Article ID Journal Published Year Pages File Type
6470259 Electrochimica Acta 2017 11 Pages PDF
Abstract

•3D in-situ h-CNF/CNS/Fe3C@Fe3O4 was constructed using ferrocene and oleic acid by a solventless one-step process.•h-CNF/CNS/Fe3C@Fe3O4 exhibited higher specific capacitance of 327 F g−1 at 5 mV s−1 and 210 F g−1 at 10 mV s−1, and superior retention of 108% after 6000 cycles at 100 mV s−1.•Carbon nanoshell comprising h-CNF and CNS well encapsulates Fe3C@Fe3O4 core materials and this sturdy structure endows high cycle stability up to 6000 cycles.

Herein, 3D in-situ hollow carbon fiber/carbon nanosheet/Fe3C@Fe3O4 (h-CNF/CNS/Fe3C@Fe3O4) was constructed using ferrocene and oleic acid by a solventless one-step process that did not require additional filtering, neutralization, drying, or calcination steps. The iron-oleate chelating structure that self-assembled during annealing facilitated the fabrication of 3D in-situ h-CNF/CNS/Fe3C@Fe3O4 by undergoing graphitization at 600 °C. This carbon shell of the 3D in-situ h-CNF/CNS/Fe3C@Fe3O4 was derived from the two cyclopentadienyl rings in ferrocene. This hybrid material made from economically cheap oleic acid exhibited superior supercapacitive behavior: high specific capacitance of 327 F g−1 at 5 mV s−1 and 210 F g−1 at 10 mV s−1, good rate capability of 60 F g−1 at 10 A g−1 (compared to 70 F g−1 at 1 A g−1 for pure Fe3O4), and superior retention of 108% after 6000 cycles at 100 mV s−1. These superior supercapacitive properties were ascribed to the 3D graphitic h-CNF/CNS for enhancing electrical conductivity and the carbonaceous shell over Fe3C@Fe3O4 core for buffering the bulk expansion of iron-related particles.

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