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

CN111326788AActive Publication Date: 2020-06-23HUAZHONG UNIV OF SCI & TECH
3 Cites 14 Cited by

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Publication Date
2020-06-23

Smart Images

  • Figure 1
    Figure 1
  • Figure 2
    Figure 2
  • Figure 3
    Figure 3
Patent Text Reader

Abstract

The invention belongs to the related field of polymer electrolyte systems. The invention discloses a single-ion polymer electrolyte system as well as a preparation method and application thereof. Thesingle-ion polymer electrolyte system is composed of a single-ion polymer electrolyte and a metal salt, wherein the single-ion polymer electrolyte is obtained by carrying out reversible addition-fragmentation chain transfer polymerization reaction on three monomers including a single-ion conductor lithium salt containing a p-styrenesulfonyl group, UPyMA containing quadruple hydrogen bonds and methoxypolyethylene glycol methacrylate. According to the invention, the key structure and related composition in the single-ion polymer electrolyte system, the overall process flow of the preparation method and other aspects are optimally designed; and, compared with the prior art, the invention is advantageous in that not only can the phenomenon that a polymer electrolyte system is easy to crack bebetter solved, but also the metal ion transference number and the ionic conductivity can be remarkably improved, and meanwhile, the growth of metal dendrites is effectively inhibited, so that the polymer electrolyte is particularly suitable for the field of metal ion batteries such as lithium ion batteries.
Need to check novelty before this filing date? Find Prior Art

Description

technical field

[0001] The invention belongs to the related field of polymer electrolyte systems, and more specifically relates to a single-ion polymer electrolyte system and its preparation method and application. Background technique

[0002] Electrolyte is one of the key materials of lithium-ion batteries, and its chemical composition and structure directly affect the performance of lithium-ion batteries. At present, commercial lithium-ion batteries are still dominated by organic liquid electrolytes, but liquid electrolytes contain a large amount of flammable, explosive and volatile organic solvents, which bring many problems to the safety performance of lithium-ion batteries. Compared with liquid electrolytes, solid electrolytes have better safety performance, especially polymer electrolyte systems can be rationally designed according to different battery performance requirements, and then endow the electrolyte with multiple functions, making polymer electrolyte systems ...

Examples

Embodiment approach

[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...