JP6411268B2 - Non-aqueous electrolyte additive, non-aqueous electrolyte, and electricity storage device - Google Patents

Description

  The present invention relates to an additive for non-aqueous electrolyte, a non-aqueous electrolyte, and an electricity storage device.

  In recent years, research on non-aqueous electrolyte secondary batteries represented by lithium ion batteries has been extensively conducted as interest in solving environmental problems and realizing a sustainable recycling society has increased. Lithium ion batteries have high working voltage and energy density, and are therefore used as power sources for notebook computers and mobile phones. Since lithium ion batteries have a higher energy density than lead batteries and nickel cadmium batteries, realization of higher capacity of the batteries is expected.

  However, the lithium ion battery has a problem that the capacity of the battery decreases as the charge / discharge cycle progresses. The cause of the decrease in capacity is, for example, the decomposition of the electrolyte solution due to the electrode reaction, the decrease in the impregnation property of the electrolyte into the electrode active material layer, and the decrease in the lithium ion intercalation efficiency with a long charge / discharge cycle. It is thought that this is caused by

  Methods for adding various additives to an electrolytic solution have been studied as a method for suppressing a decrease in battery capacity associated with a charge / discharge cycle. Additives are generally decomposed during the first charge and discharge to form a film called a solid electrolyte interface (SEI) on the electrode surface. Since the SEI is formed in the first charge / discharge cycle, lithium ions can move back and forth through the SEI while suppressing the consumption of electricity for the decomposition of the electrolyte during the subsequent charge / discharge. That is, it is considered that the formation of SEI plays a major role in suppressing the deterioration of the secondary battery when the charge / discharge cycle is repeated and improving the battery characteristics, storage characteristics, load characteristics, and the like.

  Examples of the additive for the electrolytic solution include cyclic monosulfonic acid esters in Patent Documents 1 to 3, sulfur-containing aromatic compounds in Patent Document 4, disulfide compounds in Patent Document 5, and disulfonic acids in Patent Documents 6 to 9. Each ester is disclosed. Patent Documents 10 to 15 disclose cyclic carbonates or cyclic sulfones, Patent Document 16 discloses a compound having a nitrogen-containing cyclic group and an electron-withdrawing group, and Patent Document 17 discloses an electrolytic solution containing a compound containing a sulfonic acid amide group. doing.

JP 63-102173 A JP 2000-003724 A JP 11-339850 A JP 05-258753 A JP 2001-052735 A JP 2009-038018 A JP-A-2005-203341 JP 2004-281325 A JP 2005-228631 A Japanese Unexamined Patent Publication No. 04-87156 Japanese Patent Laid-Open No. 10-50342 Japanese Patent Application Laid-Open No. 08-45545 JP 2001-6729 A JP 63-102173 A Japanese Patent Laid-Open No. 05-074486 JP 2014-127354 A JP 2014-194866 A

Geun-Chang, Hyung-Jin Kim, Seung-ll Yu, Song-Hui Jun, Jong-Wook Choi, Myung-Hwan Kim. Journal of The Electrochemical Society, 147, 12, 4391 (2000)

  A compound having a low lowest unoccupied molecular orbital (LUMO) energy is an excellent electron acceptor and is considered to be able to form a stable SEI on the surface of an electrode such as a nonaqueous electrolyte secondary battery (for example, non Patent Document 1).

  Although some of conventional additives such as compounds disclosed in Patent Documents 1 to 9 exhibit low LUMO energy, they are chemically unstable and easily deteriorate due to the influence of moisture and temperature. Had. For example, although a disulfonic acid ester compound exhibits low LUMO energy, it has a low stability to moisture and easily deteriorates. Therefore, when it is stored for a long period of time, it is necessary to strictly control the moisture content and temperature. In general, the lithium ion battery is required to have a heat resistant temperature of about 60 ° C. and the lithium ion capacitor is about 80 ° C. Therefore, the improvement of the non-aqueous electrolyte additive used in the electricity storage device at high temperature is It was one of the important issues.

