材料科学
兴奋剂
阴极
氧化物
离子
掺杂剂
溶解
容量损失
过渡金属
相变
化学工程
电极
光电子学
冶金
热力学
阳极
物理化学
催化作用
有机化学
化学
工程类
生物化学
物理
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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