Add like
Add dislike
Add to saved papers

TFSI and TDI Anions: Probes for Solvate Ionic Liquid and Disproportionation-Based Lithium Battery Electrolytes.

Highly concentrated electrolytes based on Li-salts and chelating solvents, such as glymes, are promising as electrolytes for lithium batteries. This is due to their unique properties, such as higher electrochemical stabilities, compliance with high-voltage electrodes, low volatility and flammability, and inertness toward aluminum current collector corrosion. The nature of these properties originates from the molecular-level structure created in either solvate ionic liquids (SILs) or the less common ionic aggregates by disproportionation reactions. The nature of the anion plays a crucial role, and here, we present a computational study using TFSI and TDI anions as probes, revealing increasing differences upon increased salt concentration. TFSI-based electrolytes preferably form SILs, while TDI-based electrolytes form ionic aggregates. The latter lead to an unexpected creation of "free" cationic species even at (very) high salt concentrations and thus promise of ample lithium ion transport.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app