  In addition, in the case of an electrolytic solution containing a conventional additive, when the power storage device is used over a long period of time while repeating the charge / discharge cycle, the battery characteristics of the power storage device are likely to be deteriorated. There was a need for improvement.

  The electrolyte solutions described in Patent Documents 10 to 14 can suppress irreversible capacity reduction to some extent by SEI generated on the negative electrode surface by electrochemical reductive decomposition. However, although the SEI formed by the additive in these electrolytes is excellent in the performance of protecting the electrode, it is not sufficient in terms of strength to withstand long-term use. When the SEI is decomposed or the SEI is cracked, the surface of the negative electrode is exposed, and the electrolytic solution solvent is decomposed to deteriorate the battery characteristics. The electrolytic solution using the vinylene carbonate-based compound described in Patent Document 15 as an additive generates carbon dioxide and other gases when vinylene carbonate is decomposed on the electrode, resulting in a decrease in battery performance. It had the problem of being connected. The gas generation is particularly remarkable when a charge / discharge cycle is repeated at a high temperature or for a long time.

  As described above, the additive for non-aqueous electrolyte has room for further improvement in terms of storage stability, cycle characteristics for maintaining performance when a charge / discharge cycle is repeated, or suppression of gas generation.

  Accordingly, a main object of the present invention is to provide an additive for a non-aqueous electrolyte that has high storage stability and enables improvement of cycle characteristics and suppression of gas generation for an electricity storage device.

  The present inventors have found that a compound containing a specific partial structure exhibits low LUMO energy and is chemically stable. Furthermore, the present inventors can obtain excellent cycle characteristics and suppress gas generation when the compound is used as an additive for a non-aqueous electrolyte in an electricity storage device such as a non-aqueous electrolyte secondary battery. As a result, the present invention has been completed.

  That is, one aspect of the present invention provides a non-aqueous electrolyte additive containing a compound represented by the following formula (1) or formula (2).

In formula (1) or formula (2), X ¹ , X ² and X ³ each independently represent an optionally substituted methylene group, sulfonyl group or carbonyl group. In formula (1) or formula (2), Y ¹ and Y ² each independently represent an optionally substituted hydrocarbon group having 1 to 6 carbon atoms.

  The compound represented by formula (1) or formula (2) contains a large number of polar groups containing N, O, S, etc., when the cyclic amide or cyclic sulfonamide is opened upon electrochemical reduction. It is thought that SEI is formed. Such SEI containing a large number of polar groups including N, O, S and the like can exhibit excellent ionic conductivity, and thus is considered to be a very high performance SEI. Moreover, it is thought that the compound represented by Formula (1) or Formula (2) forms SEI by ring-opening polymerization of cyclic amide or cyclic sulfonamide, respectively. The formation of SEI makes it difficult for SEI to break down during charging and discharging, and electrolyte decomposition, improves battery characteristics such as cycle characteristics, charge and discharge capacity, and internal resistance, and exhibits gas generation suppression effects. It is thought to do.

  ADVANTAGE OF THE INVENTION According to this invention, while having high storage stability, regarding an electrical storage device, the additive for nonaqueous electrolyte solutions which makes it possible to improve cycling characteristics and to suppress gas generation is provided. The non-aqueous electrolyte additive according to some embodiments is stable SEI (solid electrolyte interface) on the electrode surface when used in power storage devices such as non-aqueous electrolyte secondary batteries and electric double layer capacitors. Thus, battery characteristics such as cycle characteristics, charge / discharge capacity, and internal resistance can be improved.

It is sectional drawing which shows one Embodiment of an electrical storage device.

  Hereinafter, preferred embodiments of the present invention will be described in detail. However, the present invention is not limited to the following embodiments.

The additive for nonaqueous electrolysis according to the present embodiment contains one or more compounds represented by the following formula (1) or formula (2).

