or more. The thickness needs to be 10 μm or more. Further, the air permeability of the separator needs to be 500 seconds / 100 ml or less in order to improve the load characteristics, more preferably 400 seconds / 100 ml or less, and most preferably 350 seconds / 100 ml or less. Moreover, since it will become easy to produce an internal short circuit when too small, it is preferable to set it as 50 second / 100 ml or more, More preferably, it is 100 second / 100 ml or more, Most preferably, it is 200 second / 100 ml or more.

The strength of the separator is preferably 6.8 × 10 ⁷ N / m ² or more, more preferably 9.8 × 10 ⁷ N / m ² or more as the tensile strength in the MD direction. However, the upper limit of the tensile strength in the MD direction is usually restricted by the material, and in the case of a polyethylene separator, the upper limit is about 10 ⁸ N / m ² .

  Further, the tensile strength in the TD direction is preferably smaller than the tensile strength in the MD direction, and the ratio S2 / S1 of the tensile strength S2 in the TD direction to the tensile strength S1 in the MD direction is preferably 0.95 or less. 0.9 or less is more desirable, 0.5 or more is desirable, and 0.7 or more is more desirable. This is because heat shrinkage at 150 ° C. in the TD direction can be suppressed while maintaining the puncture strength described below.

  The puncture strength of the separator is preferably 2.9 N or more, and more preferably 3.9 N or more. The higher the piercing strength, the more difficult the battery is short-circuited. However, the upper limit is usually restricted by the material, and in the case of a polyethylene separator, the upper limit is about 10N. The puncture strength of the separator was measured by reading the maximum load until the semi-circular pin having a diameter of 1 mm and a tip shape of a radius of 0.5 mm was pierced through the separator at 2 mm / s and penetrated.

  The smaller the heat shrinkage rate of the separator, the less likely that an internal short circuit will occur. Therefore, it is desirable to use a separator with a heat shrinkage rate as small as possible, more preferably 10% or less, and particularly preferably 5% or less. Used. Examples of such a separator include a microporous polyethylene film “F20DHI” (trade name) manufactured by Tonen Chemical Corporation.

  Moreover, in order to suppress the thermal contraction of the separator, the separator may be heat-treated at a temperature of about 120 ° C. in advance.

As the positive electrode active material used for the positive electrode, lithium composite oxides such as LiCoO ₂ , LiMn ₂ O ₄ , and LiNiO ₂ whose open circuit voltage during charging is 4 V or more on the basis of Li are preferably used. In these active materials, part of Co, Ni, and Mn may be substituted with different elements. When Ge, Ti, Ta, Nb, and Yb are included as the substitution element, the content of the substitution element is desirably 0.001 atomic% or more, more desirably 0.003 atomic% or more, and 3 atomic% or less. Is desirable, and 1 atomic% or less is more desirable.

When the specific surface area of the positive electrode active material is large, load characteristics are improved, but safety is lowered. In the present invention, even an active material having a certain specific surface area can be used more safely, and any active material having a specific surface area of up to about 1 m ² / g can be used without any particular problem. In addition, the lower limit value of the specific surface area is preferably 0.2 m ² / g or more.

In addition, it is more desirable that a lithium salt is present in advance in the positive electrode active material. This is because coexistence of an aromatic compound and a lithium salt causes the positive electrode to have ion conductivity, improving the uniform reactivity of the electrode and further improving safety. Examples of the lithium salt include inorganic lithium salts such as LiBF ₄ and LiClO ₄ , C ₄ F ₉ SO ₃ Li, C ₈ F ₁₇ SO ₃ Li, (C ₂ F ₅ SO ₂ ) ₂ NLi, and (CF ₃ SO _2). Organic lithium salts such as (C ₄ F ₉ SO ₂ ) NLi, (CF ₃ SO ₂ ) ₃ CLi, C ₆ H ₅ SO ₃ Li, and C ₁₇ H ₃₅ COOLi can be used. From the viewpoint of thermal stability and safety, an organic lithium salt is desirable, and in consideration of ion dissociation properties, a fluorine-containing organic lithium salt is desirable.

