尖晶石
材料科学
阴极
氧气
化学工程
氧化还原
插层(化学)
涂层
阳极
析氧
电化学
纳米技术
无机化学
电极
物理化学
化学
冶金
有机化学
工程类
作者
Xudong Zhang,Ji‐Lei Shi,Jia‐Yan Liang,Ya‐Xia Yin,Jienan Zhang,Xiqian Yu,Yu‐Guo Guo
标识
DOI:10.1002/adma.201801751
摘要
Abstract Lithium‐rich layered oxides with the capability to realize extraordinary capacity through anodic redox as well as classical cationic redox have spurred extensive attention. However, the oxygen‐involving process inevitably leads to instability of the oxygen framework and ultimately lattice oxygen release from the surface, which incurs capacity decline, voltage fading, and poor kinetics. Herein, it is identified that this predicament can be diminished by constructing a spinel Li 4 Mn 5 O 12 coating, which is inherently stable in the lattice framework to prevent oxygen release of the lithium‐rich layered oxides at the deep delithiated state. The controlled KMnO 4 oxidation strategy ensures uniform and integrated encapsulation of Li 4 Mn 5 O 12 with structural compatibility to the layered core. With this layer suppressing oxygen release, the related phase transformation and catalytic side reaction that preferentially start from the surface are consequently hindered, as evidenced by detailed structural evolution during Li + extraction/insertion. The heterostructure cathode exhibits highly competitive energy‐storage properties including capacity retention of 83.1% after 300 cycles at 0.2 C, good voltage stability, and favorable kinetics. These results highlight the essentiality of oxygen framework stability and effectiveness of this spinel Li 4 Mn 5 O 12 coating strategy in stabilizing the surface of lithium‐rich layered oxides against lattice oxygen escaping for designing high‐performance cathode materials for high‐energy‐density lithium‐ion batteries.
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