In formula (1) or formula (2), X ¹ , X ² and X ³ each independently represent an optionally substituted methylene group, sulfonyl group or carbonyl group. In formula (1) or formula (2), Y ¹ and Y ² each independently represent an optionally substituted hydrocarbon group having 1 to 6 carbon atoms. In formula (1), X ³ may be a methylene group or a carbonyl group, and in formula (2), X ³ may be a methylene group, a sulfonyl group or a carbonyl group.

As a compound represented by Formula (1) or Formula (2), X ¹ , X ² and X ³ may each independently be a sulfonyl group or a carbonyl group. In such a case, the compound represented by the formula (1) or the formula (2) has a low resistance by having two ring-opening polymerization sites and containing a sulfonyl group or a carbonyl group. Since SEI can be formed, effects such as further improvement of battery characteristics and suppression of gas generation are easily obtained.

In formula (1) or formula (2), the hydrocarbon group having 1 to 6 carbon atoms which may be substituted as Y ¹ and Y ² may contain multiple bonds or may be cyclic. Such optionally substituted good 1 to 6 carbon atoms hydrocarbon _{group, -CH 2 CH 2 -, -} CHFCHF -, - CH 2 CH 2 CH 2 -, - CH = CH -, - C 6 H _4- and the like can be mentioned.

  The compound represented by Formula (1) or Formula (2) is, for example, from Formula (3-1), Formula (3-2), Formula (3-3), or Formula from the viewpoints of availability and reactivity. The compound represented by (3-4) may be sufficient.

In Formula (3-1), Formula (3-2), Formula (3-3), and Formula (3-4), X ¹ and X ² , and Y ¹ may be Formula (1) or Formula (2). ^{X 1} and ^{X 2} in, and is synonymous with those illustrated with respect to ^{Y 1.}

  Examples of the compound represented by formula (1) or formula (2) include phthalimide-1-carboxylic acid-2,5-dioxopyrrolidine, 2,5-pyrroldione-1-carboxylic acid-2,5-dioxo. Pyrrolidine, 2,5-dioxopyrrolidine-1-carboxylic acid-2,5-dioxopyrrolidine, o-benzsulfonimide-1-carboxylic acid-2,5-dioxopyrrolidine, benzoimide-1-carboxylic acid-phthalimide 2,5-pyrroldione-1-carboxylic acid-phthalimide, 2,5-dioxopyrrolidine-1-carboxylic acid-phthalimide, o-benzsulfonimide-1-carboxylic acid-phthalimide, and the like.

  Since the compound of formula (1) or formula (2) exhibits low LUMO energy that is susceptible to electrochemical reduction, a non-aqueous electrolyte containing these as additives for non-aqueous electrolyte is non-aqueous electrolyte 2 When used in an electricity storage device such as a secondary battery, stable SEI can be formed on the electrode surface to improve battery characteristics such as cycle characteristics, charge / discharge capacity, and internal resistance. Moreover, since the compound of Formula (1) or Formula (2) is stable with respect to moisture and temperature changes, the non-aqueous electrolyte additive and the non-aqueous electrolyte containing the compound are stored at room temperature for a long period of time. Is possible.

  The LUMO energy of the compound represented by formula (1) or formula (2) may be −3.0 eV or more, or 0.0 eV or less. When the LUMO energy is −3.0 eV or more, it is possible to further avoid the formation of SEI showing high resistance on the negative electrode due to excessive decomposition of the compound. When the LUMO energy is 0.0 eV or less, more stable SEI can be more easily formed on the negative electrode surface. From the same viewpoint, the LUMO energy may be -2.9 eV or more, or -0.5 eV or less. A person skilled in the art can find a compound exhibiting LUMO energy within these numerical ranges without undue trial and error within the range defined by the formula (1) or the formula (2).

  In this specification, “lowest unoccupied molecular orbital (LUMO) energy” is a value calculated by combining the semi-empirical molecular orbital calculation method PM3 and the density functional method B3LYP method. Specifically, the LUMO energy can be calculated using Gaussian 03 (Revision B.03, software manufactured by Gaussian, USA).

