Single-ion polymer electrolyte system as well as preparation method and application thereof
A single ion and polymer technology, applied in non-aqueous electrolytes, solid electrolytes, electrolyte immobilization/gelation, etc., can solve problems such as concentration polarization, hinder lithium ion migration, and reduce battery cycle performance
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[0078] According to a preferred embodiment of the present invention, the chemical structural formula of the single ion conductor lithium salt containing p-styrenesulfonyl group is:
[0079]
[0080] According to another preferred embodiment of the present invention, the chemical structural formula of the UPyMA containing quadruple hydrogen bonds is:
[0081]
[0082] The chemical structural formula of described polyethylene glycol monomethyl ether methacrylate is:
[0083]
[0084] According to another preferred embodiment of the present invention, in the above-mentioned single-ion polymer electrolyte system, the molar ratio of the lithium salt to the ethoxy structural unit in the single-ion polymer electrolyte is preferably set to 1:5-1 :50. In addition, the relative molecular mass of the polyethylene glycol monomethyl ether methacrylate is preferably set at 200-1000.
[0085] The second aspect of the present invention is to provide a preparation method of a single...
Embodiment 1
[0152] Add 60mL of N,N-dimethylformamide into a 250mL two-necked round-bottomed flask, stir at 0°C for more than 30 minutes, then drop 50mL of thionyl chloride into N,N-dimethylformamide through a constant pressure dropping funnel in the amide solution. Under 0°C and argon atmosphere, with mechanical stirring, slowly add 0.1 mol p-styrene sodium sulfonate solid powder into the above solution. After the sodium p-styrene sulfonate was completely dissolved, it was stirred for 2 hours at 0°C under an argon atmosphere, and then stirred for another 6 hours at room temperature under an argon atmosphere, and the resulting reaction solution was placed in a refrigerator at 4°C overnight. The reaction solution was dissolved in deionized water, extracted with dichloromethane, anhydrous MgSO 4 Drying, suction filtration, rotary evaporation, and drying gave p-styrenesulfonyl chloride, which was dissolved in anhydrous acetonitrile for later use.
[0153] Dissolve 0.1mol benzenesulfonamide,...
Embodiment 2
[0158] Add 60 mL of tetrahydrofuran into a 250 mL two-necked round-bottom flask, stir at 0°C for 30 minutes, and then drop 50 mL of thionyl chloride into the tetrahydrofuran solution through a constant pressure dropping funnel. Under 0°C and argon atmosphere, with mechanical stirring, slowly add 0.1 mol p-styrene sodium sulfonate solid powder into the above solution. After the sodium p-styrenesulfonate was completely dissolved, the mixture was stirred at 0° C. under an argon atmosphere for 1 hour, and then stirred at room temperature under an argon atmosphere for another 30 minutes to obtain a reaction solution. The reaction solution was dissolved in deionized water, extracted with dichloromethane, anhydrous MgSO 4 Drying, suction filtration, rotary evaporation, and drying gave p-styrenesulfonyl chloride, which was dissolved in anhydrous acetonitrile for later use.
[0159] Dissolve 0.1 mol of trifluoromethanesulfonamide, 0.2 mol of 4-dimethylaminopyridine and 0.3 mol of trie...
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