JP5034300B2 - Method for producing positive electrode for non-aqueous electrolyte secondary battery and non-aqueous electrolyte secondary battery using them - Google Patents

Description

  The present invention relates to a nonaqueous electrolyte secondary battery, and more specifically, a positive electrode for a nonaqueous electrolyte secondary battery excellent in moisture resistance without impairing charge / discharge characteristics, a method for producing the same, and a nonaqueous electrolyte secondary battery using the same. Next battery.

  Lithium ion secondary batteries, which are representative of non-aqueous electrolyte secondary batteries, have the characteristics of being light weight, high electromotive force, and high energy density, so mobile phones, digital cameras, video cameras, laptop computers, etc. As a power source for driving various types of portable electronic devices and mobile communication devices, demand is expanding.

And the lithium ion secondary battery is comprised from the positive electrode which consists of lithium containing complex oxide, the negative electrode containing the positive electrode active material which occludes / releases metal lithium, lithium alloy, or lithium ion, and electrolyte. Furthermore, lithium-containing composite oxides such as Li _x CoO ₂ and Li _x NiO ₂ (x varies depending on the charge / discharge of the battery) used as the positive electrode can be used for Co ⁴⁺ Ni ⁴⁺ is included.

  Due to this, in the manufacturing process of the positive electrode, the decomposition reaction of the electrolyte involving the lithium-containing composite oxide is promoted by the adsorption of moisture in the air on the surface, and sufficient charge is generated by the generation of gas in the battery. Discharge cycle characteristics and storage characteristics at high temperatures cannot be obtained.

  Thus, in general, the positive electrode and the like are manufactured in a dry air atmosphere in order to prevent adsorption of moisture in the air, but this limits the reduction in productivity and manufacturing cost.

  As a method for solving this problem, many proposals have been made to suppress the generation of gas in the battery by the positive electrode to which moisture or the like is adsorbed, and to improve the charge / discharge cycle characteristics and the storage characteristics at high temperatures.

  For example, in order to prevent the lithium-containing composite oxide of the positive electrode material from being deteriorated by the influence of moisture, the surface of the lithium-containing composite oxide fine particles or the surface of the positive electrode is provided with a coating of a water repellent material. A technique is disclosed (for example, see Patent Document 1).

In addition, in order to solve the problem that a part of the occluded lithium ions cannot be released due to a side reaction that occurs at the electrode interface when the lithium ions are occluded in the electrode, the charge / discharge cycle characteristics are deteriorated. Or the technique etc. which process a negative electrode with a silane compound or a fluorine-type surfactant are disclosed (for example, refer patent document 2).
Japanese Patent Laid-Open No. 11-224664 JP-A-11-354104

  However, in the conventional method for producing a positive electrode, it is necessary to apply a positive electrode mixture paste containing a positive electrode active material to a current collector and then press it to adjust the thickness of the positive electrode. May break due to pressure from the press.

  Therefore, as shown in Patent Document 1 and Patent Document 2, even if the positive electrode active material is treated with a silane coupling agent during preparation, the positive electrode active material is broken by the pressing process and reacts with moisture at the fracture surface. The positive electrode active material is decomposed, and gas may be generated during charging and discharging of the battery.

  Hereinafter, a conventional method for manufacturing a positive electrode will be described with reference to FIG.

  6A is a partially enlarged view of a cross section of the positive electrode after applying a positive electrode mixture paste containing a positive electrode active material on a current collector in a conventional positive electrode manufacturing process, and FIG. 6B is a pressing process. It is sectional drawing which shows the state of the subsequent positive electrode active material typically.

  As shown in FIG. 6A, the surface of the positive electrode active material 61 is previously coated with a silane coupling agent 62.

  However, as shown in FIG. 6 (b), a part of the positive electrode active material 61 is broken by the pressure during the pressing process, and the fracture surface 63 is exposed to be easily reacted with moisture and the like. That is, there is a possibility that a fracture surface of the positive electrode active material that comes into contact with moisture in the atmosphere occurs after the pressing step regardless of whether or not the positive electrode active material is treated with the coupling agent before the pressing step. Further, when the powdered positive electrode active material is not previously treated with a coupling agent, it is in a state in which it does not easily react with moisture in the atmosphere because it is coated with a binder in the state of the positive electrode before the pressing step. However, the pressing step causes a fracture surface in the positive electrode active material, and is likely to react with moisture.

  For this reason, in the conventional manufacturing process of the positive electrode, the silane coupling agent 62 cannot be disposed in the vicinity of the surface of the fracture surface 63, so that the reaction with moisture or the like on the fracture surface 63 of the positive electrode active material 61 cannot be prevented.

  Therefore, after pressing the positive electrode, it is necessary to strictly manage the storage environment such as storing the positive electrode in a low humidity environment until the positive electrode is wound and the battery is assembled, which is a major issue from the viewpoint of improving productivity. .

  That is, depending on the humidity environment in the process of handling the positive electrode, the positive electrode active material reacts with water to generate decomposition products such as hydroxide. A non-aqueous electrolyte secondary battery produced using a positive electrode in which the positive electrode active material absorbs water and forms decomposition products reacts with the non-aqueous electrolyte to generate carbon dioxide, etc. To do. As a result, the non-aqueous electrolyte secondary battery cannot obtain sufficient charge / discharge cycle characteristics, and the reliability such as deformation due to expansion and storage characteristics decreases at high temperatures.

  Furthermore, even in a room temperature environment, the generation of gas causes the battery case to expand, which causes the quality to deteriorate.

  The present invention solves the above-described problems, and provides a nonaqueous electrolyte secondary battery positive electrode for realizing a nonaqueous electrolyte secondary battery excellent in charge / discharge cycle characteristics, a method for producing the same, and a nonaqueous solution using the same. An object is to provide an electrolyte secondary battery.

In order to achieve the above object, a positive electrode for a non-aqueous electrolyte secondary battery according to the present invention includes a current collector and a positive electrode mixture layer formed on the current collector, and reversibly converts lithium ions as the positive electrode mixture layer. And a silane coupling agent that is present at least near the surface of the fracture surface of the positive electrode active material produced by pressing and prevents reaction with moisture. Thereby, the positive electrode for nonaqueous electrolyte secondary batteries with high productivity and excellent storage characteristics and charge / discharge cycle characteristics can be realized.

