Revisiting of Tetragonal NaVPO4F: A High Energy Density Cathode for Sodium-Ion Batteries

被引:26
|
作者
Ling, Moxiang [1 ,2 ]
Lv, Zhiqiang [1 ,2 ]
Li, Fan [2 ,3 ]
Zhao, Junmei [4 ]
Zhang, Huamin [1 ]
Hou, Guangjin [1 ]
Zheng, Qiong [1 ]
Li, Xianfeng [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Div Energy Storage, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, CAS Key Lab Green Proc & Engn, Beijing 100190, Peoples R China
关键词
tetragonal NaVPO4F; high energy density; sodium ion batteries; cathodes; crystal structure; ELECTROCHEMICAL PERFORMANCE; PRUSSIAN BLUE; PROMISING CATHODE; SUPERIOR CATHODE; ELECTRODE; LITHIUM; MECHANISM; INSIGHTS; CAPACITY; NANORODS;
D O I
10.1021/acsami.0c08846
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Tetragonal NaVPO4F has been regarded as an ideal cathode for sodium-ion batteries because of its high average plateau (3.8 V) and theoretical specific capacity (143 mA h g(-1)). However, the Na-storage performance is still hindered by unsatisfying thermal stability and poor conductivity. Herein, a stable tetragonal NaVPO4F has been synthesized by a novel solvent thermal method using a carbon coating precursor. The as-prepared NaVPO4F@C nanocomposite delivers a capacity of 133 mA h g(-1) at 0.2 C, corresponding to an excellent energy density of 509 W h kg(-1) ; when coupled with an HC anode, the full cell still displays an outstanding performance of 124 mA h g(-1) at 0.05 C. Fast Na+ diffusion kinetics (DNa+ = 10(-12) to 10(-10) cm(2) s(-1)) and small volume change (4.4%) are exploited, which ensures good rate trait and cycling stability of tetragonal NaVPO4F. Further, the Na+ extraction-insertion mechanism has been explored by analyzing the crystal structure change during in situ X-ray powder diffraction cycles.
引用
收藏
页码:30510 / 30519
页数:10
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