Sulfamide Isocyanate Electrolyte Additive for Low-Impedance Interface Films
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Solution Overview
Problem
Lithium secondary batteries face performance degradation due to the oxidation, decomposition, and high impedance of the electrolyte solution, especially at high temperatures, which affects the cycle life and stability of the battery.
Innovation Solution
An isocyanate electrolyte solution additive containing a sulfamide structural group is introduced, which forms a stable interface film on electrodes, reducing impedance and acting as a stabilizing agent to inhibit acidity and chroma increases in the electrolyte solution, thereby enhancing the battery's high-temperature performance and cycle stability.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If traditional carbonic ester electrolyte solution is used to form interface film on electrodes, then a protective film is formed, but the impedance of the interface film becomes too high which attenuates electrochemical performance
Solution Approach 1:
The patent changes the chemical composition parameters of the electrolyte solution by introducing specific additives (cyclic carboxylate and its derivative) to modify the interface film properties. This resolves the contradiction by adjusting the electrolyte composition to form a film with lower impedance while maintaining stability.
Solution Approach 2:
The patent creates a composite interface film system by combining traditional carbonic ester with cyclic carboxylate additives. This composite approach allows the film to simultaneously achieve good stability and reduced impedance, resolving the contradiction between film protection and ion transport.
2Productivity
If sulfur-containing additives like ethylene sulfate (DTD) are used to reduce battery impedance, then high temperature and low temperature performance improve, but thermostability deteriorates causing degradation of acid value and chroma
Solution Approach 1:
The patent introduces cyclic carboxylate as an intermediary substance that mediates between the sulfur-containing additive and the electrolyte system. This intermediary forms a stable interface film that prevents direct degradation reactions, allowing impedance reduction while maintaining thermostability.
Solution Approach 2:
The cyclic carboxylate additive acts as a sacrificial component that preferentially reacts to form stable films, protecting the main electrolyte solution from degradation. This disposable-like behavior of the additive resolves the stability issue while maintaining performance benefits.
3Object-affected harmful factors
If film forming additives are used to improve interface film performance, then impedance is reduced, but the comprehensive performance requirements of the battery become harder to meet due to various additive interactions
Solution Approach 1:
The cyclic carboxylate additive performs multiple functions simultaneously: it forms protective interface films, reduces impedance, and stabilizes the electrolyte solution. This multi-functionality resolves the contradiction by achieving multiple performance improvements with a single additive rather than requiring complex additive combinations.
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
The additive improves the cycle performance and high-temperature storage capabilities of lithium-ion batteries by forming a stable interface film and reducing internal resistance, while maintaining the electrolyte solution's stability and preventing discoloration and acidity increases.
Implementation Method 1
forming a stable interface film on the surface of an electrode
Implementation Method 2
the electrolyte solution to oxidize, decompose and degrade the battery
Implementation Method 3
acting as a stabilizing agent to inhibit acidity and chroma increases in the electrolyte solution
Data Source
AI summary
An isocyanate electrolyte solution additive containing a sulfamide structural group has a structure of formula I:where R1 and R2 are identical or different, R1 and R2 are each independently selected from methyl, ethyl, butyl, methoxy, methanesulfonyl, ethanesulfonyl, fluorosulfonyl, trifluoromethanesulfonyl, perfluoroethylsulfonyl, benzenesulfonyl, alkyl-containing benzenesulfonyl, cyano/fluorobenzenesulfonyl and alkoxy-containing benzenesulfonyl, and R1 and R2 can be linked to form one of five-membered ring or six-membered ring.