  If the positive electrode for nonaqueous electrolyte secondary batteries of this invention is used, reaction with the water | moisture content of the positive electrode active material in a positive electrode can be suppressed, and generation | occurrence | production of the gas in a nonaqueous electrolyte secondary battery can be suppressed. Therefore, it is possible to provide a positive electrode for a nonaqueous electrolyte secondary battery that is excellent in storage characteristics and charge / discharge cycle characteristics and has high productivity, a method for producing the same, and a nonaqueous electrolyte secondary battery using the same.

1st invention of this invention is a manufacturing method of the positive electrode for nonaqueous electrolyte secondary batteries, Comprising: The positive mix layer containing the positive electrode active material which occludes / releases lithium ion reversibly on a collector is provided. And a step of pressing the positive electrode mixture layer to a predetermined thickness and impregnating the surface of the fracture surface of the positive electrode active material generated by the pressing with a silane coupling agent.

By this method, in the step of pressing the positive electrode mixture layer, by impregnating the positive electrode mixture layer with the silane coupling agent, the silane coupling agent is also applied in the vicinity of the surface of the fracture surface of the positive electrode active material fractured in the pressing step. can be applied, by suppressing the reaction between the positive electrode active material and water, Ru can achieve excellent charge-discharge cycle characteristics.

The second aspect of the present invention includes a positive electrode for a nonaqueous electrolyte secondary battery according to the first invention, a non-aqueous electrolyte secondary battery comprising a negative electrode and a nonaqueous electrolyte.

  Thereby, a nonaqueous electrolyte secondary battery excellent in storage characteristics and charge / discharge cycle characteristics can be obtained.

  Hereinafter, embodiments of the present invention will be described with reference to the drawings. The present invention is not limited to the contents described below as long as it is based on the basic characteristics described in this specification.

(Embodiment)
FIG. 1 is a partially developed perspective view of a nonaqueous electrolyte secondary battery according to an embodiment of the present invention.

  As shown in FIG. 1, a rectangular nonaqueous electrolyte secondary battery (hereinafter also referred to as “battery”) includes a negative electrode 1, a positive electrode 2 that faces the negative electrode 1 and reduces lithium ions during discharge, The separator 3 is interposed between the negative electrode 1 and the positive electrode 2 and prevents direct contact between the negative electrode 1 and the positive electrode 2. The negative electrode 1 and the positive electrode 2 are wound together with the separator 3 to form an electrode group 4. And the electrode group 4 is accommodated in the battery case 5 with the nonaqueous electrolyte (not shown). Further, on the upper part of the electrode group 4, for example, a resin frame 11 that separates the electrode group 4 and the sealing plate 6 and isolates the positive electrode lead 7 and the negative electrode lead 9 is disposed. In addition, in the opening of the battery case 5 that is also used as the positive electrode external connection terminal, a negative electrode external connection terminal 10 that connects the negative electrode lead 9 to an external device and a liquid injection port sealing that seals a nonaqueous electrolyte liquid injection port A sealing plate 6 having a portion 8 is provided. And the negative electrode 1 consists of a collector and a negative mix layer, and the positive electrode 2 has a collector and a positive mix layer.

  Below, the positive electrode for nonaqueous electrolyte secondary batteries in embodiment of this invention is demonstrated in detail using FIG.

  FIG. 2 is a conceptual cross-sectional view of positive electrode mixture layer 22 constituting positive electrode 2 for a nonaqueous electrolyte secondary battery in the embodiment of the present invention. Normally, the positive electrode mixture layer 22 is formed on both surfaces of a current collector (not shown), but FIG. 2 shows only the structure of one side of the current collector, and the positive electrode mixture layer 22 has at least a positive electrode active layer. The material 23 is composed of a silane coupling agent 24 and a binder 25 existing in the vicinity of the surface. In the drawing, the positive electrode active material 23 is shown as being coated with the silane coupling agent 24. However, for example, moisture may be present in the vicinity of the positive electrode active material 23 so as not to contact the positive electrode active material 23. Needless to say.

  The present invention is that the silane coupling agent 24a is also present in the vicinity of the fracture surface 23a of the positive electrode active material 23 crushed in the pressing step as shown in FIG.

Here, as the positive electrode mixture layer 22 constituting the positive electrode 2 together with the current collector, a lithium-containing composite oxide (Ni / Co-based Li composite oxide such as LiCoO ₂ , LiNiO ₂ , Li ₂ MnO ₄ , or a mixture or composite compound thereof) or the like is included as the positive electrode active material 23.

In addition to the above, as the positive electrode active material 23, an olivine type lithium phosphate represented by a general formula of LiMPO ₄ (M = V, Fe, Ni, Mn), Li ₂ MPO ₄ F (M = V, Fe, Lithium fluorophosphate represented by the general formula of Ni, Mn) can also be used. Further, a part of these lithium-containing compounds may be substituted with a different element. You may surface-treat with a metal oxide, lithium oxide, a electrically conductive agent, etc.

  The form of the lithium-containing composite oxide is not particularly limited. For example, the case where the positive electrode active material 23 is formed in a primary particle state and the case where the positive electrode active material 23 composed of secondary particles in which a plurality of primary particles are aggregated are formed. is there.

  The positive electrode mixture layer 22 further contains a conductive agent and a binder as the binder 25. And as the conductive agent, natural graphite and artificial graphite graphite, acetylene black, ketjen black, channel black, furnace black, lamp black, thermal black and other carbon black, conductive fiber such as carbon fiber and metal fiber , Metal powders such as carbon fluoride and aluminum, conductive whiskers such as zinc oxide and potassium titanate, conductive metal oxides such as titanium oxide, and organic conductive materials such as phenylene derivatives.

  Examples of the binder include polyvinylidene fluoride (PVDF), polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, polyacrylic acid methyl ester, poly Acrylic acid ethyl ester, polyacrylic acid hexyl ester, polymethacrylic acid, polymethacrylic acid methyl ester, polymethacrylic acid ethyl ester, polymethacrylic acid hexyl ester, polyvinyl acetate, polyvinylpyrrolidone, polyether, polyethersulfone, hexafluoro Polypropylene, styrene-butadiene rubber, carboxymethyl cellulose, etc. can be used.

  Two types selected from tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkyl vinyl ether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid, and hexadiene A copolymer of the above materials may be used. Two or more selected from these may be mixed and used.

  As the current collector used for the positive electrode 2, aluminum (Al), carbon, conductive resin, or the like can be used. Further, any of these materials may be surface-treated with carbon or the like.

