Tethered molecular sorbents: Enabling metal-sulfur battery cathodes

Lin Ma, Houlong Zhuang, Yingying Lu, Surya S. Moganty, Richard G. Hennig, Lynden A. Archer

Research output: Contribution to journalArticle

61 Scopus citations

Abstract

A rechargeable battery that uses sulfur at the cathode and a metal (e.g., Li, Na, Mg, or Al) at the anode provides perhaps the most promising path to a solid-state, rechargeable electrochemical storage device capable of high charge storage capacity. It is understood that solubilization in the electrolyte and loss of sulfur in the form of long-chain lithium polysulfides (Li2Sx, 2 < x < 8) has hindered development of the most studied of these devices, the rechargeable Li-S battery. Beginning with density-functional calculations of the structure and interactions of a generic lithium polysulfide species with nitrile containing molecules, it is shown that it is possible to design nitrilerich molecular sorbents that anchor to other components in a sulfur cathode and which exert high-enough binding affinity to Li2Sx to limit its loss to the electrolyte. It is found that sorbents based on amines and imidazolium chloride present barriers to dissolution of long-chain Li2Sx and that introduction of as little as 2 wt% of these molecules to a physical sulfur-carbon blend leads to Li-S battery cathodes that exhibit stable long-term cycling behaviors at high and low charge/discharge rates.

Original languageEnglish (US)
Article number1400390
JournalAdvanced Energy Materials
Volume4
Issue number17
DOIs
StatePublished - Dec 1 2014
Externally publishedYes

Keywords

  • Lithium-nitrile interactions
  • Lithium-sulfur batteries
  • Molecular sorbents
  • Sequestering lithium polysulfide

ASJC Scopus subject areas

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

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