4.8 Article

Design of Nanostructured Heterogeneous Solid Ionic Coatings through a Multiscale Defect Model

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 8, 期 8, 页码 5687-5693

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b12030

关键词

solid electrolyte interphase; space charge; density functional theory; defect; ionic conduction; heterogeneous interface

资金

  1. U.S. Department of Energy [DE-AC02-05CH11231, 7056410]
  2. National Science Foundation (Powering the Kentucky Bioeconomy for a Sustainable Future) [1355438]
  3. Center for Computational Sciences at University of Kentucky
  4. Department of Energy
  5. Office Of The Director
  6. Office of Integrative Activities [1355438] Funding Source: National Science Foundation

向作者/读者索取更多资源

Understanding of the electrical conduction, that is, ionic and electronic conduction, through the solid electrolyte interphase (SEI) is critical to the design of durable lithium-ion batteries (LIEs) with high rate capability and long life. It is believed that an ideal SEI should not only be an ionic conductor, but also an electronic insulator: In this study, we present a theoretical design of an artificial SET consisting of lithium fluoride (LiF) and lithium carbonate (Li2CO3) on a LIB anode based on a newly developed density functional theory (DFT) informed space charge model. We demonstrate that the migration of lattice Li ions from LiF phase to form Li interstitials in Li2CO3 is energetically favorable near the LiF/Li2CO3 interface. At equilibrium, this interfacial defect reaction establishes a space charge potential across the interface, which causes the accumulation of ionic carriers but the depletion of elctronic carriers near the LiF,Li2CO3 interface. To utilize this space charge effect, we propose a computationally designed, nanostructured artificial SEI structure with high, density of interfaces of LiF and Li2CO3 perpendicular to the electrode. On the basis of this structure, the influences of grain size and volume ratio of the two phases were studied. Our results reveal that reducing the grain size of Li2CO3 in the nanostructured composite can promote ionic carriers and increase the ionic conductivity through the composite SEI by orders of magnitude. At the same time,: the electronic conductivity is reduced due to electron depletion near the LiF/Li2CO3 interface. Furthermore, an optimal volume fraction that ensures high ionic and low electronic conduction was predicted.

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