Electrolyte solvent and electrolyte solution for oxo-salt lithium cathode active material, and lithium ion secondary battery
An electrolyte solution and secondary battery technology, applied in secondary batteries, circuits, electrical components, etc., can solve the problems of easy desorption of oxygen, decomposition, poor thermal stability of lithium cobalt oxide, etc.
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Embodiment 1
[0160]
[0161] (Synthesis of N,N-diethyl-N-2-methoxyethylamine (N,N-diethyl-N-2-methoxyethylamine))
[0162] Using a 100 mL autoclave, N,N-diethylamine (35.0 g, 478 mmol) and chloroethyl methyl ether (22.6 g, 239 mmol) were reacted at 120° C. for 48 hours. The solid salt formed was filtered off and the residue (filtrate) was distilled under reduced pressure using a 25 cm Vigreux column. to the resulting amine 1 H-NMR measurement, its chemical shift is δ (ppm) 3.45-3.42 (t, 2H), 3.31 (s, 3H), 2.52-2.50 (t, 2H), 2.34-2.31 (t, 2H), 2.22 (s ,3H), 1.45-1.38(m,2H), 1.31-1.22(m,2H), 0.89-0.85(t,3H), it can be confirmed that N,N-diethyl-N-2-methyl Oxyethylamine.
[0163] (Synthesis of N-butyl-N-methyl-N-2-methoxyethylamine (N-butyl-N-methyl-N-2-methoxyethylamine))
[0164] Using a 100 mL autoclave, react N-butyl-N-methylamine (34.0 g, 390 mmol) with chloroethyl methyl ether (18.5 g, 196 mmol) at 130° C. for 48 hours. The solid salt formed was filtered and removed, and the resi...
Embodiment 2
[0198]
[0199] (Synthesis of (N,N,N-tri(2-methoxyethyl)amine)
[0200] Using a 100 mL autoclave, bis(2-methoxyethyl)amine (50.0 g, 375 mmol) was reacted with chloroethyl methyl ether (18.0 g, 190 mmol) at 140° C. for 48 hours. Filter and remove the solid salt formed in the reaction, and use a 25 cm Webster column to distill the remaining filtrate under reduced pressure. figure 1 shows the amines obtained by distillation 1 H-NMR spectrum. like figure 1 As shown, the detailed results of its chemical shift are δ (ppm) 3.45-3.41(t, 6H), 3.30(s, 9H), 2.75-2.72(t, 6H), which confirms that N, N, N - Tris(2-methoxyethyl)amine.
[0201]
[0202] (Synthesis of Ionic Liquid [2-1])
[0203] Using a 50mL autoclave, using methanol as a solvent (10mL), make N,N,N-tris(2-methoxyethyl)amine (9.1g, 48mmol) synthesized in Example 2 and bromoethane (11.2g , 104mmol) at 60°C for 24 hours. The resulting bromide was washed with ether. The washed bromide was recrystallized twice with ace...
Embodiment 3
[0217]
[0218] (Synthesis of N,N-di(2-methoxyethyl)-N-2-ethoxyethylamine (N,N-di-(2-methoxyethyl)-N-2-ethoxyethylamine))
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