Electrochemical activation, voltage decay and hysteresis of Li-rich layered cathode probed by various cobalt content

被引:40
作者
Wu, Yingqiang [1 ,2 ]
Xie, Leqiong [2 ]
He, Xiangming [3 ]
Zhuo, Linhai [4 ]
Wang, Limin [1 ]
Ming, Jun [1 ,5 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Jilin, Peoples R China
[2] Huadong Inst Lithium Ion Battery, Zhangjiagang 215600, Peoples R China
[3] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
[4] Taishan Univ, Coll Chem & Chem Engn, Tai An 271021, Shandong, Peoples R China
[5] King Abdullah Univ Sci & Technol, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
关键词
Cathode; Lithium battery; Cobalt-doping; Electrochemical activation; Voltage decay; LITHIUM; PERFORMANCE; ELECTRODES; CHEMISTRY; BATTERIES; ENERGY; OXIDES; FADE; MN; NI;
D O I
10.1016/j.electacta.2018.01.181
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The high capacity of Li-rich layered cathode materials have attracted great attention for the greater energy density lithium ion (Li-ion) batteries, but the understanding of knowledge associated with electrochemical behaviours are still needed to improve their performances further. In this study, different amount of Co content is designed in Li-rich layered compounds (0.5Li(2)MnO(3)center dot 0.5LiMn(0.5-x)Ni(0.5-x)Co(2x)O(2), 0 <= x <= 0.2), and the stepwise electrochemical activation process is applied to explore the features. We discover that the substitution of Co3+ ions can accelerate the electrochemical activation of Li2MnO3 component, and the Co-doped compound delivers much higher capacities even they suffer an apparent voltage decay comparing to the Co-free one. Besides, a fast metal ions migration exists (e. g., from the metastable tetrahedral site to the lower energy cubic site) in initial dozens of cycles (e. g., 30 cycles at 0.1C); thereafter, they likely return to the original octahedral site, as demonstrated in the voltage decay and hysteresis analysis. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
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