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Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
Published on: June 7, 2018
Crystal polymorphism: dependence of oxygen diffusion through 2D ordered Co nanocrystals.
Zhijie Yang1, Jianhui Yang, Johanna Bergström
1Université Pierre et Marie Curie, UMR 7070, LM2N, 4 place Jussieu, 75005 Paris, France. marie-paule.pileni@upmc.fr.
Different crystalline structures of cobalt (Co) nanoparticles influence their oxidation behavior. Cobalt polymorphs transform into various Co-CoO or CoO nanostructures when exposed to oxygen at high temperatures.
Area of Science:
- Materials Science
- Nanotechnology
- Chemistry
Background:
- Cobalt nanoparticles exhibit diverse crystalline structures (polymorphs).
- Controlling nanoparticle structure is key to understanding their reactivity.
- Oxidation behavior of nanomaterials is highly dependent on their phase and morphology.
Purpose of the Study:
- To investigate the effect of different cobalt nanoparticle crystalline structures on their oxidation products.
- To correlate specific cobalt polymorphs with distinct Co-CoO and CoO nanostructures formed upon oxidation.
Main Methods:
- Synthesis of 8 nm cobalt nanoparticles using reverse micelles, organometallic decomposition, and hot injection.
- Controlled oxidation of cobalt nanoparticles at elevated temperatures.
- Characterization of resulting nanostructures using electron microscopy and diffraction techniques (implied).
Main Results:
- Polycrystalline face-centered cubic (fcc) cobalt nanoparticles formed Co-CoO yolk-shell or CoO hollow structures.
- Amorphous cobalt nanoparticles yielded Co-CoO core-shell structures.
- Hexagonal close-packed (hcp) cobalt nanoparticles produced Co-CoO nanoparticles.
- Epsilon (ε) phase cobalt nanocrystals resulted in CoO hollow nanoparticles.
Conclusions:
- The crystalline structure of cobalt nanoparticles dictates the outcome of their oxidation.
- Specific cobalt polymorphs lead to predictable Co-CoO and CoO nanostructures, offering pathways for material design.
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