  The average particle diameter of the positive electrode active material 23 or the Ni / Co-based Li composite oxide particles is not particularly limited, but is preferably 1 to 30 μm, and particularly preferably 10 to 30 μm. The average particle size can be measured by, for example, a wet laser particle size distribution measuring device manufactured by Microtrack. In this case, a 50% value (median value: D50) on a volume basis can be regarded as the average particle diameter.

The lithium-containing composite oxide is represented by a general formula: Li _x M _1-y L _y O ₂ , and the general formula satisfies 0.85 ≦ x ≦ 1.25 and 0 ≦ y ≦ 0.50, and the element M Is at least one selected from the group consisting of Ni and Co, and the element L is at least one selected from the group consisting of alkaline earth elements, transition metal elements, rare earth elements, group IIIb elements and IVb elements It is. The element L gives the lithium-containing composite oxide an effect of improving thermal stability.

  In the case of 0 <y, the lithium-containing composite oxide preferably contains at least one selected from the group consisting of Al, Mn, Ti, Mg, Zr, Nb, Mo, W, and Y as the element L.

  These elements may be contained alone as the element L in the lithium-containing composite oxide, or two or more thereof may be contained. In particular, Al is suitable as the element L because of its strong bonding force with oxygen. Also preferred are Mn, Ti and Nb. The element L may include Ca, Sr, Si, Sn, B, etc., but is more preferably used in combination with Al, Mn, Ti, Nb, or the like.

  The range of x representing the Li content varies depending on the charge / discharge of the battery. The range of x in the complete discharge state (initial state) may be 0.85 ≦ x ≦ 1.25, but more preferably 0.93 ≦ x ≦ 1.1.

  The range of y representing the content of the element L may be 0 ≦ y ≦ 0.50, but considering the balance of capacity, cycle characteristics, thermal stability, etc., 0 <y ≦ 0.50 is preferable, It is particularly preferable that 0.001 ≦ y ≦ 0.35.

  When the element L contains Al, the atomic ratio a of Al to the total of Ni, Co, and element L is preferably 0.005 ≦ a ≦ 0.1, and 0.01 ≦ a ≦ 0.08. Further preferred.

  When the element L contains Mn, the atomic ratio b of Mn with respect to the sum of Ni, Co, and the element L is preferably 0.005 ≦ b ≦ 0.5, and 0.01 ≦ b ≦ 0.35. Is more preferred.

  When the element L includes at least one selected from the group consisting of Ti and Nb, the atomic ratio c of Ti and / or Nb with respect to the sum of Ni, Co and element L is 0.001 ≦ c ≦ 0.1 0.001 ≦ c ≦ 0.08 is particularly preferable.

  The lithium composite oxide constituting the positive electrode active material may be primary particles or secondary particles formed by aggregation of a plurality of primary particles. Further, a plurality of types of positive electrode active materials may be aggregated to form secondary particles.

  Below, the manufacturing method of the positive electrode for nonaqueous electrolyte secondary batteries in embodiment of this invention is demonstrated.

  First, a positive electrode active material pretreated with a silane coupling agent or a positive electrode active material not pretreated with a silane coupling agent, and a conductive material and a binder are dispersed and prepared to prepare a positive electrode mixture paste.

  Next, the prepared positive electrode mixture paste is applied onto a current collector and dried to form a positive electrode mixture layer.

  Next, the formed positive electrode mixture layer and the current collector are pressed to form a positive electrode having a predetermined thickness.

  Then, in the final pressing step of pressing the positive electrode mixture layer, for example, the positive electrode mixture layer is impregnated with the silane coupling agent by the processing method 1 to the processing method 3 described below.

  Even when the positive electrode active material is not previously treated with a silane coupling agent, the treatment method 1 to the treatment method 3 described below is used to treat the silane coupling agent in the state of the positive electrode. The effect of suppressing the reaction between moisture and the positive electrode active material can be enhanced.

  Here, the silane coupling agent has at least one organic functional group and a plurality of bonding groups in the molecule. Organic functional groups have various hydrocarbon skeletons. The bonding group is hydrolyzed to give a hydroxyl group Si—OH bonded directly to the metal element. Examples of the organic functional group include an alkyl group, a mercaptopropyl group, and a trifluoropropyl group. Examples of the linking group include hydrolyzed alkoxy groups.

  And the process by a silane coupling agent is what advances an alcohol dehydration reaction between the hydroxyl group which exists in the surface of a positive electrode active material, and the coupling group of a silane coupling agent. The presence or absence of treatment with a silane coupling agent on the surface of the positive electrode active material can be confirmed, for example, by forming a metal element-O-Si bond on the surface of the lithium nickelate-based composite oxide.

  In consideration of the reactivity with the hydroxyl group on the particle surface of the positive electrode active material, the silane coupling agent preferably has an alkoxy group as a linking group. Furthermore, the silane coupling agent preferably has at least one of a mercapto group, an alkyl group, and a fluoro group in the organic functional group from the viewpoint of suppressing side reactions with the electrolytic solution.

  The silane coupling agent may be impregnated directly on the positive electrode, and is not particularly limited, but suitable organic solvents such as ketones such as dioxane, acetone and methyl ethyl ketone (MEK), ethers such as tetrahydrofuran (THF), ethanol and the like These alcohols may be diluted with N-methyl-2-pyrrolidone (NMP), silicone oil, or the like.

  Thereby, the positive electrode for nonaqueous electrolyte secondary batteries excellent in storage characteristics is obtained.

  Hereinafter, treatment method 1 to treatment method 3 in which the surface of the positive electrode mixture layer is impregnated with the silane coupling agent will be described in detail with reference to FIGS. 3 to 5.

(Processing method 1)
First, the processing method 1 is demonstrated using FIG.

  FIG. 3 is a cross-sectional view illustrating a step of impregnating the positive electrode mixture layer with the silane coupling agent in the processing method 1.

  As shown in FIG. 3, first, two transfer rolls 32 containing a silane coupling agent are provided in contact with two rolling rolls 31, respectively.

  Next, the positive electrode 2 is roll-pressed by the rolling roll 31 so that the total thickness becomes 160 μm, and the silane coupling agent 26 transferred from the transfer roll 32 to the rolling roll 31 is applied to the surface of the positive electrode mixture layer of the positive electrode 2. Apply.

  By the above method, as shown in FIG. 2, the silane coupling agent 26 is impregnated so as to exist in the vicinity of the surface of the positive electrode active material 23 and the surface of the fracture surface 23a generated by the roll press.

