4.6 Article

Revealing the Role of Liquid Electrolytes in Cycling of Garnet-Based Solid-State Lithium-Metal Batteries

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JOURNAL OF PHYSICAL CHEMISTRY C
卷 -, 期 -, 页码 -

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AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.2c02074AJ

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  1. National Research Council of Canada (NRC) under the Low Emission Aviation Program (LEAP) [A1-026222]
  2. Office of Energy Research & Development (OERD)

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Researchers introduced a carbonate-based liquid electrolyte to lower the resistance at the garnet electrolyte/cathode interface and improve the performance of solid-state lithium-metal batteries (SS-LMBs). By using scanning transmission X-ray microscopy and X-ray absorption spectroscopy, they studied the role of liquid electrolytes at the interface and discovered the formation and chemical composition of two interphases. They also found that the liquid electrolyte decomposes during cycling into fluoride species, oxides, and carbonates, which contribute to the formation of the solid-liquid electrolyte interphase. Based on the synergy between interphases, they demonstrated the potential application of a new hybrid electrolyte approach in SS-LMBs, achieving high capacity retention after multiple cycles.
Solid-state lithium-metal batteries (SS-LMBs) suffer from the very high resistance at the garnet electrolyte/cathode interface that hampers their commercialization. Herein, a carbonate-based liquid electrolyte (LE) is introduced at the interface of a Li6.5La2.9Ba0.1Zr1.4Ta0.6O12 (LLBZTO) garnet/LiNi0.6Mn0.2Co0.2O2 (NMC 622) cathode to lower the interfacial resistance and improve the battery performance. In this work, we conducted a thorough study on the role of liquid electrolytes at the interface using scanning transmission X-ray microscopy (STXM) associated with X-ray absorption spectroscopy (XAS). As a result, we have shown new data related to the formation and the chemical composition of the two formed interphases: a solid-liquid electrolyte interphase (SLEI) and the cathode-electrolyte interphase (CEI). Furthermore, we have presented evidence that LE decomposes during cycling into fluoride species including LiF and LaF3, oxides like Li2O, and carbonates (i.e., Li2CO3) as the main components of in situ-formed SLEI. Based on the synergy between SLEI and CEI, we demonstrate Li| garnet|LE|NMC 622 cells cycled with an initial discharge capacity of 168 mAh g(-1 )and a capacity retention of similar to 82% after 28 cycles. We expect that our study of SLEI will accelerate the implementation of a new hybrid electrolyte (solid garnet and liquid electrolyte) approach in SS-LMBs.

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