Bimetal Substitution Enabled Energetic Polyanion Cathode for Sodium-Ion Batteries.
Qing-Yuan ZhaoJiang-Yu LiMeng-Jie ChenHongrui WangYu-Ting XuXiao-Feng WangXin MaQing WuXiongwei WuXian-Xiang ZengPublished in: Nano letters (2022)
The practical application of Na-superionic conductor structured materials is hindered by limited energy density and structure damage upon activating the third Na + . We propose a bimetal substitution strategy with cheaper Fe and Ni elements for costive vanadium in the polyanion to improve both ionic and electronic conductivities, and a single two-phase reaction during Na + intercalation/deintercalation and much reduced Na + diffusion barrier are uncovered by ex-situ X-ray diffraction and density functional theory calculations. Thus, the obtained cathode, Na 3 Fe 0.8 VNi 0.2 (PO 4 ) 3 , shows excellent electrochemical performances including high specific capacity (102.2 mAh g -1 at 0.1C), excellent rate capability (79.3 mAh g -1 at 20C), cycling stability (84.6% of capacity retention over 1400 cycles at 20C), low-temperature performance (89.7 mAh g -1 at 2C and -10 °C), and structure stability in an extended voltage window for the third Na + utilization. A competitive energy density of ≈287 Wh kg -1 for full batteries based on cathode and anode materials is also confirmed.
Keyphrases
- ion batteries
- density functional theory
- molecular dynamics
- reduced graphene oxide
- oxidative stress
- signaling pathway
- solar cells
- high resolution
- ionic liquid
- metal organic framework
- magnetic resonance imaging
- mass spectrometry
- magnetic resonance
- electron microscopy
- molecular dynamics simulations
- high intensity
- transition metal