  Hereinafter, a case where the positive electrode active material is previously treated with a silane coupling agent will be referred to as processing method 1a, and a case where the positive electrode active material is not previously treated with a silane coupling agent will be described as processing method 1b.

(Processing method 2)
Next, processing method 2 will be described with reference to FIGS. 4 (a) and 4 (b).

  4A and 4B are cross-sectional views for explaining the impregnation step of the silane coupling agent in the positive electrode mixture layer in the processing method 2.

  First, as shown in FIG. 4A, the positive electrode 2 is roll-pressed by two rolling rolls 31 so that the total thickness becomes 160 μm.

  Next, the two transfer rolls 32 containing the silane coupling agent 26 are brought into contact with the surface of the positive electrode mixture layer of the rolled positive electrode 2 to apply the silane coupling agent. Below, this is demonstrated as the processing method 2a.

  As another method, as shown in FIG. 4B, the silane coupling agent 26 is applied to the surface of the positive electrode mixture layer of the positive electrode 2 rolled using the spray nozzle 42 by spraying from above and below. May be. Below, this is demonstrated as the processing method 2b.

  In the processing method 1 or the processing method 2 described above, the amount of the silane coupling agent 26 impregnated on the surface and fracture surface of the positive electrode active material is the amount contained in the transfer roll 32 or the discharge amount from the injection nozzle 42. It is possible to adjust by controlling.

(Processing method 3)
Next, processing method 3 will be described with reference to FIG.

  FIG. 5 is a cross-sectional view illustrating a step of impregnating the positive electrode mixture layer with the silane coupling agent in the processing method 3.

  First, as shown in FIG. 5, the positive electrode 2 is roll-pressed by two rolling rolls 31 so that the total thickness becomes 160 μm.

  Next, the rolled positive electrode 2 is introduced into an immersion tank 52 filled with the silane coupling agent 54 and immersed in the silane coupling agent 54.

  Next, a silane coupling agent 54 is applied to the surface of the positive electrode mixture layer and discharged from the immersion tank 52.

  Next, the application amount is controlled by removing excess silane coupling agent with an inert gas 58 such as argon gas ejected from the ejection nozzle 56.

  By the above treatment methods, the positive electrode for a nonaqueous electrolyte secondary battery in the embodiment of the present invention is produced.

  The step of impregnating the silane coupling agent is preferably performed in a short time, for example, within 30 seconds, at the same time or after the formation of the fracture surface of the positive electrode active material by pressing.

  The silane coupling agent used in each of the above treatment methods may be impregnated directly on the positive electrode, and is not particularly limited, but suitable organic solvents such as ketones such as dioxane, acetone and methyl ethyl ketone (MEK), tetrahydrofuran (THF) It may be used after diluting with ethers such as ethanol, alcohols such as ethanol, N-methyl-2-pyrrolidone (NMP), silicone oil and the like.

Here, the positive electrode 2 used in the embodiment of the present invention have the general formula _{Li x M y N 1-y} O 2 ( where, M and N, Co, Ni, Mn, Cr , Fe, Mg, Al And a positive electrode composite comprising a lithium-containing composite oxide represented by M ≠ N and 0.98 ≦ x ≦ 1.10, 0 ≦ y ≦ 1), at least one selected from the group consisting of Zn and Zn It is preferable that the agent layer 22 is supported on a current collector made of Al or an Al alloy.

  As the positive electrode mixture layer 22, it is preferable that a conductive agent is added in an amount of 0.2 to 50 wt%, particularly 0.2 to 30 wt% of the positive electrode active material.

  In addition, as a collector used for the negative electrode 1, metal foil, such as stainless steel, nickel, copper, and titanium, a thin film of carbon or a conductive resin, or the like can be used. Further, surface treatment may be performed with carbon, nickel, titanium or the like.

The negative electrode mixture layer contains at least a negative electrode active material capable of occluding and releasing lithium ions. As this negative electrode active material, a carbon material such as graphite or amorphous carbon can be used. Alternatively, a material such as silicon (Si) or tin (Sn) that can store and release a large amount of lithium ions at a base potential lower than that of the positive electrode active material can be used. If it is such a material, the effect of the present invention can be exerted by any of a simple substance, an alloy, a compound, a solid solution, and a composite negative electrode active material containing a silicon-containing material and a tin-containing material. In particular, a silicon-containing material is preferable because it has a large capacity density and is inexpensive. That is, as a silicon-containing material, Si, SiO _x (0.05 <x <1.95), or any of these, B, Mg, Ni, Ti, Mo, Co, Ca, Cr, Cu, Fe, Mn An alloy, a compound, a solid solution, or the like in which a part of Si is substituted with at least one element selected from the group consisting of Nb, Ta, V, W, Zn, C, N, and Sn can be used. As the tin-containing material, Ni ₂ Sn ₄ , Mg ₂ Sn, SnO _x (0 <x <2), SnO ₂ , SnSiO ₃ , LiSnO, or the like can be applied.

These materials may constitute the negative electrode active material alone, or may be composed of a plurality of types of materials. Examples of constituting the negative electrode active material by the plurality of types of materials include a compound containing Si, oxygen and nitrogen, and a composite of a plurality of compounds containing Si and oxygen and having different constituent ratios of Si and oxygen. It is done. Among these, SiO _x (0.3 ≦ x ≦ 1.3) is preferable because it has a large discharge capacity density and an expansion coefficient lower than that of Si.

  The negative electrode mixture layer includes a composite negative electrode active material in which carbon nanofibers (hereinafter referred to as “CNF”) are attached to the surface of a negative electrode active material capable of at least occluding and releasing lithium ions. Since CNF adheres to or adheres to the surface of the negative electrode active material, resistance to current collection is reduced in the battery, and high electron conductivity is maintained.

  The negative electrode mixture layer further contains a binder. Examples of the binder include polyvinylidene fluoride (PVDF), polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, polyacrylic acid methyl ester, and polyacrylic. Acid ethyl ester, polyacrylic acid hexyl ester, polymethacrylic acid, polymethacrylic acid methyl ester, polymethacrylic acid ethyl ester, polymethacrylic acid hexyl ester, polyvinyl acetate, polyvinylpyrrolidone, polyether, polyethersulfone, hexafluoropolypropylene Styrene-butadiene rubber, carboxymethyl cellulose, and the like can be used. Two types selected from tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkyl vinyl ether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid, and hexadiene A copolymer of the above materials may be used.

