Publications by authors named "Xi-Xi Feng"

Article Synopsis
  • Rechargeable lithium-sulfur (Li-S) batteries show promise for high-energy storage, but their conventional reactions often lead to unstable intermediates.
  • *Over the past decade, various strategies have been developed to improve the stability and efficiency of these batteries through nonconventional electrochemical reactions.
  • *Our research group has focused on a top-down approach, exploring reactions at molecular and subatomic levels, which has led to valuable insights and potential advancements in battery materials.
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The prosperity of the lithium-ion battery market is dialectically accompanied by the depletion of corresponding resources and the accumulation of spent batteries. It is an urgent priority to develop green and efficient battery recycling strategies for helping ease resources and environmental pressures at the current stage. Here, we propose a mild and efficient lithium extracting strategy based on potential controllable redox couples.

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Lithium-sulfur batteries are considered a promising "beyond Li-ion" energy storage technology. Currently, the practical realization of Li-S batteries is plagued by rapid electrochemical failure of S cathodes due to aggravated polysulfide dissolution and shuttle in the conventional liquid ether-based electrolytes. A gel polymer electrolyte obtained by in situ polymerization of liquid electrolyte solvent at the cathode-electrolyte interface has been proven an effective strategy to prevent polysulfide shuttle.

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In Li-ion batteries, functional cosolvents could significantly improve the specific performance of the electrolyte, for example, the flame retardancy. In case the cosolvent shows strong Li-coordinating ability, it could adversely influence the electrochemical Li-intercalation reaction of the electrode. In this work, a noncoordinating functional cosolvent was proposed to enrich the functionality of the electrolyte while avoiding interference with the Li storage process.

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