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Na-Rich Disordered Rock Salt Oxyfluoride Cathode Materials for Sodium Ion Batteries AITranslate

Helmholtz Institute Ulm (HIU);Helmholtz Institute Ulm (HIU);Helmholtz Institute Ulm (HIU); Karlsruhe Institute of Technology (KIT);SOLEIL Synchrotron, F-91192 Gif-sur-Yvette; Karlsruhe Institute of Technology (KIT)
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Publisher: ACS
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Abstract AITranslate

The existing classes of Na-based cathode materials and their chemistries are still limited, mainly with respect to the increasing demand for alternative post-Li technologies. In this letter, a newly synthesized Na-rich disordered rock salt (DRS) oxyfluoride with the nominal composition Na2MnO2F is reported as a cathode candidate for Na-ion batteries (SIBs). Rietveld refinement analysis confirmed that the synthesized compound has a DRS structure with larger lattice compared to Li-rich homologues. During the first cycle, up to 1.7 Na+/f.u. can be extracted at a slow rate, while a better capacity retention and cycling stability are obtained at high rate, reminiscent of electrode–electrolyte interaction. Further, X-ray absorption fine structure (operando and ex situ) confirmed the Mn oxidation state evolution upon cycling in agreement with the cyclic voltammetry redox profile, emphasizing the reversible Na+ (de)insertion and change of the Mn local ordering. This work is an additional input to the limited series of cathode candidates for SIBs.

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DOI:https://doi.org/10.1021/acsmaterialslett.2c00906

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Citation Information:

The existing classes of Na-based cathode materials and their chemistries are still limited, mainly with respect to the increasing demand for alternative post-Li technologies. In this letter, a newly synthesized Na-rich disordered rock salt (DRS) oxyfluoride with the nominal composition Na2MnO2F is reported as a cathode candidate for Na-ion batteries (SIBs). Rietveld refinement analysis confirmed that the synthesized compound has a DRS structure with larger lattice compared to Li-rich homologues. During the first cycle, up to 1.7 Na+/f.u. can be extracted at a slow rate, while a better capacity retention and cycling stability are obtained at high rate, reminiscent of electrode–electrolyte interaction. Further, X-ray absorption fine structure (operando and ex situ) confirmed the Mn oxidation state evolution upon cycling in agreement with the cyclic voltammetry redox profile, emphasizing the reversible Na+ (de)insertion and change of the Mn local ordering. This work is an additional input to the limited series of cathode candidates for SIBs.

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GB/T 7714-2015 [1] Yasaman Shirazi Moghadam, Abdel El Kharbachi, Yang Hu, et al. ACS Materials Letters, 2023(5). DOI:10.1021/acsmaterialslett.2c00906.
MLA [1] Yasaman Shirazi Moghadam, et al., ACS Materials Letters, no. 5, 2023, https://doi.org/10.1021/acsmaterialslett.2c00906.
APA [1] Yasaman Shirazi Moghadam, Abdel El Kharbachi, Yang Hu, Kai Wang, Stéphanie Belin, & Maximilian Fichtner. (2023). ACS Materials Letters(5). https://doi.org/10.1021/acsmaterialslett.2c00906
IEEE [1] Yasaman Shirazi Moghadam, Abdel El Kharbachi, Yang Hu, Kai Wang, Stéphanie Belin, and Maximilian Fichtner, ACS Materials Letters, no. 5, 2023, doi: 10.1021/acsmaterialslett.2c00906.