材料科学
阴极
相(物质)
化学工程
氧化物
相变
工作(物理)
复合氧化物
钠
化学物理
拉伤
无机化学
降级(电信)
离子
纳米技术
原位
自行车
氧化锰
氧化铁
结构稳定性
过渡金属
作者
Tiandu Sheng,Jian Li,Lihua Wang,Haiying Nie,Shili Gan,Yun Zheng,Jiujun Zhang,Ting‐Liang Xie
摘要
ABSTRACT The irreversible O3‐P3 phase transition in layered sodium oxide cathodes leads to severe volumetric strain and capacity fading. While recent progress via high‐entropy design or dual‐phase structuring has improved structural stability, these strategies primarily focus on suppressing rather than guiding the phase transition pathway. Herein, we propose an “intermediate phase engineering” concept in a high‐entropy O3‐type cathode, Na 0.9 Ni 0.32 Zn 0.08 Co 0.1 Fe 0.1 Mn 0.3 Ti 0.1 O 2 (Na9NZCFMT), which enables the spontaneous formation of a strain‐buffering OP2 intermediate phase at 3.8 V. Unlike conventional approaches that suppress phase transitions, the OP2 phase acts as a structural buffer that actively guides oxygen‐layer gliding along an ordered, low‐strain pathway, reducing the volumetric strain from 6.86% to 3.12%. Through integrated in situ XRD, XAS, STEM, and DFT calculations, we unravel the formation condition and buffering mechanism of this OP2 phase: The local coordination environment modulated by specific elements lowers the energy barrier for its formation, leading to a thermodynamically favored and kinetically accessible intermediate state. The cathode exhibits highly reversible structural evolution and anionic redox, delivering 91.5% capacity retention after 100 cycles. This work offers a generalizable strategy for designing stable high‐voltage layered cathodes.
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