兴奋剂
阴极
材料科学
空位缺陷
掺杂剂
相(物质)
离子
扩散
钠
氧化物
相变
分析化学(期刊)
化学工程
化学
结晶学
光电子学
物理化学
凝聚态物理
热力学
冶金
色谱法
有机化学
工程类
物理
作者
Ashmitha Anilkumar,Neeraja Nair,Shantikumar V. Nair,Baskar Senthilkumar
标识
DOI:10.1016/j.est.2023.108291
摘要
P2 and O3-type sodium layered oxides (NaxTMO2) have been considered as most promising cathodes for sodium-ion batteries. The P2-type oxides are superior to O3 in terms of fast Na diffusion and high-rate kinetics. However, the deficient Na (x < 0.7) in the P2-structure has low initial charge capacity and it limits practical application. In addition to Na deficiency, P2-O2 phase transition and Na+/vacancy ordering degrades the performance during cycling. To address this issue, dual doping strategy can be employed, synergistic effect of the dopants can mitigate both the Na+/vacancy ordering and the P2-O2 phase transitions. Herein, effect of LiCu dual doping in P2-type Na0.67Ni0.33Mn0.67O2 is systematically investigated. Dual doped high-Na P2-type cathode achieved high capacity ~110 mAh g−1 with a cycling stability of ~85 % even following 200 cycles. Remarkably, the voltage profile is completely changed from multiple plateaus to a slow gradient which indicates a solid-solution pathway. Li present in TM layer and the strong CuO binding can suppress the irreversible P2-O2 phase transition. Structural analysis has ensured that there is no O2/OP4 phase formation during the charge up to 4.2 V. The present result reflects that the sufficient sodium and structural stabilization can improve the performance of P2-type cathodes.
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