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Prolonging the Cycle Stability of Anion Redox P3-Type Na 0.6 Li 0.2 Mn 0.8 O 2 through Al 2 O 3 Atomic Layer Deposition Surface Modification.

Zhenxiao LingLangyuan WuChaogen HuXiaodong QiLunjie QinJiaqi PanXiao-Gang Zhang
Published in: ACS applied materials & interfaces (2024)
Sodium-ion batteries (SIBs) are becoming an alternative option for large-scale energy storage systems owing to their low cost and abundance. The lattice oxygen redox (LOR), which has the potential to increase the reversible capacity of materials, has promoted the development of high-energy cathode materials in SIBs. However, the utilization of oxygen anion redox reactions usually results in harmful lattice oxygen release, which hastens structural deformation and declines electrochemical performance, severely hindering their practical application. Herein, a ribbon-ordered superstructured P3-type Na 0.6 Li 0.2 Mn 0.8 O 2 (NLMO) cathode with a uniform Al 2 O 3 coating through atomic layer deposition (ALD) was synthesized. The cycling stability and rate capability of the materials were improved by a proper thickness of the Al 2 O 3 layer. Differential electrochemical mass spectrometry (DEMS) results clearly suggest that the Al 2 O 3 coating can inhibit the CO 2 release caused by the highly active surface of the NLMO material. Moreover, the results of transmission electron microscopy (TEM) and etching X-ray photoelectron spectroscopy (XPS) show that the Al 2 O 3 coating can effectively prevent electrolyte and electrode side reactions and the dissolution of Mn. This surface engineering strategy sheds light on the way to prolong the cycling stability of anionic redox cathode materials.
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