Published November 2023 | Version v1
Journal article

High sulfur loading and capacity retention in bilayer garnet sulfurized-polyacrylonitrile/lithium-metal batteries with gel polymer electrolytes

  • 1. Maryland Energy Innovation Institute, The University of Maryland, College Park, MD, 20742 (United States)
  • 2. Department of Materials Science and Engineering, The University of Maryland, College Park, MD, 20742 (United States)
  • 3. Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, MD, 20899 (United States)

Description

The cubic-garnet (Li7La3Zr2O12, LLZO) lithium-sulfur battery shows great promise in the pursuit of achieving high energy densities. The sulfur used in the cathodes is abundant, inexpensive, and possesses high specific capacity. In addition, LLZO displays excellent chemical stability with Li metal; however, the instabilities in the sulfur cathode/LLZO interface can lead to performance degradation that limits the development of these batteries. Therefore, it is critical to resolve these interfacial challenges to achieve stable cycling. Here, an innovative gel polymer buffer layer to stabilize the sulfur cathode/LLZO interface is created. Employing a thin bilayer LLZO (dense/porous) architecture as a solid electrolyte and significantly high sulfur loading of 5.2 mg cm2, stable cycling is achieved with a high initial discharge capacity of 1542 mAh g1 (discharge current density of 0.87 mA cm2) and an average discharge capacity of 1218 mAh g1 (discharge current density of 1.74 mA cm2) with 80% capacity retention over 265 cycles, at room temperature (22 °C) and without applied pressure. Achieving such stability with high sulfur loading is a major step in the development of potentially commercial garnet lithium-sulfur batteries. (© 2023 The Authors. Advanced Energy Materials published by Wiley‐VCH GmbH)

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Energy Materials
Journal Volume
13
Journal Issue
42
Journal Page Range
p. 1-10
ISSN
1614-6832
CODEN
ADEMBC

Optional Information

Notes
AID: 2301656