TY - JOUR
T1 - Unlocking long-term cycling of ultrahigh‑nickel NCM cathodes at high voltage by boron-induced lattice stabilization
AU - Feng, Ziliang
AU - Luo, Peng
AU - Zhang, Quanyi
AU - Yu, Ziru
AU - Yu, Le
AU - Guo, Xiaohua
AU - Song, Wei Li
AU - Liu, Yongkang
AU - Zhang, Bao
AU - Zhang, Enfeng
AU - Dong, Peng
AU - Zhang, Yingjie
AU - Zhang, Yannan
N1 - Publisher Copyright:
© 2026 Elsevier Inc.
PY - 2026/10/15
Y1 - 2026/10/15
N2 - High‑nickel LiNi0.90Co0.05Mn0.05O2 (NCM9055), endowed with exceptional energy density, has emerged as one of the core cathode candidates for lithium-ion batteries in electric vehicles, portable electronic devices, and stationary energy storage systems. However, under high charging voltage conditions, severe cationic mixing and the reduction of Ni2+ migration energy barriers can induce irreversible phase transformation from the layered structure to a defective rock-salt phase. This degradation pathway critically compromises the structural integrity and electrochemical reversibility of the material. In this work, B3+ was successfully incorporated into the lattice via solid-state sintering, forming strong B-O covalent bonds with oxygen ions. These bonds raise the migration energy barrier for Ni2+ and anchor lattice oxygen, synergistically suppressing cation disorder and oxygen release. Additionally, the introduced boron creates a “riveting effect” within the crystal lattice, enhancing mechanical stability during electrochemical cycling. As a result, the modified material demonstrates markedly enhanced electrochemical performance when doped with boron at a molar ratio of 1% (relative to Ni + Co + Mn). At 1C with a high charging cutoff voltage of 4.5 V, it retains 77.58% of its capacity after 500 cycles, substantially outperforming the unmodified cathode (61.12%). Superior durability is also observed at the high rate of 5C over 700 cycles. This work demonstrates that boron-induced lattice stabilization constitutes a promising and mechanistically grounded strategy for developing next-generation, structurally robust, high-voltage ultra-high‑nickel cathode materials.
AB - High‑nickel LiNi0.90Co0.05Mn0.05O2 (NCM9055), endowed with exceptional energy density, has emerged as one of the core cathode candidates for lithium-ion batteries in electric vehicles, portable electronic devices, and stationary energy storage systems. However, under high charging voltage conditions, severe cationic mixing and the reduction of Ni2+ migration energy barriers can induce irreversible phase transformation from the layered structure to a defective rock-salt phase. This degradation pathway critically compromises the structural integrity and electrochemical reversibility of the material. In this work, B3+ was successfully incorporated into the lattice via solid-state sintering, forming strong B-O covalent bonds with oxygen ions. These bonds raise the migration energy barrier for Ni2+ and anchor lattice oxygen, synergistically suppressing cation disorder and oxygen release. Additionally, the introduced boron creates a “riveting effect” within the crystal lattice, enhancing mechanical stability during electrochemical cycling. As a result, the modified material demonstrates markedly enhanced electrochemical performance when doped with boron at a molar ratio of 1% (relative to Ni + Co + Mn). At 1C with a high charging cutoff voltage of 4.5 V, it retains 77.58% of its capacity after 500 cycles, substantially outperforming the unmodified cathode (61.12%). Superior durability is also observed at the high rate of 5C over 700 cycles. This work demonstrates that boron-induced lattice stabilization constitutes a promising and mechanistically grounded strategy for developing next-generation, structurally robust, high-voltage ultra-high‑nickel cathode materials.
KW - Durable high-voltage operation
KW - Excellent long-cycle performance
KW - Mechanical stability reinforcement
KW - Mitigating lattice oxygen loss
KW - Suppression of cation mixing
UR - https://www.scopus.com/pages/publications/105038033731
U2 - 10.1016/j.jcis.2026.140659
DO - 10.1016/j.jcis.2026.140659
M3 - Article
AN - SCOPUS:105038033731
SN - 0021-9797
VL - 720
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
M1 - 140659
ER -