Published September 28, 2020 | Version v1
Journal article

Beyond the polysulfide shuttle and Lithium dendrite formation. Addressing the sluggish sulfur redox kinetics for practical high-energy Li-S batteries

  • 1. Chemical Science and Engineering Division, Argonne National Laboratory, Lemont, IL, 60439 (United States)
  • 2. Department of Mechanical and Aerospace Engineering, The Hong Kong University of Science and Technology, Kowloon (China)
  • 3. IRMC, Imam Abdulrahman Bin Faisal University (IAU), Dammam, 34212 (Saudi Arabia)
  • 4. Materials Science and Engineering, Stanford University, Stanford, CA, 94305 (United States)

Description

Electrolyte modulation simultaneously suppresses polysulfide the shuttle effect and lithium dendrite formation of lithium-sulfur (Li-S) batteries. However, the sluggish S redox kinetics, especially under high S loading and lean electrolyte operation, has been ignored, which dramatically limits the cycle life and energy density of practical Li-S pouch cells. Herein, we demonstrate that a rational combination of selenium doping, core-shell hollow host structure, and fluorinated ether electrolytes enables ultrastable Li stripping/plating and essentially no polysulfide shuttle as well as fast redox kinetics. Thus, high areal capacity (>4 mAh cm2) with excellent cycle stability and Coulombic efficiency were both demonstrated in Li metal anode and thick S cathode (4.5 mg cm2) with a low electrolyte/sulfur ratio (10 μL mg1). This research further demonstrates a durable Li-Se/S pouch cell with high specific capacity, validating the potential practical applications. (© 2020 Wiley‐VCH GmbH)

Additional details

Identifiers

Publishing Information

Journal Title
Angewandte Chemie (International Edition)
Journal Volume
59
Journal Issue
40
Journal Page Range
p. 17634-17640
ISSN
1433-7851
CODEN
ACIEF5