B-doped and La4NiLiO8-coated Ni-rich cathode with enhanced structural and interfacial stability for lithium-ion batteries

被引:35
作者
Lingjun Li [1 ]
Lizhi Fu [1 ]
Miao Li [2 ]
Chu Wang [1 ]
Zixiang Zhao [3 ]
Shangchen Xie [1 ]
Haichen Lin [4 ]
Xianwen Wu [5 ]
Haodong Liu [4 ]
Li Zhang [6 ]
Qiaobao Zhang [2 ]
Lei Tan [3 ]
机构
[1] School of Materials Science and Engineering, Changsha University of Science and Technology
[2] Department of Materials Science and Engineering, College of Materials, Xiamen University
[3] School of Energy and Power Engineering, Changsha University of Science and Technology
[4] Chemical Engineering, UC San Diego
[5] School of Chemistry and Chemical Engineering, Jishou University
[6] College of Chemistry and Chemical Engineering, Xiamen University
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TM912 [蓄电池]; TQ131.11 [];
学科分类号
0808 ; 0817 ;
摘要
Ni-rich layered oxides are considered promising cathodes for advanced lithium-ion batteries(LIBs) in the future, owing to their high capacity and low cost. However, the issues on structural and interfacial stability of Ni-rich cathodes still pose substantial obstacles in the practical application of advanced LIBs.Here, we employ a one-step method to synthesize a B-doped and La4NiLiO8-coated LiNi0.825Co0.115Mn0.06O2(BL-1) cathode with reliable structure and interface, for the first time. The La4NiLiO8coating layer can prevent cathodes from electrolyte assault and facilitate Li+diffusion kinetics.Moreover, B-doping can effectively restrain the pernicious H2-H3phase transition and adjust the orientation of primary particles to a radial alignment, which is obstructive to the arise of microcracks induced by the change of anisotropic volume. Specifically, when tested in pouch cells, the BL-1 cathode exhibits outstanding capacity retention of 93.49% after 500 cycles at 1 C. This dual-modification strategy dramatically enhances the stability of the structure and interface for Ni-rich cathode materials, consequently accelerating the commercialization process of high-energy–density LIBs.
引用
收藏
页码:588 / 594
页数:7
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