材料科学
兴奋剂
阴极
氧化物
离子
钠
无机化学
氧化钠
化学工程
光电子学
冶金
物理化学
有机化学
化学
工程类
作者
Sidra Jamil,Farhan Mudasar,Tiange Yuan,Muhammad Fasehullah,Ghulam Ali,Keun Hwa Chae,Oleksandr Voznyy,Yiqiang Zhan,Maowen Xu
标识
DOI:10.1021/acsami.3c15667
摘要
Mn-rich P2-type layered oxide cathode materials suffer from severe capacity loss caused by detrimental phase transition and transition metal dissolution, making their implementation difficult in large-scale sodium-ion battery applications. Herein, we introduced a high-valent Sb5+ substitution, leading to a biphasic P2/O3 cathode that suppresses the P2–O2 phase transformation in the high-voltage condition attributed to the stronger Sb–O covalency that introduces extra electrons to the O atom, reducing oxygen loss from the lattices and improving structural stability, as confirmed by first-principle calculations. Besides, the enhanced Na+ diffusion kinetics and thermodynamics in the modified sample are associated with the enlarged lattice parameters. As a result, the proposed cathode delivers a discharge capacity of 142.6 mAh g–1 at 0.1C between 1.5 and 4.3 V and excellent performance at a high mass loading of 8 mg cm3 with a specific capacity of 131 mAh g–1 at 0.2C. Furthermore, it also possesses remarkable rate capability (90.3 mAh g–1 at 5C), specifying its practicality in high-energy-density sodium-ion batteries. Hence, this work provides insights into incorporating high-valent dopants for high-performance Mn-rich cathodes.
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