JP2009009703A - Organic solid electrolyte and secondary battery using this - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an organic solid electrolyte of high ion conductivity which does not react with an electrochemical active material, and a secondary battery using the electrolyte. <P>SOLUTION: The organic solid electrolyte is characterized by being composed by compounding a polymer substance which is obtained by polymerizing or copolymerizing a monomer shown by a formula (1) CH<SB>2</SB>=CHCOO-(CH<SB>2</SB>)<SB>2</SB>-CN and/or a monomer shown by a formula (2) CH<SB>2</SB>=C(CH<SB>3</SB>)COO-(CH<SB>2</SB>)<SB>2</SB>-CN and an inorganic ion salt. Since the organic solid electrolyte uses the polymer substance which has high ion conductivity and has no hydroxide group, there can be provided a secondary battery that is not accompanied the generation of gas in the substance and has a great industrial value when used, for example, as the secondary battery. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention is a solid electrolyte having high ionic conductivity useful for batteries, electrochromic devices, sensors, actuators, etc., in particular, an organic solid electrolyte using a polymer material obtained by polymerizing or copolymerizing a monomer having a cyano group And a secondary battery using the same.

In recent years, interest in batteries, particularly secondary batteries, or batteries, has increased. The applications are wide-ranging, such as mobile phones, portable video cameras, portable computers, electric vehicles and the like. Particularly lithium ion secondary batteries, Ni-MH batteries with a conventional, Ni-Cd batteries, than a battery using an aqueous electrolyte solution such as H ₂ SO ₄ -Pb batteries, advantageously has a high voltage and energy density Because it is used. However, since a lithium ion secondary battery uses an organic electrolyte, it has safety problems such as ignition and explosion.

  On the other hand, a battery that does not use an electrolytic solution, that is, a battery that uses an electrolyte made of an ion conductive solid has been studied. As an example, lithium perchlorate is dissolved in polyethylene oxide (Patent Document 1: Japanese Patent Laid-Open No. 2-56870). However, since the ionic conductivity is not sufficient and the contact resistance between the positive electrode and the negative electrode is high, there is no practicality. However, since then, research on ion-conducting polymer materials has been actively conducted.

Compared to inorganic materials, organic materials have advantages such as a low specific gravity, easy molding, and a flexible and thin film can be easily obtained. On the other hand, the required characteristics as a general solid electrolyte including a polymer substance solid electrolyte are (1) moldability, (2) high ionic conductivity, (3) stability, that is, it does not react with an electrochemically active substance. The importance is in the order of (2), (3), and (1). As organic substances that have been studied in the past, there are many polyethylene derivatives due to the above-mentioned circumstances, and dielectrics are systems in which additives are added to polyvinylidene fluoride or polyacrylonitrile, and conductivity σ = 10 ⁻⁷ to 10 ⁻⁵ (S / cm). These conventional polymer substances did not sufficiently satisfy the above required characteristics to satisfy the practical purpose of the battery and the like expected to be applied as an organic solid electrolyte. For example, polyethylene oxide derivatives have a problem of crystallization at a low temperature. For dielectrics, polyvinylidene fluoride has a relative dielectric constant of 9.2, and polyacrylonitrile has a dielectric constant of 8.0. Since a large amount of electrolyte cannot be contained, a solid electrolyte having a small number of carrier ions and high ion conductivity has not been obtained.

  Further, Patent Document 2 (Japanese Patent Laid-Open No. 4-363869) is exemplified as an application of a dielectric having a cyano group as a solid electrolyte. This shows a polymer substance obtained by substituting polyvinyl alcohol, polysaccharides and derivatives thereof with a cyanoethyl group, and shows relatively high ionic conductivity in a system using lithium ions. Patent Document 3 (Japanese Patent Laid-Open No. 9-50824) discloses a gel electrolyte using a dielectric material having a cyano group, and also shows a relatively high ionic conductivity in a system using lithium ions. ing. These dielectrics having a cyano group sufficiently satisfy the above (1) and satisfy (2) to some extent, but the required properties of not reacting with the electrochemically active substance of (3) are insufficient. there were. These dielectric materials having a cyano group are obtained by substituting all the hydroxyl groups with cyanoethyl groups, which are obtained by substituting the hydroxyl groups with cyanoethyl groups. Is difficult at present, and a certain proportion of hydroxyl groups remain. Further, when these dielectric materials having a cyano group are used as a material for a lithium ion secondary battery, it is inevitable that gas is generated due to an alcoholate reaction between a hydroxyl group and lithium ions.