  A conductive additive or a binder such as polyvinylidene fluoride is appropriately added to these positive electrode active materials to form a positive electrode mixture. Using this positive electrode mixture, a current collector material such as a metal foil is used as a core material to finish a molded body to obtain a positive electrode. The conductive material for the positive electrode is preferably a carbon material, and the amount used is preferably 5% by mass or less, more preferably 3% by mass or less based on the total mass of the positive electrode material. Moreover, 1.5 mass% or more is desirable from the point of ensuring electroconductivity.

  On the other hand, the negative electrode active material used for the negative electrode may be any material capable of reversibly doping and dedoping lithium ions. For example, natural graphite, pyrolytic carbons, cokes, glassy carbons, organic polymer compounds Carbonaceous materials such as fired bodies, mesocarbon microbeads, carbon fibers, activated carbon, and the like can be used. Alternatively, an alloy such as Si, Sn, or In, or a compound such as an oxide or nitride that can be charged and discharged at a low potential close to Li may be used. Further, similarly to the positive electrode, it is more desirable to previously have a lithium salt present in the negative electrode active material in order to form a stable protective film on the electrode surface and suppress the reaction between the electrode and the electrolyte.

  Next, embodiments of the present invention will be described with reference to the drawings. FIG. 1 is a plan view schematically showing an example of a non-aqueous secondary battery used in the present invention, and FIG. 2 is a vertical cross-sectional view of the AA portion of the non-aqueous secondary battery shown in FIG. . In FIGS. 1 and 2, a rectangular battery is shown, where T is thickness, W is width, and H is height. The same applies to a laminated battery.

  In FIG. 2, the positive electrode 1 and the negative electrode 2 are wound in a spiral shape via a separator 3 and then pressed so as to be flattened to form a flat electrode structure 6 in a rectangular battery case 4. Contained with electrolyte. However, in FIG. 2, in order to avoid complication, a metal foil, an electrolytic solution, and the like as a current collector used for manufacturing the positive electrode 1 and the negative electrode 2 are not illustrated.

  The battery case 4 is formed of an aluminum alloy or the like and serves as a battery exterior material. The battery case 4 also serves as a positive electrode terminal. Further, an insulator 5 made of a polytetrafluoroethylene sheet or the like is disposed at the bottom of the battery case 4, and the positive electrode 1 and the negative electrode are formed from the flat electrode structure 6 including the positive electrode 1, the negative electrode 2, and the separator 3. A positive electrode lead body 7 and a negative electrode lead body 8 connected to one end of each of the two are drawn out. A terminal plate 11 made of stainless steel or the like is attached to a cover plate 9 made of aluminum alloy or the like for sealing the opening of the battery case 4 via an insulating packing 10 made of polypropylene or the like. A lead plate 13 made of stainless steel or the like is attached via 12. Further, the lid plate 9 is inserted into the opening of the battery case 4, and the joint of the two is welded so that the opening of the battery case 4 is sealed and the inside of the battery is sealed.

  In the above embodiment, the positive electrode lead body 7 is directly welded to the lid plate 9 so that the battery case 4 and the lid plate 9 function as a positive electrode terminal, the negative electrode lead body 8 is welded to the lead plate 13, and the lead The terminal 11 functions as a negative electrode terminal by conducting the negative electrode lead body 8 and the terminal 11 through the plate 13. However, depending on the material of the battery case 4, the positive electrode and the negative electrode are reversed. In some cases.

  Next, an embodiment of the electronic device of the present invention will be described. The electronic device according to the present embodiment incorporates the non-aqueous secondary battery and uses the built-in non-aqueous secondary battery, so even if the charging control mechanism does not work well, the battery does not generate much heat. It can prevent the loss of sex. That is, in a conventional battery having a high capacity by using a thin separator, the battery itself generates heat due to an internal short circuit that occurs when the battery temperature rises, and the battery temperature further rises. For this reason, an electronic device incorporating such a battery is easily damaged by heat generation of the battery, and the influence is particularly remarkable in an electronic device having a large charging current of 0.6 A or more. However, since the non-aqueous secondary battery of the present invention suppresses the occurrence of an internal short circuit at a high temperature, the above problem hardly occurs and the reliability of the electronic device can be improved.

