High-Entropy Doping Boosts Ion/Electronic Transport of Na4Fe3(PO4)2(P2O7)/C Cathode for Superior Performance Sodium-Ion Batteries

被引:87
作者
Ge, Xiaochen [1 ]
Li, Huangxu [2 ]
Li, Jie [1 ]
Guan, Chaohong [3 ]
Wang, Xu [1 ]
He, Liang [1 ]
Li, Simin [1 ]
Lai, Yanqing [1 ]
Zhang, Zhian [1 ]
机构
[1] Cent South Univ, Engn Res Ctr, Hunan Prov Key Lab Nonferrous Value Added Met, Sch Met & Environm,Minist Educ Adv Battery Mat, Changsha 410083, Peoples R China
[2] City Univ Hong Kong, Dept Chem, Kowloon, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[3] Shanghai Jiao Tong Univ Shanghai, Univ Michigan Shanghai Jiao Tong Univ Joint Inst, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
fast-charging capacity; high-entropy doping; mixed phosphate cathode materials; sodium-ion batteries; IRON; MN;
D O I
10.1002/smll.202302609
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fe-based mixed phosphate cathodes for Na-ion batteries usually possess weak rate capacity and cycle stability challenges resulting from sluggish diffusion kinetics and poor conductivity under the relatively low preparation temperature. Here, the excellent sodium storage capability of this system is obtained by introducing the high-entropy doping to enhance the electronic and ionic conductivity. As designed high-entropy doping Na4Fe2.85(Ni,Co,Mn,Cu,Mg)(0.03)(PO4)(2)P2O7 (NFPP-HE) cathode can release 122 mAh g(-1) at 0.1 C, even 85 mAh g(-1) at ultrahigh rate of 50 C, and keep a high retention of 82.3% after 1500 cycles at 10 C. Besides, the cathode also exhibits outstanding fast charge capacity in terms of the cyclability and capacity with 105 mAh g(-1) at 5 C/1 C, corresponding 94.3% retention after 500 cycles. The combination of in situ X-ray diffraction, density functional theory, conductive-atomic force microscopy, and galvanostatic intermittent titration technique tests reveal that the reversible structure evolution with optimized Na+ migration path and energy barrier boost the Na+ kinetics and improve the interfacial electronic transfer, thus improving performance.
引用
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页数:10
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