Non-aqueous electrolyte solution and lithium secondary battery including the same
The present invention relates to a non-aqueous electrolyte solution including a non-aqueous organic solvent, a lithium salt, and an oligomer represented by Formula 1 described in the present specification, and a lithium secondary battery including the same. Since the non-aqueous electrolyte solution according to an embodiment of the present invention may reduce gas, such as CO or CO 2 , generated in the secondary battery during high-temperature storage, it may further improve high-temperature stability of the lithium secondary battery.
1. A non-aqueous electrolyte solution comprising:
a lithium salt;
a non-aqueous organic solvent; and
an oligomer represented by Formula 1 as an additive:
wherein, in Formula 1,
R 1 to R 3 are each independently a fluorine-substituted or unsubstituted alkylene group having 1 to 4 carbon atoms,
R 4 and R 5 are each independently an aliphatic hydrocarbon group or an aromatic hydrocarbon group,
R 6 and R 7 are each independently an alkyl group having 1 to 10 carbon atoms or,
R 8 and R 9 are each independently an alkyl group having 1 to 10 carbon atoms or,
R 10 is an aliphatic hydrocarbon group or an aromatic hydrocarbon group,
R 11 is an alkylene group having 1 to 3 carbon atoms,
R 12 is hydrogen or an alkyl group having 1 to 2 carbon atoms,
n is an integer of 1 to 70, and
m is an integer of 1 to 3.
2. The non-aqueous electrolyte solution of claim 1 , wherein, in the oligomer represented by Formula 1,
the aliphatic hydrocarbon groups of R 4 , R 5 , and R 10 comprise an alicyclic hydrocarbon group or a linear hydrocarbon group,
wherein the alicyclic hydrocarbon group is at least one selected from the group consisting of a substituted or unsubstituted cycloalkylene group having 4 to 20 carbon atoms; a substituted or unsubstituted cycloalkylene group having 4 to 20 carbon atoms which contains an isocyanate group (NCO); a substituted or unsubstituted cycloalkenylene group having 4 to 20 carbon atoms; and a substituted or unsubstituted heterocycloalkylene group having 2 to 20 carbon atoms, and
wherein the linear hydrocarbon group is at least one selected from the group consisting of a substituted or unsubstituted alkylene group having 1 to 20 carbon atoms; a substituted or unsubstituted alkylene group having 1 to 20 carbon atoms which contains an isocyanate group (NCO); a substituted or unsubstituted alkoxylene group having 1 to 20 carbon atoms; a substituted or unsubstituted alkenylene group having 2 to 20 carbon atoms; and a substituted or unsubstituted alkynylene group having 2 to 20 carbon atoms, and
the aromatic hydrocarbon groups of R 4 , R 5 , and R 10 comprise a substituted or unsubstituted arylene group having 6 to 20 carbon atoms; or a substituted or unsubstituted heteroarylene group having 2 to 20 carbon atoms.
3. The non-aqueous electrolyte solution of claim 1 , wherein the oligomer represented by Formula 1 comprises an oligomer represented by Formula 1a:
[Formula 1a]
wherein, in Formula 1a,
R 4 and R 5 are each independently an aliphatic hydrocarbon group,
R 8 and R 9 are each independently,
R 10 is an aliphatic hydrocarbon group,
R 11 is an alkylene group having 1 to 3 carbon atoms,
R 12 is hydrogen or an alkyl group having 1 to 2 carbon atoms,
n is an integer of 10 to 20, and
m is an integer of 1 to 2.
4. The non-aqueous electrolyte solution of claim 3 , wherein the oligomer represented by Formula 1a comprises an oligomer represented by Formula 1a-1:
[Formula 1a- 1 ]
wherein, in Formula 1a-1,
n is an integer of 10 to 20.
5. The non-aqueous electrolyte solution of claim 1 , wherein the oligomer represented by Formula 1 is included in an amount of 0.5 wt % to 20 wt % based on a total weight of the non-aqueous electrolyte solution.
6. The non-aqueous electrolyte solution of claim 5 , wherein the oligomer represented by Formula 1 is included in an amount of 1 wt % to 10 wt % based on the total weight of the non-aqueous electrolyte solution.
7. The non-aqueous electrolyte solution of claim 1 , wherein the oligomer represented by Formula 1 has a weight-average molecular weight (Mw) of 1,000 g/mol to 10,000 g/mol.
8. The non-aqueous electrolyte solution of claim 7 , wherein the oligomer represented by Formula 1 has a weight-average molecular weight (Mw) of 3,000 g/mol to 8,000 g/mol.
9. The non-aqueous electrolyte solution of claim 8 , wherein the oligomer represented by Formula 1 has a weight-average molecular weight (Mw) of 3,000 g/mol to 5,000 g/mol.
10. A lithium secondary battery comprising a negative electrode, a positive electrode, a separator disposed between the negative electrode and the positive electrode, and
the non-aqueous electrolyte solution of claim 1 .
11. The non-aqueous electrolyte solution of claim 1 , wherein the non-aqueous organic solvent is selected from the group consisting of an ether-based solvent, an ester-based solvent, an amide-based solvent, and mixtures of two or more thereof.
12. The non-aqueous electrolyte solution of claim 11 , wherein the ester-based solvent is selected from the group consisting of a cyclic carbonate compound, a linear carbonate compound, a linear ester compound, a cyclic ester compound, and mixtures of two or more thereof.
13. The non-aqueous electrolyte solution of claim 12 , wherein the cyclic carbonate compound is selected from the group consisting of ethylene carbonate (EC), propylene carbonate (PC), 1,2-butylene carbone, 2,3-butylene carbonate, 1,2-pentylene carbonate, 2,3-pentylene carbonate, vinylene carbonate, fluoroethylene carbonate (FEC), and mixtures of two or more thereof.
14. The non-aqueous electrolyte solution of claim 12 , wherein the linear carbonate compound is selected from the group consisting of dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate, ethylmethyl carbonate (EMC), methylpropyl carbonate, ethylpropyl carbonate, and mixtures of two or more thereof.