Sb-Doped Biphasic P2/O3-Type Mn-Rich Layered Oxide Cathode Material for High-Performance Sodium-Ion Batteries
- Authors
- Jamil, Sidra; Mudasar, Farhan; Yuan, Tiange; Fasehullah, Muhammad; Ali, Ghulam; Chae, Keun Hwa; Voznyy, Oleksandr; Zhan, Yiqiang; Xu, Maowen
- Issue Date
- 2024-03
- Publisher
- American Chemical Society
- Citation
- ACS Applied Materials & Interfaces, v.16, no.12, pp.14669 - 14679
- Abstract
- 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 cm(3 )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.
- Keywords
- OXYGEN REDOX CHEMISTRY; HIGH-ENERGY; PHASE-TRANSITION; HIGH-CAPACITY; LONG-LIFE; NI; CO; NA2/3NI1/3MN2/3O2; SUBSTITUTION; STABILITY; high-valent dopants; Mn-rich layered oxides; P2/O3 biphasic structure; robust oxygen framework; sodium-ion batteries
- ISSN
- 1944-8244
- URI
- https://pubs.kist.re.kr/handle/201004/149539
- DOI
- 10.1021/acsami.3c15667
- Appears in Collections:
- KIST Article > 2024
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