Decoupling slab gliding and lattice contraction in Na layered oxides to enable high-voltage Na-ion batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41519780.
- Also identified by DOI 10.1038/s41467-025-68238-7 and PMC identifier 12891617.
- Licence recorded as CC BY-NC-ND.
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Abstract
Layered transition metal oxide cathodes (Na<sub>x</sub>TMO<sub>2</sub>) demonstrate a classic type of cathode for Sodium-ion batteries (SIBs), however their practical application faces a long-standing challenge of irreversible phase transitions at high voltages, which causes unsatisfied specific energy and cycling stability, particularly for P-type (Na<sup>+</sup> located at prismatic sites) cathodes. This phenomenon is conventionally ascribed to the Na<sup>+</sup> re-coordination from prismatic to octahedral (O-type) configuration upon Na<sup>+</sup> extraction, whereby the TMO<sub>2</sub> slab gliding and abrupt c-lattice change are always coupled, and a straightforward solution to this situation remains elusive. Here, we reveal that, the TMO<sub>2</sub> slab gliding and the lattice contraction can be decoupled, and the rapid lattice contraction under high state-of-charge underlies the fundamental origin for the irreversible phase transitions. By pre-engineering 15.8% O-type stacking faults to a P-type Na<sub>0.7</sub>Mn<sub>0.8</sub>Ni<sub>0.2</sub>O<sub>2</sub>, the dramatic volume variation and irreversible phase transitions at high voltage (4.5 V vs. Na<sup>+</sup>/Na) can be primarily eliminated. This work advances the understanding on the phase transitions at deep desodiation states, and paves up a feasible way to realize high-energy layered oxides.