Cost-effective synthesis of sulfide-based solid electrolytes without using Li2S

Authors
Jang, Yong-JinSeo, HyungeunLee, Young-SuCho, WoosukCho, Young WhanKim, Jae-Hun
Issue Date
2024-06
Publisher
Elsevier BV
Citation
Journal of Alloys and Compounds, v.989
Abstract
Solid electrolytes possess highly attractive potential which can improve safety properties and achieve high energy density when they replace the conventional liquid electrolytes in Li -ion batteries. Sulfide-based solid electrolytes have received considerable attention owing to their high ionic conductivities and good wettability due to their soft nature. These materials are typically synthesized using Li 2 S as a precursor. However, Li 2 S is expensive and thus cannot be widely used to prepare sulfide-based solid electrolytes for all -solid -state batteries (ASSBs). Here, we propose a novel approach to synthesize a sulfide-based solid electrolyte without using Li 2 S as a precursor. In this method, the starting powders of Li 2 O, Mg, and S were converted into Li 2 S and MgO by ball milling. The Li 2 S-MgO composite was then sequentially milled with P 2 S 5 and LiBH 4 , and a BH 4 -substituted thiophosphate solid electrolyte was synthesized. The resulting Li 3 PS 4 -LiBH 4 -MgO composite exhibited a high ionic conductivity of 7.2 mS cm -1 at 25 degrees C, and the ASSB prepared using the solid electrolyte functioned well. The thiophosphate local structure of the prepared samples was examined by Raman and 31 P solid -state nuclear magnetic resonance spectroscopies. Although the ionic conductivity slightly decreased upon MgO addition, the thiophosphate local structure was maintained. Moreover, the presence of MgO improved the chemical stability of the electrolyte in air.
Keywords
LITHIUM ION CONDUCTIVITY; SUPERIONIC CONDUCTORS; STABILITY; CRYSTALLIZATION; PERFORMANCE; IMPROVEMENT; BATTERIES; LI3PS4; Sulfide-based electrolyte; Thiophosphate; Solid electrolyte; All -solid -state battery; Lithium sulfide
ISSN
0925-8388
URI
https://pubs.kist.re.kr/handle/201004/149958
DOI
10.1016/j.jallcom.2024.174294
Appears in Collections:
KIST Article > 2024
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