阴极
材料科学
氧化物
离子键合
格子(音乐)
晶体结构
氧气
单晶
化学工程
离子
结晶学
无机化学
化学
冶金
物理化学
有机化学
工程类
物理
声学
作者
Lijuan Hou,Qi Liu,Xinyuan Chen,Qiang Yang,Fengling Zhang,Daobin Mu,Li Li,Feng Wu,Renjie Chen
标识
DOI:10.1016/j.jpowsour.2024.234439
摘要
Single crystal Ni-rich layered oxide cathode materials enjoy better stability compared to polycrystalline materials, exhibiting good prospects in high energy density lithium-ion batteries. However, the poorer structure stability and rate performance are faced for the future large-scale application of single crystal Ni-rich layered oxide cathode material. The synergistic effect of Al and Ti is studied by in-situ differential electrochemical mass spectrometry (DEMS) and in-situ X-ray diffraction (XRD) combination with density functional theory (DFT) calculations to reveal the phase stabilization mechanism, improving the cycling stability of high voltage Ni-rich single crystal Li(Ni0·83Co0·12Mn0.05)O2 cathode material. It is indicated that bonding energy between the transition metal and oxygen atoms in the layered oxide are increased by introduction of Al and Ti elements, enhancing the stability of lattice oxygen and increasing the diffusion rate of Li+. The Al3+ can inhibit cation mixing, while Ti4+ can optimize the layered structure, which reduces structural failure caused by reaction heterogeneity, enhancing the cycling and rate performance of the cathode material in 4.5 V high voltage. The outstanding stably 500 cycles are obtained with capacity retention rate of 71.8%, compared to the unmodified sample with only 35.1% capacity.
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