General synthesis of yolk-shelled Fe Q @Carbon (Q = S, Se, P) film for high performance anode of sodium-ion batteries

阳极 材料科学 电极 化学工程 硒化物 纳米技术 储能 离子 化学 冶金 有机化学 工程类 物理化学 功率(物理) 物理 量子力学
作者
Xiaojun Wang,Haichang Li,Changmeng Xu,Hongran Sun,Fan Cheng,Wenming Song,Huifang Li,Jiangshan Gao,Zhiming Liu,Yan He
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:901: 163577-163577 被引量:12
标识
DOI:10.1016/j.jallcom.2021.163577
摘要

Sodium-ion batteries (SIBs) have attracted widespread attention because of the economic benefit of low-cost and abundance of sodium resources. Iron-based electrodes (sulfide, selenide and phosphide) that operate through conversion mechanism have shown huge potential for excellent sodium-ion storage. However, the problems related with serious volume expansion and lack of general synthesis methods of iron-based materials shorten the cycle life and hindered their application in SIBs. Herein, a general synthetic strategy of electrospinning process was developed to achieve the yolk-shelled FexQy@C (Q = S, Se and P) film for binder-free anode of high-performance SIBs. Such method has more precursor materials to choose from and is highly scalable. More importantly, the designed electrodes have a unique yolk-shell structure and a three-dimensional conductive network. When applied as a binder-free anode of SIBs, all three samples exhibit outstanding sodium storage performance (FeS2@C-40: remaining 280 mAh g−1 after 400 cycles at 1 A g−1, Fe7Se8@C-40: remaining 186.5 mAh g−1 after 200 cycles at 0.1 A g−1 and FeP4@C-40: remaining 205 mAh g−1 after 1000 cycles at 0.5 A g−1). Therefore, the scalability and universality of this general synthetic strategy can open up a new direction for the exploration of high-energy density and flexible electrode materials.
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