Slow-Released Cationic Redox Activity Promoted Stable Anionic Redox and Suppressed Jahn-Teller Distortion in Layered Sodium Manganese Oxides.
Ao ZengJianyue JiaoHong ZhangEnyue ZhaoTao HeZhenbang XuXiaoling XiaoPublished in: ACS applied materials & interfaces (2024)
Manganese-based layered oxides are considered promising cathodes for sodium ion batteries due to their high capacity and low-cost manganese and sodium resources. Triggering the anionic redox reaction (ARR) can exceed the capacity limitation determined by conventional cationic redox. However, the unstable ARR charge compensation and Jahn-Teller distortion of Mn 3+ ions readily result in structural degradation and rapid capacity fade. Here, we report a P2-type Na 0.8 Li 0.2 Mn 0.7 Cu 0.1 O 2 cathode that shows a capacity retention of 84.5% at 200 mA/g after 200 cycles. Combining in situ X-ray diffraction and multi other ex situ characterizations, we reveal that the enhanced cycling stability is ascribed to a slow release of cationic redox activity which can well suppress the Jahn-Teller distortion and favor the ARR reversibility. Furthermore, density-functional theory calculations demonstrate that the inhibited interlayer migration and reduced band gap facilitate the stability and kinetic behavior of ARR. These findings provide a perspective for designing high-energy-density cathode materials with ARR activity.
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