TY - JOUR
T1 - Strain engineering of particles and interfaces for long-life stable LiNi0.8Co0.1Mn0.1O2 cathodes
AU - Feng, Ziliang
AU - Guo, Xiaohua
AU - Zhang, Bao
AU - Liu, Yongkang
AU - Zhang, Enfeng
AU - Luo, Peng
AU - Zhang, Quanyi
AU - Dong, Peng
AU - Song, Wei Li
AU - Zhang, Yingjie
AU - Zhang, Yannan
N1 - Publisher Copyright:
Copyright © 2026. Published by Elsevier B.V.
PY - 2026/3
Y1 - 2026/3
N2 - High-nickel layered cathode materials undergo structural degradation caused by enlarged internal stress arising from Li+/Ni2+ cation mixing and lattice oxygen release, which accelerates capacity decay and raises safety concerns. To mitigate this stress, a rational design of LiNi0.8Co0.1Mn0.1O2 (NCM811) was developed through precise strain engineering by Mo6+ and Sb3+ co-doping. Compared with pristine NCM811, the incorporation of Sb3+ significantly reduced the lattice distortion, thereby enabling stable and reversible Li+ de/intercalation and suppressing the migration from Ni2+ to Li+ sites. Meanwhile, Mo6+ doping established stronger Mo–O coordination in the bulk and formed electrochemically stable Li2MoO4 at the interfaces, which decreased the bulk stress by reducing oxygen release and simultaneously enhanced resistance to electrolyte corrosion. Thus, this strain-engineering strategy produced robust NCM811 lattice and interface structures, favorable for the construction of stable particles and thinner, more homogeneous cathode-electrolyte interfaces. The assembled pouch full cell (∼0.8 Ah) achieved a markedly improved capacity retention ∼93 % after 1000 cycles at 1 C (capacity retention ∼69 % after 500 cycles in the pouch cell assembled with pristine NCM811), compared with the state-of-the-art values typically below 85 %. This strategy provides an effective route for developing stable Ni-rich cathodes for long-term lithium-ion batteries.
AB - High-nickel layered cathode materials undergo structural degradation caused by enlarged internal stress arising from Li+/Ni2+ cation mixing and lattice oxygen release, which accelerates capacity decay and raises safety concerns. To mitigate this stress, a rational design of LiNi0.8Co0.1Mn0.1O2 (NCM811) was developed through precise strain engineering by Mo6+ and Sb3+ co-doping. Compared with pristine NCM811, the incorporation of Sb3+ significantly reduced the lattice distortion, thereby enabling stable and reversible Li+ de/intercalation and suppressing the migration from Ni2+ to Li+ sites. Meanwhile, Mo6+ doping established stronger Mo–O coordination in the bulk and formed electrochemically stable Li2MoO4 at the interfaces, which decreased the bulk stress by reducing oxygen release and simultaneously enhanced resistance to electrolyte corrosion. Thus, this strain-engineering strategy produced robust NCM811 lattice and interface structures, favorable for the construction of stable particles and thinner, more homogeneous cathode-electrolyte interfaces. The assembled pouch full cell (∼0.8 Ah) achieved a markedly improved capacity retention ∼93 % after 1000 cycles at 1 C (capacity retention ∼69 % after 500 cycles in the pouch cell assembled with pristine NCM811), compared with the state-of-the-art values typically below 85 %. This strategy provides an effective route for developing stable Ni-rich cathodes for long-term lithium-ion batteries.
KW - Cationic disordering
KW - Electrochemical performance
KW - Nickel-rich cathode materials
KW - Oxygen release
KW - Strain engineering
UR - https://www.scopus.com/pages/publications/105028965678
U2 - 10.1016/j.ensm.2026.104924
DO - 10.1016/j.ensm.2026.104924
M3 - Article
AN - SCOPUS:105028965678
SN - 2405-8297
VL - 86
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 104924
ER -