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 and trifluoromethanesulfonate salts in a pyrrolidinium-based ionic liquid has been 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+ 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[Ni0.8Co0.1Mn0.1]O2 (NCM811) positive electrode.
Supplementary materials
Title
Entropy-driven 60 mol% Li Electrolyte
Description
Experimental and additional data
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