阴极
阳极
材料科学
电化学
兴奋剂
镍
过渡金属
锰
电解质
碱金属
空位缺陷
钠离子电池
离子
分析化学(期刊)
无机化学
电极
化学
结晶学
冶金
光电子学
物理化学
催化作用
有机化学
法拉第效率
生物化学
色谱法
作者
Xu Wang,Zixiang Yang,Mikhail Pugach,Ning Fu,Yujia Cai,Qinghua Zhang,Yang Hou,Zhizhen Ye,Jianguo Lü
出处
期刊:Small methods
[Wiley]
日期:2025-05-29
卷期号:10 (2): e2500478-e2500478
标识
DOI:10.1002/smtd.202500478
摘要
P2-Na0.67Ni0.33Mn0.67O2 is regarded as a viable cathode material for sodium ion batteries due to its high theoretical energy density. However, it also has challenges that impair its electrochemical performance, like the P2-O2 phase transition, the strong Jahn-Teller distortion effect, and the Na+/vacancy ordering at high voltage. Here, an approach is proposed to use the Cu/Li binary doping modification of P2-Na0.67Ni0.33Mn0.67O2, which stabilizes the cathode structure by introducing Li into alkali metal sites and Cu at transition metal sites. Due to its anti-site doping, Li acts as an interlayer stationary point that suppresses the relative slip of the TMO2 layer under high pressure and produces a solid solution reaction that is nearly zero phase transition. The assembled full-cell devices with Na0.67Li0.1Ni0.18Cu0.05Mn0.67O2 cathode and commercial hard carbon anode can deliver a high energy density of 379.3 Wh kg-1. In addition, due to the proposed unique dual-site doping, the full-cell also exhibits excellent cycling stability, which maintains a capacity retention rate of 84% and 71% over 200 and 1000 cycles at 1 C and 10 C, respectively. As a result, the proposed doping technique offers an effective approach to designing cathode materials with excellent cycling stability.
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