  A person skilled in the art can synthesize the compound of formula (1) or formula (2) by combining the usual reactions using available raw materials. For example, the compound of Formula (1) or Formula (2) can be synthesized by a method in which a cyclic imide compound is reacted with a corresponding chloroformate in the presence of a base.

  The additive for non-aqueous electrolyte according to the present embodiment may contain other general components such as a compound that can contribute to SEI formation in addition to the compound of formula (1) or formula (2). Good. Or you may use the compound of Formula (1) or Formula (2) itself as an additive for non-aqueous electrolytes. The additive for non-aqueous electrolyte according to the present embodiment may contain other general components as long as the effects of the present invention are not impaired. Other common components include, for example, vinylene carbonate (VC), fluoroethylene carbonate (FEC), 1,3-propane sultone (PS), negative electrode protective agent, positive electrode protective agent, flame retardant, overcharge inhibitor, etc. Is mentioned.

  The non-aqueous electrolyte according to this embodiment contains the additive for non-aqueous electrolyte, a non-aqueous solvent, and an electrolyte. The content of the additive for nonaqueous electrolyte (or the compound of formula (1) or formula (2)) in this nonaqueous electrolyte is 0.005% by mass or more based on the total mass of the nonaqueous electrolyte. It may be 10% by mass or less. When the content is 0.005% by mass or more, stable SEI is easily formed by an electrochemical reaction on the electrode surface. When the content is 10% by mass or less, the non-aqueous electrolyte additive can be easily dissolved in the non-aqueous solvent. In addition, by not excessively increasing the content of the additive for nonaqueous electrolyte, an increase in viscosity of the nonaqueous electrolyte can be suppressed, and ion mobility can be particularly ensured. If the mobility of ions is not sufficiently ensured, the conductivity of the non-aqueous electrolyte cannot be sufficiently ensured, and the charge / discharge characteristics of the electricity storage device may be hindered. From the same viewpoint, the lower limit of the content of the additive for non-aqueous electrolyte (or the compound of formula (1) or formula (2)) may be 0.01% by mass.

  The non-aqueous electrolyte may contain two or more additives for non-aqueous electrolyte (two or more compounds that form SEI). In this case, the total content of the non-aqueous electrolyte additive may be 0.005% by mass or more and 10% by mass or less based on the total mass of the non-aqueous electrolyte. Examples of other additives include vinylene carbonate (VC), fluoroethylene carbonate (FEC), and 1,3-propane sultone (PS).

  As the non-aqueous solvent, an aprotic solvent can be selected from the viewpoint of keeping the viscosity of the obtained non-aqueous electrolyte low. The aprotic solvent is at least one selected from the group consisting of cyclic carbonate, chain carbonate, aliphatic carboxylic acid ester, lactone, lactam, cyclic ether, chain ether, sulfone, nitrile, and halogen derivatives thereof. It may be. Among these, as the aprotic solvent, a cyclic carbonate and / or a chain carbonate can be selected.

  Examples of the cyclic carbonate include ethylene carbonate, propylene carbonate, and butylene carbonate. Examples of the chain carbonate include dimethyl carbonate, diethyl carbonate, and ethyl methyl carbonate. Examples of the aliphatic carboxylic acid ester include methyl acetate, ethyl acetate, methyl propionate, ethyl propionate, methyl butyrate, methyl isobutyrate, and methyl trimethyl acetate. Examples of lactones include γ-butyrolactone. Examples of the lactam include ε-caprolactam and N-methylpyrrolidone. Examples of the cyclic ether include tetrahydrofuran, 2-methyltetrahydrofuran, tetrahydropyran, and 1,3-dioxolane. Examples of the chain ether include 1,2-diethoxyethane and ethoxymethoxyethane. Examples of the sulfone include sulfolane. Examples of nitriles include acetonitrile. Examples of the halogen derivative include 4-fluoro-1,3-dioxolan-2-one, 4-chloro-1,3-dioxolan-2-one, 4,5-difluoro-1,3-dioxolan-2-one Is mentioned. These nonaqueous solvents may be used alone or in combination of two or more. These nonaqueous solvents are particularly suitable for use in non-aqueous electrolyte secondary batteries such as lithium ion batteries and electric double layer capacitors such as lithium ion capacitors.

