Unlocking the high-capacity operation of P2-type cathode through bifunctional spectator ions substitution

• Published in: Journal of power sources Vol. 613; p. 234925
• Main Authors: Jiang, Wenjia, Ren, Qiaochu, Hu, Teli, Hu, Hai, Huang, Zhifeng, Li, Zhou, Liu, Shaoxiong, Pei, Yi, Liu, Li
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.09.2024
• Subjects: Bifunctional spectator ions; High-capacity; Sodium-ion batteries; High-capacity; Bifunctional spectator ions; Sodium-ion batteries
• ISSN: 0378-7753
• DOI: 10.1016/j.jpowsour.2024.234925

The high specific capacity of the P2-type cathode endowed by the synergistic cation and anion redox makes it one of the most promising cathode materials for sodium-ion batteries (NIBs). However, the structural rearrangement and the irreversible oxygen release under highly desodiated states engender stability issues upon high-capacity operation. Herein, we show specifically how the structural degradation of the P2-type cathode is effectively stabilized by the substitution of bifunctional spectator ions. The rational incorporation of Ti and Si ions triggers the “pillar effect” and “inductive effect”, which eliminates the P2-O2/P2-P2′ structural evolution and mitigates the irreversible oxygen oxidation. Benefited from the highly reversible anion redox, the obtained Na0·67Li0·21Mn0·59Si0·01Ti0·19O2 represents a high reversible capacity of 220 mAh g−1 at 0.1C (20 mA g−1) within a Na-metal half-cell. Ex-situ XRD reveals a solid solution reaction without the formation of additional phases among the charge/discharge process, thus favoring stable cycling performance for up to 200 cycles at 2.5C (with a capacity retention rate of 88 %). This work shows, not only the specific strategies for improving the electrochemical performance of cathode materials, but also offers insights into the intrinsic mechanisms underlying the performance enhancement achieved through spectator ion substitution. •Ti4+ and Si4+ triggered the “pillar effect” and “inductive effect”.•P2-O2/P2-P2′ phase degradation and oxygen release were inhibited.•A high capacity of 220 mAh g−1 at 20 mA g−1 was obtained.