4.8 Article

Reversible Mn2+/Mn4+ double redox in lithium-excess cathode materials

Journal

NATURE
Volume 556, Issue 7700, Pages 185-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-018-0015-4

Keywords

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Funding

  1. Robert Bosch LLC
  2. Umicore Specialty Oxides and Chemicals
  3. Assistant Secretary for Energy Efficiency and Renewable Energy, Vehicle Technologies Office, of the U.S. Department of Energy under the Advanced Battery Materials Research (BMR) Program [DE-AC02-05CH11231]
  4. Argonne National Laboratory [DE-AC02-06CH11357]
  5. DOE Office of Science User Facility [DE-AC02-05CH11231]
  6. Office of Science, Office of Basic Energy Sciences, of the US DOE [DE-AC02-05CH11231]
  7. National Science Foundation [ACI-1548562]
  8. NSF Graduate Research Fellowship [DGE-1106400]
  9. Assistant Secretary for Energy Efficiency and Renewable Energy, Vehicle Technologies Office, of the US DOE under the Advanced Battery Materials Research (BMR) Program [DEAC02-05CH11231]

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There is an urgent need for low-cost, resource-friendly, high-energy-density cathode materials for lithium-ion batteries to satisfy the rapidly increasing need for electrical energy storage. To replace the nickel and cobalt, which are limited resources and are associated with safety problems, in current lithium-ion batteries, high-capacity cathodes based on manganese would be particularly desirable owing to the low cost and high abundance of the metal, and the intrinsic stability of the Mn4+ oxidation state. Here we present a strategy of combining high-valent cations and the partial substitution of fluorine for oxygen in a disordered-rocksalt structure to incorporate the reversible Mn2+/Mn4+ double redox couple into lithium-excess cathode materials. The lithium-rich cathodes thus produced have high capacity and energy density. The use of the Mn2+/Mn4+ redox reduces oxygen redox activity, thereby stabilizing the materials, and opens up new opportunities for the design of high-performance manganese-rich cathodes for advanced lithium-ion batteries.

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