Tri-functionalized Li2B4O7 coated LiNi0.5Co0.2Mn0.3O2 for boosted performance lithium-ion batteries

被引:15
作者
Deng, Ruihua [1 ,2 ]
Tao, Jianming [1 ]
Zhong, Wenhao [1 ]
Wen, Lang [1 ]
Yang, Yanmin [1 ]
Li, Jiaxin [1 ,2 ]
Lin, Yingbin [1 ,2 ]
机构
[1] Fujian Normal Univ, Coll Phys & Energy, Fuzhou 350117, Peoples R China
[2] Fujian Prov Solar Energy Convers & Energy Storage, Fuzhou 350117, Peoples R China
关键词
Lithium -ion batteries; Cathode; Li plus -ion conductor; Work function; Dielectric polarization; RICH CATHODE MATERIALS; ENHANCED ELECTROCHEMICAL PROPERTIES; LAYERED OXIDE CATHODE; NI-RICH; SURFACE MODIFICATION; MECHANISM; KINETICS;
D O I
10.1016/j.jallcom.2023.168767
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Building stable interfacial structure is regarded as an effective strategy to enhance structure stability and facilitate Li+ migration. Herein, LiNi0.5Co0.2Mn0.3O2 (NCM523) cathode materials are surface-modified with amorphous Li2B4O7 (LBO) Li+-conductor with high relative permittivity. Comparing to pristine NCM, sur-face-modified electrodes exhibit a significant improvement in capacity retention and rate capability, deli-vering a reversible capacity of 163.4 mAh center dot g-1 and 87.6 % capacity retention over 100 cycles at 1 C. Besides the protection from HF-attack, enlarged crystal lattice volume by boron-doping and Li+-conductor char-acteristic of Li2B4O7 is beneficial for Li+-ion diffusion in NCM523 and reduces charge transfer resistance. In addition, the reduced work function induced by Li2B4O7-coating is helpful for the suppression of the electrolyte oxidation, the enhanced rate capability and improved cyclic stability in terms of interfacial stability. Moreover, dielectric polarization field induced by high-permittivity Li2B4O7 at NCM523-Li2B4O7- electrolyte triple-phase interface would synergistically facilitate Li-ion migration across electric double -layer. Our work would provide a new insight into the enhanced performance of cathode material surface -modified by Li+-conductor with large relative permittivity.(c) 2023 Elsevier B.V. All rights reserved.
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页数:10
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