4.8 Article

Quantifying inactive lithium in lithium metal batteries

Journal

NATURE
Volume 572, Issue 7770, Pages 511-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41586-019-1481-z

Keywords

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Funding

  1. Office of Vehicle Technologies of the US Department of Energy through the Advanced Battery Materials Research (BMR) Program (Battery500 Consortium) [DE-EE0007764]
  2. US National Science Foundation (NSF) [ECCS-1542148]
  3. NSF Major Research Instrumentation Program [CHE-1338173]
  4. US Department of Energy, Office of Science, Basic Energy Science (BES) [DE FG02 87ER-45332]

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Lithium metal anodes offer high theoretical capacities (3,860 milliampere-hours per gram)(1), but rechargeable batteries built with such anodes suffer from dendrite growth and low Coulombic efficiency (the ratio of charge output to charge input), preventing their commercial adoption(2,3). The formation of inactive ('dead') lithium- which consists of both (electro)chemically formed Li+ compounds in the solid electrolyte interphase and electrically isolated unreacted metallic Li-0 (refs(4,5))-causes capacity loss and safety hazards. Quantitatively distinguishing between Li+ in components of the solid electrolyte interphase and unreacted metallic Li-0 has not been possible, owing to the lack of effective diagnostic tools. Optical microscopy(6), in situ environmental transmission electron microscopy(7,8), X-ray microtomography(9) and magnetic resonance imaging(10) provide a morphological perspective with little chemical information. Nuclear magnetic resonance(11), X-ray photoelectron spectroscopy(12) and cryogenic transmission electron microscopy(13,14) can distinguish between Li+ in the solid electrolyte interphase and metallic Li-0, but their detection ranges are limited to surfaces or local regions. Here we establish the analytical method of titration gas chromatography to quantify the contribution of unreacted metallic Li-0 to the total amount of inactive lithium. We identify the unreacted metallic Li-0, not the (electro)chemically formed Li+ in the solid electrolyte interphase, as the dominant source of inactive lithium and capacity loss. By coupling the unreacted metallic Li-0 content to observations of its local microstructure and nanostructure by cryogenic electron microscopy (both scanning and transmission), we also establish the formation mechanism of inactive lithium in different types of electrolytes and determine the underlying cause of low Coulombic efficiency in plating and stripping (the charge and discharge processes, respectively, in a full cell) of lithium metal anodes. We propose strategies for making lithium plating and stripping more efficient so that lithium metal anodes can be used for next-generation high-energy batteries.

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