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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 (Na 0.8 Li 0.03 Mg 0.05 Ni 0.28 Fe 0.05 Mn 0.54 Ti 0.05 O 2 ) 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–Na 0.8 Li 0.03 Mg 0.05 Ni 0.28 Fe 0.05 Mn 0.54 Ti 0.05 O 2 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.
Zhu et al. (Mon,) studied this question.
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