Boosting Fast Sodium Ion Storage by Synergistic Effect of Heterointerface Engineering and Nitrogen Doping Porous Carbon Nanofibers

阳极 材料科学 电化学 碳纳米纤维 静电纺丝 多孔性 纳米纤维 纳米技术 化学工程 储能 锂(药物) 兴奋剂 碳纤维 离子 电极 复合材料 化学 光电子学 碳纳米管 物理化学 有机化学 内分泌学 工程类 物理 功率(物理) 复合数 医学 量子力学 聚合物
作者
Qi Zhang,Yaping Zeng,Changsheng Ling,Liu Wang,Zhiyong Wang,Tian‐E Fan,Heng Wang,Jianrong Xiao,Xinyu Li,Baihua Qu
出处
期刊:Small [Wiley]
卷期号:18 (13) 被引量:52
标识
DOI:10.1002/smll.202107514
摘要

Heterointerface engineering with multiple electroactive and inactive supporting components is considered an efficient approach to enhance electrochemical performance for sodium-ion batteries (SIBs). Nevertheless, it is still a challenge to rationally design heterointerface engineering and understand the synergistic effect reaction mechanisms. In this paper, the two-phase heterointerface engineering (Sb2 S3 and FeS2 ) is well designed to incorporate into N-doped porous hollow carbon nanofibers (Sb-Fe-S@CNFs) by proper electrospinning design. The obtained Sb-Fe-S@CNFs are used as anode in SIBs to evaluate the electrochemical performance. It delivers a reversible capacity of 396 mA h g-1 after 2000 cycles at 1 A g-1 and exhibits an ultra-long high rate cycle life for 16 000 cycles at 10 A g-1 . The admirable electrochemical performance is mainly attributed to the following reasons: The porous carbon nanofibers serve as an accelerator of the electrons/ions and a buffer to alleviate volume expansion upon long cyclic performance. The abundant phase boundaries of Sb2 S3 /FeS2 exert low Na+ adsorption energy and greatly promote the charge transfer in the internal electric field calculated by first-principle density functional theory. Therefore, the as-prepared Sb-Fe-S@CNFs represents a promising candidate for an efficient anode electrode material in SIBs.
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