  Patent Document 4 (JP-A-3-74419) exemplifies a radical copolymer of vinyl ethers and cyanoethyl acrylate (the following formula (1)) or cyanoethyl methacrylate (the following formula (2)). It is difficult to obtain a polymer having a sufficient degree of polymerization.

JP-A-2-56870 JP-A-4-363869 Japanese Patent Laid-Open No. 9-50824 Japanese Patent Laid-Open No. 3-74419

  The present invention has been made in view of the above circumstances, and an object thereof is to provide a highly ionic conductive organic solid electrolyte that does not react with an electrochemically active substance and a secondary battery using the same.

  As a result of intensive studies to solve the above-mentioned problems, the present inventor showed good ion conductivity when a cyano group-containing compound having no hydroxyl group was used as an organic substance constituting the organic solid electrolyte. The inventors have found that an organic solid electrolyte that does not react with an electrochemically active substance can be obtained, and have completed the present invention.

Accordingly, the present invention provides the following organic solid electrolyte and a secondary battery using the same.
Claim 1:
An organic material obtained by combining a polymer material obtained by polymerizing or copolymerizing a monomer represented by the following formula (1) and / or a monomer represented by the following formula (2) with an inorganic ion salt: Solid electrolyte.
_{CH 2 = CHCOO- (CH 2)} 2 -CN (1)
_{CH 2 = C (CH 3)} COO- (CH 2) 2 -CN (2)
Claim 2:
2. The organic solid electrolyte according to claim 1, wherein a molar ratio of the formulas (1) and (2) in the polymer substance is 100: 0 to 50:50.
Claim 3:
The organic solid electrolyte according to claim 1 or 2, wherein the inorganic ion salt contains at least one inorganic ion salt containing Li element.
Claim 4:
The secondary battery which has arrange | positioned the organic solid electrolyte of any one of Claims 1-3 between the positive electrode and the negative electrode.

  Since the organic solid electrolyte of the present invention uses not only high ionic conductivity but also a polymer substance having no hydroxyl group, for example, when used in a secondary battery, the organic solid electrolyte is substantially free from gas generation 2. A secondary battery can be provided, and the industrial value is great.

  Since the organic solid electrolyte of the present invention contains a polymer material having a cyano group, it has a very high relative dielectric constant compared to an organic material containing a normal polymer material, and can reduce the electrostatic energy of inorganic ions. Useful, promotes dissociation of the electrolyte, can be combined in large amounts, and can be an organic solid electrolyte having high ionic conductivity.

Specifically, it is obtained by polymerizing or copolymerizing a monomer represented by the following formula (1) and / or a monomer represented by the following formula (2), and having a dimethylformamide as a solvent at a concentration of 20% by mass. It is a polymer substance having a viscosity of 30 to 8000 mPa · s.
_{CH 2 = CHCOO- (CH 2)} 2 -CN (1)
_{CH 2 = C (CH 3)} COO- (CH 2) 2 -CN (2)

The polymer material is produced by radical polymerization of the monomer represented by the formula (1) and / or the monomer represented by the formula (2) using a radical polymerization initiator.
Here, as the radical polymerization initiator, those usually used may be used, but 2,2′-azobisisobutyronitrile, 2,2′-azobis (2,4-dimethylvaleronitrile), 2,2′- Examples thereof include azo-based catalysts such as azobis-2-methylbutyronitrile and peroxide-based catalysts such as benzoyl peroxide.

  Since the polymer substance according to the present invention has a cyano group in its molecular structure, an azo polymerization initiator having a nitrile group is particularly preferable as the radical polymerization initiator. The addition amount of a polymerization initiator is 0.005-0.02 as mole number ratio with respect to the mole number of monomer whole quantity. If the addition amount of the polymerization initiator is too small, the polymerization may not proceed sufficiently due to radical deactivation, etc., and if it is too large, it becomes difficult to control the polymerization reaction, and the degree of polymerization of the resulting polymer substance is high. It may be difficult to use for subsequent use, for example, it becomes very insoluble in a solvent.

