Abstract
Nickel-rich LiNi x Co y Mn z O 2 (x ≥ 80%) cathode materials have good commercial prospects in lithium-ion batteries because of high energy density. However, defects in Ni-rich cathodes, which arise from structural instability and surface erosion by electrolyte during the charge/discharge processes, impair electrochemical performance. We propose a simple co-precipitation and in situ coating method to form aluminum‑titanium co-doped, Li 3 PO 4 -coated LiNi 0.83 Co 0.11 Mn 0.06 O 2 (NCM) material to eliminate defects in Ni-rich cathodes. Transmission electron microscopy and X-ray diffraction suggested that a 4-nm thick film was formed on the surface of NCM particles. The electrochemical properties of the modified NCM material were improved: (i) NCMAl 0.3x Ti 1.7x @(Li 3 PO 4 ) 3x (x = 0.0036) achieved a specific discharge capacity of 166.4 mAh g −1 after 100 charge/discharge cycles, compared with the discharge capacity of 125.8 mAh g −1 for unmodified NCM. The retention rate was enhanced from 72.4% for NCM to 91.0% for modified NCM. (ii) The modified NCM had a higher initial discharge capacity from 81.3% to 87.9% and improved cyclic stability, lower Li + /Ni 2+ cation mixing, and higher ionic conductivity. • The LiNi 0.83 Co 0.11 Mn 0.06 (NCM) was co-doped with Al Ti and coated with Li 3 PO 4 . • Co-precipitation enabled one-step completion of doping and in situ coating. • Stabilizing the reversibility of the H 2 → H 3 phase transition reduced capacity fading. • Modified NCM delivered 91% capacity retention rate at 1C versus 72.4% for unmodified NCM.
Published Version
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