Sodium-ion batteries (SIBs) have captured widespread attention for grid-scale energy storage owing to the wide distribution and low cost of sodium resources. Delivery of high energy density with stable retention remains a challenge in developing cathode candidates for rechargeable SIBs. Inspired by the concept of "cationic potential", here, we present a hierarchical crystalline domain in hexagonal particles with target chemical composition (Na0.8Li0.03Mg0.05Ni0.28Fe0.05Mn0.54Ti0.05O2) from the inner bulk O3 phase (71.1 wt %) to the outer P2-type shell (28.9 wt %) of the structure. Benefiting from the mitigated mechanical stress of the predominant bulk O3 phase under the protection of the surficial P2 crystalline domain at the microscale during Na+ (de)intercalation, the brittle fracture, plastic yielding, and structural damage of the bulk O3 phase are effectively prohibited during battery cycling, thereby achieving good structural integrity. As a consequence, the biphasic P2/O3-Na0.8Li0.03Mg0.05Ni0.28Fe0.05Mn0.54Ti0.05O2 material exhibits satisfactory electrochemical properties, with a high energy density of 506 Wh kg-1 and good capacity retention of 85.5% over 200 cycles. This work highlights the importance of tailoring the crystalline domain to mitigate the reaction-induced stress and particle fracture of layered biphasic cathode materials for high-energy SIBs.
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