363570 Solvothermal Route Based in Situ Carbonization to Fe3O4@C As Anode Material for Lithium Ion Battery

Thursday, November 20, 2014: 2:22 PM
International 8 (Marriott Marquis Atlanta)
Gen Chen, Litao Yan, Meng Zhou and Hongmei Luo, Chemical Engineering Department, New Mexico State University, Las Cruces, NM

Magnetite (Fe3O4) is a very promising candidate as an anode material in rechargeable lithium ion battery (LIBs) because of its ability to store up to eight Li per formula unit via reversible reactions, resulting in a high theoretical capacity of 924 mAh g-1. Moreover, advantages such as low cost, ease of synthesis and environmental friendliness make it a promising candidate for large scale commercial applications for LIBs. However, Fe3O4 suffers from poor conductivity, large volume change and voltage hysteresis during the electrochemical reaction, which strongly limits its practical application. For the fact that carbon in its own feature exhibits several interesting properties, including electronic conductivity, high surface area, tunable porous structure, etc., the combination of Fe3O4nanostructures and different forms of carbon materials show promising potential in the preparation of composite anode materials.

In this work, a high pressure and temperature based solvothermal route was developed for the synthesis of Fe3O4 with carbon as a composite anode for LIBs. The carbon in products was a result of the in situ carbonization of organic components under high pressure (24.0 MPa) and temperature (350 °C). Composites with different amounts of carbon were prepared by annealing the solvothermal products at different temperature. Taking advantage of the high theoretical capacity of Fe3O4 and favorable characteristics of carbon, a capacity of about 610 mAh g-1 after 100 cycles was achieved for the composite with 54.6% carbon. The carbon amount depended electrochemical performance was also investigated. The Fe3O4@C composite can be used as an alternative anode material and the introduced synthetic strategy may provide further insights into the preparation of inorganic oxides coupled with carbon via in situ carbonization of organic components.


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