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Ball mill assisted synthesis of cobalt–iron sulfide/N-doped carbon for high performance asymmetric supercapacitors
Cobalt–iron sulfides supported on N-doped carbon were synthesized as energy storage material using ball milling followed by carbonization. As-synthesized materials were structurally analyzed by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, scanning electron microscopy, and...
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Published in: | Journal of applied electrochemistry 2020-11, Vol.50 (11), p.1119-1128 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Cobalt–iron sulfides supported on N-doped carbon were synthesized as energy storage material using ball milling followed by carbonization. As-synthesized materials were structurally analyzed by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy. Furthermore, cobalt–iron sulfides supported on N-doped carbon were coated on Ni foam, and their electrochemical performance was tested in a 3-M KOH electrolyte. The as-fabricated Co–Fe–S-2 electrode registered a specific capacitance of 1252 F g
−1
at 1 A g
−1
and also showed capacitance retention of 66.4% at 20 A g
−1
. In addition, asymmetric supercapacitors (ASC) were fabricated using the as-synthesized electrode materials and it had a voltage window of 0
–
1.6 V. Among them, the activated carbon (AC)//Co–Fe–S-2 ASC device showed maximum specific capacitance of 169.3 F g
−1
at 1 A g
−1
, and it registered maximum energy density of 59.6 Wh kg
−1
at power density of 0.796 kW kg
−1
. The AC//Co–Fe–S-2 device delivered a rate capability of 55.6% at 30 A g
−1
, and it reveals a capacitance retention of 76.3% over 5000 cycles. Herein we also found that ball-milling-assisted synthesis of Co–Fe–S-2 electrode material is a promising candidate for high-performance ASCs.
Graphic abstract |
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ISSN: | 0021-891X 1572-8838 |
DOI: | 10.1007/s10800-020-01466-5 |