  If necessary, natural graphite such as flake graphite, graphite such as artificial graphite and expanded graphite, carbon blacks such as acetylene black, ketjen black, channel black, furnace black, lamp black and thermal black, carbon fiber Conductive agents such as conductive fibers such as metal fibers, metal powders such as copper and nickel, and organic conductive materials such as polyphenylene derivatives may be mixed in the negative electrode mixture layer.

  Moreover, as a non-aqueous electrolyte (not shown), an electrolyte solution in which a solute is dissolved in an organic solvent, or a so-called polymer electrolyte layer containing these and non-fluidized with a polymer can be applied.

  When using at least an electrolyte solution, a separator 3 such as a nonwoven fabric or a microporous film made of polyethylene, polypropylene, aramid resin, amideimide, polyphenylene sulfide, polyimide, or the like is used between the positive electrode 2 and the negative electrode 1, and the electrolyte solution is used for this. Is preferably impregnated. Further, the inside or the surface of the separator 3 may contain a heat resistant filler such as alumina, magnesia, silica, and titania. Apart from the separator 3, a heat-resistant layer composed of these fillers and a binder similar to that used for the positive electrode 2 and the negative electrode 1 may be provided.

The non-aqueous electrolyte material is selected based on the redox potential of the positive electrode active material and the negative electrode active material. Solutes preferably used for the non-aqueous electrolyte include LiPF ₆ , LiBF ₄ , LiClO ₄ , LiAlCl ₄ , LiSbF ₆ , LiSCN, LiCF ₃ SO ₃ , LiN (CF ₃ CO ₂ ), LiN (CF ₃ SO ₂ ) _2. LiAsF ₆ , LiB ₁₀ Cl ₁₀ , lower aliphatic lithium carboxylate, LiF, LiCl, LiBr, LiI, chloroborane lithium, bis (1,2-benzenediolate (2-)-O, O ′) lithium borate, Bis (2,3-naphthalenedioleate (2-)-O, O ') lithium borate, bis (2,2'-biphenyldiolate (2-)-O, O') lithium borate, bis (5-fluoro 2-oleate-1-benzenesulfonic acid -O, O ') borate borate salts such as _{lithium, (CF 3 SO 2) 2} NLi _{LiN (CF 3 SO 2) (} C 4 F 9 SO 2), can be applied salts used in _{(C 2 F 5 SO 2)} 2 NLi, lithium tetraphenyl borate, etc., generally lithium battery.

  Furthermore, the organic solvent for dissolving the salts includes ethylene carbonate (EC), propylene carbonate, butylene carbonate, vinylene carbonate, dimethyl carbonate (DMC), diethyl carbonate, ethyl methyl carbonate (EMC), dipropyl carbonate, methyl formate, Methyl acetate, methyl propionate, ethyl propionate, dimethoxymethane, γ-butyrolactone, γ-valerolactone, 1,2-diethoxyethane, 1,2-dimethoxyethane, ethoxymethoxyethane, trimethoxymethane, tetrahydrofuran, 2- Tetrahydrofuran derivatives such as methyltetrahydrofuran, dimethyl sulfoxide, 1,3-dioxolane, dioxolane derivatives such as 4-methyl-1,3-dioxolane, formamide, Acetamide, dimethylformamide, acetonitrile, propylnitrile, nitromethane, ethyl monoglyme, phosphate triester, acetate ester, propionate ester, sulfolane, 3-methylsulfolane, 1,3-dimethyl-2-imidazolidinone, 3-methyl 2-Oxazolidinone, propylene carbonate derivatives, ethyl ether, diethyl ether, 1,3-propane sultone, anisole, mixtures of one or more such as fluorobenzene, and the like, commonly used in lithium batteries Applicable.

  Furthermore, vinylene carbonate, cyclohexyl benzene, biphenyl, diphenyl ether, vinyl ethylene carbonate, divinyl ethylene carbonate, phenyl ethylene carbonate, diallyl carbonate, fluoroethylene carbonate, catechol carbonate, vinyl acetate, ethylene sulfite, propane sultone, trifluoropropylene carbonate, Additives such as dibenisofuran, 2,4-difluoroanisole, o-terphenyl, m-terphenyl may be included.

The non-aqueous electrolyte is composed of one or more kinds of polymer materials such as polyethylene oxide, polypropylene oxide, polyphosphazene, polyaziridine, polyethylene sulfide, polyvinyl alcohol, polyvinylidene fluoride, polyhexafluoropropylene, and the like. May be used as a solid electrolyte. Moreover, you may mix with the said organic solvent and use it in a gel form. Further, lithium nitride, lithium halide, lithium oxyacid _{salt, Li 4 SiO 4, Li 4} SiO 4 -LiI-LiOH, Li 3 PO 4 -Li 4 SiO 4, Li 2 SiS 3, Li 3 PO 4 -Li Inorganic materials such as ₂ S—SiS ₂ and phosphorus sulfide compounds may be used as the solid electrolyte.

  Here, in the present embodiment, as shown in FIG. 1, a rectangular battery is used as the nonaqueous electrolyte secondary battery, and the amount of gas generated is evaluated by a change in the thickness of the battery case. Note that the expansion of the battery case due to the gas generated by the reaction of the positive electrode active material with moisture does not result from the shape of the battery, but a non-aqueous electrolyte secondary battery having a flat battery such as a button battery or other shapes. This also occurs in the same way.

  Specific examples in the embodiment of the present invention will be described below.

Example 1
(Preparation of positive electrode)
First, 1 kg of powdered LiCoO ₂ (average particle size 12 μm) as a positive electrode active material and 1 kg of dioxane containing 5% by weight of methyltrimethoxysilane (KBM13 manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent, After stirring at 0 ° C., it was vacuum dried at 120 ° C. to obtain powdered LiCoO ₂ .

Next, 1 kg of the obtained positive electrode active material mainly composed of powdered LiCoO ₂ was mixed with N-methyl-2-pyrrolidone (NMP) of PVDF (# 1320, solid content 12% by weight) manufactured by Kureha Chemical Co., Ltd. ) A positive electrode mixture paste was prepared by stirring at 30 ° C. for 30 minutes using a double-arm kneader together with 0.5 kg of the solution, 40 g of acetylene black and an appropriate amount of NMP.

  Next, the obtained positive electrode mixture paste was applied to both surfaces of a 20 μm thick aluminum foil serving as a current collector, dried at 120 ° C. for 15 minutes, and then roll-pressed so that the total thickness of the positive electrode was 160 μm. did. The roller diameter used in the roll press was 40 cm in diameter, and the linear pressure indicating the press pressure was 10,000 N / cm.

