4.8 Article

Degradation Mechanisms in Li2VO2F Li-Rich Disordered Rock-Salt Cathodes

Journal

CHEMISTRY OF MATERIALS
Volume 31, Issue 16, Pages 6084-6096

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.9b00829

Keywords

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Funding

  1. European Union [711792]
  2. Swedish Research Council [2016-03545]
  3. STandUP for Energy
  4. EU [730872]
  5. Swedish Research Council [2016-03545] Funding Source: Swedish Research Council

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The increased energy density in Li-ion batteries is particularly dependent on the cathode materials that so far have been limiting the overall battery performance. A new class of materials, Li-rich disordered rock salts, has recently been brought forward as promising candidates for next-generation cathodes because of their ability to reversibly cycle more than one Li-ion per transition metal. Several variants of these Li-rich cathode materials have been developed recently and show promising initial capacities, but challenges concerning capacity fade and voltage decay during cycling are yet to be overcome. Mechanisms behind the significant capacity fade of some materials must be understood to allow for the design of new materials in which detrimental reactions can be mitigated. In this study, the origin of the capacity fade in the Li-rich material Li2VO2F is investigated, and it is shown to begin with degradation of the particle surface that spreads inward with continued cycling.

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