Abstract

The success of the rechargeable Li-S cell is limited in part by the dissolution of lithium-polysulfide in the electrolyte. Remarkably, it is found that removal of the conventional membrane separator in a Li-S cell improves sulfur utilization and cycling performance, whether the sulfur is initially contained in the cathode or electrolyte. An optimized cell design yields discharge capacities as high as 980 mA h g-1 after 100 cycles.

Highlights

  • Advanced energy storage systems are increasingly reliant on rechargeable lithium ion batteries (LIBs)

  • Secondary batteries with significantly higher energy densities compared to current LIBs are required for meeting these needs

  • We studied the surface of the carbon cathode exposed to chemically synthesized high-order lithium polysulfide intermediates (Li-PS) species in the presence of LiTFSI

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Summary

Introduction

Advanced energy storage systems are increasingly reliant on rechargeable lithium ion batteries (LIBs). We reported that integration of nitrile-containing additives in the sulfur cathode of a Li–S cell limits Li-PS loss to the electrolyte via strong interactions between Li+ and the lone pair of electrons on nitrogen containing species.[23] Figure 3 compares the galvanostatic cycling performance and discharge profiles at a fixed rate of C/5 of conventional Li–S cells in which the cathode is a physical mixture of 50 wt% sulfur, 40% carbon, and 10% binder and a conventional polypropylene material as separator.

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