假电容
阳极
钠
兴奋剂
纳米颗粒
材料科学
化学工程
阴极
电化学
碳纤维
纳米技术
电极
化学
复合材料
冶金
超级电容器
光电子学
复合数
物理化学
工程类
作者
Zhenxiao Lu,Yanjun Zhai,Nana Wang,Yaohui Zhang,Pan Xue,Meiqing Guo,Bin Tang,Di Huang,Wenxian Wang,Zhongchao Bai,Shi Xue Dou
标识
DOI:10.1016/j.cej.2019.122455
摘要
FeS2 is a promising electrode material for sodium ion batteries (SIBs) because of its high theoretical capacity, rich reserves, and eco-friendly nature. In this study, N and S doped (N, S-co-doped) carbon fibers (CFs) encapsulated FeS2 nanoparticles (5–12 nm) and adherent FeS2 nanoflakes (denoted as FeS2@CF-NS), were synthesized by electrostatic spinning and subsequent thermal treatment. In this structure, the FeS2 nanoparticles and the FeS2 nanoflakes shorten the Na+ diffusion distance; the N, S co-doping and defect-rich sites in the carbon fibers accelerate the Na+/e− transmission and buffer the volume expansion during the Na-FeS2 conversion reaction. These merits synergistically contribute to the notable sodium storage performance of FeS2@CF-NS. As anode for Na-ion half batteries, the FeS2@CF-NS exhibits high capacity (637.1 mAh/g at 1 A/g after 400 cycles) and excellent rate capacity (431.1 mAh/g at 5 A/g). Kinetic analysis confirms that this composite structure stimulates the pseudocapacitance Na+ storage mechanism and enables a capacitive contribution ratio as high as 92.7% with respect to the total capacity. In combination with Na3V2(PO4)3-C cathode, the FeS2@CF-NS also achieves remarkably high specific capacity (561.1 mAh/g at 1 A/g after 500 cycles) and stable cyclability (338.6 mAh/g at 5 A/g after 5000 cycles) in full cells.
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