Design of an Amphiphilic Anion toward High Loading Solid‐State Lithium Metal Battery

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Authors: Paul Neumann, Leire Meabe, Lorena García, Nerea Herran‐Diaz de Argote, Rafael del Olmo, David Fraile‐Insagurbe, Maria Carmen Morant‐Miñana, Margaud Lécuyer, Marc Deschamps, Heng Zhang, Michel Armand, María Martinez‐Ibañez
Cited by: 1
References: 60

Abstract

Abstract To improve the performance of all‐solid‐state lithium metal batteries (ASSLMBs), it is indispensable to work on lithium salt chemistries beyond the well‐known lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), which shows a low lithium‐ion transference number ( T Li + , ≈0.2) and induces a poor solid–electrolyte interphase (SEI). Herein, the design and synthesis of a new asymmetric lithium salt are reported in which one trifluoromethyl group of LiTFSI is replaced by a dihexylamino group to obtain lithium (trifluoromethanesulfonyl)( N ‐ N ‐dihexylsulfamoyl)imide {Li[N(SO 2 CF 3 )(SO 2 N( n ‐C 6 H 13 ) 2 )], LiC 6,6 TFSI}, seeking for a double effect in the electrolyte: 1) to improve cyclability by tuning the transport properties through the reduction of anion mobility; and 2) to ensure compatibility between the polar and non‐polar components of the cathode by developing an anion with amphipathic nature. The solid polymer electrolyte (SPE) based on LiC 6,6 TFSI and poly(ethylene oxide) (PEO) offers a reduced anion diffusivity leading to high T Li + values (≈0.52). Owing to the high T Li + and the amphipathic nature of the salt, the as‐obtained SPE empowers the Li||LiFePO 4 cells with good capacity retention under stringent working conditions (e.g., a relatively high cathode areal loading of ≈1.8 mAh cm −2 ; high current rates of 1 mA cm −2 ).

Fields of Study & Subjects

Advanced Battery Materials and Technologies Advancements in Battery Materials Inorganic Chemistry and Materials

Publication details

Journal / source
Small
Publisher
Wiley
Volume
22
Issue
7
Pages
e07567–e07567
Publication date
14 January 2026
Language
EN