Three dimensionally ordered macroporous (3DOM) Li4Ti5O12 was successfully prepared by a
colloidal crystal templating process. Colloidal crystal consisting of monodisperse polystyrene
particles (1 9m diameter) was used as a template for the synthesis of macroporous Li4Ti5O12. A
precursor sol consisting of titanium isopropoxide and lithium acetate was injected into the template,
and it was calcined at high temperatures. A macroporous membrane of Li4Ti5O12 with
inverse-opal structure was obtained. The prepared material had a spinel-related crystallographic
structure. The interconnected pores with uniform size (0.8 9m) were clearly observed on entire
part of the membrane. The electrochemical properties of the 3DOM Li4Ti5O12were characterized
with cyclic voltammetry and glavanostatic charge-discharge in an organic electrolyte containing a
lithium salt. 3DOM Li4Ti5O12 exhibited a discharge capacity of 160 mA h g-1 at the electrode
potential of 1.55 V vs. Li/Li+ due to the solid state redox of Ti3+/4+ accompanying with Li+ ion
insertion and extraction. The discharge capacity was close to the theoretical capacity (167 mA h
g-1). This means that the Li+ insertion and extraction took place at all part of the 3DOM Li4Ti5O12
membrane.
Three-dimensionally ordered macroporous (3DOM) silicon-doped La0.8K0.2CoO3 perovskite catalysts were successfully prepared by a colloidal crystal templating method. The catalysts showed a well-ordered macroporous structure and exhibited high activity for soot removal.
Three dimensionally ordered macroporous sol-gel bioactive glasses (3DOM-BGs)are a type of biomaterial that is both bioactive and resorbable. In this study, 80 % SiO2 – 20 % CaO (molar fraction) 3DOM-BG particles were prepared using a colloidal crystal templating method via a sol-gel process. The as-prepared 3DOM-BG particles can quickly convert to a calcium-deficient, bone-like apatite after soaking in a simulated body fluid (SBF). MC3T3-E1 osteoblastic cells were cultured in the presence of 3DOM-BG particles. Preliminary results from cell studies showed that 3DOM-BG particles are not cytotoxic and are compatible with
MC3T3-E1 osteoblast-like cells in vitro.