Cited time in webofscience Cited time in scopus

All-Solid-State Lithium Batteries: Li+-Conducting Ionomer Binder for Dry-Processed Composite Cathodes

Title
All-Solid-State Lithium Batteries: Li+-Conducting Ionomer Binder for Dry-Processed Composite Cathodes
Author(s)
Hong, Seung-BoLee, Young-JunKim, Un-HyuckBak, CheolLee, Yong MinCho, WoosukHah, Hoe JinSun, Yang-KookKim, Dong-Won
Issued Date
2022-03
Citation
ACS Energy Letters, v.7, no.3, pp.1092 - 1100
Type
Article
Keywords
MORPHOLOGYFIREHIGH-ENERGY-DENSITYION BATTERIESSOLVENTELECTROLYTEMICROSTRUCTURE
ISSN
2380-8195
Abstract
All-solid-state lithium batteries (ASSLBs) are considered promising alternatives to current lithium-ion batteries as their use poses less of a safety risk. However, the fabrication of composite cathodes by the conventional slurry (wet) process presents technical challenges, such as limited stability of sulfide electrolytes against organic solvents and the increase of ionic resistance due to the use of insulating polymer binder. Herein, we develop a composite cathode fabricated using a solvent-free (dry) process. The composite cathode is prepared with a Li+-conducting ionomer binder, poly(tetrafluoroethylene-co-perfluoro(3-oxa-4-pentenesulfonic acid)) lithium salt. The ionomer facilitates Li+ transport and ensures good interfacial contact between the active material (LiNi0.7Co0.1Mn0.2O2), conducting carbon, and solid electrolyte (Li6PS5Cl) during cycling. Consequently, an ASSLB featuring a composite cathode with an ionomer delivers a high discharge capacity of 180.7 mAh g-1 (3.05 mAh cm-2) at 0.1 C and demonstrates stable cycling performance, retaining 90% of its initial capacity after 300 cycles at 0.5 C. © 2022 American Chemical Society.
URI
http://hdl.handle.net/20.500.11750/16508
DOI
10.1021/acsenergylett.1c02756
Publisher
American Chemical Society
Files in This Item:

There are no files associated with this item.

Appears in Collections:
Department of Energy Science and Engineering Battery Materials & Systems LAB 1. Journal Articles

qrcode

  • twitter
  • facebook
  • mendeley

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE