High-entropy engineering enables O3-type layered oxide with high structural stability and reaction kinetic for sodium storage

被引:0
|
作者
Wang, Xiong [1 ]
Kang, Qiaoling [2 ]
Sun, Jiaze [1 ]
Yang, Zheng [2 ]
Bai, Zhenchao [2 ]
Yan, Lijing [2 ]
Meng, Xianhe [2 ]
Wan, Chubin [3 ]
Ma, Tingli [1 ]
机构
[1] Kyushu Inst Technol, Grad Sch Life Sci & Syst Engn, 2-4 Hibikino, Aizu Wakamatsu, Kitakyushu 8080196, Japan
[2] China Jiliang Univ, Coll Mat & Chem, Hangzhou 310018, Peoples R China
[3] Univ Sci & Technol Beijing, Phys Dept, Beijing 100083, Peoples R China
关键词
ION; SUBSTITUTION; CATHODE;
D O I
10.1016/j.jcis.2025.137438
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
O3-type layered oxides are considered promising cathode materials for sodium-ion batteries (SIBs) due to their high theoretical capacity, but they often face issues with structural instability and poor sodium-ion diffusion, leading to rapid capacity fading. In this work, we introduce a high-entropy approach combined with synergistic multi-metal effects to address these limitations by enhancing both the structural stability and reaction kinetics. A novel O3-type layered high-entropy cathode material, Na0.9Fe0.258Co0.129Ni0.258Mn0.258Ti0.097O2 (TMO5), which was synthesized via a straightforward solid-phase method for easy mass production. Experimental analysis combined with in/ex-situ characterization verifies that high-entropy metal ion mixing contributes to the improved reversibility of the redox reaction and O3-P3-O3 phase transition behaviors, as well as the enhanced Na+ diffusivity. Benefit from the advantage of structure and composition, the TMO5 exhibits a higher initial specific capacity of 159.6 mAh g-1 and an impressive capacity retention of 85.6 % after 100 cycles at 2 C with the specific capacity of 110.1 mAh g-1. This work showcases high-entropy O3-type layered oxides as a promising pathway for achieving robust, high-performance SIB cathodes.
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页数:11
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