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Layered lithium nickel oxide (LiNiO2) is a promising cathode for high-energy lithium batteries, yet its conventional high-temperature solid-state (HS) synthesis inevitably involves an “ordered layered → disordered rocksalt → ordered layered” phase transformation, leading to structural defects and limited electrochemical performance. Here, we report a low-temperature reaction–high-temperature crystallization (LR–HC) strategy that decouples lithiation from crystallization, enabling topotactic conversion of Ni(OH)2 into highly ordered LiNiO2 while bypassing the detrimental rocksalt intermediate. The LR–HC, product crystallized at 700 °C for only 1 h, exhibits an exceptionally low rocksalt phase content on the surface and delivers an initial discharge capacity exceeding 220 mAh·g−1 with an initial Coulombic efficiency above 90%. Remarkably, it retains 72.48% of its capacity after 200 cycles at 0.5 C, far outperforming the HS counterpart (53.10%). Operando X-ray diffraction (XRD) during cycling further demonstrates that the enhanced stability originates from a reduced c-axis contraction (4.19% vs. 6.43%) and a more reversible H2–H3 phase transition. The LR–HC strategy also proves versatile for synthesizing other high-nickel layered oxides (e.g., Ni95Co5 and Ni95Mn5), offering mechanistic insights into defect suppression and structural ordering for advanced cathode materials.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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