The electrolyte constituting the non-aqueous electrolyte may be a lithium salt that serves as a source of lithium ions. Among them, the _{electrolyte, LiAlCl 4, LiBF 4, LiPF} 6, LiClO 4, LiAsF 6, and may be at least one selected from the group consisting of LiSbF _6. It is possible to improve the ionic conductivity of the degree of dissociation is high electrolyte, even from the viewpoint of that function to suppress performance deterioration of the electric storage device according to long-term use by oxidation reduction characteristics, as an electrolyte, LiBF ₄ and / Alternatively, LiPF ₆ may be selected. These electrolytes may be used alone or in combination of two or more. LiBF ₄ and LiPF ₆ can be combined with one or more cyclic carbonates and chain carbonates as non-aqueous solvents. In particular, LiBF ₄ and / or LiPF ₆ may be combined with ethylene carbonate and diethyl carbonate.

  The concentration of the electrolyte in the nonaqueous electrolytic solution may be 0.1 mol / L or more, or 2.0 mol / L or less. When the concentration of the electrolyte is 0.1 mol / L or more, it is easy to sufficiently ensure the conductivity of the nonaqueous electrolytic solution. Therefore, it is easy to obtain stable discharge characteristics and charge characteristics of the electricity storage device. When the electrolyte concentration is 2.0 mol / L or less, an increase in the viscosity of the nonaqueous electrolytic solution can be suppressed, and the mobility of ions can be secured particularly easily. If the ion mobility is not sufficiently ensured, the conductivity of the electrolyte cannot be sufficiently ensured, and the charge / discharge characteristics of the electricity storage device may be hindered. From the same viewpoint, the concentration of the electrolyte may be 0.5 mol / L or more, or 1.5 mol / L or less.

  The electricity storage device according to this embodiment is mainly composed of the non-aqueous electrolyte, a positive electrode, and a negative electrode. Specific examples of the electricity storage device include a non-aqueous electrolyte secondary battery (such as a lithium ion battery) and an electric double layer capacitor (such as a lithium ion capacitor). The nonaqueous electrolytic solution according to the present embodiment is particularly effective in applications of lithium ion batteries and lithium ion capacitors.

  FIG. 1 is a cross-sectional view schematically showing an embodiment of an electricity storage device. An electricity storage device 1 shown in FIG. 1 is a non-aqueous electrolyte secondary battery. The electricity storage device 1 includes a positive electrode plate 4 (positive electrode), a negative electrode plate 7 (negative electrode) opposed to the positive electrode plate 4, a non-aqueous electrolyte solution 8 disposed between the positive electrode plate 4 and the negative electrode plate 7, And a separator 9 provided in the water electrolyte 8. The positive electrode plate 4 includes a positive electrode current collector 2 and a positive electrode active material layer 3 provided on the nonaqueous electrolyte solution 8 side. The negative electrode plate 7 includes a negative electrode current collector 5 and a negative electrode active material layer 6 provided on the nonaqueous electrolyte solution 8 side. As the nonaqueous electrolytic solution 8, the nonaqueous electrolytic solution according to the above-described embodiment can be used. In FIG. 1, a non-aqueous electrolyte secondary battery is shown as the electricity storage device, but the electricity storage device to which the non-aqueous electrolyte can be applied is not limited to this, and other electricity storage devices such as an electric double layer capacitor. It may be.

  The positive electrode current collector 2 and the negative electrode current collector 5 may be metal foils made of a metal such as aluminum, copper, nickel, and stainless steel, for example.