  Furthermore, regarding the mounting form of the non-aqueous secondary battery to the electronic device, safety can be improved by incorporating the non-aqueous secondary battery having a square shape or laminate shape into the electronic device while being pressed in the thickness direction. Can improve. Normally, when a battery is overcharged due to a failure of a device or the like, the battery swells, the electrode body inside the battery is deformed, the current is concentrated and energized, and the battery tends to generate heat locally. With the mounting configuration according to the present invention, the battery is less likely to swell, the deformation of the electrode is suppressed, and the current concentration is reduced, so that the heat generation of the battery can also be suppressed. The pressure of the battery in the electronic device is preferably pressed by a surface smaller than the battery side surface, and the pressed area is preferably 95% or less, more preferably 80% or less, and 50% or less of the battery side surface. Is most desirable. Further, if the battery is pressed around the center of the side surface of the battery, it is more effective, and it is preferable that the battery is pressed at 5 g or more in the initial state. Further, the pressure is more preferably 100 g or more, most preferably 500 g or more, but if it is too large, the electrode body may be damaged, so 5 kg or less is desirable. The vicinity of the center of the battery side means W is the width of the battery side, H is the height, a rectangle with a small width W / 2 and height H / 2 is the center of the side, and the diagonal of the side of the battery and the diagonal of the small rectangle Is the center side of the small rectangle.

  Further, in an electronic device incorporating a non-aqueous secondary battery in the above form, it is more desirable to use an electrolyte containing an aromatic compound as the non-aqueous electrolyte of the non-aqueous secondary battery, and the separator It is more desirable to use a separator having a thickness of 5 to 20 μm and an air permeability of 500 seconds / 100 ml or less. Furthermore, it is most desirable to incorporate the above-described non-aqueous secondary battery of the present invention in the electronic device in the above-described form. This is because when the battery is overcharged in an electronic device, the aromatic compound in the non-aqueous electrolyte reacts, and a gradual short circuit is likely to occur, so the substantial overcharge current is reduced and the overcharge This is because the maximum battery surface temperature at that time decreases. If the separator is thin, the electrodes are close to each other, and a gentle short circuit is more likely to occur.

  Electronic devices that can incorporate the non-aqueous secondary battery are not particularly limited, and portable electronic devices such as mobile phones, notebook computers, PDAs, and small medical devices, and with a battery backup function. Various electronic devices such as office equipment and medical equipment can be given.

  Next, the present invention will be described more specifically with reference to examples. However, the present invention is not limited only to the following examples.

Example 1
A mixed solvent of ethylene carbonate and methyl ethyl carbonate in a volume ratio of 1: 2 is prepared, LiPF ₆ is dissolved in the mixed solvent at a concentration of 1.2 mol / l, and aromatic compounds cyclohexylbenzene and fluorobenzene are dissolved therein. And 1,3-propane sultone are added so as to have a content of 4% by mass of cyclohexylbenzene, 3% by mass of fluorobenzene, and 2% by mass of 1,3-propane sultone with respect to the total mass of the electrolyte. A liquid was prepared.

Separately, LiCo _0.995 Ge _0.005 O ₂ having a specific surface area of 0.5 m ² / g as a positive electrode active material, carbon as a conductive additive, and (C ₂ F ₅ SO ₂ ) ₂ NLi as a lithium salt. The positive electrode mixture slurry was mixed at a mass ratio of 97.9: 2: 0.1, and this mixture was mixed with a solution of polyvinylidene fluoride as a binder dissolved in N-methylpyrrolidone. Was made. After passing this positive electrode mixture slurry through a filter to remove large particles, the positive electrode current collector made of a strip-shaped aluminum foil having a thickness of 15 μm is uniformly coated on the both surfaces and dried, and then compressed by a roller press. After forming, it was cut and the lead body was welded to produce a strip-like positive electrode. Note that the positive electrode mixture was not applied to the portion not facing the negative electrode. The positive electrode current collector used here contained 1% by mass of Fe and 0.15% by mass of Si, the purity of aluminum was 98% by mass or more, and the tensile strength was 185 N / mm ² .

