Electrode for a secondary battery and secondary battery comprising the same
View Patent ↗Disclosed is an electrolyte for a secondary battery comprising an electrolyte salt and an electrolyte solvent, the electrolyte further comprising a lactam-based compound substituted with an electron withdrawing group (EWG) at the nitrogen position thereof. The electrolyte allows formation of a firm and dense SEI film on the surface of an anode, minimizes irreversible oxidative decomposition at a cathode, and thus can provide a battery with significantly improved lifespan, stability and high temperature characteristics.
1. An electrolyte for a secondary battery comprising an electrolyte salt and an electrolyte solvent, the electrolyte further comprising a lactam-based compound substituted with an electron withdrawing group (EWG) at a nitrogen position thereof, wherein the electron withdrawing group is selected from the group consisting of cyano group (CN), nitro group (NO 2 ), methanesulfonyl group (SO 2 CH 3 ), phenylsulfonyl group (SO 2 Ph), trifluoromethanesulfonyl group (SO 2 CF 3 ), pentafluoroethanesulfonyl group (SO 2 C 2 F 5 ), pentafluorophenyl group (C 6 F 5 ), ethyl ketone group (COC 2 H 5 ), trifluoromethyl group and methyl ester group (COOCH 3 ).
2. The electrolyte for a secondary battery as claimed in claim 1 , wherein the lactam-based compound is a compound capable of being reduced on a surface of an anode of a secondary battery to form a solid electrolyte interface (SEI) film, and has an increased reduction potential due to the EWG substituent at the nitrogen position.
3. The electrolyte for a secondary battery as claimed in claim 1 , wherein the lactam-based compound has an increased oxidation potential due to the EWG substituent at the nitrogen position.
4. The electrolyte for a secondary battery as claimed in claim 1 , wherein the lactam-based compound substituted with an electron withdrawing group at the nitrogen position is used in an amount of 0.05˜10 parts by weight based on 100 parts by weight of the electrolyte.
5. A secondary battery comprising a cathode, an anode and an electrolyte as defined in claim 1 , wherein the electrolyte comprises a lactam-based compound substituted with an electron withdrawing group (EWG) at a nitrogen position thereof, wherein the electron withdrawing group is selected from the group consisting of cyano group (CN), nitro group (NO 2 ), methanesulfonyl group (SO 2 CH 3 ), phenylsulfonyl group (SO 2 Ph), trifluoromethanesulfonyl group (SO 2 CF 3 ), pentafluoroethanesulfonyl group (SO 2 C 2 F 5 ), pentafluorophenyl group (C 6 F 5 ), ethyl ketone group (COC 2 H 5 ), trifluoromethyl group and methyl ester group (COOCH 3 ).
6. The secondary battery as claimed in claim 5 , wherein the lactam-based compound is a compound capable of being reduced on a surface of an anode of a secondary battery to form a solid electrolyte interface (SEI) film, and has an increased reduction potential due to the EWG substituent at the nitrogen position.
7. The secondary battery as claimed in claim 5 , wherein the lactam-based compound has an increased oxidation potential due to the EWG substituent at the nitrogen position.
8. The secondary battery as claimed in claim 5 , wherein the lactam-based compound substituted with an electron withdrawing group at the nitrogen position is used in an amount of 0.05˜10 parts by weight based on 100 parts by weight of the electrolyte.
9. The secondary battery as claimed in claim 5 , wherein a cathode and/or an anode is an electrode comprising a solid electrolyte interface (SEI) film partially or totally formed on a surface thereof, the SEI film being a reduced form of a lactam-based compound substituted with an electron withdrawing group at a nitrogen position thereof, wherein the electron withdrawing group is selected from the group consisting of cyano group (CN), nitro group (NO 2 ), methanesulfonyl group (SO 2 CH 3 ), phenylsulfonyl group (SO 2 Ph), trifluoromethanesulfonyl group (SO 2 CF 3 ), pentafluoroethanesulfonyl group (SO 2 C 2 F 5 ), pentafluorophenyl group (C 6 F 5 ), ethyl ketone group (COC 2 H 5 ), trifluoromethyl group and methyl ester group (COOCH 3 ).
10. A method for controlling a reduction potential or oxidation potential of a lactam-based compound, the method comprising,
varying an electron donating property of a substituent introduced to a nitrogen position of the lactam-based compound, wherein the substituent is selected from the group consisting of cyano group (CN), nitro group (NO 2 ), methanesulfonyl group (SO 2 CH 3 ), phenylsulfonyl group (SO 2 Ph), trifluoromethanesulfonyl group (SO 2 CF 3 ), pentafluoroethanesulfonyl group (SO 2 C 2 F 5 ), pentafluorophenyl group (C 6 F 5 ), ethyl ketone group (COC 2 H 5 ), trifluoromethyl group and methyl ester group (COOCH 3 ).
11. The method as claimed in claim 10 , wherein the method is for increasing a reduction potential or oxidation potential of the lactam-based compound by using an electron withdrawing group (EWG) as the substituent introduced to a nitrogen position of the lactam-based compound.