Single-crystalline and uniform nanopolyhedra, nanorods, and nanocubes of cubic CeO2 were selectively prepared by a hydrothermal method at temperatures in the range of 100-180 degrees C under different NaOH concentrations, using Ce(NO3)3 as the cerium source. According to high-resolution transmission electron microscopy, they have different exposed crystal planes: {111} and {100} for polyhedra, {110} and {100} for rods, and {100} for cubes. During the synthesis, the formation of hexagonal Ce(OH)3 intermediate species and their transformation into CeO2 at elevated temperature, together with the base concentration, have been demonstrated as the key factors responsible for the shape evolution. Oxygen storage capacity (OSC) measurements at 400 degrees C revealed that the oxygen storage takes place both at the surface and in the bulk for the as-obtained CeO2 nanorods and nanocubes, but is restricted at the surface for the nanopolyhedra just like the bulk one, because the {100}/{110}-dominated surface structures are more reactive for CO oxidation than the {111}-dominated one. This result suggests that high OSC materials might be designed and obtained by shape-selective synthetic strategy.
By decomposing Zn(OH)4
2- or Zn(NH3)4
2+ precursor in various solvents at suitable reaction
conditions, zinc oxide with a diversity of well-defined morphologies was synthesized.
Flowerlike ZnO built up by nanorods was obtained by treating Zn(OH)4
2- precursor in water
at 180 °C for 13 h. Whereas a replacement of the solvent by n-heptane yields snow flakelike
ZnO. The prismlike and the prickly spherelike ZnO were also prepared, respectively, by
decomposing Zn(NH3)4
2+ or Zn(OH)4
2- in ethanol at 100 °C for 13 h. The rodlike ZnO was
produced at 180 °C under the same condition for preparing prickly spherelike product.
Besides these typical samples, ZnO in other morphologies was studied manipulatively by
changing the reaction conditions of our solution route. Systematical condition-dependent
experiments were compared comprehensively to reveal the formation and detailed growth
process of ZnO nanosized crystallites and aggregates. The experimental results studied by
X-ray diffraction, transmission electron microscopy, and scanning electron microscopy
indicated that the solvent, precursor, solution basicity, and reaction temperature as well as
time are responsible for the variations of ZnO morphologies.
Phosphate ions play a crucial role not only for the formation of the spindlelike precursors of the single‐crystalline hematite nanotubes that were synthesized by a facile hydrothermal method. They are also important for the adsorption and coordination effects. The mechanism of tube formation was deduced through EM observations as a coordination‐assisted dissolution process (see picture).
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