Trace doping realizing superior electrochemical performance in P2-type Na0.50Li0.08Mn0.60Co0.16Ni0.16O2 cathode for sodium-ion batteries

被引:0
|
作者
Hongying Hou [1 ]
Jinxu Qiu [1 ,2 ]
Bao Li [2 ]
Liang Wang [2 ]
Zhuangzhuang Zhang [2 ]
Mengmin Jia [2 ]
Xiaobing Lai [2 ]
Mingming Han [2 ]
Pengyao Yan [2 ]
Dai-Huo Liu [2 ]
Dongmei Dai [2 ]
Bao Wang [3 ]
机构
[1] Faculty of Material Science and Engineering, Kunming University of Science and Technology
[2] Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions,Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University
[3] State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
D O I
暂无
中图分类号
TM912 [蓄电池];
学科分类号
0808 ;
摘要
P2-type layered oxides are receiving significant interest due to their superior structure and intrinsic performances. There are strenuous attempts to balance the structure stability, phase transition as well as desirable electrochemical performances by inducing anion/cation ions, changing morphology, adjusting valence, etc. In this work, several same-period elements of Sc, Ti, V, Cr, Fe, Cu and Zn are doped into Na0.50Li0.08Mn0.60Co0.16Ni0.16O2cathodes, which are manipulated by ions radii and valence state, further studied by operando X-ray powder diffraction patterns(XRD). As a result, the Cu2+doped cathode performed higher rate capacities(as high as 86 m Ah/g even at 10 C) and more stable structures(capacity retention of ~89.4% for 100 cycles), which owing to the synergistic effect among the tightened TMO2layer, enlarged d-spacing, reduce O–O electrostatic repulsion, ameliorate lattice distortion as well as mitigate ordering of Na+/vacancy.
引用
收藏
页码:413 / 417
页数:5
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