Next, a negative electrode was produced as follows. d ₀₀₂ = 0.335 nm and graphite having an average particle diameter of 15 μm and (C ₂ F ₅ SO ₂ ) ₂ NLi as a negative electrode active material, and a solution in which vinylidene fluoride as a binder is dissolved in N-methylpyrrolidone And the negative electrode active material were mixed to prepare a negative electrode mixture slurry. Here, the ratio of (C ₂ F ₅ SO ₂ ) ₂ NLi was 0.1% by mass with respect to the mass of graphite. After passing this negative electrode mixture slurry through a filter to remove large particles, the negative electrode current collector made of a strip-shaped copper foil having a thickness of 10 μm is uniformly coated on the both surfaces and dried, and then compressed by a roller press. After forming, it was cut and the lead body was welded to produce a strip-shaped negative electrode. The negative electrode mixture application part of the negative electrode is made 1 mm larger in the width direction than the positive electrode mixture application part of the positive electrode and about 5 mm in the longitudinal direction, but does not face the positive electrode during other winding times. The portion was not coated with the negative electrode mixture. This is because the safety of the battery is also improved by setting the size of the positive electrode mixture application portion to be equal to or less than the size of the negative electrode mixture application portion. Here, the density of the negative electrode mixture portion of the negative electrode was 1.55 g / cm ³ .

The belt-like positive electrode and the belt-like negative electrode were made into a microporous polyethylene film “F20DHI” (air permeability: 344 seconds / 100 ml, puncture strength: 4.5 N, porosity: 39. 4%, MD direction tensile strength: 1.3 × 10 ⁸ N / m ² , TD direction tensile strength: 1.1 × 10 ⁸ N / m ² , thermal shrinkage at 150 ° C. in TD direction: 5% ) And wound into a flat shape to obtain an electrode laminate. Thereafter, the periphery of the electrode laminate is fixed with tape, and the electrode laminate is inserted into a battery aluminum alloy can having a thickness of 4 mm, a width of 30 mm, and a height of 48 mm as outer dimensions, and welding of the lead body and a lid plate for sealing Laser welding was performed.

  Next, the prepared electrolyte is poured into the battery case from the inlet, and after the electrolyte has sufficiently permeated the separator and the like, the inlet is sealed, precharged and aged, as shown in FIG. A prismatic non-aqueous secondary battery was fabricated. In addition, the capacity | capacitance of the non-aqueous secondary battery of a present Example is 600 mAh.

(Example 2)
A nonaqueous secondary battery was produced in the same manner as in Example 1 except that fluorobenzene was not added to the electrolytic solution.

(Comparative Example 1)
A nonaqueous secondary battery was produced in the same manner as in Example 2 except that cyclohexylbenzene was not added to the electrolytic solution.

(Comparative Example 2)
As a separator, a microporous polyethylene film having a thickness of 20 μm and a thermal shrinkage ratio of 34% at 150 ° C. in the TD direction (air permeability: 240 seconds / 100 ml, tensile strength in the MD direction: 1.4 × 10 ⁸⁾ N / m ² , tensile strength in TD direction: 1.3 × 10 ⁸ N / m ² ) A non-aqueous secondary battery was fabricated in the same manner as in Example 2.

(Comparative Example 3)
As a separator, a microporous polyethylene film having a thickness of 20 μm and an air permeability of 590 sec / 100 ml (MD direction tensile strength: 1.3 × 10 ⁸ N / m ² , TD direction tensile strength: 9.3 A nonaqueous secondary battery was produced in the same manner as in Example 2 except that × 10 ⁷ N / m ² and the thermal shrinkage rate at 150 ° C. in the TD direction: 10% were used.

(Comparative Example 4)
As a separator, a microporous polyethylene film having a thickness of 25 μm (air permeability: 650 sec / 100 ml, MD direction tensile strength: 1.1 × 10 ⁸ N / m ² , TD direction tensile strength: 1.0 × A nonaqueous secondary battery was fabricated in the same manner as in Example 2 except that 10 ⁸ N / m ² and the thermal shrinkage rate at 150 ° C. in the TD direction: 20%) were used.

