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Stabilization of Li-Rich Disordered Rocksalt Oxyfluoride Cathodes by Particle Surface Modification.


ABSTRACT: Promising theoretical capacities and high voltages are offered by Li-rich disordered rocksalt oxyfluoride materials as cathodes in lithium-ion batteries. However, as has been discovered for many other Li-rich materials, the oxyfluorides suffer from extensive surface degradation, leading to severe capacity fading. In the case of Li2VO2F, we have previously determined this to be a result of detrimental reactions between an unstable surface layer and the organic electrolyte. Herein, we present the protection of Li2VO2F particles with AlF3 surface modification, resulting in a much-enhanced capacity retention over 50 cycles. While the specific capacity for the untreated material drops below 100 mA h g-1 after only 50 cycles, the treated materials retain almost 200 mA h g-1. Photoelectron spectroscopy depth profiling confirms the stabilization of the active material surface by the surface modification and reveals its suppression of electrolyte decomposition.

SUBMITTER: Naylor AJ 

PROVIDER: S-EPMC7493205 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Stabilization of Li-Rich Disordered Rocksalt Oxyfluoride Cathodes by Particle Surface Modification.

Naylor Andrew J AJ   Källquist Ida I   Peralta David D   Martin Jean-Frederic JF   Boulineau Adrien A   Colin Jean-François JF   Baur Christian C   Chable Johann J   Fichtner Maximilian M   Edström Kristina K   Hahlin Maria M   Brandell Daniel D  

ACS applied energy materials 20200529 6


Promising theoretical capacities and high voltages are offered by Li-rich disordered rocksalt oxyfluoride materials as cathodes in lithium-ion batteries. However, as has been discovered for many other Li-rich materials, the oxyfluorides suffer from extensive surface degradation, leading to severe capacity fading. In the case of Li<sub>2</sub>VO<sub>2</sub>F, we have previously determined this to be a result of detrimental reactions between an unstable surface layer and the organic electrolyte. H  ...[more]

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