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One-step solution process toward formation of Li6PS5Cl argyrodite solid electrolyte for all-solid-state lithium-ion batteries.

Authors :
Zhang, Zhixia
Zhang, Long
Liu, Yanyan
Yan, Xinlin
Xu, Bo
Wang, Li-min
Source :
Journal of Alloys & Compounds. Jan2020, Vol. 812, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

Solution-processability is one of the merits of sulfide solid electrolytes because it is a facile and scalable process to construct a thin electrolyte coating layer on active material powders to reduce the interfacial resistance. Herein the argyrodite-type Li 6 PS 5 X is synthesized by an one-step solution-process method with ethanol, which avoids the multi-step processes and toxic solvent adopted in other reported works, and greatly reduces the processing time. The as-synthesized Li 6 PS 5 Cl has room temperature ionic conductivity of 0.21 mS cm−1 and comparable Li-dendrite suppression ability to solid-state-sintered Li 6 PS 5 Cl, despite of the unavoidable impurities due to the use of the protic solvent. By coating Li 6 PS 5 Cl on LiCoO 2 particles with the one-step solution process, the assembled all-solid-state battery exhibits higher capacity and better rate capability than the uncoated baseline battery. The improved electrochemical performance is attributed to a well-maintained interfacial resistance during cycling by the interfacial architecture, though the performance is not good yet and need to be further improved. The one-step solution-process method can be used for coating cathode materials. Image 1 • One-step solution-process synthesis is optimized for preparation of Li 6 PS 5 X. • Li 6 PS 5 Cl is synthesized with one-step solution process from raw materials. • The interfacial performance is enhanced by the thin and uniform electrolyte coating. • An improved cycling stability is achieved from the coated all-solid-state cell. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
812
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
139191363
Full Text :
https://doi.org/10.1016/j.jallcom.2019.152103