Substituting Na for Excess Li in Li1+x(Ni0.6Mn0.4)1-xO2 Materials

被引:0
作者
Rathore, Divya [1 ]
Perez, Harold Smith [1 ]
Monchesky, Ian [1 ]
Vain, Fanny [2 ]
Xiao, Penghao [1 ,2 ]
Yang, Chongyin [1 ,2 ]
Dahn, J. R. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 4R2, Canada
[2] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
NMC640; batteries; -; Li-ion; sodium and lithium; DFT calculations; lower cost; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; OXIDE; SIMULATION; SYSTEM;
D O I
10.1149/1945-7111/ad6937
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
NMC640, a series of Li1+x(Ni0.6Mn0.4)(1-x)O-2 materials, are important Co-free mid-Ni cathode materials for Li-ion batteries, offering high energy density and better cost-efficiency than Ni-rich counterparts. These materials require excess Li compared to stoichiometric composition to improve the electrochemical performance in terms of rate capability and cycling stability. Although lithium-to-transition metal ratios up to 1.15 can be used to optimize the performance, less than 80% of this lithium is electrochemically active during cycling up to a 4.4 V upper cut off. This study explores whether some percentage of the inactive Li can be replaced by sodium to make these materials more cost-effective and bring potential improvements in electrochemical performance. Various amounts of excess Li were substituted by sodium in the structure. The results show that sodium can be integrated into the layered oxide structure without forming any impurity phases and effectively decreases the cation mixing observed in these layered structures. However, this does compromise cycling stability and rate capability. Na tends to occupy Li sites rather than transition metal sites, resulting in electrochemical instability and capacity loss. Even though excess Li is not electrochemically active, it cannot be effectively replaced by sodium without compromising battery performance of Li1+x(Ni0.6Mn0.4)(1-x)O-2 materials.
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页数:8
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