Despite these advantages, Li4Ti5O12 is limited for use of LIBs due to its low electronic conductivity (10-13 S cm-1), which leads to poor rate capabiltiy.1 Several effective ways to improve the rate capability of Li4Ti5O12 have been reported, including reduction of the particle size to the nanoscale, doping Li, Ti, or O sites with small amounts of metal or nonmetal ions, surface modification or carbon coating, and its incorporation into composites with carbonaceous materials.2
Among the various carbonaceous materials, reduced graphene oxide (RGO) or graphene nanosheets has attracted considerable interest as electrode materials for electrochemical energy storage because of their unique properties such as high electronic conductivity, large surface area, and good mechanical properties. Some recent studies have demonstrated the excellent rate capability and cycle stability of Li4Ti5O12/RGO nanocomposites.3 However, previously reported Li4Ti5O12/RGO nanocomposites mostly have 2-dimension morphologies with low tap density.3 The 2-dimentional Li4Ti5O12/RGO nanocomposites are not suitable for commercial use because their low tap density limits the volumetric energy density. Therefore, a simple and facile synthesis of micrometer-sized spherical Li4Ti5O12/RGO composites with a high tap density and superior rate capability is highly desirable.
In this study, we report one-pot synthesis of micrometer-sized spherical Li4Ti5O12/RGO with high tap density, wherein the initial Li-Ti-O/RGO precursor is fabricated by the spray drying method in the presence of all precursors in a solution. Upon subsequent heat treatment, phase-pure micrometer-sized spherical Li4Ti5O12/RGO with high tap density was successfully synthesized. More detailed on the synthetic procedure, morpology, electrochemical and structural properties of micrometer-sized spherical Li4Ti5O12/RGO will be presented at the meeting.
References
[1] S. G. Doo et al, J. Am. Chem. Soc., 2008, 130, 14930
[2] N. Ohta et al, Adv. Mater., 2006, 18, 2226
[3] H. K. Kim et al, Electrochem. Commun., 2010, 12, 1768