Abstract
Sodium-based P2-type layered cathodes are of interest for sodium-ion batteries due to their fast Na+transport and good cycling reversibility at elevated voltages. However, their low sodium content and irreversible Na loss on the anode side limit their practical use. Here, a self-compensated P2-Na0.8Li0.06□0.04Ni0.23Mn0.67O2(P2-NLNM-Va) is developed with approximately 4% cation vacancies in the transition metal layer to regulate lattice oxygen activity during charge and counterbalance anode-side Na loss. The vacancies activate additional charge capacity without sacrificing discharge capacity, rate capability, or air/cycling stability. As a result, the full cells of P2-NLNM-Va//hard carbon exhibit an initial discharge capacity of 100.6 mAh/g and retain 83% capacity after 300 cycles, compared with 80.2 mAh/g and 62% for the vacancy-free counterpart. This self-compensation strategy raises energy density by about 20% to 245 Wh/kg (total mass of cathode and anode), offering a route toward practical P2-type oxide-based sodium-ion batteries.
| Original language | English |
|---|---|
| Pages (from-to) | 6064-6073 |
| Number of pages | 10 |
| Journal | ACS Energy Letters |
| Volume | 10 |
| DOIs | |
| State | Published - 2025 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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