4.5 Article

A novel mixed ether-based electrolyte for lithium-sulfur batteries with Li anode protection by dual salts

Journal

SUSTAINABLE ENERGY & FUELS
Volume 6, Issue 15, Pages 3658-3668

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2se00647b

Keywords

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Funding

  1. Wuhan University
  2. Key R&D program of Hubei [2021BAA173]

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In this study, the electrolyte for lithium-sulfur batteries has been optimized by using a mixed THF and DPE system, which successfully inhibits the shuttle effect of lithium polysulfides and improves the coulombic efficiency of lithium deposition/stripping. This work provides a new design strategy for the electrolyte of lithium-sulfur batteries and demonstrates excellent performance.
Lithium-sulfur batteries (LSB) are regarded as one of the next-generation energy storage systems with a high energy density. However, the shuttle effect of lithium polysulfides (LiPSs) and irreversible consumption of the Li anode prevent the practical application of Li-S batteries. In this work, a mixed tetrahydrofuran (THF) and dipropyl ether (DPE) based electrolyte has been optimized for Li-S batteries. Due to the common-ion effect, the LiPS solubility has been significantly inhibited when the sulfur cathode is operating in a concentrated electrolyte containing an optimized solvent system with weak dissolving power. And no self-discharge effect occurred in the cells with these electrolytes during a 10 day storage. Besides, the coulombic efficiency (CE) for Li deposition/stripping has been improved by optimizing the ratio of dual lithium salts. Impressively, Li||Cu half-cells can run stably for more than 500 cycles with a high CE (>99.3%). For these reasons, a Li-SeSPAN cell with a L1L2TE-1382 electrolyte demonstrates an excellent capacity retention (>94% after 500 cycles) with an ultrathin (50 mu m) Li metal anode. With a good compatibility of the optimized electrolyte for both the Li metal anode and sulfur cathode, this work provides a new design strategy for the electrolyte for lithium-sulfur batteries.

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