Growth of Well-Defined Cubic Hematite Single Crystals: Oriented Aggregation and Ostwald Ripening

• Published in: Crystal growth & design 2008-04, Vol.8 (4), p.1372-1376
• Main Authors: Jia, Baoping, Gao, Lian
• Format: Article
• Language: English
• Subjects: Cross-disciplinary physics: materials science; rheology; Exact sciences and technology; Growth from solutions; Materials science; Methods of crystal growth; physics of crystal growth; Nanoscale materials and structures: fabrication and characterization; Physics; Quantum wires; Theory and models of crystal growth; physics of crystal growth, crystal morphology and orientation
• ISSN: 1528-7483; 1528-7505
• DOI: 10.1021/cg070300t

Single-crystalline α-Fe2O3 submicron cubes with a well-defined shape have been successively synthesized via a simple hydrothermal process. X-ray diffraction patterns, transmission electron microscopy, field emission scanning electron microscopy, and selected area electron diffraction patterns were applied to characterize the as-synthesized samples. The results indicate that the growth of single-crystalline α-Fe2O3 cubes can be attributed to cooperation of two principal mechanisms: oriented aggregation and Ostwald ripening. At the beginning, α-Fe2O3 nanorods were first fabricated and formed cube-like aggregation following a “one-dimensional (1D) → three-dimensional (3D)” mode, in which these nanorods orientedly aggregated on the surfaces of some cores by sharing common {012} faces. Then, the resulting polycrystalline aggregates would fuse into a single crystal, in which Ostwald ripening process was expected to carry out because oriented aggregation alone cannot result in well-defined α-Fe2O3 cubes. The extended particle would further attract free-standing α-Fe2O3 nanorods to orientedly attach on their surface, and the fusion process was repeated until nanorods were completely consumed. This kind of cooperation of two basic mechanisms may give us a new insight into the growth of α-Fe2O3 crystals and opens a new way for controllable synthesis of other well-defined crystals in morphology and dimensionality.