An epitaxial surface heterostructure anchoring approach for high-performance Ni-rich layered cathodes

被引:0
作者
Sun, Weili [1 ]
Tan, Junbin [1 ]
Li, Jianlin [4 ]
Zhang, Qingqing [1 ]
Sun, Xiao-Guang [2 ]
Liu, Kai [5 ]
Li, Cheng [3 ]
Huang, Yongsheng [1 ]
Mu, Wenyu [1 ]
Zheng, Shijian [1 ]
Dai, Sheng [2 ,6 ]
机构
[1] Hebei Univ Technol, Sch Mat Sci & Engn, Tianjin Key Lab Mat Laminating Fabricat & Interfac, Tianjin 300130, Peoples R China
[2] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37831 USA
[3] Oak Ridge Natl Lab, Neutron Scattering Div, Oak Ridge, TN 37830 USA
[4] Argonne Natl Lab, Appl Mat Div, Lemont, IL 60439 USA
[5] Tianjin Univ Technol, Sch Mat Sci & Engn, Tianjin 300384, Peoples R China
[6] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
来源
JOURNAL OF ENERGY CHEMISTRY | 2025年 / 105卷
基金
中国国家自然科学基金;
关键词
Ni-rich layered oxides; Rock-salt nanolayer; Heteroatom anchoring; Lattice oxygen reversibility; Lithium-ion batteries; LITHIUM-ION BATTERIES; OXIDE CATHODE; TRANSITION;
D O I
10.1016/j.jechem.2025.01.053
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Nickel-rich (Ni >= 90%) layered oxides materials have emerged as a promising candidate for next- generation high-energy-density lithium-ion batteries (LIBs). However, their widespread application is hindered by structural fatigue and lattice oxygen loss. In this work, an epitaxial surface rock-salt nano- layer is successfully developed on the LiNi0.9Co0.1O2 sub-surface via heteroatom anchoring utilizing high-valence element molybdenum modification. This in-situ formed conformal buffer phase with a thickness of 1.2 nm effectively suppresses the continuous interphase side-reactions, and thus maintains the excellent structure integrity at high voltage. Furthermore, theoretical calculations indicate that the lattice oxygen reversibility in the anion framework of the optimized sample is obviously enhanced due to the higher content of O 2p states near the Fermi level than that of the pristine one. Meanwhile, the stronger Mo-O bond further reduces cell volume alteration, which improves the bulk structure stability of modified materials. Besides, the detailed charge compensation mechanism suggests that the average oxidation state of Ni is reduced, which induces more active Li+ participating in the redox reactions, boosting the cell energy density. As a result, the uniquely designed cathode materials exhibit an extraordinary discharge capacity of 245.4 mAh g-1 at 0.1 C, remarkable rate performance of 169.3 mAh g-1 at 10 C at 4.5 V, and a high capacity retention of 70.5% after 1000 cycles in full cells at a high cut-off voltage of 4.4 V. This strategy provides an valuable insight into constructing distinctive heterostructure on highperformance Ni-rich layered cathodes for LIBs. (c) 2025 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:158 / 169
页数:12
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