  The batteries of Examples 1-2 and Comparative Examples 1-4 were charged at a constant current at room temperature (20 ° C.) until the battery voltage reached 4.2 V at a current value of 0.12 A (0.2 C), and 2V constant voltage charge was performed, and the charge was terminated when 7 hours had elapsed after the start of charge. Next, it was discharged to 3 V at 0.12 A (0.2 C). The positive electrode potential during charging was approximately 4.3 V based on lithium. Further, after charging under the above charging conditions, the discharge capacity was measured by discharging to 3 V at 1.2 A (2 C), and the load characteristics were evaluated by the ratio of the discharge capacity at 2 C to the discharge capacity at 0.2 C. did. The results are shown in Table 1. In Table 1, the load characteristic (%) is indicated by (discharge capacity at 2C / discharge capacity at 0.2C) × 100.

  In addition to the batteries used in the above measurement, each of the five batteries in Examples 1 and 2 and Comparative Examples 1 to 4 was charged to 4.25 V at 0.2 C, and then charged at a constant voltage at 4.25 V. The charging was completed 7 hours after the start of charging. After completion of charging, the battery is placed in an explosion-proof thermostat, heated from room temperature (20 ° C) to 150 ° C at a rate of 5 ° C / min, and a battery is held at 150 ° C for 60 minutes. The surface temperature of each battery was measured, and the maximum temperature reached was measured for the surface temperature of each battery. Table 1 shows the maximum value among the maximum temperatures reached for each battery as the maximum battery temperature.

  The batteries of Example 1 and Example 2 use an electrolytic solution containing an aromatic compound in the range of 2 to 15% by mass as the nonaqueous electrolytic solution, and have the MD direction and the TD direction as the separator, and the TD direction. If a separator having a thermal shrinkage rate of 150% at 150 ° C. or less, a thickness of 5 to 20 μm, and an air permeability of 500 seconds / 100 ml or less is used, only load characteristics are excellent. Therefore, the internal short circuit of the battery when the battery was exposed to a high temperature could be suppressed, and the temperature rise of the battery itself could be suppressed. In particular, the battery of Example 1 in which a compound having an alkyl group bonded to an aromatic ring and a compound having a halogen group bonded to an aromatic ring showed excellent characteristics.

  On the other hand, the batteries of Comparative Example 1 in which the aromatic compound was not contained in the electrolyte solution and Comparative Example 2 using a separator having a thermal shrinkage rate at 150 ° C. in the TD direction of greater than 30% were heated at 150 ° C. The maximum battery temperature at 5 ° C was higher than in Example 1 and Example 2, and the stability at high temperature was lowered. In particular, the battery of Comparative Example 2 having a large thermal shrinkage rate of the separator exceeded the measurement limit of 180 ° C., and the temperature of the battery rose, making it unsuitable for use at high temperatures. In addition, the load characteristics of the batteries of Comparative Example 3 using a separator with an air permeability of greater than 500 seconds / 100 ml and Comparative Example 4 using a separator with a thickness of more than 20 μm were significantly reduced.

  Next, the batteries of Example 1 and Comparative Example 1 were incorporated as power sources in a mobile phone “C451H” (trade name) manufactured by Hitachi, Ltd., and the following tests were performed. Assuming that the protection circuit and the charging circuit are damaged, the protection circuit, the PTC, and the voltage control circuit are not functioned, and then charged to a voltage of 12 V at a current value of 1 A, and then constant voltage charging at 12 V was performed ( Test A). As a result, in the mobile phone using the battery of Example 1 of the present invention, the appearance and deformation of the mobile phone were not observed after the test was completed.

  Next, the battery of Example 1 produced in the same manner is mounted on the mobile phone, and a plastic plate having a thickness of 1 mm, a width of 15 mm, and a length of 24 mm from the battery cover on the back of the mobile phone is centered on the center of the side of the battery Was applied to the position corresponding to the above, 500 g of pressure was applied to the portion in the thickness direction of the battery, and overcharge was performed in the same manner as above (Test B). As a result, in test B, the battery was less likely to generate heat than in test A, and the maximum battery temperature during overcharge was reduced by 18 ° C.