  In order to control the polymerization reaction, it is also possible to use a chain transfer agent such as lauryl mercaptan. In this case, the addition amount of the chain transfer agent is 0.05 to 1.0 as a mole number ratio to the mole number of the polymerization initiator. If the addition amount of the chain transfer agent is less than this, there are disadvantages such as difficulty in controlling the polymerization reaction depending on the addition amount of the polymerization initiator, and if it is more than this, the polymerization reaction may not proceed sufficiently.

  As the polymerization method, generally known methods such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization can be used. Examples of the polymerization solvent in the case of solution polymerization include acetone, N, N′-dimethylformamide, esters, ethers, etc., but any solvent that can dissolve the monomer and does not inhibit the polymerization reaction. There is no particular limitation. Considering the purification step after the polymerization reaction, a solvent that is miscible with the crystallization solvent and miscible with water is preferable. In this respect, acetone, N, N′-dimethylformamide, and the like are preferable. In addition, although the monomer concentration in the polymerization solvent is not particularly limited, when the polymerization reaction is performed as solution polymerization, if the monomer concentration in the polymerization solvent is too dilute, the polymerization reaction may not sufficiently proceed. % Or more is preferable. When no polymerization solvent is used, bulk polymerization is performed.

  Although the homopolymer of cyanoethyl acrylate of formula (1) tends to have a high relative dielectric constant and a low softening temperature, the homopolymer of cyanoethyl methacrylate of formula (2) is less than the homopolymer of cyanoethyl acrylate. The dielectric constant tends to be low and the softening temperature tends to be high. Regarding the relative dielectric constant, when cyanoethyl acrylate and cyanoethyl methacrylate are compared as monomers, the content of cyanoethyl groups that are dipole groups is higher in cyanoethyl acrylate than in cyanoethyl methacrylate. On the other hand, regarding the softening temperature, when comparing acrylate homopolymers and methacrylate homopolymers, it is a well-known fact that methacrylate homopolymers are generally higher, and the same applies to polymers of cyanoethyl monomers. is there.

  Since it is considered that the polymer substance of the present invention functions as an ion conductive solid electrolyte by a cyanoethyl group which is a dipole group, it is considered that the higher the relative dielectric constant, the higher the ionic conductivity. In addition, if the softening temperature is too high, the solid electrolyte layer during driving is inferior in flexibility and may not show stable performance. Therefore, the molar ratio of the formulas (1) and (2) in the polymer material is 100: 0-50: 50, preferably 90: 10-50: 50 is preferred. When the molar ratio of the formula (2) is larger than this, the softening temperature may be increased and the relative dielectric constant may be lowered.

The organic solid electrolyte of the present invention can be obtained by combining an inorganic ion salt in addition to the above polymer substance. The inorganic ion salt is not particularly limited as long as it is used for an ordinary electrochemical element as an ion conductive metal salt, but at least one of Li, Na, K, Cs, Ag, Cu and Mg. Contains elements. Specifically, LiClO ₄ , LiI, LiSCN, LiBF ₄ , LiAsF ₅ , LiCF ₃ SO ₃ , LiPF ₄ , NaI, NaSCN, NaBr, NaPF ₅ , KI, KSCN, KPF ₅ , KAsF ₅ , CsSCN, CsPF ₅ , AgNO ₃ , CuC ₁₂ Mg (ClO ₄ ) ₂ , Rb ₄ I _1.75 Cl _3.25 , Li (CF ₃ SO ₂ ) ₂ N, Li (C ₂ F ₅ SO ₂ ) ₂ N, Li (CF ₃ SO ₂ ) ₂ C, _{li (C 2 F 5 SO 2} ) 3 C and the like, which are used alone or in combination of two or more thereof.

  Moreover, the addition amount of the inorganic ion salt is preferably 0.01 to 50% by mass, particularly preferably 0.1 to 30% by mass with respect to the mass of the polymer substance. When the addition amount of the inorganic ion salt is less than this, the ion concentration is too low to obtain practical conductivity, and when it is too much, ions may not be dissolved in the polymer substance and may be precipitated.

