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Engineering of Electrolyte Solution in Governing the Stability of Sodium Metal Anode for Room Temperature Sodium-Sulfur Batteries

Authors
Park, HyeonaKim, HyerimKim, Jae-MinKang, HyokyeongKansara, ShivamSun, ZhaoweiAgostini, MarcoRizell, JosefMatic, AleksandarXiong, ShizhaoSun, Yang-KookHwang, Jang-Yeon
Issue Date
Feb-2026
Publisher
AMER CHEMICAL SOC
Citation
ACS ENERGY LETTERS, v.11, no.2, pp 1751 - 1760
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
ACS ENERGY LETTERS
Volume
11
Number
2
Start Page
1751
End Page
1760
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/214930
DOI
10.1021/acsenergylett.5c03325
ISSN
2380-8195
Abstract
The charge storage properties of room temperature sodium-sulfur (Na-S) batteries are dependent on the electrolyte chemistry, which dictates the interfacial stability between electrode and electrolyte. Here, we introduce a localized high-concentration electrolyte (LHCE) consisting of 6 M sodium bis(fluorosulfonyl)imide in 1,2-dimethoxyethane and diluted with bis(2,2,2-trifluoroethyl)ether in a 1:1.5 molar ratio for Na-S batteries. This LHCE consists of a highly aggregated solvation shell over strongly interacting Na+-FSI- ion pairs and minimal free solvent. Such a solvation structure enables the formation of an inorganic-rich solid electrolyte interphase on the Na metal anode, which suppresses dendrite growth. Moreover, the LHCE shows compatibility with sulfurized polyacrylonitrile (SPAN) cathode without dissolution of soluble Na-polysulfides during cycling. Coupled with a SPAN cathode and 50 mu m of Na metal anode, the pouch-type Na-S battery using the LHCE delivers an areal capacity of 2.6 mAh cm-2 and cycling stability after 300 cycles at 1 C.
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