Synthesis of FeS-impregnated heteroatom-doped carbon nanofibers assisted by one-step vulcanization for superior sodium storage

材料科学 静电纺丝 法拉第效率 化学工程 杂原子 碳纳米纤维 硫化 电化学 纳米纤维 碳化 阳极 氧化还原 碳纤维 纳米技术 复合材料 电极 化学 碳纳米管 有机化学 天然橡胶 冶金 扫描电子显微镜 聚合物 戒指(化学) 物理化学 工程类
作者
Yifu Chen,Yue Bao,Haihui Wang,Xiang Yao,Haihui Wang
出处
期刊:Journal of Alloys and Compounds [Elsevier]
卷期号:888: 161513-161513 被引量:1
标识
DOI:10.1016/j.jallcom.2021.161513
摘要

Severe volume changes during sodiation/desodiation and the sluggish sodium reaction kinetics of FeS limit its applications in high-performance sodium-ion batteries (SIBs). To solve these problems, free-standing FeS nanocrystallites-impregnated porous N, S-doped carbon nanofibers ([email protected]) is fabricated through an electrospinning technique combined with one-step vulcanization. During the vulcanization, the Fe precursor containing as-spun film is carbonized and sulfurated, and the carbon matrix is functionalized by S-containing oxygen groups meanwhile. The obtained free-standing and flexible [email protected] film can be directly used as anode for SIBs without slurry-casting. The film exhibits prominent electrochemical property because low electronic conductivity and aggregation of FeS particles are resolved by introducing well-distributed FeS nanocrystallites into the conductive carbon nanofibers network. In addition, the film exhibits good structural stability with limited volume changes during cycling due to the buffer effects of CNFs. The film shows a high specific capacity of 530 mA h g−1 at 0.2 A g−1 with a high initial Coulombic efficiency of 86.2%. Additionally, with enhanced surface-dominant pseudocapacitive redox reactions, which facilitate charge transfer and ion diffusion, the [email protected] delivers capacities of 367 and 278 mA h g−1 at 10 and 30 A g−1, respectively, maintaining long cycling stability with a high capacity retention rate of 87.6% after 700 cycles at 10 A g−1.

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