Improved electrochemical performances of Ni-rich LiNi0.83Co0.12Mn0.5O2 by Mg-doping

被引:119
作者
Lv, Yeting [1 ]
Cheng, Xu [1 ]
Qiang, Wenjiang [1 ]
Huang, Bingxin [1 ]
机构
[1] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
关键词
Ni-rich cathode; Coprecipitation; Cycle stability; Mg-doping; Cracks; LITHIUM-ION BATTERIES; LINI0.8CO0.1MN0.1O2 CATHODE MATERIALS; POSITIVE ELECTRODE MATERIAL; CYCLING PERFORMANCE; RATE CAPABILITY; DEGRADATION; GENERATION; SUBSTITUTION; STABILITY; MAGNESIUM;
D O I
10.1016/j.jpowsour.2020.227718
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
Ni-rich layered oxide LiNi0.83Co0.12Mn0.05O2 (NCM) has advantages of high energy density, low price, and so on. However, the application of NCM is impeded by low cycle stability. To address this issue, (Ni0.83Co0.12Mn0.05)(1-x)Mg-x(OH)(2) is coated on (Li0.83Co0.12Mn0.05)(OH)(2) precursor particles with coprecipitation method, which ensures full and uniform coverage of precursor particle by the coating layer. Mg2+ ions evenly distribute in the cathode particles due to the diffusion during sintering. The pristine and doped cathodes are cycled in a voltage range of 2.8-4.5 Vat 1C. NCM exhibits an initial discharge capacity of 201.8 mAh g(-1) and capacity retention of 74.0% after 200 cycles, and NCM particles have been fractured by the cycle process. Mg doping could significantly improve the cycle stability, where 0.96 at% Mg-doped sample achieves the best electrochemical performance. The Mg-doped sample delivers an initial discharge capacity of 199.7 mAh g(-1) and capacity retention of 87.2%. The structural integrity of the Mg-doped particles is retained after cycles, which agrees well with the enhanced cycle stability.
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页数:9
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共 44 条
[1]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[2]   Effect of surface modification using a sulfate-based surfactant on the electrochemical performance of Ni-rich cathode materials [J].
Chae, Bum-Jin ;
Yim, Taeeun .
MATERIALS CHEMISTRY AND PHYSICS, 2018, 214 :66-72
[3]   Divalent cation incorporated Li(1+x)MMgxO2(1+x) (M = Ni0.75Co0.25):: viable cathode materials for rechargeable lithium-ion batteries [J].
Chang, CC ;
Kim, JY ;
Kumta, PN .
JOURNAL OF POWER SOURCES, 2000, 89 (01) :56-63
[4]   Al-Doped Li[Ni0.78Co0.1Mn0.1Al0.02]O2 for High Performance of Lithium Ion Batteries [J].
Do, Su Jung ;
Santhoshkumar, P. ;
Kang, Suk Hyun ;
Prasanna, K. ;
Jo, Yong Nam ;
Lee, Chang Woo .
CERAMICS INTERNATIONAL, 2019, 45 (06) :6972-6977
[5]   Improved cyclic stability of LiNi0.8Co0.1Mn0.1O2 via Ti substitution with a cut-off potential of 4.5 V [J].
Du, Rui ;
Bi, Yujing ;
Yang, Wenchao ;
Peng, Zhe ;
Liu, Meng ;
Liu, Yang ;
Wu, Baoming ;
Yang, Bangcheng ;
Ding, Fei ;
Wang, Deyu .
CERAMICS INTERNATIONAL, 2015, 41 (05) :7133-7139
[6]   Structural, electrochemical and Li-ion transport properties of Zr-modified LiNi0.8Co0.1Mn0.1O2 positive electrode materials for Li-ion batteries [J].
Gao, Shuang ;
Zhan, Xiaowen ;
Cheng, Yang-Tse .
JOURNAL OF POWER SOURCES, 2019, 410 :45-52
[7]   Surface layer design of cathode materials based on mechanical stability towards long cycle life for lithium secondary batteries [J].
Hu, Xitao ;
Qiang, Wenjiang ;
Huang, Bingxin .
ENERGY STORAGE MATERIALS, 2017, 8 :141-146
[8]   Influence of Mg2+ doping on the structure and electrochemical performances of layered LiNi0.6Co0.2-xMn0.2MgxO2 cathode materials [J].
Huang, Zhenjun ;
Wang, Zhixing ;
Guo, Huajun ;
Li, Xinhai .
JOURNAL OF ALLOYS AND COMPOUNDS, 2016, 671 :479-485
[9]   Excellent rate capability of Mg doped Li[Li0.2Ni0.13Co0.13Mn0.54]O2 cathode material for lithium-ion battery [J].
Jin, Xue ;
Xu, Qunjie ;
Liu, Haimei ;
Yuan, Xiaolei ;
Xia, Yongyao .
ELECTROCHIMICA ACTA, 2014, 136 :19-26
[10]   Understanding the Degradation Mechanisms of LiNi0.5Co0.2Mn0.3O2 Cathode Material in Lithium Ion Batteries [J].
Jung, Sung-Kyun ;
Gwon, Hyeokjo ;
Hong, Jihyun ;
Park, Kyu-Young ;
Seo, Dong-Hwa ;
Kim, Haegyeom ;
Hyun, Jangsuk ;
Yang, Wooyoung ;
Kang, Kisuk .
ADVANCED ENERGY MATERIALS, 2014, 4 (01)