  There are no particular restrictions on the method of combining at least one polymer substance of the present invention with an inorganic ion salt. For example, at least one of the polymer and copolymer of the present invention and an inorganic ion salt may be combined with a solvent such as acetone as necessary. A method of dissolving and dissolving uniformly in a film, forming a film and drying, a method of mechanically kneading at least one of the polymer and copolymer shown in the present invention and inorganic ions at room temperature or under heating is arbitrarily selected. be able to. In addition, when a film is formed by a solution method, a solid electrolyte membrane can be obtained by heating under reduced pressure. However, liquid electrolytes used for general lithium ion secondary batteries such as ethylene carbonate, propylene carbonate, dimethyl It can also be carried out by dissolving in a non-aqueous electrolyte such as carbonate, diethyl carbonate, methyl ethyl carbonate, γ-butyrolactone. At this time, it is possible to obtain a solid electrolyte membrane dried by heating under reduced pressure, but by leaving an appropriate arbitrary amount of solvent, the dissolved amount of the ion conductive metal salt in the polymer substance of the present invention And the mobility of metal ions dissolved in the polymer substance can be improved.

Further, the same effect can be obtained by adding an appropriate amount of the above non-aqueous electrolyte later and impregnating the solid electrolyte membrane obtained by drying. Further, since it is known that the volume resistivity of a general polymer substance such as polyester is as high as 10 ¹⁵ (Ω · cm) or more, even polyvinylidene fluoride having a relatively high relative dielectric constant is 10 ^14. Whereas it is about (Ω · cm), the volume resistivity of the polymer substance of the present invention is as low as about 10 ¹² (Ω · cm). A reduction effect is expected.

Next, the secondary battery of the present invention will be described.
The secondary battery of the present invention is formed by arranging the organic solid electrolyte between a positive electrode and a negative electrode.

As the positive electrode active material used for the positive electrode, CuO, Cu ₂ O, Ag ₂ O, CuS, CuSO ₂ , TiS, SiO ₂ , SnO, V ₂ O ₅ , V ₆ O ₁₃ , VO _x , Nb ₂ O ₅ Bi ₂ O ₃ , CrO ₃ , Cr ₂ O ₃ , MoO ₃ , MoS ₂ , WO ₃ , SeO ₂ , MnO ₂ , Mn ₂ O ₄ , Fe ₂ O ₃ , FeO, Fe ₃ O ₄ , Ni ₂ O ₃ Examples thereof include, but are not limited to, metal compounds such as NiO and CoO ₂ and conductive polymer substances such as polypyrrole and polyacene.

  Examples of the negative electrode active material used for the negative electrode include alkali metals, alkali alloys, compounds shown as the positive electrode active material, and carbon materials. As the alkali metal and the alkali alloy, Li series such as Li, Li—Al, Li—Mg, Li—Al—Ni is particularly preferable. Furthermore, when producing a positive electrode and a negative electrode, it is common to add a binder, a conductive agent, and the like, and the materials used are not particularly limited.

  Hereinafter, specific embodiments of the present invention will be described in more detail based on examples and comparative examples.

[Example 1]
A three-necked flask (500 ml) having a condenser and a stirrer was purged with nitrogen, and 70 g of 2-cyanoethyl acrylate monomer distilled by a normal vacuum distillation method was added. Next, 163 g of acetone subjected to dehydration treatment as a polymerization solvent, 2,2′-azobisisobutyronitrile as a radical initiator were added so that the molar ratio with respect to the monomer was 0.01, and further 0.20 as a chain transfer agent. 001 mole of lauryl mercaptan was added. A nitrogen introduction tube was connected, and the reaction was performed at a reaction temperature of 60 ° C. under a reaction time of 300 minutes. After completion, the mixture is cooled to room temperature, the reaction solution is precipitated in an excess amount of methanol, and the precipitate is dissolved in acetone and precipitated with an excess amount of methanol several times, and then the purified precipitate is dried. And about 63 g of poly (2-cyanoethyl acrylate) having a viscosity of 20% by mass using dimethylformamide as a solvent, a viscosity at 20 ° C. of 305 mPa · s, a relative dielectric constant of 40 ° C./1 kHz of about 18, and a softening temperature of about 30 ° C. Obtained.

