Non-aqueous electrolyte solution and non-aqueous electrolyte secondary battery employing the same
US-2016164143-A1 · Jun 9, 2016 · US
US10756384B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10756384-B2 |
| Application number | US-201615768137-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 14, 2016 |
| Priority date | Oct 22, 2015 |
| Publication date | Aug 25, 2020 |
| Grant date | Aug 25, 2020 |
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The present invention provides an electrolytic solution capable of providing an electrochemical device (e.g., a lithium ion secondary battery) or a module that is less likely to generate gas even in high-temperature storage and has high capacity retention even after high-temperature storage. The present invention relates to an electrolytic solution which may contain a compound represented by Y21R21C—CY22R22 wherein R21 and R22 may be the same as or different from each other, and are each H, an alkyl group, or a halogenated alkyl group; Y21 and Y22 may be the same as or different from each other, and are each —OR23 or a halogen atom; and R23 is H, an alkyl group, or a halogenated alkyl group.
Opening claim text (preview).
The invention claimed is: 1. An electrolytic solution comprising: a compound (1) represented by formula (1): wherein R 11 and R 13 are each individually a halogenated C1-C5 alkyl group and R 12 and R 14 are H; and X 11 and X 12 are individually O or S, and wherein the electrolytic solution contains the compound (1) in an amount of 0.001 mass ppm to 10000 mass ppm relative to the electrolytic solution. 2. The electrolytic solution according to claim 1 , further comprising a solvent, wherein the solvent contains a carbonate. 3. The electrolytic solution according to claim 1 , further comprising a solvent, wherein the solvent contains an acyclic ether. 4. The electrolytic solution according to claim 1 , further comprising at least one lithium salt (X) selected from the group consisting of: a compound (3) represented by formula (3): wherein X 31 and X 32 may be the same as or different from each other, and are each —H, —F, —O, —OCN, an alkyl group which may optionally have an ether bond, a fluorinated alkyl group which may optionally have an ether bond, an alkoxy group which may optionally have an ether bond, or a fluorinated alkoxy group which may optionally have an ether bond; X 31 and X 32 may be bonded to each other to form a ring; and a is an integer of 1 to 3; a compound (4) represented by formula (4): wherein X 41 is —H, —F, —Cl, an alkyl group which may optionally have an ether bond, a fluorinated alkyl group which may optionally have an ether bond, an alkoxy group which may optionally have an ether bond, or a fluorinated alkoxy group which may optionally have an ether bond; a compound (5) represented by formula (5): wherein X 51 is —H, —F, —Cl, an alkyl group which may optionally have an ether bond, a fluorinated alkyl group which may optionally have an ether bond, an alkoxy group which may optionally have an ether bond, or a fluorinated alkoxy group which may optionally have an ether bond; and a compound (6) represented by formula (6): wherein X 61 is —H, —F, —Cl, an alkyl group which may optionally have an ether bond, a fluorinated alkyl group which may optionally have an ether bond, an alkoxy group which may optionally have an ether bond, or a fluorinated alkoxy group which may optionally have an ether bond. 5. The electrolytic solution according to claim 1 , further comprising at least one cyclic dicarbonyl compound selected from the group consisting of: a compound represented by formula (7): wherein A a+ is a metal ion, a hydrogen ion, or an onium ion; a is an integer of 1 to 3; b is an integer of 1 to 3; p is b/a; n 73 is an integer of 1 to 4; n 71 is an integer of 0 to 8; n 72 is 0 or 1; Z 71 is a transition metal or an element in Group III, IV, or V of the periodic table; X 71 is O, S, a C1-C10 alkylene group, a C1-C10 halogenated alkylene group, a C6-C20 arylene group, or a C6-C20 halogenated arylene group, where the alkylene group, the halogenated alkylene group, the arylene group, and the halogenated arylene group each may have a substituent or a hetero atom in the structure, and n 73 X 71 s may be bonded to each other when n 72 is 1 and n 73 is 2 to 4; L 71 is a halogen atom, a cyano group, a C1-C10 alkyl group, a C1-C10 halogenated alkyl group, a C6-C20 aryl group, a C6-C20 halogenated aryl group, or —Z 73 Y 73 , where the alkylene group, the halogenated alkylene group, the arylene group, and the halogenated arylene group each may have a substituent or a hetero atom in the structure, and n 71 L 71 s may be bonded to each other to form a ring when n 71 is 2 to 8; Y 71 , Y 72 , and Z 73 are each individually O, S, NY 74 , a hydrocarbon group, or a fluorinated hydrocarbon group; and Y 73 and Y 74 are each individually H, F, a C1-C10 alkyl group, a C1-C10 halogenated alkyl group, a C6-C20 aryl group, or a C6-C20 halogenated aryl group, where the alkyl group, the halogenated alkyl group, the aryl group, and the halogenated aryl group each may have a substituent or a hetero atom in the structure, and when there are multiple Y 73 s or Y 74 s, the Y 73 s and Y 74 s may be bonded to each other to form a ring; and a compound (8) represented by (8): wherein n 81 is 0 or 1; n 82 is 0 or 1; Z 81 is a transition metal or an element in Group III, IV, or V in the periodic table; X 81 is O, S, a C1-C10 alkylene group, a C1-C10 halogenated alkylene group, a C6-C20 arylene group, or a C6-C20 halogenated arylene group, where the alkylene group, the halogenated alkylene group, the arylene group, and the halogenated arylene group each may have a substituent or a hetero atom in the structure; Y 81 and Y 82 are each individually O, S, NY 84 , a hydrocarbon group, or a fluorinated hydrocarbon group; and Y 84 is H, a C1-C10 alkyl group, a C1-C10 halogenated alkyl group, a C6-C20 aryl group, or a C6-C20 halogenated aryl group, where the alkyl group, the halogenated alkyl group, the aryl group, and the halogenated aryl group each may have a substituent or a hetero atom in the structure, and when there is multiple Y 84 s, the Y 84 s may be bonded to each other to form a ring. 6. The electrolytic solution according to claim 1 , further comprising at least one compound containing a multiple bond between a heteroatom other than an oxygen atom and an adjacent atom in a molecule selected from the group consisting of compounds represented by formula (9-1) to formula (9-3): wherein X 91 is O or N, M 91 is C, P, S, or N, and Z 91 is N or may be absent, but L 91 -C═O, where N is absent, M 91 is C, and X 91 is 0, is excluded; L 91 is a halogen atom or an oxygen atom, or R, OR, ORR′, ORR′O, SR, NR, SiR, or OSiR that may contain a halogen atom; R and R′ are each a C1-C10 alkyl group, a C1-C10 alkylene group, a C1-C10 alkene group, a C1-C10 alkyne group, a C1-C10 haloalkyl group, a C1-C10 haloalkylene group, a C1-C10 haloalkene group, a C1-C10 haloalkyne group, or a C1-C10 cycloalkyl group; R and R′ may form a ring together; n 91 is an integer of 1 to 3; and m 91 is or 2. 7. The electrolytic solution according to claim 1 , further comprising a compound containing structure represented by any of —CN, —N═C═O, 8. The electrolytic solution according to claim 1 , further comprising at least one compound containing a multiple bond between a hetero atom other than an oxygen atom and an adjacent atom in a molecule selected from the group consisting of: a compound (10) represented by formula (10): NC—R 101 —(CN) n101 wherein R 101 is a monovalent to trivalent hydrocarbon group or a monovalent to trivalent halogenated hydrocarbon group; and n 101 is an integer of 0 to 2; a compound (11) represented by formula (11): OCN—R 111 —(NCO) n101 wherein R 111 is a monovalent or divalent hydrocarbon
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