Rational Design of Yolk-Shell Zn-Co-Se@N-Doped Dual Carbon Architectures as Long-Life and High-Rate Anodes for Half/Full Na-Ion Batteries

被引:69
作者
Feng, Jian [1 ]
Luo, Shao-hua [1 ,2 ,3 ,4 ]
Yan, Sheng-xue [1 ]
Zhan, Yang [1 ,3 ,4 ]
Wang, Qing [1 ,3 ,4 ]
Zhang, Ya-hui [1 ,3 ,4 ]
Liu, Xin [1 ,3 ,4 ]
Chang, Long-jiao [5 ]
机构
[1] Northeastern Univ, Sch Mat Sci & Engn, Shenyang 110819, Peoples R China
[2] Northeastern Univ, State Key Lab Rolling & Automat, Shenyang 110819, Peoples R China
[3] Northeastern Univ Qinhuangdao, Sch Resources & Mat, Qinhuangdao 066004, Hebei, Peoples R China
[4] Key Lab Dielect & Electrolyte Funct Mat Hebei Pro, Qinhuangdao 066004, Hebei, Peoples R China
[5] Bohai Univ, Sch New Energy, Jinzhou 121013, Peoples R China
基金
中国国家自然科学基金;
关键词
binary metal selenide; long-term cycling; n-doped dual carbon; sodium ion batteries; yolk-shell architecture; SODIUM STORAGE; LITHIUM; DODECAHEDRON; PERFORMANCE; COBALT;
D O I
10.1002/smll.202101887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal selenides (TMSs) have emerged as prospective anode materials for sodium ion batteries (SIBs), owing to their considerable theoretical capacity and intrinsic high electronic conductivity. Whereas, TMSs still suffer from poor rate capability and inferior cycling stability induced by sluggish kinetics and severe volume changes during de/sodiation processes. Herein, a hierarchical composite consisting of a zinc-cobalt bimetallic selenide yolk and nitrogen-doped double carbon shell (denoted as Zn-Co-Se@NDC) is engineered and fabricated successfully. The architecture of the as-fabricated material improves the Na-ion storage performance via increasing the electron transfer kinetics, accommodating volume expansion, and mitigating the generation of by-products. As expected, the Zn-Co-Se@NDC electrode delivers superior sodium storage performance with long cycling stability (344.5 mAh g(-1) at 5.0 A g(-1) over 2000 long-term cycles) and high-rate performance (319.2 mAh g(-1) at 10.0 A g(-1)). Meanwhile, the NVP@C//Zn-Co-Se@NDC full SIB cells are constructed successfully, retaining 96.3% of its initial capacity at 0.5A g(-1) after 200 loops. The outstanding electrochemical performance and the construction of hybrid SIBs will have far-reaching influences on the development of the various rechargeable batteries.
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页数:12
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