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The effects of dual modification on structure and performance of P2-type layered oxide cathode for sodium-ion batteries

机译:双重改性对钠离子电池P2型分层氧化物阴极结构和性能的影响

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摘要

As the competitive cathode material of sodium-ion batteries (SIBS), P2-type Na0.67Ni0.33Mn0.67O2 (NMO) possesses high theoretical specific capacity and high operating voltage. However, it suffers from severe capacity fading caused by the unfavorable P2-O2 phase transition during charge/discharge cycling process. Moreover, the HF formed by the reaction of electrolyte salts with trace water molecules causes the voltage decay of NMO. Herein, the dual-modification strategy of Mg substitution for transition metal in bulk structure and NaTi2 (PO4)(3) surface coating layer is designed to solve above defects. It has been found that Mg substitution can stabilize the bulk structure and enlarge the slab-spacing, while the NASICON-type NaTi2(PO4)(3) coating layer can stabilize the interface, prevent the HF impact and facilitate the Na+ migration at the cathode-electrolyte interface. Additionally, the combination of Mg substitution and NaTi2(PO4)(3) coating can restrain particle crack and exfoliation. The results show that the as-prepared material by dual-modification technology exhibits excellent cycling stability (77.4% capacity retention after 200 cycles at a rate of 1 C) and good rate performance (106.8 mAh g(-1) at a rate of 5 C). Accordingly, the dual-modification strategy provides a new horizon for design and development of the high-performance layered oxide cathode materials of SIBS.
机译:作为钠离子电池(SIBS)的竞争阴极材料,P2型NA0.67NI0.33MN0.67O2(NMO)具有高理论特异性容量和高工作电压。然而,它受到充电/放电循环过程中不利的P2-O2相转变引起的严重容量衰落。此外,通过电解质盐与痕量水分子反应形成的HF导致NMO的电压衰减。这里,散装结构中的过渡金属的Mg替换的双重修饰策略和Nati2(PO4)表面涂层设计用于解决上述缺陷。已经发现Mg取代可以稳定散装结构并扩大平板间距,而Nasicon型Nati2(PO4)(3)涂层可以稳定界面,防止HF撞击并促进阴极的Na +迁移 - 电解液界面。另外,Mg替代和Nati2(PO4)(3)涂层的组合可以抑制颗粒裂纹和剥离。结果表明,双重改性技术的原制材料表现出优异的循环稳定性(以1℃的速度为200次循环后77.4%的容量保留)和良好的速率性能(106.8mAhg(-1),速率为5 C)。因此,双重修改策略提供了用于设计和开发SIBs的高性能层状氧化物阴极材料的新地平线。

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