AI Article Synopsis

  • P2-type Fe- and Mn-based layered sodium transition metal oxides are potential materials for sodium batteries, offering high energy density and low costs, but struggle with poor structural reversibility and rapid capacity decline.
  • Real-time studies reveal that during the battery's discharge, an intermediate OP4 phase forms before transitioning to an irreversible ramsdellite phase, which hampers performance.
  • The findings suggest that stabilizing the crystal structure through substitutions or chemical modifications could enhance the cycling performance of these materials.

Article Abstract

P2-type Fe- and Mn-based layered sodium transition metal oxides are promising positive electrode materials for sodium batteries due to their high energy density and low costs of the constituting transition metals. However, poor structural reversibility and fast capacity decay have prevented their breakthrough so far. Herein, the real-time dynamic phase transitions and capacity fading mechanism of the P2 NaFeMnO positive electrode are revealed by operando X-ray diffraction, operando/ex situ X-ray absorption spectroscopy, neutron powder diffraction, and neutron pair distribution functions. Upon the desodiation process, a layered OP4 phase with long-range order is found as an intermediate state. With further deep desodiation, the formation of a Na-depleted ramsdellite phase with a short coherent length of 30 Å is observed for the first time. However, the transition from OP4 to ramsdellite is considered to be irreversible due to the breakdown of the layered structural characteristics, resulting in poor cycling performance in a variety of Fe-based layered sodium transition metal oxides. This work suggests that stabilizing the crystal structure by substitution or chemical modification can be a favorable strategy to avoid the degradation of positive electrodes and thus to improve the cycling performance.

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Source
http://dx.doi.org/10.1021/acsami.9b18109DOI Listing

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