  Thereafter, the positive electrode mixture layer of the positive electrode that was roll-pressed was impregnated by treatment method 1a using methyltrimethoxysilane (KBM13 manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent. Thereafter, it was heated at 120 ° C. and dried.

  Then, the obtained positive electrode was cut into a width that could be inserted into a rectangular battery case having a height of 50 mm, a width of 34 mm, and a thickness of 5 mm to obtain a positive electrode provided with a positive electrode lead.

  The positive electrode was produced in an environment where the dew point can be maintained at −50 ° C. or lower.

(Preparation of negative electrode)
First, 3 kg of artificial graphite was added to 200 g of BM-400B (dispersion of modified styrene-butadiene rubber having a solid content of 40% by weight), 50 g of carboxymethyl cellulose (CMC), and an appropriate amount of water, manufactured by Nippon Zeon Co., Ltd. The mixture was stirred with a kneader to prepare a negative electrode mixture paste.

  Next, the obtained negative electrode mixture paste was applied on both sides of a 12 μm thick copper foil serving as a current collector, dried at 120 ° C., and rolled so that the total thickness of the negative electrode was 160 μm.

  Then, the obtained negative electrode was cut into a width that could be inserted into a rectangular battery case having a height of 50 mm, a width of 34 mm, and a thickness of 5 mm to obtain a negative electrode having a negative electrode lead.

(Production of battery)
First, the negative electrode 1 and the positive electrode 2 produced as described above were wound through a separator 3 to form a spiral electrode group 4. Here, as separator 3, a composite film of polyethylene and polypropylene (2300 manufactured by Celgard Co., Ltd., thickness 25 μm) was used.

  Next, the opening part of the battery case 5 was sealed with the sealing plate 6 provided with the negative electrode external connection terminal 10, and after the nonaqueous electrolyte was injected from the liquid injection port, it was sealed with the liquid injection port sealing part 8. In this manner, a rectangular battery having a height of 50 mm, a width of 34 mm, and a thickness of 5 mm was produced. The design capacity of the battery was 900 mAh.

  A non-aqueous electrolyte secondary battery having a positive electrode manufactured by the above method is referred to as Sample 1.

(Example 2)
Sample 2 is a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material.

(Example 3)
Sample 3 is a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material.

Example 4
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and trifluoropropyltrimethoxysilane (KBM7103 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. A non-aqueous electrolyte secondary battery produced by the same method as in Example 4 is designated as sample 4.

(Example 5)
The same as Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and dimethyldimethoxysilane (KBM22 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. A non-aqueous electrolyte secondary battery produced by the method is designated as sample 5.

(Example 6)
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material, and methyltriethoxysilane (KBE13 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. The nonaqueous electrolyte secondary battery produced by the method is designated as Sample 6.

(Example 7)
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and decyltrimethoxysilane (KBM3103 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. The nonaqueous electrolyte secondary battery produced by the method is designated as Sample 7.

(Example 8)
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and hexyltrimethoxysilane (KBM3063 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. The nonaqueous electrolyte secondary battery produced by the method is designated as Sample 8.

Example 9
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and hexyltriethoxysilane (KBE3063 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. The nonaqueous electrolyte secondary battery produced by the method is designated as sample 9.

(Example 10)
Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and phenyltrimethoxysilane (KBM103 manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the silane coupling agent. The nonaqueous electrolyte secondary battery produced by the method is designated as sample 10.

(Example 11)
First, using the treatment method 1b, a positive electrode active material (average particle size 12 μm) mainly composed of LiCoO ₂ not previously treated with a silane coupling agent was roll-pressed in the same manner as in Example 3. Sample 11 is a nonaqueous electrolyte secondary battery using a positive electrode prepared by impregnating methyltrimethoxysilane as a silane coupling agent on the surface of the positive electrode mixture layer of the positive electrode.

(Example 12)
Sample 12 is a nonaqueous electrolyte secondary battery produced by the same method as in Example 11 except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material.

(Example 13)
Sample 13 is a nonaqueous electrolyte secondary battery produced by the same method as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material.

(Example 14)
Non-aqueous produced by the same method as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and trifluoropropyltrimethoxysilane was used as the silane coupling agent. The electrolyte secondary battery is referred to as Sample 14.

(Example 15)
A nonaqueous electrolyte secondary produced by the same method as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and dimethyldimethoxysilane was used as the silane coupling agent. The battery is designated as sample 15.

(Example 16)
The nonaqueous electrolyte 2 was prepared in the same manner as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and methyltriethoxysilane was used as the silane coupling agent. The secondary battery is designated as Sample 16.

(Example 17)
The nonaqueous electrolyte 2 was prepared by the same method as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and decyltrimethoxysilane was used as the silane coupling agent. The secondary battery is designated as sample 17.

(Example 18)
The nonaqueous electrolyte 2 was prepared by the same method as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and hexyltrimethoxysilane was used as the silane coupling agent. The secondary battery is designated as sample 18.

(Example 19)
The nonaqueous electrolyte 2 was prepared in the same manner as in Example 11 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and phenyltrimethoxysilane was used as the silane coupling agent. The next battery is designated as sample 19.

(Example 20)
First, by using the processing method 2a, a positive electrode mixture layer of a positive electrode that was pressed by pressing a porous roller sufficiently impregnated with a silane coupling agent against the surface of the positive electrode was impregnated. Then, the obtained positive electrode was heated at 120 ° C. and dried. At this time, the roller diameter used in the roll press was 40 cm in diameter, and the linear pressure indicating the press pressure was 10,000 N / cm.

  That is, a sample 20 is a nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that the positive electrode was treated using the treatment method 2a.

(Example 21)
A sample of a nonaqueous electrolyte secondary battery produced by the same method as in Example 20 except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material and methyltrimethoxysilane was used as the silane coupling agent. 21.

(Example 22)
The nonaqueous electrolyte 2 was prepared in the same manner as in Example 20 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and methyltrimethoxysilane was used as the silane coupling agent. The secondary battery is designated as Sample 22.

(Example 23)
A nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that the positive electrode was treated using the treatment method 3 is referred to as Sample 23.

  As specific treatment method 3, after the positive electrode after pressing is impregnated with a silane coupling agent, an argon gas having a dew point of −100 ° C. or less is blown onto the positive electrode surface, whereby an extra silane coupling agent attached to the positive electrode surface. Removed.

