Na/Co dual-doped olivine LiMn0.6Fe0.4PO4 cathode with superior reaction kinetics for Li-ion batteries

被引:1
|
作者
Wang, Pengxu [1 ]
Zhang, Erdong [2 ]
Fang, Yaoguo [2 ]
Chen, Yihong [2 ]
Yu, Haifeng [1 ]
Zhang, Ya [2 ]
Cheng, Qian [2 ]
Jiang, Hao [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] Shanghai Xuanyi New Energy Dev Co Ltd, Shanghai 201800, Peoples R China
基金
中国博士后科学基金;
关键词
LiMn0.6Fe0.4PO4; Element doping; Rate performance; Li-ion batteries; LITHIUM; PERFORMANCE; CHALLENGES; LIFEPO4;
D O I
10.1007/s10008-024-06043-w
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Olivine-type lithium manganese iron phosphate (LMFP) has been a promising cathode for Li-ion batteries (LIB) owing to its superior safety performance and low cost, yet the intrinsic low ionic/electronic conductivities result in large electrochemical polarization and inferior rate performance. Herein, we report a LMFP with high-power Li-storage capability through a Na/Co co-doped strategy. The Na+ with a larger ionic radius (1.02 & Aring;) locates at Li-sites, effectively widening the Li+ diffusion channel to improve the Li-ion transfer dynamic. The Co2+ located at transition metal sites (TM-sites) can lower the band gap to improve the electronic conductivity, while it can also alleviate the increase in the b-axis parameter to shorten the Li+ transfer path. Accordingly, the concurrently improved ionic/electronic transfer rate endows the superior rate performance of LMFP, with a high reversible capacity of 113.5 mAh g(-1) at 5 C, much higher than the pristine sample (only 79.5 mAh g(-1)). The modified LMFP also displays excellent cycling stability, maintaining 97.1% of its initial capacity after 1000 cycles at 1 C.
引用
收藏
页码:4303 / 4310
页数:8
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