Low-Cost Zinc Substitution of Iron-Based Prussian Blue Analogs as Long Lifespan Cathode Materials for Fast Charging Sodium-Ion Batteries

被引:79
|
作者
Zhang, Hang [1 ]
Peng, Jian [1 ]
Li, Lin [2 ]
Zhao, Yanan [3 ]
Gao, Yun [4 ]
Wang, Jiazhao [1 ]
Cao, Yuliang [3 ]
Dou, Shixue [1 ]
Chou, Shulei [2 ]
机构
[1] Univ Wollongong, Inst Superconducting & Elect Mat, Australian Inst Innovat Mat, Innovat Campus,Squires Way, North Wollongong, NSW 2522, Australia
[2] Wenzhou Univ, Inst Carbon Neutralizat, Coll Chem & Mat Engn, Wenzhou 325035, Zhejiang, Peoples R China
[3] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan, Peoples R China
[4] Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
element optimization; long lifespans; phase transitions; Prussian blue analogs; sodium-ion batteries; SUPERIOR CATHODE; HEXACYANOFERRATE;
D O I
10.1002/adfm.202210725
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Iron-based Prussian blue analogs (Fe-PBAs) are extensively studied as promising cathode materials for rechargeable sodium-ion batteries owing to their high theoretical capacity, low-cost and facile synthesis method. However, Fe-PBAs suffer poor cycle stability and low specific capacity due to the low crystallinity and irreversible phase transition during excess sodium-ion storage. Herein, a modified co-precipitation method to prepare highly crystallized PBAs is reported. By introducing an electrochemical inert element (Zn) to substitute the high-spin Fe in the Fe-PBAs (ZnFeHCF-2), the depth of charge/discharge is rationally controlled to form a highly reversible phase transition process for sustainable sodium-ion storage. Minor lattice distortion and highly reversible phase transition process of ZnFeHCF-2 during the sodium-ions insertion and extraction are proved by in-situ tests, which have significantly impacted the cycling stability. The ZnFeHCF-2 shows a remarkably enhanced cycling performance with capacity retention of 58.5% over 2000 cycles at 150 mA g(-1) as well as superior rate performance up to 6000 mA g(-1) (fast kinetics). Furthermore, the successful fabrication of the full cell on the as-prepared cathode and commercial hard carbon anode demonstrates their potential as high-performance electrode materials for large-scale energy storage systems.
引用
收藏
页数:8
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