尖晶石
材料科学
电解质
电化学
氧化还原
阴极
氧气
氧化物
离子
化学工程
表面改性
无机化学
电极
物理化学
化学
有机化学
工程类
冶金
作者
Han‐xin Wei,Yu‐ming Liu,Yu‐hong Luo,Ying‐de Huang,Lin‐bo Tang,Zhen‐yu Wang,Cheng Yan,Jing Mao,Kehua Dai,Qing Wu,Xiahui Zhang,Junchao Zheng
标识
DOI:10.1002/adfm.202307583
摘要
Abstract Anionic redox activity can trigger structural instability in Li‐rich Mn‐based cathodes. Lattice oxygen activity can be tuned through liquid acid‐induced spinel phases and oxygen vacancies. However, the liquid‐acid‐modified surface is still attacked by the electrolyte. Besides, the underlying mechanism of spinel phase suppression of lattice oxygen activity is controversial. Here, a solid acid strategy for modification is proposed and the underlying mechanism is investigated in detail. Unique solid acid can in situ generate an interface protection layer and remarkably stabilize the structure. Theoretical calculations and experimental characterizations reveal that the spinel phase suppresses the irreversible loss of lattice oxygen by decreasing the O 2p non‐bonding energy level and enriching electrons at the layered/spinel phase interface. The inert layer on the surface prevents highly active O n− from being attacked by electrolytes. The obtained material exhibits significantly reduced irreversible lattice oxygen release and improved electrochemical performance. After 300 cycles, a slow capacity fading of 0.177 mAh g −1 per cycle and suppressed voltage fading are achieved. This study reveals the regulation method and mechanism for the anion activity of oxide cathodes in next‐generation Li‐ion batteries.
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