Boosting the anchoring and catalytic capability of MoSfor high-loading lithium sulfur batteries

Zheng Long Xu, Nicolas Onofrio, Jian Wang

Research output: Journal article publicationJournal articleAcademic researchpeer-review

2 Citations (Scopus)

Abstract

A high sulfur loading and low electrolyte/sulfur ratio are considered prerequisites for practical high-energy lithium sulfur batteries (LSBs); however, shuttling and the sluggish conversion of flooded polysulfides make it challenging to achieve the full utilization of active materials with an extended cyclic life. Herein, we explore 1T MoS2nanodots as powerful electrocatalyst to overcome this issue. Electrochemical and synchrotronin situX-ray diffraction characterizations revealed that 1T MoS2nanodots with numerous active sites are favored to trap and propel the redox reactions for polysulfides. First-principle calculations indicated that the surface and Mo-terminated edges of 1T MoS2provide stronger anchor sites for Li2S, a lower Li-S decomposition barrier, and faster Li ion migration than those for the 2H phase, which suggest the unique catalytic property for edge-rich 1T MoS2nanodots in LSBs. In the presence of a small amount of 1T MoS2nanodots, porous carbon/Li2S6cathodes exhibited remarkable electrochemical performance retaining a capacity of 9.3 mA h cm−2over 300 cycles under high sulfur loading of 12.9 mg cm−2and a low electrolyte/sulfur ratio of 4.6 μL mg−1, which rivals the performance of the state-of-the-art LSBs. Our combined experimental and theoretical analyses rationalized the use of nanodot catalysts in high energy rechargeable batteries.

Original languageEnglish
Pages (from-to)17646-17656
Number of pages11
JournalJournal of Materials Chemistry A
Volume8
Issue number34
DOIs
Publication statusPublished - 14 Sep 2020

ASJC Scopus subject areas

  • Chemistry(all)
  • Renewable Energy, Sustainability and the Environment
  • Materials Science(all)

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