DOI QR코드

DOI QR Code

Synthesis of Li2MnSiO4 by Solid-state Reaction

고상반응법을 이용한 Li2MnSiO4 합성

  • Kim, Ji-Su (Department of Materials Science and Engineering, Kunsan National University) ;
  • Shim, Joong-Pyo (Department of Nano and Chemical Engineering, Kunsan National University) ;
  • Park, Gyung-Se (Department of Chemistry, Kunsan National University) ;
  • Sun, Ho-Jung (Department of Materials Science and Engineering, Kunsan National University)
  • Received : 2012.03.27
  • Accepted : 2012.04.18
  • Published : 2012.05.01

Abstract

Synthesis of $Li_2MnSiO_4$ was attempted by the conventional solid-state reaction method, and the phase formation behavior according to the change of the calcination condition was investigated. When the mixture of the three source materials, $Li_2O$, MnO and $SiO_2$ powders, were used for calcination in air, it was difficult to develop the $Li_2MnSiO_4$ phase because the oxidation number of $Mn^{2+}$ could not be maintained. Therefore, two-step calcination was applied: $Li_2SiO_3$ was made from $Li_2O$ and $SiO_2$ at the first step, and $Li_2MnSiO_4$ was synthesized from $Li_2SiO_3$ and MnO at the second step. It was easy to make $Li_2MnSiO_3$ from $Li_2O$ and $SiO_2$. $Li_2MnSiO_4$ single phase was developed by the calcination at $900^{\circ}C$ for 24 hr in Ar atmosphere as the oxidation of $Mn^{2+}$ was prevented. However, the $Li_2MnSiO_4$ was ${\gamma}-Li_2MnSiO_4$, one of the polymorph of $Li_2MnSiO_4$, which could not be used as the cathode materials in Li-ion batteries. By applying the additional low temperature annealing at $400^{\circ}C$, the single phase ${\beta}-Li_2MnSiO_4$ powder was synthesized successfully through the phase transition from ${\gamma}$ to ${\beta}$ phase.

Keywords

References

  1. A. Nyten, A. Abouimrane, M. Armand, T. Gustafsson, and J. O. Thomas, Electrochem. Commun., 7, 156 (2005). https://doi.org/10.1016/j.elecom.2004.11.008
  2. R. Dominko, M. Bele, M. Gaberscek, A. Meden, M. Remskar, and J. Jamnik, Electrochem. Commun., 8, 217 (2006). https://doi.org/10.1016/j.elecom.2005.11.010
  3. R. Dominko, M. Bele, A. Kokalj, M. Gaberscek, and J. Jamnik, J. Power Sources, 174, 457 (2007). https://doi.org/10.1016/j.jpowsour.2007.06.188
  4. I. Belharouak, A. Abouimrane, and K. Amine, J. Phys. Chem., C113, 20733 (2009).
  5. C. Deng, S. Zhang, B. L. Fu, S. Y. Yang, and L. Ma, Mater. Chem. Phys., 120, 14 (2010). https://doi.org/10.1016/j.matchemphys.2009.11.027
  6. S. Claus, H. Lkeykamp, and W. Smykatz-Kloss, J. Nuclear Mater., 230, 8 (1996). https://doi.org/10.1016/0022-3115(96)00022-0
  7. D. Cruz, S. Bulbulian, E. Lima, and H. Pfeiffer, J. Solid State Chem., 179, 909 (2006). https://doi.org/10.1016/j.jssc.2005.12.020
  8. V. V. Politaev, A. A. Petrenko, V. B. Nalbandyan, B. S. Medvedev, and E. S. Shvetsova, J. Solid State Chem., 180, 1045 (2007). https://doi.org/10.1016/j.jssc.2007.01.001
  9. A. R. West and F. P. Glasser, J. Solid State Chem., 4, 20 (1972). https://doi.org/10.1016/0022-4596(72)90127-2