(Example 24)
A sample of a nonaqueous electrolyte secondary battery produced by the same method as in Example 23, except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material and methyltrimethoxysilane was used as the silane coupling agent. 24.

(Example 25)
The nonaqueous electrolyte 2 was prepared by the same method as in Example 23 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material and methyltrimethoxysilane was used as the silane coupling agent. The secondary battery is designated as sample 25.

(Example 26)
A nonaqueous electrolyte secondary battery produced by the same method as in Example 1 except that LiCoO ₂ was used as the positive electrode active material and the positive electrode was treated by the treatment method 2a using trifluoropropyltrimethoxysilane as the silane coupling agent. Is designated as sample 26.

(Example 27)
A non-aqueous electrolyte secondary battery produced by the same method as in Example 26 is used as sample 27 except that LiMn _1/3 Ni _1/3 CoO ₂ is used as the positive electrode active material.

(Example 28)
A non-aqueous electrolyte secondary battery produced by the same method as in Example 26 is used as sample 28 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ is used as the positive electrode active material.

(Example 29)
A non-aqueous electrolyte secondary battery manufactured by the same method as in Example 26 is used as sample 29 except that the positive electrode is processed using processing method 3.

(Example 30)
A non-aqueous electrolyte secondary battery produced by the same method as in Example 29 is used as sample 30 except that LiMn _1/3 Ni _1/3 CoO ₂ is used as the positive electrode active material.

(Example 31)
A non-aqueous electrolyte secondary battery produced by the same method as in Example 29 is used as sample 31 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ is used as the positive electrode active material.

(Example 32)
Treatment using LiNi _0.80 Co _0.15 Al _0.05 O ₂ as a positive electrode active material and applying methylmethoxysilane as a silane coupling agent so as to wet the surface of the positive electrode mixture layer from the injection nozzle A non-aqueous electrolyte secondary battery produced by the same method as in Example 1 except that the positive electrode was treated by Method 2b was designated as Sample 32.

  Next, a nonaqueous electrolyte secondary battery used as a comparative example will be described.

  In the following, the method in which the positive electrode active material is not pretreated with a silane coupling agent and the silane coupling agent is not impregnated even during roll press is referred to as treatment method 4, and the positive electrode active material is pretreated with a silane coupling agent and roll press. A method that does not sometimes impregnate the silane coupling agent will be described as treatment method 5.

(Comparative Example 1)
Produced by the same method as in Example 1 except that the positive electrode mixture layer whose thickness was adjusted by roll pressing a positive electrode mixture layer using LiCoO ₂ that has not been treated with a silane coupling agent by treatment method 4 is used. The nonaqueous electrolyte secondary battery thus obtained is designated as sample C1.

(Comparative Example 2)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 1 except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material is referred to as Sample C2.

(Comparative Example 3)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 1 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material is referred to as Sample C3.

(Comparative Example 4)
According to treatment method 5, 5% by weight methyltrimethoxysilane as a silane coupling agent was added to dioxane and diluted, and LiCoO ₂ was added and kneaded as a positive electrode active material powder to this solution, followed by stirring at 80 ° C., A non-electrode produced by the same method as in Example 1 except that a positive electrode mixture layer was formed using a powdered positive electrode active material obtained by vacuum drying at 120 ° C., and a positive electrode whose thickness was adjusted by roll pressing was used. The water electrolyte secondary battery is designated as sample C4.

(Comparative Example 5)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 4 except that LiMn _1/3 Ni _1/3 CoO ₂ was used as the positive electrode active material is referred to as Sample C5.

(Comparative Example 6)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 4 except that LiNi _0.80 Co _0.15 Al _0.05 O ₂ was used as the positive electrode active material is designated as Sample C6.

(Comparative Example 7)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 6 except that trifluoropropyltrimethoxysilane was used as the silane coupling agent was designated as Sample C7.

(Comparative Example 8)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 6 is used as sample C8 except that dimethyldimethoxysilane is used as the silane coupling agent.

(Comparative Example 9)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 6 is used as sample C9 except that methyltriethoxysilane is used as the silane coupling agent.

(Comparative Example 10)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 6 is used as sample C10 except that decyltrimethoxysilane is used as the silane coupling agent.

(Comparative Example 11)
A nonaqueous electrolyte secondary battery produced by the same method as in Comparative Example 6 is used as sample C11 except that hexyltrimethoxysilane is used as the silane coupling agent.

  The positive electrode treated by each of the above treatment methods was stored under the following storage environment conditions (A) and (B), and the non-aqueous square samples of Sample 1 to Sample 32 and Sample C1 to Sample C11 were prepared. The following evaluation was performed on the electrolyte secondary battery.

(Environmental conditions for positive electrode storage)
(A) 12 hours storage at a dew point of −50 ° C. (B) 12 hours storage at a temperature of 25 ° C. and a relative humidity of 50% (battery evaluation method)
(1) Cycle characteristics Each square nonaqueous electrolyte secondary battery was charged and discharged under the following conditions at an environmental temperature of 45 ° C.

  The maximum current value was 0.9 A, and constant voltage charging was performed at 4.2 V. The termination condition was 50 mA. Pause for 30 minutes after charging.

  Thereafter, the battery was discharged at a constant current of 0.9 A, and the end condition was 3.0 V. The pause between charging and discharging was 30 minutes.

  The charge / discharge cycle was defined as one cycle, which was repeated 500 times. And the value which expressed the ratio of the discharge capacity of the 500th cycle with respect to the discharge capacity of the 1st cycle in percentage was calculated | required as a capacity maintenance rate (%).

(2) Battery thickness measurement After discharging each square-shaped non-aqueous electrolyte secondary battery of each of the above Examples and Comparative Examples to 3.0 V under a constant current condition of 50 mA at 25 ° C. environmental temperature, Paused for 30 minutes. Thereafter, the battery was charged at 200 mA for 4 hours and then allowed to stand at 45 ° C. ambient temperature for 10 hours. Further, the battery taken out from the 45 ° C. environment was cooled in a 25 ° C. temperature environment until the battery temperature reached 25 ° C., and the battery thickness at the battery temperature of 25 ° C. was measured.

  The specifications and evaluation results of Sample 1 to Sample 32 are shown in (Table 1), and the specifications and evaluation results of Sample C1 to Sample C11 are shown in (Table 2).

