4.6 Article

Enabling the high capacity of lithium-rich anti-fluorite lithium iron oxide by simultaneous anionic and cationic redox

Journal

NATURE ENERGY
Volume 2, Issue 12, Pages 963-971

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41560-017-0043-6

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Funding

  1. Centre for Electrochemical Energy Science, an Energy Frontier Research Centre - US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11]
  2. DOE, Office of Science by Argonne National Laboratory - US DOE [DE-AC02-06CH11357]
  3. National Energy Research Scientific Computing Center, a DOE Office of Science User Facility - Office of Science of the US Department of Energy [DE-AC02-05CH11231]

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Anionic redox reactions in cathodes of lithium-ion batteries are allowing opportunities to double or even triple the energy density. However, it is still challenging to develop a cathode, especially with Earth-abundant elements, that enables anionic redox activity for real-world applications, primarily due to limited strategies to intercept the oxygenates from further irreversible oxidation to O-2 gas. Here we report simultaneous iron and oxygen redox activity in a Li-rich anti-fluorite Li5FeO4 electrode. During the removal of the first two Li ions, the oxidation potential of O2- is lowered to approximately 3.5 V versus Li+/Li-0, at which potential the cationic oxidation occurs concurrently. These anionic and cationic redox reactions show high reversibility without any obvious O2 gas release. Moreover, this study provides an insightful guide to designing high-capacity cathodes with reversible oxygen redox activity by simply introducing oxygen ions that are exclusively coordinated by Li+.

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