High capacity electrospun MgFe2O4–C composite nanofibers as an anode material for lithium ion batteries

D., Narsimulu and B. Nageswara, Rao and E. S., Srinadhu and N., Satyanarayana (2018) High capacity electrospun MgFe2O4–C composite nanofibers as an anode material for lithium ion batteries. Chemistry Select, 3 (27). ISSN 2365-6549

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Abstract

MgFe2O4 -C composite nanofibers were prepared via electrospinning technique followed by carbonization at 600 8C.
Thermogravimetric-differential thermal analysis (TG-DTA) results showed ignition, decomposition and carbonization temperatures of the as-grown fibers. Formation of the nanocrystalline phase of the MgFe2O4 over the amorphous phase of the carbon fibers sample was confirmed from the analysis of the measured XRD results. FE-SEM images of the as-spun and calcined fibers sample showed that the formation of one dimensional (1-D) MgFe2O4 -C composite nanofibers and the formed 1-D nanofibers were well interconnected with high porous structured morphology. The electrochemical properties of the MgFe2O4 -C composite nanofibers sample were tested as an anode material for lithium-ion battery. Lithium-ion battery made up of the newly developed MgFe2O4 -C composite nanofibers sample, used as an anode material, showed discharge capacity of 575 mAh g @1 at a current density of 100 mA g @1 after 20th cycles. Further, the discharge capacity of the lithium-ion battery also measured at a high current density of 1 A g @1 and it was found to be 433 mAh g @1 even after 85 cycles. Also, the lithium-ion battery showed exceptional reversible capacity with the coulombic efficiency of 99.6% even after 85 cycles at a high current density of 1 A g @1 . Hence the electrochemical properties suggest that the newly developed MgFe2O4 -C composite nanofibers can be used as high capacity anode materials for lithiumion batteries

Item Type: Article
Subjects: AC Rearch Cluster
Depositing User: Unnamed user with email techsupport@mosys.org
Date Deposited: 14 Dec 2023 05:07
Last Modified: 14 Dec 2023 12:02
URI: https://ir.vignan.ac.in/id/eprint/537

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