Citation: CHENG Feng, HUANG Ke-Long, LIU Su-Qin, FANG Xue-Song, ZHANG Xin. Surfactant Carbonization to Synthesize a Fe3O4/C Composite and Its Electrochemical Performance[J]. Acta Physico-Chimica Sinica, ;2011, 27(06): 1439-1445. doi: 10.3866/PKU.WHXB20110607
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Oleic acid-capped α-Fe2O3 nanoparticles were initially prepared as precursors by a simple hydrothermal method. Fe3O4/C nanocomposites were synthesized by annealing the precursor at 500 °C for 1 h under an Ar atmosphere. The surface organic groups and core phase structure of the samples were characterized by Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD), respectively. Scanning electron microscopy (SEM) was used to observe their morphology. The existence of carbon was confirmed by elemental analysis, energy-dispersive X-ray (EDX) spectroscopy and high-resolution transmission electron microscopy (HRTEM). Cyclic voltammetry (CV) and galvanostatic discharge/charge measurements were used to evaluate the electrochemical performance of the as-prepared Fe3O4/C nanocomposites. The results showed that Fe3O4/C nanocomposites were spindles alike with a length of about 200 nm and a diameter of about 100 nm. A carbon layer of 1-2 nm in thickness was coated on the surface of the Fe3O4 nanocrystals and the carbon content was 1.956% (mass fraction). As anode materials for lithium-ion batteries, the composite exhibited excellent cycling performance (691.7 mAh·g-1 after 80 cycles at 0.2C (1C=928 mA·g-1)) and rate capability (520 mAh·g-1 after 20 cycles at 2C). Compared with commercial Fe3O4 particles, the remarkably improved electrochemical performance of the Fe3O4/C composites was attributed to in situ carbon coating, which prevented nanoparticle aggregation, increased electronic conductivity and stabilized the solid electrolyte interface (SEI) films.
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