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@ARTICLE{Kundu:916121,
      author       = {Kundu, Sumana and Kraytsberg, Alexander and Ein-Eli, Yair},
      title        = {{R}ecent development in the field of ceramics solid-state
                      electrolytes: {I}—oxide ceramic solid-state electrolytes},
      journal      = {Journal of solid state electrochemistry},
      volume       = {26},
      number       = {9},
      issn         = {1432-8488},
      address      = {New York},
      publisher    = {Springer},
      reportid     = {FZJ-2022-05952},
      pages        = {1809 - 1838},
      year         = {2022},
      abstract     = {Many elements in the periodic table form ionic compounds;
                      the crystal lattices of such compounds contain cations and
                      anions, which are arranged in the way that these cations and
                      anions form two interpenetrated sub-lattices (cation and
                      anion sub-lattices). Up to now, a number of ionic compounds
                      are known, in which cations or anions are fairly mobile
                      within the corresponding sub-lattice; these compounds are
                      termed as “solid-state electrolytes”. Many solid-state
                      electrolytes with such moveable cations and moveable anions
                      are known to date. Following the footsteps of the
                      established Li-ion battery technology, an interest in the
                      Li+-conducting solid-state electrolytes appears, and
                      all-solid-state lithium battery has started its journey to
                      accompany the reigning counterpart. The valence and ionic
                      radius of ions, the crystal structure, and intrinsic defects
                      of the material are the prime properties of the solid-state
                      electrolytes, which determine the ion mobility in the
                      crystal framework. There are a number of solid-state
                      electrolyte structures that demonstrate high Li+-mobility
                      and high Li+ conductivity (Li+ superconductors) in the range
                      of 10−2 to 10−3 S/cm at room temperature, which is
                      comparable to the ionic conductivity of 1 M LiPF6
                      (~ 10−2 S/cm), but the conductivity can dwindle highly
                      by up to 5–6 orders of magnitude within the different
                      materials that belonged to the same crystal structure
                      family. Moreover, the surface or interface properties are
                      also crucial factors in tailoring the ionic conductivity of
                      practical polycrystalline solid electrolytes. The
                      interfacial properties and compatibility with electrode
                      materials have a high impact on the performance of
                      electrochemical cells with solid electrolytes. Although the
                      potential window of many solid electrolytes is high enough,
                      there are solid electrolytes which are unstable at low
                      operating potentials while others are not stable towards the
                      cathodes; these features result in the appearance of
                      non-conductive interface layers resulting in a low
                      interfacial charge–transfer kinetics. In this review, we
                      discuss the latest advancements in the field of Li-ion
                      conducting electrolytes from the points of their fundamental
                      properties. The latest achievements in the fields of cell
                      design and improvements of (solid-state
                      electrolytes)/(various anodes) and (solid-state
                      electrolytes)/(various cathodes) compatibilities are
                      considered as well.},
      cin          = {IEK-9},
      ddc          = {540},
      cid          = {I:(DE-Juel1)IEK-9-20110218},
      pnm          = {1223 - Batteries in Application (POF4-122)},
      pid          = {G:(DE-HGF)POF4-1223},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000817847000001},
      doi          = {10.1007/s10008-022-05206-x},
      url          = {https://juser.fz-juelich.de/record/916121},
}