The positive electrode active material layer 3 contains a positive electrode active material. The positive electrode active material may be a lithium-containing composite oxide. Specific examples of the lithium-containing composite oxide _{includes LiMnO 2, LiFeO 2, LiCoO 2} , LiMn 2 O 4, Li 2 FeSiO 4, LiNi 1/3 Co 1/3 Mn 1/3 O 2, and LiFePO _4.

  The negative electrode active material layer 6 contains a negative electrode active material. The negative electrode active material may be a material that can occlude and release lithium, for example. Specific examples of such materials include carbon materials such as graphite and amorphous carbon, and oxide materials such as indium oxide, silicon oxide, tin oxide, zinc oxide and lithium oxide. The negative electrode active material may be a lithium metal or a metal material capable of forming an alloy with lithium. Specific examples of metals that can form alloys with lithium include Cu, Sn, Si, Co, Mn, Fe, Sb, and Ag. A binary or ternary alloy containing these metals and lithium can also be used as the negative electrode active material. These negative electrode active materials may be used alone or in combination of two or more.

  For example, the separator 9 may be a porous film made of polyethylene, polypropylene, fluororesin, or the like.

  Specific forms such as the shape and thickness of each member constituting the power storage device can be set as appropriate by those skilled in the art. The configuration of the power storage device is not limited to the embodiment of FIG. 1 and can be changed as appropriate.

  Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to these examples.

1. Preparation of non-aqueous electrolyte (Example 1)
Ethylene carbonate (EC) and diethyl carbonate (DEC) are mixed at a volume ratio of EC: DEC = 30: 70 to prepare a mixed non-aqueous solvent, to which LiPF ₆ is added at 1.0 mol / L as an electrolyte. It dissolved so that it might become a density | concentration. To the obtained solution, the compound 1 shown in Table 1 was added as an additive for non-aqueous electrolyte solution to prepare a non-aqueous electrolyte solution. The content ratio of the additive for non-aqueous electrolyte (Compound 1) was 0.5% by mass based on the total mass of the non-aqueous electrolyte.

(Example 2)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the content ratio of Compound 1 was 1.0% by mass.

(Example 3)
The nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 2 shown in Table 1 and the content ratio was 1.0% by mass. did.

Example 4
The nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 3 shown in Table 1 and the content ratio was 1.0% by mass. did.

(Example 5)
A nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 4 shown in Table 1 and the content ratio was 1.0% by mass. did.

(Example 6)
A nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 5 shown in Table 1 and the content ratio was 1.0% by mass. did.

(Example 7)
The nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 6 shown in Table 1 and the content ratio was 1.0% by mass. did.

(Example 8)
The nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 7 shown in Table 1 and the content ratio was 1.0% by mass. did.

Example 9
The nonaqueous electrolyte solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolyte solution was changed from compound 1 to compound 8 shown in Table 1 and the content ratio was 1.0% by mass. did.

(Comparative Example 1)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that Compound 1 was not added.

(Comparative Example 2)
A non-aqueous electrolyte was prepared in the same manner as in Example 1 except that the additive for non-aqueous electrolyte was changed from Compound 1 to 1,3-propane sultone and the content ratio was 1.0% by mass. .

(Comparative Example 3)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from compound 1 to vinylene carbonate (VC) and the content ratio was 1.0% by mass.

(Comparative Example 4)
A nonaqueous electrolytic solution was prepared in the same manner as in Comparative Example 3 except that the content of vinylene carbonate (VC) was 2.0% by mass.

(Comparative Example 5)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from Compound 1 to fluoroethylene carbonate (FEC) and the content ratio was 1.0% by mass. .

(Comparative Example 6)
A nonaqueous electrolytic solution was prepared in the same manner as in Comparative Example 5 except that the content ratio of fluoroethylene carbonate (FEC) was 2.0% by mass.

