材料科学
阴极
离子键合
兴奋剂
纳米颗粒
离子
动力学
无机化学
纳米技术
物理化学
化学
光电子学
量子力学
物理
有机化学
作者
Taotao Zeng,Peng Gao,Zeyan Zhou,Changling Fan,Zhixiao Liu,Fuquan Zhang,Jinshui Liu,Jilei Liu
标识
DOI:10.1016/j.ensm.2023.103125
摘要
The practical applications of LiMn0.8Fe0.2PO4 have been greatly limited due to its low electrical conductivity and inferior electrochemical reaction kinetics. Herein, a Ni-doped strategy has been employed to optimize the morphology of LiMn0.8Fe0.2PO4 nanoparticles with preferred growth orientation, leads to improved electrical/ionic conductivity and electrode kinetic. Compared with pristine sample (Ni-D0), the electrical conductivity, ion diffusion coefficient and exchange current density of 5 mol% Ni-doped sample (Ni-D5) are obviously increased to 9.57 × 10−2 S cm−1, 3.301 × 10−11 cm2 s−1, and 0.339 mA cm−2, respectively. The first principle calculations also confirmed the enhanced electrical conductivity of LiMn0.8Fe0.15Ni0.05PO4@C. Meanwhile, Ni-D5 exhibits good rate capability and cycling stability. Furthermore, the operando XRD analysis demonstrated its highly structural stability and reversible properties. Therefore, the Ni-doped strategy is considered a promising and effective modification approach to enhance the Li-storage capability of LiMn0.8Fe0.2PO4 cathode for high performance rechargeable second batteries.
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