Issue 104, 2014

One-step solvothermal preparation of Fe3O4/graphene composites at elevated temperature and their application as anode materials for lithium-ion batteries

Abstract

A one-step high-temperature solvothermal process (can be used up to 400 °C) has been explored for the preparation of Fe3O4/graphene composites. The influence of high temperature (>230 °C) on the structure, morphology and electrochemical properties of the resulting Fe3O4/graphene composites was investigated by XRD, SEM, TEM and N2 adsorption–desorption measurements. Electrochemical performances of the as-prepared Fe3O4/graphene composites at different temperatures were evaluated in coin-type cells as anode materials for lithium-ion batteries. In comparison with the traditional solvothermal method (<240 °C), the high-temperature method does not require an additional calcination process yet it still could result in Fe3O4/graphene composites with pure phase and excellent electrochemical properties. A preferred solvothermal temperature of 280 °C has been deduced based on a series of control experiments. The Fe3O4/graphene composite derived at 280 °C exhibited a high reversible capacity of 907 mA h g−1 at 0.1 C (92.6 mA g−1) even after 65 cycles, showing outstanding cycle stability. It also exhibited a high rate capability of 410 mA h g−1 at 2 C (1852 mA g−1). The role of the graphene substrates in improving the electrochemical properties of the composite is discussed based on the morphology, structure, phase and electrochemical property studies.

Graphical abstract: One-step solvothermal preparation of Fe3O4/graphene composites at elevated temperature and their application as anode materials for lithium-ion batteries

Article information

Article type
Paper
Submitted
22 Aug 2014
Accepted
31 Oct 2014
First published
03 Nov 2014

RSC Adv., 2014,4, 59981-59989

Author version available

One-step solvothermal preparation of Fe3O4/graphene composites at elevated temperature and their application as anode materials for lithium-ion batteries

L. Jing, A. Fu, H. Li, J. Liu, P. Guo, Y. Wang and X. S. Zhao, RSC Adv., 2014, 4, 59981 DOI: 10.1039/C4RA09079A

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