(Comparative Example 7)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from Compound 1 to phthalimide and the content ratio was 1.0% by mass.

(Comparative Example 8)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from Compound 1 to maleimide and the content ratio was 1.0% by mass.

(Comparative Example 9)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from Compound 1 to succinimide and the content ratio was 1.0% by mass.

(Comparative Example 10)
A nonaqueous electrolytic solution was prepared in the same manner as in Example 1 except that the additive for nonaqueous electrolytic solution was changed from Compound 1 to saccharin and the content ratio was 1.0% by mass.

2. Evaluation (calculation of LUMO energy)
The LUMO (lowest unoccupied molecular orbital) energies of compounds 1-8 used in the examples were determined by semi-empirical molecular orbital calculation with Gaussian 03 software. The calculated LUMO energy is shown in Table 1.

(Stability)
The compounds 1 to 8 used in the Examples and the fluoroethylene carbonate (FEC) used in Comparative Examples 5 and 6 are left for 90 days in a constant temperature and humidity environment with a temperature of 40 ± 2 ° C. and a humidity of 75 ± 5%. It used for the preservation | save test. The ¹ H-nuclear magnetic resonance spectrum ( ¹ H-NMR) of each non-aqueous electrolyte additive before and after the storage test was measured, and the stability of each compound was evaluated according to the following criteria. Table 2 shows the stability evaluation results.
○: There was no peak changes in ¹ H-NMR spectrum before and after the storage test.
Δ: Slight peak change in ¹ H-NMR spectrum was confirmed before and after the storage test.
X: A clear peak change in the ¹ H-NMR spectrum was confirmed before and after the storage test.

  As shown in Table 2, the fluoroethylene carbonate (FEC) used in Comparative Examples 5 and 6 was considered to be partially hydrolyzed and had poor stability. On the other hand, the compounds 1 to 8 used in the examples were hardly changed and excellent in stability.

(Preparation of non-aqueous electrolyte secondary battery)
LiMn ₂ O ₄ as a positive electrode active material and carbon black as a conductivity imparting agent were dry mixed. The obtained mixture was uniformly dispersed in N-methyl-2-pyrrolidone (NMP) in which polyvinylidene fluoride (PVDF) was dissolved as a binder to prepare a slurry. The obtained slurry was applied to both surfaces of an aluminum metal foil (square shape, thickness 20 μm). After the coating film was dried to remove NMP, the whole was pressed to obtain a positive electrode sheet having an aluminum metal foil as a positive electrode current collector and a positive electrode active material layer formed on both surfaces thereof. The solid content ratio in the positive electrode active material layer of the obtained positive electrode sheet was a mass ratio, and was positive electrode active material: conductivity imparting agent: PVDF = 90: 5: 5.
As the negative electrode sheet, a commercially available graphite-coated electrode sheet (manufactured by Hosen Co., Ltd., trade name: electrode sheet negative electrode single layer) was used.
In various non-aqueous electrolytes obtained in Examples and Comparative Examples, a polyethylene separator was laminated in the order of a negative electrode, a separator, a positive electrode, a separator, and a negative electrode to prepare a battery element. After inserting this battery element into a bag made of a laminate film in which both surfaces of aluminum (thickness: 40 μm) were coated with a resin layer while projecting positive and negative terminals, Examples 1-9 and Comparative Examples 1-10 Each non-aqueous electrolyte obtained in (1) was poured into a bag and vacuum-sealed to produce a sheet-like non-aqueous electrolyte secondary battery. Furthermore, in order to improve the adhesiveness between electrodes, a sheet-like battery was sandwiched between glass plates and pressed to prepare a non-aqueous electrolyte secondary battery (sheet-type secondary battery).