The obtained poly (2-cyanoethyl acrylate) 2 g was dissolved in 10g of acetone and uniformly mixed with it to a 3g of acetone was dissolved LiClO ₄ in 0.8 g. This solution was cast on a Teflon (registered trademark) plate, and the sample was allowed to stand at room temperature for 24 hours to remove excess solvent, and then dried under reduced pressure at 60 ° C./24 hours to obtain a thickness of about 50 μm. An ion conductive solid electrolyte membrane was obtained. The obtained film was transparent and LiClO ₄ was uniformly mixed.

This film is cut into a disk shape with a diameter of 10 mm, electrodes are formed by sandwiching a stainless steel plate on both sides, and using an AC impedance measuring device multifrequency LCR meter model 4192A (manufactured by Yokogawa Hewlett Packard) with a frequency of 5 Hz to 5 MHz. Ion conductivity was calculated by computer processing of the complex impedance display. As a result, a value of 1.1 × 10 ⁻³ (S / cm) was obtained at 25 ° C.

For the positive electrode, a mixture of LiCoO ₂ and Ketjen Black in a mass ratio of 90: 1 and a solution of 2 g of poly (2-cyanoethyl acrylate) dissolved in 10 g of acetone are mixed at a mass ratio of 1: 2. did. This mixture was cast on a positive electrode current collector plate made of aluminum, and prepared by heating and drying in a nitrogen atmosphere. The negative electrode was prepared by pressure bonding lithium metal to a stainless current collector.

  The obtained ion conductive solid electrolyte membrane was sandwiched between the prepared positive electrode and negative electrode, and heat-pressed at 80 ° C. in a nitrogen atmosphere so that the thickness of the ion conductive solid electrolyte membrane was 25 μm.

The secondary battery produced by the above procedure was placed in a stainless steel pressure vessel, purged with nitrogen, and then sealed at normal pressure. Then, until the battery voltage reached 4.2V with a current of 0.1 mA / cm ^2, repeated 300 times that the voltage discharge at 0.1 mA / cm ² current until 2.75V As a result, no increase in the internal pressure in the container was observed.

[Example 2]
The same operation as in Example 1 was carried out except that 2-cyanoethyl acrylate monomer and 2-cyanoethyl methacrylate monomer were adjusted to a molar ratio of 1: 1 so that the total amount was 73.92 g, and dimethylformamide was used as a solvent. About 66 g of a 20 mass% copolymer having a viscosity at 20 ° C. of 355 mPa · s, a relative dielectric constant of 40 ° C./1 kHz of about 15, and a softening temperature of about 50 ° C. was obtained.

Except using the obtained copolymer, it carried out similarly to Example 1, and obtained the ion conductivity value of 0.9x10 < ^-3 > (S / cm) at 25 degreeC. Further, as in Example 1, no increase in internal pressure was observed in the pressure vessel containing the battery.

[Comparative Example 1]
Evaluation was performed in the same manner as in Example 1 except that cyanoethyl polyvinyl alcohol (CR-V manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the ion conductive polymer substance. The cyanoethyl polyvinyl alcohol used has a relative dielectric constant of about 23 ° C. at 40 ° C./1 kHz, a softening temperature of about 30 ° C., and has about 20 mol% of hydroxyl groups in the molecule.

The ionic conductivity value was as low as 8 × 10 ⁻⁵ (S / cm) at 25 ° C., and as in Example 1, the pressure in the pressure vessel containing the battery was found to increase by about 5%.

Claims (4)

An organic material obtained by combining a polymer material obtained by polymerizing or copolymerizing a monomer represented by the following formula (1) and / or a monomer represented by the following formula (2) with an inorganic ion salt: Solid electrolyte.
_{CH 2 = CHCOO- (CH 2)} 2 -CN (1)
_{CH 2 = C (CH 3)} COO- (CH 2) 2 -CN (2)   2. The organic solid electrolyte according to claim 1, wherein a molar ratio of the formulas (1) and (2) in the polymer substance is 100: 0 to 50:50.   The organic solid electrolyte according to claim 1 or 2, wherein the inorganic ion salt contains at least one inorganic ion salt containing Li element.   The secondary battery which has arrange | positioned the organic solid electrolyte of any one of Claims 1-3 between the positive electrode and the negative electrode.