Abstract
The artificial graphite materials were prepared by carbonizing coal tar pitch using two methods, namely, one- and two-step processes, and all sintered samples were graphitized at 2800 °C. Effects of different heat treatments on the performance of the samples were characterized by scanning electron microscopy, transmission electron microscopy (TEM), X-ray diffraction, Brunauer–Emmett–Teller, electrochemical impedance spectroscopy (EIS), particle size analysis, polarized light microscopy, and charge–discharge measurements. All samples show a typical graphite crystalline structure; moreover, the degree of graphitization (g factor) and crystallite size along the c-axis (L c ) were calculated from (002) peak. The polarized light microscopy indicates that the coke with carbonization at 700 °C has an obvious wide domain (D) optical structure, while that with two-step sintering at 400 and 700 °C has a mixed optical structures of wide D, flow domains, and mosaics. TEM analysis revealed a number of irregular graphene layer images which are caused by the defects of graphite. EIS shows that the sample carbonized by two-step has a larger diffusion coefficient than the sample carbonized at 700 °C by one step. Higher carbonization temperature leads to better cycle performance as the temperature increasing from 500 to 700 °C in the one-step route. Specifically, the charge (Li+ extraction) capacity at the 50th cycle increases from 318 mA h g−1 to 357 mA h g−1. The results show that the rate performance of the artificial graphite is improved with the addition of the presintering at 400 °C.
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This work was financially sponsored by the Major Special Project of Science and Technology of Hunan Province (grant number 2011FJ1005) and Fundamental Research Funds for the Central Universities (grant number 2010QZZD0101)).
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Huang, S., Guo, H., Li, X. et al. Carbonization and graphitization of pitch applied for anode materials of high power lithium ion batteries. J Solid State Electrochem 17, 1401–1408 (2013). https://doi.org/10.1007/s10008-013-2003-9
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DOI: https://doi.org/10.1007/s10008-013-2003-9