Published in

Wiley, Advanced Energy Materials, 10(12), 2022

DOI: 10.1002/aenm.202103444

Links

Tools

Export citation

Search in Google Scholar

Dual‐Ion Flux Management for Stable High Areal Capacity Lithium–Sulfur Batteries

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

AbstractControlling the interaction between multiple ion fluxes is a major challenge that hampers the adoption of post‐Li intercalation battery systems, which offer a multifold increase in energy density over existing technologies. Here, a dual‐ion flux management strategy is introduced to simultaneously control the distribution of Li and polysulfide ions in high‐energy Li–S batteries. This approach enables long‐term use of high S‐loading cathodes with 13.6 mgsulfur cm−2, achieving 9 mAh cm−2 areal capacity with 73% capacity retention for 1000 charging/discharging cycles. The battery system relies on the use of a multiscale membrane, with comparable size to existing battery separators, which simultaneously acts as an atomic redisperser for Li ions, dielectric and mechanical separator, polysulfide barrier, and extended cathode. Combined characterization and modeling reveal that the membrane is stable down to <1.0 V versus Li+/Li and result in a uniform Li‐ion flux to the anode and effective polysulfide confinement and reutilization. The potential of this approach for application is demonstrated by the fabrication of stable pouch cells with a horizontal surface of 40 cm2 and 6.8 mAh cm−2 capacity. These findings provide an exemplification of the potential for effective multi‐ion flux management for future energy storage and emerging electrochemical systems.