4.8 Article

Nanostructured ligament and fiber Al-doped Li7La3Zr2O12 scaffolds to mediate cathode-electrolyte interface chemistry

Journal

JOURNAL OF POWER SOURCES
Volume 513, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2021.230551

Keywords

LLZO scaffolds; Cubic phase; Electrospinning; Composite cathodes; Cathode-electrolyte interface

Funding

  1. US Department of Energy (DOE) [DE-AC05-00OR22725]
  2. Office of Energy Efficiency and Renewable Energy Advanced Manufacturing Office
  3. DOE Office of Basic Energy Sciences, Division of Materials Science and Engineering
  4. Laboratory Directed Research and Development Program at Oak Ridge National Laboratory

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Electrospun Al-LLZO scaffold structures were synthesized and used as additives in a LiNi0.6Mn0.2Co0.2O2 composite cathode. The morphology of the Al-LLZO scaffold was found to affect the long-term cycling stability and rate performance of the cells, with uniformly dispersed fibers resulting in improved cathode electrolyte interface formation and cycling performance.
Scaffold structures of electrospun aluminum-substituted lithium lanthanum zirconate Li7La3Zr2O12 (Al-LLZO) were synthesized and used as an additive in a LiNi0.6Mn0.2Co0.2O2 composite cathode. The scaffolds were crystalized in the cubic phase after calcination at 700 degrees C. The Al-LLZO scaffold morphology was dependent on the precursor formulation (aqueous and dimethylformamide. The aqueous precursors resulted in scaffolds of densely coalesced ligaments, whereas the dimethylformamide precursors resulted in high-aspect ratio nanofiber scaffolds. The long-term cycling stability and rate performance of the cells were found to depend on the Al-LLZO scaffold morphology. The uniformly dispersed Al-LLZO fibers resulted in a more stable cathode electrolyte interface formation through the reduced decomposition of the LiPF6 salt during cycling, resulting in a better high-rate and long-term cycling performance.

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