复合数
材料科学
兴奋剂
电导率
离子电导率
扩散
带隙
电化学
离子
密度泛函理论
离子键合
功率密度
分析化学(期刊)
化学工程
纳米技术
化学物理
复合材料
物理化学
光电子学
计算化学
化学
热力学
电解质
电极
功率(物理)
工程类
有机化学
物理
色谱法
作者
Baofeng Zhang,Xiaoning Ma,Wenqiang Hou,Wei Yuan,Lixia He,Yang Ou,Yuebo Liu,Jie Wang,Youlong Xu
标识
DOI:10.1021/acsaem.2c02035
摘要
LiFePO 4 with ultrahigh rate ability and enhanced electronic/ionic conductivity can be achieved by element doping. However, the role of substitution on the electronic/ionic conductivity and size effect on the electrochemical performance are still open. Here, LiFePO 4 particles (LC-LFP) with tuned sizes are synthesized via La and Ce co-doping, delivering a capacity of 91.9 mAh g –1 under 200 C. In addition, LC-LFP exhibit a power density as high as 57.6 kW kg –1 when the energy density is nearly 300 Wh kg –1 owing to the 10 5 enhancement of inherent conductivity and 10 5 Li + diffusion ability. DFT results suggest that La and Ce co-doping would not only facilitate free Li + ions to extrude out of the unit cell due to the structure distortion but also generate extra middle-gap states to boost the carrier concentration. Furthermore, it appears that atoms on the surface of the particles tend to decrease the band gap and lower the conduction band compared to the atoms in the bulk. This work demonstrates and discloses a promising strategy to enhance the rate performance of LiFePO 4 by element co-doping.
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