Fluorinated hybrid solid-electrolyte-interphase for dendrite-free lithium deposition.

Nat Commun

Department of Electrical Engineering and Computer Science, Center for Advanced Photovoltaics and Sustainable Energy, South Dakota State University, Brookings, SD, 57007, USA.

Published: January 2020

AI Article Synopsis

  • Lithium metal anodes are highly sought after for their potential capacity, but issues like dendrite growth and unstable interfaces hinder their use.
  • Researchers have developed a simple, cost-effective method to create an artificial interphase on lithium anodes by using a tin-containing electrolyte.
  • This artificial layer enhances lithium-ion diffusion, reduces dendrite formation, and allows for efficient lithium storage and plating, leading to improved stability and performance in lithium cells compared to traditional lithium anodes.

Article Abstract

Lithium metal anodes have attracted extensive attention owing to their high theoretical specific capacity. However, the notorious reactivity of lithium prevents their practical applications, as evidenced by the undesired lithium dendrite growth and unstable solid electrolyte interphase formation. Here, we develop a facile, cost-effective and one-step approach to create an artificial lithium metal/electrolyte interphase by treating the lithium anode with a tin-containing electrolyte. As a result, an artificial solid electrolyte interphase composed of lithium fluoride, tin, and the tin-lithium alloy is formed, which not only ensures fast lithium-ion diffusion and suppresses lithium dendrite growth but also brings a synergistic effect of storing lithium via a reversible tin-lithium alloy formation and enabling lithium plating underneath it. With such an artificial solid electrolyte interphase, lithium symmetrical cells show outstanding plating/stripping cycles, and the full cell exhibits remarkably better cycling stability and capacity retention as well as capacity utilization at high rates compared to bare lithium.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941966PMC
http://dx.doi.org/10.1038/s41467-019-13774-2DOI Listing

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