用精细的多组分调制策略抑制Na0.67Ni0.33Mn0.67O2中的P2-O2相变和Na+/空位有序化

Guanglin Wan, Yanxu Chen, Bo Peng, Lai Yu, Xinyi Ma, Nazir Ahmad, Genqiang Zhang
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引用次数: 0

摘要

P2型Na0.67Ni0.33Mn0.67O2是一种很有前途的钠离子电池正极,具有高比容量和高空气电阻的特点,但由于钠离子脱嵌过程中P2-O2发生了灾难性的相变和Na+/空位有序化,其循环稳定性和倍率性能不理想,阻碍了其未来的实际应用。本文提出了一种精细的多组分调制策略来同时解决这两个问题,其中引入Li+和Ti4+分别取代Ni2+和Mn4+,而Na+含量也根据电荷平衡原理设计。因此,设计的阴极(Na0.72Ni0.28Li0.05Mn0.57Ti0.10O2)在1 200次循环后的C以及82.7的可观的速率性能 毫安时 g−1在5 C.原位X射线衍射测量表明,破坏性的P2-O2相变被抑制并转化为具有优异可逆性的P2-Z相变,以及具有更好Na+/空位无序的平滑充电/放电曲线。此外,与硬碳阳极匹配的全电池提供了263.4的优异能量密度 Wh 37.3时为kg−1 W kg−1,具有很强的实用性。我们的工作提出了一种合理设计层状氧化物阴极组件并实现钠离子电池优异性能的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Suppressing the P2-O2 phase transition and Na+/vacancy ordering in Na0.67Ni0.33Mn0.67O2 by a delicate multicomponent modulation strategy

Suppressing the P2-O2 phase transition and Na+/vacancy ordering in Na0.67Ni0.33Mn0.67O2 by a delicate multicomponent modulation strategy

P2-type Na0.67Ni0.33Mn0.67O2 is a promising cathode for sodium-ion batteries with features of high specific capacity and air resistance, whereas its cycling stability and rate performance are dissatisfactory suffering from the disastrous P2-O2 phase transition and Na+/vacancy ordering during sodium-ion de/intercalation, which makes it an obstruction for future practical applications. Herein, a delicate multicomponent modulation strategy is proposed to tackle these two issues simultaneously, in which Li+ and Ti4+ are introduced to replace the Ni2+ and Mn4+, respectively, whereas the Na+ content is also designed according to the principle of charge balance. Consequently, the designed cathode (Na0.72Ni0.28Li0.05Mn0.57Ti0.10O2) can deliver an enchanting cycling stability of 80% at 1 C after 200 cycles along with a considerable rate performance of 82.7 mAh g−1 at 5 C. In situ X-ray diffraction measurement demonstrates the destructive P2-O2 phase transition is suppressed and converted into a P2-Z phase transition with superior reversibility as well as smooth charge/discharge curves with better Na+/vacancy disordering. In addition, the full cell matched with hard carbon anode delivers an excellent energy density of 263.4 Wh kg−1 at 37.3 W kg−1, exhibiting great practicality. Our work presents a mean to rationally design the component of layered oxide cathode and achieve fabulous performance for sodium ion batteries.

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