Cesium doping to improve the electrochemical performance of layered Li1.2Ni0.13Co0.13Mn0.54O2 cathode material

被引:35
作者
Ding, Xiang [1 ,2 ]
Li, Yi-xuan [1 ,2 ]
Deng, Miao-miao [1 ,2 ]
Wang, Shuo [1 ,2 ]
Aqsa, Yasmin [1 ,2 ]
Hu, Qiao [1 ,2 ]
Chen, Chun-hua [1 ,2 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Mat Energy Convers, Dept Mat Sci & Engn, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Anhui, Peoples R China
基金
美国国家科学基金会;
关键词
Li-rich cathode; Cesium doping; Lithium ion diffusion coefficient; Rate capability; LI-RICH; SURFACE MODIFICATION; OXIDE CATHODES; LI1.2MN0.54CO0.13NI0.13O2; STABILITY;
D O I
10.1016/j.jallcom.2019.03.297
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
Aiming to improve the rate capability and cycling stability, cesium doped Li-rich cathode materials Li1.2-xCsxNi0.13Co0.13Mn0.54O2 (x = 0, 0.012, 0.036, 0.060, 0.096) are synthesized by a sol-gel method and a subsequent calcination process. The optimal Cs+ content is found to be x = 0.060. After Cesium doping to Li+ sites, the enlarged interplanar spacing of (003) plane, which is confirmed by high resolution transmission electron microscopy, can accelerate the Li+ diffusion during the lithiation/delithiation process at the interface of electrode/electrolyte. The obtained Cs-doped Li-rich sample with x = 0.060 exhibits much improved electrochemical performance compared with the bare, especially the rate capability (148 mAh g(-1) compared to 50 mAh g(-1) at 10 C). The first discharge capacity is much enhanced from 250 to 281 mAh g(-1) at 0.1 C with a heightened coulombic efficiency from 72% to 81%. XRD, SEM, TEM, elemental mapping, EDS and ICP-AES are adopted to characterize the morphologies and structures. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 108
页数:9
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