Back to Search Start Over

Entropy-Driven 60 mol% Li Electrolyte for Li Metal-Free Batteries.

Authors :
Wu S
Nishigaki Y
Hagiwara R
Hwang J
Matsumoto K
Source :
Small (Weinheim an der Bergstrasse, Germany) [Small] 2024 Sep 10, pp. e2405007. Date of Electronic Publication: 2024 Sep 10.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Highly Li-concentrated electrolytes are acknowledged for their compatibility with Li metal negative electrodes and high voltage positive electrodes to achieve high-energy Li metal batteries, showcasing stable and facile interfaces for Li deposition/dissolution and high anodic stability. This study aims to explore a highly concentrated electrolyte by adopting entropy-driven chemistry for Li metal-free (so-called anode-free) batteries. The combination of lithium bis(fluorosulfonyl)amide (LiFSA) and lithium trifluoromethanesulfonate (LiOTf) salts in a pyrrolidinium-based ionic liquid is found to significantly modify the coordination structure, resulting in an unprecedented 60 mol% Li concentration and a low solvent-to-salt ratio of 0.67:1 in the electrolyte system. This novel 60 mol% Li electrolyte demonstrates unique coordination stricture, featuring a high ratio of monodentate-anion structures and aggregates, which facilitates an enhanced Li <superscript>+</superscript> transference number and improved anodic stability. Moreover, the developed electrolyte provides a facile de-coordination process and leads to the formation of an anion-based solid electrolyte interface, which enables stable Li deposition/dissolution properties and demonstrates excellent cycling stability in the Li metal-free full cell with a Li[Ni <subscript>0.8</subscript> Co <subscript>0.1</subscript> Mn <subscript>0.1</subscript> ]O <subscript>2</subscript> (NCM811) positive electrode.<br /> (© 2024 Wiley‐VCH GmbH.)

Details

Language :
English
ISSN :
1613-6829
Database :
MEDLINE
Journal :
Small (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
39252636
Full Text :
https://doi.org/10.1002/smll.202405007