Ternary NASICON-typed Na3.8MnV0.8Zr0.2(PO4)3 cathode with stable Mn2+/Mn3+ redox and fast sodiation/desodiation kinetics for Na-ion batteries

被引:45
作者
Tang, Ao [1 ]
Zhang, Shu [2 ]
Lin, Weiguang [3 ]
Xiao, Dongdong [3 ]
Ma, Jun [2 ]
Shang, Chaoqun [1 ]
Yan, Min [1 ]
Zhang, Zhanhui [1 ]
Chen, Changlian [1 ]
Huang, Zhiliang [1 ]
Aifantis, Katerina E. [4 ]
Hu, Pu [1 ]
Cui, Guanglei [2 ]
机构
[1] Wuhan Inst Technol, Sch Mat Sci & Engn, Hubei Key Lab Plasma Chem & Adv Mat, Wuhan 430205, Peoples R China
[2] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao Ind Energy Storage Res Inst, Qingdao 266101, Peoples R China
[3] Chinese Acad Sci, Inst Phys, Huairou Div, Beijing 101400, Peoples R China
[4] Univ Florida, Dept Mech & Aerosp Engn, Gainesville, FL 32603 USA
基金
中国国家自然科学基金;
关键词
Sodium-ion batteries; NASICON; Mn-based cathode; Substitution; Na4MnV(PO4)(3); DIFFUSION;
D O I
10.1016/j.ensm.2023.03.024
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
Rechargeable sodium-ion batteries (SIBs) have attracted great attention as potential application in grid energy storage but are plagued by lacks of promising cathode materials with both excellent cycling stability and rate capability. Herein A novel ternary NASICON Na3.8MnV0.8Zr0.2(PO4)(3) is fabricated and tested as a cathode material. By Partial substitution with Zr4+, the obtained Na3.8MnV0.8Zr0.2(PO4)(3), delivering a capacity retention of 83.5% after 1000 cycles at 2 C, and an impressive rate capacity of 73.1 mAh g(-1) at 20 C and 66.8 mAh g(-1) at 60 C. Electron microscopy, x-ray diffraction, cyclic voltammetry, and first principle calculations show that this superior rate capability can be attributed to the broadened Na-ion channels and high Na-ion diffusivity. Furthermore, the volume expansion upon Na-ion de-insertion is lower than other NASICON materials (only 4.9%), which facilitates the structural integrity over cycling. This work paves the way in producing greener, high-power and long-life Na-ion batteries.
引用
收藏
页码:271 / 278
页数:8
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