(Evaluation of discharge capacity maintenance ratio and internal resistance ratio)
For each of the obtained nonaqueous electrolyte secondary batteries, at 25 ° C., the charge rate was 0.3 C, the discharge rate was 0.3 C, the charge end voltage was 4.2 V, and the discharge end voltage was 2.5 V. A charge / discharge cycle test was conducted. Table 3 shows the discharge capacity retention rate (%) after 200 cycles and the internal resistance ratio after 200 cycles.
“Discharge capacity maintenance rate after 200 cycles (%)” is the ratio (percentage) of the discharge capacity (mAh) after the 200 cycle test to the discharge capacity (mAh) after the 10 cycle test. The “internal resistance ratio after 200 cycles” is the relative value of the resistance after the 200 cycle test when the resistance before the cycle test is 1.

(Measurement of gas generation amount)
Separately from the batteries used in the cycle test, non-aqueous electrolyte secondary batteries having the same configuration including the electrolytes of the examples and comparative examples were prepared. This battery was charged to 4.2 V at 25 ° C. with a current corresponding to 0.2 C, and then discharged to 3 V with a current corresponding to 0.2 C for 3 cycles to stabilize the battery. Next, after charging the battery to 4.2 V again at a charge rate of 0.3 C, the battery was stored at a high temperature of 60 ° C. and 168 hours. Then, it cooled to room temperature, measured the volume of the battery by Archimedes method, and calculated | required the gas generation amount from the volume change before and behind a preservation | save.

  From Table 3, the non-aqueous electrolyte secondary battery using the non-aqueous electrolyte solution of each example containing compounds 1 to 8 which are compounds of formula (1) or formula (2) is a non-aqueous electrolyte solution of a comparative example. It can be seen that the discharge capacity retention rate during the cycle test is higher than that of the non-aqueous electrolyte secondary battery using the. Moreover, from Table 4, the nonaqueous electrolyte secondary battery using the nonaqueous electrolyte solution of each Example containing the compounds 1 to 8 which are the compounds of the formula (1) or the formula (2) has less gas generation. I understand. This strongly suggests that the compound of formula (1) or formula (2) forms a stable SEI for charge / discharge cycles and high temperature storage when used in non-aqueous electrolyte secondary batteries. doing. Moreover, it was confirmed that the compound of Formula (1) or Formula (2) is excellent also in the point that there is little increase in internal resistance by a charging / discharging cycle.

  DESCRIPTION OF SYMBOLS 1 ... Power storage device (nonaqueous electrolyte secondary battery), 2 ... Positive electrode current collector, 3 ... Positive electrode active material layer, 4 ... Positive electrode plate, 5 ... Negative electrode current collector, 6 ... Negative electrode active material layer, 7 ... Negative electrode Plate, 8 ... non-aqueous electrolyte, 9 ... separator.

Claims (8)

The additive for non-aqueous electrolyte containing the compound represented by following formula (1) or following formula (2).

[In Formula (1) or Formula (2), X ¹ , X ² and X ³ each independently represent an optionally substituted methylene group, sulfonyl group or carbonyl group. In formula (1) or formula (2), Y ¹ and Y ² each independently represent an optionally substituted hydrocarbon group having 1 to 6 carbon atoms. ] The additive for non-aqueous electrolyte according to claim ¹ , wherein X ¹ , X ² and X ³ are each independently a sulfonyl group or a carbonyl group.   A nonaqueous electrolytic solution containing the additive for nonaqueous electrolytic solution according to claim 1, a nonaqueous solvent, and an electrolyte.   The nonaqueous electrolytic solution according to claim 3, wherein the nonaqueous solvent is an aprotic solvent.   The nonaqueous electrolytic solution according to claim 3 or 4, wherein the electrolyte contains a lithium salt.   An electrical storage device provided with the nonaqueous electrolyte solution as described in any one of Claims 3-5, a positive electrode, and a negative electrode.   A lithium ion battery comprising the nonaqueous electrolytic solution according to any one of claims 3 to 5, and a positive electrode and a negative electrode.   A lithium ion capacitor comprising the nonaqueous electrolytic solution according to any one of claims 3 to 5, and a positive electrode and a negative electrode.

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