Isostructural and Multivalent Anion Substitution toward Improved Phosphate Cathode Materials for Sodium-Ion Batteries

被引:119
作者
Wang, Mei-Yi [1 ]
Guo, Jin-Zhi [2 ]
Wang, Zhi-Wei [1 ]
Gu, Zhen-Yi [2 ]
Nie, Xue-Jiao [1 ]
Yang, Xu [1 ]
Wu, Xing-Long [1 ,2 ]
机构
[1] Northeast Normal Univ, Natl & Local United Engn Lab Power Batteries, Fac Chem, Changchun 130024, Jilin, Peoples R China
[2] Northeast Normal Univ, Minist Educ, Key Lab UV Light Emitting Mat & Technol, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
anionic substitution; cathode materials; Na-super-ionic conductors; phosphate materials; sodium-ion batteries; NA3V2(PO4)(3); CARBON; PERFORMANCE; GRAPHENE;
D O I
10.1002/smll.201907645
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyanion-type phosphate materials are highly promising cathode candidates for next-generation batteries due to their excellent structural stability during cycling; however, their poor conductivity has impeded their development. Isostructural and multivalent anion substitution combined with carbon coating is proposed to greatly improve the electrochemical properties of phosphate cathode in sodium-ion batteries (SIBs). Specifically, multivalent tetrahedral SiO44- substitute for PO43- in Na3V2(PO4)(3) (NVP) lattice, preparing the optimal Na3.1V2(PO4)(2.9)(SiO4)(0.1) with high-rate capability (delivering a high capacity of 82.5 mAh g(-1) even at 20 C) and outstanding cyclic stability (approximate to 98% capacity retention after 500 cycles at 1 C). Theoretical calculation and experimental analyses reveal that the anion-substituted Na3.1V2(PO4)(2.9)(SiO4)(0.1) reduces the bandgap of NVP lattice and enhanced its structural stability, Na+-diffusion kinetics and electronic conductivity. This strategy of multivalent and isostructural anion substitution chemistry provides a new insight to develop advanced phosphate cathodes.
引用
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页数:10
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