New insights on the reaction mechanism and charge contribution of NaNiF3 perovskite as an anode for sodium-ion batteries

被引:6
作者
Ch, Liliana T. Lopez [1 ]
Medina, Alejandro [2 ]
Jaramillo, Franklin [1 ]
Calderon, Jorge A. [1 ]
Lavela, Pedro [2 ]
Tirado, Jose L. [2 ]
机构
[1] Univ Antioquia, Fac Ingn, Ctr Invest Innovac & Desarrollo Mat CIDEMAT, Calle 70 52-21, Medellin, Colombia
[2] Univ Cordoba, Inst Univ Invest Quim Fina & Nanoquim IUNAN, Grp PAIDI FQM288 Quim & Electroquim Mat Inorgan QU, Dept Quim Inorgan Ingn Quim, Campus Rabanales,Edificio Marie Curie, Cordoba, Cordoba, Argentina
关键词
NaNiF3; Perovskite; Anode; Conversion mechanism; Sodium-ion batteries; Capacitive behavior; ELECTRODE MATERIALS; ELECTROCHEMICAL PERFORMANCE; ENERGY-STORAGE; LOW-COST; LITHIUM; FLUORIDE; INTERCALATION; NANOCOMPOSITE; CATHODE;
D O I
10.1016/j.electacta.2023.142341
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Sodium-ion battery is a growing technology that has become a major focus of attention for energy storage of smart electric grids and renewable energy because of the enormous availability of sodium and its low cost of production. Particularly, the perovskite structure is an attractive material due to its novel properties in energy applications, such as good ionic mobility, low cost, facile route of synthesis, and fabrication. In the present work, an electrode based on NaNiF3 nanostructured perovskite active materials was explored as an anode for sodium-ion battery application. The morphology and microstructure of NaNiF3 perovskite were optimized using trisodium citrate dehydrated and microwave heating. Here a remarkable first capacity of c.a. 376 mA h g(-1) of the optimized electrode was obtained in the first discharge. The ex-situ XRD and electrochemical characterization of the active material allow proposing a reaction mechanism by conversion processes during the discharge and identifying a capacitive contribution of around 25% to the total current at 20 mV s(-1).
引用
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页数:11
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