Abstract

Carbonate-based electrolytes demonstrate safe and stable electrochemical performance in lithium-sulfur batteries. However, only a few types of sulfur cathodes with low loadings can be employed and the underlying electrochemical mechanism of lithium-sulfur batteries with carbonate-based electrolytes is not well understood. Here, we employ in operando X-ray absorption near edge spectroscopy to shed light on a solid-phase lithium-sulfur reaction mechanism in carbonate electrolyte systems in which sulfur directly transfers to Li2S without the formation of linear polysulfides. Based on this, we demonstrate the cyclability of conventional cyclo-S8 based sulfur cathodes in carbonate-based electrolyte across a wide temperature range, from −20 °C to 55 °C. Remarkably, the developed sulfur cathode architecture has high sulfur content (>65 wt%) with an areal loading of 4.0 mg cm−2. This research demonstrates promising performance of lithium-sulfur pouch cells in a carbonate-based electrolyte, indicating potential application in the future.

Highlights

  • Carbonate-based electrolytes demonstrate safe and stable electrochemical performance in lithium-sulfur batteries

  • We demonstrated that an alucone-coated commercial C–S cathode can reversibly cycle in carbonate electrolyte[7]

  • This research reveals the underlying mechanism of Li–S batteries in carbonate electrolytes and promotes their practical application

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Summary

Introduction

Carbonate-based electrolytes demonstrate safe and stable electrochemical performance in lithium-sulfur batteries. A few commonalities exist across the literature for the sulfur cathodes in carbonate-based electrolyte: (1) confinement of shortchain sulfur molecules within a microporous structure or strong chemical bonding to a polymeric host, resulting in (2) very limited sulfur mass content (mostly

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