  From (Table 1) and (Table 2), when the positive electrode was stored under storage conditions (A), no significant difference was observed in the battery thickness and capacity retention rate between sample 1 to sample 32 and sample C1 to sample C11. . This is because the positive electrode active material of the positive electrode does not react with moisture because there is no moisture in the surrounding environment under these conditions.

  However, when the positive electrode was stored under storage conditions (B), a large difference in battery thickness and capacity retention rate was measured depending on the presence or absence of the silane coupling agent treatment and the treatment method.

  That is, in Sample 1 to Sample 32, there was no significant difference in battery thickness and capacity retention rate depending on the positive electrode active material, the silane coupling agent, and the treatment method. On the other hand, in Samples C1 to C11, when the positive electrode was allowed to stand under storage conditions (B), the battery thickness was large, and the decrease in the capacity retention rate after the cycle characteristics test was also large. This is because the silane coupling agent does not exist near the fracture surface, that is, near the surface of the new positive electrode active material due to the rupture of the positive electrode active material that occurs during the roll press of the positive electrode. It is.

However, from comparison between sample 1 and sample 11 and sample C1 and sample C4, the positive electrode active material is not treated even in the storage environment (A) and the storage environment (B) even if the positive electrode active material is previously treated with a silane coupling agent. In addition, even when the positive electrode was not treated with a silane coupling agent, the change in battery thickness and the decrease in the capacity retention rate were small compared to the samples prepared in other comparative examples. This is because even if a fracture surface is generated in the positive electrode active material by the roll press, since the positive electrode active material is LiCoO ₂ , the reactivity with moisture is small.

In Sample C2, Sample C3, and Sample C5 to Sample C11, the positive electrode active material is a lithium-containing composite oxide containing nickel and is easily decomposed by moisture. Therefore, in the sample using the positive electrode produced in the storage environment (B), the increase in the battery thickness due to the generation of gas and the decrease in the capacity retention rate after the charge / discharge cycle test are large, and the tendency is that the nickel content is large. It is remarkable. In particular, in the case of Sample C6 to Sample C11 having a positive electrode using LiNi _0.80 Co _0.15 Al _0.05 O ₂ as a positive electrode active material, it does not contain nickel regardless of the type of silane coupling agent used. Compared with sample C1, the capacity retention rate is extremely reduced.

  On the other hand, in each sample in the example of the present invention, as is clear from (Table 1), in the storage environment (B) as compared with the storage environment (A), the above-mentioned deterioration of the property is not recognized, and the roll It was confirmed that the treatment of the silane coupling agent on the fracture surface of the positive electrode active material generated by pressing had a remarkable effect.

  This is because the reaction between moisture and the positive electrode active material is suppressed by the presence of the silane coupling agent in the vicinity of the surface of the fracture surface of the positive electrode active material. Thereby, generation | occurrence | production of the decomposition gas from a positive electrode active material is suppressed, As a result, a high capacity | capacitance maintenance factor can be hold | maintained even if a charge / discharge cycle test is repeated 500 cycles.

  And the effect is exhibited also in the lithium containing complex oxide containing nickel as a positive electrode active material which can implement | achieve a high capacity | capacitance, and can obtain the nonaqueous electrolyte secondary battery which has a high capacity | capacitance density.

  Further, comparing the sample 22 and the sample 32, regardless of the treatment method such as the treatment method 2a applied with a roller in which the positive electrode is impregnated with the silane coupling agent or the treatment method 2b applied by the spray method, the battery thickness There was no change or difference in capacity maintenance rate, and it was found that both are effective treatment methods.

  In the embodiment of the present invention, an example in which the present invention is applied to a wound prismatic non-aqueous electrolyte secondary battery has been described. However, the shape of the battery according to the present invention is not limited to a square, The present invention can also be applied to flat batteries, wound cylindrical batteries, laminated coin batteries, and laminated batteries. Further, although the battery for a small device has been studied, it is needless to say that it is effective for a large-sized and large-capacity battery such as a power source for electric vehicles and power storage.

  The present invention reversibly occludes and releases lithium ions as a positive electrode mixture layer in a positive electrode for a non-aqueous electrolyte secondary battery including a current collector and a positive electrode mixture layer formed on the current collector. A positive electrode active material is used, and a silane coupling agent is disposed near the surface of the positive electrode active material and the surface of the fracture surface of the positive electrode active material. With such a configuration, since the reaction between the fracture surface of the positive electrode active material and moisture can be suppressed in the battery manufacturing process, it is not necessary to strictly manage the storage of the positive electrode, and it is excellent in high capacity. A non-aqueous electrolyte secondary battery having charge / discharge cycle characteristics can be manufactured at low cost and with high productivity.

1 is a partially developed perspective view of a nonaqueous electrolyte secondary battery in an embodiment of the present invention. Partial sectional drawing of the positive electrode in embodiment of this invention Partial sectional drawing which shows the process of the processing method 1 of the positive electrode silane coupling agent in embodiment of this invention (A) Partial sectional view showing the process of the positive electrode silane coupling agent treatment method 2a in the embodiment of the present invention (b) The positive electrode silane coupling agent treatment method 2b process in the same embodiment Partial sectional view Partial sectional drawing which shows the process of the processing method 3 of the positive electrode silane coupling agent in embodiment of this invention (A) Partial sectional view of a conventional positive electrode (b) Partial sectional view of a conventional positive electrode after the pressing step

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Negative electrode 2 Positive electrode 3 Separator 4 Electrode group 5 Battery case 6 Sealing plate 7 Positive electrode lead 8 Injection hole sealing part 9 Negative electrode lead 10 Negative electrode external connection terminal 11 Frame body 22 Positive electrode mixture layer 23 Positive electrode active material 23a Broken surface 24, 24a, 26, 54 Silane coupling agent 25 Binder 31 Roll roll 32 Transfer roll 42, 56 Injection nozzle 52 Immersion tank 58 Inert gas

Claims (2)

Forming a positive electrode mixture layer containing a positive electrode active material that reversibly occludes / releases lithium ions on a current collector;
A step of pressing the positive electrode mixture layer to a predetermined thickness and impregnating a silane coupling agent in the vicinity of the surface of the fracture surface of the positive electrode active material generated at least by the pressing ;
The manufacturing method of the positive electrode for nonaqueous electrolyte secondary batteries characterized by including. A nonaqueous electrolyte secondary battery comprising a positive electrode for a nonaqueous electrolyte secondary battery obtained by the production method according to claim 1, a negative electrode, and a nonaqueous electrolyte.

Images