Zhang Xu-Dong, Shi Ji-Lei, Liang Jia-Yan, Yin Ya-Xia, Zhang Jie-Nan, Yu Xi-Qian, Guo Yu-Guo
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing, 100190, P. R. China.
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Adv Mater. 2018 May 28:e1801751. doi: 10.1002/adma.201801751.
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 Mn O 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 oxidation strategy ensures uniform and integrated encapsulation of Li Mn O 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 Mn O 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.
具有通过阳极氧化还原以及经典阳离子氧化还原实现超高容量能力的富锂层状氧化物引起了广泛关注。然而,涉及氧的过程不可避免地导致氧框架的不稳定,并最终导致表面晶格氧释放,从而导致容量下降、电压衰减和动力学性能不佳。在此,研究发现通过构建尖晶石LiMn₂O₄涂层可以缓解这一困境,该涂层在晶格框架中固有稳定,可防止富锂层状氧化物在深度脱锂状态下释放氧。可控的KMnO₄氧化策略确保了LiMn₂O₄的均匀且完整的包覆,且与层状核心具有结构相容性。由于该涂层抑制了氧的释放,优先从表面开始的相关相变和催化副反应因此受到阻碍,Li脱嵌过程中的详细结构演变证明了这一点。这种异质结构正极表现出极具竞争力的储能性能,包括在0.2C下循环300次后容量保持率为83.1%、良好的电压稳定性和良好的动力学性能。这些结果突出了氧框架稳定性的重要性以及这种尖晶石LiMn₂O₄涂层策略在稳定富锂层状氧化物表面以防止晶格氧逸出方面的有效性,这对于设计用于高能量密度锂离子电池的高性能正极材料至关重要。