4.8 Article

High-performance N-methyl-N-propylpiperidinium bis (trifluoromethanesulfonyl)imide/poly(vinylidene fluoride-hexafluoropropylene) gel polymer electrolytes for lithium metal batteries

期刊

JOURNAL OF POWER SOURCES
卷 403, 期 -, 页码 127-136

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2018.09.080

关键词

Lithium metal battery; Ionic liquid gel polymer electrolyte; Ionic conductivity; Interfacial chemistry; Freestanding

资金

  1. Department of Chemistry Startup at Virginia Tech
  2. ORAU Ralph E. Powe Junior Faculty Enhancement Award
  3. Project of Natural Science Foundation of Heilongjiang Province of China [B2015004]
  4. China Scholarship Council

向作者/读者索取更多资源

Ionically conductive polymer electrolytes represent a class of safe and environment-friendly electrolytes for next generation alkali metal batteries. Understanding the interplay between composition-driven interfacial processes and battery performance can fundamentally inform the design of polymer electrolytes for practical applications. In this study, we fabricate lithium metal batteries based on transparent free-standing ionic liquid gel polymer electrolytes (ILGPEs) and LiFePO4 cathodes. We develop the ILGPEs using a composite of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP), N-methyl-N-propylpiperidinium bis(trifluoromethanesulfonyl) imide (PP13TFSI), and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). A thorough compositional optimization shows that the lithium ion conductivity of the ILGPE increases with the increase of PP13TFSI and LiTFSI, reaching maxima of 1.3 mS cm(-1) at 23 degrees C and 5.82 mS cm(-1) at 80 degrees C when the ILGPE contains 60 wt% PP13TFSI and 20 wt% LiTFSI. The optimized ILGPE exhibits excellent interfacial stability against the lithium metal, as signified by the stable interfacial resistance upon long-term storage. The LiFePO4 vertical bar ILGPE vertical bar Li cells can deliver superior battery performance with a practical capacity approaching 89.5% of the theoretical capacity and capacity retention of 95.0% after 200 cycles. The formation of the electrode-electrolyte interphases takes place primarily during the initial cycles, which likely accounts for the activation period observed in LiFePO4 vertical bar ILGPE vertical bar Li cells.

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