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Phosphorus-doped lithium- and manganese-rich layered oxide cathode material for fast charging lithium-ion batteries

Authors :
Kang, Yuqiong
Guo, Xingang
Guo, Zhiwu
Li, Jiangang
Zhou, Yunan
Liang, Zheng
Han, Cuiping
He, Xiangming
Zhao, Yun
Tavajohi Hassan Kiadeh, Naser
Li, Baohua
Kang, Yuqiong
Guo, Xingang
Guo, Zhiwu
Li, Jiangang
Zhou, Yunan
Liang, Zheng
Han, Cuiping
He, Xiangming
Zhao, Yun
Tavajohi Hassan Kiadeh, Naser
Li, Baohua
Publication Year :
2021

Abstract

Owing to their high theoretical specific capacity and low cost, lithium- and manganese-rich layered oxide (LMR) cathode materials are receiving increasing attention for application in lithium-ion batteries. However, poor lithium ion and electron transport kinetics plus side effects of anion and cation redox reactions hamper power performance and stability of the LMRs. In this study, LMR Li1.2Mn0.6Ni0.2O2 was modified by phosphorus (P)-doping to increase Li+ conductivity in the bulk material. This was achieved by increasing the interlayer spacing of the lithium layer, electron transport and structural stability, resulting in improvement of the rate and safety performance. P5+ doping increased the distance between the (003) crystal planes from ∼0.474 nm to 0.488 nm and enhanced the structural stability by forming strong covalent bonds with oxygen atoms, resulting in an improved rate performance (capacity retention from 38% to 50% at 0.05 C to 5 C) and thermal stability (50% heat release compared with pristine material). First-principles calculations showed the P-doping makes the transfer of excited electrons from the valence band to conduction band easier and P can form a strong covalent bond helping to stabilize material structure. Furthermore, the solid-state electrolyte modified P5+ doped LMR showed an improved cycle performance for up to 200 cycles with capacity retention of 90.5% and enhanced initial coulombic efficiency from 68.5% (pristine) or 81.7% (P-doped LMR) to 88.7%.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1280631802
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.jechem.2021.04.026