Hard templating pathways for the synthesis of nanostructured porous Co3O4

被引:322
作者
Rumplecker, Anja
Kleitz, Freddy
Salabas, Elena-Lorena
Schueth, Ferdi
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
[2] Univ Laval, Dept Chem, Laval, PQ G1K 7P4, Canada
关键词
D O I
10.1021/cm0610635
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The present study is concerned with the nanocasting preparation of Co3O4 nanostructures employing two-dimensional (2D) hexagonal SBA-15 and three-dimensional (3D) cubic KIT-6 as hard templates. The influence of framework connectivity of the parent silica and loading of the cobalt source are studied in detail. Structures can be tailored as isolated or randomly organized Co3O4 nanowires or as highly ordered mesoporous Co3O4 networks retaining the symmetry of the silica parent using 2D hexagonal parent materials. Applying cubic KIT-6 silica with suitable wall thickness and degree of framework interconnectivity as a template, we can vary the pore size of mesostructured Co3O4 from 3 nm up to values as high as 10 nm. To verify the influence of surface properties and texture, we employed different mesoporous silicas that were conventionally calcined at 550 degrees C and equivalent silica materials microwave treated in the presence of a concentrated H2O2/HNO3 mixture. The parent silica materials and the resulting Co3O4 were characterized in detail at different steps during the templating route by nitrogen physisorption measurements and powder X-ray diffraction. Transmission electron microscopy and scanning electron microscopy investigations were performed to visualize the structure and morphology of the nanocast materials, and thermogravimetry-differential thermal analyses (TG-DTA) were done to follow the formation of Co3O4. With our method, preparation of nanocast Co3O4 is highly reproducible, regardless of template shapes and sizes, which makes the pathway much more versatile for a great variety of templates.
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页码:485 / 496
页数:12
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