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Weakly Polar Ether‐Aided Ionic Liquid Electrolyte Enables High‐Performance Sodium Metal Batteries over Wide Temperature Range.

Authors :
Liu, Yang
Lu, Suwan
Wang, Zhicheng
Xu, Jingjing
Weng, Shixiao
Xue, Jiangyan
Tu, Haifeng
Zhang, Fengrui
Liu, Lingwang
Gao, Yiwen
Li, Hong
Zheng, Jieyun
Wu, Xiaodong
Source :
Advanced Functional Materials. 7/10/2024, Vol. 34 Issue 28, p1-9. 9p.
Publication Year :
2024

Abstract

Sodium (Na) metal batteries (SMBs) have attracted many attentions because of high specific capacity and low redox potential. However, SMBs encounter several crucial challenges including Na dendrites growth, severe interfacial side reactions and safe issues from liquid organic electrolyte. In this study, a non‐flammable 1,2‐bis (1,1,2,2‐tetrafluoroethoxy) ethane (TFEE) aided ionic liquid (IL) electrolyte (TILE) is reported with sodium bis(trifluoromethylsulfonyl)imide (NaTFSI) salt and N‐methyl‐N‐propylpyrrolidinium bis(fluorosulfonyl)imide ([Py13][FSI]) IL solvent. The IL solvent contains plentiful organic cations and anions, which helps to provide a cationic shielding effect by [Py13]+ cations and regulate the Na+ solvation structure with more FSI− and TFSI− anions. The unique solvation structure of Na+ facilitates a stable inorganic‐rich solid electrolyte interphase (SEI), effectively inhibiting unstable Na deposition and suppressing side reactions between the electrolyte and Na‐metal in SMBs. Therefore, the Na3V2(PO4)3 (NVP)||Na cells with TILE can deliver good rate capability and superior cycling performance with capacity retention of 95.5% and Coulombic efficiency of ≈99.9% after 2000 cycles at 5C rate and 25 °C. The high‐voltage NaNi0.33Fe0.33Mn0.33O2(NFM)||Na cells with TILE can also deliver good cycling performance with capacity retention of 92% after 150 cycles in the voltage range of 2.0–4.1 V at 0.5C rate and 25 °C. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
34
Issue :
28
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
178355017
Full Text :
https://doi.org/10.1002/adfm.202312295