  On the other hand, when the test A and the test B were performed in the same manner as described above using the battery of Comparative Example 1, both of the mobile phones were damaged and did not function normally.

  In the above test, the protection circuit, the PTC, and the voltage control circuit were not functioned, but it goes without saying that the reliability of the electronic device is further improved by adding each protection function.

  As described above, the present invention can improve the safety of an electronic device by incorporating a rectangular or laminated nonaqueous secondary battery into the electronic device while being pressed in the thickness direction.

It is a top view which shows typically an example of the non-aqueous secondary battery used for this invention. It is a longitudinal cross-sectional view of the AA part of the non-aqueous secondary battery shown in FIG.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Positive electrode 2 Negative electrode 3 Separator 4 Battery case 5 Insulator 6 Electrode laminated body 7 Positive electrode lead body 8 Negative electrode lead body 9 Cover plate 10 Insulation packing 11 Terminal 12 Insulator 13 Lead body

Claims (13)

An electronic device comprising a positive electrode, a negative electrode, a separator, and a non-aqueous electrolyte, and including a non-aqueous secondary battery formed in a square shape or a laminate shape,
The non-aqueous secondary battery is pressed in the thickness direction,
The positive electrode and the negative electrode are laminated via the separator to constitute an electrode laminate,
The non-aqueous electrolyte contains 2 to 15% by mass of an aromatic compound with respect to the total mass of the electrolyte,
The separator has an MD direction and a TD direction, and a thermal shrinkage rate at 150 ° C. in the TD direction is 30% or less,
The separator has a thickness of 5 to 20 μm and an air permeability of 500 seconds / 100 ml or less,
Charge to 4.25V at 0.2C, then charge at constant voltage at 4.25V for 7 hours, then place in an explosion-proof thermostat and increase from 20 ° C to 150 ° C at a rate of 5 ° C / min. An electronic device characterized by having a maximum surface temperature of a battery surface temperature of 165 ° C. or lower during a test in which the battery is held at 150 ° C. for 60 minutes. The electronic device according to claim 1 , wherein the aromatic compound is a compound in which an alkyl group is bonded to an aromatic ring and a compound in which a halogen group is bonded to an aromatic ring. The non-aqueous electrolyte contains 0.5 to 8% by mass of a compound having an alkyl group bonded to an aromatic ring with respect to the total mass of the electrolyte, and a compound having a halogen group bonded to an aromatic ring to the total mass of the electrolyte. The electronic device of Claim 1 which contains 1-12 mass% with respect to. The electronic device according to claim 1 , wherein the non-aqueous electrolyte includes a solvent having a —SO ₂ — bond. The secondary battery, based on the total volume of the electrolyte comprises 40% by volume or more of chain carbonate and less than 90 vol%, and, in claim 1 containing 1% by volume or more of a cyclic carbonate less than 80 vol% The electronic device described. The electronic device according to claim 1 , wherein the tensile strength in the MD direction of the separator is 6.8 × 10 ⁷ N / m ² or more. For the MD direction of the tensile strength S1 of the separator, the ratio S2 / S1 in the TD direction of the tensile strength S2 is an electronic device according to claim 1 is 0.5 to 0.95. The electronic device according to claim 1 , wherein the puncture strength of the separator is 2.9 N or more. The electronic device according to claim 1 , wherein the positive electrode includes a lithium composite oxide as a positive electrode active material. The electronic device according to claim 9 , wherein the positive electrode active material has a specific surface area of 1 m ² / g or less. The electronic device according to claim 1 , wherein the positive electrode includes a carbon material as a conductive additive, and the amount of the carbon material used is 5% by mass or less based on the total mass of the positive electrode material. The electronic device according to claim 1 , wherein the negative electrode includes a material capable of reversibly doping and dedoping lithium ions as a negative electrode active material. The electronic device according to claim 1 , wherein at least one selected from the positive electrode and the negative electrode includes a lithium salt in advance.

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